Conder Jason, Jalalizadeh Mehregan, Luo Hong, Bess Amanda, Sande Steven, Healey Michael, Unger Michael A
Geosyntec Consultants, Huntington Beach, CA, United States.
Exponent, Exponent, Los Angeles, CA, United States.
Environ Adv. 2021 Apr;3. doi: 10.1016/j.envadv.2021.100032. Epub 2021 Jan 6.
Decades of research have shown that the concentration of freely dissolved PAH (C in sediment correlates with PAH bioavailability and toxicity to aquatic organisms. Passive sampling techniques and models have been used for measuring and predicting C respectively, but these techniques require weeks for analytical chemical measurements and data evaluation. This study evaluated the performance of a portable, field-deployable antibody-based PAH biosensor method that can provide measurements of PAH C within a matter of minutes using a small volume of mechanically-extracted sediment porewater. Four sediments with a wide range of PAHs (ΣPAH 2.4 to 307 mg/kg) derived from petroleum, creosote, and mixed urban sources, were analyzed via three methods: 1) bulk chemistry analysis; 2) sediment passive sampling; and 3) biosensor analysis of mechanically-extracted sediment porewater. Mean ΣPAH C determined by the biosensor for the four sediments (3.1 to 55 μg/L) were within a factor of 1.1 (on average) compared to values determined by the passive samplers (2.0 to 52 μg/L). All mean values differed by a factor of 3 or less. The biosensor was also useful in identifying sediments that are likely to be non-toxic to benthic invertebrates. In two of the four sediments, biosensor results of 20 and 55 μg/L exceeded a potential risk-based screening level of 10 μg/L, indicating toxicity could not be ruled out. PAH Toxic Units (ΣTU) measured in these two sediments using the passive sampler C results were also greater than the ΣTU threshold of 1 (6.7 and 5.8, respectively), confirming the conclusions reached with the biosensor. In contrast, the other two sediments were identified as non-toxic by both the biosensor (3.1 and 4.3 μg/L) and the passive sampler (ΣTUs of 0.34 and 0.039). These results indicate that the biosensor is a promising tool for rapid screening of sediments potentially-impacted with PAHs.
数十年的研究表明,沉积物中自由溶解的多环芳烃(PAH)浓度(C)与PAH对水生生物的生物有效性和毒性相关。被动采样技术和模型分别用于测量和预测C,但这些技术需要数周时间进行分析化学测量和数据评估。本研究评估了一种基于抗体的便携式现场可部署PAH生物传感器方法的性能,该方法使用少量机械提取的沉积物孔隙水,能在几分钟内提供PAH C的测量值。通过三种方法分析了四种来自石油、杂酚油和混合城市源且PAHs含量范围广泛(总PAH为2.4至307 mg/kg)的沉积物:1)整体化学分析;2)沉积物被动采样;3)对机械提取的沉积物孔隙水进行生物传感器分析。生物传感器测定的四种沉积物的平均总PAH C(3.1至55 μg/L)与被动采样器测定的值(2.0至52 μg/L)相比,平均相差1.1倍以内。所有平均值相差3倍或更小。该生物传感器在识别可能对底栖无脊椎动物无毒的沉积物方面也很有用。在四种沉积物中的两种中,生物传感器测得的结果为20和55 μg/L,超过了基于潜在风险的筛选水平10 μg/L,表明不能排除毒性。使用被动采样器C结果在这两种沉积物中测得的PAH毒性单位(总TU)也大于总TU阈值1(分别为6.7和5.8),证实了生物传感器得出的结论。相比之下,另外两种沉积物通过生物传感器(3.1和4.3 μg/L)和被动采样器(总TU分别为0.34和0.039)均被鉴定为无毒。这些结果表明,该生物传感器是快速筛选可能受PAHs影响的沉积物的一种有前途的工具。