Dissolved gaseous mercury formation and mercury volatilization in intertidal sediments.

Intertidal sediments of Tagus estuary regularly experiences complex redistribution due to tidal forcing, which affects the cycling of mercury (Hg) between sediments and the water column. This study quantifies total mercury (Hg) and methylmercury (MMHg) concentrations and fluxes in a flooded mudflat as well as the effects on water-level fluctuations on the air-surface exchange of mercury. A fast increase in dissolved Hg and MMHg concentrations was observed in overlying water in the first 10min of inundation and corresponded to a decrease in pore waters, suggesting a rapid export of Hg and MMHg from sediments to the water column.

Sulfonylurea herbicides in an agricultural catchment basin and its adjacent wetland in the St. Lawrence River basin.

The use of sulfonylurea herbicides (SU) has increased greater than 100 times over the past 30 years in both Europe and North America. Applied at low rates, their presence, persistence and potential impacts on aquatic ecosystems remain poorly studied. During late-spring to early fall in 2009-2011, concentrations of 9 SU were assessed in two agricultural streams and their receiving wetland, an enlargement of the St.

Variation in peak growing season net ecosystem production across the Canadian Arctic.

Tundra ecosystems store vast amounts of soil organic carbon, which may be sensitive to climatic change. Net ecosystem production, NEP, is the net exchange of carbon dioxide (CO(2)) between landscapes and the atmosphere, and represents the balance between CO(2) uptake by photosynthesis and release by decomposition and autotrophic respiration. Here we examine CO(2) exchange across seven sites in the Canadian low and high Arctic during the peak growing season (July) in summer 2008.

Mercury in sediments and vegetation in a moderately contaminated salt marsh (Tagus Estuary, Portugal).

Depth variations of total mercury (Hg) and methylmercury (MeHg) concentrations were studied in cores from non-colonized sediments, sediments colonized by Halimione portulacoides, Sarcocorniafruticosa and Spartina maritima and belowground biomass, in a moderately contaminated salt marsh (Tagus Estuary, Portugal). Concentrations in belowground biomass exceeded up to 3 (Hg) and 15 (MeHg) times the levels in sediments, and up to 198 (Hg) and 308 (MeHg) times those found in aboveground parts. Methylmercury in colonized sediments reached 3% of the total Hg, 50 times above the maximum values found in non-colonized sediments.

Mercury transport between sediments and the overlying water of the St. Lawrence River area of concern near Cornwall, Ontario.

Contaminated sediments in the St. Lawrence River remain a difficult problem despite decreases in emissions. Here, sediment and pore water phases were analyzed for total mercury (THg) and methyl mercury (MeHg) and diffusion from the sediment to the overlying water was 17.

Tropospheric H(2) budget and the response of its soil uptake under the changing environment.

Molecular hydrogen (H(2)) is an indirect greenhouse gas present at the trace level in the atmosphere. So far, the sum of its sources and sinks is close to equilibrium, but its large-scale utilization as an alternative energy carrier would alter its atmospheric burden. The magnitude of the emissions associated with a future H(2)-based economy is difficult to predict and remains a matter of debate.

Sediment processes and mercury transport in a frozen freshwater fluvial lake (Lake St. Louis, QC, Canada).

An open-bottom and a closed-bottom mesocosm were developed to investigate the release of mercury from sediments to the water column in a frozen freshwater lake. The mesoscosms were deployed in a hole in the ice and particulate mercury (Hg(P)) and total dissolved mercury (TDHg) were measured in sediments and in water column vertical profiles. In addition, dissolved gaseous mercury (DGM) in water and mercury water/airflux were quantified.

Methylated mercury species in marine waters of the Canadian high and sub Arctic.

Distribution of total mercury (THg), gaseous elemental Hg(0) (GEM), monomethyl Hg (MMHg), and dimethyl Hg (DMHg) was examined in marine waters of the Canadian Arctic Archipelago (CAA), Hudson Strait, and Hudson Bay. Concentrations of THg were low throughout the water column in all regions sampled (mean +/- standard deviation; 0.40 +/- 0.

