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ENVIRONMENTAL EXPOSURE ASSESSMENT<br />

Such site-specific assessments should only be used when it is known that all the emissions<br />

emanating from the particular point in the life-cycle e.g. manufacture, arise from a limited<br />

number of specific <strong>and</strong> identifiable sites. In these circumstances each specific point of release<br />

will need to be assessed individually. If it is not possible to make this judgement, then the default<br />

assumptions should be applied. In site-specific assessments, due account can be taken of the true<br />

dilution available to the given emission as well as the impact of degradation, volatilisation, etc.<br />

in the derivation of the PEC. Normally, only dilution <strong>and</strong> adsorption to suspended sediment need<br />

to be considered but site-specific conditions may indicate that local distribution models can be<br />

used.<br />

It must be noted that with the assumption of complete mixing of the effluent in the surface water<br />

no account is taken of the fact that in reality in the mixing zone higher concentrations will occur.<br />

For situations with relatively low dilution factors this mixing-zone effect can be accepted. For<br />

situations with very high dilution factors, however, the mixing zones may be very long <strong>and</strong> the<br />

overall area that is impacted by the effluent be<strong>for</strong>e it is completely mixed can be very<br />

substantial. There<strong>for</strong>e, in case of site-specific assessments the dilution factor that is applied <strong>for</strong><br />

calculation of the local concentration in surface water should not be greater than 1000.<br />

If no measured data are available on the partition coefficient between suspended matter <strong>and</strong><br />

water, Kpsusp, it can be estimated from the Koc of the substance, determined <strong>for</strong> other sorbents<br />

like soil or sediments (Section 2.3.5) by taking into account different organic carbon contents of<br />

the media.<br />

For some substances it may be possible that PECs are calculated in water which are in excess of<br />

the water solubility. These results need to be interpreted carefully on a case-by-case basis. The<br />

concentration in surface water will not be corrected, but the result needs to be flagged. The PEC<br />

has to be interpreted based on the effects found in the aquatic toxicity tests.<br />

In a situation where a substance is released through several point sources into the same river, the<br />

resulting cumulative concentration may in a first approach be estimated by assuming it to be<br />

released from one point source. If this PEC leads to “concern” then refined approaches may be<br />

used, such as river flow models, e.g. OECD (1992a) which address the specific emission pattern<br />

as well as river parameters.<br />

The local concentration in surface water is calculated as follows.<br />

76<br />

Clocal<br />

Explanation of symbols<br />

water<br />

=<br />

( 1+<br />

Kp<br />

susp<br />

Clocaleff<br />

- 6<br />

• SUSPwater<br />

•10<br />

)<br />

•<br />

DILUTION<br />

Clocaleff concentration of the substance in the STP effluent [mg . l -1 ] eq. (33)<br />

Kpsusp solids-water partitioning coefficient of suspended matter [l . kg -1 ] eq. (23)<br />

SUSPwater concentration of suspended matter in the river [mg . l -1 ] 15<br />

DILUTION dilution factor [-] 10<br />

Clocalwater local concentration in surface water during emission episode [mg . l -1 ]<br />

(45)

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