MOE Key Laboratory of Pollution Processes and Environmental Criteria, College of Environmental Science and Engineering, Nankai University, Tianjin 300071, China.
Environ Toxicol Chem. 2010 Jun;29(6):1248-55. doi: 10.1002/etc.154.
Bioturbation by the burrowing crab Helice tiensinensis was investigated to determine its impact on polycyclic aromatic hydrocarbon (PAH)-contaminated estuarine sediments. The concentrations of 16 U.S. Environmental Protection Agency (U.S. EPA) priority PAHs in sediment and pore water from a crab bed (including surface and burrow samples) and a control area, as well as in crabs, were measured. The total concentration of the 16 U.S. EPA priority PAHs in surface sediment of the crab bed (average 2,772 ng/g dry weight) was significantly higher than in the control area (1,173 ng/g dry weight). In the crab bed, the total concentration of PAHs in burrow sediment (1,239 ng/g dry weight) was lower than in surface sediment, and a similar trend was found for most of the individual PAHs, except for indeno[1,2,3-cd]pyrene, and benzo[ghi]perylene. The enhanced PAH desorption in the burrow, which could be attributed to the increase in dissolved organic matter in pore water as well as the mechanical mixing by the crab, is expected to increase PAH flux to the sea. In addition to increased flushing to the sea, incorporation of PAHs in crab biomass and metabolism of PAHs by the crab, stimulated microbial degradation, was proposed as an ignorable factor that lowered the PAH concentration in burrow sediment, because crab bioturbation increases the abundance and activity of microorganisms through several means. Log K(OW) and log K(OC) correlated well for individual PAHs in sediment in the control area, although this correlation was poor for sediments in the crab bed. The log biota-sediment accumulation factor (BSAF) of PAHs exhibited a negative relationship with log K(OW), suggesting that the bioaccumulation of sorbed PAHs was controlled primarily by their bioavailability.
研究了穴居蟹(Helice tiensinensis)的生物扰动对受多环芳烃(PAH)污染的河口沉积物的影响。测量了来自蟹床(包括表面和洞穴样本)和对照区的沉积物和孔隙水中的 16 种美国环保署(USEPA)优先 PAH 的浓度,以及蟹体内的浓度。蟹床表面沉积物中 16 种 USEPA 优先 PAH 的总浓度(平均 2772ng/g 干重)明显高于对照区(1173ng/g 干重)。在蟹床中,洞穴沉积物中 PAH 的总浓度(1239ng/g 干重)低于表面沉积物,大多数单个 PAH 也呈现出类似的趋势,除了茚并[1,2,3-cd]芘和苯并[ghi]苝。洞穴中 PAH 的解吸增强,这可能归因于孔隙水中溶解有机质的增加以及蟹的机械混合,预计会增加 PAH 向海的通量。除了向海的冲洗增加外,PAH 被蟹吸收并代谢,以及蟹的生物扰动通过多种方式增加了微生物的丰度和活性,被认为是降低洞穴沉积物中 PAH 浓度的一个可忽略的因素。在对照区沉积物中,个别 PAH 的 log K(OW) 和 log K(OC) 相关性较好,尽管在蟹床沉积物中相关性较差。PAH 的生物浓缩因子(BSAF)与 log K(OW) 呈负相关,表明吸附态 PAH 的生物累积主要受其生物可利用性控制。