Source characterization using compound composition and stable carbon isotope ratio of PAHs in sediments from lakes, harbor, and shipping waterway

Molecular compositions and compound specific stable carbon isotope ratios of polycyclic aromatic hydrocarbons (PAH) isolated from sediments were used to characterize possible sources of contamination at an urban lake, a harbor, a shipping waterway, and a relatively undisturbed remote lake in the northwest United States. Total PAH concentrations in urban lake sediments ranged from 66.0 to 16,500 microg g(-1) dry wt. with an average of 2600 microg g(-1), which is approximately 50, 100, and 400 times higher on average than PAH in harbor (48 microg g(-1) on average), shipping waterway (26 microg g(-1)), and remote lake (7 microg g(-1)) sediments, respectively. The PAH distribution patterns, methyl phenanthrene/phenanthrene ratios, and a pyrogenic index at the sites suggest a pyrogenic origin for PAHs. Source characterization using principal component analysis and various molecular indices including C2-dibenzothiophenes/C2-phenanthrenes, C3-dibenzothiophenes/C3-phenanthrenes, and C2-chrysenes/C2-phenanthrenes ratios, was able to differentiate PAH deposited in sediments from the four sites. The uniqueness of the source of the sediment PAHs from urban lake was also illustrated by compound specific stable carbon isotope analysis. It was concluded that urban lake sediments are accumulating PAH from sources that are unique from contamination detected at nearby sites in the same watershed.     

Chemical and ecotoxicological assessment of polycyclic aromatic hydrocarbon--contaminated sediments of the Niger Delta, Southern Nigeria

The extent of environmental contamination and sources of polycyclic aromatic hydrocarbons (PAHs) compounds to sediments of the Niger Delta, Nigeria were assessed using combined chemical analysis and toxicity bioassay techniques. Concentrations of two- to six-ring PAHs of molecular mass 128-278 and toxicity to Vibrio fischeri and Lemna minor are considered in this investigation. Levels of the sum of the 16 USEPA priority pollutant PAHs varied from 20.7 to 72.1 ng/g dry weight. Sediment PAH levels were highest in samples collected from Delta Steel located at the outskirts of Warri, and Quality control centre, Ughelli West; with total PAH concentrations of 72.1 and 67.5 ng/g dry weight, respectively. The overall levels of PAHs in this study are low compared to other regions and reveal moderate PAHs pollution in the sediments of the Niger Delta. Two- and three-ring aromatic hydrocarbons predominated in almost all the sediments, which indicate a petrogenic origin. The sediment total PAH (PAHtot) concentration, normalized to organic carbon content (OC), ranged from 120.2 to 1.99 ng PAHtot/mg OC; and showed distinctively that the sedimentary organic matter of the sample from Delta Steel is highly contaminated with PAHs, and had a value of 120.2 ng PAHtot/mg OC. The toxicity bioassays indicated that the sample collected from Warri Refinery Area (SDWRR) was the most toxic to V. fischeri, with an EC50 value of 0.45 mg sediment equiv./mL test medium; and samples from Ogunu (SDOGN) and Warri Refinery area (SDWRR) showed high toxicity to L. minor, with percent inhibitions of 42.6% and 33.67%, respectively, after 7 days of exposure. The total PAH concentrations showed no correlation with toxicity bioassays, and thereby implied that chemical analysis of PAHs cannot be an indicator of sediment toxicity.     

Determination of polycyclic aromatic hydrocarbons in sediments and mussels from Saudafjord, W. Norway, by glass capillary gas chromatography.

Polycyclic aromatic hydrocarbons (PAH) have been determined, by glass capillary gas chromatography, in two species of bivalves (Mytilus edulis and Modiolus modiolus) and sediments of Saudafjorden, Norway. The PAH observed are derived from waste effluents from a ferro alloy smelter. Up to 34 PAH compounds were identified, including some reported to be carcinogenic. The concentrations decreased rapidly with distance from the source and with sediment depth, but could be traced more than 15 km from the source. Relative abundance of various PAH did not change significantly in the mussels collected from the head to the mouth of the fjord. In the sediments, however, phenanthrene increased from minor importance to dominance towards the mouth, whereas the relative content of anthracene and benzo [a]pyrene decreased. The results are compared with observations from other marine localities and discussed in relation to transport processes, biodegradation and chemical transformation in the sediments.     

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.     

