Hg Monitoring Research Articles

Rhamphotheca as a useful indicator of mercury in seabirds

The evaluation of mercury (Hg) toxicity in wildlife species has prompted a search for sensitive indicators to accurately measure the body burden of Hg. Despite the extensive use of feathers as an indicator of Hg in birds, they do not appear to be an entirely suitable indicator of the extent of contamination in certain conditions and bird species since Hg levels are influenced by the growth period, timing of the last moult and migration. This research aimed to evaluate rhamphotheca as a potential indicator of environmental Hg concentrations in seabirds. We used culled yellow-legged gulls (Larus michahellis) (n = 20) and determined THg in rhamphotheca and feathers. We distinguished between upper and lower rhamphotheca, and divided each one into 16 equal portions along the culmen to analyse their THg content spatially. In each bird, THg was also determined in primary (P1) and secondary (S8) feathers and compared with rhamphotheca. The median (25th, 75th percentile) rhamphotheca Hg concentration was 13.44 (9.63, 17.46) μg/g, which was twofold higher than in the feathers 7.56 (4.88, 12.89) μg/g. Median THg in rhamphotheca was significantly higher (p < 0.05) in females 15.05 (10.35, 23.04) μg/g than in males 12.34 (8.57, 15.19) μg/g, whereas no differences (p > 0.05) were found in the feathers. No significant differences in Hg levels were found between upper and lower beak mandibles or along either. In contrast, significant differences in Hg concentrations were found between the P1 and S8 feathers (mean, 12.04 vs. 6.04 μg/g). No correlation was found between Hg content in rhamphotheca and feathers. Mercury levels in rhamphotheca exhibited stronger significant relationships with weight (R2 = 0.568), length (R2 = 0.524) and culmen (R2 = 0.347) than the levels in the feathers, which showed no correlation. Overall, our results suggest that rhamphotheca is a suitable tissue indicator for Hg monitoring in gulls; however, further studies are needed to extend our research to other bird species.

A National-Scale Assessment of Mercury Bioaccumulation in United States National Parks Using Dragonfly Larvae As Biosentinels through a Citizen-Science Framework.

We conducted a national-scale assessment of mercury (Hg) bioaccumulation in aquatic ecosystems, using dragonfly larvae as biosentinels, by developing a citizen-science network to facilitate biological sampling. Implementing a carefully designed sampling methodology for citizen scientists, we developed an effective framework for a landscape-level inquiry that might otherwise be resource limited. We assessed the variation in dragonfly Hg concentrations across >450 sites spanning 100 United States National Park Service units and examined intrinsic and extrinsic factors associated with the variation in Hg concentrations. Mercury concentrations ranged between 10.4 and 1411 ng/g dry weight across sites and varied among habitat types. Dragonfly total Hg (THg) concentrations were up to 1.8-fold higher in lotic habitats than in lentic habitats and 37% higher in waterbodies with abundant wetlands along their margins than those without wetlands. Mercury concentrations in dragonflies differed among families but were correlated (r2 > 0.80) with each other, enabling adjustment to a consistent family to facilitate spatial comparisons among sampling units. Dragonfly THg concentrations were positively correlated with THg concentrations in both fish and amphibians from the same locations, indicating that dragonfly larvae are effective indicators of Hg bioavailability in aquatic food webs. We used these relationships to develop an integrated impairment index of Hg risk to aquatic ecosytems and found that 12% of site-years exceeded high or severe benchmarks of fish, wildlife, or human health risk. Collectively, this continental-scale study demonstrates the utility of dragonfly larvae for estimating the potential mercury risk to fish and wildlife in aquatic ecosystems and provides a framework for engaging citizen science as a component of landscape Hg monitoring programs.

Mercury in fish from streams and rivers in New York State: Spatial patterns, temporal changes, and environmental drivers.

