长江河口硅和磷生源要素质量浓度的变化特征

根据近年来长江河口区域内大通水文站的记录和近期在长江入海河口区上海段多个采样点的生源要素质量浓度实测数据,比较水中可溶性硅酸盐和磷酸盐的质量浓度,分析在长江入海河口区水中硅和磷元素含量的主要变化特征.结果表明,长江水中的硅酸盐和磷酸盐从长江入海河口进入大海的过程中,其质量浓度有降低的趋势,它们在长江入海河口的多年的质量浓度变化趋势是相反的.长江入海河口区域上游的磷酸盐质量浓度升高幅度较大,而硅酸盐变化不大,硅酸盐、磷酸盐质量浓度在长江河口区进入海洋的过程中迅速降低.      

蒽降解菌与铜绿假单胞菌融合子的特性研究

将蒽降解菌An815和绿色荧光蛋白标记铜绿假单胞菌(Pseudomonas aeruginosa/EGFP)P原生质体融合,得到了既能高效降解蒽,又能产生生物表面活性剂的融合子F。研究了它的形态特征、生理生化特性、产表面活性剂的能力、对蒽的降解性能及生长繁殖情况。结果表明,融合子菌落和菌体形态,产脓青素,荧光色素的特性类似于铜绿假单胞菌亲本,但其大多生理生化特性酷似An815亲本而不同于铜绿假单胞菌亲本;融合子有较好产表面活性剂的能力,72 h内将表面张力由70.2 mN/m降至36.5mN/m;在蒽的反应体系中,32h内融合子和亲本An815对蒽的降解转化率分别为86.7%,59.4%,融合子对蒽的降解速率比An815提高了27.3%;在蒽的反应体系中融合子和亲本生长曲线相似。     

岩溶环境对多环芳烃迁移转化的影响

从水文地质条件、地貌环境和地球化学环境等3个方面,综述了岩溶环境对多环芳烃(PAHs)迁移转化的影响。针对研究现状及存在的不足,提出了未来可能的研究趋势,包括不同气候条件下发育的岩溶系统的对比研究、不同气候条件和不同岩溶系统快速流和慢速流对PAHs迁移的贡献、碳酸盐岩与PAHs相互作用的机理,以及有机质对PAHs迁移行为的影响。     

气相色谱-串联质谱法测定沉积物中多环芳烃

采用ASE法提取沉积物中16种多环芳烃,以固相萃取法净化提取液,用气相色谱-串联质谱法测定。通过优化测定条件,使方法在5.00μg/L~1 600μg/L范围内线性良好,方法检出限为0.15μg/kg~0.66μg/kg。空白石英砂的加标回收率为61.9%~121%,7次测定结果的RSD为2.6%~11.1%。     

灌河口表层土壤多环芳烃污染调查

为了解灌河口工业区表层土壤中多环芳烃的污染水平及健康风险。于2017年4月份在灌河口化工园区、火力发电厂和钢铁工业园区采集30个表层土壤样品,利用气相色谱-质谱联用仪(GC-MS)对16种优控ω(PAH)进行了检测。结果表明,30个采样点16种PAH的ω(T-PAHs)总为1 212.8~12 264.5 ng/g,平均值为3 504.8 ng/g。其中单体PAH以Fl为主,平均比例高达19.4%,其次为Pyr(16.7%)和B[a]P(9.6%)。单体PAH相关性分析表明了污染物来源的一致性,主要来源于本地工业区原油、生物质和煤的燃烧过程。根据加拿大土壤环境质量标准,灌河口工业区87%的土壤PAHs污染超过了安全值,存在潜在的生态风险。     

珠江口表层水中多环芳烃的分布特征及健康风险评估

分别于2015年2、5、8、11月在珠江八大入海口采集表层水体样品,应用固相萃取富集法对该区域表层水体中16种USEPA优控多环芳烃(PAHs)的时空分布特征进行分析,并利用终生致癌风险增量模型(ILCR)对该区域的饮水健康风险进行评价。结果表明:珠江口4个季度所采集的水样中,∑15PAHs的浓度范围为18.0~50.3 ng/L,含量处于中等水平。其中7种强致癌性∑7PAHs的浓度范围为1.53~3.73 ng/L,占∑15PAHs的5.89%~11.1%,∑15PAHs和∑7PAHs在枯水期(2、11月)样品中明显高于丰水期(5、8月)。就组成特征而言,各采样点PAHs以3、4环为主。珠江口表层水中非致癌类PAHs的危害商数值为0.99×10~(-5)~2.73×10~(-5),远低于USEPA规定的阈值(1);致癌类PAHs产生的健康风险为6.50×10~(-8)~2.37×10~(-7),其中Ba P导致的饮水途径健康风险最高,所有点位致癌类PAHs的健康风险均低于USEPA推荐的对致癌物质最大可接受风险水平(10~(-6)),表明珠江口表层水中PAHs尚不具备严重的致癌风险,但是仍然存在潜在的健康风险,需要重点控制和管理。     

