Effects of oil dispersants on settling of marine sediment particles and particle-facilitated distribution and transport of oil components

This work investigated effects of three model oil dispersants (Corexit EC9527A, Corexit EC9500A and SPC1000) on settling of fine sediment particles and particle-facilitated distribution and transport of oil components in sediment-seawater systems. All three dispersants enhanced settling of sediment particles. The nonionic surfactants (Tween 80 and Tween 85) play key roles in promoting particle aggregation. Yet, the effects varied with environmental factors (pH, salinity, DOM, and temperature). Strongest dispersant effect was observed at neutral or alkaline pH and in salinity range of 0–3.5 wt%. The presence of water accommodated oil and dispersed oil accelerated settling of the particles. Total petroleum hydrocarbons in the sediment phase were increased from 6.9% to 90.1% in the presence of Corexit EC9527A, and from 11.4% to 86.7% for PAHs. The information is useful for understanding roles of oil dispersants in formation of oil-sediment aggregates and in sediment-facilitated transport of oil and PAHs in marine eco-systems.     

The effects of adsorptive materials on microbial community composition and PAH degradation at the sediment capewater interface

Capping with layers of inert or adsorptive materials is used to control the release of polycyclic aromatic hydrocarbons(PAH)in sediment but little is known about microbial degradation processes in these materials.A rich native microbial community inhabits the sediment bed,and capping media can influence enrichment and biodegradation activity of benthic microorganisms.The aim of this study was to evaluate the effects of capping media(sand,organoclay,and powdered activated carbon[PAC])on microbial communities under oxic conditions typical of the capewater interface,where naphthalene degradation(model PAH)is likely to be maximized.Bench scale experiments compared naphthalene concentrations,nahAc biomarker abundance,microbial community composition,and cellular attachment in systems amended with adsorptive and non-adsorptive capping materials.Results indicate that activated carbon promoted and enhanced bioactivity;PAC treatments showed high biodegradation rates,nahAc biomarker levels,and attached biological growth consistent with enrichment of the PAHdegrading genus Pseudomonae.In contrast,sand did not enhance biological activity compared to media-free systems.Naphthalene strongly influenced microbial community composition at the species level in all treatments except organoclay,which promoted biological signatures commonly associated with impeding degradation activity.Data overall suggest that adsorptive capping materials can both promote(PAC)and inhibit(organoclay)bioactivity in the surficial layer of caps,indicating that media selection is critical to the design of bioactive capping systems.     

Complex conductivity response to microbial growth and biofilm formation on phenanthrene spiked medium

Several laboratory studies have recently demonstrated the utility of geophysical methods for the investigation of microbial-induced changes over contaminated sites. However, it remains difficult to distinguish the effects due to the new physical properties imparted by microbial processes, to bacterial growth, or to the development of bacterial biofilm. We chose to study the influence of biofilm formation on geophysical response using complex conductivity measurements (0.1-1000 Hz) in phenanthrene-contaminated media. Biotic assays were conducted with two phenanthrene (PHE) degrading bacterial strains: Burkholderia sp (NAH1), which produced biofilm and Stenophomonas maltophilia (MATE10), which did not, and an abiotic control. Results showed that bacterial densities for NAH1 and MATE10 strains continuously increased at the same rate during the experiment. However, the complex conductivity signature showed noticeable differences between the two bacteria, with a phase shift of 50 mrad at 4 Hz for NAH1, which produced biofilm. Biofilm volume was quantified by Scanning Confocal Laser Microscopy (SCLM). Significant correlations were established between phase shift decrease and biofilm volume for NAH1 assays. Results suggest that complex conductivity measurements, specifically phase shift, can be a useful indicator of biofilm formation inside the overall signal of microbial activity on contaminated sites.     

http://www.sciencedirect.com/science/article/pii/S1674987112000424

Subcooled liquid solubility is the water solubility for a hypothetical state of liquid.It is an important parameter for multicomponent nonaqueous phase liquids(NAPLs) containing polycyclic aromatic hydrocarbons(PAHs),which can exist as liquids even though most of the solutes are solid in their pure form at ambient temperature.So far,subcooled liquid solubilities were estimated from the solid water solubility and fugacity ratio of the solid and(subcooled) liquid phase,but rarely derived from experimental data.In our study,partitioning batch experiments were performed to determine the subcooled liquid solubility of PAHs in NAPL-water system.For selected PAH,a series of batch experiments were carried out at increased mole fractions of the target component in the NAPL and at a constant NAPL/ water volume ratio.The equilibrium aqueous PAH concentrations were measured with HPLC and/or GCMS. The subcooled liquid solubility was derived by extrapolation of the experimental equilibrium aqueous concentration to a mole fraction of unity.With the derived subcooled liquid solubility,the fugacity ratio and enthalpy of fusion of the solute were also estimated.Our results show a good agreement between the experimentally determined and published data.     

