WorldWideScience

Sample records for hg concentration showing

  1. Importance of Dissolved Neutral Hg-Sulfides, Energy Rich Organic Matter and total Hg Concentrations for Methyl Mercury Production in Sediments

    Science.gov (United States)

    Drott, A.; Skyllberg, U.

    2007-12-01

    Methyl mercury (MeHg) is the mercury form that biomagnifies to the greatest extent in aquatic food webs. Therefore information about factors determining MeHg concentrations is critical for accurate risk assessment of contaminated environments. The concentration of MeHg in wetlands and sediments is the net result of: 1) methylation rates, 2) demethylation rates, and 3) input/output processes. In this study, the main controls on Hg methylation rates and total concentrations of MeHg, were investigated at eight sites in Sweden with sediments that had been subjected to local Hg contamination either as Hg(0), or as phenyl-Hg. Sediments were selected to represent a gradient in total Hg concentration, temperature climate, salinity, primary productivity, and organic C content and quality. Most sediments were high in organic matter content due to wood fibre efflux from pulp and paper industry. The pore water was analysed for total Hg, MeHg, DOC, H2S(aq), pH, DOC, Cl and Br. The chemical speciation of Hg(II) and MeHg in pore water was calculated using equilibrium models. Potential methylation and demethylation rates in sediments were determined in incubation experiments at 23° C under N2(g) for 48 h, after addition of isotopically enriched 201Hg(II) and Me204Hg. In all surface (0-20 cm) sediments there was a significant (pproduction overruled degradation and input/output processes of MeHg in surface sediments, and that % MeHg in surface sediments may be used as a proxy for net production of MeHg. To our knowledge, these are the first data showing significant positive relationships between short term (48 h) MeHg production and longer term accumulation of MeHg, across a range of sites with different properties (1). If MeHg was not normalized to total Hg, the relationship was not significant. For sub-sets of brackish waters (pproductivity freshwaters (pproductivity freshwater (p=0.048, n=6), the sum of neutral Hg-sulfides [Hg(SH)20 (aq)] and [HgS0 (aq)] in the sediment pore

  2. Using MOF-74 for Hg2+ removal from ultra-low concentration aqueous solution

    Science.gov (United States)

    Xiong, Yang Yang; Li, Jian Qiang; Gong, Le Le; Feng, Xue Feng; Meng, Li Na; Zhang, Le; Meng, Pan Pan; Luo, Ming Biao; Luo, Feng

    2017-02-01

    Mercury (Hg2+) ions have very high toxicity and widely spread as environmental pollutants. At present, many efforts have been taken to remove the hazardous materials of mercury(II) by adsorption, and it is highly desirable to develop a novel adsorbent with high adsorptive capacities. However it is still a big challenge to remove the ultra-low-concentration mercury ions from water. In this paper, MOF-74-Zn is explored for such function, showing high removal rate of Hg(II) from water without any pretreatment, especially for the ultra-trace Hg(II) ions in the ppb magnitude with the removal rate reaching to 54.48%, 69.71%, 72.26% when the initial concentration of Hg(II) is 20ppb, 40ppb, 50ppb, respectively.

  3. Spatial Distribution of Mercury (Hg Concentration in Agricultural Soil and Its Risk Assessment on Food Safety in China

    Directory of Open Access Journals (Sweden)

    Shanqian Wang

    2016-08-01

    Full Text Available Soil mercury (Hg pollution in some areas of China is a serious problem and has aroused a lot of attention on a local scale. However, there are few studies on Hg pollution on a national scale. This study collected 444 published papers during 2005–2015 on Hg concentrations in agricultural soil throughout China, under seven land uses, namely: dry land, paddy field, vegetable field, tea garden, orchard, traditional Chinese medicine field and tobacco field, to assess the spatial distribution of Hg concentration and evaluate its influence on food safety. The averaged Hg concentration (0.108 mg/kg was higher than its background (0.065 mg/kg, but much lower than the guidelines (GB15618-1995 II for crop production. The spatial distribution of Hg throughout China showed great variability, with some hotspots due to Hg related mining and smelting activities. According to the Environment Quality Standard for soil in China (GB15618-1995 II, 4.2% of agricultural soil should be abandoned due to Hg pollution, and 2.0% faced a high risk of Hg pollution.

  4. Hg concentrations in fish from coastal waters of California and Western North America

    Science.gov (United States)

    Davis, Jay; Ross, John; Bezalel, Shira; Sim, Lawrence; Bonnema, Autumn; Ichikawa, Gary; Heim, Wes; Schiff, Kenneth C; Eagles-Smith, Collin A.; Ackerman, Josh

    2016-01-01

    The State of California conducted an extensive and systematic survey of mercury (Hg) in fish from the California coast in 2009 and 2010. The California survey sampled 3483 fish representing 46 species at 68 locations, and demonstrated that methylHg in fish presents a widespread exposure risk to fish consumers. Most of the locations sampled (37 of 68) had a species with an average concentration above 0.3 μg/g wet weight (ww), and 10 locations an average above 1.0 μg/g ww. The recent and robust dataset from California provided a basis for a broader examination of spatial and temporal patterns in fish Hg in coastal waters of Western North America. There is a striking lack of data in publicly accessible databases on Hg and other contaminants in coastal fish. An assessment of the raw data from these databases suggested the presence of relatively high concentrations along the California coast and in Puget Sound, and relatively low concentrations along the coasts of Alaska and Oregon, and the outer coast of Washington. The dataset suggests that Hg concentrations of public health concern can be observed at any location on the coast of Western North America where long-lived predator species are sampled. Output from a linear mixed-effects model resembled the spatial pattern observed for the raw data and suggested, based on the limited dataset, a lack of trend in fish Hg over the nearly 30-year period covered by the dataset. Expanded and continued monitoring, accompanied by rigorous data management procedures, would be of great value in characterizing methylHg exposure, and tracking changes in contamination of coastal fish in response to possible increases in atmospheric Hg emissions in Asia, climate change, and terrestrial Hg control efforts in coastal watersheds.

  5. Hg concentrations and related risk assessment in coral reef crustaceans, molluscs and fish from New Caledonia

    Energy Technology Data Exchange (ETDEWEB)

    Chouvelon, Tiphaine [Littoral Environnement et Societes (LIENSs), UMR 6250, CNRS-Universite La Rochelle, 2 Rue Olympe de Gouges, F-17042 La Rochelle Cedex 01 (France); Warnau, Michel [International Atomic Energy Agency-Marine Environment Laboratories (IAEA-MEL), 4 Quai Antoine Ier, MC-98000 (Monaco); Churlaud, Carine [Federation de Recherche en Environnement pour le Developpement Durable (FR-EDD), FR CNRS 3097, Centre Commun d' Analyses, 5 Perspectives de l' Ocean, F-17071 La Rochelle Cedex 9 (France); Bustamante, Paco [Littoral Environnement et Societes (LIENSs), UMR 6250, CNRS-Universite La Rochelle, 2 Rue Olympe de Gouges, F-17042 La Rochelle Cedex 01 (France)], E-mail: pbustama@univ-lr.fr

    2009-01-15

    There is a dramatic lack of data on Hg levels in marine organisms from tropical areas, and in particular from New Caledonia. For the first time, this study reports the total Hg concentrations in the tissues of several marine taxa from the New Caledonian lagoon. Seafood from both wild and farmed populations was considered. Hg concentrations varied over three orders of magnitudes according to factors including species, age (size/weight), trophic level, lifestyle and geographical origin. Taking into account the edible tissues, estimations of the amount of flesh that should be consumed by a 60-kg person to reach the Hg Provisional Tolerable Weekly Intake (PTWI) reveal acceptable risk for Human health in general. However, a risk was clearly identified in one site of the lagoon (i.e. Grande Rade) where high Hg concentrations were measured. These concentrations were higher than values reported in the current literature. - This work reports the first assessment of Hg levels in edible organisms from the New Caledonian lagoon and the associated risk linked to their consumption by Human.

  6. Anadromous char as an alternate food choice to marine animals: A synthesis of Hg concentrations, population features and other influencing factors

    Energy Technology Data Exchange (ETDEWEB)

    Evans, Marlene S., E-mail: marlene.evans@ec.gc.ca [Environment Canada, Water Science and Technology Directorate, 11 Innovation Blvd., Saskatoon SK S7N 3H5 (Canada); Muir, Derek C.G. [Environment Canada, Water Science and Technology Directorate, 867 Lakeshore Rd., Burlington, ON L7R 4A6 (Canada); Keating, Jonathan [Environment Canada, Water Science and Technology Directorate, 11 Innovation Blvd., Saskatoon SK S7N 3H5 (Canada); Wang, Xiaowa [Environment Canada, Water Science and Technology Directorate, 867 Lakeshore Rd., Burlington, ON L7R 4A6 (Canada)

    2015-03-15

    This study was conducted to confirm sporadic measurements made over the late 1970s to the early 1990s which determined that mercury (Hg) concentrations were low in anadromous char across Arctic and subarctic Canada including northern Québec and Labrador. Over 2004–2013, anadromous char populations across northern Canada were investigated at 20 sites for Hg concentrations and life history characteristics. Hg concentrations were extremely low in anadromous char muscle, typically < 0.05 μg/g (wet weight) and, at each location, generally increased with fish length, age and nitrogen isotope (δ{sup 15}N) ratio and decreased with condition factor and %lipid; correlations with carbon isotope (δ{sup 13}C) ratio were inconsistent. Location and year were significant variables influencing Hg concentrations over the study area; longitude and latitude also were significant influencing variables. Char length, weight, age, condition factor and lipid content explained additional variance. A tendency towards higher Hg concentrations with increasing latitude may be partially related to decreasing growth of char towards the north. However, Hg concentrations in char were positively correlated with growth rates suggesting that Hg concentrations in char also were higher in the more productive study areas, including to the west where mainland riverine inputs of terrestrial carbon, nutrients, and Hg were greater. The data base for assessing time trends in char was limited by the small number of years investigated at most locations, variable fish size across years, small sample size, etc. Where temporal trends were detected, they were of increase on the long term (1970s, 1980s or early 1990s to the present) but of decrease on the short term (early 2000s to present) with Nain (Labrador) showing the converse pattern. Higher Hg concentrations were also related to lower condition factor and cooler springs. Hg concentrations in anadromous char are compared with other terrestrial, aquatic

  7. Manifold and method of batch measurement of Hg-196 concentration using a mass spectrometer

    Science.gov (United States)

    Grossman, M.W.; Evans, R.

    1991-11-26

    A sample manifold and method of its use has been developed so that milligram quantities of mercury can be analyzed mass spectroscopically to determine the [sup 196]Hg concentration to less than 0.02 atomic percent. Using natural mercury as a standard, accuracy of [+-]0.002 atomic percent can be obtained. The mass spectrometer preferably used is a commercially available GC/MS manufactured by Hewlett Packard. A novel sample manifold is contained within an oven allowing flow rate control of Hg into the MS. Another part of the manifold connects to an auxiliary pumping system which facilitates rapid clean up of residual Hg in the manifold. Sample cycle time is about 1 hour. 8 figures.

