Dissolved Gaseous Mercury Production at a Marine Aquaculture Site in the Mercury-Contaminated Marano and Grado Lagoon, Italy.

Dissolved gaseous mercury (DGM) production was examined in relation to ultraviolet radiation within a marine aquaculture site in the contaminated Marano and Grado Lagoon (Italy). The measured rates of DGM production relative to time elapsed (17.06 and 20.68 pg h-1, respectively) were substantially (6-20 times) higher than what has been observed in other marine Hg studies. We measured similar levels of DGM relative to dissolved total mercury (THgD) (0.84%-8.91%) at these sites in comparison to uncontaminated marine sites, however relative to other moderately-contaminated marine sites in Portugal the % DGM/THgD was high. These results suggest a substantial capacity for Hg volatilization from these highly contaminated lagoons to the atmosphere due to photoreduction mechanisms.

Effect of forced aeration on the biogeochemical cycle of nutrients and metal(loid)s as a remedy for hypoxia in a permanently stratified estuary (Gulf of Trieste, northern Adriatic Sea).

The Timavo River estuary (northern Adriatic Sea) is characterised by strong thermohaline stratification that keeps the deep waters hypoxic. The consequence is an harmful algal bloom at the surface in summer that can be mitigated with a forced aeration system installed at the bottom to improve water oxygenation. The nutrient and metal(loid) cycle was investigated, before and during reoxygenation, using an in situ benthic chamber coupled with sampling and analyses of the water column, sediments and porewater. Dissolved oxygen (DO) decreased along the water column and quickly within the benthic chamber when aeration was not in operation, resulting in hypoxia (2.29 mg L-1) at the bottom and consequent increase in nutrient and metal(loid) concentrations. In contrast, DO levels increased during the activation of the forced aeration system, which proved effective in mitigating oxygen depletion and the efflux of metal(loid)s and nutrients into the overlying water.

Gaseous mercury evasion from bare and grass-covered soils contaminated by mining and ore roasting (Isonzo River alluvial plain, Northeastern Italy).

High amounts of mercury (Hg) can be released into the atmosphere from soil surfaces of legacy contaminated areas as gaseous elemental mercury (Hg0). The alluvial plain of the Isonzo River (NE Italy) suffered widespread Hg contamination due to the re-distribution of Hg-enriched material discharged by historical cinnabar mining at the Idrija mine (Slovenia), but an assessment of Hg0 releases from the soils of this area is still lacking. In this work, Hg0 fluxes at the soil-air interface were evaluated using a non-steady state flux chamber coupled with a real-time Hg0 analyser at 6 sites within the Isonzo River plain. Measurements were performed in summer, autumn, and winter both on bare and grass-covered soil plots at regular time intervals during the diurnal period. Moreover, topsoils were analysed for organic matter content and Hg total concentration and speciation. Overall, Hg0 fluxes tracked the incident UV radiation during the sampling periods with daily averages significantly higher in summer (62.4 ± 14.5-800.2 ± 178.8 ng m-2 h-1) than autumn (15.2 ± 4.7-280.8 ± 75.6 ng m-2 h-1) and winter (16.9 ± 7.9-187.8 ± 62.7 ng m-2 h-1) due to higher irradiation and temperature, which favoured Hg reduction reactions. In summer and autumn significant correlations were observed between Hg0 fluxes and soil Hg content (78-95% cinnabar), whereas this relationship was not observed in winter likely due to relatively low emissions found in morning measurements in all sites coupled with low temperatures. Finally, vegetation cover effectively reduced Hg0 releases in summer (∼9-68%) and autumn (∼41-78%), whereas the difference between fluxes from vegetated and bare soils was not evident during winter dormancy due to scarce soil shading. These results suggest the opportunity of more extended spatial monitoring of Hg0 fluxes particularly in the croplands covering most of the Isonzo River alluvial plain and where bare soils are frequently disturbed by agricultural practices and directly exposed to radiation.

Dissolved gaseous mercury production and sea-air gaseous exchange in impacted coastal environments of the northern Adriatic Sea.

