Abstract
Contamination from polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs) in the shallow water areas of the Venice Lagoon (415 km2) was investigated in the surface (0–5 cm) and sub-surface (5–10 cm) sediments by collecting cores from 380 sites. The concentrations of 14 PAHs (USEPA priority pollutants) and seven PCB indicator congeners were analysed with high-performance liquid chromatography (HPLC) and capillary gas chromatography (GC), respectively. PAH and PCB concentrations ranged from 2.75 to 9980 ng g−1 d.w. and from 0.01 to 60.1 ng g−1 d.w., respectively. Their concentrations never exceeded the probable effect level (PEL) stipulated in the respective quality guidelines. In addition, the average total PAH levels expressed as B[a]P toxicity equivalents (total TEQ) were lower in the sediments of the Venice Lagoon than in other literature-reported zones in the Mediterranean. PAH profiles and ratios showed that they originated not only largely from high-temperature pyrolytic processes attributable primarily to the burning of fossil fuels but also partly from petroleum spillage. Comparison of tetra-to-hepta PCB congeners enabled the PCB profiles observed in the lagoon environment to be characterised as Aroclor 1254 and 1260 (1:1). Compared to other marine coastal areas and harbours in the Mediterranean, the Venice Lagoon sediments showed a low mean value but a wide range of concentrations. The estimation of PAH and PCB inventories indicated the low contribution of atmospheric deposition relative to local sources.
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Introduction
Polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs) are ubiquitous, persistent organic compounds, both regarded as priority pollutants by the U.S. Environmental Protection Agency (EPA). PAHs enter the marine environment mainly from anthropogenic sources by various processes: incomplete combustion at higher temperatures of recent and fossil organic matter (pyrolytic origin), slow maturation of organic matter under certain geochemical conditions (petrogenic origin), and short-term diagenetic degradation of biogenic precursors (diagenesis) (Neff, 1979). PCBs were once widely used in a variety of industrial products, including heat exchangers and dielectric fluids, pesticides, ink, paints, paper, and plastics (UNEP 1999).
In Italy, PCBs were produced from the 1940s, reaching a peak in the 1970s (12,000 t for the decade), until 1984, with a cumulative national production of approximately 31,000 t (Maroni et al., 1991; Breivik et al. 2002). Although they have been banned in the majority of industrial countries for several decades, PCBs are still widely found in the marine environment (Covaci et al. 2002; Letcher et al. 2010).
The Venice Lagoon has been affected by various anthropogenic pollutants, including PAHs and PCBs, particularly since the development of the industrial zone of Porto Marghera in the 1930s. The industrial zone reached its maximum development in 1965 (229 industrial facilities and ca. 33,000 employees) but started to decline in the 1970s along with heavy industry in general.
Due to their hydrophobic character, PAHs and PCBs have a tendency to adsorb to organic matter particles, especially carbonaceous geosorbents (Ghosh et al. 2003; Cornelissen et al. 2005) and to accumulate in sediments. Several investigations have been conducted in the Venice Lagoon in order to assess the presence of PAHs and PCBs in the surface sediments. The first survey of the whole lagoon was performed in 1997, sampling from 67 sites located in the shallow water areas (MAV 1999). The sediments of specific lagoon areas were also investigated by Van Vleet et al. 1988; Fossato et al. 1998; Frignani et al. 2001; Moret et al. 2001; Frignani et al. 2003; Secco et al. 2005; Zonta et al. 2005a; Guerzoni et al. 2007; Zonta et al. 2007.
The aim of the present study was to assess the level of contamination and the distribution of PAHs and PCBs throughout the shallow water sediments of the Venice Lagoon before the construction of the MOSE system. MOSE (MOdulo Sperimentale Elettromeccanico, i.e. experimental electromechanical module) is designed to defend Venice and the lagoon from flooding at high tide. It consists of mobile barriers, installed in the seabed in the lagoon’s three seaward inlets, which temporarily seal off the lagoon from the Adriatic Sea during high tide events (Scotti 2005). Preliminary works at the inlets began in 2003 and are now in their final stages. The works imply a modification of hydrological conditions and sediment displacement in the vicinity of the inlets and, once in operation, the system is expected to increase water residence time in the lagoon (Ferrarin et al. 2013). It is not clear how these changes will modify the transport and transfer of pollutants within the water body and affect the characteristics of the surface sediments. The information acquired with this study aims to provide a snapshot of the sediment contamination right before a seaward open lagoon is transformed and begins a “new era” of tidal regulation.