  8. Concentration of Cd, Pb, Hg, and Se in Different Parts of Human Breast Cancer Tissues

    Directory of Open Access Journals (Sweden)

    Mehrnoosh Mohammadi

    2014-01-01

    Full Text Available Breast cancer is the major cause of cancer morbidity and mortality between women in the world. Metals involved in environmental toxicology are closely related to tumor growth and cancer. On the other hand, some metals such as selenium have anticarcinogenic properties. The aim of this study is to determine the concentration of cadmium, lead, mercury, and selenium in separated parts of tegmen, tumor, tumor adiposity, and tegmen adiposity of 14 breast cancer tissues which have been analyzed by graphite furnace atomic absorption (AA-670 and ICP-OES (ULTIMA 2CE. Our results show that Se and Hg have maximum and minimum concentration, respectively. Statistical analysis reveals no significant differences between metal accumulations in different parts of cancer tissues (P>0.05 and this observation might be due to the close relation of separated parts of fatty breast organ. Thus, we could conclude that a high level of these heavy metals is accumulated in Iranian cancerous breasts and their presence can be one of the reasons of cancer appearance.

  9. Analysis of carrier concentration, lifetime, and electron mobility on p-type HgCdTe

    Science.gov (United States)

    Yoo, Sang Dong; Kwack, Kae Dal

    1998-03-01

    Minority carrier transport characteristics of vacancy-doped p-type HgCdTe such as carrier concentration, lifetime, and mobility are investigated. In the calculation of the carrier concentration two acceptor levels—a donor level and a trap level—were taken into account. The acceptor levels have been described by two models—two independent singly ionized levels and a divalent level with two ionization energies. When each model was examined by calculating electron mobility as a function of temperature, the latter was found to be more accurate. Electron mobility as a function of majority carrier concentration was also presented for both n-type and p-type HgCdTe with 0.225 Cd mole fraction. Steady state electron lifetime was computed assuming the acceptor levels and the trap level would act as Schokley-Read-Hall type recombination centers. The calculated results using the divalent acceptor model were in good agreement with the experimental data.

  10. Contrasting Food Web Factor and Body Size Relationships with Hg and Se Concentrations in Marine Biota

    Science.gov (United States)

    Karimi, Roxanne; Frisk, Michael; Fisher, Nicholas S.

    2013-01-01

    Marine fish and shellfish are primary sources of human exposure to mercury, a potentially toxic metal, and selenium, an essential element that may protect against mercury bioaccumulation and toxicity. Yet we lack a thorough understanding of Hg and Se patterns in common marine taxa, particularly those that are commercially important, and how food web and body size factors differ in their influence on Hg and Se patterns. We compared Hg and Se content among marine fish and invertebrate taxa collected from Long Island, NY, and examined associations between Hg, Se, body length, trophic level (measured by δ15N) and degree of pelagic feeding (measured by δ13C). Finfish, particularly shark, had high Hg content whereas bivalves generally had high Se content. Both taxonomic differences and variability were larger for Hg than Se, and Hg content explained most of the variation in Hg:Se molar ratios among taxa. Finally, Hg was more strongly associated with length and trophic level across taxa than Se, consistent with a greater degree of Hg bioaccumulation in the body over time, and biomagnification through the food web, respectively. Overall, our findings indicate distinct taxonomic and ecological Hg and Se patterns in commercially important marine biota, and these patterns have nutritional and toxicological implications for seafood-consuming wildlife and humans. PMID:24019976

  11. [Concentration of Hg, Pb, Cd, Cr and As in liver Carcharhinus limbatus (Carcharhiniformes: Carcharhinidae) captured in Veracruz, Mexico].

    Science.gov (United States)

    Mendoza-Díaz, Fernando; Serrano, Arturo; Cuervo-López, Liliana; López-Jiménez, Alejandra; Galindo, José A; Basañez-Muñoz, Agustin

    2013-06-01

    Pollution by heavy metals in marine ecosystems in the Gulf of Mexico is one of the hardest conservation issues to solve. Sharks as top predators are bioindicators of the marine ecosystem health, since they tend to bioaccumulate and biomagnify contaminants; they also represent a food source for local consumption. Thus, the objective of this study was to study the possible presence of heavy metals and a metalloid in livers of Carcharhinus limbatus. For this, a total of 19 shark livers were taken from animals captured nearby Tamihua, Veracruz, Mexico from December 2007 to April 2008. 12 out of the 19 captured sharks were males, one was an adult female, three were juvenile males, and three juvenile females. Four heavy metals (Hg, Pb, Cd, and Cr) and one metaloid (As) were analyzed in shark livers using an atomic absorption spectrophotometry with flame and hydride generator. Our results showed that the maximum concentrations found were: Hg = 0.69 mg/kg, Cd = 0.43 mg/kg, As = 27.37 mg/kg, Cr = 0.70 mg/kg. The minimum concentrations found were: As = 14.91 mg/kg, Cr = 0.35 mg/kg. The Pb could not be determined because the samples did not have the spectrophotometer minimum detectable amount (0.1 mg/kg). None of the 19 samples analyzed showed above the permissible limits established by Mexican and American laws. There was a correlation between shark size and Cr and As concentration (Pearson test). The concentration of Cr and As was observed to be higher in bigger animals. There was not a significant difference in heavy metals concentration between juveniles and adults; however, there was a difference between males and females. A higher Cr concentration was found in females when compared to males. None of the samples exceed the maximum limit established by the laws of Mexico and the United States of America. Much longer studies are needed with C. limbatus and other species caught in the region, in order to determine the degree of contaminants exposure in aquatic ecosystems

  12. The average concentrations of As, Cd, Cr, Hg, Ni and Pb in residential soil and drinking water obtained from springs and wells in Rosia Montana area.

    Data.gov (United States)

    U.S. Environmental Protection Agency — The average concentrations of As, Cd, Cr, Hg, Ni and Pb in n=84 residential soil samples, in Rosia Montana area, analyzed by X-ray fluorescence spectrometry are...

  13. The influence of external subsidies on diet, growth and Hg concentrations of freshwater sport fish: implications for management and fish consumption advisories

    Science.gov (United States)

    Lepak, J.M.; Hooten, M.B.; Johnson, B.M.

    2012-01-01

    Mercury (Hg) contamination in sport fish is a global problem. In freshwater systems, food web structure, sport fish sex, size, diet and growth rates influence Hg bioaccumulation. Fish stocking is a common management practice worldwide that can introduce external energy and contaminants into freshwater systems. Thus, stocking can alter many of the factors that influence Hg concentrations in sport fish. Here we evaluated the influence of external subsidies, in the form of hatchery-raised rainbow trout Oncorhynchus mykiss on walleye Sander vitreus diet, growth and Hg concentrations in two freshwater systems. Stocking differentially influenced male and female walleye diets and growth, producing a counterintuitive size-contamination relationship. Modeling indicated that walleye growth rate and diet were important explanatory variables when predicting Hg concentrations. Thus, hatchery contributions to freshwater systems in the form of energy and contaminants can influence diet, growth and Hg concentrations in sport fish. Given the extensive scale of fish stocking, and the known health risks associated with Hg contamination, this represents a significant issue for managers monitoring and manipulating freshwater food web structures, and policy makers attempting to develop fish consumption advisories to protect human health in stocked systems.

  14. Determination of total selenium in geological samples by HG-AFS after concentration with thiol cotton fiber

    Institute of Scientific and Technical Information of China (English)

    FAN Haifeng; WEN Hanjie; HU Ruizhong; CHANG Bin

    2008-01-01

    Standard reference material and different geological samples were dissolved by system A (the mixture of nitric and perchloric acids) and system B (mixture of nitric, perchloric and hydrofluoric acids), and total Se in all samples was measured by hydride-generation atomic fluorescence spectrometry (HG-AFS) after concentration with thiol cotton fiber (TCF). The analytical results obtained by the two digestion method are in good agreement (within the limit of errors) for most of the samples, particularly for those having recommended values. The Se concentrations determined by the two methods are of no difference, and the correlation coefficient is 0.9986; the relative standard deviation (RSD) for the determination of 0.04 (g/g Se is 10.2%. The recovery rates of systems A and B by the standard-addition method were 96%-106% and 99%-104%, respectively.

  15. International system of units traceable results of Hg mass concentration at saturation in air from a newly developed measurement procedure.

    Science.gov (United States)

    Quétel, Christophe R; Zampella, Mariavittoria; Brown, Richard J C; Ent, Hugo; Horvat, Milena; Paredes, Eduardo; Tunc, Murat

    2014-08-05

    Data most commonly used at present to calibrate measurements of mercury vapor concentrations in air come from a relationship known as the "Dumarey equation". It uses a fitting relationship to experimental results obtained nearly 30 years ago. The way these results relate to the international system of units (SI) is not known. This has caused difficulties for the specification and enforcement of limit values for mercury concentrations in air and in emissions to air as part of national or international legislation. Furthermore, there is a significant discrepancy (around 7% at room temperature) between the Dumarey data and data calculated from results of mercury vapor pressure measurements in the presence of only liquid mercury. As an attempt to solve some of these problems, a new measurement procedure is described for SI traceable results of gaseous Hg concentrations at saturation in milliliter samples of air. The aim was to propose a scheme as immune as possible to analytical biases. It was based on isotope dilution (ID) in the liquid phase with the (202)Hg enriched certified reference material ERM-AE640 and measurements of the mercury isotope ratios in ID blends, subsequent to a cold vapor generation step, by inductively coupled plasma mass spectrometry. The process developed involved a combination of interconnected valves and syringes operated by computer controlled pumps and ensured continuity under closed circuit conditions from the air sampling stage onward. Quantitative trapping of the gaseous mercury in the liquid phase was achieved with 11.5 μM KMnO4 in 2% HNO3. Mass concentrations at saturation found from five measurements under room temperature conditions were significantly higher (5.8% on average) than data calculated from the Dumarey equation, but in agreement (-1.2% lower on average) with data based on mercury vapor pressure measurement results. Relative expanded combined uncertainties were estimated following a model based approach. They ranged from 2

  16. A rare 3D chloro-laced Mn(II) metal-organic framework to show sensitive probing effect to Hg2+

    Science.gov (United States)

    Ming, Mei; Bai, Na

    2017-10-01

    Two 3D Mn(II) metal-organic frameworks (MOFs), [Mn(L-Cl)(DMA)](H2O) (1) and Mn(L-CH3)(DMA) (2) (H2L-Cl = 2,2'-dichloro-4,4'-azodibenzoic acid, H2L-CH3 = 2,2'-dimethyl-4,4'-azodibenzoic acid) were synthesized under similar solvothermal condition. Both MOFs crystallize in the orthorhombic system and show the 3D rod-packing networks in 2-fold interpenetrated pattern with sra topology. Due to the different substituent laces of MOFs (-Cl vs -CH3), only MOF 1 shows highly selective and sensitive fluorescence sensing effect for detecting Hg2+ ion.

