Subedi Bikram, Yun Sehun, Jayaraman Saro, Bergen Barbara J, Kannan Kurunthachalam
Wadsworth Center, New York State Department of Health, Empire State Plaza, P.O. Box 509, Albany, NY, 12201-0509, USA.
Environ Monit Assess. 2014 Aug;186(8):5273-84. doi: 10.1007/s10661-014-3776-8. Epub 2014 Apr 30.
Blue mussels (Mytilus edulis) and sediments collected from 1991 to 2005 from New Bedford Harbor (NBH), MA, were analyzed for two polycyclic musks (HHCB or Galaxolide® and AHTN or Tonalide®), polybrominated diphenyl ethers (PBDEs), polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs), and organochlorine pesticides (OCPs). HHCB and AHTN were found in mussel tissues at mean concentrations of 836 and 376 ng/g lipid weight (lw), respectively, which were two- to seven-fold higher than those found at a reference site. Mean concentrations of HHCB and AHTN in NBH sediments were 12 and 6.3 ng/g dry weight (dw), respectively. Four- and five-ringed PAHs, such as phenanthrene, anthracene, fluoranthene, and pyrene, collectively accounted for 61 % of the ∑PAHs concentrations in mussels from NBH. Mean ΣPCB concentrations in mussels from upper and lower NBH were 942 and 182 μg/g lw, respectively, and were dominated by tetra- and penta-chlorobiphenyl congeners, collectively accounting for 61 % of the ΣPCB concentrations. The mean concentration of ∑PBDEs in mussels from NBH was 277 ng/g lw, and no significant difference existed in the concentrations between upper and lower NBH. DDTs were the major OCP found in mussels, found at a mean concentration of 778 ng/g lw. The concentrations of HHCB, AHTN, ΣPBDEs, ΣPAHs, and DDTs in mussels decreased significantly (r (2) ≥ 0.56, p ≤ 0.052) from 1991 to 2005. The concentrations of PCBs and chlordanes did not exhibit a decreasing trend in mussel tissues (r (2) < 0.50; p > 0.076) from 1991 to 2005. Based on the temporal trends in the concentrations of HHCB, AHTN, ∑PAHs, and ∑PBDEs found in mussels from NBH, it was estimated that between 5.5 and 12 years were required for the concentrations of these compounds to decrease by half (i.e., environmental halving time) of the levels found in 1991.
对1991年至2005年期间从马萨诸塞州新贝德福德港(NBH)采集的蓝贻贝(紫贻贝)和沉积物进行了分析,检测其中两种多环麝香(六氯环六烷或佳乐麝香®和六溴环十二烷或吐纳麝香®)、多溴二苯醚(PBDEs)、多环芳烃(PAHs)、多氯联苯(PCBs)和有机氯农药(OCPs)的含量。在贻贝组织中发现六氯环六烷和六溴环十二烷的平均浓度分别为836和376纳克/克脂重(lw),比在一个参考地点发现的浓度高出两至七倍。NBH沉积物中六氯环六烷和六溴环十二烷的平均浓度分别为12和6.3纳克/克干重(dw)。四环和五环多环芳烃,如菲、蒽、荧蒽和芘,共同占NBH贻贝中总多环芳烃浓度的61%。NBH上游和下游贻贝中多氯联苯的平均总浓度分别为942和182微克/克脂重,且以四氯和五氯联苯同系物为主,共同占多氯联苯总浓度的61%。NBH贻贝中多溴二苯醚的平均总浓度为277纳克/克脂重,NBH上下游的浓度无显著差异。滴滴涕是在贻贝中发现的主要有机氯农药,平均浓度为778纳克/克脂重。从1991年到2005年,贻贝中六氯环六烷、六溴环十二烷、多溴二苯醚总含量、多环芳烃总含量和滴滴涕的浓度显著下降(r (2) ≥ 0.56,p ≤ 0.052)。1991年至2005年期间,贻贝组织中多氯联苯和氯丹的浓度没有呈现下降趋势(r (2) < 0.50;p > 0.076)。根据在NBH贻贝中发现的六氯环六烷、六溴环十二烷、多环芳烃总含量和多溴二苯醚总含量的时间趋势,估计这些化合物浓度降低一半(即环境半衰期)至1991年发现水平所需的时间为5.5至12年。