Mercury (Hg) concentrations in freshwater fish across the state of New York frequently exceed guidelines considered harmful to humans and wildlife, but statewide distribution and temporal changes are not well known for the state's streams and rivers. We analyzed existing data to describe recent spatial patterns, identify key environmental drivers, and assess temporal changes. Size classes within sportfishes and prey fishes formed 'functional taxa' (FT), and standardized scores were generated from 2007-2016 data for 218 sites. Muscle Hg in ≥1 sportfish FT exceeded human-health guidelines of 50 ng/g (sensitive populations) and 300 ng/g (general population, GP) at 93 and 56% of sites, respectively, but exceeded 1000 ng/g (a state threshold) at only 10% of sites. Whole-body Hg in ≥1 prey fish FT exceeded wildlife thresholds of 40 ng/g and 100 ng/g at 91 and 51% of sites, respectively. Environmental drivers of recent spatial patterns include extent of forest cover and storage, the latter an indicator of wetlands. Standardized Hg scores increased with increasing atmospheric Hg deposition and storage across rural 'upland' regions of New York. However, scores were not related to atmospheric deposition in more-developed 'lowland' regions due to the limited methylation potential of urban landscapes. Comparisons of 2010-2015 sportfish Hg concentrations with those of 1998 and 2000-2005 showed inconsistent temporal changes both among and within eight sites examined. Some recent stream and river fish Hg spatial patterns differed from those of lake-based studies, highlighting the importance of New York's flowing waters to future Hg monitoring and risk assessment.

Influence of size on total mercury (THg), methyl mercury (MeHg), and stable isotopes of N and C in green turtles (Chelonia mydas) from NE Brazil.

The green turtle (Chelonia mydas) is known to present an herbivorous diet as an adult; however, juveniles may have an omnivore habit, and these changes in food preference may affect the uptake and accumulation of pollutants, such as mercury (Hg). In order to better understand the influence of this ontogenetic shift on Hg accumulation, this study evaluates the concentrations of total mercury (THg), methyl mercury (MeHg), and stable isotopes of carbon and nitrogen (δ13C and δ15N) in a group of juveniles of the green turtle. Tissue samples (liver, kidney, muscle, and scutes) were sampled from 47 turtles stranded dead on the coast of Bahia, NE, Brazil, between 2009 and 2013. The turtles analyzed showed a size range of 24.9-62.0cm and an average of 36.4 ± 7.2cm of curved carapace length. The scutes showed to be a viable method for Hg monitoring in the green turtles. The concentrations of THg and MeHg decreased with increasing size. The isotope values of δ15N and δ13C did not show a clear relationship with the size, suggesting that the green turtles used in our work would be occupying similar trophic levels, and foraging habitat.

Mercury bioaccumulation in freshwater fishes of the Chesapeake Bay watershed.

Chemical contaminants are a threat to the Chesapeake Bay watershed, with mercury (Hg) among the most prevalent causes of impairment. Despite this, large-scale patterns of Hg concentrations, and the potential risks to fish, wildlife, and humans across the watershed, are poorly understood. We compiled fish Hg data from state monitoring programs and recent research efforts to address this knowledge gap and provide a comprehensive assessment of fish Hg concentrations in the watershed's freshwater habitats. The resulting dataset consisted of nearly 8000 total Hg (THg) concentrations from 600 locations. Across the watershed, fish THg concentrations spanned a 44-fold range, with mean concentrations varying by 2.6- and 8.8-fold among major sub-watersheds and individual 8-digit hydrological units, respectively. Although, mean THg concentrations tended to be moderate, fish frequently exceeded benchmarks for potential adverse health effects, with 45, 48, and 36% of all samples exceeding benchmarks for human, avian piscivore, and fish risk, respectively. Importantly, the percentage of fish exceeding these benchmarks was not uniform among species or locations. The variation in fish THg concentrations among species and sites highlights the roles of waterbody, landscape, and ecological processes in shaping broad patterns in Hg risk across the watershed. We outline an integrated Hg monitoring program that could identify key factors influencing Hg concentrations across the watershed and facilitate the implementation of management strategies to mitigate the risks posed by Hg.

Development of a new binding phase for the diffusive gradients in thin films technique based on an ionic liquid for mercury determination.

