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.     

Eine neue elektrochemische Methode zur Bestimmung von Bromidionen in natürlichen Gewässern

A New Electrochemical Method for the Determination of Bromide in Natural Waters Formation of poorly soluble Hg(I)-halides at the polarized mercury electrode was used for the development of a new electrochemical method for determination of bromide in mixed chloride and bromide solutions. Interferences due to anions, surface-active agents, and suspended matter present in natural waters were not found. The applicability of the method to natural waters was tested in the Krka River estuary in Croatia. The mass ratio Br/chlorinity = 3.320·10^?3 was calculated on the basis of recorded bromide concentrations in the estuary. As the relationship is linear, conservative behaviour of bromide ions in the Krka River estuary may be assumed.     

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.     

The distribution and inventory of total and methyl mercury in Kuwait Bay

Sediment (surface and core) sampling was conducted during the period from August 96-December 98 from intertidal and offshore areas in Kuwait Bay. The highest (and most variable) concentrations of total mercury (T-Hg; 36500+/-34930 ng g(-1)) are encountered around the previous industrial outfall where sediments are disturbed by shipping activities. The concentrations of T-Hg are lower in the Shuwaikh Port area (650+/-210 ng g(-1)) and continue to decrease towards the northern coastline of Kuwait Bay (average concentrations in the wider Bay region are 50+/-30 ng g(-1)). These values are still above background concentrations of 15-20 ng g(-1). Calculation of the total inventory of mercury in all the surface sediments of the studied area indicates that approximately 22.5 ton is present which is similar to the estimated industrial discharges of approximately 20 ton suggesting that the contamination is largely confined to the Bay and that releases to the wider Gulf region are small. The distributions of MeHg are similar to those of T-Hg and represent ranges between 0.23% and 0.5% of the T-Hg indicating that surface sediments within Kuwait Bay contain approximately 80 kg of this chemical.     

Evaluation of diffusive gradients in thin-films (DGTs) as a monitoring tool for the assessment of the chemical status of transitional waters within the Water Framework Directive

In this contribution, the potential use of diffusive gradients in thin-films (DGTs) for the chemical evaluation of transitional water bodies within the Water Framework Directive (WFD) has been studied. The water metal concentration has been evaluated in 13 estuaries in the southeastern Bay of Biscay. The DGTs were deployed in triplicate at two stations in each estuary, delimiting the tidal influence. The DGT results were in the ranges of 2-1570 ng L(-1) for cadmium, 66-515 ng L(-1) for copper, 30-3650 ng L(-1) for nickel and 0.8-95.5 μg L(-1) for zinc. The DGTs provided reliable average labile metal concentrations in highly dynamic systems that were comparable with DGT measurements in coastal and estuarine waters worldwide. In addition, it was possible to discriminate those estuaries more susceptible to environmental impacts, being consistent with the historical contamination of each estuary. Based on the obtained results, a sampling strategy for the monitoring of transitional water bodies using DGTs is proposed.     

Trace metals, PAHs, and PCBs in sediments from the Jobos Bay area in Puerto Rico

This study provides baseline information on the extent of contamination in sediments of the Jobos Bay estuary and surrounding areas in Puerto Rico. Sediments from Jobos Bay area (n = 14) had higher overall average concentrations than those from La Parguera area (n = 5, used as reference site), in μg/g dw, for As (17 vs 9), Cu (29 vs 14), Pb (11 vs 4), and Zn (64 vs 28); and in %, for Fe (2.6 vs 0.6). Sediments (n = 8) screened for PAHs and PCBs exhibited total concentrations (ng/g dw) that ranged from 40.4 to 1912, and from not detected to 11.21, respectively. The quality of sediments of Jobos Bay could be classified as low to moderate pollution. The proximity to anthropogenic sources of contamination warrants a monitoring program for inorganic and organic pollutants in Jobos Bay area for an effective coastal management program of this tropical ecosystem.     