The objectives of the study were to (i) provide a detailed picture of the distribution of PAH and PCB concentrations in the surface (0–5-cm depth) and sub-surface (5–10 cm) sediments of the Venice Lagoon before the entry into service of the MOSE system; (ii) derive indications of the potential sources from the proportions of specific PAH and PCB compounds; (iii) compare the contribution of atmospheric deposition derived from previous studies to the overall accumulation of PAHs and PCBs in surface sediments; (iv) evaluate the potential toxic risk due to their presence in surface sediments together with the carcinogenic risk due to PAHs; and (v) compare sediment contamination in the Venice Lagoon with other coastal areas in Italy and the Mediterranean Sea.
Materials and methods
Study site
The Venice Lagoon (Fig. 1), which has a surface area of 550 km2 and a mean water depth of about 1 m, is made up of islands, tidal marshes, mudflats, and a complex network of tidal channels. Shallow water areas account for ca. 75% of the whole surface area (ca. 415 km2). The lagoon is linked to the Adriatic Sea by three inlets (Lido, Malamocco, and Chioggia), which enable the exchange of water and sediments during tidal cycles. The mean excursion is 30 and 80 cm in neap and spring tide conditions, respectively. The drainage basin, with a total area of ca. 1850 km2 and a population of about one million inhabitants, hosts important urban areas, intensive husbandry activities, and industrial districts (Zonta et al. 2005b). Twelve main tributaries drain the catchment, providing a mean freshwater discharge of about 35.5 m3/s to the lagoon (Zuliani et al. 2005). In addition to the pollutant load from the watershed (Collavini et al. 2005) and from the industrial zone by direct discharge or surface runoff, other pollution sources for the lagoon include waste waters from the inhabited islands (the most important being Venice, Murano, and Chioggia), water traffic, and atmospheric deposition. Located in the industrial area (Fusina) is a multi-fuel (coal and refuse-derived fuel) power plant built in the 1960s.
The various morphological units of the lagoon (Zonta et al. 1995) are affected by the impact of human activities to differing degrees, depending on local water dynamics and their position with respect to the main pollution sources (Zonta et al. 2018).
Sample collection
Sediment cores were collected at 380 sites distributed throughout the shallow areas of the lagoon (Fig. 1) in early 2008. The density of sampling sites was higher in areas where a higher pollution level was expected (i.e. around the cities of Venice, Murano, and Chioggia, in the proximity of Porto Marghera industrial district and near the mouths of the principal freshwater tributaries). The large number of sampling sites ensured coverage of at least one site every 2 km2.
Three 50-cm-long cores were collected in each site using a piston corer and sectioned in the field. This study considered the surface (0–5 cm) and sub-surface (5–10 cm) layers, labelling them A and B, respectively. In a companion study, the samples were analysed for grain-size, total and organic carbon (TOC, OC), and heavy metals (Zonta et al. 2018).
Sample preparation
In the laboratory, triplicate samples from each depth interval were merged and sieved through a 1-mm mesh to remove any debris and thoroughly homogenised. An aliquot of sample was subsequently air dried in the dark at room temperature for 48 h on hexane-rinsed aluminium foil and then finely ground in an agate mortar. It should be noted that this procedure may lead to a concentration loss of the more volatile PAHs (Beriro et al. 2014).
