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Volltext : R&D-Project - Identification of organic compounds in the North and Baltic Seas

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Table  10:  Overview  of  sPCA  levels  in  selected  environmental  matrices  at  the  start  of  this  project.

Sample

Sampling  location

Sampling  date

sPCA  concentration

Reference

Air

Spitsbergen,
Norway

1999

9-57  pg/m 3

Borgen  et  al.
2000

Air

Egbert,  Canada

1990

65-924  pg/m 3

Stern  and  Tomy,
2000

Freshwater  biota

different  locations,
Norway

not  specified

108-3700  ng/g  fat

Borgen  et  al.
2001

Freshwater
particulate  matter

different  locations,
Germany

not  specified

69-860  ng/g  dry
weight

Maulshagen  et
al.,  2003

Marine  sediments

different  locations,
Canada

not  specified

4.52-135  ng/g  dry
weight

Tomy  et  al,
1999a

5.2.2  Chlordane
The  pesticide  technical  chlordane  was  first  synthesised  in  1945  by  Kearns  et.  al  (1945),
and  its  commercial  production  started  in  1946  by  Vesicol  Corporation.  About  70’000
tons  were  manufactured  between  1960  and  1988  (Dearth  and  Hites,  1991).  Technical
chlordane  was  neither  manufactured  in  Europe  nor  in  Japan  (Falandysz  et  al,  1994),  but
was  commercially  available  in  Germany  around  1950.  In  1976,  the  pesticide  was
removed  from  the  German  market.  First  restrictions  on  the  use  of  technical  chlordane  in
the  United  States  were  decided  in  1978  by  the  US  Environmental  Protection  Agency.  In
1983,  it  was  only  allowed  to  be  used  to  control  underground  termites  (WHO,  1984).
Technical  chlordane  is  a  contact  and  stomach  pesticide  (WHO,  1984)  with  a  broad
spectrum.  It  was  mainly  used  for  building  protection,  ornamental  lawns  and  trees,
drainage  ditches,  but  also  to  protect  crops  like  com  and  potatoes  (WHO,  1984).
5.2.2.1  Structures
147  compounds  could  be  identified  in  technical  chlordane  (Dearth  and  Hites,  1991).
Main  constituents  are  about  24  %  trans-chlordane,  19  %  cA-chlordane,  9  %  ychlordene,
  7  %  heptachlor,  7  %  trans-nonachlor,  3  %  a-chlordene,  3  %  [3-chlordene,
1  %  chlordane  and  19.5  %  related  compounds  including  cA-nonachlor  (Bussart  and
Schor,  1948).  Figure  1  shows  the  structure  of  the  main  chlordane  congeners  and
metabolites.
            
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