Total,methyl and organic mercury in sediments of the Southern Baltic Sea

Distribution of sedimentary mercury in the Southern Baltic was investigated. Sediment samples were collected from the Southern Baltic in the period from 2009 to 2011, and concentrations of sedimentary total mercury (average 102 ng/g, range 5.8–225 ng/g) and methyl mercury (average 261 pg/g, range 61–940 pg/g) were measured in the manner that the influence of both patchiness and seasonal changes were assessed. Moreover, sedimentary mercury extracted with organic solvent- the so-called organic mercury was also analyzed (average 425 pg/g, range 100–1440 pg/g). There is a statistically significant dependence between organic mercury and both methyl mercury and total mercury concentrations in the sediments. Methyl mercury contribution to total mercury varied from 0.12% to 1.05%, while organic mercury contributed to 2% of total concentration on average. The area studied, although mercury concentrations exceed threefold the geochemical background, can be regarded as moderately contaminated with mercury, and methylmercury.     

Dioxin-like compounds in sediments from the Daliao River Estuary of Bohai Sea: distribution and their influencing factors

The concentrations, compositional profiles, and potential ecological risk of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs), polychlorinated biphenyls (PCBs) and polychlorinated naphthalenes (PCNs) in sediments of the Daliao River Estuary were investigated. Total concentrations of PCDD/Fs, PCBs, and PCNs were in the range of 11.3-133.2 ng/kg dry weight (dw), 1 971-37 632 ng/kg dw and 33.1-284.4 ng/kg dw, respectively. The total TEQ values varied from 0.37 to 4.08 ng/kg dw, with the dominant contributions by PCDD/Fs, then by PCBs and PCNs. The spatial distributions of PCDD/Fs, PCBs and PCNs in the river estuary were much related to hydrodynamic conditions. The risk of contamination to the deeper sea was increased in the flood seasons. Moreover, our data confirmed that both organic matter in sediments and molecular properties of dioxin-like compounds were the factors which strongly influenced the partition behavior of these dioxin-like compounds between sediments and water phase in the estuarine zone.     

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.     

Indicators of sediment and biotic mercury contamination in a southern New England estuary

Total mercury (Hg) and methylmercury (MeHg) were analyzed in near surface sediments (0-2 cm) and biota (zooplankton, macro-invertebrates, finfish) collected from Narragansett Bay (Rhode Island/Massachusetts, USA) and adjacent embayments and tidal rivers. Spatial patterns in sediment contamination were governed by the high affinity of Hg for total organic carbon (TOC). Sediment MeHg and percent MeHg were also inversely related to summer bottom water dissolved oxygen (DO) concentrations, presumably due to the increased activity of methylating bacteria. For biota, Hg accumulation was influenced by inter-specific habitat preferences and trophic structure, and sediments with high TOC and percent silt-clay composition limited mercury bioavailability. Moreover, hypoxic bottom water limited Hg bioaccumulation, which is possibly mediated by a reduction in biotic foraging, and thus, dietary uptake of mercury. Finally, most biota demonstrated a significant positive relationship between tissue and TOC-normalized sediment Hg, but relationships were much weaker or absent for sediment MeHg. These results have important implications for the utility of estuarine biota as subjects for mercury monitoring programs.     

An Estimation of the Mercury Content in the Waters of the Pomeranian Baltic-Shore-Area

In the catchment area of the Pomeranian Bay an average mercury concentration of 178 ng/l in precipitation was determined. Eight different flowing waters showed mean concentrations between 105 ng/l (?upawa) and 500 ng/l (Odra), a pronounced annual cycle having been demonstrated for the concentrations and for the freights with the minimum in February/March and the maximum in August/September. The total freight of the eight rivers amounts to 19.5 t/a, the share of the Wisla being 11 t/a. The ratio between the mercury precipitation of 335 to 410 μg/m²a Hg and the run-off varies of 30 … 75 μg/m²a Hg for the individual river basins between 0.08 and 0.21. In the Baltic Sea, the mercury concentrations are 40 ng/l in the open sea, 50 ng/l in the coastal region and 290 … 390 ng/l near the estuaries. Trough the eight investigated rivers about 48 km³/a water run off into the Baltic Sea with about 20 t/a Hg. The total introduction of Hg into the Baltic Sea is estimated at 100 t/a with the river water, 35 t/a with precipitation and 35 t/a with dust.     

