BSEP116B Biodiversity in the Baltic Sea - Helcom
BSEP116B Biodiversity in the Baltic Sea - Helcom
BSEP116B Biodiversity in the Baltic Sea - Helcom
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Heavy metals<br />
Heavy metals, such as mercury and cadmium<br />
which are specifically addressed by <strong>the</strong> BSAP, are<br />
widely used <strong>in</strong> <strong>in</strong>dustrial products and processes.<br />
As an example, mercury is extensively used <strong>in</strong> <strong>the</strong><br />
chlor-alkali <strong>in</strong>dustry and cadmium <strong>in</strong> metal <strong>in</strong>dustries.<br />
Significant amounts of atmospherically transported<br />
heavy metals orig<strong>in</strong>ate from distant sources outside<br />
<strong>the</strong> <strong>Baltic</strong> <strong>Sea</strong> catchment area. For cadmium, lead<br />
and mercury, <strong>the</strong> proportion of distant sources<br />
located outside <strong>the</strong> HELCOM area was larger than<br />
half of <strong>the</strong> total emissions <strong>in</strong> 1996–2000 (HELCOM<br />
2005b). A large part of <strong>the</strong> waterborne <strong>in</strong>puts of<br />
heavy metals also orig<strong>in</strong>ates from non-HELCOM<br />
countries <strong>in</strong> <strong>the</strong> catchment area (HELCOM 2007f).<br />
For cadmium, lead and mercury, non-HELCOM<br />
countries accounted for 5% to 13% of total river<strong>in</strong>e<br />
transboundary <strong>in</strong>puts (HELCOM 2007f).<br />
Annual emissions of heavy metals from HELCOM<br />
countries to air have decreased dur<strong>in</strong>g <strong>the</strong> period<br />
from 1990 to 2006 by 47% for cadmium, 45% for<br />
mercury, and 86% for lead (Gusev 2008a) (Figure<br />
6.6.1). S<strong>in</strong>ce <strong>the</strong> mid-1990s, river<strong>in</strong>e heavy metal<br />
loads, especially those of cadmium and lead, have<br />
also decreased <strong>in</strong> several countries (Knuuttila <strong>in</strong><br />
prep.).<br />
The total atmospheric deposition of heavy metals<br />
<strong>in</strong>to <strong>the</strong> <strong>Baltic</strong> <strong>Sea</strong> dur<strong>in</strong>g 2006 was 7.1 tonnes of<br />
cadmium, 3.4 tonnes of mercury and about 234<br />
tonnes of lead (Gusev 2008b). The Belt <strong>Sea</strong> and<br />
Kattegat were <strong>the</strong> sub-bas<strong>in</strong>s receiv<strong>in</strong>g <strong>the</strong> highest<br />
amounts of heavy metal deposition. The reported<br />
waterborne loads to <strong>the</strong> <strong>Baltic</strong> <strong>Sea</strong> <strong>in</strong> 2006<br />
amounted to 47.5 tonnes of cadmium, 10.8 tonnes<br />
of mercury and 274.2 tonnes of lead (Knuuttila <strong>in</strong><br />
prep.).<br />
Organic pollutants<br />
The ma<strong>in</strong> source or pathway to <strong>the</strong> <strong>Baltic</strong> mar<strong>in</strong>e<br />
environment of tributylt<strong>in</strong> (TBT) and triphenylt<strong>in</strong><br />
(TPhT) is <strong>the</strong>ir use as anti-foulants on ship hulls<br />
and subsequent direct release to seawater. On<br />
<strong>the</strong> o<strong>the</strong>r hand, <strong>the</strong> ma<strong>in</strong> pathways of pentabromodiphenyl<br />
e<strong>the</strong>r (pentaBDE), octabromodiphenyl<br />
e<strong>the</strong>r (octaBDE) and decabromodiphenyl e<strong>the</strong>r<br />
(decaBDE), hexabromocyclododecane (HBCDD),<br />
perfluorooctane sulfonate (PFOS), perfluoroocta-<br />
HELCOM countries emissions,% of 1990<br />
120<br />
100<br />
80<br />
60<br />
40<br />
20<br />
0<br />
1990<br />
1991<br />
Cadmium Lead Mercury<br />
1992<br />
1993<br />
1994<br />
1995<br />
1996<br />
1997<br />
1998<br />
Figure 6.6.1. Total annual emissions (as % of 1990 emissions) of<br />
cadmium (Cd), mercury (Hg), and lead (Pb) to air from HELCOM<br />
countries <strong>in</strong> 1990–2006 (Gusev 2008a).<br />
noic acid (PFOA), short-cha<strong>in</strong> chlor<strong>in</strong>ated paraff<strong>in</strong>s<br />
(SCCP), and medium-cha<strong>in</strong> chlor<strong>in</strong>ated paraff<strong>in</strong>s<br />
(MCCP) to <strong>the</strong> <strong>Baltic</strong> <strong>Sea</strong> are via municipal<br />
and <strong>in</strong>dustrial wastewaters and <strong>the</strong> atmosphere.<br />
Municipal and <strong>in</strong>dustrial wastewaters are also <strong>the</strong><br />
ma<strong>in</strong> sources of nonylphenols (NP), nonylphenol<br />
ethoxylates (NPE), octylphenols (OP), and octylphenol<br />
ethoxylates (OPE). The ma<strong>in</strong> pathways<br />
of endosulfan are via rivers receiv<strong>in</strong>g losses from<br />
agricultural land and from atmospheric deposition<br />
due to <strong>the</strong> application of agricultural pesticides<br />
conta<strong>in</strong><strong>in</strong>g endosulfan. Discharges from landfills<br />
and via storm water can be significant for some of<br />
<strong>the</strong> substances mentioned above (HELCOM 2007a,<br />
2007g, HELCOM 2009b).<br />
The net annual atmospheric deposition of polychlor<strong>in</strong>ated<br />
dibenzo-p-diox<strong>in</strong>s/polychlor<strong>in</strong>ated<br />
dibenzofurans (PCDD/Fs) to <strong>the</strong> surface of <strong>the</strong><br />
<strong>Baltic</strong> <strong>Sea</strong> has decreased by 59% dur<strong>in</strong>g <strong>the</strong> period<br />
1990–2006. At <strong>the</strong> sub-bas<strong>in</strong> level, <strong>the</strong> most significant<br />
decrease <strong>in</strong> PCDD/F deposition has been<br />
observed <strong>in</strong> <strong>the</strong> Belt <strong>Sea</strong> (73%) and Kattegat<br />
(65%). Currently, <strong>the</strong> highest levels of PCDD/F<br />
deposition over <strong>the</strong> <strong>Baltic</strong> <strong>Sea</strong> have been observed<br />
for <strong>the</strong> Belt <strong>Sea</strong> and <strong>the</strong> lowest deposition fluxes<br />
for <strong>the</strong> Gulf of Bothnia (Gusev 2008c).<br />
6.6.2 Occurrence and impacts of<br />
hazardous substances on <strong>Baltic</strong><br />
biodiversity<br />
For many organic contam<strong>in</strong>ants, a full assessment<br />
of <strong>the</strong>ir levels and effects <strong>in</strong> <strong>Baltic</strong> mar<strong>in</strong>e biota is<br />
not possible ow<strong>in</strong>g to <strong>the</strong> lack of monitor<strong>in</strong>g and<br />
ecotoxicological data.<br />
1999<br />
2000<br />
2001<br />
2002<br />
2003<br />
2004<br />
2005<br />
2006<br />
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