The extraction was performed using a Microwave Sample Preparation System (Multiwave 3000, Anton Paar Graz, Austria), in accordance with EPA recommendations (USEPA 2007a). Two grams of dried sediment was accurately weighed into lined microwave extraction vessels, and a 25-ml 1:1 acetone/hexane solvent mixture was added. Vessels were then assembled as instructed by the manufacturer, and the extraction was conducted for 15 min at 110 °C and up to 10 bars. Once cooled to room temperature, the extracts were filtered and rinsed with the same solvent mixture and then concentrated in a rotating evaporator (Rotavapor-R Buchi, Switzerland). Sulphur compounds were removed by soaking the extracts with activated copper powder.
Purification and fractionation were performed by eluting extracts through glass chromatography columns packed with silica gel/alumina/florisil (4 + 4 + 1 g). The first fraction, intended for PCB analysis, was eluted with 25 ml of n-hexane, while the second fraction, intended for PAH analysis, was eluted with 30 ml of 4:1 n-hexane/methylene chloride solvent mixture (Fossato et al. 1996, 1998). After concentration with a rotary evaporator, samples were ready for instrumental analysis.
PAH quantification
Concentrations of 14 USEPA priority PAHs (naphthalene (Naph), acenaphtene (Ace), fluorene (Fl), phenanthrene (Phe), anthracene (Ant), fluoranthene (Ft), pyrene (Py), benzo(a)anthracene (B[a]A), chrysene (Chy), benzo(b)fluoranthene (B[b]Ft), benzo(k)fluoranthene (B[k]Ft), benzo(a)pyrene (B[a]Py), dibenzo(a,h)antracene (diB[a,h]A), and benzo(g,h,i)perylene (B[g,h,i]Per)) were measured using a high-performance liquid chromatograph (PE 200, USA) coupled to a programmed fluorescence detector (HP 1046A, USA). The column used was a reverse-phase Supelcosil LC-PAH (L = 150 mm ϕ = 3 cm, particles-size = 5 μm). Linear gradient elution was executed with acetonitrile-water mixture as mobile phase at a flow rate of 0.8 ml min−1. The composition of the gradient started with 40% acetonitrile held constant for 4 min, rising to 100% over 11 min, and then held constant for other 10 min. The column compartment was thermo-stated at 40 °C. A wavelength programme was developed to enable optimal detection of all compounds (Table 1).
PCB quantification
PCB concentrations were measured by capillary gas chromatography (Carlo Erba Fractovap 4160, Italy) fitted with electron capture detectors (ECD) on a 15-m Varian VF-5-ms capillary column (0.15-mm ID, 0.15-μm film). The injector was used in splitless mode and held at 270 °C. After a conditioning period of 4 min, the column was held at 80 °C for 1 min, rising to 280 °C at a rate of 9.5 °C min−1, and held at 280 °C for 4 min. The ECD temperature was maintained at 330 °C. The flow-rate of carrier (hydrogen) and make-up (nitrogen) gases was 0.6 and 30 ml min−1, respectively. Total PCB concentration was determined as the sum of 7 congeners (52, 101, 110, 118, 138, 153, 180), which are appropriate indicators for a range of PCB patterns in various sample matrices and are most suitable for risk assessment of “non-dioxin-like PCBs” (EFSA 2005). In Italy, more than 90% of the production of PCBs was destined for oil for transformers, containing Aroclor mixtures 1254 and 1260 (Maroni et al. 1991; Rachdawong and Christensen 1997), in which CB-28 represents a negligible fraction (Bedard and May 1996; Newman et al. 1998). In order to ensure a more realistic estimate of total PCBs, as an alternative to CB-28, we thus determined CB-110, which accounts for 10% of total weight in Aroclor 1254 (Newman et al. 1998). The concentration was also given as total Aroclors, calculated as the sum of a 1:1 1254–1260 mixture.