Impacts of pollution derived from ship wrecks on the marine environment on the basis of s/s “Stuttgart” (Polish coast, Europe)

In 1943 the German hospital ship s/s Stuttgart (Lazaretschiff “C”) was sunk close to the port of Gdynia (Gulf of Gdańsk — Polish coast). This and other actions (undertaken after the war to remove the wreck) led to pollution of the sea bottom with oil derivatives.During our studies (2009) 11 surface sediment and water samples were collected as well as sediment core samples at 4 locations in order to determine the concentration levels of priority pollutants belonging to polycyclic aromatic hydrocarbons (PAH) and polychlorinated biphenyls (PCB). The concentrations of 16 PAH and 7 PCB were analysed with GC-MS. ΣPAH varied between 11.54 ± 0.39 and 206.7 ± 6.5 mg/kg dry weight in the surface sediments, and from 0.686 ± 0.026 to 1291 ± 53 mg/kg dry weight in the core samples. Contamination in the core samples collected may reach a depth of at least 230-240 cm (deepest sample studied). The PAH-group profiles in all surface sediment samples suggest a pyrolytic source of PAH, while the results obtained for core samples indicate a mixed pattern of pyrolytic and petrogenic inputs of PAH. Results obtained may suggest also that fuel residues being present at sea bottom is not crude oil derived but results from coal processing (synthetic fuel). The sum of PCB in surface sediments ranged from 0.761 ± 0.068 to 6.82 ± 0.28 μg/kg dry weight (except for sampling point W2, where ΣPCB was 108.8 ± 4.4 μg/kg dry weight). The strong correlation between PAH and PCB levels, and the fact that PCB are present only in the surface sediments, suggest that the compounds in these sediments got there as a result of emission from urban areas, entering the aquatic environment via atmospheric deposition. PCB levels in the sediment core samples were generally very low and in most cases did not exceed the method quantification limit.     

A non-lethal chemically based approach to investigate the quality of harbour sediments

A non-lethal chemically based approach was used to investigate the quality of harbour sediments receiving combined road runoff and sewage effluents. A previous investigation of the behaviour of the amphipod Corophium volutator linked polycyclic aromatic hydrocarbons (PAH) in sediments corresponding to the probable effects levels listed in the sediment quality guidelines of the Canadian Council of the Marine Environment to a sediment avoidance response. Since the amphipods did not biotransform contaminants, bioaccumulation was the only fate pursued to examine the bioavailability of PAH. For five Halifax Harbour sediments, a relationship was established between the threshold effects level representing the amphipods' avoidance response and the bioaccumulation of PAH. A body burden of 0.3-1.1 mumol/kg (wet weight) was determined for the sum of abundant parental PAH in amphipods exposed to sediments that initiated the behavioural effect. PAH were much more available from spiked sediments than from field sediments, with biota-sediment accumulation factors of 2.2-7.8 compared to <0.01-0.3, respectively. Animals exposed to PAH-spiked sediments avoided contaminated sediments when their body burden was up to seven times higher than observed with field sediments. This latter result and two exposures to sediments collected further away from sewage discharges point to a role for unidentified chemicals in the body burden and behaviour relationship. Further research is warranted to develop this promising assessment tool.     

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.     

PAHs in sediments of the Black River and the Ashtabula River, Ohio: source apportionment by factor analysis

Sources of polycyclic aromatic hydrocarbons (PAHs) in the Black River and Ashtabula River sediments were apportioned using a factor analysis (FA) model with nonnegative constraints. Source profiles, contributions (microg/g) and percent contributions are determined with no prior knowledge of sources. The FA model includes scaling and backscaling of data with average PAH concentrations, without sample normalization. The present work is a follow-up to studies that used a chemical mass balance model to apportion sources to the same data sets. Literature source profiles, modified based on gas/particle partitioning of individual PAHs, from nine PAH sources were considered for comparison. FA results for a three-source solution indicate traffic (58%), coke oven (26%), and wood burning/coal tar (16%) are the primary PAH sources to Black River sediments. The primary PAH sources to the Ashtabula River sediments are traffic (51%), coke oven (44%), and wood burning (5%). This work supports the previous studies of Black River and Ashtabula River PAHs by CMB model. In addition, FA provides a more realistic fit to Ashtabula River model data by eliminating 100% contributions from one source.     

