A comparison of anthropogenic mercury pollution in Kastela Bay (Croatia) with pristine estuaries in Ore (Sweden) and Krka (Croatia)

Anthropogenic mercury pollution was studied in Kastela Bay (Croatia), 10 years after chloralkaline plant (PVC) stopped production. The concentration of total mercury determined in sediments which are composed mainly of calcite and quartz, are in the range 14,280-30,400 ng/g. The values are higher than reported in the literature for Elbe and Seine estuaries and also above 25,000 ng/g used for criterion in remediation project in Minamata Bay. The concentration of methylmercury 6.05-36.74 ng/g are typical for slightly to highly contaminated estuarine sediments. The low ratio of methylmercury to total mercury found in sediments of Kastela Bay is in the range 0.04-0.18%. It can be explained that in this region predominate conditions which do not promote in-situ methylation. Sediments were found to be highly anoxic. Concentrations of total mercury in unfiltered surface waters are in the range 69-145 ng/l and in unfiltered bottom waters in the range 230-1,418 ngl(-1). High concentrations found in bottom waters suggest that either resuspension or partial dissolution of sediments takes place. An experiment performed on filtered and unfiltered waters showed that about 85% of total mercury in surface water and almost 100% in bottom water was retained on 45 microm filters. To demonstrate contrasts, two pristine estuaries from norths and south Europe were studied. Silicious sediments of Ore estuary (Sweden) and calcareous sediments of Krka estuary (Croatia) have total mercury concentrations close to accepted background level. The ratio of methylmercury to total mercury is < or = 1% in all samples with one exception. The highest observed ratio (2.70%) was in the surface sediment from E2 station in Krka estuary measured in March 2000. This location is suitable for studying methylmercury formation in pristine environment.     

Depth profiles of lithogenic and anthropogenic mercury in the sediments from Thane Creek,Mumbai, India

Mercury（Hg） is well known as one of the most toxic elements to man.The coastal environments adjacent to industrial areas are reported to often be contaminated with mercury.Mercury becomes more toxic in the form of methylmercury（Me-Hg） which is converted from inorganic mercury in aqueous systems by microbial activity and can bio-magnify through the food chain.A simple method for the determination of total mercury and methylmercury in sediments was optimized by slightly modifying an old method using the direct mercury analyzer technique.Core sediment samples from Thane Creek,Mumbai,India were collected and analysed for total mercury and methylmercury.The Hg concentration in the creek varied between 0.54 to 16.03 μg g~（-1） while Me-Hg concentrations ranged between0.04 to 1.07 μg g~（-1）.In surface sediment,mercury concentrations ranged from 4.33 μg g~（-1） to 12.16μg g~（-1）.Total organic carbon content was found to be around 2 percent in different layers of the sediments.The enrichment factors,which indicate the extent of pollution in sediments,were estimated to range from 26 to 50 at different locations in the creek.Lithogenic and anthropogenic concentrations of mercury in the creek were also determined to compare the impact of anthropogenic and natural sources.Anthropogenic inventories were about 5-70 times more in concentration than the lithogenic in the different core sediments.     

New assessment of organic mercury formation in highly polluted sediments in the Lenga estuary,Chile

Anomalously high levels of mercury in sediment in the Lenga estuary, Chile are comparable to the most contaminated sites previously reported elsewhere. Total mercury (Hg_total) concentrations range from 0.5 to 129 mg kg⁻¹ and organic mercury (Hg_org) from 11 to 53 μg kg⁻¹. The highest levels are in areas near the previous wastewater outfall of a chlo-alkali plant. The results show that the proportion of Hg_org/Hg_total in the sediment varies by more than two orders of magnitude (0.02–5.7%) according to the concentration of Hg_total. No correlation between the concentration of Hg_org and Hg_total was found. The lack of correlation does contrast with the findings of other authors in culture media. Our results indicate that even at very high concentrations of Hg_total and organic matter do not influence organic mercury formation in estuary sediments. The disparity in Hg_total and Hg_org concentrations also attests to environmental differences in the formation.     