The northern Adriatic Sea is well known for mercury (Hg) contamination mainly due to historical Hg mining which took place in Idrija (Slovenia). The formation of dissolved gaseous mercury (DGM) and its subsequent volatilisation can reduce the amount of Hg available in the water column. In this work, the diurnal patterns of both DGM production and gaseous elemental Hg (Hg0) fluxes at the water-air interface were seasonally evaluated in two selected environments within this area, a highly Hg-impacted, confined fish farm (VN: Val Noghera, Italy) and an open coastal zone less impacted by Hg inputs (PR: Bay of Piran, Slovenia). A floating flux chamber coupled with a real-time Hg0 analyser was used for flux estimation in parallel with DGM concentrations determination through in-field incubations. Substantial DGM production was observed at VN (range = 126.0-711.3 pg L-1) driven by both strong photoreduction and possibly dark biotic reduction, resulting in higher values in spring and summer and comparable concentrations throughout both day and night. Significantly lower DGM was observed at PR (range = 21.8-183.4 pg L-1). Surprisingly, comparable Hg0 fluxes were found at the two sites (range VN = 7.43-41.17 ng m-2 h-1, PR = 0-81.49 ng m-2 h-1), likely due to enhanced gaseous exchanges at PR thanks to high water turbulence and to the strong limitation of evasion at VN by water stagnation and expected high DGM oxidation in saltwater. Slight differences between the temporal variation of DGM and fluxes indicate that Hg evasion is more controlled by factors such as water temperature and mixing conditions than DGM concentrations alone. The relative low Hg losses through volatilisation at VN (2.4-4.6% of total Hg) further confirm that static conditions in saltwater environments negatively affect the ability of this process in reducing the amount of Hg retained in the water column, therefore potentially leading to a greater availability for methylation and trophic transfer.

Environmental impact of potentially toxic elements on soils, sediments, waters, and air nearby an abandoned Hg-rich fahlore mine (Mt. Avanza, Carnic Alps, NE Italy).

The decommissioned fahlore Cu-Sb(-Ag) mine at Mt. Avanza (Carnic Alps, Italy) is a rare example of exploited ore deposits, as the tetrahedrite (Cu6[Cu4(Fe,Zn)2]Sb4S13) is the main ore mineral found. This multi-compartmental geochemical characterisation approach provides one of the first case studies regarding the geochemical behaviour and fate of Hg, Sb, As, Cu, and other elements in solid and water matrices and of Hg in the atmosphere in an environment affected by the mining activity of a fahlore ore deposit. Elevated concentrations of the elements (Cu, Sb, As, Pb, Zn, Hg) associated with both (Zn-Hg)-tetrahedrite and to other minor ore minerals in mine wastes, soils, and stream sediments were observed. Concentrations in waters and stream sediments greatly decreased with increasing distance from the mining area and the Igeo index values testify the highest levels of sediment contamination inside the mine area. Thallium and Ge were associated with the "lithogenic component" and not to sulfosalt/sulphide minerals. Although mine drainage water often slightly exceeded the national regulatory limits for Sb and As, with Sb being more mobile than As, the relatively low dissolved concentrations indicate a moderate stability of the tetrahedrite. The fate of Hg at the investigated fahlore mining district appeared similar to cinnabar mining sites around the world. Weak solubility but the potential evasion of gaseous elemental mercury (GEM) into the atmosphere also appear to be characteristics of Hg in fahlore ores. Although GEM concentrations are such that they do not present a pressing concern, real-time field surveys allowed for the easy identification of Hg sources, proving to be an effective, suitable high-resolution indirect approach for optimising soil sampling surveys and detecting mine wastes and mine adits.

Concentration of mercury in human hair and associated factors in residents of the Gulf of Trieste (North-Eastern Italy).

