Variation Of Total Gaseous Mercury Research Articles

Katabatic Wind and Sea-Ice Dynamics Drive Isotopic Variations of Total Gaseous Mercury on the Antarctic Coast.

Clarifying the sources and fates of atmospheric mercury (Hg) in the Antarctic is crucial to understand the global Hg circulation and its impacts on the fragile ecosystem of the Antarctic. Herein, the annual variations in the isotopic compositions of total gaseous Hg (TGM), with 5-22 days of sampling duration for each sample, were presented for the first time to provide isotopic evidence of the sources and environmental processes of gaseous Hg around the Chinese Great Wall Station (GWS) in the western Antarctic. Different from the Arctic tundra and lower latitude areas in the northern hemisphere, positive δ202Hg (0.58 ± 0.21‰, mean ± 1SD) and negative Δ199Hg (-0.30 ± 0.10‰, mean ± 1SD) in TGM at the GWS indicated little impact from the vegetation-air exchange in the Antarctic. Correlations among TGM Δ199Hg, air temperature, and ozone concentrations suggested that enhanced katabatic wind that transported inland air masses to the continental margin elevated TGM Δ199Hg in the austral winter, while the surrounding marine surface emissions controlled by sea-ice dynamics lowered TGM Δ199Hg in the austral summer. The oxidation of Hg(0) might elevate Δ199Hg in TGM during atmospheric Hg depletion events but have little impact on the seasonal variations of atmospheric Hg isotopes. The presented atmospheric Hg isotopes were essential to identify the transport and transformation of atmospheric Hg and further understand Hg cycling in the Antarctic.

Current understanding of the driving mechanisms for spatiotemporal variations of atmospheric speciated mercury: a review

Abstract. Atmospheric mercury (Hg) is a global pollutant and thought to be the main source of mercury in oceanic and remote terrestrial systems, where it becomes methylated and bioavailable; hence, atmospheric mercury pollution has global consequences for both human and ecosystem health. Understanding of spatial and temporal variations of atmospheric speciated mercury can advance our knowledge of mercury cycling in various environments. This review summarized spatiotemporal variations of total gaseous mercury or gaseous elemental mercury (TGM/GEM), gaseous oxidized mercury (GOM), and particulate-bound mercury (PBM) in various environments including oceans, continents, high elevation, the free troposphere, and low to high latitudes. In the marine boundary layer (MBL), the oxidation of GEM was generally thought to drive the diurnal and seasonal variations of TGM/GEM and GOM in most oceanic regions, leading to lower GEM and higher GOM from noon to afternoon and higher GEM during winter and higher GOM during spring–summer. At continental sites, the driving mechanisms of TGM/GEM diurnal patterns included surface and local emissions, boundary layer dynamics, GEM oxidation, and for high-elevation sites mountain–valley winds, while oxidation of GEM and entrainment of free tropospheric air appeared to control the diurnal patterns of GOM. No pronounced diurnal variation was found for Tekran measured PBM at MBL and continental sites. Seasonal variations in TGM/GEM at continental sites were attributed to increased winter combustion and summertime surface emissions, and monsoons in Asia, while those in GOM were controlled by GEM oxidation, free tropospheric transport, anthropogenic emissions, and wet deposition. Increased PBM at continental sites during winter was primarily due to local/regional coal and wood combustion emissions. Long-term TGM measurements from the MBL and continental sites indicated an overall declining trend. Limited measurements suggested TGM/GEM increasing from the Southern Hemisphere (SH) to the Northern Hemisphere (NH) due largely to the vast majority of mercury emissions in the NH, and the latitudinal gradient was insignificant in summer probably as a result of stronger meridional mixing. Aircraft measurements showed no significant vertical variation in GEM over the field campaign regions; however, depletion of GEM was observed in stratospherically influenced air masses. In examining the remaining questions and issues, recommendations for future research needs were provided, and among them is the most imminent need for GOM speciation measurements and fundamental understanding of multiphase redox kinetics.

Seasonal Variations of Total Gaseous Mercury at a French Coastal Mediterranean Site

The seasonal variation and spatial distribution of atmospheric particles at three islands in the Taiwan Strait were investigated. Atmospheric particles (PM10) were collected at three offshore islands (i.e., Kinmen islands, Matsu islands, and Penghu Islands) and two coastal regions (i.e., Xiamen and Fuzhou) in the years of 2008–2012. Field sampling results indicated that the average PM10 concentrations at the Kinmen islands were generally higher than other sampling sites, suggesting that a superimposition phenomenon was regularly observed during the air pollution episodes at Kinmen Islands and Xiamen region. PM10 samples were analyzed for their chemical composition, including water-soluble ions, metallic elements, and carbonaceous content. The most abundant water-soluble ionic species of PM10 were recognized as SO42–, NO3–, and NH4+, indicating that PM10 was mainly composed of secondary inorganic aerosols. Although natural crustal elements dominated the metallic content of PM10, the most abundant anthropogenic metals of PM10 were Zn and Pb. Enrichment factor calculations showed that Ni, Cr, and Zn were the enriched elements emitted mainly from anthropogenic sources. Moreover, the OC concentration of PM10 was always higher than that of EC at all sampling sites. High OC/EC ratios of PM10 were commonly observed at the sampling sites on the Matsu Islands, the Fuzhou region, and the Penghu Islands. Source apportionment results indicated that vehicular exhausts were the main source of PM10, and followed by industrial boilers, secondary aerosols, soil dusts, biomass burning, petrochemical plants, steel plants, oceanic spray, and cement plants at the island and coastal sampling sites in the Taiwan Strait. Highlights ► Investigation of 2 years of TGM at a French coastal Mediterranean site. ► Daily variations of TGM are observed, due to local industrial or urban activities. ► Seasonal variations are due to the dispersion of pollutants in the troposphere. ► High TGM concentrations are due to air masses coming from local or regional sources.