  17. Microbial Oxidation of Hg(0) - Its Effect on Hg Stable Isotope Fractionation and Methylmercury Production

    Energy Technology Data Exchange (ETDEWEB)

    Yee, Nathan [Rutgers Univ., New Brunswick, NJ (United States); Barkay, Tamar [Rutgers Univ., New Brunswick, NJ (United States); Reinfelder, John [Rutgers Univ., New Brunswick, NJ (United States)

    2016-06-28

    relationship between Hg concentrations and rates of denitrification in enrichment cultures. In part III of our project, we examined in more detail the effects of microbial interactions on Hg transformations. We discovered that both sulfate reducing and iron reducing bacteria coexist in freshwater sediments and both microbial groups contribute to mercury methylation. We showed that mercury methylation by sulfate reducing and iron reducing bacteria are temporally and spatially separated processes. We also discovered that methanogens can methylate mercury. We showed that Methanospirillum hungatei JF-1 methylated Hg at comparable rates, but with higher yields, than those observed for sulfate-reducing bacteria and iron-reducing bacteria. Finally, we demonstrated that syntrophic interactions between different microbial groups increase mercury methylation rates. We showed that Hg methylation rates are stimulated via inter-species hydrogen and acetate transfer (i) from sulfate-reducing bacteria to methanogens and (ii) from fermenters to the sulfate-reducing bacteria. In part IV of the project, we studied Hg bioavailability and Hg isotope fractionation. We demonstrated that thiol-bound Hg is bioavailable to mercury resistant bacteria. We found that uptake of Hg from Hg-glutathione and Hg-cysteine complexes does not require functioning glutathione and cystine/cysteine transport systems. We demonstrated that a wide range of methylmercury complexes (e.g. MeHgOH, MeHg-cysteine, and MeHg-glutathione) are bioavailable to mercury resistant bacteria. The rate of MeHg demethylation varies more between different species of mercury resistant bacteria than among MeHg complexes. We showed that microbial demethylation of MeHg depends more on the species of microorganism than on the types and relative concentrations of thiols or other MeHg ligands present. Finally, we demonstrated that Hg methylation by Geobacter sulfurreducens PCA and Desulfovibrio desulfuricans ND132 imparts mass

  18. Microbial Oxidation of Hg(0) - Its Effect on Hg Stable Isotope Fractionation and Methylmercury Production

    Energy Technology Data Exchange (ETDEWEB)

    Yee, Nathan [Rutgers Univ., New Brunswick, NJ (United States); Barkay, Tamar [Rutgers Univ., New Brunswick, NJ (United States); Reinfelder, John [Rutgers Univ., New Brunswick, NJ (United States)

    2016-06-28

    relationship between Hg concentrations and rates of denitrification in enrichment cultures. In part III of our project, we examined in more detail the effects of microbial interactions on Hg transformations. We discovered that both sulfate reducing and iron reducing bacteria coexist in freshwater sediments and both microbial groups contribute to mercury methylation. We showed that mercury methylation by sulfate reducing and iron reducing bacteria are temporally and spatially separated processes. We also discovered that methanogens can methylate mercury. We showed that Methanospirillum hungatei JF-1 methylated Hg at comparable rates, but with higher yields, than those observed for sulfate-reducing bacteria and iron-reducing bacteria. Finally, we demonstrated that syntrophic interactions between different microbial groups increase mercury methylation rates. We showed that Hg methylation rates are stimulated via inter-species hydrogen and acetate transfer (i) from sulfate-reducing bacteria to methanogens and (ii) from fermenters to the sulfate-reducing bacteria. In part IV of the project, we studied Hg bioavailability and Hg isotope fractionation. We demonstrated that thiol-bound Hg is bioavailable to mercury resistant bacteria. We found that uptake of Hg from Hg-glutathione and Hg-cysteine complexes does not require functioning glutathione and cystine/cysteine transport systems. We demonstrated that a wide range of methylmercury complexes (e.g. MeHgOH, MeHg-cysteine, and MeHg-glutathione) are bioavailable to mercury resistant bacteria. The rate of MeHg demethylation varies more between different species of mercury resistant bacteria than among MeHg complexes. We showed that microbial demethylation of MeHg depends more on the species of microorganism than on the types and relative concentrations of thiols or other MeHg ligands present. Finally, we demonstrated that Hg methylation by Geobacter sulfurreducens PCA and Desulfovibrio desulfuricans ND132 imparts mass

  19. Luminescence and influence of defect concentration on excitons in $^{197}\\!$Hg / $^{197}\\!$Au-doped CdTe

    CERN Document Server

    Hamann, J; Deicher, M; Filz, T; Ostheimer, V; Strasser, F; Wolf, H; Wichert, T

    1999-01-01

    CdTe, implanted with $^{197}\\!$Hg ions, which decay to $^{197}\\!$Au with a half-life of 64.1 h, was investigated by photoluminescence (PL) spectroscopy. The results unambiguously verify the assignments of both, the donor–acceptor pair transition at 1.335 eV, which corresponds to an acceptor level with E$\\scriptstyle_{A}$=263 meV, and the recombination of excitons bound to neutral acceptors at 1.57606 eV to single Au atoms on Cd sites. In addition, the dependence of the intensities of excitonic lines on the defect concentration was investigated quantitatively. The observed intensities are well explained, assuming that a defect can only bind an exciton if there is no additional defect within the volume of the bound exciton. The ratio between the exciton radii of the Cu and Au-bound excitons R$\\scriptscriptstyle^\\textrm{Cu}_{exc}$ / R$\\scriptscriptstyle^\\textrm{Au}_{exc}$ = 1.2$\\pm$0.2 obtained from this model is in good agreement with the ratio derived from the diamagnetic shift parameters of the two correspo...

  20. Concentrations of As, Ca, Cd, Co, Cr, Cu, Fe, Hg, K, Mg, Mn, Mo, Na, Ni, Pb, and Zn in uruguayan rice determined by atomic absorption spectrometry

    Directory of Open Access Journals (Sweden)

    Mario E. Rivero Huguet

    2011-04-01

    Full Text Available The United Nations General Assembly declared the year 2004 the International Year of Rice and the concept "Rice is life". The largest nutritional problems occurring globally are protein-energy malnutrition, and Ca, Fe, I, Zn, and vitamin A deficiency. In this report, 49 rice samples (Oryza sativa L. were digested by dry ashing in order to determine As, Cd, Cr, and Pb by ETA-AAS; while Ca, Co, Cu, Fe, K, Mg, Mo, Mn, Na, Ni, and Zn were determined by FAAS; and Hg by CV-AAS using microwave-assisted decomposition. The following concentration ranges were obtained for Ca (9.1-15 mg/100 g, Cd (2.30-4.12 µg/kg, Co (41-60 µg/kg, Cu (1.33-180 mg/kg, Fe (4.41-7.15 mg/kg, K (167-217 mg/100 g, Mg (45-121 mg/100 g, Mo (0.52-0.97 mg/kg, Mn (5.45-25.4 mg/kg, Na (0.95-2.50 mg/100g, Ni (0.53-0.72 mg/kg, and Zn (5.86-12.6 mg/kg. Mean recoveries of elements from fortified rice were: 87±12% for As, 95.3±8.9% for Ca, 106.2±7.7% for Cd, 103.3±6.5% for Co, 89.4±8.1% for Cr, 99.3±4.6% for Cu, 103±10% for Fe, 96.3±9.3% for Hg, 95.4±12% for K, 98.3±8.0% for Mg, 93.4±7.8% for Mo, 95.3±9.9% for Mn, 89±12% for Na, 90.3±9.7% for Ni, 91.2±5.5% for Pb and 92.0±9.4% for Zn. The concentrations of the minerals and microelements studied fall within the typical range of rice grown around the world. Potassium was the most abundant mineral, followed by Mg and Ca; among microelements, the concentrations of Cu, Fe, Mo, Mn, Na, and Zn in rice were outstanding. It was also found that the milling process highly affects the K, Mg, Mn, Na, and Zn concentrations, while it has little influence on Ca, Co, Cu, and Fe. On the other hand, there is a loss of Ca, Fe, and Mn during the parboiling process. Recent studies have shown the potential to exploit the genetic variation of rice seeds with regard to the concentration of some minerals (Ca, Fe, Zn, etc. without affecting yield or adding new traits. All rice samples tested showed lower levels of As, Cd, Hg, and Pb in comparison

  1. Determination of Hg{sup 2+} by on-line separation and pre-concentration with atmospheric-pressure solution-cathode glow discharge atomic emission spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Li, Qing [Shanghai Institute of Ceramics, Chinese Academy of Science, Shanghai 200050 (China); Zhang, Zhen [Shanghai Institute of Ceramics, Chinese Academy of Science, Shanghai 200050 (China); School of Materials Science and Engineering, Shanghai University, Shanghai 200072 (China); Wang, Zheng, E-mail: wangzheng@mail.sic.ac.cn [Shanghai Institute of Ceramics, Chinese Academy of Science, Shanghai 200050 (China)

    2014-10-03

    Highlights: • A modified SBA-15 mesoporous silica (SH-SBA-15) was synthesized as a sorbent. • On-line SPE combined with SCGD-AES based on FIA was used to detect Hg{sup 2+} firstly. • A simple, low-cost Hg{sup 2+} analysis in a complex matrix was established. • The sensitive detection of Hg{sup 2+} was achieved with a detection limit of 0.75 μg L{sup −1}. - Abstract: A simple and sensitive method to determine Hg{sup 2+} was developed by combining solution-cathode glow discharge atomic emission spectrometry (SCGD-AES) with flow injection (FI) based on on-line solid-phase extraction (SPE). We synthesized L-cysteine-modified mesoporous silica and packed it in an SPE microcolumn, which was experimentally determined to possess a good mercury adsorption capacity. An enrichment factor of 42 was achieved under optimized Hg{sup 2+} elution conditions, namely, an FI flow rate of 2.0 mL min{sup −1} and an eluent comprised of 10% thiourea in 0.2 mol L{sup −1} HNO{sub 3}. The detection limit of FI–SCGD-AES was determined to be 0.75 μg L{sup −1}, and the precision of the 11 replicate Hg{sup 2+} measurements was 0.86% at a concentration of 100 μg L{sup −1}. The proposed method was validated by determining Hg{sup 2+} in certified reference materials such as human hair (GBW09101b) and stream sediment (GBW07310)

  2. Dielectric functions and carrier concentrations of Hg{sub 1−x}Cd{sub x}Se films determined by spectroscopic ellipsometry

    Energy Technology Data Exchange (ETDEWEB)

    Lee, A. J.; Peiris, F. C., E-mail: peirisf@kenyon.edu [Department of Physics, Kenyon College, Gambier, Ohio 43022 (United States); Brill, G.; Doyle, K. [U.S. Army Research Laboratory, Adelphi, Maryland 20783-1197 (United States); Myers, T. H. [Department of Physics, Texas State University, San Marcos, Texas 78666 (United States)

    2015-08-17

    Spectroscopic ellipsometry, ranging from 35 meV to 6 eV, was used to determine the dielectric functions of a series of molecular beam epitaxy-grown Hg{sub 1−x}Cd{sub x}Se thin films deposited on both ZnTe/Si(112) and GaSb(112) substrates. The fundamental band gap as well as two higher-order electronic transitions blue-shift with increasing Cd composition in Hg{sub 1−x}Cd{sub x}Se, as expected. Representing the free carrier absorption with a Drude oscillator, we found that the effective masses of Hg{sub 1−x}Cd{sub x}Se (grown on ZnTe/Si) vary between 0.028 and 0.050 times the free electron mass, calculated using the values of carrier concentration and the mobility obtained through Hall measurements. Using these effective masses, we determined the carrier concentrations of Hg{sub 1−x}Cd{sub x}Se samples grown on GaSb, which is of significance as films grown on such doped-substrates posit ambiguous results when measured by conventional Hall experiments. These models can serve as a basis for monitoring Cd-composition during sample growth through in-situ spectroscopic ellipsometry.