Distribution and Sources of Polycyclic Aromatic Hydrocarbon （PAH） in Marine Environment of China

1INTRODUCTIONPolycyclicaromatichydrocarbons (PAHs)depo sit edinmarineenvironmentsfromavarietyofsourcessuchaswastewater,industrialanddomesticdischarges,andoilspills.Themajorityofthesesourcesfrompetrogenicoriginischaracterizedbyadominanceoflowmolecularweightaromaticcompounds,especiallynaphthaleneandalkylatedPAHs(Sportoletal.,1 983 ) .Crudeoilanditsrefinedproductssuchasgasoline,keroseneandotherfu eloilshaveahighcontentofalkylatedPAHsduetotheirslowformationattemperatureslowerthanthatofcomb…     

A laboratory and field comparison of sediment polycyclic aromatic hydrocarbon bioaccumulation by the cosmopolitan estuarine polychaete Streblospio benedicti (Webster)

Polycyclic aromatic hydrocarbon (PAH) bioaccumulation by the polychaete worm Streblospio benedicti (Webster) was measured under exposure to PAH-contaminated sediments in the field and for 28 d in the laboratory. Streblospio benedicti collected from field sediments contaminated at 2.94, 1.07, and l.52 μg g⁻¹ fluoranthene (FLU), benz[a]anthracene (BAA), and benzo[a]pyrene (BAP), bioaccumulated those PAHs at 1.53, 0.215, and 0.332 μg g⁻¹, while worms isolated from less contaminated field sediments (0.399, 0.228, 0.288 μg g⁻¹ FLU, BAA, and BAP) had FLU, BAA, and BAP body burdens of 0.543, 0.236, and 0.083 μg g⁻¹. Worms incubated for 28 d in PAH-spiked sediments (1.52, 0.991, 0.504 μg g⁻¹ FLU, BAA, and BAP) bioaccumulated those PAHs at 0.382, 0.966, and 0.602 μg g⁻¹, respectively. Data normalization to organism lipid and sediment organic carbon (biota-sediment accumulation factors [BSAFs] strongly suggest that Streblospio PAH bioaccumulation was directly related to percent sediment organic carbon, but BSAFs were substantially lower than predicted by equilibrium partitioning theory. BSAFs decreased with increasing PAH log K_ow, in worms collected from field sediments, but in spiked sediments BSAFs increased with increasing PAH hydrophobicity. This disparity may have been caused by insufficient spiked-sediment equilibration time (1.5h) in the case of the laboratory test sediments.     

Sources of polycyclic aromatic hydrocarbons in marine sediments from southern and northern areas of the Norwegian continental shelf

Variability in levels and sources of polycyclic aromatic hydrocarbons (PAH) in sediments from one large sea area off the coast of northern Norway (“North area”, NA) have been compared to similar data from another large area off the coast of southern Norway (“South area”, SA). Samples from NA were collected at the Norwegian continental shelf in south-western Barents Sea and north-eastern Norwegian Sea. Samples from SA were from the Norwegian Trench and the Skagerrak. Sediment cores have been dated, characterised by grain size distribution (GS) and organic carbon content (TOC), and the composition of PAH and geochemical biomarkers (alkanes and triterpanes) studied to provide an insight into the different sources of PAH. Generally, PAH levels are higher in sediments from SA compared to NA. A mixture of pyrogenic and petrogenic sources contribute to PAH levels in SA, while the contents of petrogenic PAH is negligible in surface sediments in NA. At some locations in NA, petrogenic PAH levels are elevated in the deepest sediment layers from pre-industrial times, indicating a natural input of petroleum through seepage. Occurrence of elevated levels of microbial hopanoids (hopenes) in the deepest sediment layers at some locations both in the north and the south indicate the presence of petroleum.     

Pollution characteristics of polycyclic aromatic hydrocarbons （PAHs） in oily sludge from the Zhongyuan Oilfield and its peripheral soils

The purpose of this study is to determine the degree of contamination caused by polycyclic aromatic hydrocarbons (PAHs) in oily sludge and soils around it in the Zhongyuan Oilfield. The contents of polycyclic aromatic hydrocarbons in oily sludge samples were determined with HPLC. The contents of PAHs of oily sludge from three different oil production plants vary from high to low in the order of the Wenming oily sludge dumping site of No. 3 Oil Production Plant (3W)>the Mazhai oily sludge dumping site of No. 3 Oil Production Plant (3M)>the Wen’er oily sludge dumping site of No. 4 Oil Production Plant (4W). Naphthalene, acenaphthylene, acenaphthene, fluorine and phenanthrene are the major pollutants of PAHs in oily sludge. The contents of PAHs in soil samples around the oily sludge dumping sites vary widely from 434.49 to 2408.8 ng/g. Naphthalene, acenaphthene, fluorine, phenanthrene and pyrene are the characteristic factors of PAHs in soil samples of 3M and 3W, and naphthalene, acenaphthene, fluorine and phenanthrene are the characteristic factors of PAHs in soil samples of 4W. According to these data and the ratios of Fl/Py, PAHs in oily sludge samples come mainly from petrogenic sources, and soil samples are divided into petrogenic soil samples and mixed-source soil samples, and both petrogenic and pyrogenic soil samples in terms of the sources of PAHs. The classification by Nemero index P indicates that soils around the oily sludge dumping sites have been seriously polluted.     

多环芳烃类标准物质使用时效性评价

为对半挥发性有机化合物标准物质的正确使用提供指导,选用美国ChemSevice公司生产的PPH-10RPM"甲醇中16种多环芳烃混合标准物质",将其分装于2 mL聚四氟乙烯衬盖棕色螺口样品瓶中于-18℃避光贮存,采用气相色谱-火焰离子化检测器方法测试各个特性量值随贮存时间的变化。结果表明,标准物质各个特性量测量的标准偏差在0.3~4.0μg/mL,最大相对标准偏差为3.92%。在置信度为95%时,2χ-检验表明测试结果的精密度适当,评价的测试方法可行;标准物质各特性量值在(100.0±7.2)μg/mL时,测量的偏差不显著。分装后的标准物质至多可保存80天,具体的保存期限还应结合标准物质所剩的有效期确定。