Pesticides in the atmosphere across Canadian agricultural regions.

The Canadian Atmospheric Network for Currently Used Pesticides (CANCUP) was the first comprehensive, nationwide air surveillance study of pesticides in Canada. This paper presentsthe atmospheric occurrence and distribution of pesticides including organochlorine pesticides (OCPs), organophosphate pesticides (OPPs), acid herbicides (AHs), and neutral herbicides (NHs) during the spring to summer of 2004 and 2005 across agricultural regions in Canada. Atmospheric concentrations of pesticides varied within years and time periods, and regional characteristics were observed including the following: (i) highest air concentrations of several herbicides (e.

Critical review of mercury fates and contamination in the Arctic tundra ecosystem.

Mercury (Hg) contamination in tundra region has raised substantial concerns, especially since the first report of atmospheric mercury depletion events (AMDEs) in the Polar Regions. During the past decade, steady progress has been made in the research of Hg cycling in the Polar Regions. This has generated a unique opportunity to survey the whole Arctic in respect to Hg issue and to find out new discoveries.

Pesticides in fluvial wetlands catchments under intensive agricultural activities.

A survey on pesticides (73 compounds) in the Bay St. François wetland and its catchment (part of the wetlands of Lake St. Pierre area [St.

Isolation of Streptomyces sp. PCB7, the first microorganism demonstrating high-affinity uptake of tropospheric H2.

Microbial-mediated soil uptake accounts for approximately 80% of the global tropospheric dihydrogen (H(2)) sinks. Studies conducted over the last three decades provide indirect evidences that H(2) soil uptake is mediated by free soil hydrogenases or by unknown microorganisms that have a high affinity for H(2). The exact nature of these hypothetical free soil enzymes or of H(2)-consuming microorganisms remains elusive because the activity has never been observed in pure culture.

Pesticides measured in air and precipitation in the Yamaska Basin (Québec): occurrence and concentrations in 2004.

Air and precipitation samples were collected and analyzed for 91 pesticides or metabolites from May to September 2004 at St. Damase, an agricultural site located in Yamaska basin in Québec, Canada. A broad range of pesticides was detected during this experiment where 40 different compounds were measured.

The ebullition of hydrogen, carbon monoxide, methane, carbon dioxide and total gaseous mercury from the Cornwall Area of Concern.

This paper reports the first ebullitive fluxes of hydrogen (H2), carbon monoxide (CO), methane (CH4), carbon dioxide (CO2) and total gaseous mercury (TGM) from the Cornwall Area of Concern (CAC). Although sediments were contaminated with mercury, bubbling was a negligible source of mercury for the global atmosphere. Indeed, the average emission of TGM through ebullition was 0.

Abiotic source of reactive organic halogens in the sub-arctic atmosphere?

Recent theoretical studies indicate that reactive organic iodocarbons such as CH2I2 would be extremely effective agents for tropospheric Arctic ozone depletion and that iodine compounds added to a Br2/BrCl mixture have a significantly greater ozone (and mercury) depletion effect than additional Br2 and BrCl molecules. Here we report the first observations of CH2I2, CH2IBr, and CH2ICl in Arctic air, as well as other reactive halocarbons including CHBr3, during spring at Kuujjuarapik, Hudson Bay. The organoiodine compounds were present atthe highest levels yet reported in air.

Estimation and mapping of wet and dry mercury deposition across northeastern North America.

Whereas many ecosystem characteristics and processes influence mercury accumulation in higher trophic-level organisms, the mercury flux from the atmosphere to a lake and its watershed is a likely factor in potential risk to biota. Atmospheric deposition clearly affects mercury accumulation in soils and lake sediments. Thus, knowledge of spatial patterns in atmospheric deposition may provide information for assessing the relative risk for ecosystems to exhibit excessive biotic mercury contamination.

