Evaluation of Polycyclic Aromatic Hydrocarbons Contamination in the Sediments of the Johor Strait,Peninsular Malaysia

In May 2013, sediment samples were collected from five stations in the Straits of Johor, near the southern tip of Peninsular Malaysia, in order to evaluate the distribution and sources of polycyclic aromatic hydrocarbons (PAHs). The concentrations of 16 United States Environmental Protection Agency PAHs varied from 650.5 to 1441.2 ng g ^?1 dry weight (dw) with a mean value of 985.5 ng g ^?1 dw. PAHs can be classified as moderate level pollution in the collected samples. When comparing PAHs in this study with that of the sediment quality guidelines (SQGs), it was found that the total PAHs, low molecular weight (LMW), and high molecular weight (HMW) PAHs might incur minimal adverse biological effects. The diagnostic ratios of individual PAHs indicated both petrogenic and pyrogenic origins with predominantly pyrogenic sources, the findings of which are further supported by the results from principal component analysis (PCA). The PCA results reveal contributions of 44.44%, 32.3%, and 18.96% for traffic-related, coal combustion, and petroleum-related products, respectively. These findings indicate that the effective monitoring and significant improvement resulting from the implementation of environmental regulations in Malaysia might have caused a shift in the source of petroleum hydrocarbons in the Straits of Johor's aquatic ecosystems from petrogenic to pyrogenic origins.     

Source Apportionment and Risk Assessment of Polycyclic Aromatic Hydrocarbons (PAHs) in Surface Sediments from Upper Reach of Huaihe River,China

Fifteen priority PAHs in 16 sediments from upper reach of Huaihe River collected in 2007 were measured. Source apportionment derived from PCA/MLR indicated that the highest contribution to ΣPAHs was from biomass burning (34.1%), followed by coal combustion (29.7%), vehicular emission (25.8%), and coke oven origin (10.4%). Risk assessment for each identified source was quantitatively calculated by combining the benzo[a]pyrene equivalent (BaPE) with estimated source contribution. The results showed that coal combustion posed the highest toxic risk, with BaPE value of 13.1 ng g^?1 dw, and the BaPE values for biomass burning, vehicular emission and coke oven were 5.6 ng g^?1 dw, 7.8 ng g^?1 dw, and 4.1 ng g^?1 dw, respectively. The distributions of contribution for total PAHs burden and BaPE of each identified source showed similar pattern among different sampling sites.     

Concentrations and Source Identification of Polycyclic Aromatic Hydrocarbons (PAHs) in Mangrove Sediments from North of Persian Gulf

The concentrations of 16 Environmental Protection Agency (EPA) priority polyaromatic hydrocarbons (PAHs) were quantified in surface sediments from Hormozgan Province mangroves, south of Iran in dry and wet seasons. Sampling stations were selected in Laft and Khamir mangroves with international importance. Polyaromatic hydrocarbons varied from 75.24 ± 11.24 to 581.94 ± 637.39 ng/g dry weight basis. Pollution sources and their contribution for polyaromatic hydrocarbons pollution in sediments of Hormozgan mangroves were appointed based on molecular ratios and statistical methods, including principal components analysis (PCA) and multiple linear regression/principal components analysis (PCA/MLR) tests. Both of pyrogenic and petrogenic sources contributed in detected concentrations of PAHs. Contribution percentages of pyrogenic and petrogenic origins were estimated at 73.20 and 26.79%, respectively. Temporal variations showed that sediments contained higher levels of ∑PAHs in wet season than dry time. However, the mean detected ∑PAHs was lower than international quality guidelines; the high concentration of PAHs was found in Laft mangrove, suggesting the presence of PAH polluted localized area.     