Quality control
PAHs and PCBs were identified by matching retention times and quantified from the calibration curves established for each compound by analysing four external standards. For PCBs, according to EPA Method 8082A (USEPA 2007b), congener identification was confirmed for a selected number of samples, with a second analysis on a 30-m Zebron ZB capillary column (0.25-mm ID, 0.25-μm film). The average determination coefficients R2 of the calibration curves were greater than 0.99 for both PAHs and PCBs, and the relative standard deviations of the calibration factors were always below 20% (average 10%). The linear ranges of responses were assessed from levels close to the detection limit through three orders of magnitude, for both the categories of compounds. Blanks and calibration verification with standards at one or more concentrations were run frequently for the entire procedure. Blank results indicated that the analytical procedure was free from contamination as the concentration of all compounds examined was at or near the noise level and showed no evidence of carryover. Check standards were on average within 10 and 7% of the nominal value for PAHs and PCBs, respectively.
The detection limits were 0.05–0.10 and 0.05 ng/g for PAHs and PCBs, respectively. Recovery and accuracy were validated with IAEA-417 and IAEA-159 certified sediment sample reference materials, obtaining values in the range 75–108% for all PAHs except naphthalene and 85–112% for PCBs. Naphthalene exhibited lower and more variable recovery (20–40%), due to losses in the two-rotovapor steps, and thus, results for this compound are not presented here.
Laboratory methods were also validated over time by intercalibration procedures (IAEA 2001, 2007, 2012), obtaining Z scores in the range 0.95–0.99 and 0.60–0.72, for PAHs and PCBs, respectively.
Data processing and statistics
For statistical processing, we choose to fill in the values below the detection limit (n.r.) with values equal to half the detection limit. This option represents a reasonable compromise between solutions that underestimate (n.r. = 0) or overestimate (n.r. = detection limit) the true value. It is also reasonable from a health/toxicity perspective, easier to perform than other more complex statistical approaches, and in agreement with the findings of various studies reported in the literature (Menichini and Viviano 2004). Correlation analysis was performed on log-transformed data sets. The frequency distributions of the elements and basic statistics were analysed with the Statistica 6.0 (Statsoft, 2001) software package for Windows.
The distribution maps of the concentrations were represented as contour plots based on Geographic Information System (GIS) technology (software QGIS). In order to reduce the bias of the mean concentrations due to the non-uniform spatial distribution of sampling sites, weighted means were calculated by an inverse distance weighted method (IDW) that takes into account the area between concentration isolines. This method was also used for calculating PAH and PCB inventories in layers A and B. The dry bulk density of sediments was calculated from porosity (Nafe and Drake 1961).
Results and discussion
Spatial distribution of PAHs and PCBs
Total PAH concentrations (Table 2) ranged from 3.6 to 9980 ng/g in layer A (0–5 cm) and from 2.8 to 7458 ng/g in layer B (5–10 cm). Concentrations in both layers (Fig. 2) were highest near the city of Chioggia, in the southern lagoon, with mean values of 2300 ng/g. In this area, sediment quality is affected by urban waste discharge and road and boat traffic, being close to the harbour of the second largest fishing fleet in Italy. High values were also measured around the city of Venice and the islands of Murano and Burano, along the main shipping channels connecting the mainland and the industrial area to Venice, in the vicinity of a shipyard on the Pellestrina shore and to the south of the industrial area. Comparable values were observed in the south-western sector of the lagoon (Dogaletto) near the mainland, which is influenced by the discharge of freshwater tributaries, and downwind of the Romea highway, a very busy road that connects Venice to Ravenna. A further contribution to the increase of PAH could also be the input caused by fish feeding (Hellou et al. 2005; Berntssen et al. 2015), practiced in a series of important fishing farms located near the area.
Total PCB concentrations ranged from < d.l. (detection limit) to 47.8 ng/g in layer A and from < d.l. to 60.1 ng/g in layer B (Table 2). The spatial distributions of PCB concentrations in layers A and B are shown in Fig. 3. The highest values were measured at sites near the city of Chioggia, as observed for PAH concentrations. High concentrations were also measured between the Porto Marghera industrial area and the city of Venice, to the north of Venice and Murano, and at the mouth of the Osellino Canal. Medium-to-low contamination was observed in an extensive area to the southeast of Venice airport. Enhanced PCB concentrations in the run-off water from Gdansk airport in Poland were reported by Sulej et al. (2011) and in airport soils in Croatia (Vasilić et al. 2004). We presume that this large area is moderately contaminated with PCBs delivered by run-off or atmospheric deposition from Venice airport. There were practically no differences between the distributions of concentrations in layers A and B, which confirms the absence of new sources since PCB production was banned in 1984.