  3. Mercury methylation in paddy soil: source and distribution of mercury species at a Hg mining area, Guizhou Province, China

    Science.gov (United States)

    Zhao, Lei; Anderson, Christopher W. N.; Qiu, Guangle; Meng, Bo; Wang, Dingyong; Feng, Xinbin

    2016-04-01

    Rice paddy plantation is the dominant agricultural land use throughout Asia. Rice paddy fields have been identified as important sites for methylmercury (MeHg) production in the terrestrial ecosystem and a primary pathway of MeHg exposure to humans in mercury (Hg) mining areas. We compared the source and distribution of Hg species in different compartments of the rice paddy during a complete rice-growing season at two different typical Hg-contaminated mining sites in Guizhou province, China: an abandoned site with a high Hg concentration in soil but a low concentration in the atmosphere and a current-day artisanal site with a low concentration in soil but a high concentration in the atmosphere. Our results showed that the flux of new Hg to the ecosystem from irrigation and atmospheric deposition was insignificant relative to the pool of old Hg in soil; the dominant source of MeHg to paddy soil is in situ methylation of inorganic Hg (IHg). Elevated MeHg concentrations and the high proportion of Hg as MeHg in paddy water and the surface soil layer at the artisanal site demonstrated active Hg methylation at this site only. We propose that the in situ production of MeHg in paddy water and surface soil is dependent on elevated Hg in the atmosphere and the consequential deposition of new Hg into a low-pH anoxic geochemical system. The absence of depth-dependent variability in the MeHg concentration in soil cores collected from the abandoned Hg mining site, consistent with the low concentration of Hg in the atmosphere and high pH of the paddy water and irrigation water, suggested that net production of MeHg at this site was limited. We propose that the concentration of Hg in ambient air is an indicator for the risk of MeHg accumulation in paddy rice.

  4. Determination of Hg(2+) by on-line separation and pre-concentration with atmospheric-pressure solution-cathode glow discharge atomic emission spectrometry.

    Science.gov (United States)

    Li, Qing; Zhang, Zhen; Wang, Zheng

    2014-10-03

    A simple and sensitive method to determine Hg(2+) was developed by combining solution-cathode glow discharge atomic emission spectrometry (SCGD-AES) with flow injection (FI) based on on-line solid-phase extraction (SPE). We synthesized l-cysteine-modified mesoporous silica and packed it in an SPE microcolumn, which was experimentally determined to possess a good mercury adsorption capacity. An enrichment factor of 42 was achieved under optimized Hg(2+) elution conditions, namely, an FI flow rate of 2.0 mL min(-1) and an eluent comprised of 10% thiourea in 0.2 mol L(-1) HNO3. The detection limit of FI-SCGD-AES was determined to be 0.75 μg L(-1), and the precision of the 11 replicate Hg(2+) measurements was 0.86% at a concentration of 100 μg L(-1). The proposed method was validated by determining Hg(2+) in certified reference materials such as human hair (GBW09101b) and stream sediment (GBW07310).

  5. Hg0 absorption in potassium persulfate solution

    Institute of Scientific and Technical Information of China (English)

    YE Qun-feng; WANG Cheng-yun; WANG Da-hui; SUN Guan; XU Xin-hua

    2006-01-01

    The aqueous phase oxidation of gaseous elemental mercury (Hg0) by potassium persulfate (KPS) catalyzed by Ag+was investigated using a glass bubble column reactor. Concentration of gaseous mercury and potassium persulfate were measured by cold vapor atom absorption (CVAA) and ion chromatograph (IC), respectively. The effects of pH value, concentration of potassium persulfate and silver nitrate (SN), temperature, Hg0 concentration in the reactor inlet and tertiary butanol (TBA), free radical scavenger, on the removal efficiency of Hg0 were studied. The results showed that the removal efficiency of Hg0 increased with increasing concentration of potassium persulfate and silver nitrate, while temperature and TBA were negatively effective. Furthermore, the removal efficiency of Hg0 was much better in neutral solution than in both acidic and alkaline solution. But the influence of pH was almost eliminated by adding AgNO3. High Hg0 concentration has positive effect. The possible reaction mechanism of gaseous mercury was also discussed.

  6. Temporal changes in Hg, Pb, Cd and Zn environmental concentrations in the southern Baltic Sea sediments dated with 210Pb method

    Directory of Open Access Journals (Sweden)

    Tamara Zalewska

    2015-01-01

    Full Text Available The article presents data on heavy metal – Hg, Pb, Cd and Zn – distribution in the layers of marine sediments from the off-shore areas of the southern Baltic Sea: Gdańsk Deep, SE Gotland Basin and Bornholm Deep. Depth profiles of metal concentrations were converted to time-based profiles using the 210Pb dating method and verified by 137Cs distribution in the vertical profile. The linear sedimentation rates in the Gdańsk Deep and SE Gotland Basin are similar, 0.18 cm yr−1 and 0.14 cm yr−1, respectively, while the region of the Bornholm Deep is characterized by a greater sedimentation rate: 0.31 cm yr−1. Regarding anthropogenic pressure, Gdańsk Deep receives the largest share among the analyzed regions. The maximal metal concentrations detected in this area were Zn – 230 mg kg−1, Pb – 77 mg kg−1, Cd – 2.04 mg kg−1 and Hg – 0.27 mg kg−1. The least impact of anthropogenic pressure was noticeable in SE Gotland Basin. The combination of sediment dating with the analysis of vertical distribution of heavy metals in sediments benefited in the determination of target metal concentrations used in environmental status assessments. Reference values of heavy metal concentrations in marine sediments were determined as: Zn – 110 mg kg−1, Pb – 30 mg kg−1, Cd – 0.3 mg kg−1 and Hg – 0.05 mg kg−1 from the period of minor anthropogenic pressure. Basing on the determined indices: enrichment factor (EF, geoaccumulation indicator (Igeo and contamination factor (CF the status of marine environment was assessed regarding the pollution with heavy metals.

  7. Final report on CCQM-K70: Determination of Hg in natural water at a concentration level required by the European environmental quality standard (EQS)

    Science.gov (United States)

    Schiel, Detlef; Rienitz, Olaf

    2011-01-01

    This comparison 'Hg in natural water' was a follow-up to the pilot studies CCQM-P100.1 and CCQM-P100.2. The aim of this comparison was to demonstrate the capability of national metrology institutes to measure the Hg mass concentration in a natural water sample at the very low concentration level of γ(Hg) ≈ 70 ng/L as required by the EQS. In this way it served to help implement the European Water Framework Directive (WFD). This comparison was an activity of the Inorganic Analysis Working Group (IAWG) of CCQM and was piloted by Physikalisch-Technische Bundesanstalt (PTB, Braunschweig, Germany) with the help of the co-organizers Bundesanstalt für Materialforschung und -prüfung (BAM, Berlin, Germany), Laboratoire National de Métrologie et d'Essais (LNE, Paris, France), and the Joint Research Centre-Institute for Reference Materials and Measurements (EC-JRC-IRMM, Geel, Belgium). The following laboratories participated in this key comparison (in alphabetical order): BAM (Germany) EC-JRC-IRMM (European Union) KRISS (Republic of Korea) LGC (United Kingdom) LNE (France) NIST (United States of America) NMIA (Australia) NRC (Canada) PTB (Germany) SP (Sweden) The majority of participants applied isotope dilution mass spectrometry (IDMS) using sector field or quadrupole inductively coupled plasma MS (ICP-MS) in combination with cold vapour (CV) generation as the analytical technique. NRC reported a combined result of ID-CV-ICP-MS and CV atomic absorption spectrometry (CV-AAS). SP applied a standard addition method on a sector field ICP-MS, while BAM made use of an external 5-point calibration on a CV atomic fluorescence spectrometer (AFS). The key comparison reference value (KCRV) was agreed upon during the IAWG meeting in April 2010 at BIPM as the sum of the added Hg content calculated from the gravimetric sample preparation and the Hg matrix content of the water used for sample preparation (determined and validated on two independent pathways). Accordingly the degrees

  8. Removal of Hg~0 with sodium chlorite solution and mass transfer reaction kinetics

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    The absorption behavior of Hg0 was studied experimentally by using sodium chlorite solution(NaClO2) as the absorbent in a bubble reactor.Primary influencing factors on removal efficiency of Hg0 such as NaClO2 concentration,pH,reaction temperature and the concentration of Hg0 were investigated.The results indicated that 72.91% of Hg0 removal efficiency could be achieved in acidic NaClO2 solution.The removal mechanism of Hg0 was proposed by analyzing of Hg2+ concentration in ab-sorption solution after reaction and comparing the electrode potentials between NaClO2 species and Hg2+/Hg0.The experimental results of mass transfer-reaction kinetics on oxidation of Hg0 by NaClO2 solution showed that with the increase of NaClO2 concentration and the decrease of pH value,the enhancement factor(E) and ratio of KG(Hg0)/kG(Hg0) increased and the liquid phase mass transfer resistance decreased,which is benefit to the mass transfer adsorption reaction.Although the increase of reaction temperature could improve the enhancement factor(E),but the ratio of KG(Hg0)/kG(Hg0) decreased;as a result,the liquid phase mass transfer resistance increased,therefore,the reaction rate for removal of Hg0 decreased.

  9. Immunomodulation the marine green mussel Perna viridis exposed to sub-lethal concentrations of Cu and Hg.

    Science.gov (United States)

    Thiagarajan, R; Gopalakrishnan, S; Thilagam, H

    2006-10-01

    Environmental pollution is a growing concern and, more importantly, pollution of the aquatic ecosystem is alarming. Marine pollution may be one of the reasons for disease incidence in marine organisms, which is caused due to adverse effects of pollutants on the immune system. Bivalves are commonly used as bio-indicators of marine pollution, and immunomodulation due to toxicants is one of the important bio-markers used. Perna viridis too have been used as a bio-indicator, but this study is, to our knowledge, a first report on immunomodulation produced by metals, in P. viridis. Animals were exposed to copper and mercury at their sub-lethal concentrations of 20 microg L(-1) and 10 microg L(-1), respectively. Immune parameters including phenoloxidase, reactive oxygen species generation, and phagocytosis were monitored. The study period was for 25 days (chronic long-term exposure) and objectives established whether metals produced immunomodulation and to understand the effects of long-term exposure on immunomodulation. Results showed that both metals adversely affected immune parameters studied and, interestingly, there appears to be some level of recovery (depuration) from the toxic effects of metals.

  10. Mercury (Hg) in meteorites: variations in abundance, thermal release profile, mass-dependent and mass-independent isotopic fractionation

    CERN Document Server

    Meier, Matthias M M; Marty, Bernard

    2016-01-01

    We have measured the concentration, isotopic composition and thermal release profiles of Mercury (Hg) in a suite of meteorites, including both chondrites and achondrites. We find large variations in Hg concentration between different meteorites (ca. 10 ppb to 14'000 ppb), with the highest concentration orders of magnitude above the expected bulk solar system silicates value. From the presence of several different Hg carrier phases in thermal release profiles (150 to 650 {\\deg}C), we argue that these variations are unlikely to be mainly due to terrestrial contamination. The Hg abundance of meteorites shows no correlation with petrographic type, or mass-dependent fractionation of Hg isotopes. Most carbonaceous chondrites show mass-independent enrichments in the odd-numbered isotopes 199Hg and 201Hg. We show that the enrichments are not nucleosynthetic, as we do not find corresponding nucleosynthetic deficits of 196Hg. Instead, they can partially be explained by Hg evaporation and redeposition during heating of ...