Three Centuries of Polycyclic Aromatic Hydrocarbons and Teriterpane Records In Tebrau Strait,Malaysia; Recent Pollution Concern in a Pristine Marine Environment

In the last century, application of fossil fuel as the primary source of energy caused environmental pollution in many countries including Malaysia. Polycyclic Aromatic Hydrocarbons (PAHs) are an important class of petroleum contamination. Two sediment cores were collected from the Tebrau Strait at the southern part of Peninsular Malaysia near the border line to Singapore, where entering into the South China Sea. The samples were sliced in certain intervals, extracted with Dichloromethane in Soxhlet apparatus, cleaned and fractionated in 2-steps column chromatography, and analyzed in Gas Chromatography – Mass Spectrometry. The results showed that PAHs input were started soon after World War II and exponentially increased from 1980 onward by 310 ng/g d. w., in comparison it was negligible and probably nature derived during 18^th and 19^th century. The application of compound-specific ratios and pentacyclic teriterpanes suggested the vicinity of sources that atmospherically transported to the sampling locations. They were originated from combusted oil of Southeast Asian and the Middle East, polluting urban sediment and street dusts prior to final deposition. Biomass burning appeared historically as a predominant minor background pollution of both cores. Remarkably, crankcase oil was not traced in this study while it was reported as a predominant source in Malaysia. This study suggested ocean-going ships and Singapore International Airport as the main sources of petroleum pollution in recent decades since there was insignificant rural development surrounding the studied area.     

LONG TERM MONITORING OF POLYCYCLIC AROMATIC HYDROCARBONS (PAHS) IN BLUE MUSSELS (Mytilus edulis) FROM A REMOTE SCOTTISH LOCATION

Farmed mussels have been collected on a monthly basis since 1999 from a remote site on the west coast of Scotland for polycyclic aromatic hydrocarbon (PAHs) analysis with the aim of establishing background concentrations as a benchmark against which to assess any environmental incident. Total PAH (2- to 6-ring parent and alkylated) concentrations ranged from 12.5 to 151.2 μg kg^?1 wet weight. Seasonal trends were evident with concentrations being significantly higher for samples collected between November and March compared to those collected between April and October. By taking the median of medians for each of these time periods two background concentrations are suggested for the total PAH concentrations (2- to 6-ring PAHs parent and alkylated); for April to October: 31.2 μg kg^?1 wet weight and for November to March: 62.9 μg kg^?1 wet weight. Individual PAH concentrations were mainly below the OSPAR Background Assessment Concentrations (BACs), where they are specified, and were only exceeded for the heavier 4- and 5-ring PAHs (fluoranthene, pyrene, benz[a]anthracene and benzo[a]pyrene) in samples collected between November and March. Differences were also seen in the PAH profiles with season. Mussels collected between November and March had a higher proportion of the heavier PAHs compared to mussels collected in the summer and autumn.     

Isolation and Characterization of Phenanthrene-Degrading Bacteria from PAHs Contaminated Mangrove Sediment of Thane Creek in Mumbai,India

Polycyclic aromatic hydrocarbons (PAHs), including phenanthrene, are commonly found as pollutants in soils, estuarine, and sediments, as well as in terrestrial and other aquatic ecosystems. In this context, the phenanthrene-degrading bacteria were isolated and characterized in contaminated mangrove surface sediment, on the coast of Thane Creek, Mumbai, India by enrichment method, using phenanthrene as the sole source of carbon and energy. The phylogenetic diversity of the isolates were evaluated by 16S rRNA gene analysis and characterized as Bacillus mojavensis strain KSS001, Bacillus firmus strain KSS002, Bacillus flexus strain KSS003, Bacillus vietnamensis strain KSS004, and Bacillus amyloliquefaciens strain KSS005. Each isolate was grown on the phenanthrene up to 100 mg/L and the biodegradation ability was evidenced using a gas chromatography–flame ionization detector. Further, the mean value of phenanthrene degradation by 5 bacterial isolates after incubation in mineral salt medium for 7 days was 63% at 100 mg/L. The study reports that mangrove sediments of Thane Creek, Mumbai, contain a diverse population of phenanthrene-degrading bacteria that have the potential and capability to degrade PAHs contaminated sites, and are consequently recommended for bioremediation.     