On the whole-lagoon scale, no significant differences between sediment layers A and B were found for either total PAH or total PCB concentrations (Wilcoxon test p = 0.06 and p = 0.39, respectively).
However, significant differences between the two layers were seen in some areas of the lagoon. Specifically, the areas in front of the mouth of the Dese river and near the Pellestrina shipyard had lower values in layer A than layer B; while in the area in front of the fish farms, the reverse was found.
In addition, concentrations of PAHs with five or more aromatic rings (B[b]Ft, B[k]Ft, B[a]Py and B[ghi]P) were significantly higher in layer B than layer A (Wilcoxon test p = 0.03, 0.02, 0.04, 0.01, respectively). This might be due to their higher resistance to biodegradation compared to low molecular weight compounds (Cerniglia 1992). No significant differences with depth were observed for individual PCB congeners.
Analysis of correlation among TOC, grain-size, and both organic pollutant concentrations, performed on log-transformed values did not show significant relationships (p > 0.05).
The mean concentration of PAHs in the sediments of the Venice Lagoon (Fig. 4, left) was lower than that of the highly contaminated area of Taranto (Mar Piccolo, Gulf of Taranto; Cardellicchio et al. 2006, 2007) and those of other harbour areas, such as Napoli, Italy (Sprovieri et al. 2007), Rovinj, Croatia (Bihari et al. 2006), and harbours in southern France (Baumard et al. 1998). It was comparable to values reported for coastal areas, such as the Gulf of Trieste, Italy (Notar et al. 2001) and the Istanbul Strait, Turkey (Karacik et al. 2009), but was higher compared to the values found in other lagoon systems (Trabelsi and Driss 2005; Perra et al. 2009; Acquavita et al. 2014). The range of concentrations measured in the sediments of the Lagoon of Venice was wide (4 orders of magnitude), with the highest values comparable to those of the above-mentioned harbours.
Mean PCB concentration (Fig. 4, right) was lower than the values reported for the inner channels of the industrial zone of the Venice Lagoon (Frignani et al. 2001), Mar Piccolo near Taranto, Italy (Cardellicchio et al. 2007), Keratsini harbour, Greece (Galanopoulou et al. 2005), and Alexandria harbour, Egypt (Barakat et al. 2002), but higher than values reported for coastal areas, such as the Caspian Sea (De Mora et al. 2004) and Adriatic Coast, Albania (Koci 1998). PCB concentration was lower than values reported for other Mediterranean lagoons (Mandalakis et al. 2014; Jayed et al. 2015).
Estimation of toxicological and carcinogenic risk
Sediment quality guidelines (SQGs) provide a scientifically valid basis for evaluating the potential effects of sediment-associated contaminants on aquatic organisms. The threshold effects level (TEL) and probable effects level (PEL) (MacDonald et al. 1996) have been used to estimate the potential effect of PAHs and PCBs in the surface sediments (0–5 cm) on the biota of the Venice Lagoon, as have the limits for Venice sediment established by the Ministry of the Environment (Ministero dell’Ambiente 1993). The latter system identifies four classes corresponding to increasingly strict constraints for sediment disposal: non-polluted (A), moderately polluted (B), polluted (C), and highly polluted (> C). Table 3 shows the percentage distribution of samples with respect to SQGs and national limits.
The PEL was never exceeded by PAHs or PCBs, and the TEL was exceeded only in a small number of sites for PAHs (8, i.e. 2.1%) and PCBs (10, i.e. 2.6%), highlighting the absence in the lagoon of zones where effective incidence on biota would be expected. Although the concentrations never exceeded the “B” limit, it is worth noting that 5.8 and 19% of sites would respectively be considered as moderately polluted due to PAH and PCB concentrations if the sediment was to be subjected to disposal after dredging.