  11. 烟台近海海域经济类海洋生物体内Sn、Hg的含量分析%Study on Concentrations of Sn, Hg in Some Edible Marine Organisms in Yantai Coastal Areas

    Institute of Scientific and Technical Information of China (English)

    邵立娜; 任宗明; 张高生; 陈琳琳; 刘东艳; 王子健; 赵建平

    2011-01-01

    To evaluate the contamination of Sn and Hg in the seafood in Yantai coastal areas,three kinds of wild shrimps and crabs were collected from three zones located in the coast in July ,2009. At the same time, seven kinds of mollusks were purchased from the local market. The concentrations of Sn and Hg in the samples were analyzed using an Agilent 7500i inductively coupled plasma-mass spectrometer (ICP-MS). The results showed that Sn and Hg concentrations in all the samples were different,with the ranges of 0.375-0.570 mg· kg -1 and 0.060-0.340 mg· kg -1 ( d.w.) and the average values of 0.470 and 0.140 mg· kg -1, respectively. For the mollusk samples, Concha ostreae was highly enriched with Sn, with the value of 0.570 mg·kg-1, while Mytilus edulis was obviously enriched with Hg,with the value of 0.340 mg·kg-1. The value of P1 was 1.13, which indicated that Mytilus edulis was seriously polluted. The concentrations of Sn and Hg in Chamys farreri and Sol sricus were the lowest, respectively. For the collected samples, the average concentrations of Sn and Hg in Oratosquilla oratoria ,Alpheus brevicristatus and Carpilius convexus in the background area were all lower than those in sewage outfall area and port area, the average concentrations of Sn were 0.520 mg·kg-1 ( port area) ,0.470 mg·kg -1 (sewage outfall area) and 0.290 mg· kg -1 ( background area ), the average concentrations of Hg were: 0.160 mg·kg -1 ( port area ),0.157 mg· kg-1 (sewage outfall area)and 0.137 mg·kg-1 (background area). Compared with other reports, the Sn level in the studied marine organisms was moderate ,but the Hg level was a little higher. However, the concentrations of Sn and Hg in the studied marine seafood were all below the limit for agriculture product safety requirements for non-environmental pollution products, except Hg in Mytilus edulis (the national standards of Sn haven't been established). The results suggested that the coastal areas studied were not significantly

  12. Enrichment of Pb, Hg and Cr in cultured carp otolith

    African Journals Online (AJOL)

    AJL

    2012-01-26

    Jan 26, 2012 ... record the pollution condition at the sampling time. ... aquatic organisms are aquatic algae, zooplankton .... element cannot show that Hg concentration in otolith ..... from Atlantic croaker along an estuarine pollution gradient.

  13. Hg transfer from contaminated soils to plants and animals

    NARCIS (Netherlands)

    Rodrigues, S.M.; Henriques, B.; Reis, A.T.; Duarte, A.C.; Pereira, E.; Romkens, P.F.A.M.

    2012-01-01

    Understanding the transfer of mercury (Hg) from soil to crops is crucial due to Hg toxicity and Hg occurrence in terrestrial systems. Previous research has shown that available Hg in soils contributes to plant Hg levels. Plant Hg concentrations are related to soil conditions and plant characteristic

  14. Culturable associated-bacteria of the sponge Theonella swinhoei show tolerance to high arsenic concentrations

    Directory of Open Access Journals (Sweden)

    Ray eKeren

    2015-02-01

    Full Text Available Sponges are potent filter feeders and as such are exposed to high fluxes of toxic trace elements, which can accumulate in their body over time. Such is the case of the Red Sea sponge Theonella swinhoei, which has been shown to accumulate up to 8500 mg/Kg of the highly toxic element arsenic. T. swinhoei is known to harbor a multitude of sponge-associated bacteria, so it is hypothesized that the associated-bacteria will be tolerant to high arsenic concentration. This study also investigates the fate of the arsenic accumulated in the sponge to test if the associated-bacteria have an important role in the arsenic accumulation process of their host, since bacteria are key players in the natural arsenic cycle. Separation of the sponge to sponge cells and bacteria enriched fractions showed that arsenic is accumulated by the bacteria. Sponge-associated, arsenic-tolerant bacteria were cultured in the presence of 5 mM of either arsenate or arsenite (equivalent to 6150 mg/Kg arsenic, dry weight. The 54 isolated bacteria were grouped to 15 OTUs and isolates belonging to 12 OTUs were assessed for tolerance to arsenate at increased concentrations up to 100 mM. Eight of the 12 OTUs tolerated an order of magnitude increase in the concentration of arsenate, and some exhibited external biomineralization of arsenic-magnesium salts. The biomineralization of this unique mineral was directly observed in bacteria for the first time. These results may provide an explanation for the ability of the sponge to accumulate considerable amounts of arsenic. Furthermore arsenic-mineralizing bacteria can potentially be used for the study of bioremediation, as arsenic toxicity affects millions of people worldwide.

  15. Modeling interactions of Hg(II) and bauxitic soils.

    Science.gov (United States)

    Weerasooriya, Rohan; Tobschall, Heinz J; Bandara, Atula

    2007-11-01

    The adsorptive interactions of Hg(II) with gibbsite-rich soils (hereafter SOIL-g) were modeled by 1-pK surface complexation theory using charge distribution multi-site ion competition model (CD MUSIC) incorporating basic Stern layer model (BSM) to account for electrostatic effects. The model calibrations were performed for the experimental data of synthetic gibbsite-Hg(II) adsorption. When [NaNO(3)] > or = 0.01M, the Hg(II) adsorption density values, of gibbsite, Gamma(Hg(II)), showed a negligible variation with ionic strength. However, Gamma(Hg(II)) values show a marked variation with the [Cl(-)]. When [Cl(-)] > or = 0.01M, the Gamma(Hg(II)) values showed a significant reduction with the pH. The Hg(II) adsorption behavior in NaNO(3) was modeled assuming homogeneous solid surface. The introduction of high affinity sites, i.e., >Al(s)OH at a low concentration (typically about 0.045 sites nm(-2)) is required to model Hg(II) adsorption in NaCl. According to IR spectroscopic data, the bauxitic soil (SOIL-g) is characterized by gibbsite and bayerite. These mineral phases were not treated discretely in modeling of Hg(II) and soil interactions. The CD MUSIC/BSM model combination can be used to model Hg(II) adsorption on bauxitic soil. The role of organic matter seems to play a role on Hg(II) binding when pH>8. The Hg(II) adsorption in the presence of excess Cl(-) ions required the selection of high affinity sites in modeling.

  16. Impacts of forest harvesting on mobilization of Hg and MeHg in drained peatland forests on black schist or felsic bedrock.

    Science.gov (United States)

    Ukonmaanaho, Liisa; Starr, Mike; Kantola, Marjatta; Laurén, Ari; Piispanen, Juha; Pietilä, Heidi; Perämäki, Paavo; Merilä, Päivi; Fritze, Hannu; Tuomivirta, Tero; Heikkinen, Juha; Mäkinen, Jari; Nieminen, Tiina M

    2016-04-01

    Forest harvesting, especially when intensified harvesting method as whole-tree harvesting with stump lifting (WTHs) are used, may increase mercury (Hg) and methylmercury (MeHg) leaching to recipient water courses. The effect can be enhanced if the underlying bedrock and overburden soil contain Hg. The impact of stem-only harvesting (SOH) and WTHs on the concentrations of Hg and MeHg as well as several other variables in the ditch water was studied using a paired catchment approach in eight drained peatland-dominated catchments in Finland (2008-2012). Four of the catchments were on felsic bedrock and four on black schist bedrock containing heavy metals. Although both Hg and MeHg concentrations increased after harvesting in all treated sites according to the randomized intervention analyses (RIAs), there was only a weak indication of a harvest-induced mobilization of Hg and MeHg into the ditches. Furthermore, no clear differences between WTHs and SOH were found, although MeHg showed a nearly significant difference (p = 0.06) between the harvesting regimes. However, there was a clear bedrock effect, since the MeHg concentrations in the ditch water were higher at catchments on black schist than at those on felsic bedrock. The pH, suspended solid matter (SSM), dissolved organic carbon (DOC), and iron (Fe) concentrations increased after harvest while the sulfate (SO4-S) concentration decreased. The highest abundances of sulfate-reducing bacteria (SRB) were found on the sites with high MeHg concentrations. The biggest changes in ditch water concentrations occurred first 2 years after harvesting.

  17. High removal efficacy of Hg(II) and MeHg(II) ions from aqueous solution by organoalkoxysilane-grafted lignocellulosic waste biomass.

    Science.gov (United States)

    Saman, Norasikin; Johari, Khairiraihanna; Song, Shiow-Tien; Kong, Helen; Cheu, Siew-Chin; Mat, Hanapi

    2017-03-01

    An effective organoalkoxysilanes-grafted lignocellulosic waste biomass (OS-LWB) adsorbent aiming for high removal towards inorganic and organic mercury (Hg(II) and MeHg(II)) ions was prepared. Organoalkoxysilanes (OS) namely mercaptoproyltriethoxylsilane (MPTES), aminopropyltriethoxylsilane (APTES), aminoethylaminopropyltriethoxylsilane (AEPTES), bis(triethoxysilylpropyl) tetrasulfide (BTESPT), methacrylopropyltrimethoxylsilane (MPS) and ureidopropyltriethoxylsilane (URS) were grafted onto the LWB using the same conditions. The MPTES grafted lignocellulosic waste biomass (MPTES-LWB) showed the highest adsorption capacity towards both mercury ions. The adsorption behavior of inorganic and organic mercury ions (Hg(II) and MeHg(II)) in batch adsorption studies shows that it was independent with pH of the solutions and dependent on initial concentration, temperature and contact time. The maximum adsorption capacity of Hg(II) was greater than MeHg(II) which respectively followed the Temkin and Langmuir models. The kinetic data analysis showed that the adsorptions of Hg(II) and MeHg(II) onto MPTES-LWB were respectively controlled by the physical process of film diffusion and the chemical process of physisorption interactions. The overall mechanism of Hg(II) and MeHg(II) adsorption was a combination of diffusion and chemical interaction mechanisms. Regeneration results were very encouraging especially for the Hg(II); this therefore further demonstrated the potential application of organosilane-grafted lignocellulosic waste biomass as low-cost adsorbents for mercury removal process.

  18. Northern European trees show a progressively diminishing response to increasing atmospheric carbon dioxide concentrations

    CSIR Research Space (South Africa)

    Waterhouse, JS

    2004-04-01

    Full Text Available 1895-1994 of three tree species growing across northern Europe to increases in atmospheric CO2 concentrations using parameters derived from stable carbon isotope ratios of trunk cellulose. Using the isotope data, values of intrinsic water-use efficiency...

  19. Uptake of Hg2+ by picocyanobacteria in natural water from four Andean lakes

    Directory of Open Access Journals (Sweden)

    Diéguez M.C.

    2014-07-01

    Full Text Available In lake food webs, planktonic bacteria and algae represent the greatest bioconcentration step for Hg2+ and monomethyl-Hg (MeHg. As they are the most abundant organisms in planktonic trophic webs and also the main food resource for herbivorous plankton, they can mobilize large amounts of Hg to higher trophic levels. In Andean Patagonian lakes (Argentina, dissolved organic matter (DOM concentration and character, coupled with photo-reactions, play a central role in the complexation of Hg2+ in the water column and can even regulate the uptake of Hg2+ by planktonic algae. In this investigation we evaluated the DOM character of natural waters (NW from four Andean lakes and studied its influence on the uptake of 197Hg2+ in a strain of the picocyanobacteria Synechococcus by using Hg2+ labeled with 197Hg2+. The uptake of radiolabeled Hg2+ by Synechococcus showed different magnitude in NW of lakes Moreno, El Trébol, Morenito and Escondido. Increasing lake DOM concentration reduced the bioavailability of Hg2+ as indicated by the lower uptakes rates found in NW with higher complexity and concentration of the DOM pool. Uptakes of Hg2+ by this picocyanobacteria contrasted among NW from pelagic (surface and bottom and littoral compartments of Lake Escondido which suggest that the entry of this metal may be highly variable even in the same environment. The study of the uptake of radiolabeled Hg2+ in a set of dilutions of NW from Lake Escondido demonstrated that the bioavailability of Hg2+ decrease with increasing DOM concentration.

