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Bio - Bio Project - European Soil Portal - Europa

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was derived from a French approach developed by<br />

INRA [2] . Every area was equally divided in 9 sub-units<br />

having 6.6 m side. Litter, roots, stones and other coarse<br />

material were removed before sampling. The different<br />

horizons have been sampled and the 9 sub samples of<br />

each horizon were mixed together in a homogeneous<br />

mean sample. Moreover, three different depths were<br />

sampled: 0-5 cm, 0-15 cm and 15-30 cm [3] .<br />

Figure 4 - Sampling scheme<br />

<strong>Soil</strong> samples collection has been performed<br />

contemporarily with the AM-1 sampling campaign of<br />

the Pavia <strong>Project</strong>, by specialized technicians of the <strong>Soil</strong><br />

& Waste Unit of JRC Ispra.<br />

Figure 5 - delimitation and subdivision of the sampled area<br />

Figure 6 and 7 - Sampling operations<br />

EUR 22245 EN (2006) <strong>Bio</strong>-<strong>Bio</strong> <strong>Project</strong><br />

39<br />

Each of the 9 soil samples (3 areas and 3 depths) was<br />

homogenized and then divided in 4 sub-samples. First<br />

aliquot was utilized for the determination of total<br />

mercury content, total and organic carbon, pH<br />

measurement and macro-elements determination. The<br />

second has been delivered to the technicians of the<br />

University Sacro Cuore in Piacenza for the heavy<br />

metals determination.<br />

Another part, after air drying, was delivered to the<br />

Experimental Institute of Plants Nutrition in Rome for<br />

microbiological analysis and evaluation of PCBs<br />

concentration (analysis performed by the Health<br />

Superior Institute in Rome). The fourth fraction of soil,<br />

frozen and preserved in dark glass bottles, was used for<br />

the determination of dioxins’ concentration.<br />

3.2 Sampling<br />

Based on the aforementioned profile information, the<br />

disturbed soil samples were obtained manually using<br />

an Auger device; an example can be seen in Figures 8<br />

and 9.<br />

Figure 8and 9 - Examples of an Auger sampling device<br />

4. Analysis and results<br />

4.1 Used methods<br />

When possible, ISO procedures were applied to the<br />

samples for the requested analysis. In case no ISO<br />

procedures were available, internal methods of analysis<br />

were followed. These internal methods have been<br />

developed for similar sample types by our laboratories,<br />

both tested and proofed with Reference Materials.<br />

Quality Control was ensured by the parallel analysis of<br />

several replicates of appropriate matrices-matching<br />

Certificate Reference Materials. The mercury<br />

analytical method was recently benchmarked on<br />

International scale [4] and proofed to be fully under<br />

control and traceable to the SI (IRMM 2003). For<br />

every single analysis the ISO procedure is hereby<br />

indicated, as well as a short resume of the procedure<br />

itself.<br />

4.2 Sample pre treatment and preparation<br />

According with ISO 11464 Procedure [5] , after storage<br />

at 4°C and prior to analysis, samples were dried in

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