Jager Tjalling, Baerselman Rob, Dijkman Ellen, de Groot Arthur C, Hogendoorn Elbert A, de Jong Ad, Kruitbosch Jantien A W, Peijnenburg Willie J G M
Laboratory for Ecotoxicology, National Institute of Public Health and the Environment (RIVM), PO Box 1, NL-3720 BA Bilthoven, The Netherlands.
Environ Toxicol Chem. 2003 Apr;22(4):767-75.
The bioavailability of polycyclic aromatic hydrocarbons (PAHs) for earthworms (Eisenia andrei) was experimentally determined in seven field-polluted soils and 15 soil-sediment mixtures. The pore-water concentration of most PAHs was higher than predicted. However, most of the compound was associated with dissolved organic carbon (DOC) and not directly available for uptake by earthworms. The apparent sorption could be reasonably predicted on the basis of interactions with DOC; however, the biota-soil accumulation factors (BSAFs) for earthworms were up to two orders of magnitude lower than predicted by equilibrium partitioning. The large variability between sites was not fully explained by differences in sorption. Experimental results indicate that the pool of freely dissolved PAHs in the pore water became partially depleted because of uptake by the earthworms and that bioaccumulation is thus also influenced by the kinetics of PAH desorption and mass transport. A pilot study with Lumbricus rubellus showed that steady-state body residues were well correlated to E. andrei. Current results show that depositing dredge spoil on land may lead to increased bioavailability of the lower-molecular-weight PAHs. However, risk assessment can conservatively rely on equilibrium partitioning, but accurate prediction requires quantification of the kinetics of bioavailability.
在七种受田间污染的土壤和15种土壤 - 沉积物混合物中,通过实验测定了多环芳烃(PAHs)对蚯蚓(安德爱胜蚓)的生物有效性。大多数PAHs的孔隙水浓度高于预测值。然而,大部分化合物与溶解有机碳(DOC)结合,蚯蚓无法直接摄取。基于与DOC的相互作用,可以合理预测表观吸附;然而,蚯蚓的生物群 - 土壤积累因子(BSAFs)比平衡分配预测值低达两个数量级。不同地点之间的巨大差异不能完全由吸附差异来解释。实验结果表明,由于蚯蚓的摄取,孔隙水中自由溶解的PAHs池部分耗尽,因此生物累积也受PAH解吸动力学和质量传输的影响。一项对红色正蚓的初步研究表明,稳态体内残留量与安德爱胜蚓有很好的相关性。目前的结果表明,在陆地上堆放疏浚弃土可能会导致低分子量PAHs的生物有效性增加。然而,风险评估可以保守地依赖平衡分配,但准确的预测需要对生物有效性动力学进行量化。