Mobility Of Mercury In Soils Research Articles

Mobility of mercury in soil and its transport into the sea.

Mercury (Hg) is deposited temporarily in soil and can be remobilised into rivers and seas. Given that rivers are a significant part of the mercury budget in the southern Baltic region (inland sea located in northern Europe) and meteorological changes (e.g. intense rain, drought) are observed more frequently, it is important to recognize the factors affecting the cycling of bioavailable Hg forms. The aim of this study was to identify the processes influencing the changes of labile and stabile mercury proportion in soil and the potential impact on the outflow of labile Hg into fluvial systems. For this purpose, soil samples, river sediments, and river water were collected from the Reda River (southern Baltic Sea catchment area) during the 2015 hydrologic year. The material was analysed for total and particulate mercury content and Hg forms, by a thermo-desorption method. The analysis showed that due to changes of meteorological and hydrological conditions Hg can enter rivers and then be introduced into the marine environment in various forms. On the one hand due to high precipitation events washing out of labile (i.e. bond with halogenides, MeHg, HgSO4), Hg forms into the river can be enhanced which affects increasing of availability of the most dangerous Hg form in the water systems. On the other hand the same event can cause the limitation of bioavailable mercury forms by a conversion of labile Hg into the most stable one (HgSO4 ➔ HgS) under anaerobic conditions.

Impact of hydrotechnical works on outflow of mercury from the riparian zone to a river and input to the sea

The aim of this research was to assess the impact of hydrotechnical works within the riverbed and riparian zone on the mobility of mercury in soil and its outflow to the river and the sea. Deepening and reconstruction of the riverbed or the cutting of reeds, influenced the fate of mercury in the river system. However, only activitis that disturbed the riperian zone increased mobilization of Hg in soils. Hg transformations in these places were controled by inflow of fresh organic matter in soil and sediments as well as by oxidation-reduction potential. In areas where reducing conditions occurred, mercury released from the soil was incorporated into the sediment. However, in areas where oxidizing conditions prevailed in the sediment, mercury flowing out of the soil occurred mainly in dissolved form and most of it was transported downstream from where it could reach the sea.

Speciation and Mobility of Mercury in Soils Contaminated by Legacy Emissions from a Chemical Factory in the Rhône Valley in Canton of Valais, Switzerland

Legacy contamination of soils and sediments with mercury (Hg) can pose serious threats to the environment and to human health. Assessing risks and possible remediation strategies must consider the chemical forms of Hg, as different Hg species exhibit vastly different environmental behaviors and toxicities. Here, we present a study on Hg speciation and potential mobility in sediments from a chemical factory site, and soils from nearby settlement areas in the canton of Valais, Switzerland. Total Hg ranged from 0.5 to 28.4 mg/kg in the soils, and 3.5 to 174.7 mg/kg in the sediments, respectively. Elemental Hg(0) was not detectable in the soils by thermal desorption analysis. Methylmercury, the most toxic form of Hg, was present at low levels in all soils (<0.010 mg/kg; <0.8% of total Hg). Sequential extractions and thermal desorption analyses suggested that most of the Hg in the soils was present as “matrix-bound Hg(II)”, most likely associated with soil organic matter. For factory sediments, which contained less organic matter, the results suggested a higher fraction of sulfide-bound Hg. Batch extractions in different CaCl2 solutions revealed that Hg solubility was low overall, and there was no Hg-mobilizing effects of Ca2+ or Cl− in solution. Only in some of the factory sediments did high CaCl2 concentrations result in increased extractability of Hg, due to the formation of Hg-chloride complexes. Additional experiments with soil redox reactors showed that even mildly reducing conditions led to a sharp release of Hg into solution, which may be highly relevant in soils that are prone to periodic water saturation of flooding.

Mobility of mercury in soil as affected by soil physicochemical properties

Purpose The interaction of mercury with organic matter was studied on three soils with distinct physical-chemical compositions (Fluvisol, Luvisol, and Chernozem) and three vermicomposts based on various bio-waste materials (digestate, kitchen waste with woodchips, and garden bio-waste).