The carcinogenicity of certain PAHs, due to the production of active metabolites that can covalently bind to DNA (USEPA 1993), has been documented (Harvey 1991, 1997). The toxicity of PAHs is expressed in terms of toxic equivalency factors (TEFs) with respect to benzo[a]pyrene, the latter being the only known potentially carcinogenic PAH for which toxicological data are sufficient for derivation of a carcinogenic potency factor (Peters et al. 1999).
TEF values for benzo[a]anthracene, benzo[a]pyrene, benzo[b]fluoranthene, benzo[k]fluoranthene, dibenzo[a,h]anthracene, and chrysene are 0.1, 1, 0.1, 0.01, 1, and 0.001, respectively (USEPA 1993). The total toxic benzo[a]pyrene equivalent (total TEQ) of the mixture was then calculated from the sum of the concentrations of individual compounds (conci) multiplied by their relative toxicity (TEFi):
where
In this study, total TEQ calculated for sediment layer A varied from 0.3 to 1070, with a mean of 39. The PAH congeners contributing most to total TEQ were (in order): BaPy (69.0%) > BbFt (13.3%) > diBahA (10.8%) > BaA (6.3%) > BkFt (0.5%) > Chy (0.1%).
The mean total TEQ was lower than the majority of values reported in other studies (Table 4). Nevertheless, the maximum total TEQ value suggested that the most PAH-polluted areas of the Venice Lagoon represented a possible hazard.
PAH and PCB composition and sources
Each type of source gives rise to characteristic PAH patterns, making it possible to infer the processes that generate the compounds (Soclo et al. 2000). PAH profiles and ratios have been widely used to detect PAH sources (Gogou et al. 1996; Mantis et al. 2005; Rossini et al. 2007; Sprovieri et al. 2007). In this study, to minimise possible confusion due to differences in volatility, water solubility, adsorption, and degradation by photo-oxidation, profiles and ratio calculations were restricted to PAHs within a given molecular mass (Yunker et al. 2002).
To determine their relative composition, PAHs were subdivided into five isomer groups: the mean concentrations of isomers with molecular masses of 178, 202, 228, 252, and 276 were calculated. The concentration of isomers decreased in the order 202 > 252 > 228 > 178 > 276; this profile is commonly observed in sediments adjacent to urbanised and industrialised areas. PAHs with a mass of 178 and 202 predominate in kerosene and diesel exhaust fumes. In gasoline and diesel soot, mass 202 or 252 is generally the dominant constituent (Rogge et al. 1993; Wang et al. 1999; Oros and Simoneit 2000). Hence, a PAH profile dominated by masses 202 and 252 (usually with mass 202 predominant) is indicative of pyrolytic PAHs of anthropogenic origin (Gogou et al. 1996).
The ratios of PAH isomers with molecular masses of 178 and 202 are also commonly used to distinguish between combustion and petroleum sources (Budzinski et al. 1997; Soclo et al. 2000), while isomers with a molecular mass of 228 are often used to corroborate the assignment of combustion sources (Yunker and Macdonald 2003).
When the primary PAH source is combustion, the less stable or kinetic PAH isomers tend to be enhanced with respect to the more stable or thermodynamic PAH isomers of the same molecular mass (Yunker and Macdonald 1995).
For isomers with a molecular mass of 178, anthracene/anthracene + phenanthrene ratios below 0.1 are usually taken as an indication of unburned petroleum, while a ratio higher than 0.1 indicates a dominance of combustion effects (Yunker and Macdonald 2003). For isomers with a molecular mass of 202, low fluoranthene/fluoranthene + pyrene ratios (< 0.4) indicate petroleum, intermediate ratios (0.4–0.5) indicate combustion of liquid fossil fuel (petrol and crude oil), whereas ratios > 0.5 are characteristic of grass, wood, or coal combustion (Yunker and Macdonald 2003). Ratios > 0.5 are also often observed in atmospheric deposition samples (Rossini et al. 2007, Gambaro et al. 2009).
