Allan Ian John, Vrana Branislav, de Weert Jasperien, Kringstad Alfhild, Ruus Anders, Christensen Guttorm, Terentjev Petr, Green Norman Whitaker
Norwegian Institute for Water Research (NIVA), Gaustadalléen 21, 0349, Oslo, Norway.
RECETOX, Masaryk University, Brno, Kamenice 753/5, 625 00, Brno, Czech Republic.
Sci Rep. 2021 May 27;11(1):11231. doi: 10.1038/s41598-021-90457-3.
The identification and prioritisation of water bodies presenting elevated levels of anthropogenic chemicals is a key aspect of environmental monitoring programmes. Albeit this is challenging owing to geographical scales, choice of indicator aquatic species used for chemical monitoring, and inherent need for an understanding of contaminant fate and distribution in the environment. Here, we propose an innovative methodology for identifying and ranking water bodies according to their levels of hydrophobic organic contaminants (HOCs) in water. This is based on a unique passive sampling dataset acquired over a 10-year period with silicone rubber exposures in surface water bodies across Europe. We show with these data that, far from point sources of contamination, levels of hexachlorobenzene (HCB) and pentachlorobenzene (PeCB) in water approach equilibrium with atmospheric concentrations near the air/water surface. This results in a relatively constant ratio of their concentrations in the water phase. This, in turn, allows us to (i) identify sites of contamination with either of the two chemicals when the HCB/PeCB ratio deviates from theory and (ii) define benchmark levels of other HOCs in surface water against those of HCB and/or PeCB. For two polychlorinated biphenyls (congener 28 and 52) used as model chemicals, differences in contamination levels between the more contaminated and pristine sites are wider than differences in HCB and PeCB concentrations endorsing the benchmarking procedure.
识别和优先处理人为化学物质含量较高的水体是环境监测计划的一个关键方面。尽管由于地理尺度、用于化学监测的指示水生物种的选择以及了解污染物在环境中的归宿和分布的内在需求,这具有挑战性。在此,我们提出了一种创新方法,用于根据水体中疏水性有机污染物(HOCs)的含量对水体进行识别和排名。这基于一个独特的被动采样数据集,该数据集是在10年期间通过在欧洲地表水水体中暴露硅橡胶获得的。我们用这些数据表明,在远离污染源的地方,水中六氯苯(HCB)和五氯苯(PeCB)的含量在空气/水表面附近接近与大气浓度的平衡。这导致它们在水相中的浓度比相对恒定。反过来,这使我们能够:(i)当HCB/PeCB比值偏离理论值时,识别受这两种化学物质中任何一种污染的地点;(ii)根据HCB和/或PeCB的含量确定地表水其他HOCs的基准水平。对于用作模型化学物质的两种多氯联苯(同系物28和52),污染较严重的地点和原始地点之间的污染水平差异比HCB和PeCB浓度差异更大,这支持了基准程序。