Distribution and mobility of mercury in soils of a gold mining region, Cuyuni river basin, Venezuela

An extensive and remote gold mining region located in the East of Venezuela has been studied with the aim of assessing the distribution and mobility of mercury in soil and the level of Hg pollution at artisanal gold mining sites. To do so, soils and pond sediments were sampled at sites not subject to anthropological influence, as well as in areas affected by gold mining activities. Total Hg in regionally distributed soils ranged between 0.02mgkg−1 and 0.40mgkg−1, with a median value of 0.11mgkg−1, which is slightly higher than soil Hg worldwide, possibly indicating long-term atmospheric input or more recent local atmospheric input, in addition to minor lithogenic sources. A reference Hg concentration of 0.33mgkg−1 is proposed for the detection of mining affected soils in this region. Critical total Hg concentrations were found in the surrounding soils of pollutant sources, such as milling-amalgamation sites, where soil Hg contents ranged from 0.16mgkg−1 to 542mgkg−1 with an average of 26.89mgkg−1, which also showed high levels of elemental Hg, but quite low soluble+exchangeable Hg fraction (0.02–4.90mgkg−1), suggesting low Hg soil mobility and bioavailability, as confirmed by soil column leaching tests. The vertical distribution of Hg through the soil profiles, as well as variations in soil Hg contents with distance from the pollution source, and Hg in pond mining sediments were also analysed.

Distribution and mobility of mercury in soils from an old mining area in Mieres, Asturias (Spain)

Mercury content in soils near abandoned mine wastes in the mercury mining area of Mieres (Asturias, Spain) is highly elevated as a result of the long period of mining and abundant Hg production. In this work, an evaluation of Hg concentration, distribution, and mobility in three soil samples from the immediate vicinity of a chimney used for vapour evacuation during pyrometallurgical treatment of the ore was carried out. For that purpose, total Hg contents were determined for the original samples and their grain-size subsamples. The study of mercury mobility in the original samples and in the different particle-size subsamples was made by the application of a sequential extraction method. Results showed that Hg concentration in soils decreases directly with the distance from the chimney and the dispersion of Hg is not influenced by the topographic height of the site tested. The sample collected in the base of the chimney exhibited appreciable amounts of mobile Hg. In general, a higher Hg concentration was found for the finest particle-size subsamples. Hg mobility was found to be higher for quite developed soils. The sample collected downstream from the chimney showed a significant Hg mobile content as a result of a more intensive weathering. An increase of Hg mobility at decreasing particle size was found in all three analysed samples.

Binding and mobility of mercury in soils contaminated by emissions from chlor-alkali plants.

Chlor-alkali plants are known to be an important source of Hg emissions to the atmosphere and related contamination of soils in their vicinity. In the present study, the results of Hg speciation and mobility of Hg in soils affected by Hg emissions from three chlor-alkali plants are compared. Solid phase mercury speciation analyses was carried out using a mercury-thermo-desorption technique with the aim of distinguishing elemental Hg [Hg(0)] from Hg(II)-binding forms. Mercury species in soil leachates were distinguished using an operationally defined method, which is based on the reactivity of soluble Hg compounds. Results show that the Hg(0) emitted from the plants could not be detected in any of the investigated soils. This indicates quantitative re-emission or oxidation of this Hg species in the atmosphere or soils. In most soils Hg was predominately bound to organic matter. Only in sandy soils deficient in organic matter was Hg, to a larger extent, sorbed onto mineral soil components. Leachable Hg in most soils occurred as non-reactive, soluble organic Hg complexes such as fulvic acid-bound Hg, and reach their highest values (90 microg kg(-1)) in soils rich in organic matter. Concentrations of reactive, soluble Hg compounds were highest in sandy soils where the content of organic matter was low. Leachability of Hg was found to be inhibited in soils with a high content of clayey soil components. The distribution of Hg in soil profiles suggests that migration of Hg to deeper soil layers (approx. 20 cm) is most effective if Hg is bound to soluble organic complexes, whereas reactive Hg or weak Hg complexes are effectively retained in the uppermost soil layer (5 cm) through sorption on mineral surfaces.