Polycyclic aromatic hydrocarbons (PAHs) in bottom sediments of the Kara Sea shelf,Gulf of Ob and Yenisei Bay

PAH concentration and distribution has been examined in surface sediments samples from the Kara Sea, Russia. The study includes 13 samples from the South-eastern Kara Sea shelf, one sample from the south-western part of the sea, 4 samples from the Baydaratskaya Bay, 5 samples from the Gulf of Ob and 4 samples from the Yenisei Bay, collected in August-September 1993-1994. Cluster analysis and principal component analysis (PCA) were used to identify common patterns and possible sources of PAHs. The total PAH concentration (sum of two- to six-ring aromatic hydrocarbons) in the Kara Sea sediments was generally lower than in the Barents Sea sediments and comparable to the levels in the Pechora and White seas. Two- and three-ring aromatic hydrocarbons predominated in Kara Sea sediments, which indicate a relatively stronger petrogenic origin than that in the adjacent seas. The highest total PAH concentrations within the Kara Sea were found in sediments from the Yenisei Bay and in the South-western part of the Kara Sea in the Eastern Novaya Zemlya Trough. The PAHs of the Yenisei Bay sediments were dominated by perylene and PAHs of petrogenic origin, but had also a strong indication of PAHs of pyrogenic origin. The dominating PAH group in the South-western part of the Kara Sea were four- to six-ring aromatic hydrocarbons, indicating pyrogenic origin. Perylene levels were high in all the Kara Sea samples, and highest levels were found in areas of strong terrigenous influence. The most probable source is decaying peat products being transported to the Kara Sea by both large and small rivers.     

Polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs) in sediments from the Mersey Estuary, U.K

Sediments from the Mersey Estuary were analysed for polycylic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs). Total PAH concentrations ranged from 626 to 3766 microg/kg and total PCB concentrations ranged from 36 to 1409 microg/kg. These concentrations are intermediate in comparison to other U.K estuaries with similar histories of industrialisation and urbanisation. The distribution of individual PAHs were consistent throughout the Mersey Estuary, this together with molecular indices suggests mainly pyrolitic inputs, augmented by a variety of industrial petrogenic sources. Comparison of tri-to-hepta PCB congeners revealed multiple sources and inputs throughout the estuary. A sediment core collected in close proximity to Garston Docks revealed the take-off, peak pollutant input and recent decline of PCB pollution. However, a second depth profile of sediments at Ellesmere Port showed little change in total or individual PCB concentrations due to extensive sediment reworking and mixing.     

Polycyclic aromatic hydrocarbons (PAHs) in agricultural soil and vegetables from Tianjin

Several types of vegetables were collected from two contaminated sites in Tianjin, China. The bulk soil and the rhizosphere soil samples were also collected from the same plots. Sixteen PAHs in the samples were measured. The total concentrations of PAH16 in the bulk soil from the two sites were 1.08 and 6.25 microg/g, respectively, with similar pattern. The concentrations of PAH16 and individual compounds in the rhizosphere were significantly higher than those in the bulk soil with mean values of 2.25 and 7.82 microg/g for the two sites, respectively. The contents of both total and dissolved organic matter in the rhizosphere were also higher than those in the bulk soil. Almost all PAH compounds studied were detected in both roots and aerial parts of the vegetables studied. Abundance of higher molecular weight PAHs in vegetable, however, was lower than that in soil. Concentrations of PAH16 in vegetable were higher than those reported in the literature for other areas. It appears that agricultural soils and vegetables in Tianjin, especially those from the site located immediately next to an urban district and irrigated with wastewater for several decades, are severely contaminated by PAHs. Among the eight types of vegetable studied, the highest concentration of PAHs was found in cauliflower. By average, the concentration of PAH16 in the aerial part of vegetables was 6.5 times higher as that in vegetable root, suggesting that foliar uptake is the primary transfer pathway of PAHs from environment to vegetables.     

