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

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(1974) used thermodynamics to argue that Pb-orthophosphates (e.g., pyromorphite) represented<br />

the most stable Pb phase in many soils and sediments. He further suggested that, because <strong>of</strong> the<br />

extremely low solubility <strong>of</strong> Pb-phosphate minerals, Pb deposition could potentially reduce<br />

phosphorous availability. Olson and Skogerboe (1975) reported that solid-phase PbSO4<br />

dominated gasoline-derived Pb speciation in surface soils from Colorado, Missouri, and Chicago,<br />

while Santillan-Medrano and Jurinak (1975) suggested that Pb(OH)2, Pb(PO4)2, and PbCO3<br />

could regulate Pb speciation in soils. However, insoluble organic material can bind strongly to<br />

Pb and prevent many inorganic phases from ever <strong>for</strong>ming in soils (Zimdahl and Skogerboe,<br />

1977).<br />

The vertical distribution and mobility <strong>of</strong> atmospheric Pb in soils was poorly documented<br />

prior to 1986. Chapter 6 <strong>of</strong> the 1986 AQCD cited a few references suggesting that atmospheric<br />

Pb is retained in the upper 5 cm <strong>of</strong> soil (Reaves and Berrow, 1984). Techniques using radiogenic<br />

Pb isotopes had been developed to discern between gasoline-derived Pb and natural, geogenic<br />

(native) Pb, but these techniques were mostly applied to sediments (Shirahata et al., 1980) prior<br />

to the 1986 <strong>Lead</strong> AQCD. Without using these techniques, accurate determinations <strong>of</strong> the depth-<br />

distribution and potential migration velocities <strong>for</strong> atmospherically delivered Pb in soils were<br />

largely unavailable.<br />

Several technological advances, combined with the expansion <strong>of</strong> existing technologies<br />

after 1986 resulted in the publication <strong>of</strong> a large body <strong>of</strong> literature detailing the speciation,<br />

distribution, and geochemical behavior <strong>of</strong> gasoline-derived Pb in the terrestrial environment.<br />

Most notably, the development <strong>of</strong> selective chemical extraction (SCE) procedures as a rapid and<br />

inexpensive means <strong>for</strong> partitioning Pb into different soil and sediment phases (e.g., Pb-oxides,<br />

Pb-humate, etc.) has been exploited by a number <strong>of</strong> researchers (Tessier et al., 1979; Johnson<br />

and Petras, 1998; Ho and Evans, 2000; Scheckel et al., 2003). Also, since 1986, several workers<br />

have exploited synchrotron-based XAS in order to probe the electron coordination environment<br />

<strong>of</strong> Pb in soils, organic matter, organisms, and sediments (Manceau et al., 1996; Xia et al., 1997;<br />

Trivedi et al., 2003). X-ray absorption studies can be used <strong>for</strong> the in-situ determination <strong>of</strong> the<br />

valence state <strong>of</strong> Pb and can be used to quantify Pb speciation in a variety <strong>of</strong> untreated samples.<br />

Biosensors, which are a relatively new technology coupling biological material, such as an<br />

enzyme, with a transducer, <strong>of</strong>fer a new, simple, and inexpensive means <strong>for</strong> quantifying available<br />

Pb in ecosystems (Verma and Singh, 2005). Advances in voltammetric, diffusive gradients in<br />

AX7-23

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