Polychlorinated Biphenyls in Sediments from Sicilian Coastal Area (Scoglitti) using Automated Soxhlet,GC-MS,and Principal Component Analysis

A methodology for the PAHs and PCBs congener determination in sediment samples has been revised. We determined the distributions of PAHs and PCBs in the superficial sediments of the Scoglitti (Italy) coastal area to provide data for comparison with other marine systems and to hypothesize the sources. Extraction yield, for PCB, was never less than 60% in most cases, while for PAHs, utilizing perdeuterated surrogate standard (benz[a]anthracene-d₁₂ and anthracene-d₁₀) was never less than 72%. The total concentration of the 16 PAHs investigated, expressed as the sum of concentrations, ∑PAHs, varied from 1–5087 μg/kg of dry matrix, while the ∑ PCBs ranged from detection limit to 36 μg/kg of dry matrix. Linear relationships were found between PAHs concentration and organic matter percentages (R² = 0.60) and water content and organic matter percentages (R² = 0.87). Isomeric ratios were used for discriminating between pyrolitic and petroleum origin. The principal component analysis (PCA) has been conduced to discriminate the different sampling sites in internal or external harbor area.     

Source and Toxicological Assessment of Polycyclic Aromatic Hydrocarbons in Sediments from Imo River,Southeastern Nigeria

Polycyclic aromatic hydrocarbons (PAHs) in sediments from the Imo River were analyzed to characterize their sources and assess their toxicity potential. The total PAH concentrations ranged from 409.43 to 41,198 ng/g dw with standard deviation of 4,796 ± 1,941. This wide variation reflects a localized contamination in the study area. The inadequacy in the use of traditional isomeric ratios for PAHs source characterization in sediment from tropical environments with shallow water depth of < 10 m was highlighted. A more robust principal component analysis coupled with n-alkanes unresolved complex mixture profiles approach to apportioned specific chemical signatures to samples was proposed. This approach differentiated stations that were heavily—from those that were mildly—impacted by oil and discriminated among stations that were influenced by pyrogenic sources. Effect range low (ERL) and effect range median (ERM) as well as risk quotients (RQwcs) revealed that only naphthalene, flourene, dibenzo(a,h)anthracene and low molecular weight PAHs were implicated with ERL and ERM exceeding the US National Oceanic and Atmospheric Administration's limit of concern and RQwcs > 1, as compounds of concern. The maximum toxicity equivalency value of 179.81 ng/g TEQs_carc measured for the illegal petroleum refinery site indicated that this site requires some control measure and remedial action.     

DETERMINATION OF POLYCYCLIC AROMATIC HYDROCARBONS (PAHs) IN SEDIMENTS AND BENTHOS COLLECTED ON THE COAST OF CHIBA

Eight polycyclic aromatic hydrocarbons (PAHs) including benzo[a]pyrene were analyzed in sediment and benthos collected on the coast of Chiba Prefecture in Japan by gas chromatography-mass spectrometry (GC/MS). The total concentration of the PAHs ranged from 8 to 18 μ g/kg-dry in the sediments and from 36 to 59 μ g/kg-wet in the benthos, Mactra quadrangularis, Scoletoma nipponica, and Arenicola basiliensis. The PAH composition in the sediments and the benthos was similar at four sampling points and dominated by phenanthrene (Phe), fluoranthene (Flu), and pyrene (Pyr). The ratios of abundance of Flu to that of Pyr, Flu/Pyr, and of Phe/anthracene suggest that the PAHs in the benthos are derived from the combustion of fossil fuels. The ratio, R, of the PAH concentration in the benthos to that in the sediment is 2.0 for Scoletoma nipponica and 1.8 for Arenicola basiliensis in average, indicating that the bioaccumulation is not significant in the benthos. However, the R value for perylene in Scoletoma nipponica was 3.7 times as large as the average.     