Laboratory and field studies of the accumulation of inorganic mercury by the mussel Mytilus edulis (L.)

Laboratory and field experiments have been used to indicate the relative importance of mercury in dissolved and particulate phases as sources of mercury to mussels in a contaminated estuary. Laboratory experiments have demonstrated that mussels can accumulate inorganic mercury from sea-water, phytoplankton, and suspended sediment. Following exposure, concentrations were normally higher in the gills, digestive gland, and kidneys than in the adductor muscle, mantle, and foot, and the distribution of mercury between organs varied according to source. The relative bioavailabilities of inorganic mercury in water, phytoplankton, and sediment are estimated to be in the ratios 10:5:1. Mussels exposed for four weeks in a mercury-contaminated estuary accumulated primarily inorganic mercury from suspended sediment at the seaward end of the estuary, but further upstream uptake from solution and of methylmercury compounds were more important.     

Mercury pollution sources in sediments of Patos Lagoon Estuary,Southern Brazil

Present study has continued the investigation on distribution of mercury in estuarine sediments of Patos Lagoon which began whilst assessing the after-effect of enormous accidental discharge of sulfuric acid into the estuary. An attempt to evaluate the contribution of anthropogenic effluents on mercury pollution in sediments was undertaken. The effluents from Rio Grande City sewages were categorized into four groups based on their sources. Comparison of mercury concentrations from those, indicated that domestic effluent was prevalent. Apparent geographic controls of effluent locations enriched in mercury on zones of polluted estuarine sediments were also revealed. Insufficient control on waste collecting and absence of sewage treatment are considered the principal causes of mercury pollution in estuarine sediments.     

Total mercury,methyl mercury and sulphide in river carron sediments

Total mercury, methyl mercury and sulphide contents of River Carron sediments (Lothian, Scotland) have been determined. Total mercury concentrations are comparable to other mercury polluted estuaries in the UK, but the methyl mercury values for low-sulphide Carron sediments are generally higher. It has been found that methyl mercury levels are initially in direct proportion to the sulphide concentrations of the sediments but beyond sulphide concentrations of 1.8 mg g^?1 the methyl mercury levels decline sharply.     

Plutonium occurrence and phase distribution in sediments of the Wyre estuary,northwest England

The occurrence of plutonium isotopes derived from the Windscale reprocessing facility discharges and weapons test fallout in intertidal sediments of the Wyre estuary, northwest England, is reported. Windscale plutonium appears to be slowly transported to the estuary in association with sedimentary material, and its distribution in surface and buried sediments is controlled by the variations in organic matter content of the sediments and/or their grain size characteristics. Results from chemical leaching experiments suggest that very little plutonium is ion exchangeable or in humic substances, but it is in other organic and Fe/Mn hydrous oxide fractions of the sediments. Plutonium shows a similar depositional behaviour to mercury which enters the Wyre directly in local industrial discharges.     

Evidence of methylmercury production and modification of the microbial community structure in estuary sediments contaminated with wastewater treatment plant effluents

The Seine’s estuary (France) waters are the receptacle of effluents originating from wastewater treatment plants (WWTP). In this estuary, mudflats are deposition zones for sediments and their associated contaminants, and play an essential role in the mercury (Hg) biogeochemical cycle mainly due to indigenous microorganisms. Microcosms were used to assess the impact of WWTP-effluents on mercury methylation by monitoring Hg species (total dissolved Hg in porewater, methylmercury and total mercury) and on microbial communities in sediments. After effluent amendment, methylmercury (MeHg) concentrations increased in relation with the total Hg and organic matter content of the WWTP-effluents. A correlation was observed between MeHg and acid-volatile-sulfides concentrations. Quantification of sulfate-reducing microorganisms involved in Hg methylation showed no increase of their abundance but their activity was probably enhanced by the organic matter supplied with the effluents. WWTP-effluent spiking modified the bacterial community fingerprint, mainly influenced by Hg contamination and the organic matter amendment.     