Polycyclic aromatic hydrocarbons (PAHs), nitrated PAHs and oxygenated PAHs in ambient air of the Marseilles area (South of France): concentrations and sources

Ambient measurements (gas+particle phases) of 15 polycyclic aromatic hydrocarbons (PAHs), 17 nitrated PAHs (NPAHs) and 9 oxygenated PAHs (OPAHs) were carried out during July 2004 on three different sites (urban, sub-urban and rural) in the region of Marseilles (South of France). Atmospheric concentrations of these classes of polyaromatics are great of interest because of their high potential mutagenicity and carcinogenicity. OPAH concentrations were of the same order of magnitude as those of PAHs while NPAH concentrations were one to two orders lower. 9-Fluorenone and 9,10-anthraquinone were the most abundant OPAHs, accounting for about 60% and 20% of the total OPAH concentration. Respectively 1-and 2-nitronaphthalene were the most abundant NPAHs and were accounting for about 30-50% and 15-30% of the total NPAH concentration. NPAHs and OPAHs concentration levels were consistent with the characteristics of the sampling sites. Study of source specific ratios (2-nitrofluoranthene/1-nitropyrene) clearly showed those primary NPAH sources influence the urban and sub-urban sites whereas production of secondary NPAHs by gas phase reactions was prevalent at the rural site. The study of NPAH and OPAH sources suggested that gasoline engines were an important source of such compounds Whereas the dominant source of 1-nitropyrene, 2-nitrofluorene, 6-nitrochrysene and benz[a]anthracene-7,12-dione seems to be diesel vehicles. Finally, 9,10-anthraquinone presents a double origin: primary diesel emission and photochemical processes. Formation of 9,10-anthraquinone from anthracene ozonation was shown at the rural site. Further investigations will be necessary in order to discriminate when (before or during the sampling) the OPAHs are formed.     

Polycyclic aromatic hydrocarbons in nearshore marine sediments of Australia.

The occurrence and fate of polycyclic aromatic hydrocarbons (PAH) in nearshore marine sediments of Australia is discussed. Available information indicates that PAH are accumulating in the sediments and organisms of estuaries and harbours with both highly urbanized/industrialized and non-urban catchments. PAH levels in polluted sediments are similar to those of grossly polluted areas of Japan, North America and Europe, however PAH sources cannot be identified from the information available. PAH appear to persist in reducing environments, while in relatively pristine environments that have been previously exposed to PAH, conditions are probably favourable for the aerobic degradation of PAH by microorganisms.     

Source apportionment of polycyclic aromatic hydrocarbons (PAHs) in surface sediments of the Huangpu River, Shanghai, China

We applied cluster analysis and principal component analysis (PCA) with multivariate linear regression (MLR) to apportion sources of polycyclic aromatic hydrocarbons (PAHs) in surface sediments of the Huangpu River in Shanghai, China, based on the measured PAH concentrations of 32 samples collected at eight sites in four seasons in 2006. The results indicate that petrogenic and pyrogenic sources are the important sources of PAHs. Further analysis shows that the contributions of coal combustion, traffic-related pollution and spills of oil products (petrogenic) are 40%, 36% and 24% using PCA/MLR, respectively. Pyrogenic sources (coal combustion and traffic related pollution) contribute 76% of anthropogenic PAHs to sediments, which indicates that energy consumption is a predominant factor of PAH pollution in Shanghai. Rainfall, the monsoon and temperature play important roles in the distinct seasonal variation of PAH pollution, such that the contamination level of PAHs in spring is significantly higher than in the other seasons.

Brief

We apportion PAHs in surface sediments of the Huangpu River and show that coal combustion, traffic-related pollution, and petroleum spillage are the major sources.     

Polycyclic aromatic hydrocarbons (PAHs) in urban surface dust of Guangzhou, China: Status, sources and human health risk assessment

Ninety-six urban surface dust samples collected from Guangzhou, a typical urban center in South China, were analyzed for 16 PAHs (2-6 rings). ∑ PAHs concentrations in the urban surface dust ranged from 0.84 to 12.3 μg/g with a mean of 4.80 μg/g. High molecular weight compounds (4-6 rings) contributed to 62 to 94% of ∑ PAHs mass in the surface dust samples. Four hotspots with highest ∑ PAHs were identified via kriging prediction mapping, representing the highly-urbanized regions: central downtown, highway and industrial area. Two major origins of PAHs inputs to urban surface dust were identified as vehicle emissions (51.9%) and coal combustion (26.8%). The 95% UCL of Incremental Lifetime Cancer Risk (ILCR) due to human exposure to urban surface dust PAHs in central South China was 3.03 × 10⁻⁶ for children and 2.92 × 10⁻⁶ for adults.     