  20. Benzoxazinoid concentrations show correlation with Fusarium Head Blight resistance in Danish wheat varieties

    DEFF Research Database (Denmark)

    Søltoft, Malene; Jørgensen, Lise N.; Svensmark, Bo;

    2008-01-01

    Fusarium Head Blight (FHB) is a destructive disease that affects the grain yield and quality of cereals. The relationship between the natural defense chemicals benzoxazinoids and the FHB resistance of field grown winter wheat varieties was investigated. FHB resistance was assessed by the inoculat......Fusarium Head Blight (FHB) is a destructive disease that affects the grain yield and quality of cereals. The relationship between the natural defense chemicals benzoxazinoids and the FHB resistance of field grown winter wheat varieties was investigated. FHB resistance was assessed...... by the inoculation of wheat ears with mixtures of Fusarium avenaceum, Fusarium culmorum, Fusarium graminearum, and Microdochium nivale. The benzoxazinoids detected in the highest concentration were 2,4-dihydroxy-7-methoxy-(2H)-1,4-benzoxazin-3(4H)-one (3.7-9.4 mu mol/kg DW) and 2-hydroxy-7-nnethoxy-(2H)-1...

  1. Selective Hg(II) adsorption from aqueous solutions of Hg(II) and Pb(II) by hydrolyzed acrylamide-grafted PET films.

    Science.gov (United States)

    Rahman, Nazia; Sato, Nobuhiro; Sugiyama, Masaaki; Hidaka, Yoshiki; Okabe, Hirotaka; Hara, Kazuhiro

    2014-01-01

    Selective Hg(II) adsorption from aqueous solutions of Hg(II) and Pb(II) using hydrolyzed acrylamide (AAm)-grafted polyethylene terephthalate (PET) films was examined to explore the potential reuse of waste PET materials. Selective recovery of Hg(II) from a mixture of soft acids with similar structure, such as Hg(II) and Pb(II), is important to allow the reuse of recovered Hg(II). An adsorbent for selective Hg(II) adsorption was prepared by γ-ray-induced grafting of AAm onto PET films followed by partial hydrolysis through KOH treatment. The adsorption capacity of the AAm-grafted PET films for Hg(II) ions increased from 15 to 70 mg/g after partial hydrolysis because of the reduction of hydrogen bonding between -CONH2 groups and the corresponding improved access of metal ions to the amide groups. The prepared adsorbent was characterized by Fourier transform infrared spectroscopy and scanning electron microscopy. The absorbent film showed high selectivity for the adsorption of Hg(II) over Pb(II) throughout the entire initial metal concentration range (100-500 mg/L) and pH range (2.2-5.6) studied. The high selectivity is attributed to the ability of Hg(II) ions to form covalent bonds with the amide groups. The calculated selectivity coefficient for the adsorbent binding Hg(II) over Pb(II) was 19.2 at pH 4.5 with an initial metal concentration of 100 mg/L. Selective Hg(II) adsorption equilibrium data followed the Langmuir model and kinetic data were well fitted by a pseudo-second-order equation. The adsorbed Hg(II) and Pb(II) ions were effectively desorbed from the adsorbent film by acid treatment, and the regenerated film showed no marked loss of adsorption capacity upon reuse for selective Hg(II) adsorption.

  2. Hg SOIL GAS AND Hg SOIL DISTRIBUTION AROUND FORMER „ZRINSKI“ MINE ON MT. MEDVEDNICA, CROATIA

    Directory of Open Access Journals (Sweden)

    Nataša Jug

    2008-12-01

    Full Text Available The purpose of this study is to present the field and laboratory researches, statistical analyses and graphical displays of the results of Hg soil gas and Hg soil distribution in the area around former mining site „Zrinski“ on Mt. Medvednica. The values of overall Hg concentrations in the soil gas show lognormal distribution, and their spatial distribution outlines the connection with the present Pb-Ag-Zn mineralization and confirms anthropogenic origin of uneven landscape relief (waste rock clusters. Regression analysis of the dependence between Hg contents in the soil gas and the distance from the mine entrance (correlation coefficient r also points to the considerable spatial dependence. Hg soil contents show as well distribution similar to lognormal, and there is a slight correlation when compared with Hg soil gas content. Concentrations are mostly within background values, except in the immediate vicinity of the mine entrance where the values are significantly higher due to the mineralization influence concentrated in the waste-rock clusters. Soil pollution caused by mercury is of local character with the spreading tendency to the south-west because of the dominant relief influence. Mercury found in the soil of the research location derives from the present mineral body and former mining activities, while possible anthropogenic atmospheric inputs from remote sources can not be proven on the basic of conducted research studies (the paper is published in Croatian.

  3. [Using atomic fluorescence spectrometry to study the spatial distribution of As and Hg in orchard soils].

    Science.gov (United States)

    Zhao, Xi-Mei; Lü, Chun-Yan; Liu, Qing; Zhu, Xi-Cun

    2014-02-01

    Aqua regia digestion, double channels-atomic fluorescence spectrometry method was used to determine the concentrations of As and Hg in orchard soils of Qixia City - the main apple production area of Shandong province. Validate The detection limitation, accuracy and precision of the method were validated, the spatial distribution was analyzed, and the characteristics of As and Hg pollution in Qixia orchard soils were assessed. The results showed that the range of As concentration in Qixia soils is between 2.79 and 20.93 mg x kg(-1), the average concentration is 10.59 mg x kg(-1), the range of Hg concentration in Qixia soil is between 0.01 and 0.79 mg x kg(-1), the average concentration is 0.12 mg x kg(-1). The variation of As concentration in soils is small, whereas that of Hg concentration is large. Frequency distribution graphics of As and Hg showed that the concentration of As in soils is according with the normal distribution approximately and the concentrations are mostly between 7 and 15 mg x kg(-1), the concentration of Hg in soil isn't according with the normal distribution and the concentrations are mostly between 0.03 and 0.21 mg x kg(-1). The correlations between the concentrations of As or Hg in soils and the nutrient are not significant and there is no significant correlation even between As and Hg. Based on the environmental technical terms for green food production area, the As concentration in orchard soil of Qixia City is at clean level, but there are 4.76% of sample points with Hg pollution index exceeding 1, and this should be attracted the attention of the administrators.

  4. Sediment accumulation and mercury (Hg) flux in Avicennia marina forest of Deep Bay, China

    Science.gov (United States)

    Li, Ruili; Chai, Minwei; Guo, Meixian; Qiu, Guo Yu

    2016-08-01

    To investigate the rate of sediment accumulation and mercury (Hg) flux in Avicennia marina forest of Deep Bay, China, sediment cores were analyzed. The results showed that Hg concentrations were much higher at all depths compared to the background level. A high correlation between Hg and total organic carbon (TOC) indicated their similar anthropogenic origin. Sedimentation rate was estimated to be 1.38 cm a-1 by 210Pb geochronology. The increase in the mass sediment accumulation rates was rapid (range: 0.5-0.94 g cm-2 a-1), and the Hg fluxes ranged between 76 and 116 ng cm-2 a-1 during the last three decades. The reduction in both Hg concentrations and flux during the last decade may be due to the adoption of contamination control policies. Our results support the notion that the Hg fluxes determined from the sediment cores reveal the effects of anthropogenic influences from the areas around Deep Bay.

  5. Mercury (Hg) in meteorites: Variations in abundance, thermal release profile, mass-dependent and mass-independent isotopic fractionation

    Science.gov (United States)

    Meier, Matthias M. M.; Cloquet, Christophe; Marty, Bernard

    2016-06-01

    We have measured the concentration, isotopic composition and thermal release profiles of Mercury (Hg) in a suite of meteorites, including both chondrites and achondrites. We find large variations in Hg concentration between different meteorites (ca. 10 ppb to 14,000 ppb), with the highest concentration orders of magnitude above the expected bulk solar system silicates value. From the presence of several different Hg carrier phases in thermal release profiles (150-650 °C), we argue that these variations are unlikely to be mainly due to terrestrial contamination. The Hg abundance of meteorites shows no correlation with petrographic type, or mass-dependent fractionation of Hg isotopes. Most carbonaceous chondrites show mass-independent enrichments in the odd-numbered isotopes 199Hg and 201Hg. We show that the enrichments are not nucleosynthetic, as we do not find corresponding nucleosynthetic deficits of 196Hg. Instead, they can partially be explained by Hg evaporation and redeposition during heating of asteroids from primordial radionuclides and late-stage impact heating. Non-carbonaceous chondrites, most achondrites and the Earth do not show these enrichments in vapor-phase Hg. All meteorites studied here have however isotopically light Hg (δ202Hg = ∼-7 to -1) relative to the Earth's average crustal values, which could suggest that the Earth has lost a significant fraction of its primordial Hg. However, the late accretion of carbonaceous chondritic material on the order of ∼2%, which has been suggested to account for the water, carbon, nitrogen and noble gas inventories of the Earth, can also contribute most or all of the Earth's current Hg budget. In this case, the isotopically heavy Hg of the Earth's crust would have to be the result of isotopic fractionation between surface and deep-Earth reservoirs.

  6. HCN Producing Bacteria Enable Sensing Of Non-Bioavailable Hg Species by the Whole Cell Biosensor

    Science.gov (United States)

    Horvat, M.; Rijavec, T.; Koron, N.; Lapanje, A.

    2015-12-01

    Bacteria play an important role in Hg transformation reactions. The production of cyanide (HCN) and other secondary metabolites seems to be key elements involved in these transformations. Current hypotheses link the role of HCN production to growth inhibition of nonHCN producing competitor organisms (role of an antimicrobial agent). Our past investigations showed that HCN production did not correlate with antimicrobial activity and since pK value of HCN is very high (pK = 9,21), it can be expected that most of the produced HCN is removed from the microenvironment. This way, the expected inhibitory concentrations can hardly be reached. Accordingly, we proposed a new concept, where the ability of complexation of transient metals by HCN served as a regulation process for the accessibility of micro-elements. In our study, we focused on the presence of HCN producing bacteria and carried it out in the Hg contaminated environment connected to the Idrija Mercury Mine, Slovenia. We characterised the isolates according to the presence of Hg resistance (HgR), level of HCN production and genetic similarities. In laboratory setups, using our merR whole cell based biosensor, we determined the transformation of low bioavailable Hg0 and HgS forms into bioavailable Hg by these HCN producing bacteria. We observed that HgR strains producing HCN had the highest impact on increased Hg bioavailability. In the proposed ecological strategy HgR HCN producing bacteria increase their competitive edge over non-HgR competitors through the increase of Hg toxicity. Due to their activity, Hg is made available to other organisms as well and thus enters into the ecosystem. Finally, using some of the characteristics of bacteria (e.g. Hg resistance genetic elements), we developed a fully automated sensing approach, combining biosensorics and mechatronics, to measure the bioavailability of Hg in situ.