Determining bioavailable trace concentrations of mercury (Hg) in water is still a challenging analytical task. In this study, we report a methodology for determining labile Hg in natural waters using newly developed sorbents. Silicon dioxide at a nanoparticle range (Si-np) and cellulose powder at a microparticle range (Cel-p), both modified with the ionic liquid trioctylmethylammonium thiosalicylate (TOMATS), have been tested as sorbents (sorb-TOMATS) for Hg(II) uptake from solution. These novel sorb-TOMATS materials were characterized, and parameters affecting the uptake were examined. A similar Hg(II) uptake efficiency (97%) and binding capacity (9mg Hg/g) was obtained for both sorb-TOMATS, while only a 25% of Hg(II) was taken up using non-impregnated materials. Moreover, these sorb-TOMATS were effectively embedded in agarose gel and were tested as a novel binding phase for the Diffusive Gradients in Thin Films (DGT) technique. Research revealed Si(np)-TOMATS sorbent as a suitable binding phase in the DGT technique for Hg(II) measurements, since it also allowed the efficient elution of the bound Hg(II). This new binding phase showed strong linear correlation between the accumulated Hg(II) mass and deployment time, which is in agreement with the DGT principle. In summary, this novel sorbent has a great potential to improve Hg monitoring in natural waters when integrated it in the DGT design.

Determining optimal sampling strategies for monitoring mercury and reproductive success in common loons in the Adirondacks of New York.

The common loon (Gavia immer), a top predator in the freshwater food web, has been recognized as an important bioindicator of aquatic mercury (Hg) pollution. Because capturing loons can be difficult, statistical approaches are needed to evaluate the efficiency of Hg monitoring. Using data from 1998 to 2016 collected in New York's Adirondack Park, we calculated the power to detect temporal changes in loon Hg concentrations and fledging success as a function of sampling intensity. There is a tradeoff between the number of lakes per year and the number of years needed to detect a particular rate of change. For example, a 5% year-1 change in Hg concentration could be detected with a sampling effort of either 15 lakes per year for 10 years, or 5 lakes per year for 15 years, given two loons sampled per lake per year. A 2% year-1 change in fledging success could be detected with a sampling effort of either 40 lakes per year for 15 years, or 30 lakes per year for 20 years. We found that more acidic lakes required greater sampling intensity than less acidic lakes for monitoring Hg concentrations but not for fledging success. Power analysis provides a means to optimize the sampling designs for monitoring loon Hg concentrations and reproductive success. This approach is applicable to other monitoring schemes where cost is an issue.

Total and methyl mercury distribution in water, sediment, plankton and fish along the Tapajós River basin in the Brazilian Amazon

Mercury (Hg) is known as one of the major contaminants in the Amazon. The Tapajós River basin, in the Brazilian Amazon, has diverse anthropogenic activities which increase Hg concentrations in the aquatic ecosystem. Moreover, high concentrations of Hg are naturally found in this basin. Distribution of total (THg) and methyl (MeHg) mercury were assessed in unfiltered water (n = 47), suspended particulate matter (SPM, n = 30), superficial sediment (BS, n = 29), plankton (n = 28) and fishes (n = 129) from the Tapajós River basin. Suspended particles were the main carrier of Hg in the water column and sediment. Increased erosion, prompted by anthropic activities, led to higher Hg concentrations in water from the most impacted areas. Hg is transported mainly in particulate matter; thus, anthropic disturbances influence Hg concentrations downstream. Limnological parameters such as organic matter content influenced MeHg concentrations in water, plankton and sediment of the Tapajós basin. Hg methylation in total plankton was more efficient in lakes (13-66%) than in Tapajós River main channel (2-14%). Biotic and abiotic factors interact in a complex way in the aquatic ecosystem, making Hg concentrations to vary in food web. Gold mining and deforestation probably increase Hg levels in the Tapajós basin. Thus, in addition to Hg monitoring, prevention and remediation efforts should be focused on soil and sediment erosion control.

Songbird feathers as indicators of mercury exposure: high variability and low predictive power suggest limitations.