Aerobic biodegradation and inhibition kinetics of poly‐aromatic hydrocarbons (PAHs) in a petrochemical industry wastewater in the presence of biosurfactants

BACKROUND: In Izmir, Turkey, wastewaters from the petrochemical industry are treated using conventional activated sludge systems. A significant proportion of poly‐aromatic hydrocarbons (PAHs) with high‐molecular weights remains in this treatment system and inhibits the biological activity. Biosurfactants increase PAHs degradation by enhancing the solubility of the petroleum components. The aerobic inhibition kinetics of PAHs has not previously been investigated in the presence of biosurfactants for a real petrochemical industry wastewater. RESULTS: Among the kinetic models used (Monod‐type, zero, first‐order and second‐order) it was found that the Monod kinetic was effective for describing the biodegradation of PAHs in petrochemcal industry wastewater in the presence of three biosurfactants, namely Rhamnolipid (RD), Surfactine (SR) and Emulsan (EM) in an aerobic activated sludge reactor (AASR). The maximum PAH removal rate (R_max) and specific growth rate of PAH degrading bacteria (µ_max) increased, while the half saturation concentration of PAH (K_s) decreased at 15 mg L^?1 RD concentration compared with the control without biosurfactant at a sludge retention time (SRT) of 25 days. CONCLUSION: PAH oxidation is typified by competitive inhibition at RD concentrations > 15 mg L^?1 resulting in increases in K_s values with PAH accumulation. Low inhibition constant (K_ID) values reflect difficulties in the metabolizability of PAHs. Metabolite production decreased at RD = 25 mg L^?1 in the PAHs indeno (1,2,3‐cd) pyrene (IcdP), flourene (FLN), phenanthrene (PHE) and benzo(a)pyrene (BaP). Copyright © 2011 Society of Chemical Industry     

Fatty acid metabolism in young oysters,Crassostrea gigas: Polyunsaturated fatty acids

Tetraselmis suecica andDunaliella tertiolecta were grown for 24 hr in the presence of¹⁴C sodium bicarbonate and then fed separately to batches of juvenile oysters,Crassostrea gigas, for 3 days.D. tertiolecta contained fatty acids no longer than C₁₈; 22∶6ω3 was absent inT. suecica. Analysis of the oyster fatty acids by radio gas chromatography (GC) showed that oysters were able to incorporate some of the dietary¹⁴C label into long-chain fatty acids not supplied in the diet, e.g., C₂₀ and C₂₂ mono- and polyunsaturated fatty acids, and particularly 20∶5ω3. However, the low¹⁴C incorporation into fatty acids longer or more unsaturated than those supplied in the diet suggests that elongation and desaturation activity in young oysters is not sufficient to sustain optimum growth.     

Sorption of polycyclic aromatic hydrocarbons from aqueous solution by hexadecyltrimethylammonium bromide modified fibric peat

BACKGROUND: Fibric peat was modified by hexadecyltrimethylammonium bromide (HTAB) to improve its performance in sorption of polycyclic aromatic hydrocarbons (PAHs). The raw fibric peat (P‐R) and surfactant modified peat (P‐HTAB) were characterized by capillary rise test to determine the effect of HTAB on surface hydrophobicity. Effect of contact time was also investigated. Batch sorption data were fitted to the Freundlich model and pseudo‐second‐order model for isotherm and kinetics study. RESULTS: P‐HTAB had a more hydrophobic surface than P‐R. After modification, the sorption coefficients (K_OC) of naphthalene, phenanthrene and pyrene on fibric peat increased from 1590, 29661 and 204171 mL g^?1 to 2006, 52410 and 358569 mL g^?1, respectively; the sorption rate constants of naphthalene, phenanthrene and pyrene increased from 0.00057, 0.00036 and 0.00051 g µg^?1 min^?1 to 0.00062, 0.00140 and 0.00155 g µg^?1 min^?1, respectively. The sorption coefficients of PAHs were positively correlated with the octane‐water partition coefficients of PAHs. CONCLUSIONS: The hydrophobicity of fibric peat was enhanced through modification by HTAB, which resulted in the improved sorption rate and sorption capacity for PAHs. The sorption performance of P‐HTAB reveals that it is an effective biosorbent for PAHs and has potential for treatment of wastewater containing hydrophobic organic contaminants. Copyright © 2010 Society of Chemical Industry     