Input and behaviour of linear alkylbenzenesulphonates (LAS) in a stratified estuary

Input and distribution of linear alkylbenzenesulphonates (LAS) in the highly stratified Krka River estuary were studied during 1990–1991. Determinations of individual LAS homologues in wastewater and estuarine waters were performed using reversed-phase high-performance liquid chromatography (HPLC) with spectrofluorimetric detection. The investigated municipal wastewaters contained LAS homologues with alkyl-chain lengths from C₁₀ to C₁₃ at total concentrations in the range of 285–1041 μg l⁻¹. Total LAS input via wastewaters into ibenik Harbour, the most polluted part of the estuary, was estimated at 12.6 kg day⁻¹. A relatively large fraction of total LAS, depending on the wastewater particle load, was found in particulate form (11–59%). Distributions of the individual homologues in dissolved and particulate fractions were rather different, the latter being significantly enriched in higher homologues (C₁₂, C₁₃). The LAS concentration in the estuary was quite low (0.2–23.9 μg l⁻¹) which was caused chiefly by a strong and fast dilution process. However, characteristic vertical distribution of LAS in the estuarine water column indicated that the wastewater plume spreads almost exclusively in the upper (brackish) layer. The concentration maxima were observed in the surface microlayer and at the brackish water/seawater boundary.     

Distribution and origins of polycyclic aromatic hydrocarbons (PAHs) in riverine, estuarine, and marine sediments in Thailand

To assess the status of polycyclic aromatic hydrocarbon (PAH) contamination in coastal and riverine environments in Thailand, we collected 42 surface sediment samples from canals, a river, an estuary, and coastal areas in Thailand in 2003 and analyzed them for PAHs with 3-7 benzene rings by gas chromatography-mass spectrometry (GC-MS). The total concentration of PAHs ranged from 6 to 8399 ng/g dry weight. The average total PAH concentrations were 2290+/-2556 ng/g dry weight (n=8) in canals, 263+/-174 (n=11) in the river, 179+/-222 (n=9) in the estuary, and 50+/-56 (n=14) in coastal areas. Comparison of the concentration range with a worldwide survey of sedimentary PAH concentrations ranked PAH contamination in Thai sediments as low to moderate. The ratio of the sum of methylphenanthrenes to phenanthrene (MP/P ratio) allows discrimination of PAH sources between petrogenic (>2) and pyrogenic (<0.5) origins. Sediments from urban canals in Bangkok showed the highest PAH concentrations and petrogenic signatures (MP/P=1.84+/-0.98 [n=6] in canal sediments) with abundant alkylated PAHs, indicating major sources of petrogenic PAHs in the city. To identify the sources of the petrogenic inputs in Thailand, we analyzed triterpanes, biomarkers of petroleum pollution, in the sediment samples and in potential source materials. Hopane profiles were remarkably uniform throughout the nation, suggesting a diffuse single source (e.g. automobiles). Molecular profiles of hopanes and PAHs in sediments from the urban canals were similar to those in street dust, indicating that street dust is one of the major sources of petrogenic PAHs in the urban area. On the other hand, low levels of PAHs (approximately 50 ng/g) with a pyrogenic signature (MP/P ratio approximately 0.5) were widely recorded in remote areas of the coast and the Chao Phraya River. These pyrogenic PAHs may be atmospherically transported throughout the nation. Middle and lower reaches of the Chao Phraya River, the river mouth, and the upper Gulf of Thailand showed intermediate concentrations and profiles of PAHs, indicating mixtures of petrogenic and pyrogenic origins. Perylene was abundant in sediments, representing up to approximately 60% of total identified PAHs. High inputs of soil due to frequent heavy rains could contribute to the high perylene abundance in the sediments. Sedimentary PAH concentrations decreased offshore with a half distance of approximately 10 km in the upper Gulf off the mouth of the Chao Phraya River. This is probably due to active deposition of laterally transported riverborne particles.     