For isomers with a molecular mass of 228, benz(a)anthracene/benz(a)anthracene + chrysene ratios < 0.20 imply petroleum, from 0.20 to 0.35 either petroleum or combustion and > 0.35 combustion (Yunker and Macdonald 2003).
The present study showed the clear dominance of combustion sources in the Venice Lagoon, with more than 73% of samples simultaneously fulfilling the three criteria for the ratios mentioned above. This feature is also supported by the presence of acenaphthene in 95% of samples, which is specific to combustion sources (Yunker and Macdonald 1995).
Among the zones of the lagoon with a higher presence of PAHs in the surface sediment, five areas with three different source patterns were identified (Fig. 5).
Sediments in zones LF1 and LF2 showed a distribution of isomers dominated by classes 202 and 252 (with 202 > 252 and 178 isomers making up around 10%). They were also characterised by a 202 ratio < 0.5. Given the intense boat traffic in these zones, sediment showed the characteristic PAH fingerprint for liquid fossil fuel combustion.
The two zones CD1 and CD2 showed a distribution of isomers similar to the previous two, but the 202 ratio was always > 0.5, indicating a prevalence of coal combustion sources and/or the occurrence of significant atmospheric deposition (Rossini et al. 2007). Both areas are located downwind of the industrial zone and the Fusina power plant.
In contrast, the 178 and 252 isomers are dominant in the sediments of zone CO, which is under the direct influence of the industrial zone. The 202 ratio was mostly > 0.5 and the 178 isomers accounted for almost 30%, suggesting the combined effects of combustion and unburned oil.
As observed in other studies (e.g. Viñas et al. 2010, León et al. 2014), the distribution of PAHs in sediment seems to be dependent on proximity of emission sources rather than on sediment characteristics.
Regarding PCB congeners, the most abundant (24 and 23%) were two hexachlorobiphenyls (CB-138 and CB-153), followed by two pentachlorobiphenyls (CB-101 and CB-110) and a heptachlorobiphenyl (CB-180), accounting for 13, 13, and 12%, respectively. The resulting PCB pattern (hexa-PCBs > penta-PCBs > hepta-PCBs > tetra-PCBs) is in agreement with what has been reported by other authors for the Venice Lagoon (Secco et al. 2005) and for other Mediterranean zones (Galanopoulou et al. 2005, Castro-Jiménez et al. 2008). A different composition was found in other areas (Jayed et al. 2015) in which lower chlorinated PCBs (3–4 Cl atoms) were predominant. This could be due either to the different grain-size and organic matter content of the sediment (Pierard et al. 1996) or to the different composition of the main sources.
To evaluate the similarity of the PCB pattern with that of the principal commercial mixtures, the composition (weight %) of chlorobiphenyl PCB homologues in the sediment samples was compared with that of Aroclors 1254 and 1260 (Fig. 6). The comparison confirmed that a 1:1 mixture of 1254 + 1260 best represents the PCB composition of the lagoon sediments, as suggested previously (Frignani et al. 2001).
PAH and PCB inventories
Given the high number of sampling sites, our results were suitable for reliable quantification of PAHs and PCBs in the shallow water sediments of the Venice Lagoon. The inventories were calculated for both surface (0–5 cm) and sub-surface (5–10 cm) sediment layers (Table 5).
A comparison of the amounts of PAHs and PCBs in the surface sediment and rates of atmospheric deposition was tentatively carried out for the northern basin of the Venice Lagoon. The northern basin (shown in Fig. 1) is the only part of the lagoon that is mainly in deposition conditions (Sarretta et al. 2010), and we assumed that the total PAH and PCB atmospheric fallout accumulated in sediments.
The estimated amounts of PAHs and PCBs in the surface sediments (layer A) of the northern basin were 2770 and 34 kg, respectively. On the basis of literature data (Cochran et al. 1998; Ciavola et al. 2002; Bellucci et al. 2007; Zonta et al. 2018), the mean sedimentation rate in this basin was assumed to be 0.2 cm year−1, and thus, the 5-cm surface sediments would be accumulated in about 25 years.