Although feathers are commonly used to monitor mercury (Hg) in avian populations, their reliability as a sampling matrix has not been thoroughly assessed for many avian species, including most songbirds (Order Passeriformes). To better understand relationships between total Hg (THg) concentrations in feathers and other tissues for birds in the thrush and sparrow families, we (1) examined variation in THg concentrations among tissues, including feathers from six different tracts, nails, liver, and muscle; (2) tested relationships between THg concentrations in the various feather tracts and those in internal tissues from the same birds, to assess the predictive power of feather THg, and; (3) compared these relationships to those between THg concentrations in nails and internal tissues, to assess the viability of nails as a non-lethal sampling alternative. THg concentrations in all feather tracts and nails were consistently higher than those in the liver and muscle, and THg was higher in the thrushes than the sparrows. When comparing feather tracts, we observed high variation within some individuals, suggesting that estimates of Hg exposure could vary depending on which feather was sampled. Despite this variation, feather type had little effect on the predictive power of feather THg concentrations, which ranged from extremely weak in the sparrows (0.09 ≤ R2 ≤ 0.16) to moderate (0.29 ≤ R2 ≤ 0.42) in the thrushes. Alternatively, we found that nail samples better predicted internal tissue THg concentrations in both the thrushes (0.44 ≤ R2 ≤ 0.48) and sparrows (0.70 ≤ R2 ≤ 0.78). Nails have been used to monitor Hg in mammals and reptiles, but their reliability as a sampling matrix for monitoring Hg in avian populations has yet to be assessed for most taxa. While nails exhibit stronger relationships to internal tissue THg concentrations, they may not be an effective sampling option for all avian species because the collection of sizable nail samples could harm living birds, particularly small songbirds. However, this method may be reasonable for retrospective museum studies. Overall, our results suggest that, despite their current use in the literature, feathers are not a suitable sampling matrix for Hg monitoring in some songbird species.

New Electrochemical Sensor for Hg(II) Trace Detection in Natural Waters: Electrode Functionalization with Gold Nanoparticles and Diazonium Salts

Mercury (Hg) represents a growing environmental and health major concern. It originates from natural sources and mainly from anthropogenic processes and it is widely distributed in the natural media. According to the last Global Mercury Assessment (2013), annual global emissions from both sources were estimated to be from 5,000 to 8,000 metric tons per year. Among the different mercury species released to the environment, methylmercury (MeHg) is considered as the most toxic form due to its ability to bioaccumulate, being then threatening even at very low concentrations.Its presence depends onHg(II) bioavailability and global amount.This explains the urgent need to ensure a continuous Hg(II) monitoring. Many efforts have been made in order to develop reliable systems able to deliver quick data and to comply with low detection limits, in accordance with the threshold value delivered by the World Health Organization (1µg L-1/ 5 nM). Spectroscopic techniques such as CV-AFS and CV-AAS are routinely used for Hg(II) determination. Although these methods can afford good sensitivity and low concentrations determination, they require sample preparation step, complex procedures and expensive material, which limits their use for on-site measurements. In this context, electrochemical sensors present excellent candidates for in situ Hg(II) trace analysis, taking in account their numerous advantages compared to spectroscopic techniques: easier handling, simple procedure, low energy consuming, low cost material and portability. In this work, we will propose a new electrochemical approach aiming to conceive and optimize an electrochemical Hg(II) sensor. The method consists in the functionalization of a glassy carbon electrode (GC) with gold nanoparticles (AuNPs) and Diazonium Salts. The main idea is to combine the interesting properties of both AuNPs and Diazonium salts. AuNPs were chosen for their electrocatalytic effect, large surface area, mass transport enhancement and for the strong affinity to mercury which will improve the sensor sensitivity. On the other hand, diazonium salts are used to improve the sensor stability by anchoring the AuNPs to the GC surface. First, nanometricorganic layer were grafted of the polished GC surface, by electrochemical reduction of 1.5 mM4-thiophenol diazonium (SH) using Constant Potential Electrolysis (CPE) in 0.1 M HCl solution at -0.55 V for 300 seconds. Electrochemical characterization performed by Cyclic Voltammetry (CV) and redox probes (ferricyanide and hexaamineruthenium(III)) revealed a total suppression of the signal, confirming the formation of a continuous blocking layer. This was confirmed by Atomic Force Microscopy (AFM)used to estimate the layer thickness, which was found to be 4 nm. Second, AuNPs were electrodeposited, for the first time, onto the diazonium multilayer by CPE in NaNO3 solution containing 0.25 mM HAuCl4for 300 seconds. Once more, redox probes were used to characterize the resulting interface and a total signal restauration and enhancement was observed after AuNPs electrodeposition, which highlights the effective AuNPs onto the organic layers. Field emission gun scanning microscopy (FEG-SEM) was used to provided further evidence and to quantify particle size and density of the AuNPs deposits. Both size and density are dependent on the CPE duration. Small homogeneous AuNPs with 27±3 nm average diameter and 158 NPs/µm2density were observed when the CPE was carried out during 300 seconds, while larger particles with 63±6 nm average diameter and lower density (63 NPs/µm2) were obtained when a longer CPE duration (600 seconds) is used. Finally, AuNPs were activated by cyclic voltammetry in H2SO4 prior to Hg(II) detection in order to homogenize the surface and to rearrange the crystallographic plans of the AuNPs. Herein, the well-known gold oxides reduction peak was observed and used to calculate the electroactive surface area (ESA) of the functionlized electrode. The electrochemical response of the final generated GC/SH/AuNPs interface towards Hg(II) was recorded by Square Wave Anodic Stripping Voltammetry (SWASV) in 0.01 M HCl solution containing different amounts of Hg(II). The SWASV procedure consists on the Hg(II) preconcentration at the electrode surface followed by the preconcentrated Hg(0) reoxidation in Hg(II). Under optimized conditions, and for a preconcentration time of 300 seconds, a well-defined peak, corresponding to Hg(0) reoxidation, was observed around 0.5 V/ECS. The sensor showed a linearity range from 1 up to 10 nM and allowed to reach picomolar level. The stability in HCl, phosphate buffer and air was also studied over several weeks: Once a week, the activation procedure was performed and followed by Hg(II) determination in order to evaluate the analytical performances of the sensor over time. Finally, Hg(II) detection assays were conducted in natural water samples collected from different sampling points. Figure 1