Spatial and vertical distribution of polycyclic aromatic hydrocarbons in mangrove sediments

The distribution and historical changes of polycyclic aromatic hydrocarbons (PAHs) contamination in mangrove sediments in Hong Kong SAR were investigated. Surface sediments (2-3 cm) collected from four mangrove swamps exhibited significant spatial variations in concentrations of total PAH (with SigmaPAHs ranging from 56 to 3758 ng g(-1) dry wt), as well as the composition of 16 USEPA priority PAH compounds. Within a small swamp with an area of 0.68 ha, the total PAH concentrations also differed from sampling site to site, indicating that the PAH contamination is localized and confined to a very small area within the same swamp. Discharges from municipal and industrial wastewater, urban runoff, oil leakage from boats and ships, and accidental oil spill are possible sources of the PAH contamination. The sediment depth profiles reveal that the surface sediment layer (0-5 cm) had lower total PAH concentrations than that in the bottom layer (15-20 cm), and PAH composition also changed with the sediment layers. Based on the estimated annual sediment deposition rate in Hong Kong SAR of around 0.4-0.5 cm, the present findings suggest that the PAH contamination was most serious between 1958 and 1979 but started to decline thereafter. Such decline was probably due to changes in petroleum usage in urban areas and a better control of wastewater discharges from 1980 onwards in this region.     

Source apportionment of PAHs in dated sediments from the Black River,Ohio

Black River, OH, is contaminated with polycyclic aromatic hydrocarbons (PAHs) from coke ovens of a US Steel Corp. Plant. Closing of a coking plant in 1983 and environmental dredging of the sediments during 1989 and 1990 has reduced the PAH levels significantly. This study quantifies the decrease, and consider source apportionment of PAHs in Black River sediments using chemical mass balance modeling. Five vibra cores collected in 1998 and dated using 210Pb and 137Cs, were analyzed for 18 PAHs. The cores had total PAH concentrations between 250 and 0.10 ppm. PAH maxima occur in 1949, 1969, in accordance with regional historical inputs (core BR4), and in 1991 due to remediation (BR6). Coke oven emissions (CO), highway dust (HWY), and wood burning (WB) are likely sources. The CO source (6-92% of total PAHs) is maximal in 1954, and again in 1992-1994 due to the exposure and redistribution of older contaminated sediments during dredging, and decreases thereafter. There is minimal CO content in 1985 (BR4), 2 yr after closure of the coking plant. The HWY contribution (2-86%) is high during 1969-1988, and increases again after 1993. The WB source is less than 23%, and exhibits a minimum (2%) around 1979 (BR4). There is evidence of aerobic biodegradation or photolysis in the sediment of phenanthrene (PhA) at PhA concentrations >500 ppb.     

PAH content, toxicity and genotoxicity of coastal marine sediments from the Rovinj area, Northern Adriatic, Croatia

Surface marine sediments collected from 8 sampling sites within the Rovinj coastal area, Northern Adriatic, Croatia, were used for determining priority pollutant polycyclic aromatic hydrocarbons (PAHs) and toxic/genotoxic potential of sediment organic extracts. Total PAH concentrations ranged from 32 microg/kg (protected area) to 13.2 mg/kg dry weight (harbor) and showed clear differences between pristine, urban industrial and harbor areas. PAHs distribution revealed their pyrogenic origin with some biogenic influence in harbor. At all sampling sites sediment extracts showed toxic potential that was consistent with the sediment type. No correlation between toxicity measured by Microtox assay and concentrations of individual or total PAHs was found. Noncytotoxic dose of sediment extracts showed no genotoxic potential in bacterial umu-test. DNA damage is positively related to total PAHs at 4 sampling sites (S-1, S-2, S-3, S-6), but the highest DNA damage was not observed at the site with the highest total sediment PAH content (S-5).     

Native polycyclic aromatic hydrocarbons (PAH) in coals - A hardly recognized source of environmental contamination

Numerous environmental polycyclic aromatic hydrocarbon (PAH) sources have been reported in literature, however, unburnt hard coal/ bituminous coal is considered only rarely. It can carry native PAH concentrations up to hundreds, in some cases, thousands of mg/kg. The molecular structures of extractable compounds from hard coals consist mostly of 2-6 polyaromatic condensed rings, linked by ether or methylene bridges carrying methyl and phenol side chains. The extractable phase may be released to the aquatic environment, be available to organisms, and thus be an important PAH source. PAH concentrations and patterns in coals depend on the original organic matter type, as well as temperature and pressure conditions during coalification. The environmental impact of native unburnt coal-bound PAH in soils and sediments is not well studied, and an exact source apportionment is hardly possible. In this paper, we review the current state of the art.     

