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EFFECTS ASSESSMENT<br />

3.3.2 Effects assessment <strong>for</strong> substances with intermittent release<br />

For substances subject to intermittent release (see Section 2.3.3.4 <strong>for</strong> the definition of<br />

intermittent release), a single exposure event may be of only short duration. At least <strong>for</strong> dynamic<br />

systems such as rivers, the likelihood of long-term effects arising from such exposure is low, the<br />

principal risk being that of short-term toxic effects. Thus, the risk assessment should be based on<br />

a no-effect-concentration <strong>for</strong> intermittent release. In extrapolating to such a PNECwater,<br />

intermittent, there<strong>for</strong>e, generally only short-term effects need to be considered. It is there<strong>for</strong>e<br />

proposed that, to derive a PNECwater, intermittent <strong>for</strong> such situations, an assessment factor of<br />

100 be normally applied to the lowest L(E)C50 of at least three short-term tests from three<br />

trophic levels. The assessment factor is designed to take account of the uncertainty that exists in<br />

extrapolating from the results of short-term laboratory toxicity tests to short-term effects that can<br />

be anticipated in the ecosystems.<br />

In undertaking such an extrapolation, due account is taken of the biological variables of intra<strong>and</strong><br />

inter-species toxicity, as well as the general uncertainties in predicting ecosystem effects<br />

from laboratory data. This extrapolation should be carried out with care. Some substances may<br />

be taken up rapidly by aquatic organisms <strong>and</strong> this can lead to delayed effects even after exposure<br />

has ceased. This will generally be taken into account by the assessment factor of 100 but there<br />

may be occasions when a higher or lower factor would be appropriate. For substances with a<br />

potential to bioaccumulate the lowered assessment factor of 100 may not always be sufficient to<br />

provide adequate protection. For substances with a known non-specific mode of action, interspecies<br />

variations may be low. In such cases, a lower factor may be appropriate. In no case<br />

should a factor lower than 10 be applied to a short-term L(E)C50 value.<br />

3.4 EFFECTS ASSESSMENT FOR MICROORGANISMS IN SEWAGE<br />

TREATMENT PLANTS (STP)<br />

Since chemicals may cause adverse effects on microbial activity in STPs it is necessary to derive<br />

a PNECmicroorganisms (see Section 2.3.7). The PNECmicroorganisms will be used <strong>for</strong> the calculation of<br />

the PEC/PNEC ratio concerning microbial activity in STPs. Current test systems <strong>for</strong> measuring<br />

the effect of chemicals on microbial activity have different endpoints <strong>and</strong> different levels of<br />

sensitivity. A number of internationally accepted test systems exist (cf. table below). Available<br />

data (e.g. UBA, 1993; Reynolds et al., 1987) suggest the following order of increasing<br />

sensitivities among particular test systems: respiration inhibition test (EU Annex V C.11; OECD<br />

209, 1984f) < inhibition control in base-set tests < growth inhibition test with P. putida <<br />

inhibition of nitrification.<br />

In general, short-term measurements in the order of hours (e.g. 10 h) are preferred, in accordance<br />

with the retention time in a STP. In<strong>for</strong>mation available on the toxicity <strong>for</strong> microorganisms has<br />

also to be relevant <strong>for</strong> the endpoint considered, i.e. microbial degradation activity in a STP. Test<br />

systems such as the respiration inhibition test <strong>and</strong> the nitrification inhibition test can be used.<br />

Respiration tests using a mixed inoculum are considered more relevant than respiration<br />

inhibition tests using a single-species inoculum.<br />

The assumption that the substance under investigation is not inhibitory to the microorganisms<br />

when dosed in the test system is implicit in ready biodegradability testing (i.e., EU Annex V<br />

C.4A-F, OECD 301A-F, 1992f). Reynolds et al. (1987) report that microbial EC50 values<br />

determined <strong>for</strong> test substances using a variety of tests (Annex V C.11, OECD 209, 1984f, Annex<br />

V C.4F, Closed Bottle Test, Growth Inhibition) were found to be inhibitory in ready<br />

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