Institute of Geography and Geoecology, Karlsruhe Institute of Technology (KIT), Reinhard-Baumeister-Platz 1, 76131 Karlsruhe, Germany; Organic Geochemistry Unit (OGU), School of Chemistry, University of Bristol, Cantock's Close, Bristol BS8 1TS, United Kingdom; Institute of Geography, University of Bern, Hallerstrasse 12, 3012 Bern, Switzerland.
Institute of Geography, University of Bern, Hallerstrasse 12, 3012 Bern, Switzerland.
Sci Total Environ. 2018 Jul 15;630:83-95. doi: 10.1016/j.scitotenv.2018.02.109. Epub 2018 Feb 20.
Little is known about oxygenated polycyclic aromatic hydrocarbons (OPAHs) and azaarenes (AZAs) in forest soils. We sampled all horizons of forest soils from five locations at increasing distances from an Al plant in Slovakia, and determined their polycyclic aromatic compound (PACs) concentrations. The ∑29PAHs concentrations were highest in the Oa and lowest in the Oi horizon, while the ∑14OPAHs and ∑4AZAs concentrations did not show a consistent vertical distribution among the organic horizons. The concentration ratios of PAHs and OPAHs between deeper O horizons and their overlying horizon (enrichment factors) were positively correlated with the octanol-water partition coefficients (K) at several locations. This is attributed to the slower degradation of the more hydrophobic PACs during organic matter decomposition. PACs concentrations decreased from the organic layer to the mineral horizons. The concentrations of ∑29PAHs (2400-17,000 ng g), ∑14OPAHs (430-2900 ng g) and ∑4AZAs (27-280 ng g) in the mineral A horizon generally decreased with increasing distance from the Al plant. In the A horizons, the concentrations of ∑29PAHs were correlated with those of ∑14OPAHs (r = 0.95, p = 0.02) and ∑4AZAs (r = 0.93, p = 0.02) suggesting that bioturbation was the main transport process of PACs from the organic layer into the mineral soil. At each location, the concentrations of PACs generally decreased with increasing depth of the mineral soil. Enrichment factors of PAHs in the mineral horizons were not correlated with K, pointing at colloid-assisted transport and bioturbation. The enrichment factors of OPAHs (in mineral horizons) at a site were negatively correlated with their K values indicating that these compounds were leached in dissolved form. Compared to a study 13 years before, the concentrations of PAHs had decreased in the O horizons but increased in the A and B horizons because of soil-internal redistribution after emissions had been reduced.
关于森林土壤中的含氧多环芳烃(OPAHs)和氮杂芳烃(AZAs),人们知之甚少。我们在斯洛伐克的一家铝厂附近的五个地点,从所有土壤层次中采集样本,并测定了它们的多环芳烃化合物(PACs)浓度。∑29PAHs 浓度在 Oa 层最高,Oi 层最低,而∑14OPAHs 和∑4AZAs 浓度在有机层中没有表现出一致的垂直分布。在几个地点,深层 O 层与上覆层之间 PAHs 和 OPAHs 的浓度比(富集因子)与辛醇-水分配系数(K)呈正相关。这归因于在有机质分解过程中,疏水性 PACs 的降解速度较慢。PACs 浓度从有机层向矿质层减少。∑29PAHs(2400-17,000ngg)、∑14OPAHs(430-2900ngg)和∑4AZAs(27-280ngg)的浓度在矿质 A 层中通常随距离铝厂的增加而降低。在 A 层中,∑29PAHs 的浓度与∑14OPAHs(r=0.95,p=0.02)和∑4AZAs(r=0.93,p=0.02)的浓度相关,这表明生物扰动是 PACs 从有机层向矿质土壤传输的主要过程。在每个地点,PACs 的浓度通常随矿质土壤深度的增加而降低。矿质层中 PAHs 的富集因子与 K 无关,这表明存在胶体辅助传输和生物扰动。一个地点矿质层中 OPAHs(的富集因子)与 K 值呈负相关,表明这些化合物以溶解形式淋溶。与 13 年前的一项研究相比,由于排放量减少后土壤内部再分配,O 层中的 PAHs 浓度降低,而 A 层和 B 层中的 PAHs 浓度增加。