Possible causes of temporal fluctuations in primary production of the microphytobenthos in the Danish Wadden Sea

The effects of prior exposure to unlabelled naphthalene on the processes of uptake, tissue distribution and elimination of [1-¹⁴C] naphthalene by mussels (Mytilus edulis) were examined. Mussels collected from Whitsand Bay (S. W. England) in October 1980 were either held unexposed or exposed to unlabelled naphthalene (0.5 μg 1^?1) for 4 wk, prior to receiving a 4 h pulse of [1-¹⁴C] naphthalene in the medium (7 μg 1^?1). After 4 h exposure to [1-¹⁴C] naphthalene, the major tissues (digestive gland, gills, kidneys, mantle and remaining tissue) showed exponential depuration curves which could be resolved into two statistically significant components. The kinetics of elimination and the biological half-times of [1-¹⁴C] naphthalene in the tissues were determined. Mussels pre-exposed to unlabelled naphthalene had a significantly higher rate of elimination of [1-¹⁴C] naphthalene from the gills and kidneys. These results indicate that the toxicant, naphthalene, is actively excreted from the body by the gills and kidneys and the process is enhanced by prior exposure to the toxicant.     

Polycyclic aromatic hydrocarbons in Syrian olive oils and their likely daily intakes

The levels of 16 US Environmental Protection Agency polycyclic aromatic hydrocarbons (16 EPA PAHs) in Syrian olive oils have been determined. Forty-two samples including commercial extra virgin and virgin olive oils, and virgin olive oils from olive mills were analyzed. Only naphthalene (NAP) was detected in all olive oil samples under investigation. Among the studied 16 EPA PAHs, the highest maximum concentration was also observed for NAP (120 μg kg^?1). Moreover, three samples exceeded the European Union (EU) maximum level of 2 μg kg^?1 for benzo[a]pyrene (BaP) in oils and fats, and only one sample exceeded the EU maximum level of 10 μg kg^?1 for the sum of benz[a]anthracene, chrysene, BaP, and benzo[b]fluoranthene (PAH4). The likely daily intakes of the total sum of 16 EPA PAHs, the sum of eight genotoxic PAHs, the sum of PAH4, the BaP, and the BaP equivalent through consumption of Syrian olive oils were estimated.     

Occurrence of and risk posed by highly carcinogenic dibenzo[def,p]chrysene isomers in urban soil

Dibenzopyrene and its isomers are considered the most potent carcinogens of all polycyclic aromatic hydrocarbons tested to date. However, despite public concerns over their deleterious effects, they have not been extensively studied. The occurrence of four highly carcinogenic isomers of dibenzopyrene – dibenzo[def,p]chrysene, dibenzo[a,e]pyrene, dibenzo[a,i]pyrene, and dibenzo[a,h]pyrene in urban soil samples from Shanghai, China, have been determined in this study, as well as that of benzo[a]pyrene and coronene. A total of 14 peaks with ions at m/z 302 were detected by gas chromatography-mass spectrometry. Although the concentrations of benzo[a]pyrene and the sum of the 16 priority polycyclic aromatic hydrocarbons were greater than that of dibenzopyrene and its isomers, the carcinogenic potency of the latter was higher than that of benzo[a]pyrene. The results also indicate that the relative carcinogenic potency of the four dibenzopyrene isomers in the samples is higher than that of the 16 priority polycyclic aromatic hydrocarbons.     

Effect of the chemical composition of organic extracts from environmental and industrial atmospheric samples on the genotoxicity of polycyclic aromatic hydrocarbons mixtures

Particulate organic matter (PM) present in the atmosphere is a complex mixture of chemicals like polycyclic aromatic hydrocarbons (PAH) that may exert adverse health effects including respiratory and cardiovascular disturbances and cancer. In this study, airborne samples from environmental or industrial areas exhibiting different physicochemical composition were compared for their capacities to induce DNA damage in human hepatocytes HepG2. DNA strand breaks and DNA adducts formed by benzo[a]pyrene-7,8-dihydrodiol-9,10-epoxide (BPDE), the most reactive metabolite of the carcinogenic benzo[a]pyrene (B[a]P), were measured with the comet assay and by high-performance liquid chromatography (HPLC)/mass spectrometry, respectively. Cells were exposed to organic matter extracted from PM. Experiments were performed either at a constant concentration of B[a]P or at concentrations corresponding to fixed air volumes. Results show that industrial extracts tend to produce more benzo[a]pyrene diol epoxide-N ²-2′-deoxyguanosine (BPDE-N ²-dGuo) DNA adducts than strand breaks, whereas the opposite was observed with environmental extracts. The chemical composition of the extracts significantly impacts the nature and levels of DNA damage. The amount of B[a]P and interaction with other contaminants in the extracts need to be considered to explain the formation of DNA damage. These results emphasize the use of in vitro tests as promising and complementary tools to widely used toxic equivalent factor (TEF) approach in order to assess health hazards related to chemical exposure of the general population.     