The Gulf of Trieste (Northern Adriatic Sea, Italy) is the coastal area of the Mediterranean Sea most highly contaminated by mercury (Hg) due to fluvial inputs from the Isonzo/Soca River system, draining over 500 years' worth of cinnabar extraction activity from the Idrija mining district (Western Slovenia). The aim of this research is to investigate the concentration of Hg in hair samples taken from the general population of the Friuli Venezia Giulia (FVG) Region coastal area, as a marker of chronic exposure to Hg. Three hundred and one individuals - 119 males and 182 females - were recruited by convenience sampling in Trieste in September 2021. An amount of approximately 100 mg of hair was collected from the occipital scalp of each participant to measure the respective Hg concentrations (expressed as mg/kg). Moreover, participants completed a self-report questionnaire collecting extensive socio-demographic and life-style information. A multiple linear regression analysis was employed to investigate factors associated with increased levels of Hg concentration in hair. A mean Hg concentration in hair of 1.63 mg/kg was found, slightly above the 1.0 mg/kg threshold recommended by the WHO for pregnant women and children, although still well below the no observed adverse effects level (NOAEL) of 10 mg/kg. Among respondents, 55.6% showed a Hg concentration in hair > 1 mg/kg, 22.9% > 2 mg/kg, and 2 participants exhibited Hg levels > 10 mg/kg. The adjusted mean hair Hg level increased in those subjects who reported a preference for shellfish/crayfish/mollusks (RC = 0.35; 95%CI: 0.16; 0.55), whereas it decreased in those who reported a preference for frozen fish (RC = -0.23; 95%CI: - 0.39; - 0.06). Though a risk alert for Hg exposure for coastal residents from FVG is deemed unnecessary at this time, it is recommended that pregnant women limit their ingestion of locally caught fish to < 4 servings/month.

Gaseous Mercury Exchange from Water-Air Interface in Differently Impacted Freshwater Environments.

Gaseous exchanges of mercury (Hg) at the water-air interface in contaminated sites strongly influence its fate in the environment. In this study, diurnal gaseous Hg exchanges were seasonally evaluated by means of a floating flux chamber in two freshwater environments impacted by anthropogenic sources of Hg, specifically historical mining activity (Solkan Reservoir, Slovenia) and the chlor-alkali industry (Torviscosa dockyard, Italy), and in a pristine site, Cavazzo Lake (Italy). The highest fluxes (21.88 ± 11.55 ng m-2 h-1) were observed at Solkan, coupled with high dissolved gaseous mercury (DGM) and dissolved Hg (THgD) concentrations. Conversely, low vertical mixing and saltwater intrusion at Torviscosa limited Hg mobility through the water column, with higher Hg concentrations in the deep layer near the contaminated sediments. Consequently, both DGM and THgD in surface water were generally lower at Torviscosa than at Solkan, resulting in lower fluxes (19.01 ± 12.65 ng m-2 h-1). However, at this site, evasion may also be limited by high atmospheric Hg levels related to dispersion of emissions from the nearby chlor-alkali plant. Surprisingly, comparable fluxes (15.56 ± 12.78 ng m-2 h-1) and Hg levels in water were observed at Cavazzo, suggesting a previously unidentified Hg input (atmospheric depositions or local geology). Overall, at all sites the fluxes were higher in the summer and correlated to incident UV radiation and water temperature due to enhanced photo production and diffusivity of DGM, the concentrations of which roughly followed the same seasonal trend.

Diurnal fluxes of gaseous elemental mercury from the water-air interface in coastal environments of the northern Adriatic Sea.

A crucial step towards developing a more complete understanding of mercury (Hg) biogeochemical cycling in coastal environments is the measurement of the fluxes of gaseous elemental mercury (GEM), at the water-air interface (W-A interface). A floating flux chamber coupled with a real-time atomic adsorption spectrometer (Lumex-RA 915M) was applied to measure GEM concentrations, and to estimate the diurnal evasion flux at the W-A interface during three seasonal campaigns at four selected sites: two in a lagoon-based fish farm, one in an open lagoon environment highly impacted by long-term activities from the Idrija mercury mine (Slovenia), and an uncontaminated area of the Gulf of Trieste, the Bay of Piran (Slovenia). In this study, the regional background concentration measured at the uncontaminated site of atmospheric GEM (from 1.60 ±â€¯0.95 to 2.87 ±â€¯1.52 ng m-3) was determined. GEM fluxes at the W-A interface were found to be significantly higher during the summer (from 51.2 ±â€¯8.8 ng m-2 h-1 to 79.9 ±â€¯11.4 ng m-2 h-1) and correlated to incident solar radiation and water temperature. This finding confirms the importance of these two parameters in the photoreduction and biotic reduction of Hg2+ to dissolved gaseous mercury (DGM), which is volatile and easily released to the atmosphere in the form of GEM. These new insights will be of help for future estimates of Hg mass balance in one of the most contaminated areas in the Adriatic Sea.