  7. Chemical thermodynamics of the Hg1212 phase

    Science.gov (United States)

    Tsuchiya, Tetsuo; Fueki, Kazuo

    1997-02-01

    The single phase of Hg1212 was synthesized by the simple oxide method using starting materials containing HgO 16% in excess. Stability regions of Hg1212 and pure HgO were determined by measuring the decomposition temperature as a function of oxygen partial pressure, and thermodynamic diagrams showing the stability domains of HgO and Hg1212 were constructed. The thermodynamical condition of formation of Hg1212 was discussed using the diagrams. It was found by chemical analysis that the valence of Hg is always 2 + and the valence of Ce changes with the oxygen content. TC (zero) changed from 122 to 118 K when the oxygen content was increased from 6.10 to 6.22.

  8. Single concentration tests show synergism among Bacillus thuringiensis subsp. israelensis toxins against the malaria vector mosquito Anopheles albimanus.

    Science.gov (United States)

    Fernández-Luna, María Teresa; Tabashnik, Bruce E; Lanz-Mendoza, Humberto; Bravo, Alejandra; Soberón, Mario; Miranda-Ríos, Juan

    2010-07-01

    Bioassays of insecticidal proteins from Bacillus thuringiensis subsp. israelensis with larvae of the malaria vector mosquito Anopheles albimanus showed that the cytolytic protein Cyt1Aa was not toxic alone, but it increased the toxicity of the crystalline proteins Cry4Ba and Cry11Aa. Synergism also occurred between Cry4Ba and Cry11Aa toxins. Whereas many previous analyses of synergism have been based on a series of toxin concentrations leading to comparisons between expected and observed values for the concentration killing 50% of insects tested (LC(50)), we describe and apply a method here that enables testing for synergism based on single concentrations of toxins.

  9. Impacts of Activated Carbon Amendment on Hg Methylation, Demethylation and Microbial Activity in Marsh Soils

    Science.gov (United States)

    Gilmour, C. C.; Ghosh, U.; Santillan, E. F. U.; Soren, A.; Bell, J. T.; Butera, D.; McBurney, A. W.; Brown, S.; Henry, E.; Vlassopoulos, D.

    2015-12-01

    In-situ sorbent amendments are a low-impact approach for remediation of contaminants in sediments, particular in habitats like wetlands that provide important ecosystem services. Laboratory microcosm trials (Gilmour et al. 2013) and early field trials show that activated carbon (AC) can effectively increase partitioning of both inorganic Hg and methylmercury to the solid phase. Sediment-water partitioning can serve as a proxy for Hg and MeHg bioavailability in soils. One consideration in using AC in remediation is its potential impact on organisms. For mercury, a critical consideration is the potential impact on net MeHg accumulation and bioavailability. In this study, we specifically evaluated the impact of AC on rates of methylmercury production and degradation, and on overall microbial activity, in 4 different Hg-contaminated salt marsh soils. The study was done over 28 days in anaerobic, sulfate-reducing slurries. A double label of enriched mercury isotopes (Me199Hg and inorganic 201Hg) was used to separately follow de novo Me201Hg production and Me199Hg degradation. AC amendments decreased both methylation and demethylation rate constants relative to un-amended controls, but the impact on demethylation was stronger. The addition of 5% (dry weight) regenerated AC to soil slurries drove demethylation rate constants to nearly zero; i.e. MeHg sorption to AC almost totally blocked its degradation. The net impact was increased solid phase MeHg concentrations in some of the soil slurries with the highest methylation rate constants. However, the net impact of AC amendments was to increase MeHg (and inorganic Hg) partitioning to the soil phase and decrease concentrations in the aqueous phase. AC significantly decreased aqueous phase inorganic Hg and MeHg concentrations after 28 days. Overall, the efficacy of AC in reducing aqueous MeHg was highest in the soils with the highest MeHg concentrations. The AC addition did not significantly impact microbial activity, as

  10. [Experimental Research of Hg (II) Removal from Aqueous Solutions of HgCl2 with Nano-TiO2].

    Science.gov (United States)

    Zhou, Xiong; Zhang, Jin-yang; Wang, Ding-yong; Qin, Cai-qing; Xu, Feng; Luo Cheng-zhong; Yang, Xi

    2016-01-15

    Mercury removal from aqueous solutions of HgCl2 was studied by indoor simulation experiments, and the effects of three different diameter of particles of Nano-TiO2 ( Nano-Titanium Dioxide) at different dosage, pH, adsorption time and the initial concentration of Hg2+ on the mercury adsorption from simulated wastewater were investigated. The single factor experiments showed that the optimal conditions were: 7.5 g x L(-1) of 5 nm TiO2 or 2.0 g x L(-1) of 100 nm TiO2, pH 8.0, initial concentration of Hg2+ 15 x mg x L(-1) adsorption time 5 min, and under these conditions the adsorption rates reached 99.5% and 99.3%, relatively. When the content of 25 nm TiO2 was 10 g x L(-1), and the other conditions were pH 8.0, initial concentration of Hg2+ 15 mg x L(-1), adsorption time 60 min, the adsorption rate was 62.8%. The Hg(II) removal effects of the TiO2 particles with different diameters followed the order of 100 nm TiO2 > 5 nm TiO2 > 25 nm TiO2. Component adsorption results showed that the 5 nm TiO2 component adsorption effect was superior to its single adsorption effect, while there was little difference between 100 nm TiO2 component adsorption effect and its single adsorption effect. The results of orthogonal experiments indicated that the influencing factors of the adsorption rate followed the order of pH > the initial concentration of Hg2+ > time > dosage. The optimal experiment scheme was: pH 8.0, a dosage of 100 nm Nano-TiO2 of 2.0 g x L(-1) an initial Hg2+ concentration of 25 mg x L(-1) and adsorption time of 10 min. Under the experimental conditions, the maximum adsorption rate reached 99.9%, at the same time, the equilibrium concentration of Hg(II) was 0.033 mg x L(-1) adsorptive capacity was 26.95 mg x g(-1). The adsorption isotherm was in line with the Langmuir isotherm equation, indicating that the Hg(II) uptake by 100 nm Nano-TiO2 was typical monolayer adsorption.

  11. Assessing anthropogenic sources of mercury in soil in Wanshan Hg mining area, Guizhou, China.

    Science.gov (United States)

    Dai, Zhihui; Feng, Xinbin; Zhang, Chao; Wang, Jingfu; Jiang, Taiming; Xiao, Houjun; Li, Yu; Wang, Xun; Qiu, Guangle

    2013-11-01

    Long-term mining and smelting activities brought a series of environmental issues into soils in Wanshan mercury (Hg) mining area (WMMA), Guizhou, China. Several studies have been published on the concentrations of Hg in local soils, but a comprehensive assessment of the mass of Hg in soil induced by anthropogenic activities, as presented in this paper, has not been previously conducted. Three districts of WMMA were chosen as the study areas. We summarized previous published data and sampled 14 typical soil profiles to analyze the spatial and vertical distributions of Hg in soil in the study areas. The regional geologic background, direct and indirect Hg deposition, and Hg-polluted irrigation water were considered as the main sources of Hg contaminations in local soils. Furthermore, the enrichment factor (EF) method was applied to assess the extent of anthropogenic input of Hg to soil. Titanium (Ti) was chosen to be the reference element to calculate the EF. Generally, the elevated values of EF were observed in the upper soil layers and close to mine wastes. The total budget of Hg in soil contributed from anthropogenic sources was estimated to be 1,227 t in arable soil and 75 t in natural soil. Our data showed that arable soil was the major sink of anthropogenic Hg in the study area.

  12. Toxic effects of HgCl2 on the growth and oogonium formation in Oedogonium hatei.

    Science.gov (United States)

    Singh, H V

    2001-01-01

    The effect of mercuric chloride on the germination and growth of swarmers and subsequent induction of oogonia was studied in Oedogonium hatei Kam. (Oedogoniales, Chorophyceae). HgCl2 within the concentration range of 0.01 to 1.0 mg/l produced a progressive increase in the initiation of germination and reduction in the growth of the alga. The percentage of oogonia formed, and mature oogonia developed, decreased linearly with a rise in the concentrations of HgCl2 employed. The results showed that 1 mg/l HgCl2 was highly toxic to the growth and/or multiplication of zoospores and further development of sexual structures in O. hatei. The germination of zoospores and growth of germlings were so severely affected that induction of oogonia remained completely inhibited at 1 mg/l HgCl2. Moreover, 2 mg/l of HgCl2 was lethal to the asexual zoospores.

  13. Long-distance transport of Hg, Sb, and As from a mined area, conversion of Hg to methyl-Hg, and uptake of Hg by fish on the Tiber River basin, west-central Italy

    Science.gov (United States)

    Gray, John E.; Rimondi, Valentina; Costagliola, Pilario; Vaselli, Orlando; Lattanzi, Pierfranco

    2014-01-01

    Stream sediment, stream water, and fish were collected from a broad region to evaluate downstream transport and dispersion of mercury (Hg) from inactive mines in the Monte Amiata Hg District (MAMD), Tuscany, Italy. Stream sediment samples ranged in Hg concentration from 20 to 1,900 ng/g, and only 5 of the 17 collected samples exceeded the probable effect concentration for Hg of 1,060 ng/g, above which harmful effects are likely to be observed in sediment-dwelling organisms. Concentrations of methyl-Hg in Tiber River sediment varied from 0.12 to 0.52 ng/g, and although there is no established guideline for sediment methyl-Hg, these concentrations exceeded methyl-Hg in a regional baseline site (Sb (Sb) and for protection against chronic effects to aquatic wildlife (150 μg/L for As and 5.6 μg/L for Sb). Concentrations of Hg in freshwater fish muscle ranged from 0.052–0.56 μg/g (wet weight), mean of 0.17 μg/g, but only 17 % (9 of 54) exceeded the 0.30 μg/g (wet weight) USEPA fish muscle guideline recommended to protect human health. Concentrations of Hg in freshwater fish in this region generally decreased with increasing distance from the MAMD, where fish with the highest Hg concentrations were collected more proximal to the MAMD, whereas all fish collected most distal from Hg mines contained Hg below the 0.30 μg/g fish muscle guideline. Data in this study indicate some conversion of inorganic Hg to methyl-Hg and uptake of Hg in fish on the Paglia River, but less methylation of Hg and Hg uptake by freshwater fish in the larger Tiber River.

  14. Estimating atmospheric mercury concentrations with lichens.

    Science.gov (United States)

    Vannini, Andrea; Nicolardi, Valentina; Bargagli, Roberto; Loppi, Stefano

    2014-01-01

    The uptake kinetics of elemental gaseous Hg (Hg(0)) in three species of epiphytic lichens (Pseudevernia furfuracea, Evernia prunastri, and Xanthoria parietina) were investigated under four different Hg concentrations (10, 15, 30, and 45 μg/m(3)) and three different temperatures (10, 20, and 30 °C) with the aim of evaluating the lichen efficiency for Hg(0) accumulation and their potential use in the estimate of atmospheric concentrations of this metal in the field. The results showed that under our experimental conditions the lichens accumulated Hg according to exposure time and that the metal is not released back to the atmosphere after Hg(0) was removed from the air (clearance). Pseudevernia furfuracea showed the highest Hg accumulation capacity and Evernia prunastri showed the lowest, but in these species the metal uptake kinetics was affected by temperature. Xanthoria parietina showed an intermediate metal accumulation capacity and a Hg accumulation rate independent of temperature (in the range 10-30 °C). The use of first-order kinetics equations for Hg uptake in X. parietina and available field data on Hg bioaccumulation in this species allowed reliable estimates of atmospheric Hg concentrations in the environment.

