Distribution and sources of polycyclic aromatic hydrocarbons in surface sediments of rivers and an estuary in Shanghai, China

Concentrations, spatial distribution and sources of 17 polycyclic aromatic hydrocarbons (PAHs) and methylnaphthalene were investigated in surface sediments of rivers and an estuary in Shanghai, China. Total PAH concentrations, excluding perylene, ranged from 107 to 1707 ng/g-dw. Sedimentary PAH concentrations of the Huangpu River were higher than those of the Yangtze Estuary. The concentration of the Suzhou River was close to the average concentration of the Huangpu River. PAHs source analysis suggested that, in the Yangtze Estuary, PAHs at locations far away from cities were mainly from petrogenic sources. At other locations, both petrogenic and pyrogenic inputs were significant. In the Huangpu and Suzhou Rivers, pyrogenic input outweighed other sources. The pyrogenic PAHs in the upper reaches of the Huangpu River were mainly from the incomplete combustion of grass, wood and coal, and those in the middle and lower reaches were from vehicle and vessel exhaust.     

Sampling of airborne polycyclic aromatic hydrocarbons with semipermeable membrane devices

Semipermeable membrane devices (SPMDs) are nowadays used as passive samplers of organic pollutants. The knowledge of the sampling rate values (R_S) of each substance trapped on membranes is necessary to calculate their average concentration. Here we calculate R_S values for 16 polycyclic aromatic hydrocarbons using the comparison of active sampling method results and the amounts sequestered by SPMDs at varying exposure times.Selected article from the Regional Symposium on Chemistry and Environment, Krusevac, Serbia, June 2003, organized by Dr. Branimir Jovancicevic.     

Atmospheric deposition of polycyclic aromatic hydrocarbons near New England coastal waters

Wet and dry deposition of polycyclic aromatic hydrocarbons (PAHs) was measured at Nahant, Massachusetts, a peninsula jutting into Massachusetts Bay and Wolf Neck, a peninsula jutting into Casco Bay, Maine. Wet deposition (rain and snow) was collected in a funnel which drains into a shielded, temperature controlled receiving bottle. Dry deposition of gaseous and particulate PAHs was collected onto an exposed water surface. PAHs were analyzed by solid phase extraction and gas chromatography-mass spectrometry. Sixteen PAH species were analyzed, ranging from acenaphthylene to coronene. The mean wet deposition rate of the sum of the 16 species is 720 ng m⁻² cm⁻¹ precipitation at Nahant, and 831 ng m⁻² cm⁻¹ precipitation at Wolf Neck. Wet deposition is attributed to regional PAH emitting sources. Storm patterns appear to bring somewhat higher wet deposition of PAHs to Wolf Neck than to Nahant. The mean dry deposition rate is 95 ng m⁻² h⁻¹ at Nahant and 9.3 ng m⁻² h⁻¹ at Wolf Neck. The large difference is attributed to the fact that Nahant is close to the urban-industrial metropolitan Boston area and Logan International Airport, whereas Wolf Neck has no major PAH-emitting sources nearby. Individual measurements have an error bracket of ±30%. The Chemical Mass Balance model was used to apportion the dry deposition to source categories. At Nahant, nine samples gave valid statistical attributes with a mean apportionment: jet exhaust 35%, gasoline fueled vehicles 32%, diesel fueled vehicles 17%, wood combustion 13%, others 3%. At Wolf Neck, six samples yielded a mean apportionment: jet exhaust 30%, gasoline vehicles 28%, diesel vehicles 18%, wood combustion 16%, others 8%. There is a considerable variation between the samples. The apportionment is greatly dependent on the quality and selection of the model inputs, i.e. source signatures, which for PAHs are questionable.     

Dual <Superscript>14</Superscript>C/residue analysis method to assess the microbial accessibility of native phenanthrene in environmental samples

The aim of this work was to develop a method to assess the microbial accessibility of native phenanthrene present in soils and sediments. We developed an accelerated biodegradation assay, characterized by (a) inoculation with a sufficient number of phenanthrene-degrading microorganisms, (b) monitoring of the biodegradation activity through ¹⁴C-mineralization measurements, and (c) single-step chemical analysis of the native compound in the residue. The use of ¹⁴C-labeling allowed the determination of the time period needed for biodegradation of the bioaccessible fraction of the native chemical. The method was tested with environmental samples having a wide range of phenanthrene concentrations, i.e., from background levels (μg kg^-1) originating in soil from atmospheric deposition, to acute concentrations (g kg^-1) corresponding to industrial pollution of soils and sediments. The results showed a wide range of bioaccessibility (15–95% of the initial amount). The method can be used for the assessment of bioaccessibility involved in the management of polycyclic aromatic hydrocarbon (PAH) pollution.     