From data collected between November 1998 and July 1999, Rossini et al. (2005b) estimated the annual rates of atmospheric PAH and PCB deposition for the whole lagoon surface area (550 km2) at 104.5 and 0.52 kg, respectively, corresponding to 17.9 and 0.09 kg for the 94 km2 of the northern basin. These values can be considered as the upper limit, as the mean deposition includes values from the Porto Marghera industrial area. Based on these numbers, atmospheric deposition accounts for 16.1 and 6.6% of the total inventory of PAHs and PCBs in the sediments, respectively (Table 5). Atmospheric fallout can also be inferred from measurements at two sites located on opposite sides of the northern basin (data collected in 1998/99 (Rossini et al. 2005a), and in 2003/04 (Rossini et al. 2005b)). Using these data, the mean fallout in the northern basin was 13.8 (PAHs) and 0.06 kg/year (PCBs), respectively, accounting for 12.5 and 4.4% of the total flux into sediments. Atmospheric deposition in this semi-enclosed basin seems to be relatively less important than for the lagoon as a whole (Rossini et al. 2005a; Bettiol et al. 2005), probably because of the predominance of input from the catchment area.
Conclusions
The study provides an assessment of PAH and PCB contamination in the upper sediment layer of the Venice Lagoon, which is the most comprehensive to date. Neither PAH nor PCB concentrations represent a risk to the biota (TEL exceeded in only 2.1% of sites), although for the purposes of disposal after dredging, sediments should be considered moderately polluted in 5.8 and 19% of sites for PAH and PCB concentrations, respectively. These more polluted areas are linked to specific sources, being located around inhabited islands or in the proximity of the industrial zone, harbours, and the mouths of the lagoon’s freshwater tributaries. Slightly higher PCB concentrations in the northern part of the lagoon can possibly be attributed to runoff from Venice airport. In general, the distribution of persistent organic pollutants is thus more dependent on proximity to sources than on sediment characteristics.
A clear dominance of combustion sources is observed in the distribution of PAH concentrations on the basis of isomer ratios. Nevertheless, a signal reflecting both unburned oil sources and atmospheric fallout with the fingerprint of coal combustion is evident in specific zones of the lagoon and can be interpreted as the effect of the presence of the industrial zone.
Compared to other Mediterranean areas, PAH concentrations had lower maximum values than those measured in harbours and higher than those measured in majority of coastal systems. PCB concentrations were comparable to Mediterranean coastal sediments, but generally lower in comparison with other Mediterranean lagoons.
Based on high-density sampling, the PAH and PCB inventories in the surface layer of the whole of the shallow area of the lagoon were calculated. The estimate for the northern basin of the lagoon suggests a modest contribution of atmospheric deposition to the sediment inventory (12–16% for PAHs and 4–7% for PCBs).
The resulting picture of PAH and PCB distributions in the sediments provides a reference for future monitoring of changes that may arise as a result of the entry into service of the MOSE system, as well as the general evolution of pollution in the Venice Lagoon sediments.
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Acknowledgements
The authors thank Loris Dametto and Gianfranco Magris (CNR-ISMAR, Venice) and the SELC Company for the sediment sampling and Andrea Pesce, Federica Braga, Elisa Camatti, and Alessandro Sarretta (CNR-ISMAR, Venice) for the support given in sample treatment and chemical analyses.
Funding
The research was part of the QSEV project (Quality of sediments in the Venice Lagoon), cofunded by CNR ISMAR and the Ministero delle Infrastrutture e dei Trasporti (Provveditorato Interregionale alle OO. PP. del Veneto—Trentino Alto Adige—Friuli Venezia Giulia)—Consorzio Venezia Nuova.
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Cassin, D., Dominik, J., Botter, M. et al. PAH and PCB contamination in the sediments of the Venice Lagoon (Italy) before the installation of the MOSE flood defence works. Environ Sci Pollut Res 25, 24951–24964 (2018). https://doi.org/10.1007/s11356-018-2524-y
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DOI: https://doi.org/10.1007/s11356-018-2524-y