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MERCURY 401<br />

5. POTENTIAL FOR HUMAN EXPOSURE<br />

0.001 mg/m 3 <strong>for</strong> the vapor concentrations, indicating that it was also nonleachable <strong>and</strong> did not readily<br />

volatilize. This study also showed that concentrations of mercury in leachate could not be correlated with<br />

the concentration of mercury in the soil or in the headspace vapors (Willett et al. 1992). Mercuric sulfide<br />

has been found to strongly adsorb to soil, <strong>and</strong> even with weathering, any mercury released from the<br />

mercuric sulfide is readsorbed by the soil (Harsh <strong>and</strong> Doner 1981).<br />

The most common organic <strong>for</strong>m of mercury, methylmercury, is soluble, mobile, <strong>and</strong> quickly enters the<br />

aquatic food chain. This <strong>for</strong>m of mercury is accumulated to a greater extent in biological tissue than are<br />

inorganic <strong>for</strong>ms of mercury (Riisgard <strong>and</strong> Hansen 1990). Methylmercury in surface waters is rapidly<br />

accumulated by aquatic organisms; concentrations in carnivorous fish (e.g., pike, shark, <strong>and</strong> swordfish) at<br />

the top of both freshwater <strong>and</strong> marine food chains are biomagnified on the order of 10,000–100,000 times<br />

the concentrations found in ambient waters (Callahan et al. 1979; EPA 1984b; WHO 1990, 1991). The<br />

range in experimentally determined bioconcentration factor (BCF) values is shown in Table 5-6. The<br />

bioaccumulation potential <strong>for</strong> methylmercury in fish is influenced by the pH of the water, with a greater<br />

bioaccumulation seen in waters with lower pH (Ponce <strong>and</strong> Bloom 1991). Mercury concentrations in fish<br />

have also been negatively correlated with other water quality factors, such as alkalinity <strong>and</strong> dissolved<br />

oxygen content (Wren 1992).<br />

The biomagnification of methylmercury has been demonstrated by the elevated levels found in piscivorous<br />

fish compared with fish at lower levels of the food chain (Jackson 1991; Kohler et al. 1990; Porcella 1994;<br />

Watras <strong>and</strong> Bloom 1992). Biomagnification factors <strong>for</strong> methylmercury in the food webs of Lake Ontario<br />

were lowest <strong>for</strong> the transfer of methylmercury from mysids to amphipods (1.1), plankton to amphipods<br />

(1.8), <strong>and</strong> plankton to mysids (2.4); were intermediate <strong>for</strong> the transfer from mysids to fish (5.1) <strong>and</strong><br />

amphipods to fish (6.5); <strong>and</strong> were highest <strong>for</strong> the transfer from plankton to fish (10.4) (Evans et al. 1991).<br />

(The biomagnification of methylmercury from water through several trophic levels is compared to the<br />

biomagnification of inorganic mercury in Table 5-7.) Watras <strong>and</strong> Bloom (1992) reported that<br />

biomagnification of methylmercury in Little Rock Lake seems to be a result of two processes: the higher<br />

affinity of inorganic mercury in lower trophic level organisms <strong>and</strong> the high affinity of methylmercury in<br />

fish. Fish appear to accumulate methylmercury from both food sources <strong>and</strong> the water column. However,<br />

Hall et al. (1997) found that food was the predominant source of mercury uptake in fish. The biological<br />

concentration factor (BCF) of methylmercury in fish in Little Rock Lake was three million (Porcella<br />

1994). Mason et al. (1995) also compared bioaccumulation of inorganic mercury <strong>and</strong> methylmercury.<br />

These authors showed that passive uptake of the mercury complexes (HgCl2 <strong>and</strong> CH3HgCl) results in high

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