添加乙醇碳源对驯化菌种降解油制气废水的影响

进行了添加乙醇作为碳源强化油制气废水生物降解的研究,并利用GC／MS分析对油制气废水中芳烃类化合物的降解进行了初步研究。研究表明,共代谢基质乙醇的加入,可使菌种S-2、Y-3、XH-3、M-3对COD、氨氮、可萃取有机物等指标的去除率分别提高17．6％～25．6％、34．9％～42．8％、10．4％～14．2％;但在所采用的时间范围内,酚类化合物的去除率降低;芳烃类化合物的去除率提高15．4％～21．2％。除了维持无共代谢条件下对芳环数≤3的芳烃类化合物的良好降解能力外,对芳环数为4～6的化合物降解能力也有所提高。     

通风及营养元素对多环芳烃污染土壤修复影响

文章在无外源接种体的条件下,评估了强制通风(通风量为1.51 L/min)与营养元素对土壤中多环芳烃(PAHs)降解的交互作用。结果表明:仅靠合适的营养液配方和长时间通风可以刺激污染土壤中的土著微生物生长,并影响微生物菌群的形成。通风同时添加营养液有利于好氧菌生长、加快PAHs的降解;与通风相比,添加营养元素是影响PAHs降解的主要因素。通风和添加营养元素对3环PAHs降解影响不显著,但可促进4环、5环和6环PAHs污染物降解。60 d内,仅通风、仅添加营养元素、同时通风和添加营养元素处理的PAHs分别降解了52%、59%、67%。     

多环芳烃对卤虫无节幼体的光诱导毒性

以卤虫Ⅱ～Ⅲ龄无节幼体为实验材料,在实验室内研究4种多环芳烃的光诱导毒性,比较了在有紫外(UV)和无UV照射条件下多环芳烃对卤虫幼体的存活和几种生理生化指标的影响.结果表明:UV辐射(UVA:476 μw·cm-2;UVB:6.5 μW·cm-2)明显提高了菲、蒽、荧蒽和芘对卤虫幼体的毒性,其24 h LC50值分别是无UV照射条件下LC50值的1/139、1/182、1/102和1/88.UV照射诱导了荧蒽对卤虫幼体的氧化损伤,过氧化物酶(POD)对荧蒽的光诱导毒性较超氧化物歧化酶(SOD)敏感;卤虫幼体的丙二醛(MDA)和Na ·K -ATPase是衡量荧蒽光诱导毒性的较敏感参数.     

长江水系武汉段沉积物再悬浮过程中PAHs的释放动力学

采用沉积物再悬浮模拟装置进行了再悬浮过程中多环芳烃（PAHs）的释放动力学实验,研究了长江水系武汉段7种沉积物中PAHs的释放动力学特征,并考察了沉积物组成对PAHs释放动力学的影响.结果表明,不同剪应力作用下的沉积物再悬浮过程中,不同性质沉积物中PAHs向上覆水体的释放均符合一级动力学方程,且释放过程分为两个阶段,第...     

Sources of hydrocarbons in sediments of the Mandovi estuary and the Marmugoa harbour, west coast of India

Surface sediments were collected from various locations of the Mandovi estuary and the Marmugoa harbour. Sediments were analysed for organic carbon (OC), total lipids, n-alkanes concentration and composition. Concentrations of OC, total lipids and n-alkanes varied spatially and ranged from 1 to 2.5%, 176 to 1413 microg/g dry weight (dw) sediments, and 0.8 to 3.2 microg/g dw sediments of the Mandovi estuary, respectively; and from 0.6 to 2.9%, 233 to 1448 microg/g dw sediments, and 1.6 to 10.7 microg/g dw sediments in the Marmugoa harbour, respectively. Long chain, odd carbon n-alkanes (C(23)-C(33)) in the Mandovi estuary, whereas short chain, even carbon n-alkanes (C(11)-C(21)) in the Marmugoa harbour sediments were more abundant. The total HC concentrations, n-alkane composition, CPI, UCM and other evaluation indices suggest the dominance of terrestrial hydrocarbons in the estuarine while petroleum derived hydrocarbons in the harbour sediments. This conclusion was further supported by the abundance of hopanes with C(29) to C(34) alpha, beta compounds and steranes with C(27), C(28) and C(29) compounds in the harbour sediments.     

Characterization of dissolved organic carbon and Humic substances in the well water of the Blackfoot disease area in Taiwan

Since the early 1960s, many investigators have reported that blackfoot disease, a peripheral vascular disease, observed in southwestern Taiwan is due to drinking the higher arsenic concentration in well water. However, recent studies indicated that the relationship with blackfoot disease is not only with arsenic but also humic substances. This paper presents some results concerning the characterization (such as fluorescence, elemental composition, molecular weight and carbon distribution) of humic substances isolated from the Fuhsing well water of the blackfoot disease area. For comparison, the dissolved organic carbon (DOC) and humic substances in the normal well water from Chiuying and the Nanwan coastal water were also analyzed. In general, in the well water of the blackfoot disease area, extremely high concentrations of DOC (18.5mg/L) and fulvic acid (7.54mg/L) with high fluorescence intensity (59.1, equivalent to 0.0282uM quinine sulfate solution) and high percentages (over 50%) of low molecular weights of less than 1,000 were obtained compared with those of normal waters. C‐13 Nuclear magnetic resonance spectroscopy showed a high content (37.2%) of aromatic carbon. These higher concentrations of DOC and fulvic acid with the higher content of aromatic carbon in well water might be one of the key factors causing the blackfoot disease in Taiwan.