Characterization and Quantification of Atmospheric Mercury Sources Using Passive Air Samplers

AbstractThe Minamata Convention on Mercury (Hg) requires improved atmospheric Hg monitoring and characterization of Hg sources. Here we demonstrate how a network of passive air samplers (PASs) can be used cost effectively to determine the spatial distribution of gaseous Hg and estimate atmospheric Hg emissions at contaminated sites. Gaseous Hg concentrations were mapped around a former Hg mine in the Monte Amiata district in Italy using simultaneous deployments of PASs across local and regional spatial scale grids. The concentration maps help visualize with great detail and precision the dispersal of gaseous Hg from a contaminated site, revealing even subtle effects of wind, season, and minor sources. Emissions estimated from the empirical data (80 ± 40 and 150 ± 75 kg/year for October and July, respectively) were robust to changes in the most uncertain parameters (excess Hg in the air above the mine and advection rate) and compared well to previous estimates for this and other closed Hg mines. This PAS‐based approach has a number of advantages: (i) concurrent deployments of multiple samplers constrain concentration changes to spatial variability only, (ii) time‐averaged data over longer periods negate biases related to short‐term, infrequent measurements, (iii) more spatially representative estimates of Hg distributions and emissions can be made at a fraction of the cost, and (iv) use is easy, especially in difficult terrain. Time‐averaged data across a broad area are also most pertinent for assessing chronic human exposure, especially in terms of the inhalation of Hg by workers and residents living close to contaminated sites.

Tracing Mercury Pollution along the Norwegian Coast via Elemental, Speciation, and Isotopic Analysis of Liver and Muscle Tissue of Deep-Water Marine Fish ( Brosme brosme).

Liver and muscle tissue of tusks ( Brosme brosme) have been analyzed for their THg and MeHg concentrations and Hg isotopic signatures for tracing Hg pollution along the Norwegian coast. Clear differences between tissue types and locations were established. At five of the eight locations, the Hg concentration in muscle exceeded the maximum allowable level of 0.5 mg kg-1 wet weight. δ202Hg values in both tissue types indicated that Hg speciation affects the bulk Hg isotopic signature. Tusk liver seems to be more sensitive to immediate changes and to anthropogenic inorganic Hg, while the muscle rather reflects the Hg accumulated over a longer period of exposure. The δ202Hg values of liver and muscle also enabled different sources of Hg and exposure pathways to be distinguished. δ202Hgmuscle-δ202Hgliver showed a clear correlation with the % MeHg in tusk liver for the coastal waters, but not for the fjords. The absence of significant differences in Δ199Hg values between both tissues of tusk from the same location suggests that in vivo metabolic processes are the underlying reason for the differences in Hg speciation and in δ202Hg values. This work highlights the importance of selecting different tissues of marine fish in future Hg monitoring programs.