Variability of the dissolved nutrient (N,P, Si) concentrations in the Bay of Annaba in relation to the inputs of the Seybouse and Mafragh estuaries

Dissolved inorganic nitrogen (DIN), phosphate (PO₄) and silicic acid (Si(OH)₄) loads from the Seybouse and the Mafragh estuaries into the Bay of Annaba, Algeria, were assessed at three stations of the Bay over three years. The Seybouse inputs had high levels of DIN and PO₄, in contrast to the Mafragh estuary’s near-pristine inputs; Si(OH)₄ levels were low in both estuaries. The DIN:PO₄ molar ratios were over 30 in most samples and the Si(OH)₄:DIN ratio was less than 0.5 in the Seybouse waters, but nearly balanced in the Mafragh. The specific fluxes of Si–Si(OH)₄ (400–540 kg Si km⁻² yr⁻¹) were comparable in the two catchments, but those of DIN were several-fold higher in the Seybouse (373 kg N km⁻² yr⁻¹). The inner Bay affected by the Seybouse inputs had high levels of all nutrients, while the Mafragh plume and the outer marine station were less enriched.     

Seasonal and spatial distribution of matrix-bound phosphine and its relationship with the environment in the Changjiang River Estuary, China

Sediment is commonly considered as a source of phosphine, which is a highly toxic and reactive atmospheric trace gas. This study aims to investigate the seasonal and spatial distribution of matrix-bound phosphine (MBP) and its relationship with the environment in the Changjiang River Estuary. A total of 43 surface sediments were collected in four seasons of 2006, and concentrations of MBP and relative environmental factors were analyzed. MBP ranged from 1.93 to 94.86ngkg(-1) dry weight (dw) with an average concentration of 17.14ngkg(-1)dw. The concentrations of MBP in the upper estuary were higher than those in the lower estuary, which could be attributed to greater pollutant inputs in the upper estuary. The concentrations of MBP also varied with season, with November>August>May>February. Significant correlations existed between MBP and total phosphorus (TP), organic phosphorus (OP), inorganic phosphorus (IP), organic carbon (OC), total nitrogen (TN), the grain size, and redox potential (Eh), suggesting that these sedimentary environmental characteristics played an important role in controlling the MBP levels in the sediments. Notably, there were positive linear relationships between the concentrations of soluble reactive phosphorus (SRP), TP, and chlorophyll a (Chl a) in bottom water and MBP in sediments. These relationships might be very complicated and need further exploration. This work is the first comprehensive study of the seasonal and spatial distribution of MBP in sediments and its relationships with environmental factors in a typical estuary, and will lead to deeper understanding of the phosphorus (P) biogeochemical cycle.     

Mercury contamination history of an estuarine floodplain reconstructed from a Pb-dated sediment core (Berg River, South Africa)

Mercury deposition histories have been scarcely documented in the southern hemisphere. A sediment core was collected from the ecologically important estuarine floodplain of the Berg River (South Africa). We establish the concentration of Hg in this ²¹⁰Pb-dated sediment core at <50 ng g⁻¹ Hg_T throughout the core, but with 1.3 ng g⁻¹ methylmercury in surface sediments. The ²¹⁰Pb dating of the core provides a first record of mercury deposition to the site and reveals the onset of enhanced mercury deposition in 1970. The ratio of methylmercury to total mercury is relatively high in these sediments when compared to other wetlands.     