Distribution of benzo[a]pyrene in discrete regions of rat brain tissue using light microscopic autoradiography and gamma counting

In order to study the distribution of benzo[a]pyrene (B[a]P) in rat brain, Sprague-Dawley male rats, 21-day-old, weighted 40–50 g were given a single intravenous (iv) injection of 3.7 × 10⁵ Bq kg^?1 of ¹⁴C-B[a]P. Rats were sacrificed at 1, 6, 12, 24, or 48 h after the administration of radiolabeled B[a]P. Light microscopic autoradiography and gamma counting were used. Gamma counting and light microscopic autoradiography showed that ¹⁴C-B[a]P localized in hippocampus at 1 h, in cerebral cortex at 6 h, and corpus striatum at 24 h after treatment. After B[a]P administration, silver grains rose with time reaching a peak at 24 h and sharp decrease at 48 h. The silver grains distribution was higher in neurons than in gliocytes. Thus, B[a]P penetrated the blood-brain barrier and distributed in various regions of rat brain.     

Uptake and accumulation of naphthalene by the oyster Ostrea edulis,in a flow-through system

A flow-through system was used to follow naphthalene and naphthalene metabolite accumulation in the seawater and in the tissue of the oyster Ostrea edulis. After 72 h, 82.5% of the naphthalene carbon was recovered from the system. Glucose was added to seawater to stimulate the pathways of glucose metabolism in the oysters. Streptomycin (100 ppm) reduced microbial oxidation of naphthalene and glucose, and reduced bacterial growth. However, even in the presence of streptomycin, microbial oxidation of naphthalene was considerable. The main oxidation product recovered from seawater was ¹⁴CO₂. Radioactivity was also associated with compounds which separated by TLC with 2- and 1- naphthol. The pattern of naphthalene uptake and accumulation in oyster tissues was relatively constant after only a few hours of exposure to naphthalene. The potential of tissues to accumulate naphthalene was shown to be a function of multiple variables such as nutritional state, lipid concentration, length of exposure to naphthalene, and the external naphthalene concentration. Carbon-14-labeled metabolites derived from ¹⁴C-naphthalene were consistently recovered from digests of the oyster tissues. Non-CO₂ alkaline-soluble substances were the primary metabolites. Hexane-extractable substances, which separated by TLC with known standards of 2- and 1- naphthol, were consistently recovered from seawater and tissue digests. It was not possible to conclude that these metabolites were a result of naphthalene metabolism by oyster enzyme systems.     

UVR-induced toxicity of sludge and polycyclic aromatic hydrocarbons on seed germination and seedling growth of Triticum aestivum L.

The depletion of the ozone layer and enhancement of solar radiation may exert an adverse influence on the ecosystem. Phototoxicity of sludge and polycyclic aromatic hydrocarbons (PAHs) under ultraviolet radiation (UVR) to seedling was studied. Seeds of wheat (Triticum aestivum) were planted in sludge and PAHs (anthracene (An), benzo(a)pyrene (BaP) and pyrene (Py)) with and without UVR. Toxicity of sludge increased in the presence of UVR in wheat. UVB radiation was found to be more hazardous than UVA radiation. Results demonstrated that An, BaP and Py induced phototoxicity at various concentrations (1–10?µg/mL) under UVA (1.5?mW/cm²) or UVB (1.08?J/cm²) exposure. The pattern of phototoxicity was An?>?Py?>?BaP to shoot length, root length, and fresh weight; chlorophyll, protein content, enzyme activity of catalase and α-amylase were reduced while the activity of superoxide dismutase and starch was enhanced. Reduction in seedling growth and biochemical parameters may be related to less photosynthesis, less nutritional uptake, and distortion of root cap. Thus, the synergistic effect may be due to alterations in photosynthesis, phytohormones, or nutritional uptake.     

The deployment of γ-irradiation for reducing polycyclic aromatic hydrocarbons and microbial load in wheat kernels

Food contamination may contribute to serious human health problems. In this work, the effect of γ-irradiation 0, 5, 10, and 15 kGy doses on the removal of polycyclic aromatic hydrocarbons from wheat kernels was investigated. Additionally, variations in the contents of 16 congeners on bacterial load and other chemical parameters were studied. Polycyclic aromatic hydrocarbons concentrations were determined by high-performance liquid chromatography followed by fluorescence detection. The effects of γ-irradiation on the concentrations varied for each congener, with the highest irradiation dose being the most effective. Benzo[a]pyrene was reduced by ～50%, and the total concentration of all congeners decreased dramatically from 154 to 21 µg.kg^?1 upon 15 kGy irradiation at a dose rate of 8.49 kGy h^?1. The total bacterial load was reduced from 2.4 to < 1 log₁₀ cfu g^?1, while wheat chemical properties were not affected.     