Distribution patterns of polycyclic aromatic hydrocarbons (PAHs) in the sediments and fish at Mai Po Marshes Nature Reserve, Hong Kong

Sediment samples were collected monthly from eight shrimp shallow ponds (local name gei wais) from July 2003 to January 2004, and from mangrove swamps and inter-tidal mudflats in July and November 2003, respectively. Fish samples (tilapia) were also collected. Polycyclic aromatic hydrocarbons (PAHs) were analyzed by gas chromatography and mass spectrometry (GC/MS). The results indicated that under wet season wet deposition and suspended particulates brought in by nearby rivers, such as the Peal River, served as an important source of PAHs entering Mai Po Marshes. Total organic matter in the sediments showed significant correlations (p<0.01) with PAHs in the sediments, mainly due to the mechanism that organic matter such as humic substances increased PAH persistence by binding and occluding PAHs. Except for naphthalene, biota-sediment accumulation factors (BSAF) of the PAHs in tilapia were below 1.7, which may be caused by biotransformation and the lower uptake in fish. In addition, aqueous route dominated accumulation of non-biodegradable PAHs in tilapia because higher levels were detected in larger fish than in smaller ones. A general trend was observed that BSAFs declined with the increase of K(ow) values, which suggested that bioavailability of low K(ow) isomers was high due to higher gill transfer efficiencies (aqueous uptake) in fish but enhanced biotransformation and decreased gut assimilation (dietary uptake) resulted in decreased accumulation of more hydrophobic PAHs (high K(ow)). Lastly, viscera appeared to be a promising tissue for biomonitoring, as it contained much higher concentrations than the muscle (3.5 magnitudes), and the levels in the muscle were significantly correlated with those in the viscera (r2=0.938, p<0.0001).     

Combining data sets of organochlorines (OCs) in human plasma for the Russian Arctic

As part of AMAP's human circumpolar study of POPs, an international effort was initiated to extend coverage to communities across the Russian Arctic. Two additional laboratories were invited to join the analytical component of this effort, resulting in four participating analytical centres. Although quality assurance measures were put in place, and the level of performance of the laboratories was generally acceptable, deficiencies in the analytical protocols used were recognized subsequent to the collection and analyses of the plasma specimens. The current paper describes the criteria employed to critically appraise the four data bases and guide their integration into a single data set. Summary statistics are presented for plasma concentrations of major PCBs, p,p′-DDE, p,p′-DDT, β-HCH, and HCB for communities/regions across the arctic/subarctic Russian continent, and for one community located in the Aral Sea area of Uzbekistan (a control group). Highly exposed people were identified in the coastal communities of Chukotka, which appears mainly related to marine mammal intake, but recent pesticide use is also suspected. Other communities with intermediate levels of PCBs had relatively elevated β-HCH, p,p′-DDT and HCB concentrations and low DDE/DDT ratios (<10), suggesting recent pesticide use.     

Spatial and temporal distribution of polycyclic aromatic hydrocarbons (PAHs) in the atmosphere of Xiamen, China

An intensive sampling program was conducted from October 2008 to September 2009 at the five different environmental sites in Xiamen, Fujian Province, to study the spatial and temporal characteristics of Polycyclic Aromatic Hydrocarbons (PAHs) in the gaseous and particulate phase, respectively. The PAHs concentrations at different sites were quite distinct during four seasons. The average concentrations of PAHs in winter were about 8.4 times higher than those in spring, and the concentrations of background were 0.56 times lower than those of industrial area. In addition, the higher temperature in summer affected the particle/gas partitioning of PAHs and led to the higher concentrations of gaseous PAHs. Diagnostic ratios of PAHs, which were employed to indicate the primary sources of PAHs in Xiamen, showed that the traffic vehicle exhaust was the largest contributor and the primary source for PAHs in Xiamen, especially in urban area; while the stationary combustion processes, such as petrochemical factories and power plants, were mainly responsible for PAHs sources in the industrial areas. The health risk of PAHs in the particulate phase was higher than those of the gaseous phase at the five sampling sites. The average toxic equivalent (BaP_eq) of the benzo[a]pyrene values for PAHs were 0.14, 0.32, 1.38 and 3.59 ng m^− 3 in spring, summer, autumn and winter, respectively. Furthermore, the results of average BaP_eq in all four seasons indicated that the health risks of particulate PAHs were higher than those of the gaseous PAHs at different sampling sites.     