液液萃取-气相色谱法测定水质可萃取性石油烃C10~C40

建立了以环己烷为萃取剂、气相色谱法(氢火焰离子化检测器,FID)测定水质样品中可萃取性石油烃(C_(10)～C_(40))的分析方法。以正构烷烃混合标准溶液为定性和定量校准标准,以色谱峰面积总和与混合标准溶液总浓度建立校准曲线进行外标法定量。方法检出限为0.01 mg/L,经验证方法精密度和准确度良好。同时,分别以气相色谱法和红外光度法测定了地表水、污水处理厂出水、海水和化工废水等实际样品,对比实验结果表明,在可萃取性石油烃C_(10)～C_(40)的碳数范围内,气相色谱法的测试结果与红外光度法无明显差异,有较好的可比性。     

Effects of temperature and fertilization on total vs. active bacterial communities exposed to crude and diesel oil pollution in NW Mediterranean Sea

The dynamics of total and active microbial communities were studied in seawater microcosms amended with crude or diesel oil at different temperatures (25, 10 and 4 °C) in the presence/absence of organic fertilization (Inipol EAP 22). Total and hydrocarbon-degrading microbes were enumerated by fluorescence microscopy and Most Probable Number (MPN) method, respectively. Total (16S rDNA-based) vs. active (16S rRNA) bacterial community structure was monitored by Capillary-Electrophoresis Single Strand Conformation Polymorphism (CE-SSCP) fingerprinting. Hydrocarbons were analyzed after 12 weeks of incubation by gas chromatography-mass spectrometry. Total and hydrocarbon-degrading microbial counts were highly influenced by fertilization while no important differences were observed between temperatures. Higher biodegradation levels were observed in fertilized microcosms. Temperature and fertilization induced changes in structure of total bacterial communities. However, fertilization showed a more important effect on active bacterial structure. The calculation of Simpson's diversity index showed similar trends among temperatures whereas fertilization reduced diversity index of both total and active bacterial communities.     

Sources and distribution of polycyclic aromatic hydrocarbons in sediments from the Spanish northern continental shelf. Assessment of spatial and temporal trends

The distribution of polycyclic aromatic hydrocarbons was determined in surface sediments collected at 36 stations along the Spanish Northern continental shelf in March and September 2003, and February 2005. Concentrations of PAHs (Σ13 parent components) were in the range of 22-47528 μg/kg dw, the highest values corresponding to coastal urban-industrial hotspots and decreasing offshore. Sediment quality guidelines (SQGs) showed that concentrations of total PAHs were below the threshold effect level (TEC) in 27 stations (81%) and above in 7, two of which (Gijon and Bilbao) were above the probable effect concentration (PEC). The detailed study of diagnostic ratios suggested a rather uniform mixture of petrogenic and pyrolytic PAH sources along the continental shelf, with a slight decrease of the latter moving westwards and offshore. In order to assess the incidence of sediment sampling on the variability of the results, selected stations were also monitored in February and September 2004 and September 2005. The average field variance of the values obtained for each station was 31% that decreased to 23% when the values were normalized to TOC.     

Temperature-dependent sorption of polycyclic aromatic hydrocarbons on natural and treated sediments

In aqueous environment temperature is considered to play a significant role in the sorption process of polycyclic aromatic hydrocarbons (PAHs) and its influence on the sorption equilibrium is indicative of sorption energies and mechanisms. In this study, sorptions of five PAHs on three heterogeneous sorbents including one river sediment (YHR), one estuary sediment (YRD) and one treated sediment with organic matter removed (IM) were carried out at a range of temperature from 5 °C to 35 °C. Stronger sorptions were observed at lower temperatures, with the equilibrium sorption coefficient K_d increasing 2-5 times as the temperature decreases 30 °C. The increase of K_d value was attributed primarily to the change of PAH water solubility, which predicted 40-75% of the increase of K_d in the sorption process. To provide insight into the sorption mechanism, enthalpy change (ΔH_S) for the sorption process was calculated and the values were observed to be negative for all of the interactions, suggesting that the exothermal sorption of PAHs inversely dependents on temperature. Based on the values of ΔH_S, van der Waals forces were inferred as the main sorption mechanism for the PAHs, especially on the YHR sediment which contained more organic matter. For sorption of larger size PAHs on the sorbents with low organic matter, specific interactions were deduced to contribute to the overall sorption.