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MERCURY<br />

2. HEALTH EFFECTS<br />

parameters. Exposed monkeys were found to produce smaller or slower transitions than controls. The<br />

magnitude <strong>and</strong> stability of lever-press durations <strong>for</strong> controls <strong>and</strong> exposed monkeys were indistinguishable<br />

early in the experiment, but at the end, the exposed monkeys had longer lever-press durations <strong>and</strong> the<br />

session-to-session variability was much greater. One monkey's exposure began during the third week of<br />

gestation (earlier than any of the others) <strong>and</strong> its behavior was so erratic that some of the analyses could not<br />

be accomplished. Long-term effects of prenatal mercury vapor exposure included instability in lever-press<br />

durations <strong>and</strong> steady-state per<strong>for</strong>mance under concurrent schedules of rein<strong>for</strong>cement as well as aberrant<br />

transitions (Newl<strong>and</strong> et al. 1996).<br />

Organic Mercury. No studies were located regarding developmental effects in humans or animals after<br />

inhalation exposure to organic mercury.<br />

The highest NOAELs <strong>and</strong> all reliable LOAELs <strong>for</strong> developmental effects in each species <strong>and</strong> duration<br />

category are recorded in Table 2-1 <strong>and</strong> plotted in Figure 2-1.<br />

2.2.1.7 Genotoxic Effects<br />

There is inconclusive evidence that occupational exposure to metallic mercury <strong>and</strong> to organic <strong>and</strong> inorganic<br />

mercury compounds, primarily through inhalation, causes structural <strong>and</strong> numerical chromosome<br />

aberrations in human lymphocytes. In one study, significant increases in the frequency of acentric<br />

fragments (chromosome breaks) occurred in 4 workers exposed to high concentrations of metallic mercury<br />

<strong>and</strong> in 18 workers exposed to a mixture of mercuric chloride, methylmercuric chloride, <strong>and</strong> ethylmercuric<br />

chloride (Popescu et al. 1979). Mercury concentrations in the workplace ranged from 0.15 to 0.44 mg/m 3 ;<br />

the urinary excretion level of mercury <strong>for</strong> both exposed groups was .890 µg/L. The findings of this study<br />

are suspect because the control group was not matched <strong>for</strong> sex, smoking habits, or sample size.<br />

Additionally, one of the four individuals in the metallic mercury group had a history of benzene poisoning,<br />

which was reflected in the unusually high frequency of abnormal chromosome morphology seen in this<br />

individual. No difference in the incidence of aneuploidy was found between the exposed workers <strong>and</strong> the<br />

controls. In an earlier study, an apparent association between increased chromosome aberrations <strong>and</strong><br />

workplace exposure to mercury (as measured by urinary mercury levels) was reported (Verschaeve et al.<br />

1976). However, the study was not well controlled (i.e., not matched <strong>for</strong> sex, smoking habits, or sample<br />

size), <strong>and</strong> the only significant increase in structural aberrations occurred in the three workers exposed to<br />

ethylmercury. Significant increases in aneuploid were also noted <strong>for</strong> the exposure groups compared to the<br />

72

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