Atmospheric deposition of polycyclic aromatic hydrocarbons (PAHs) in mosses (Hypnum cupressiforme) in Hungary

The atmospheric deposition of polycyclic aromatic hydrocarbons (PAHs) was investigated in Hungary by analyzing a moss (Hypnum cupressiforme) species as a bioindicator. In the autumn of 1997, samples were collected at 29 sites distributed across Hungary. The concentrations of total PAH at these sites were in the range of 0.1567-10.45 x 10(4) microg kg(-1) with a mean value of 1.87 x 10(4) microg kg(-1). More than 99% of the total PAHs atmospheric deposition were low molecular weight PAHs (up to 3 ring compounds). The total PAH values showed no correlation with metal concentrations. However, most of the sites in this region showed a positive linear relationship between PAHs levels and traffic volume (r2 = 0.83; P < 0.001) while no relationship existed between PAH levels and population (r2 = 0.01; P > 0.1). Atmospheric deposition of PAHs at different regions in Hungary may be due to incomplete combustion of fuel. The total concentrations of PAHs were compared to the PAH levels in vegetation samples collected from different regions around the world. The highest PAHs concentrations accumulated were found in Hypnum cupressiforme than other vegetation species. A greater affinity for PAH compounds by Hypnum cupressiforme than other moss species probably caused larger amounts of accumulation. A relationship between accumulations of PAH compounds in Hypnum cupressiforme and octanol-air partition coefficients was obtained and is briefly discussed.     

HPLC determination of polycyclic aromatic hydrocarbons (PAHs) in the littoral urban sewage area of cortiou (Marseille,France)

A selective method for determining polycyclic aromatic hydrocarbons (PAHs) in sediments using solid‐phase extraction and RP‐HPLC with fluorescence and UV detection is described. The complete analytical method is used to surface sediments from the creek of Cortiou (France). Sewage from the urban area of Marseille is delivered to the creek. PAH levels in sediments (µg/g) range between 2.251 µg/g (for the benzo(a)anthracene) and 相似文献   

Health risk assessment on dietary exposure to polycyclic aromatic hydrocarbons (PAHs) in Taiyuan, China

Twenty-five kinds of seven categories of foods were sampled in December 2008 and the concentrations of 16 polycyclic aromatic hydrocarbons (PAHs) were determined. The highest level of total PAHs was detected in pork (195.30 ng/g) whereas the lowest concentration was found in milk (8.73 ng/g). The median values of B[a]P equivalent (B[a]P_eq) daily exposure doses for children, adolescents, adults and seniors of male were estimated to be 392.42, 511.01, 571.56 and 532.56 ng/d, respectively, whereas those for the above population groups of female were found to be 355.16, 440.51, 487.64 and 444.85 ng/d, respectively. The incremental lifetime cancer risk (ILCR) values at the 22.1th, 26.1th, 12.7th, 24.9th, 22.7th, 27.0th, 12.9th, and 25.5th percentiles for male children, male adolescents, male adults, male seniors, female children, female adolescents, female adults and female seniors, respectively, were larger than 10^− 6, indicating high potential carcinogenic risk, and were larger than 10^− 4 at the 74.5th, 78.7th, 60.6th, 77.4th, 75.3th, 79.5th, 60.8th and 77.9th percentiles for the above groups, respectively, which implied significant cancer risk. Sensitivity analysis found that the two variables of oral cancer slope factor of benzo(a) pyrene (SF) and the daily dietary PAH exposure level (ED) had the greater impact than that of body weight (BW) on the ILCR.     

