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

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sampl<strong>in</strong>g site <strong>and</strong> used from a cleaned cooler. At <strong>the</strong> sampl<strong>in</strong>g<br />

site on <strong>the</strong> edge <strong>of</strong> <strong>the</strong> isl<strong>and</strong>, a cleaned pre-labelled 4 L sample<br />

bottle was <strong>in</strong>stalled <strong>in</strong> <strong>the</strong> sampler which was lowered rapidly to<br />

10 metres, held open for approximately one m<strong>in</strong>ute, closed <strong>and</strong><br />

recovered. Bottle caps l<strong>in</strong>ed with cleaned FEP teflon sheet were<br />

<strong>in</strong>stalled <strong>and</strong> <strong>the</strong> bottle stored <strong>in</strong> an <strong>in</strong>sulated box for<br />

transportation back to <strong>the</strong> lab. Three replicate samples,<br />

nom<strong>in</strong>ally 8 L each, were collected for chlor<strong>in</strong>ated hydrocarbon<br />

analysis. Each sample consisted <strong>of</strong> two 4 L bottles. Three<br />

additional samples were collected for filtration for particulate<br />

organic carbon analysis on <strong>the</strong> second trip.<br />

2.2.2 Filtration <strong>and</strong> Extraction<br />

Sample bottles were shaken to resuspend settled particulate<br />

<strong>and</strong> gravity filtered through a glass fibre filter (142 mm Gelman<br />

AE) <strong>in</strong> a solvent r<strong>in</strong>sed (acetone <strong>the</strong>n dichloromethane) 4L<br />

separatory funnel. The filter was removed with cleaned forceps,<br />

folded to reta<strong>in</strong> particulates <strong>and</strong> stored frozen <strong>in</strong> a cleaned<br />

alum<strong>in</strong>um foil pouch. The filtrate was serially extracted with<br />

glass distilled hexane (10 mL <strong>the</strong>n 2 x 100 mL) <strong>and</strong> <strong>the</strong> extracts<br />

comb<strong>in</strong>ed <strong>in</strong> a 500 mL stoppered flask. This was repeated for <strong>the</strong><br />

rema<strong>in</strong><strong>in</strong>g sample bottle <strong>and</strong> <strong>the</strong> comb<strong>in</strong>ed extracts dried by<br />

st<strong>and</strong><strong>in</strong>g over anhydrous sodium sulphate for 10 m<strong>in</strong>utes. The<br />

extract was taken down by vacuum rotary evaporation at 20°C to 3<br />

mL <strong>and</strong> quantitatively transferred by pipette to a 10 mL ampoule<br />

with 3 x 1 mL hexane sample flask r<strong>in</strong>ses. After cool<strong>in</strong>g <strong>and</strong><br />

solvent vapour removal, <strong>the</strong> ampoule was sealed <strong>of</strong>f for shipment<br />

<strong>and</strong> analysis. Procedural blanks were carried through <strong>the</strong><br />

extraction us<strong>in</strong>g pre-extracted sea water as a sample.<br />

2.3 <strong>Chlor<strong>in</strong>ated</strong> <strong>Hydrocarbon</strong>s <strong>in</strong> Sea-Ice (May 1986, June 1987)<br />

A core <strong>of</strong> first year sea ice was melted out us<strong>in</strong>g <strong>the</strong> hot<br />

water ice drill with a 60 cm diameter melt<strong>in</strong>g r<strong>in</strong>g. The ice<br />

cores, approximately 1.4 m <strong>in</strong> length, were lifted out, placed

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