Improved Environmental Status: 50 Years of Declining Fish Mercury Levels in Boreal and Subarctic Fennoscandia.

Temporally (1965-2015) and spatially (55°-70°N) extensive records of total mercury (Hg) in freshwater fish showed consistent declines in boreal and subarctic Fennoscandia. The database contains 54 560 fish entries ( n: pike > perch ≫ brown trout > roach ≈ Arctic charr) from 3132 lakes across Sweden, Finland, Norway, and Russian Murmansk area. 74% of the lakes did not meet the 0.5 ppm limit to protect human health. However, after 2000 only 25% of the lakes exceeded this level, indicating improved environmental status. In lakes where local pollution sources were identified, pike and perch Hg concentrations were significantly higher between 1965 and 1990 compared to values after 1995, likely an effect of implemented reduction measures. In lakes where Hg originated from long-range transboundary air pollution (LRTAP), consistent Hg declines (3-7‰ per year) were found for perch and pike in both boreal and subarctic Fennoscandia, suggesting common environmental controls. Hg in perch and pike in LRTAP lakes showed minimal declines with latitude, suggesting that drivers affected by temperature, such as growth dilution, counteracted Hg loading and food web exposure. We recommend that future fish Hg monitoring sampling design should include repeated sampling and collection of pollution history, water chemistry, fish age, and stable isotopes to enable evaluation of emission reduction policies.

Mercury determination at trace levels using membrane preconcentration and benchtop total reflection X-ray fluorescence analysis

At present, there is a considerable interest in Hg monitoring in water samples due to its widespread occurrence and the high toxicity of most of its compounds. Hg determination in water samples by means of total reflection X-ray fluorescence spectrometry (TXRF) entails some difficulties due to the high vapour pressure and low boiling point of this element that produce evaporation and loss of Hg from the surface of the reflector during the drying process, commonly employed in sample preparation in TXRF analysis.In a former work we demonstrated the usefulness of PVC-based membranes functionalized with dithizone for Hg preconcentration. Limits of detection as low as 0.8 μg·L−1 Hg were obtained using a 1 kW TXRF system. The main goal of the present research was to improve the extraction system and to apply it in combination with low power TXRF instrumentation (50 W). In this sense, some extraction parameters as well as measurement conditions such as the volume of membrane deposited on the quartz reflector, the agitation speed during extraction, the aqueous sample volume and the measurement time were carefully evaluated to obtain the maximum sensitivity for Hg determination. Using the best analytical conditions, a limit of detection for Hg of 0.3 μg·L−1 was obtained which is adequate according to the limits of current legislation on the quality of water for human consumption. Additionally, a morphological study of the preconcentrated sample on the quartz reflector was performed by optical microscopy and information regarding Hg distribution along the membrane was obtained by μ-XRF analysis. It was found that Hg is not homogenously accumulated on the membrane and thus, the size of the membrane on the reflector is a critical parameter that has to be controlled to ensure the complete exposure of the loaded membrane to the X-ray beam. This fact is of special relevance when using this preconcentration approach in combination with micro-TXRF. Finally, to further prove applicability of the TXRF method for real water sample analysis, different types of spiked water samples were analysed.

A Study on the Total Mercury (Hg) Monitoring and Methylmercury (MeHg) Analysis method and Exposure Assessment of Methylmercury (MeHg) in Marine Products

A Study on the Total Mercury (Hg) Monitoring and Methylmercury (MeHg) Analysis method and Exposure Assessment of Methylmercury (MeHg) in Marine Products