Patterns of mercury deposition and concentration in northeastern North America (1996-2002).

Data from 13 National Atmospheric Deposition Program Mercury Monitor Network (NADP/ MDN) monitoring stations (1996-2002) and the Underhill (VT) event-based monitoring site (1993-2002) were evaluated for spatial and temporal trends. More precipitation and mercury deposition occurred in the southern and coastal MDN sites, except for the Underhill site, which received more mercury deposition than surrounding sites. Precipitation patterns varied.

Some pesticides occurrence in air and precipitation in Québec, Canada.

Air and precipitation samples were collected in three stations located in Quebec between January 1993 and March 1996 to determine spatial and seasonal variations of several organochlorine pesticides and metabolites (alpha-HCH, gamma-HCH, HCB, gamma-chlordane, DDT, DDE, Mirex). alpha-HCH, gamma-HCH, and HCB were more or less measured in large amounts at all sites, whereas gamma-chlordane, DDT, and DDE concentrations were lower and Mirex was undetectable. Higher concentrations levels were observed in air during hot spring/summer periods except for HCB, indicating a probable temperature dependence.

Scavenging of gaseous mercury by acidic snow at Kuujjuarapik, Northern Québec.

One fate of gaseous elemental mercury (GEM) in the Arctic has been identified as gas phase oxidation by halogen-containing radicals, leading to abrupt atmospheric mercury depletion concurrent with ozone depletion. Rapid deposition of oxidized mercury leads to snow enrichment in mercury. In this report, we describe experiments that demonstrate the ability of snow to directly scavenge atmospheric mercury.

Mercury in the Arctic atmosphere: an analysis of eight years of measurements of GEM at Alert (Canada) and a comparison with observations at Amderma (Russia) and Kuujjuarapik (Canada).

Eight years of gaseous elemental mercury (GEM) concentration measurements from Alert, Nunavut, Canada (between 1995 and 2002) is presented. The annual time series shows a distinct repeating seasonal pattern with an overall annual median concentration for this time period of 1.58 (S.

Atmospheric particle evolution during a nighttime atmospheric mercury depletion event in sub-Arctic at Kuujjuarapik/Whapmagoostui, Québec, Canada.

During a field experiment at Kuujjuarapik/Whapmagoostui (55.31 degrees N, 77.75 degrees W), Quebec, we observed increases of concentrations of particles with diameters larger than 0.

Modeling the atmospheric transport and deposition of mercury to the Great Lakes.

A special version of the NOAA HYSPLIT_4 model has been developed and used to estimate the atmospheric fate and transport of mercury in a North American modeling domain. Spatial and chemical interpolation procedures were used to expand the modeling results and provide estimates of the contribution of each source in a 1996 anthropogenic US/Canadian emissions inventory to atmospheric mercury deposition to the Great Lakes. While there are uncertainties in the emissions inventories and ambient data suitable for model evaluation are scarce, model results were found to be reasonably consistent with wet deposition measurements in the Great Lakes region and with independent measurement-based estimates of deposition to Lake Michigan.

Diurnal cycles of gaseous mercury within the snowpack at Kuujjuarapik/Whapmagoostui, Québec, Canada.

Mercury is a globally dispersed and toxic pollutant that can be transported far from its emission sources. In polar and subpolar regions, recent research activities have demonstrated its ability to be converted and deposited rapidly onto snow surfaces during the so-known Mercury Depletion Events (MDEs). The fate of mercury once deposited onto snow surfaces is still unclear: a part could be re-emitted to the atmosphere, the other part could contaminate water systems at the snowmelt.

Polycyclic aromatic hydrocarbons in the air in the St. Lawrence Basin (Québec).

High-volume air samples were collected from 1993 to 1996 in rural areas of Québec to investigate on the levels and the vapor-particle partitioning of polycyclic aromatic hydrocarbons (PAHs). Ranges for the mean concentrations of total PAHs (ng m(-3)) were as follows: Villeroy, 3.31-18.