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APPENDIX VIII<br />

collection), <strong>and</strong> that is generally considered to be a better estimate <strong>for</strong> the fraction that is<br />

potentially available <strong>for</strong> organisms than the total concentration;<br />

• bioavailable fraction: the fraction that is available <strong>for</strong> uptake by a specific organism. A<br />

single substrate has only one 'availability' <strong>for</strong> each of the possible physico-chemical<br />

extraction procedures. The bioavailability differs, however, per biological species. Thus,<br />

taking soil as an example, <strong>for</strong> instance <strong>for</strong> worms in a certain soil the bioavailability may be<br />

high (it is in this case the concentration in the pore water that determines uptake), while <strong>for</strong><br />

arthropods in the same soil the bioavailability may be low (uptake by the food is <strong>for</strong> these<br />

organisms the dominant uptake route);<br />

• natural background concentration: the concentration that is present due to natural causes<br />

only;<br />

• ambient background concentration: the concentration that is present due to natural<br />

background plus the immission of metals from diffuse sources of human origin 9.<br />

For soils or sediments<br />

• water extractable fraction or concentration: the fraction or the concentration of the metal<br />

that is extracted after shaking the substrate in aqueous solution (usually distilled water);<br />

• neutral-salt solution extractable fraction or concentration: the fraction or the<br />

concentration of the metal that is extracted after shaking the substrate in neutral salt<br />

solution;<br />

• pore water concentration: the concentration of the metal that is present in the pore water<br />

collected from the substrate;<br />

• pore water activity: the concentration of a metal in the aqueous fraction that is potentially<br />

biologically active (usually considered to be the concentration of metal ions that can be<br />

taken up by organisms).<br />

Exposure assessment<br />

For the assessment of metals it is in general necessary to take into account all metal species that<br />

are emitted to the environment which in the end lead to concentrations of the bioavailable<br />

species that may cause effects. In practice, a limited number of major emissions or uses<br />

predominate <strong>and</strong> these must initially be identified. The assessment will normally concentrate on<br />

the impact of these emissions since they will be the major contributors to the regional burden,<br />

but due care must be paid to the impact of local emissions of specific substances. An inventory<br />

of all relevant emission sources must be prepared <strong>and</strong> specific industry <strong>and</strong> use categories<br />

identified <strong>for</strong> assessment of both local <strong>and</strong> regional impact.<br />

Two types of emission can be identified: diffuse emissions <strong>and</strong> point source emissions. For some<br />

metal compounds, diffuse sources such as emissions from agriculture, transport, corrosion etc<br />

9 In case of soil, <strong>for</strong> all metals so-called reference lines were derived by correlating measured ambient background<br />

concentrations (total concen-trations in the soil-matrix) at a series of remote rural sites in the Netherl<strong>and</strong>s to the<br />

percentage lutum (%L) <strong>and</strong> the organic matter content (%H) of these soils (Ministry of VROM, 1994). The same<br />

approach has been followed in Fl<strong>and</strong>ers, Belgium (Ontwerp uitvoeringsbesluit, 1995). To this end the 90percentiles<br />

of the ambient background concentrations measured were used. The metal-specific parameters of the<br />

regression equations represent the strength of binding of the different metals to soils of different clay <strong>and</strong> humus<br />

contents. The reference lines are not only used to calculate ambient background concentrations at given sites, but<br />

also to enable the extrapolation of laboratory toxicity data to st<strong>and</strong>ard-soil conditions.<br />

Some typical examples of reference lines derived in The Netherl<strong>and</strong>s ([ ] = ambient background concentration in<br />

mg/kg soil, L = % lutum, H = % organic matter): [Cu] = 15 + 0.6 . (L + H) ; [Zn] = 50 + 1.5 . (2L + H) or [Ni] = 10<br />

+ L.<br />

302

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