Global evaluation and calibration of a passive air sampler for gaseous mercury

Abstract. Passive air samplers (PASs) for gaseous mercury (Hg) were deployed for time periods between 1 month and 1 year at 20 sites across the globe with continuous atmospheric Hg monitoring using active Tekran instruments. The purpose was to evaluate the accuracy of the PAS vis-à-vis the industry standard active instruments and to determine a sampling rate (SR; the volume of air stripped of gaseous Hg per unit of time) that is applicable across a wide range of conditions. The sites spanned a wide range of latitudes, altitudes, meteorological conditions, and gaseous Hg concentrations. Precision, based on 378 replicated deployments performed by numerous personnel at multiple sites, is 3.6 ± 3.0 %1, confirming the PAS's excellent reproducibility and ease of use. Using a SR previously determined at a single site, gaseous Hg concentrations derived from the globally distributed PASs deviate from Tekran-based concentrations by 14.2 ± 10 %. A recalibration using the entire new data set yields a slightly higher SR of 0.1354 ± 0.016 m3 day−1. When concentrations are derived from the PAS using this revised SR the difference between concentrations from active and passive sampling is reduced to 8.8 ± 7.5 %. At the mean gaseous Hg concentration across the study sites of 1.54 ng m−3, this represents an ability to resolve concentrations to within 0.13 ng m−3. Adjusting the sampling rate to deployment specific temperatures and wind speeds does not decrease the difference in active–passive concentration further (8.7 ± 5.7 %), but reduces its variability by leading to better agreement in Hg concentrations measured at sites with very high and very low temperatures and very high wind speeds. This value (8.7 ± 5.7 %) represents a conservative assessment of the overall uncertainty of the PAS due to inherent uncertainties of the Tekran instruments. Going forward, the recalibrated SR adjusted for temperature and wind speed should be used, especially if conditions are highly variable or deviate considerably from the average of the deployments in this study (9.89 ∘C, 3.41 m s−1). Overall, the study demonstrates that the sampler is capable of recording background gaseous Hg concentrations across a wide range of environmental conditions with accuracy similar to that of industry standard active sampling instruments. Results at sites with active speciation units were inconclusive on whether the PASs take up total gaseous Hg or solely gaseous elemental Hg primarily because gaseous oxidized Hg concentrations were in a similar range as the uncertainty of the PAS.

Mercury Bioaccumulation in Tropical Mangrove Wetland Fishes: Evaluating Potential Risk to Coastal Wildlife.

The present study, aimed at observing the total concentration of mercury (Hg) in edible finfish species with an implication to human health risk, was carried out from the Setiu mangrove wetlands on the east coast of Peninsular Malaysia. Out of 20 species observed, the highest Hg concentrations were found among carnivores-fish/invertebrate-feeders, followed by omnivores and carnivores-invertebrate-feeders, while the lowest concentrations in herbivores. The Hg concentrations varied widely with fish species and body size, from 0.12 to 2.10mg/kg dry weight. A positive relationship between body weight and Hg concentration was observed in particular for Toxotes jaculatrix and Tetraodon nigroviridis. Besides the permissible range of Hg concentration up to 0.3mg/kg (cf. United States Environmental Protection Agency (USEPA)) in majority of species, the carnivore feeders such as Acanthopagrus pacificus, Gerres filamentosus, and Caranx ignobilis have shown excess amounts (> 0.40mg/kg flesh weight) that raising concerns over the consumption by local people. However, the weekly intake of mercury-estimated through the fish consumption in all three trophic levels-suggests that the present Hg concentrations are still within the range of Provisional Tolerable Weekly Intake (PTWI) reported by the Joint FAO/WHO Expert Committee on Food Additives (JECFA). Perhaps, a multi-species design for Hg monitoring at Setiu wetlands would be able to provide further insights into the level of toxicity transfer among other aquatic organisms and thereby a strong health risk assessment for the local communities.

Cleaning and sampling protocol for analysis of mercury and dissolved organic matter in freshwater systems

Mercury (Hg), and in particular its methylated form (methylmercury, MeHg), is a hazardous substance with the potential to produce significant adverse neurological and other health effects. Enhanced anthropogenic emissions and long-range transport of atmospheric Hg have increased Hg concentrations above background levels in aquatic systems. In this context, the Minamata Convention, a global legally binding agreement that seeks to prevent human exposure to Hg, was signed and enforced by 128 countries, and today more than 90 Parties have ratified it. All these Parties have committed to develop Hg monitoring programs to report the effectiveness of the convention. For this purpose, we provide a standardized cleaning and water sampling protocol for the determination of total-Hg and MeHg in freshwaters at ambient levels. As Hg and organic matter are tightly bound, the protocol also describes sample collection for dissolved organic carbon (DOC) concentration and characterization of dissolved organic matter (DOM) composition by fluorescence spectroscopy. This protocol is highly useful to non-experts without a prior background in Hg sampling and analysis, and can serve as a useful basis for national monitoring programs. Furthermore, this protocol should help increase quantitative inventories of DOC, inorganic-Hg (IHg) and MeHg concentrations and DOM composition in freshwater, which are severely lacking at a global scale.•Provides a standardized method to collect water samples for IHg, MeHg, DOC and DOM composition from freshwater ecosystems.

