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MERCURY 229<br />

C<br />

2. HEALTH EFFECTS<br />

No MRLs were derived <strong>for</strong> acute- or intermediate-duration inhalation exposure to metallic mercury vapors.<br />

Available studies were either deficient in their reporting of details of experimental protocols <strong>and</strong> results,<br />

used an insufficient number of experimental animals, or tested only one dose/concentration level.<br />

An MRL of 0.0002 mg/m 3 has been derived <strong>for</strong> chronic-duration inhalation exposure (365 days<br />

or longer) to metallic mercury vapor.<br />

A significant increase in the average velocity of naturally occurring tremors compared to controls was<br />

observed in a group of 26 mercury-exposed workers (from 3 industries) exposed to low levels of mercury<br />

<strong>for</strong> an average of 15.3 years (range, 1–41 years) (Fawer et al. 1983). To estimate an equivalent continuous<br />

exposure concentration, the average concentration assumed <strong>for</strong> the 8 hour/day exposures was multiplied by<br />

8/24 <strong>and</strong> 5/7 (0.026 mg/m 3 x 8/24 hours/day x 5/7 days/week=0.0062 mg/m3 ). Uncertainty factors of 10 <strong>for</strong><br />

variability in sensitivity to mercury within the human population <strong>and</strong> 3 <strong>for</strong> use of a minimal-effect LOAEL<br />

in MRL derivation were then applied to the calculated 0.0062 mg/m3 value, yielding a chronic inhalation<br />

MRL of 0.2 µg/m3 . Although this MRL is based on experimental data from an adult working population,<br />

there is no experimental or clinical evidence to suggest that it would not also be sufficiently protective of<br />

neurodevelopmental effects in developing embryos/fetuses <strong>and</strong> children, the most sensitive subgroups <strong>for</strong><br />

metallic mercury toxicity.<br />

Inhaled metallic mercury is quickly absorbed through the lungs into the blood, <strong>and</strong> 70–80% is retained. Its<br />

biological half-life in humans is approximately 60 days. The half-life is different <strong>for</strong> different physiological<br />

compartments (e.g., 21 days in the head versus 64 days in the kidneys) (Hursh et al. 1976). Since the<br />

duration of exposure influences the level of mercury in the body, the exposure level reported in the Fawer et<br />

al. (1983) occupational study was extrapolated from an 8-hour day, 40-hour workweek exposure to a level<br />

equivalent to a continuous 24 hour/day, 7 day/week exposure, as might be encountered near a hazardous<br />

waste site containing metallic mercury.<br />

Gentry et al. (1998) used the neurobehavioral in<strong>for</strong>mation on a control group <strong>and</strong> one exposure group from<br />

the Fawer et al. (1983) study to derive an inhalation MRL <strong>for</strong> elemental mercury based upon a benchmark<br />

dose (BMD) analysis. Dose-response analysis could be per<strong>for</strong>med on four measures of h<strong>and</strong> tremor, with<br />

tasks per<strong>for</strong>med both at rest <strong>and</strong> with a load. The exposure level of the exposed group to metallic mercury<br />

was assumed to be the mean TWA exposure of 0.026 mg/m 3 . A physiologically based pharmacokinetic<br />

model <strong>for</strong> metallic mercury vapor was found to be linear through the region of concern from the LOAEL to

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