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Interim report of the HELCOM CORESET project

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For US EPA it is <strong>the</strong> list <strong>of</strong> 16 priority compounds quoted under 1.1.<br />

Relevance <strong>of</strong> <strong>the</strong> indicator for describing <strong>the</strong> developments in <strong>the</strong> environment<br />

Low-molecular-weight PAH compounds, containing two or three rings, are acutely toxic to a broad spectrum<br />

<strong>of</strong> marine organisms. Examples <strong>of</strong> low-molecular-weight PAHs that tend to be toxic are anthracene,<br />

fl uorene, naphthalene and phenanthrene. The high-molecular-weight PAH compounds, containing four,<br />

fi ve, and six rings, are less toxic but have greater carcinogenic potential, e.g. benzo(a)pyrene, dibenz(a,h)<br />

anthracene, benzo(b)fl uoran<strong>the</strong>ne (Kennish 1997). While PAHs can be weakly carcinogenic or noncarcinogenic,<br />

<strong>the</strong>y can modify <strong>the</strong> carcinogenic activity <strong>of</strong> o<strong>the</strong>r PAHs in complex mixtures (Marston et al.<br />

2001). Therefore, synergistic effects <strong>of</strong> PAHs can be larger than <strong>the</strong> total levels <strong>of</strong> PAHs would indicate.<br />

Higher concentrations <strong>of</strong> PAHs are also harmful to reproduction <strong>of</strong> fi sh and can damage cellular membrane<br />

structures (Knutzen 1995). When PAHs are exposed to sunlight, <strong>the</strong> mechanism known as phototoxicity is<br />

involved, producing reactive and toxic photomodifi cation products (<strong>HELCOM</strong> 2010).<br />

Anthropogenic PAH sources in <strong>the</strong> marine environment include <strong>the</strong> release <strong>of</strong> crude oil products (petrogenic<br />

source) and all types <strong>of</strong> incomplete combustion <strong>of</strong> fossil fuels—coal, oil and gas or wood and waste<br />

incineration (pyrolytic sources) (Neff 2004). Some PAHs are formed naturally, but <strong>the</strong> majority <strong>of</strong> PAHs in<br />

<strong>the</strong> marine environment come from anthropogenic activity. Each source generates a characteristic PAH<br />

pattern, enabling distinction <strong>of</strong> <strong>the</strong> sources in a sample; concentration relationships <strong>of</strong> individual PAH compounds<br />

can be used to reveal <strong>the</strong> sources <strong>of</strong> <strong>the</strong> PAH compounds (Baumard et al. 1998, Sicre et al. 1987,<br />

Yunker et al. 2002). Molecular indices calculated from both sediment and biota showed that pyrolytic<br />

sources predominate in <strong>the</strong> Baltic Sea PAH contamination. However, in <strong>the</strong> Gulf <strong>of</strong> Finland and some areas<br />

in <strong>the</strong> western Baltic Sea (Sound, Belt Sea and Kattegat), molecular indices indicated a signifi cant contribution<br />

<strong>of</strong> petrogenic PAHs. This may indicate that atmospheric deposition combined with shipping activities is<br />

<strong>the</strong> main source <strong>of</strong> PAHs in <strong>the</strong>se areas. The dominance <strong>of</strong> pyrolytic sources could be surprising in view <strong>of</strong><br />

<strong>the</strong> heavy maritime traffi c and illegal oil discharges. On <strong>the</strong> o<strong>the</strong>r hand, no reliable information is available<br />

on <strong>the</strong> airborne deposition <strong>of</strong> PAHs onto Baltic Sea surface waters (Pikkarainen 2004).<br />

Status <strong>of</strong> restrictions, bans or use<br />

The maximum levels <strong>of</strong> benzo(a(pyrene and also a sum <strong>of</strong> benzo(a)pyrene, benz(a)anthracene, benzo(b)<br />

fl uoran<strong>the</strong>ne and chrysene are regulated in food stuff according to <strong>the</strong> Commission Regulation (EC) No<br />

835/2011. There are no o<strong>the</strong>r regulations for <strong>the</strong> production or use <strong>of</strong> PAHs.<br />

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