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

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Compared to their estimated 20th-century atmospheric Pb deposition <strong>of</strong> 0.9 g Pb m Γ2 , the <strong>for</strong>est<br />

floor has retained 83% <strong>of</strong> the atmospheric Pb loadings (Johnson et al., 1995a). Johnson et al.<br />

(2004) noted that gasoline-derived Pb was a significant component <strong>of</strong> the labile Pb at the HBEF.<br />

They calculated that Pb fluxes to the HBEF by atmospheric pollution were essentially equivalent<br />

to the Pb released by mineral weathering over the past 12,000 years. Marsh and Siccama (1997)<br />

used the relatively homogenous mineral soils underneath <strong>for</strong>merly plowed land in Rhode Island,<br />

New Hampshire and Connecticut to assess the depth-distribution <strong>of</strong> atmospheric Pb. They<br />

reported that 65% <strong>of</strong> the atmospheric Pb deposited during the 20th century is in the mineral soil<br />

and 35% is in the <strong>for</strong>est floor. At their remote study site in the Sierra Nevada Mountains, Erel<br />

and Patterson (1994) reported that most <strong>of</strong> the anthropogenic Pb was associated with the humus<br />

fraction <strong>of</strong> the litter layer and soils sampled in the upper few cm.<br />

Atmospherically delivered Pb is probably present in ecosystems in a variety <strong>of</strong> different<br />

biogeochemical phases. A combination <strong>of</strong> Pb adsorbtion processes and the precipitation <strong>of</strong> Pb<br />

minerals will typically keep dissolved Pb species low in soil solution, surface waters, and<br />

streams (Sauvé et al., 2000a; Jackson et al., 2005). While experimental and theoretical evidence<br />

suggest that the precipitation <strong>of</strong> inorganic Pb phases and the adsorption <strong>of</strong> Pb on inorganic<br />

phases can control the biogeochemistry <strong>of</strong> contaminant Pb (Nriagu, 1974; Ruby et al., 1994;<br />

Jackson et al., 2005), the influence <strong>of</strong> organic matter on the biogeochemistry <strong>of</strong> Pb in terrestrial<br />

ecosystems cannot be ignored in many systems. Organic matter can bind to Pb, preventing Pb<br />

migration and the precipitation <strong>of</strong> inorganic phases (Manceau et al., 1996; Xia et al., 1997; Lang<br />

and Kaupenjohann, 2003). As the abundance <strong>of</strong> organic matter declines in soil, Pb adsorption to<br />

inorganic soil minerals and the direct precipitation <strong>of</strong> Pb phases may dominate the<br />

biogeochemistry <strong>of</strong> Pb in terrestrial ecosystems (Ostergren et al., 2000a,b; Sauvé et al., 2000a).<br />

Conclusions<br />

Advances in technology since the 1986 <strong>Lead</strong> AQCD have allowed <strong>for</strong> a quantitative<br />

determination <strong>of</strong> the mobility, distribution, uptake, and fluxes <strong>of</strong> atmospherically delivered Pb in<br />

ecosystems. Among other things, these studies have shown that industrial Pb represents a<br />

significant fraction <strong>of</strong> total labile Pb in watersheds. Selective chemical extractions and<br />

synchrotron-based X-ray studies have shown that industrial Pb can be strongly sequestered by<br />

organic matter and by secondary minerals such as clays and oxides <strong>of</strong> Al, Fe, and Mn. Some <strong>of</strong><br />

AX7-38

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