北京地区表层土壤中多环芳烃的分布特征及污染源分析

根据北京地区不同环境功能区62个样品的分析结果,讨论了研究区表层土壤中多环芳烃的分布特征及污染源类型。结果表明：（1）研究区表层土壤中检测到的多环芳烃主要包括萘、苊、菲、惹烯、三芴、荧蒽、芘、、苯并蒽、苯并[b]荧蒽、苯并[k]荧蒽、苯并[e]芘、苯并[a]芘、苝、二苯并[a,h]蒽、茚并[1,2,3–cd]芘、苯并[g,h,i]苝及其同系物;（2）不同环境功能区表层土壤中多环芳烃的组成及质量分数均存在一定的差别,16种优先控制的多环芳烃质量分数为175.1~10 344 ng.g-1,其中城市中心区表层土壤中多环芳烃的质量分数最高,交通干线附近、工矿企业附近表层土壤中PAHs的质量分数较高,林地、果园和农田表层土壤中PAHs的质量分数较低;（3）表层土壤中PAHs既有来源于石油源,也有来源于化石燃料燃烧产物的,但不同功能区二者贡献存在差别,其中农业用地（林地、果园、农田）中PAHs主要来源于石油源（或部分来源于土壤母岩中的有机质）,城区、交通干线附近及工矿企业附近表层土壤中PAHs污染源以化石燃料燃烧产物输入为主。     

Comparison between the carbon-14 and oxygen consumption method for the determination of the activity of heterotrophic bacterial populations

The activity of the heterotrophic microbial population in the saline Lake Grevelingen (The Netherlands) and the Mediterranean Etang Salses Leucate (France) was determined by measuring the oxygen consumption rate, and the uptake of ¹⁴C-labelled glycollate, pyruvate and an amino acid mixture. The maximum uptake rate of the applied organic compounds in Lake Grevelingen was generally less than 10% of the carbon mineralization rate calculated from the oxygen consumption experiments. Only for pyruvate and glycollate higher values were found of about 30 to 40% with one exceptionally high value for pyruvate of 149%. However, these higher percentages were found in winter, when the activity of the heterotrophic microbial population was very low. In Etang Salses Leucate higher maximum uptake rates of the ¹⁴C-labelled compounds were found, relating this uptake to the oxygen consumption rate. Yet the maximum uptake rate is still always lower than 35% of the carbon mineralization calculated from the oxygen uptake rate. Taking into account that maximum uptake rates were considered, the results demonstrate that the uptake of ¹⁴C-labelled organic compounds represents a serious underestimation of the activity of the bacterial population in situ. The extent of the underestimation depends on the water type. It was concluded that the determination of the heterotrophic activity by measuring oxygen consumption rates offers a better insight into the carbon mineralization process in natural waters than the uptake experiments with ¹⁴C-labelled substrates.Communication no. 228 of the Delta Institute for Hydrobiological Research, Yerseke, The Netherlands     

Multiple-time contamination of benzo(a)pyrene in soils inhibits soil enzymatic activities

Benzo[a]pyrene (B[a]P) is accumulating in soils in a low-dose cumulative manner. The objectives of this study were to investigate the effects of B[a]P on the extractable and available fractions of B[a]P and on soil enzymatic activity using multiple-time superimposed and one-time contamination approaches. Results showed that the contents of B[a]P rapidly decreased in the first 14?d and later decreased slowly from 14 to 56?d in both one-time and multiple-time contamination tests. The contents of B[a]P in the multiple-time contamination test were lower than those in the one-time test. Soil urease, sucrase and dehydrogenase activities were rapidly inhibited in the early stage (14?d) and stimulated during the rest of the incubation, and soil dehydrogenase activity was more sensitive to B[a]P contamination than the other enzymes. High concentrations of B[a]P in soil led to greater inhibition of enzymatic activity than that at low concentrations in the early period of culture. Soil enzyme activities were weakly inhibited in multiple-time compared with in one-time contamination tests and were lower in the subsurface layer than in the surface layer. Our results revealed that the multiple-time superimposed approach might be better than one-time contamination for evaluating B[a]P risk in soil.     