Sources of polycyclic aromatic hydrocarbons (PAHs) in street dust in a tropical Asian mega-city, Bangkok, Thailand

We collected samples of roadside air, automobile exhaust soot, tires, asphalt, and used engine oil in a tropical Asian mega-city, Bangkok, Thailand, and analyzed them for polycyclic aromatic hydrocarbons (PAHs) and hopanes. The concentrations and compositions of PAHs and hopanes were utilized to identify the sources of PAHs in street dust, in which high concentrations of PAHs were reported in our previous study. Weight-based concentrations of total PAHs had the following order: gasoline-powered vehicle soot (2600+/-2900 microg/g; n=4)>diesel-powered vehicle soot (115+/-245 microg/g; n=7) approximately roadside aerosols (101+/-35 microg/g; n=5) approximately used engine oil (97+/-65 microg/g; n=4) approximately tire wear particles (82+/-41 microg/g; n=5)>asphalt (2.3+/-1.6 microg/g; n=3)>street dust (1.1+/-0.8 microg/g; n=10). In cluster analysis, all the source materials fell into different clusters from that in which street dust fell, indicating that multiple source materials contribute to PAHs in the street dust. Multiple regression analysis of PAH profiles and diagnostics of hopane compositions identified tire debris as the major contributor of PAHs to street dust, followed by diesel vehicle exhaust.     

Modelling of runoff behaviour of particle-bound polycyclic aromatic hydrocarbons (PAHs) from roads and roofs

Road and roof dust was collected and samples of runoff were taken at an urban storm sewer system in a residential area in Japan. Suspended solids (SS) in the runoff samples were classified into two fractions: fine (smaller than 45 μm) and coarse (larger than 45 μm). Runoff monitoring and chemical analysis data were also used to validate a runoff model for particle-bound polycyclic aromatic hydrocarbons (PAHs) that was originally developed to explain the behaviour of SS in the same area. The model, in which roads and roofs were considered separately as impervious surfaces, expressed the SS and particle-bound PAHs runoff behaviour for fine and coarse particles very well, except during and after heavy rainfalls (more than 10 mm/h). However, the model could not explain the PAH profiles of runoff particles; the profiles of 12 PAH compounds tracked in this study were almost constant and more similar to those of road dust than roof dust throughout the event. An improved model is developed which explains the runoff behaviour by considering two types of road dust with different mobility.     

Health risk assessment for traffic policemen exposed to polycyclic aromatic hydrocarbons (PAHs) in Tianjin, China

In China, traffic policemen have to stand for several hours a day at the road intersections with high vehicle flows. To assess their exposure to airborne carcinogenic polycyclic aromatic hydrocarbons (PAHs) during their working time, a preliminary study was conducted to measure the personal exposure level to PAHs. And a probabilistic incremental lifetime cancer risk (ILCR) model together with the benzo[a]pyrene (BaP) toxic equivalents (BaP(eq)) method was used to conduct health risk assessment. Personal exposure monitors (PEM) were carried by traffic policemen to collect PM10 samples during their daily work in Tianjin, China. Meanwhile, PM100 samples were collected at the roadsides and on campus of Nankai University as comparison. PAHs species were quantitatively analyzed by GC/MS. Experimental results showed that the concentrations of total PAHs, BaP and BaP(eq) were much higher at the road intersections (867.5, 26.2, 82.4 ng m(-3)), where the traffic policemen stand during their work time, than those at the roadsides (46.6, 1.5, 5.7 ng m(-3)), and on campus (19.5, 0.7, 2.4 ng m(-3)). According to the risk assessment results, the occupational risk falls within the range from 10(-6) to 10(-3). On the basis of sensitivity analysis results, further research should be directed to give better characterization of the yearly concentration distribution of PAHs and the cancer slope factor (CSF) of BaP in order to improve the accuracy of the health risk assessment.     

Inhalation exposure of traffic police officers to polycyclic aromatic hydrocarbons (PAHs) during the winter in Beijing, China

This study concerns the use of personal samplers to evaluate the exposure of traffic police to polycyclic aromatic hydrocarbons (PAHs) during the winter of 2005 in Beijing. We measured the samples collected for gas and particulate phases PAHs with the same technique used for an earlier study during the summer of 2004, and evaluated exposure risk based on the calculated benzo(a)pyrene equivalent concentrations (BaP(eq)) of both summer and winter. The mean exposure concentrations of gaseous and particulate phase PAHs in the winter are 4300+/-2900 ng/m(3) and 750+/-1000 ng/m(3), respectively, significantly higher than those measured simultaneously at control sites and also considerably higher than the values measured during the summer. The exposure PAH profiles for police and the control subjects are similar with predominant naphthalene in gaseous phase and dominant fluoranthene, pyrene, anthracene and naphthalene in particulate phase. Large daily variations occur both in summer and winter, because of the changes in the weather conditions especially wind speed and relative humidity which tend to disperse and scavenge PAHs in air. In the winter, the average BaP(eq) value for traffic police is 82.1 ng/m(3), which is significantly higher than those for the control subjects and the national standard of 10 ng/m(3) for ambient air. Particulate phase PAHs contribute more than 90% of the total exposure risk in the winter. Annually, weighted-average probabilities of exceeding the national standard (10 ng/m(3)) are 69.3% and 20.6% for the police and the controls, respectively.     

