Signatures of chlorinated dioxins and furans along the exposure path - The relation between vegetation and soil.

Polychlorinated dibenzo-p-dioxins and dibenzo-furans (PCDD/Fs) belong to the most toxic persistent organic environmental pollutants. Therefore, knowledge about their fate along the exposure path is of special concern. In order to comprehend the transfer of PCDD/Fs across different environmental compartments, PCDD/F concentrations in plants and in soil were evaluated. Pairs of soil and plant samples were selected according to the shortest distance between sampling points. At 15 sites PCDD/F concentrations in spruce needles and in forest humus layers where compared. Summer conditions were evaluated on the basis of 8 sites with ryegrass- and grassland topsoil samples. Autumn conditions were addressed using 7 sites with curly kale and topsoil samples under grassland. Correlation analyses of the PCDD/F congener profiles for plant- and soil samples were conducted. The correlations were compared to influencing site (e.g. local temperature) and spatial as well as temporal offset parameters. No governing parameter that decisively influenced the similarity between plant and soil signature became evident. By means of the toxicity factors of TEQ-WHO, tetra- and penta-PCDD/F homologues were assigned to the group of low-chlorinated homologues (lcH), and hexa-, hepta- and octa-PCDD/F homologues to the high-chlorinated homologues (hcH). lcH and hcH are presumed to differ in solubility, volatility and rate of degradation. The ratio of lcH/hcH revealed characteristic fingerprints that enabled the differentiation of the individual PCDD/F-plant and -soil pairs. Spruce-humus pairs showed a close relation during winter exposure times, while the lower summer concentrations were not reflected in the humus layer. Kale was exposed at the beginning of the season with elevated PCDD/F immissions, and showed a closer relation to grassland topsoil than did ryegrass. lcH/hcH proved as a simple criterion that can reveal related PCDD/F fingerprints of different environmental compartments despite signal attenuation due to decomposition, volatilization and particulate transport.