Mercury health risk assessment among a young adult Lebanese population.

Mercury (Hg) exposure represents a significant public health concern at a global level. This study aims at assessing Hg exposure and risk among Lebanese young adults based on Hg biomonitoring and seafood intake. A group of 166 young adults were administered a questionnaire to assess Hg exposure and were asked to provide a hair sample. Risk assessment was performed: (1) using the US Environmental Protection Agency Hazard Quotient (HQ) model based on fish intake and previously studied local fish Hg concentrations, and (2) by determining the total hair Hg concentration (THHg) using continuous flow-chemical vapor generation atomic absorption spectrometry. Differences in THHg across demographic and exposure subgroups were tested using t test or ANOVA. Correlations between THHg concentrations, fish consumption, and HQ were determined by computing Pearson's r. Higher THHg correlated with higher consumption of Mediterranean rabbitfish/spinefoots (r=0.27; p=0.001) and geographical location (p<0.001) in the bivariate analysis, and remained significant in the adjusted multivariable linear regression model (geographical location: ß=0.255, 95%CI 0.121-0.388; rabbitfish/spinefoots consumption: ß=0.016, 95%CI 0.004-0.027). No significant correlations were found between HQ and THHg. In conclusion, this is the first study examining hair Hg levels and fish consumption in a young adult Lebanese population. Our findings constitute valuable baseline data for a local fish advisory and Hg monitoring.

BLOOD PRESSURE PHENOTYPES IN TREATED HYPERTENSIVE PATIENTS IN SUMMER AND WINTER: FOCUS ON MASKED UNCONTROLLED HYPERTENSION. Part 2. The main markers

Background. Seasonal variability of cardiovascular morbidity and mortality emphasizes the need for the development of new preventive approaches. One of them could be early diagnostics of the unfavorable blood pressure (BP) phenotypes. Aim. To evaluate markers of the masked uncontrolled hypertension (MUH) phenotype in winter and summer in ambulatory treated hypertensive patients. Material and methods . We selected patients from the database (n=477; Ivanovo and Saratov residents) according to the following criteria: regular antihypertensive treatment (AHT), clinical BP<140/90 mm Hg, available clinical and ambulatory BP monitoring (ABPM) data both in winter and summer (MUH and “optimal AHT effect” phenotypes). Results. The patients with MUH in Ivanovo had a significantly higher body mass index in comparison with patients with optimal AHT effect in winter (29.1±4.4 kg/m2 vs 27.3±3.4 kg/m2; p<0.01), and a higher level of clinical BP. Similar differences were found for clinical heart rate (HR), orthostatic BP and HR. These patients with MUH in summer had significantly higher values of clinical BP and orthostatic systolic BP. In Saratov patients, the MUH phenotype in winter was characterized by a higher prevalence in men (56% vs 38%; p<0.05), a relatively high body height and weight vs these in patients with optimal AHT effect. Similar to the patients from Ivanovo, Saratov patients with MUH in winter had higher clinical and orthostatic BP levels compared to patients with optimal AHT effect. In summer, Saratov patients with MUH had significantly higher body mass index, clinical BP, orthostatic HR and systolic BP. In multivariate analysis, MUH was associated with male sex (p<0.05), obesity Stage 1 (p<0.05) and Stage 2 (p<0.01), and diastolic BP in orthostasis (in particular, diastolic BP≥85 mmHg; p<0.0001). No significant associations were observed for season, city, and other selected factors. Conclusion. According to our study ABPM could be useful for “unmasking” of the probable MUH both in winter and in summer in patients with target clinical BP on AHT who are obese, have orthostatic diastolic BP ≥85 mmHg and especially in men. Further studies in this area are required, in particular the assessment of the prognostic value of the seasonal dynamics and interrelation of clinical and ambulatory BP.