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MERCURY 391<br />

5. POTENTIAL FOR HUMAN EXPOSURE<br />

Bullock (1997) used the Regional Lagrangian Model of Air Pollution (RELMAP) to simulate the emission,<br />

transport, chemical trans<strong>for</strong>mation, <strong>and</strong> wet <strong>and</strong> dry deposition of elemental mercury gas, divalent mercury<br />

gas, <strong>and</strong> particulate mercury from various point <strong>and</strong> area source types to develop an atmospheric mercury<br />

emissions inventory by anthropogenic source type. The results of the RELMAP model are shown in<br />

Table 5-3. On a percentage basis, various combustion processes (medical waste incinerators, municipal<br />

waste incinerators, electric utility power production [fossil fuel burning] <strong>and</strong> non-utility power <strong>and</strong> heat<br />

generation) account <strong>for</strong> 83% of all anthropogenic emissions in the United States. Overall, of the emissions<br />

produced, 41% were associated with elemental mercury vapor (Hg o ), 41% with the mercuric <strong>for</strong>m (Hg2+) ,<br />

<strong>and</strong> 18% was mercury associated with particulates.<br />

A more detailed estimate of national mercury emission rates <strong>for</strong> various categories of sources is shown in<br />

Table 5-4. As shown in this table, point sources of anthropogenic mercury emissions appear to represent<br />

the greatest contribution of mercury releases, with combustion sources representing 85% of all emissions.<br />

According to the most recent <strong>Toxic</strong>s Release Inventory (Table 5-1), in 1996, the estimated releases of<br />

17,097 pounds of mercury to the air from 31 large processing facilities accounted <strong>for</strong> about 20% of annual<br />

environmental releases <strong>for</strong> this element (TRI96 1998). This is slightly more (13%) than the estimated<br />

13,885 pounds that were released to the air in 1994 (TRI94 1996), but 35% less than the 21,288 pounds<br />

released to the air in 1991 (Table 5-2). The TRI data listed in Tables 5-1 <strong>and</strong> 5-2 should be used with<br />

some caution, since only certain types of facilities are required to report (EPA 1996f). This is not an<br />

exhaustive list.<br />

Mercury has been identified in air samples collected at 25 of the 714 NPL hazardous waste sites where it<br />

has been detected in at least one environmental medium (HazDat 1998).<br />

5.2.2 Water<br />

Natural weathering of mercury-bearing minerals in igneous rocks is estimated to directly release about<br />

800 metric tons of mercury per year to surface waters of the earth (Gavis <strong>and</strong> Ferguson 1972).<br />

Atmospheric deposition of elemental mercury from both natural <strong>and</strong> anthropogenic sources has been<br />

identified as an indirect source of mercury to surface waters (WHO 1991). Mercury associated with soils<br />

can be directly washed into surface waters during rain events. Surface runoff is an important mechanism<br />

<strong>for</strong> transporting mercury from soil into surface waters, particularly <strong>for</strong> soils with high humic content (Meili

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