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Distribution of Chlorinated Hydrocarbon Pesticides and PCBs in the ...

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Technical mixtures used previously <strong>in</strong> <strong>the</strong> nor<strong>the</strong>rn hemisphere<br />

conta<strong>in</strong>ed approximately 50 to 80% alpha-HCH (<strong>the</strong> <strong>in</strong>active <strong>and</strong><br />

stable isomer) with 8 to 15% l<strong>in</strong>dane giv<strong>in</strong>g a ratio <strong>of</strong> a1pha:gamma<br />

5 to 6. Besides <strong>the</strong> source <strong>of</strong> HCH, ratios <strong>of</strong> a1pha:gamma isomers<br />

may be altered by transformation <strong>of</strong> l<strong>in</strong>dane to <strong>the</strong> more stable a<br />

isomer on exposure to W radiation <strong>and</strong> <strong>in</strong> aerated water (Oehme <strong>and</strong><br />

Mano, 1984). High ratios <strong>in</strong> air vapour <strong>in</strong> August/September <strong>and</strong> <strong>in</strong><br />

August snow could reflect <strong>the</strong> loss <strong>of</strong> <strong>the</strong> gamma isomer by UV<br />

<strong>in</strong>duced transformation. The ratios for <strong>the</strong> HCH isomers <strong>in</strong><br />

seawater did not vary significantly between sampl<strong>in</strong>g trips,<br />

reflect<strong>in</strong>g stability <strong>of</strong> <strong>the</strong> large reservoir <strong>of</strong> HCH1s dissolved <strong>in</strong><br />

surface seawater.<br />

HCB concentrations <strong>in</strong> air vapour measured over <strong>the</strong> Ice<br />

Isl<strong>and</strong> (63 - 109 pg m'3) (Table 4.1) are similar to <strong>the</strong> lowest<br />

values reported dur<strong>in</strong>g summer <strong>of</strong>f <strong>the</strong> Norwegian Arctic coast<br />

(Oehme <strong>and</strong> Stray, 1982; Oehme <strong>and</strong> Ottar, 1984), but <strong>the</strong>y are an<br />

order-<strong>of</strong>-magnitude less than concentrations measured <strong>in</strong> air over<br />

<strong>the</strong> cont<strong>in</strong>ental U.S. <strong>and</strong> North Atlantic (Bidleman et &., 1987) .<br />

Simultaneous measurements on <strong>the</strong> Ice Isl<strong>and</strong> <strong>in</strong> August <strong>and</strong> June by<br />

staff from Bidlemanls lab at USC were 3 times higher <strong>in</strong> August<br />

1986 <strong>and</strong> about 50% higher <strong>in</strong> June 1987 (Table 3.8, Section 3.2.2).<br />

Levels measured <strong>in</strong> both air <strong>and</strong> seawater <strong>in</strong> our study were similar<br />

for <strong>the</strong> three sampl<strong>in</strong>g periods but values <strong>in</strong> snow were lower <strong>in</strong><br />

August/September. Although HCB has a vapour pressure which is low<br />

compared to many o<strong>the</strong>r organochlor<strong>in</strong>es (Table 5.1), it is a semivolatile<br />

organic compound. Decreases <strong>in</strong> concentrations dissolved<br />

<strong>in</strong> snow could arise from volatilization after deposition <strong>in</strong> <strong>the</strong><br />

early spr<strong>in</strong>g.<br />

In general, our values for most organochlor<strong>in</strong>e residues<br />

<strong>in</strong> snow <strong>in</strong> 1987 are <strong>in</strong> agreement with both USC <strong>and</strong> <strong>the</strong> National<br />

Water Quality Laboratory. Patton g& &.Is (1988) collected<br />

freshly fallen snow on <strong>the</strong> Ice Isl<strong>and</strong> <strong>in</strong> June 1987 <strong>and</strong> showed that<br />

levels <strong>of</strong> total HCH were two to six times higher than<br />

concentrations present <strong>in</strong> lloldll subsurface snow. Sublimation <strong>of</strong><br />

previously deposited hexachlorocyclo-hexanes could have depleted<br />

concentrations <strong>in</strong> snow, especially dur<strong>in</strong>g summer when air

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