Occurrence of PCBs and PAHs in an urban soil of Madrid (Spain)

Polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs) were analysed in surface soil samples collected in 2001–2002 at an open urban area of Madrid. In order to obtain representative samples, three collection points at the site were chosen. The most abundant PAHs and PCBs were phenanthrene, fluorene, pyrene, chrysene and benzo[a]pyrene and hexa- and heptachlorinated PCBs, respectively. The sum of selected PAHs (13 compounds) and PCBs (15 congeners) averaged 1 and 0.1?µg?g^?1, respectively. PCB levels in winter were 2–10 times higher than summer ones, while seasonal variation for most of PAHs were not observed. Good correlations among all PCBs were found. Five PAHs were also well correlated.     

Hydrocarbon metabolism in the intertidal fiddler crab Uca pugnax

The fiddler crab Uca pugnax was examined for its ability to metabolize foreign hydrocarbons. The microsomal mixed function oxidase system was identified in U. pugnax tissues using Aldrin epoxidation rates as the assay. Rates were slow: 96 pM Dieldrin per mg microsomal protein per hour in the hepatopancreas, 438 pM mg^-1 h^-1 in the gill, and 228 pM mg^-1 h^-1 in claw-muscle microsomes. Using standard methods, no difference in rates could be detected between crabs living in clean areas and those living in environments highly contaminated with foreign hydrocarbons. In vivo rates of naphthalene oxidation were measured and used to calculate a clearance time for U. pugnax body tissues based on the aromatic hydrocarbon content of crabs collected from an oil-polluted salt marsh. Calculated clearance time was beyond the life span of the crab. It is concluded that this minimal ability of U. pugnax to metabolize foreign hydrocarbons partially accounts for its sensitivity to oil pollution in the environment.     

渤海北部典型芳香烃类化合物污染状况及生态风险评价

为探究渤海北部海上油气区及周边近岸海域典型芳香烃类化合物污染状况,2015年5月现场采集了32个站位的海水样品,针对7种苯系物(BTEX)和17种多环芳烃(PAHs)进行测定,并采用商值法和毒性当量法对污染物开展单一和联合生态风险评估。结果显示,研究海域海水中7种苯系物总含量范围为65.1～222.6 ng·L~(-1),以甲苯含量最高,表层含量略低于底层,油气区平均含量低于周边近岸,受到陆源污染输入的影响特征明显。表层海水中ΣPAHs含量范围为98.9～356.0 ng·L~(-1),平均值为184.5 ng·L~(-1),以低环芳烃占优势,总体处于中等水平,比值法判定该海域PAHs可能主要来源于石油及其加工产品。该海域海水中苯并(a)芘的风险商RQ值大于0.1,表现出低度风险,其余3种处于可接受水平。4种芳香烃类化合物联合生态风险等级为低度风险,对生态系统具有潜在的不利影响,但不同区域仍存在一定差异性,海上石油开采与陆源输入是影响该海域个别区域生态风险较高的重要因素。     

Uptake and Dupuration of Petroleum Hydrocarbons By the Backwater Clam,Meretrix Casta Chemnitz

Meretrix casta were experimentally exposed to water soluble fractions of refined and crude oil and their rate of accumulation of the petroleum hydrocarbons including total and individual aromatics viz., naphthalene, methylnaphthalene and dimethylnaphthalene, was studied. Subsequent transfer to clean waters in the laboratory and field resulted in depuration of the accumulated hydrocarbons from tissues. in general, the rate of discharge was found to be dependent on the concentration that the animals had been earlier exposed to and also the alkylation of aromatic hydrocarbons. Occasional increases were observed in the hydrocarbon values of clams which were placed in the field, compared to their laboratory counterparts, suggesting an intermittent source of petroleum hydrocarbon input into the environment. the influence on the rate of uptake, release and retention of hydrocarbons in the clams is discussed.     

Combined ultrasound with Fenton treatment for the degradation of carcinogenic polycyclic aromatic hydrocarbons in textile dying sludge

To develop an effective method to remove the toxic and carcinogenic polycyclic aromatic hydrocarbons (CPAHs) from textile dyeing sludge, five CPAHs were selected to investigate the degradation efficiencies using ultrasound combined with Fenton process (US/Fenton). The results showed that the synergistic effect of the US/Fenton process on the degradation of CPAHs in textile dyeing sludge was significant with the synergy degree of 30.4. During the US/Fenton process, low ultrasonic density showed significant advantage in degrading the CPAHs in textile dyeing sludge. Key reaction parameters on CPAHs degradation were optimized by the central composite design as followed: H₂O₂ concentration of 152 mmol/L, ultrasonic density of 408 W/L, pH value of 3.7, the molar ratio of H₂O₂ to Fe²⁺ of 1.3 and reaction time of 43 min. Under the optimal conditions of the US/Fenton process, the degradation efficiencies of five CPAHs were obtained as 81.23% (benzo[a]pyrene) to 84.98% (benz[a]anthracene), and the benzo[a]pyrene equivalent (BaP_eq) concentrations of five CPAHs declined by 81.22–85.19%, which indicated the high potency of US/Fenton process for removing toxic CPAHs from textile dyeing sludge.     