PAH fluxes in the Laja Lake of south central Chile Andes over the last 50 years: evidence from a dated sediment core

This paper reports the occurrence of polyaromatic hydrocarbons (PAHs) deposition inferred from a sediment core of an Andean lake in south central Chile. Sediments were carefully collected from one of the deepest section of the lake and sliced every 1 cm. The samples were analyzed for PAHs, (137)Cs, (210)Pb, organic carbon and grain-size. The stratigraphic chronology and the sedimentation rates were estimated using the sedimentary signature left by the (137)Cs and (210)Pb fallout as temporal markers. PAHs were quantified by HPLC-fluorescence detection (HPLC-Fluorescence). 15 priority EPA PAHs were analyzed in this study. Based on these results, PAH deposition over the last 50 years was estimated (a period characterized by an important intervention in the area). PAH concentration ranged from 226 to 620 ng g(-1) d.w. The highest concentrations of PAHs were found in the core's bottom. The PAH profile is dominated by the presence of perylene indicating a natural source of PAH. In addition, two clear PAH deposition periods could be determined: the most recent with two-four rings PAHs, the older one with five-seven rings predomination. Determined fluxes where 71 to 972 microg m(-2) year(-1), dominated by perylene deposition. PAH levels and fluxes are lower compared to the levels found in sediments from remote lakes in Europe and North America. It is concluded that the main source of PAHs into the Laja Lake sediments are of natural origin.     

Contribution of PAHs from coal-tar pavement sealcoat and other sources to 40 U.S. lakes

Contamination of urban lakes and streams by polycyclic aromatic hydrocarbons (PAHs) has increased in the United States during the past 40 years. We evaluated sources of PAHs in post-1990 sediments in cores from 40 lakes in urban areas across the United States using a contaminant mass-balance receptor model and including as a potential source coal-tar-based (CT) sealcoat, a recently recognized source of urban PAH. Other PAH sources considered included several coal- and vehicle-related sources, wood combustion, and fuel-oil combustion. The four best modeling scenarios all indicate CT sealcoat is the largest PAH source when averaged across all 40 lakes, contributing about one-half of PAH in sediment, followed by vehicle-related sources and coal combustion. PAH concentrations in the lakes were highly correlated with PAH loading from CT sealcoat (Spearman's rho = 0.98), and the mean proportional PAH profile for the 40 lakes was highly correlated with the PAH profile for dust from CT-sealed pavement (r = 0.95). PAH concentrations and mass and fractional loading from CT sealcoat were significantly greater in the central and eastern United States than in the western United States, reflecting regional differences in use of different sealcoat product types. The model was used to calculate temporal trends in PAH source contributions during the last 40 to 100 years to eight of the 40 lakes. In seven of the lakes, CT sealcoat has been the largest source of PAHs since the 1960s, and in six of those lakes PAH trends are upward. Traffic is the largest source to the eighth lake, located in southern California where use of CT sealcoat is rare.     

Polycyclic aromatic hydrocarbons (PAHs) and organochlorines (OCs) in bottom sediments of the Guba Pechenga,Barents Sea,Russia

Surface sediment samples from the Guba Penchenga and adjacent areas: Varangerfjord, Guba Malaya Volokovaya and Guba Bol'shaya Volokovaya (south-western Barents Sea) collected in March-April 1997 were analysed for polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs), chlorinated pesticides: p,p'-DDT, p,p'-DDE, p,p'-DDD, alpha- and gamma-HCH, and hexachlorobenzene (HCB). Mean summation operator PAH (sum of the two- to six-ring PAHs) concentration in sediments from the Guba Pechenga (1481 ng/g dry wt.) was significantly higher than in sediments from adjacent areas (252 ng/g dry wt.), where PAH contamination levels were similar to reported for unpolluted sediments of the northern Norway fjords and open parts of the Barents Sea. Differences between HCB levels as well as summation operator HCH (sum of alpha- and gamma-HCH) levels found in Guba Pechenga sediments and adjacent area sediments were not significant. Concentrations of these contaminants varied in ranges 0.28-1.76 and 0.05-0.68 ng/g dry wt., respectively, and were consistent with literature data on PAH levels in sediments from the northern Norway harbours, Kola Bay (Russia) and south-eastern part of the Barents Sea. Average total DDT concentration in Guba Pechenga sediments (10.5 ng/g dry wt.) was one and 2-3 orders higher than those found in sediments from the Pechora Sea and from the seas of eastern Arctic, respectively, however, it was comparable with DDT levels reported for harbours of northern Norway and Kola Bay. Significant difference between total DDT levels in Guba Pechenga and in the adjacent areas (mean 1.8 ng/g) was found. Among compounds of DDT family, p,p'-DDT isomer prevailed in all sediment samples indicating a possible local 'fresh' DDT source. Mean summation operator PCB (sum of PCB-28, 31, 52, 101, 118, 105, 153, 138, 156, 180, 209) concentration in the Guba Pechenga sediments (12.8 ng/g dry wt.) was significantly higher than in sediments of adjacent areas (2.1 ng/g dry wt.), but it was lower in comparison with summation operator PCB levels reported for the northern Norway harbours and Kola Bay sediments. The highest levels of contaminants were found in sediments collected close to the Liinakhamari harbour. The origin of both PAHs and OCs in the Guba Pechenga sediments is a combination of local sources and long-range transport from lower latitudes.     

