A benchmark concentration analysis for manganese in drinking water and IQ deficits in children.

Background: Manganese is an essential nutrient, but in excess, can be a potent neurotoxicant. We previously reported findings from two cross-sectional studies on children, showing that higher concentrations of manganese in drinking water were associated with deficits in IQ scores. Despite the common occurrence of this neurotoxic metal, its concentration in drinking water is rarely regulated.

Radium geochemical monitoring in well waters at regional and local scales: an environmental impact indicator-based approach.

To assess radium (Ra) as a potential indicator of impact in well waters, we investigated its behavior under natural conditions using a case study approach. Ra geochemistry was investigated in 67 private wells of southeastern New Brunswick, Canada, a region targeted for potential shale gas exploitation. Objectives were to i) establish Ra baseline in groundwater; ii) characterize Ra spatial distribution and temporal variability; iii) characterize Ra partitioning between dissolved phase and particulate forms in well waters; and iv) understand the mechanisms controlling Ra mobility under natural environmental settings.

Assessment of saliva, hair and toenails as biomarkers of low level exposure to manganese from drinking water in children.

We evaluated hair, toenails, and saliva (whole and supernatant) as biomarkers of exposure to manganese (Mn) in 274 school age children (6-13 years) consuming well water in southeastern New Brunswick, Canada. Mn concentrations in tap water ranged from <0.03 to 1046μgL (geometric mean 5.

Exposure to low environmental concentrations of manganese, lead, and cadmium alters the serotonin system of blue mussels.

Serotonin plays a crucial role in mussel survival and reproduction. Although the serotonin system can be affected by metals, the effects of environmental concentrations of metals such as manganese (Mn), lead (Pd), and cadmium (Cd) have never been studied in blue mussels. The present study aimed to determine the effects of exposure to Mn, Pb, or Cd on serotonin levels, monoamine oxidase (MAO) activity, and serotonin transporter (SERT) levels in the blue mussel Mytilus edulis.

Low level exposure to manganese from drinking water and cognition in school-age children.

Background: Manganese (Mn) is an element found in the environment and certain geographic areas have elevated concentrations in soil and water du to natural conditions or anthropic activities. A growing body of data suggests that exposure to manganese in drinking water could be neurotoxic.

Objective: Firstly, we aimed to examine the association between exposure to manganese from drinking water and cognition in children consuming well water.

Quantification of Ra at environmental relevant levels in natural waters by ICP-MS: Optimization, validation and limitations of an extraction and preconcentration approach.

Radium (Ra) at environmental relevant levels in natural waters was determined by ICP-MS after an off-line pre-concentration procedure. The latter consisted of Ra selective elution from potential interfering elements (i.e.

Tracing mercury contamination sources in sediments using mercury isotope compositions.

Mercury (Hg) isotope ratios were determined in two sediment cores collected from two adjacent reservoirs in Guizhou, China, including Hongfeng Reservoir and Baihua Reservoir. Hg isotope compositions were also analyzed in a soil sample collected from the catchment of Hongfeng Reservoir and three cinnabar samples collected from the Wanshan Hg mine. Baihua Reservoir was contaminated with runoff from Guizhou Organic Chemical Plant (GOCP) when metallic Hg was used as a catalyst to produce acetic acid.

Deposition of mercury species in the Ny-Alesund area (79 degrees N) and their transfer during snowmelt.

Arctic snowpacks are often considered as temporary reservoirs for atmospheric mercury (Hg) deposited during springtime deposition events (AMDEs). The fate of deposited species is of utmost importance because melt leads to the transfer of contaminants to snowmelt-fed ecosystems. Here, we examined the deposition, fate, and transfer of mercury species (total Hg (THg) and methylmercury (MeHg)) in an arctic environment from the beginning of mass deposition of Hg during AMDEs to the full melt of the snow.

Tracing mercury contamination from the Idrija mining region (Slovenia) to the Gulf of Trieste using Hg isotope ratio measurements.

To demonstrate the power of precise isotope ratio measurements of Hg in environmental samples and, more particularly, to test the use of stable isotopes as distinct tracers of the contamination source, we investigated a well-documented system, the Hg mining region near Idrija, Slovenia. Sediments alongside the Idrijca River, the Soca/Isonzo River, and in the Gulf of Trieste were analyzed to determine the variation in Hg isotopic composition versus distance from the source. Similar Hg isotopic signatures were observed among samples collected from the rivers Idrijca, Soca/Isonzo, and around the river mouth in the Gulf of Trieste, suggesting that sediments throughout the watershed of the Soca/Isonzo River to the Gulf of Trieste are dominated by Hg exported from the headwaters of the Idrijca River.

Methylmercury speciation in the dissolved phase of a stratified lake using the diffusive gradient in thin film technique.

The diffusive gradient in thin film (DGT) technique was successfully used to monitor methylmercury (MeHg) speciation in the dissolved phase of a stratified boreal lake, Lake 658 of the Experimental Lakes Area (ELA) in Ontario, Canada. Water samples were conventionally analysed for MeHg, sulfides, and dissolved organic matter (DOM). MeHg accumulated by DGT devices was compared to MeHg concentration measured conventionally in water samples to establish MeHg speciation.

Determination of compound-specific Hg isotope ratios from transient signals using gas chromatography coupled to multicollector inductively coupled plasma mass spectrometry (MC-ICP/MS).

MeHg and inorganic Hg compounds were measured in aqueous media for isotope ratio analysis using aqueous phase derivatization, followed by purge-and-trap preconcentration. Compound-specific isotope ratio measurements were performed by gas chromatography interfaced to MC-ICP/MS. Several methods of calculating isotope ratios were evaluated for their precision and accuracy and compared with conventional continuous flow cold vapor measurements.

Mercury in aquatic sediments and soils from Croatia.

Mercury is one of the most toxic and hazardous pollutant which occurs in the environment in different chemical forms, of which methylmercury is the most dangerous. Recently it was recognised that long-term anthropogenic inputs of mercury into environment resulted in the global mercury pollution and it was concluded that action should be taken to quantify the pollution sources and reduce human-generated releases of mercury. This paper presents new data on mercury levels in aquatic sediments from about 15 Croatian rivers, lakes and estuaries.

High-precision measurement of mercury isotope ratios in sediments using cold-vapor generation multi-collector inductively coupled plasma mass spectrometry.

An on-line Hg reduction technique using stannous chloride as the reductant was applied for accurate and precise mercury isotope ratio determinations by multi-collector (MC)-ICP/MS. Special attention has been paid to ensure optimal conditions (such as acquisition time and mercury concentration) allowing precision measurements good enough to be able to significantly detect the anticipated small differences in Hg isotope ratios in nature. Typically, internal precision was better than 0.

Influence of chloride and sediment matrix on the extractability of HgS (cinnabar and metacinnabar) by nitric acid.

The extractability of metacinnabar and cinnabar, alone or in the presence of some sediment components, with various concentrations of HNO3 (1, 4, 6, and 14 M) was studied. Both forms of HgS (0.2-0.

Extractability of HgS (cinnabar and metacinnabar) by hydrochloric acid.

In this work we investigated the behaviour of pure HgS during extraction with dilute HCl to establish its extractability in 1 and 6 M HCl at the concentration level close to those occurring in natural sediments and soils. We found that neither cinnabar nor metacinnabar were soluble in 1 M HCl, whereas both were partially extracted by 6 M HCl. Metacinnabar precipitated in the laboratory was most prone to dissolution in 6 M HCl (up to 90%), followed by crystalline (commercial) metacinnabar (up to 70%) and cinnabar (up to 15%).