Bioaccumulation of polychlorinated biphenyls in mullet fish in a former ship dismantling harbour, a contaminated estuary, and nearby coastal fish farms

This study investigated the bioaccumulation of polychlorinated biphenyls (PCBs) toward mullet fish (Liza macrolepis) living in former PCB contaminated areas, the Ann-Ping harbour and the Er-Jen estuary, and fish farms located near the above two areas in 2003. The PCB body burdens of collected fish samples are proportional to the contamination level of their locations with the following rank order (greatest to least) from the Er-Jen estuary, the Ann-Ping harbour to the fish farms. Concentration of PCBs of the estuarine mullet has been approximately decreased to one-half of the peak concentration of the 1990s. Although the concentration of PCBs in farmed fish inhabiting near the two contaminated areas was greater than the average of those of fish from local fish markets in Taiwan, no particularly great contamination level was observed in their bodies. Using the less chlorinated PCB fraction (triCB + tetraCB)/total PCBs as the indicator of the origins of PCBs, fish near former contaminated areas had greater body burdens of the more chlorinated PCB congeners, while the farmed fish exhibited a PCB pattern more like that known to originate from air–water exchange with less chlorinated PCBs predominating. Although the PCB contamination has been stopped for a decade, the residual contaminants, supposedly existing in soil and sediments, still contribute to the body burden of fish residing in the estuary and the harbour.     

Total mercury in sediments and in Brazilian Ariidae catfish from two estuaries under different anthropogenic influence

Santos-São Vicente estuary, located in São Paulo State, Brazil, has a history of contamination by inorganic chemicals such as mercury (Hg). In the 1980s the Cubatão was considered one of the most polluted sites in the world as a consequence of the intense industrial activities located in the city close to the estuary. To provide data and evaluate the local biota, total mercury (THg) contents were determined in sediments and in fish, Cathorops spixii, from different areas of the Santos-São Vicente estuary. For comparison, samples were also collected in a non-polluted system with similar hydrochemistry characteristics, the Cananeia estuary. The water characteristics and THg levels in sediment and fish samples confirmed a high human influence in the Santos-São Vicente estuary. The lowest THg values, observed in Cananeia, were evidence of low anthropogenic influence. High values observed in Santos-São Vicente show the necessity for a monitoring program.     

Can Nassarius reticulatus be used as a bioindicator for Hg contamination? Results from a longitudinal study of the Portuguese coastline

The focus of this work is to explore the use of the netted whelk, Nassarius reticulatus (L.), as an indicator of mercury (Hg) contamination, by assessing the concentration of Hg in the sediments and in the whelk along the entire Portuguese coast. Total Hg concentrations ranged from below the detection limit (0.01 ng absolute mercury) up to 0.87 mg kg(-1) dry weight (dwt) in sediments and between 0.06 and 1.02 mg kg(-1) (dwt) for organisms, with no significant differences between males and females. Although organic mercury was not detected in the sediments, it represented, on average, 52% of the total Hg in the whelk tissues, and as high as 88% in some cases, suggesting mercury accumulation from dietary intake. Significant negative correlations were found between the total Hg concentrations in the sediments and the log(10) of Hg concentrations in whelk tissues males (r=-0.64; P<0.01) and females (r=-0.52; P<0.01) indicating that the species is a poor indicator of Hg contamination. Nevertheless, since the highest concentrations of organic mercury in the whelk tissues were found in the least contaminated areas, this species must be highly relevant in the trophic web, namely on the possible biomagnification of mercury. The high dietary mercury accumulation from feeding on carrion and the low bioavailability of mercury to whelks in estuarine sediments may be the basis of the mercury accumulation pattern in N. reticulatus.     

Long-term variation in mercury concentrations in estuarine organisms with changes in releases into Lavaca Bay,Texas

Mercury releases into Lavaca Bay resulted in public health notices and a fishing closure for crabs and finfish. Mercury containing wastewater discharges were halted in 1970, but sediments were contaminated with mercury. The sediments are a source of mercury to the benthic food web via methylation. Mercury in water column feeding organisms has decreased markedly. Concentrations in benthic food web organisms remain elevated. Human consumption concerns for oysters have ended, but a closure for fishing for crabs and finfish continues. Monitoring of mercury in organisms since 1977 shows a gradual downward trend in mercury in crabs and finfish, but this was not sufficient to remove the closure. Continued releases of mercury, man's activities, and resuspension of sediments keep mercury in the sediment's biologically active zone. This enables the uptake of mercury via the benthic food web. If releases are ended, it will take years for the mercury to decrease to concentrations not of concern for human consumption. If more remediation to reduce the mercury concentrations in the sediments takes place, decrease of mercury in the organisms might occur more quickly.     