Polycyclic Aromatic Hydrocarbons Determination in Grilled Beef and Chicken

ABSTRACT

Polycyclic aromatic hydrocarbons (PAHs) are principally formed as a result of thermal treatment of food, especially grilling or barbecuing. In the present study, two types of Iranian popular grilled beef and chicken dishes (kebab) were analyzed for toxic PAHs, i.e., naphthalene, fluoranthene, phenanthtrene, anthracene, pyrene, and benzo(a)pyrene applying GC/MS. The differences in PAHs concentrations among grilled beef and chicken (kebab koobide and juje kebab) were found to be significant (p < 0.05), ranging from 0.29 to 21.95 ng·g^?1. Benzo(a)pyrene was found in nearly all samples; the maximum concentration of total PAHs was 21.95 ng·g^?1 found in grilled beef (koobide Khalij fars) and the lowest was 0.29 ng·g^?1 in grilled chicken (juje kebab) of Sahel restaurant.     

POLYCYCLIC AROMATIC HYDROCARBONS IN PRODUCTS OF A BEET SUGAR FACTORY IN VOJVODINA: LEVELS AND INTAKES

The levels of 16 EPA polycyclic aromatic hydrocarbons (PAHs) were investigated in samples of sugar beets and their products representative for a beet sugar factory located in the central part of Vojvodina, the main agricultural region in Serbia. The sum of the detected PAHs ranged from 51 pg g ^?1 ww for molasses to 391 pg g ^?1 ww for dried sugar beet pulp. The concentration of benzo(a)pyrene (BaP) for all sample types was about or less than 100 pg g ^?1 ww, which is far less than the existing Serbian and EU tolerances set for some foodstuffs. The Serbian intake of BaP via total sugar consumption that ranged from 70–85 g per capita day ^?1 , was assessed to be from 0.029 to 0.035 ng kg ^?1 b.w. day ^?1 . Furthermore, the toxic equivalency factor (TEF) approach was used to estimate the carcinogenicity of PAH mixture found in analyzed samples.     

Determination of reducing power of 56 Algerian plant products using olive (Olea europaea) oil as extraction solvent

This work evaluates the efficiency of olive (Olea europaea) oil (OO) as extraction solvent (referred to here as lipophilic extraction) for reducing power (RP) determination of 56 plant materials belonging to three plant product groups: medicinal plant leaves, fruit peels and green vegetable pulps. In addition, the sample which exhibited the greatest lipophilic RP (RP_lip) value in each studied group was characterized in terms of (1) RP_aq in the case of an aqueous extraction, (2) Pearson’s correlation coefficient (r) between RP values and color parameters of CIELab system, in the case of both lipophilic and aqueous extraction, and (3) diphenylpicrylhydrazyl (DPPH) radical scavenging activity (RSA) in the case of both lipophilic and aqueous extraction. Among all investigated plant products, the wormwood (Artemisia absinthium) leaves showed the highest RP_lip (～70?mg BHT equivalents(eq.)?×?g^?1 dry weight (dw)), while among fruits and green vegetables, the arbutus-berries (Arbutus unedo) peel (～53?mg BHT eq.?×?g^?1 wet weight (ww)) and eggplant (Solanum melongena) pulp (30?mg BHT eq.?×?g^?1, ww) gave the best results, respectively. Nevertheless, RP_lip negative values were obtained in numerous investigated samples. Regarding the additional characterization, any significant correlation was found between RP_lip and color parameters, whereas a significant perfect positive correlation (p?≤?0.05, r?～?1) was found between RP_aq and certain color parameters in the case of arbutus-berries and eggplant. Furthermore, the RSA results confirmed the predominance of wormwood lipophilic extract in terms of antioxidant potential. Considering the applied lipidic extraction procedure, the resulting data reflect the antioxidant potential of OO-based plant infusions.     

