A study of PCB concentrations and fluxes in lake
sediments was conducted to test the “global fractionation” hypothesis that deposition of semivolatile
organics will decline while more volatile congeners
will be enriched in polar regions. Sediment cores
were collected from 11 remote lakes in Canada ranging
from 49° N to 82° N and were dated using excess
210Pb and 137Cs. Sediment extracts
were analyzed for
up to 90 PCB congeners by capillary GC-ECD with
confirmation by GC/high-resolution MS. Total PCB
(∑PCB) concentrations in surface slices ranged
from 2.4 to 39 ng g-1 (dry wt) and showed no
latitudinal
trend. Fluxes (ng m-2
yr-1) and inventories of ∑PCB
as well as total tetra- to octachlorobiphenyls
declined with increasing north latitude while those
for di/trichlorobiphenyls showed no latitudinal trend.
The
proportion of di/trichloro congeners of ∑PCB also
increased significantly with latitude, while total octachlorobiphenyls declined. Maximum ∑PCB concentrations were observed in subsurface slices dating
to the 1960−1970s in most lakes except those in the
high Arctic, where maxima were generally in
surface slices. The onset of elevated ∑PCB
deposition
was delayed in the high Arctic (1950−1960s) relative
to the midlatitude and sub-Arctic lakes (1930−1940s).
The high proportions of lower chlorinated congeners
and the delayed appearance of PCBs are
consistent
with predictions of the global fractionation
model.
The variation in levels of polychlorinated biphenyls (sigma PCBs), chlorobenzenes and chlorinated pesticides was studied in burbot (Lota lota) from eight remote locations along a northwesterly transect from northwestern Ontario to the Mackenzie River delta in Canada. Significant declines in concentrations of PCB congeners, DDT isomers (sigma DDT), lindane, dieldrin, and mirex in burbot liver were found with increasing north latitude. Mean sigma PCB concentrations ranged from 1,290 ng/g (lipid wt) at Lake 625, a remote lake in northwestern Ontario, to 301 ng/g in samples from the Mackenzie River at Arctic Red River, N.W.T. No significant differences in mean concentrations of toxaphene, alpha-HCH, tri- and tetrachlorobiphenyls were observed between southern and northern sampling sites. Toxaphene was the predominant organochlorine residue in northern fish samples averaging 1,400 ng/g (lipid wt) at the three most northerly sites and 1,723 ng/g at Lake 625. Airborne contamination was the only likely source of organochlorines for most of the locations surveyed. The results were consistent with the hypothesis that inputs of semi-volatile organochlorines to northern aquatic ecosystems decrease with increasing north latitude and distance from North American sources.
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