Novel method for in situ visualization of polycyclic aromatic hydrocarbons in mangrove plants

Two-photon laser confocal scanning microscopy (TPLCSM) was first used to visualize the uptake and movement of naphthalene (NAP), phenanthrene (PHE), and pyrene (PYR), from separately contaminated hydroponics solutions into living Kandelia candel (L.) Druce seedlings. With this non-destructive and non-chemical extraction technique, the experimental results revealed that three types of polycyclic aromatic hydrocarbons (PAH) were observed moving into the K. candel and its translocation to radicle, hypocotyl and leaf, and the transmission rates of these PAH in the K. candel were in the order of NAP?>?PHE?>?PYR. Data demonstrate the manner in which PAH enter, transport, and distribute within the K. candel, and provided us some valuable information on uptake and translocation mechanism of PAH. These findings may help to optimize the phytoremediation strategies of PAH in mangrove wetlands.     

烧烤场景中基于PBPK模型的人群PAHs暴露评估

为探究烧烤场景中人群多环芳烃(PAHs)的暴露特征与健康风险,使用美国环保署推荐的计算模型和基于生理的药代动力学模型(PBPK)模拟了我国人群的PAHs外暴露剂量和健康风险以及内暴露剂量变化情况。结果表明:1)普通居民和职业人群的日均苯并[a]芘等效摄入剂量为(50±3)ng·d~(-1)和(179±98)ng·d~(-1),其终生致癌风险为7.57×10~(-7)~1.28×10~(-5),均在可接受范围内;2)普通居民暴露后体内组织中PAHs内暴露标志物芘的最大浓度范围依次为肝(6.52~8.67 ng·L~(-1))肾(0.97~1.12 ng·L~(-1))静脉血(0.71~0.94 ng·L~(-1))皮肤(0.64~0.75 ng·L~(-1))脂肪(0.36~0.56 ng·L~(-1)),职业人群暴露后体内组织芘最大浓度为脂肪(2.97ng·L~(-1))皮肤(1.14 ng·L~(-1))≥肾(1.14 ng·L~(-1))肝(0.57 ng·L~(-1))静脉血(0.17 ng·L~(-1));3)膳食是普通人群的主导暴露途经,会导致肝组织浓度最大;呼吸和皮肤接触是职业人群的主导暴露途经,会导致脂肪组织浓度最大;4)暴露标志物芘的组织总富集量关系为职业人群(48 ng·d~(-1))大于普通人群(6~11 ng·d~(-1))。     

PAHs in organic film on glass window surfaces from central Shanghai,China: distribution,sources and risk assessment

Polycyclic aromatic hydrocarbons (PAHs) concentrations were analysed in the organic film on the glass surfaces of different functional areas in central Shanghai. Concentration levels of total PAHs in the organic film ranged from 1,348.5 to 4,007.9 ng m^?2. The concentration of PAHs was lowest in parks and green spaces (1,348.5 ng m^?2) and highest in traffic zones (4,007.9 ng m^?2). A concentration gradient of total PAHs was observed as follows: traffic zones > commercial areas > cultural and educational areas > parks and green spaces. The distribution of PAHs was characterised by 3–4 ring PAHs in the study areas. The most abundant PAHs were phenanthrene (20.5 %), fluorene (16.7 %), pyrene (12.4 %) and chrysene (Chry) (11.2 %). The mass of the bulk film was composed of organic and inorganic compounds and ranged from 246 to 1,288 mg m^?2. The bulk film thickness varied from 144 to 757 nm in the different functional areas. The ratios of An/178 and Fl/202 and principal component analysis suggested that PAHs came mainly from the mixed sources of fossil fuel, coal and incomplete combustion of biomass. Benzo[a]anthracene (BaA)/Chry is not suitable for use as a tracer for the transmission process of PAHs because of the rapid depletion of BaA in the organic film by photooxidation during daylight hours. The concentration of benzo[a]pyrene equivalent (BaPeq) varied from 21 to 701 ng g^?1, and the major carcinogenic contributors of the 16 PAHs were BaP, DahA, B[b/k]F and InP, accounting for 83 % of BaPeq.