Pollicipes pollicipes as a Biomonitor of PAHs Contamination in Seawaters of the Northwest Coast of Portugal

Simple, fast, and economic solid phase microextration–gas chromatography–mass spectrometry (SPME–GC–MS) methods were validated for the determination of 8 United States Environmental Protection Agency priority polycyclic aromatic hydrocarbons (PAHs: naphthalene, acenaphthylene, acenaphthene, fluorene, phenanthrene, anthracene, fluoranthene and pyrene) in coastal seawaters and soft tissues of goose barnacles Pollicipes pollicipes. Under the optimized conditions, the limits of detection ranged from 0.012 to 1.069 ng L^?1 and 0.002 to 0.061 µg kg^?1 (dry weight basis) for seawaters and soft tissues, respectively. Precision varied between 3.9% and 20.0% for seawaters and between 8.4% and 19.1% for soft tissues, which are acceptable repeatabilities for environmental analyses. Finally, the accuracy of the optimized conditions also showed suitable recoveries, varying between 81.5% and 105.5% in spiked seawater samples and between 88.0% and 103.4% in the standard reference material for organics in mussel tissues (NIST SRM 2977). These methods were applied to a monitoring program performed along the northwest coast of Portugal during four seasons in 2011 in order to assess the levels of these compounds present in coastal waters and in the tissues of goose barnacles, one food resource of high commercial value. The results showed that although the concentrations of PAHs in seawaters and P. pollicipes varied significantly along the coast and between seasons (p < 0.05), in general the concentrations in seawater can be classified as “Class II – Good/Natural Background Concentrations” during the four seasons of 2011. As for the concentrations of PAHs in P. pollicipes, they were positively correlated (p < 0.05) with their concentrations in seawater, indicating that P. pollicipes may be an adequate biomonitor species of PAHs availabilities along the coast of Portugal throughout the year.     

HYDROCARBON POLLUTION ALONG MOROCCAN COASTS AND BPH ACTIVITY IN THE MUSSEL PERNA PERNA

Specimens of the mussel Perna perna were collected along Moroccan coasts to determine the concentrations of polycyclic aromatic hydrocarbons (PAHs) bioaccumulated in the tissues, and to measure benzo[a]pyrene hydroxylase (BPH) activity. Chemical analysis of PAHs show that the Mediterranean (Nador, Martil, Tanger) and central Atlantic coasts (from Rabat to Jorf Lihoudi) are those most contaminated (351 245 ng.g^{? 1} dry weight in Tanger). The mussel contaminants were of mixed origin for most of the locations with non negligible inputs of petrogenic origin in many of them. Baseline levels of PAHs were between 6 and 55 ng.g^{? 1} dry weight. BPH activity showed significant correlation (r _s = 0.64, P < 0.05) with total PAH concentrations at the six most contaminated stations. The baseline level of BPH activity can be identified as in the range 0.1 to 13 pmol.min^{? 1}.mg prot^{? 1} along the Mediterranean and Atlantic coasts.     

