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Air Quality Criteria for Lead Volume II of II - (NEPIS)(EPA) - US ...

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to 15 years after biosolid application. The increase in metal transport is likely the result <strong>of</strong><br />

elevated dissolved organic carbon (DOC) in the amended soil. Anodic stripping voltammetry<br />

has indicated that very low percentages (2 to 18%) <strong>of</strong> the soluble metals are present as ionic or<br />

inorganic complexes (McBride, 1999; Al-Wabel et al., 2002).<br />

AX7.1.2 Distribution <strong>of</strong> Atmospherically Delivered <strong>Lead</strong> in<br />

Terrestrial Ecosystems<br />

The 1986 <strong>Lead</strong> AQCD (U.S. Environmental Protection Agency, 1986a) contains only a<br />

few minor sections that detail the speciation, distribution, and behavior <strong>of</strong> atmospherically<br />

delivered Pb in terrestrial ecosystems. The document concluded that the majority <strong>of</strong> Pb in the<br />

atmosphere at that time was from gasoline consumption: <strong>of</strong> the 34,881 tons <strong>of</strong> Pb emitted to the<br />

atmosphere in 1984, 89% was from gasoline use and minor amounts were from waste oil<br />

combustion, iron and steel production, and smelting. <strong>Lead</strong> in the atmosphere today, however, is<br />

not primarily from leaded-gasoline consumption, but results largely from iron and steel<br />

foundaries, boilers and process heaters, the combustion <strong>of</strong> fossil fuels in automobiles, trucks,<br />

airplanes, and ships, and other industrial processes (Table 2-8, Polissar et al., 2001; Newhook<br />

et al., 2003). The emission source can determine the species <strong>of</strong> Pb that are delivered to terrestrial<br />

ecosystems. For example, Pb species emitted from automobile exhaust is dominated by<br />

particulate Pb halides and double salts with ammonium halides (e.g., PbBrCl, PbBrCl2NH4Cl),<br />

while Pb emitted from smelters is dominated by Pb-sulfur species (Habibi, 1973). The halides<br />

from automobile exhaust break down rapidly in the atmosphere, possibly via reactions with<br />

atmospheric acids (Biggins and Harrison, 1979). <strong>Lead</strong> phases in the atmosphere, and<br />

presumably the compounds delivered to the surface <strong>of</strong> the earth (i.e., to vegetation and soils),<br />

are suspected to be in the <strong>for</strong>m <strong>of</strong> PbSO4, PbS, and PbO (Olson and Skogerboe, 1975; Clevenger<br />

et al., 1991; Utsunomiya et al., 2004).<br />

There are conflicting reports <strong>of</strong> how atmospherically derived Pb specifically behaves in<br />

surface soils. This disagreement may represent the natural variability <strong>of</strong> the biogeochemical<br />

behavior <strong>of</strong> Pb in different terrestrial systems, the different Pb sources, or it may be a function <strong>of</strong><br />

the different analytical methods employed. The importance <strong>of</strong> humic and fulvic acids (Zimdahl<br />

and Skogerboe, 1977; Gamble et al., 1983) and hydrous Mn- and Fe-oxides (Miller and McFee,<br />

1983) <strong>for</strong> scavenging Pb in soils are discussed in some detail in the 1986 <strong>Lead</strong> AQCD. Nriagu<br />

AX7-22

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