Seasonal fluctuations of tissue mercury contents in the European shore crab Carcinus maenas from low and high contamination areas (Ria de Aveiro, Portugal)

The main objective was to study the seasonal variation of mercury concentrations in different tissues (muscle, hepatopancreas and gills) of Carcinus maenas from low and high Hg contaminated areas, a valuable resource in temperate estuaries and a possible pathway for human uptake. Individuals of two size classes (around 35 and 55 mm cephalothorax wide) were captured monthly between March 1999 and May 2000 in two areas of Ria de Aveiro: in the main navigation channel that connects the lagoon to the sea, and in the inner lagoon area heavily contaminated by mercury (maximum Hg in sediments of 5.4 microg g(-1)). Pronounced decreases in salinity and temperature and reduced food availability in winter seemed to be the responsible for the decline of the crab condition index (0.75-0.45) in larger individuals. Muscle and hepatopancreas exhibited higher mercury concentrations than gills, with concentrations in the contaminated site ranging from 0.03 to 0.63 microg g(-1) and 0.02 to 0.34 microg g(-1), respectively. Linear regressions between muscle and hepatopancreas (r=0.94, p<0.001) and muscle and gills (r=0.97, p<0.001) suggested a rapid redistribution of mercury inside the organism. During winter, a rapid elimination of mercury was found in the three analysed tissues followed by uptake. Larger crabs presented elimination rates from 18 to 34 ng g(-1) per week, while the smaller crabs showed lower elimination rates (10-24 ng g(-1) per week). The uptake was similar in both size classes (11-15 ng g(-1) and 8.1-15 ng g(-1) per week, respectively for large and small crabs). Our results suggest that C. maenas harvested in the contaminated areas must be considered with caution, since Hg concentrations were found to exceed the threshold concentration allowed for human consumption (0.5 microg g(-1)).     

Heavy metals in surface sediments from nine estuaries along the coast of Bohai Bay,Northern China

Concentrations of heavy metals in river water and sediment were investigated in nine estuaries along the coast of Bohai Bay, Northern China. Multivariate statistical techniques such as principal component analysis and cluster analysis, in combination with metal concentration analysis and correlation analysis, were used to identify the possible sources of the metals and the pollution pattern in nine estuaries along the coast of Bohai Bay. The environmental risks of metals, evaluated by sediment quality guidelines and background values, revealed Hg contamination in the estuaries. However, levels of Cd in estuarine sediments were low, and they were less than those levels in river sediments, partly due to the high mobility and dilution of river or seawater. Cd did not contribute to sediment deposits in estuaries. High organic matter from effluents from large municipal sewage treatment plants was predominantly responsible for restricting Hg mobility from the river to Bohai Bay.     

Grain size characteristics of surface sediment and its response to the dynamic sedimentary environment in Qiantang Estuary,China

The composition and grain size characteristics of sediment in estuarine and coastal environments provide important information on the material source, hydrodynamic environment, environmental events,etc. However, few studies have focused on the sediment characteristics of the entire Qiantang Estuary,particularly, on the correlation between hydrodynamics and sediment properties. Through systematic sampling of the surface sediment in a large area of the Qiantang Estuary, the spatial distribution ch...     

Cellular energy allocation in mussels (Mytilus galloprovincialis) from the stratified estuary as a physiological biomarker

This study demonstrates the usefulness of cellular energy allocation (CEA) evaluations as a physiological biomarker to infer the occurrence of natural stress in native populations of mussels inhabiting the stratified estuary (Krka River estuary, Croatia). Sampling sites were selected based on their differences in the salinity and temperature. The CEA value was calculated as a ratio between available energy (E_a) and energy consumption (E_c). Generally, higher values of E_a were recorded in June than in November, which were especially evident in the storage components (carbohydrates and lipids), while the constitutive component (proteins) remained relatively constant. The highest E_c was recorded in mussels at estuarine site compared to coastal site, which may be caused by the energetically costly maintenance of osmotic balance. Decrease in CEA recorded in estuarine mussels may ultimately result in a lower amount of energy available for growth, reproduction, or defence against other stresses (e.g. pollution).