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MERCURY A-20<br />

APPENDIX A<br />

panel that addressed the issue of concurrent PCB exposures, the Statistics/Design Panel, noted that only 3 of<br />

208 PCB congeners were measured in the Faroe study, <strong>and</strong> stated that it “seems likely that mercury was<br />

measured more accurately than the biologically relevant PCB exposure. Consequently even if the<br />

neurological effects seen in this study were caused entirely by PCBs, it is possible that mercury would still<br />

be more highly correlated with these effects than PCBs.” The Statistics/Design Panel also said that “the<br />

best method to deal with this problem would be to study a population where exposure to PCBs is not an<br />

issue.” This statement points directly to the Seychelles study as the study most appropriate <strong>for</strong> MRL<br />

derivation.<br />

Another issue raised at Raleigh workshop concerned the taking of hair samples <strong>for</strong> determining pre-natal<br />

exposure. In the Seychelles, hair samples were collected 6 months post-partum, <strong>and</strong> segments<br />

corresponding to pregnancy were selected <strong>for</strong> analysis. In the case of the Faroese, hair samples were taken<br />

at the scalp. Regarding that, the Confounders <strong>and</strong> Variables (Epidemiology) panel stated that “Given the<br />

time it takes the Hg to be excreted into the hair, we can assume that samples collected at parturition do not<br />

cover the last 6 weeks of gestation, during which critically important neuronal proliferation <strong>and</strong><br />

differentiation is taking place.”<br />

Regarding both the Seychelles <strong>and</strong> Faroe studies, the Neurobehavioral Endpoints Panel found “no specific<br />

neurobehavioral signature injury from MeHg” in the data from either study (Seychelles or Faroe). The<br />

same panel also noted that episodic exposure in the Faroe Isl<strong>and</strong>s (1–2 fish meals/week <strong>and</strong>

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