Priority Polycyclic Aromatic Hydrocarbons (PAHs): Distribution,Possible Sources and Toxicity Equivalency in Urban Drains

Wastewater from urban areas constitutes one of the major sources of pollutants contributed to aquatic ecosystem. This study was carried out to elucidate the occurrence and possible source of US Environmental Protection Agency identified 16 priority polycyclic aromatic hydrocarbons (PAHs) in water and sediments from the urban wastewater drains in Delhi, India. A total 60 samples (water and sediment) collected during year 2011–2012, and analyzed the following USEPA methods. Water and sediment samples were extracted using liquid-liquid and ultrasonication techniques, respectively. Glass column chromatography with activated silica was used for sample extracts clean-up, followed by quantification on HPLC equipped with diode array detector at 254 nm wavelength using mixture of acetonitrule and water as mobile phase. Concentrations of total 16 PAHs (∑16PAHs) in all drain water samples ranged from 0.29–35.22 μg/L (mean ± SD, 10.83 ± 10.66 μg/L), predominated by two- and three -ring PAHs. The ∑16PAHs concentrations in all collected sediments ranged between 220–19321 μg/kg (mean±SD, 5574 ± 6820 μg/kg) dry weights. High molecular weight PAHs (≥4-ring PAHs) were dominant in sediment samples. Benzo(a)pyrene equivalent (BaPeq), a relative carcinogenic potential to the corresponding PAHs to BaP was estimated and presented. A selected number of concentration ratios of specific PAHs compounds were calculated and used to diagnose the possible sources of PAHs contamination. The diagnostic ratios reflected pyrogenic input from gasoline or diesel powered vehicular emissions as the major source of PAHs. The levels of PAHs observed in water and sediments were compared with similar studies undertaken in other regions of the world.     

Distribution,Sources, and Risk of Polycyclic Aromatic Hydrocarbons in the Core Sediments from Baiyangdian Lake,China

The burial characteristics and risks of 16 polycyclic aromatic hydrocarbons (PAHs) in core sediments from Baiyangdian Lake were investigated through gas-chromato graphy/mass spectrometry. The total concentrations of the 16 PAHs ranged from 39.48–1877.75 ng g^?1. The low-molecular-weight PAHs (two- to three-ring PAHs) were the dominant species, contributing 40.10–92.18% to the total PAHs, with a mean of 71.01%. Based on the observed molecular indices and on principal component analysis, the PAHs inputs were initially dominated by biomass and coal combustion, and atmospheric deposition and surface runoff could be the major transport pathways. The contaminated source characteristics, hydrodynamic condition, and sediment textural composition are the key factors affecting the distribution and source of PAHs. By conducting a risk quotient analysis between specific PAH concentrations and their corresponding sediment quality values, the top layer sediments were found to have a potential biological impact and relatively high toxicity. However, such impact should have no impairment. The toxic potency of PAHs in Baiyangdian Lake could be described by using the toxic equivalent of benzo[a]pyrene.     

Using Urban Streams as Drinking Water: The Potential Risk in Respect to Polycyclic Aromatic Hydrocarbons (PAHs) Content in Sediments

Several polycyclic aromatic hydrocarbons are considered carcinogenic and mutagenic. 16 of these compounds are listed as priority control pollutants by the USEPA. The present study aimed at the evaluation of the presence of PAHs in sediments of an urban stream by GC-MS. The study area was located in Indaiatuba-São Paulo-Brazil, and supplies to approximately 40,000 people of a region with limited availability of water. Therefore, this water body flowing in the urban region represents a case study of the potential risk in using this water for drinking. The results show that, in general, the sampling site near the intake of the water treatment plant for human consumption had the highest concentration of total PAHs (247.7μg kg^?1). This is the site that presents more contact with urban pollution and surface runoff from the streets. The PAHs composition pattern by ring number presented a higher proportion of hydrocarbons of 4- and 5-rings, and showed a tendency, in the majority of the samples, of predominance of the high-molecular-weight PAHs, except for samples collected on June 2011 that had a high concentration of naphthalene (a 2-ring PAH). The application of a principal component analysis helped to identify the sources of hydrocarbons as pyrogenic (PC1) and petrogenic origin (PC2). Through this statistical tool it is postulated that, in some periods, the stream was exposed to point and non-point sources of contamination, showing that this type of water supply option has a high degree of vulnerability mainly during the first rain after of a long dry period, and its consumption can cause long-term problems.