Biological half-lives of eight polycyclic aromatic hydrocarbons (PAHs) in rainbow trout (Salmo gairdneri)

Adult rainbow trout were exposed to a single oral dose containing a mixture of eight PAHs, and fish were sampled at intervals between 5–48 days after exposure. Regression analyses on whole fish indicate levels declined significantly in four of the compounds monitored. Their biological half-lives were estimated as 9 days for phenanthrene, 7 days for fluorene and anthracene and 6 days for fluoranthene. No reliable estimates could be derived for benzo[a]pyrene, benz[a]anthracene, chrysene or pyrene because of low or nondetectable concentrations at the first sample interval although it could be suggested that their half-lives would be less than several days. The data also suggested that these PAHs are poorly absorbed by trout.     

Studying associations between urinary metabolites of polycyclic aromatic hydrocarbons (PAHs) and cardiovascular diseases in the United States

The association between background, enduring environmental exposure to polycyclic aromatic hydrocarbons (PAHs) and cardiovascular diseases has not been well studied in the general population. In this study, we used the National Health and Nutrition Examination Survey (NHANES) 2001-2004 to investigate the associations between eight monohydroxy PAHs (OH-PAHs) and self-report CVD. In a logistic regression model adjusting for cigarette smoking and other covariates, phenanthrene metabolite, 2-hydroxyphennathrene (2-PHEN), was significantly associated with self-report CVD. Compared to subjects within the lowest tertile of 2-PHEN, subjects within the middle and highest tertiles had higher self-report CVD (the 2nd tertile: AOR = 1.29, 95%CI: 0.97-1.72; the 3rd tertile: AOR = 1.45, 95%CI: 1.01-2.07; p for trend = 0.04). In addition, fluorene metabolite (i.e. 2-hydroxyfluorene) also showed a marginally significant linear trend with self-report CVD (p for trend = 0.07). Further studies are necessary to explore the associations between these highly prevalent pollutants and CVD.     

Monitoring of dioxin-like, estrogenic and anti-androgenic activities in sediments of the Bizerta lagoon (Tunisia) by means of in vitro cell-based bioassays: contribution of low concentrations of polynuclear aromatic hydrocarbons (PAHs)

We used an array of in vitro cell-based bioassays to assess dioxin-like, estrogenic and (anti-)androgenic activities in organic extracts of sediments from the Bizerta lagoon, one of the largest Tunisian lagoons subjected to various anthropogenic and industrial pressures. The sediments were sampled both in winter and summer 2006 in 6 stations differently impacted and in one reference station located in the seawards entrance of Ghar el Melh lagoon. Chemical analyses of the 16 priority PAHs showed that the sediments were low to moderately contaminated (2-537 ng/g dry weight). By using the estrogen- (MELN) and androgen-responsive (MDA-kb2) reporter cell lines, significant estrogenic and anti-androgenic activities were detected only in the Menzel Bourguiba (MB) site, the most contaminated site, both in winter and summer. By using 7-ethoxyresorufin-O-deethylase (EROD) induction in the fish PLHC-1 cell line after both 4 and 24 h of cell exposure, dioxin-like activities were detected in all analysed samples. Dioxin-like activities were higher after 4 h exposure, and varied according to the sites and the sampling season. While highly significant correlation was observed between bioassay- and chemical analyses-derived toxic equivalents (TEQs), PAHs accounted for only a small part (up to 4%) of the detected biological activities, suggesting that other readily metabolised EROD-inducing compounds were present. This study argues for the use of short time exposure to assess biological TEQs in low contaminated samples and provides new induction equivalent factors (IEF(4h)) for 16 PAHs in the PLHC-1 cell line. Finally, our results stress the need to further characterise the nature of organic chemical contamination as well as its long-term impacts on aquatic wildlife in the Bizerta lagoon.