Relationships between hydrosedimentary processes and occurrence of mercury-resistant bacteria (merA) in estuary mudflats (Seine, France)

The Seine estuary (France) is one of the world's macrotidal systems that is most contaminated with heavy metals. To study the mercury-resistant bacterial community in such an environment, we have developed a molecular tool, based on competitive PCR, enabling the quantification of Gram-negative merA gene abundance. The occurrence of the Gram-negative merA gene in relation with the topology (erosion/deposit periods) and the mercury contamination of three contrasted mudflats was investigated through a multidisciplinary approach and compared with a non-anthropized site (Authie, France). The higher abundance of the Gram-negative merA gene in the Seine estuary mudflats indicates a relationship between the degree of anthropization and the abundance of the merA gene in the mudflat sediments. In the Seine mudflats, the maxima of abundance are always located in fresh sediment deposits. Therefore, the abundance is closely related with the hydrosedimentary processes, which thus seem to be determining factors in the occurrence of the Gram-negative merA gene in the surface sediments of the Seine's mudflat.     

Mercury Circulation in Aquatic Environment. Part 3: Mercury Transformations in Sediments

Two types of sediments, one of them highly polluted by the pulp and chemical industry and the other one polluted by the urban type of sewage, have been analysed for their content of methylmercury and inorganic mercury. The rate of the formation of methylmercury in sediment from inorganic mercury (II) and the decomposition of methylmercury and phenylmercury have been investigated using ²⁰³mercury compounds. It has been found that the rates of both processes depend on the experimental conditions. The quickest formation of methylmercury has been observed under the Procedure C which simulates the natural conditions. The lower the rate of demethylation of methylmercury the higher the equilibrium concentration of methylmercury which has been found in sediments.     

Mercury distribution in Douro estuary (Portugal)

Determinations of dissolved reactive and total dissolved mercury, particulate and sedimentary mercury, dissolved organic carbon (DOC), particulate organic carbon (POC) and suspended particulate matter (SPM) have been made in the estuary of river Douro, in northern Portugal. The estuary was stratified by salinity along most of its length, it had low concentrations of SPM, typically <20 mg dm(-3), and concentrations of DOC in the range <1.0-1.8 mg dm(-3). The surface waters had a maximum dissolved concentration of reactive mercury of about 10 ng dm(-3), whereas for the more saline bottom waters it was about 65 ng dm(-3). The surface waters had maximum concentrations of total suspended particulate mercury of approximately 7 microg g(-1) and the bottom waters were always <1 microg g(-1). Concentrations of mercury in sediments was low and in the range from 0.06 to 0.18 microg g(-1). The transport of mercury in surface waters was mainly associated with organic-rich particulate matter, while in bottom waters the dissolved phase transport of mercury is more important. Lower particulate organic matter, formation of chlorocomplexes in more saline waters and eventually the presence of colloids appear to explain the difference of mercury partitioning in Douro estuarine waters.     

Studies of a contaminated brackish marsh in the Hackensack Meadowlands of northeastern New Jersey: an assessment of natural recovery

Eight-Day Swamp is known to be contaminated with heavy metals, especially mercury. Sediment cores were collected to approximately 32 cm at 17 sites on four transects and analyzed at 1 or 2 cm intervals for seven metals and organic matter. Very high metal levels were found throughout the site. Long and Morgan's "effects range-median" (ER-M) was exceeded in more than 50% of slices for all elements except As. Hg had the highest concentration relative to ER-M; median Hg concentration was 72 times its ER-M. On the marsh plain, all metals showed enrichment at 14-20 cm depth of 10-40X over surficial sediments. 137Cs analysis showed sedimentation rates ranging from 0.33 to 0.50 cm yr(-1) over the last approximately 40 yr. These rates indicate that metal contamination peaks occurred in sediments deposited in the early 1960s. Thus, newer, less contaminated sediments are burying older, more contaminated layers and peak levels of contaminants are becoming less available to benthos.     