Seasonal and Diurnal Variations of Total Gaseous Mercury in Urban Houston, TX, USA

Total gaseous mercury (THg) observations in urban Houston, over the period from August 2011 to October 2012, were analyzed for their seasonal and diurnal characteristics. Our continuous measurements found that the median level of THg was 172 parts per quadrillion by volume (ppqv), consistent with the current global background level. The seasonal variation showed that the highest median THg mixing ratios occurred in summer and the lowest ones in winter. This seasonal pattern was closely related to the frequency of THg episodes, energy production/consumption and precipitation in the area. The diurnal variations of THg exhibited a pattern where THg accumulated overnight and reached its maximum level right before sunrise, followed by a rapid decrease after sunrise. This pattern was clearly influenced by planetary boundary layer (PBL) height and horizontal winds, including the complex sea breeze system in the Houston area. A predominant feature of THg in the Houston area was the frequent occurrence of large THg spikes. Highly concentrated pollution plumes revealed that mixing ratios of THg were related to not only the combustion tracers CO, CO2, and NO, but also CH4 which is presumably released from oil and natural gas operations, landfills and waste treatment. Many THg episodes occurred simultaneously with peaks in CO, CO2, CH4, NOx, and/or SO2, suggesting possible contributions from similar sources with multi-source types. Our measurements revealed that the mixing ratios and variability of THg were primarily controlled by nearby mercury sources.

Mercury emissions from flooded soils and sediments in Germany are an underestimated problem: challenges for reliable risk assessments and management strategies

Environmental pollution by mercury is a world-wide problem. Particularly floodplain ecosystems are frequently affected. One example is the Elbe River in Germany and its catchment areas; large amounts of Hg from a range of anthropogenic and geogenic sources have been accumulated in the soils of these floodplains. They serve as sink for Hg originating from the surface water of adjacent river. Today, the vastly elevated Hg contents of the floodplain soils at the Elbe River often exceed even the action values of the German Soil Conservation Law. This is especially important as Hg polluted areas at the Elbe River achieve several hundred square kilometres. Thus, authorities are coerced by law to conduct an appropriate risk assessment and to implement practical actions to eliminate or reduce environmental problems. A reliable risk assessment particularly with view to organisms (vegetation as green fodder and hay production, grazing and wild animals) to avoid the transfer of Hg into the human food chain, requires an authentic determination of Hg fluxes and their dynamics since gaseous emissions from soil to atmosphere are an important pathway of Hg. However, reliable estimates of Hg fluxes from the highly polluted floodplain soils at the Elbe River and its tributaries, and its influencing factors are scarce. For this purpose, we have developed a new method to determine mercury emissions from soils at various sites. Our objectives were i) to quantify seasonal variations of total gaseous mercury (TGM) fluxes for floodplain soils at the Elbe River, ii) to provide insights into physico-chemical processes regulating these TGM fluxes, and iii) to quantify the impacts of the controlling factors soil temperature and soil water content on Hg volatilization from a typical contaminated floodplain soil within soil microcosm experiments under various controlled temperature and moisture conditions. Our study provides insight into TGM emissions from highly Hg-polluted floodplain soils in Germany and that those emissions are an underestimated problem. Current needs for reliable risk assessments, the induced implications for authorities, and future challenges will be discussed. The presented data will contribute to a better understanding of seasonal dynamics of Hg fluxes and its controlling factors. This presentation should be of large interest for a wide international audience, such as environmental scientists and managers, applied ecologists, and authorities.

Temporal variation of total gaseous mercury in the air of Guiyang, China

Total gaseous mercury (TGM) concentrations in ambient air were monitored at an urban site in Guiyang from 23 November 2001 to 30 November 2002 using a high temporal resolution 5 min mercury vapor analyzer (Tekran 2537A). TGM concentrations follow lognormal frequency distribution pattern, and the mean TGM concentration at the measurement site is 8.40 ng m−3 on the basis of 1 year observation. TGM concentrations in Guiyang are significantly elevated compared to the continental global background values. Coal combustion from both industrial and domestic uses is estimated to be the primary atmospheric source. A seasonal distribution pattern of TGM with a descending order of winter, spring, fall, and summer was observed. The highest TGM concentration in winter is attributed to household heating using coal. A consistent diurnal distribution pattern of TGM was obtained among all seasons, and the nighttime TGM concentration is elevated compared to the daytime values. Meteorological conditions are responsible for the formation of diurnal TGM distribution pattern. Tremendous efforts are needed to reduce mercury emissions from coal combustion to decrease TGM concentrations in Guiyang.