Polycyclic aromatic hydrocarbons in fish from remote and high mountain lakes in Europe and Greenland

Polycyclic aromatic hydrocarbons (PAHs) were analysed in liver of fifty-seven individual trout distributed among seven high mountain lakes in Europe and one remote lake in Greenland. In all cases, very similar distributions were observed in which phenanthrene largely predominated and fluoranthene and pyrene were the second major compounds. These distributions were similar to those observed in the dissolved fraction of the waters studied in three of these lakes. The range of concentrations of PAH in fish liver show only a five-fold variation, which is considerably smaller than the range more than two orders of magnitude of sedimentary PAH concentrations of these lakes. No correlation between PAH content in sediments and fish liver has been found both at the level of total and individual compounds. However, lake site is the main statistically significant factor of variability between PAH concentrations in fish liver. Changes in fish species explain significant differences in liver content of some PAHs. Within lake, condition factor and liver concentration are inversely correlated. Female fish display lower average concentrations than male in all lakes but the differences are not statistically significant. No correspondence between fish age and PAH content has been observed.     

Characterization and distribution of polycyclic aromatic hydrocarbon contaminations in surface sediment and water from Gao-ping River, Taiwan

The concentrations of 16 polycyclic aromatic hydrocarbons (PAHs) in water and sediment samples collected from 12 locations in Gao-ping River, Taiwan were analyzed. Molecular ratios and principal component analysis (PCA) were used to characterize the possible pollution sources. Concentrations of total 16 PAHs (SigmaPAHs) in water samples ranged from below method detection limits (相似文献   

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.     

Phase association of polycyclic aromatic hydrocarbons in the Minjiang River Estuary, China

Persistent organic pollutants such as polycyclic aromatic hydrocarbons (PAHs) are of great concern due to their persistence, bioaccumulation and toxic effects. In this work the levels of 16 priority PAHs were determined in water, pore water, sediment, soil and vegetable samples from Minjiang River Estuary, China. Total PAH concentrations varied from 9.9 to 474 microg/l in water, 82.1 to 239 microg/l in pore water, 112 to 877 ng/g dry wt. in surficial sediments, 128 to 465 ng/g dry wt. in soil and 8600 to 111,000 ng/g dry wt. in Chinese vegetables. Overall, the mean concentrations of PAHs were present in higher levels in pore water than that in surface water, due possibly to higher concentrations of dissolved organic carbon or colloids with which the hydrophobic pollutants were strongly associated. Such a concentration gradient implies a potential flux of pollutants from sediment pore water to overlying water. Contamination was dominated by high molecular mass PAH compounds in all samples, indicating combustion-derived sources (for example, pyrolysis at high temperature). The levels of PAHs in water and vegetable were relatively high in comparison to other studies, although PAHs in sediment and soil were comparable to those found in many other similar environments. The ratios of selected PAHs indicated again that PAHs in Minjiang River Estuary were mainly derived from incomplete combustion of fossil fuel.     

Possible impacts of Hg and PAH contamination on benthic foraminiferal assemblages: an example from the Sicilian coast, central Mediterranean

The Palermo and Augusta urban/industrial areas (Sicily) are examples of contaminated coastal environments with a relatively high influx of unregulated industrial and domestic effluents. Three sediment box-cores were collected offshore of these urban/industrial areas in water depths of 60-150 m during two cruises (summers 2003/2004), dated by (210)Pb and (137)Cs, and analysed for total mercury concentration and total polycyclic aromatic hydrocarbon (PAH) concentration. Benthic foraminiferal assemblages were also examined (in terms of their distribution and morphology) to assess the potential use of benthic foraminifera as bioindicators of pollutant input and environmental change in these Mediterranean shelf environments. The Hg and PAHs vs depth profiles show a clear increase in concentration with decreasing depth. Most of the sediments are highly enriched in mercury and show concentrations more than 20 times the background mercury value estimated for sediments from the Sicily Strait. The Hg and PAH concentrations appear to be potentially hazardous, grossly exceeding national and international regulatory guidelines. A reduction in abundance of benthic foraminifera, increasing percentages of tests with various morphological deformities, and the dominance of opportunistic species in more recent sediments can be correlated to anthropogenic impact.