Estuarine ecological risk based on hepatic histopathological indices from laboratory and in situ tested fish

Juvenile Senegalese soles were exposed through 28-day laboratory and field (in situ) bioassays to sediments from three sites of the Sado estuary (W Portugal): a reference and two contaminated by metallic and organic contaminants. Fish were surveyed for ten hepatic histopathological alterations divided by four distinct reaction patterns and integrated through the estimation of individual histopathological condition indices. Fish exposed to contaminated sediments sustained more damage, with especial respect to regressive changes like necrosis. However, differences were observed between laboratory- and field-exposed animals, with the latest, for instance, exhibiting more pronounced fatty degeneration and hepatocellular eosinophilic alteration. Also, some lesions in fish exposed to the reference sediment indicate that in both assays unaccounted variables produced experimental background noise, such as hyaline degeneration in laboratory-exposed fish. Still, the field assays yielded results that were found to better reflect the overall levels of contaminants and physico-chemical characteristics of the tested sediments.     

The mobilization and deposition of mud deposits in a coastal plain estuary

Muddy sediments with their potential for containing contaminants are commonly deposited and remobilized by tidal currents in estuarine environments. We examined the mobilization and subsequent redeposition of mud in a coastal plain estuary located in the southeastern United States. Time-series data for salinity, suspended sediment concentrations and quality (percent organic matter and pigment concentrations) were obtained over a 13-hour tidal cycle. We found that fast-settling mud particles are found during the highest tidal current speeds. Particle quality analyses suggest that all the material is of similar origin, and that phaeopigment can be used as a tracer of particles in this system. These particles settle onto the bed when current speeds approach slack conditions. We speculate that the quantity of mud mobilized during neap tide is less than during spring tide resulting in an opportunity for the mud to partially consolidate on the bottom and be removed from resuspension. We further speculate that the muddy sediments are mainly derived from fringing marshes in this estuary.     

Heavy metals,organochlorine pesticides and PCBs in green mussels,mullets and sediments of river mouths in Thailand

This investigation was undertaken to determine the levels of lead, zinc, copper, cadmium, and mercury and certain organochlorines including DDT and PCBs in green mussels, mullets, and bottom sediments of the mouths of the river Mae Klong, Ta Chin, Chao Phraya, and Ban Pakong. The four river mouths are contaminated by the five heavy metals to some extent. The contamination of lead in mussels, mullets and sediments was quite obvious, at values significantly higher than those previously reported. Contamination of the other four metals in mussels and mullets was still within acceptable limits, except for mercury in the Chao Phraya river mouth which was approaching the limit. Organochlorines, especially DDT and its metabolites, are detectable in some samples of mussels, mullet, and sediments. PCBs were detectable in some samples of mussels and mullets, but none were detected in the sediments. The levels of these organochlorines are considered to be comparable to baseline levels.     

Occurrence of DDA in DDT-contaminated sediments of the Southern California Bight

DDT, DDE and some additional lipophilic derivatives are recognized contaminants in sediments of Southern California Bight (SCB). Only about 10% of total DDTs discharged into the SCB are accounted for using available monitoring data (sediment, water, and biota). DDA represented up to 0.03% DDTs (DDT/DDE/DDD) in SCB surface sediments (top 2 cm) in amounts up to 76 μg DDA/kg dry weight. Highest DDA levels were found where DDT and DDD levels were maximal at the primary wastewater outfall indicating a natural precursor-product relationship for DDT and DDA. Still culture of SCB sediment revealed limited DDA formation following DDT fortification. DDA residues have also been found in contaminated Long Island, NY sediments provided by USGS. The formation of DDA and its potential release from sediments may be significant in resolution of uncertainties concerning the natural recovery of sediments in DDT-contaminated environments.