  15. Identification of Potential Sources of Mercury (Hg in Farmland Soil Using a Decision Tree Method in China

    Directory of Open Access Journals (Sweden)

    Taiyang Zhong

    2016-11-01

    Full Text Available Identification of the sources of soil mercury (Hg on the provincial scale is helpful for enacting effective policies to prevent further contamination and take reclamation measurements. The natural and anthropogenic sources and their contributions of Hg in Chinese farmland soil were identified based on a decision tree method. The results showed that the concentrations of Hg in parent materials were most strongly associated with the general spatial distribution pattern of Hg concentration on a provincial scale. The decision tree analysis gained an 89.70% total accuracy in simulating the influence of human activities on the additions of Hg in farmland soil. Human activities—for example, the production of coke, application of fertilizers, discharge of wastewater, discharge of solid waste, and the production of non-ferrous metals—were the main external sources of a large amount of Hg in the farmland soil.

  16. HgNO3 sensitivity of AlGaN/GaN field effect transistors functionalized with phytochelating peptides

    Science.gov (United States)

    Rohrbaugh, Nathaniel; Hernandez-Balderrama, Luis; Kaess, Felix; Kirste, Ronny; Collazo, Ramon; Ivanisevic, Albena

    2016-06-01

    This study examined the conductance sensitivity of AlGaN/GaN field effect transistors in response to varying Hg/HNO3 solutions. FET surfaces were covalently functionalized with phytochelatin-5 peptides in order to detect Hg in solution. Results showed a resilience of peptide-AlGaN/GaN bonds in the presence of strong HNO3 aliquots, with significant degradation in FET ID signal. However, devices showed strong and varied response to Hg concentrations of 1, 10, 100, and 1000 ppm. The gathered statistically significant results indicate that peptide terminated AlGaN/GaN devices are capable of differentiating between Hg solutions and demonstrate device sensitivity.

  17. Electron Concentration in the Near-Surface Graded-Gap Layer of MBE n-Hg1- x Cd x Te ( x = 0.22-0.40) Determined from the Capacitance Measurements of MIS-Structures

    Science.gov (United States)

    Voitsekhovskii, A. V.; Nesmelov, S. N.; Dzyadukh, S. M.; Grigor'ev, D. V.; Lyapunov, D. V.

    2017-05-01

    Capacitance-voltage (C-V) characteristics of MIS structures based on the graded-gap n-Hg1- x Cd x Te ( x = 0.22-0.40) grown by molecular-beam epitaxy were experimentally studied in the temperature range of 9-77 K. The concentrations of majority charge carriers in the near-surface layer of the semiconductor are determined from the capacitance value at the minimum of the (C-V) characteristic due to the high-frequency behavior of the capacitance characteristics of the structures with graded-gap layers with respect to the recharge time of surface states. The electron concentration in the near-surface layer of the graded-gap n-Hg1- x Cd x Te at x = 0.22-0.23 in the working layer, found from the value of the capacitance at the minimum, considerably exceeds the integral electron concentration determined by the Hall method. With an increase in the composition in the working layer to x = 0.30-0.40, the difference in the values of the electron concentrations decreases substantially for the near-surface layers with close compositions on the surface. The results obtained are explained by the appearance of additional native defects of donor type in the near-surface graded-gap layer, and this effect is most clearly manifested at large composition gradients in the graded-gap layer. The results of processing of experimental C-V characteristics are in qualitative agreement with the results of studying the electron concentration distribution over the film thickness performed by the Hall method.

  18. Trace elements concentrations (Zn, Cu, Pb, Cd, As and Hg in the Mediterranean mussel (Mytilus galloprovincialis and evaluation of mussel quality and possible human health risk from cultivated and wild sites of the southeastern Adriatic Sea, Montenegro

    Directory of Open Access Journals (Sweden)

    Jović Mihajlo

    2011-01-01

    Full Text Available The Mediterranean mussel Mytilus galloprovincialis (L was collected from the fall 2005 to the winter 2009 from the six sites on the Montenegrin coastline. Two wild samples were collected from the open sea coastline, and two cultivated and two wild were from the Boka Kotorska Bay. The mussels soft tissue was analyzed for zinc (Zn, copper (Cu, lead (Pb, cadmium (Cd, arsenic (As and total mercury (Hg. Concentrations of these metals ranged from 135.5-210 for Zn, 6.2-14.5 for Cu, 4.0-11.5 for Pb, 1.7-2.1 for Cd, 5.8-12.4 for As and 0.11-0.51 for Hg, in mg kg-1 dry weight. The metals were found to be present in the samples at different levels, but not in concentrations higher than maximum residual levels prescribed by the European Union (EU and US Food and Drug Administration (USFDA regulations for seafood. This indicates that the consumption of wild or cultivated mussels from the studied area is safe in moderate quantities.

  19. Strong and Nonspecific Synergistic Antibacterial Efficiency of Antibiotics Combined with Silver Nanoparticles at Very Low Concentrations Showing No Cytotoxic Effect.

    Science.gov (United States)

    Panáček, Aleš; Smékalová, Monika; Kilianová, Martina; Prucek, Robert; Bogdanová, Kateřina; Večeřová, Renata; Kolář, Milan; Havrdová, Markéta; Płaza, Grażyna Anna; Chojniak, Joanna; Zbořil, Radek; Kvítek, Libor

    2015-12-28

    The resistance of bacteria towards traditional antibiotics currently constitutes one of the most important health care issues with serious negative impacts in practice. Overcoming this issue can be achieved by using antibacterial agents with multimode antibacterial action. Silver nano-particles (AgNPs) are one of the well-known antibacterial substances showing such multimode antibacterial action. Therefore, AgNPs are suitable candidates for use in combinations with traditional antibiotics in order to improve their antibacterial action. In this work, a systematic study quantifying the synergistic effects of antibiotics with different modes of action and different chemical structures in combination with AgNPs against Escherichia coli, Pseudomonas aeruginosa and Staphylococcus aureus was performed. Employing the microdilution method as more suitable and reliable than the disc diffusion method, strong synergistic effects were shown for all tested antibiotics combined with AgNPs at very low concentrations of both antibiotics and AgNPs. No trends were observed for synergistic effects of antibiotics with different modes of action and different chemical structures in combination with AgNPs, indicating non-specific synergistic effects. Moreover, a very low amount of silver is needed for effective antibacterial action of the antibiotics, which represents an important finding for potential medical applications due to the negligible cytotoxic effect of AgNPs towards human cells at these concentration levels.

  20. Strong and Nonspecific Synergistic Antibacterial Efficiency of Antibiotics Combined with Silver Nanoparticles at Very Low Concentrations Showing No Cytotoxic Effect

    Directory of Open Access Journals (Sweden)

    Aleš Panáček

    2015-12-01

    Full Text Available The resistance of bacteria towards traditional antibiotics currently constitutes one of the most important health care issues with serious negative impacts in practice. Overcoming this issue can be achieved by using antibacterial agents with multimode antibacterial action. Silver nano-particles (AgNPs are one of the well-known antibacterial substances showing such multimode antibacterial action. Therefore, AgNPs are suitable candidates for use in combinations with traditional antibiotics in order to improve their antibacterial action. In this work, a systematic study quantifying the synergistic effects of antibiotics with different modes of action and different chemical structures in combination with AgNPs against Escherichia coli, Pseudomonas aeruginosa and Staphylococcus aureus was performed. Employing the microdilution method as more suitable and reliable than the disc diffusion method, strong synergistic effects were shown for all tested antibiotics combined with AgNPs at very low concentrations of both antibiotics and AgNPs. No trends were observed for synergistic effects of antibiotics with different modes of action and different chemical structures in combination with AgNPs, indicating non-specific synergistic effects. Moreover, a very low amount of silver is needed for effective antibacterial action of the antibiotics, which represents an important finding for potential medical applications due to the negligible cytotoxic effect of AgNPs towards human cells at these concentration levels.

  1. IN VITRO STUDY OF ENTAMOEBA HISTOLYTICA CAUSATIVE AGENT OF AMOEBIASIS WITH LEMON JUICE AT DIFFERENT CONCENTRATION SHOWED ANTIAMOEBIC PROPERTIES

    Directory of Open Access Journals (Sweden)

    Shrivastava Bhanu

    2011-09-01

    Full Text Available A species of parasite protozoa Entamoeba histolytica causing amoebiasis and amoebic dysentery characteristic include a single nucleus containing a small central karyosome and peripheral chromatin that is finely and regularly beaded. This is a single celled parasitic animal, that infects predominantly humans and other primates. Amoebic infection was first described by Fedor Losch in 1875 in St. Petersburg. In 1890, Sir William Osler reported the first North American case of amoebiasis when he observed amoebae in stool in abscess fluid from physician who previously resided in Panama. So we used the Lemon juice (Citrus at different concentration against Entamoeba histolytica to treat the amoebiasis disease. Entamoeba histolytica shows the variety of growth due to the effect of Lemon juice (Citrus. Lemon juice is ingredient and it has antiamoebic properties against Entamoeba histolytica a causative agent of amoebiasis.

  2. Bioaccumulation of As, Cd, Cr, Hg(II), and MeHg in killifish (Fundulus heteroclitus) from amphipod and worm prey.

    Science.gov (United States)

    Dutton, Jessica; Fisher, Nicholas S

    2011-08-15

    Elevated metal levels in fish are a concern for the fish themselves, their predators, and possibly humans who consume contaminated seafood. Metal bioaccumulation models often rely on assimilation efficiencies (AEs) of ingested metals and loss rate constants after dietary exposure (k(ef)s). These models can be used to better understand processes regulating metal accumulation and can be used to make site-specific predictions of metal concentrations in animal tissues. Fish often consume a varied diet, and prey choice can influence these two parameters. We investigated the trophic transfer of As, Cd, Cr, Hg(II), and methylmercury (MeHg) from a benthic amphipod (Leptocheirus plumulosus) and an oligochaete (Lumbriculus variegatus) to killifish (Fundulus heteroclitus) using gamma-emitting radioisotopes. Except for MeHg, AEs varied between prey type. AEs were highest for MeHg (92%) and lowest for Cd (2.9-4.5%) and Cr (0.2-4%). Hg(II) showed the largest AE difference between prey type (14% amphipods, 24% worms). For Cd and Hg(II) k(ef)s were higher after consuming amphipods than consuming worms. Tissue distribution data shows that Cd and Hg(II) were mainly associated with the intestine, whereas As and MeHg were transported throughout the body. Calculated trophic transfer factors (TTFs) suggest that MeHg is likely to biomagnify at this trophic step at all ingestion rates, whereas As, Cd, Cr, and Hg(II) will not. Data collected in this study and others indicate that using one prey item to calculate AE and k(ef) could lead to an over- or underestimation of these parameters.

  3. Chemical thermodynamics of Hg1201 and Hg1223 phases

    Science.gov (United States)

    Tsuchiya, Tetsuo; Fueki, Kazuo; Koyama, Tadashi

    1998-03-01

    The decomposition equilibrium of Hg1201 and Hg1223 was studied using a thermomicrobalance. A thermodynamic diagram representing the stability domains of Hg1201 and Hg1223 was constructed. Using the diagram, it was shown that Hg1201 is metastable at 800°C and that Hg1223 is stable at 660°C due to the formation of an atmosphere of mercury vapor and oxygen formed by the decomposition of excess HgO. Chemical analysis revealed that the valence of Hg is +2 regardless of the oxygen content. The dependence of Tc on the oxygen content was also studied.

  4. Superconducting Hg-Based Mixed Oxides and Oxyfluorides

    Science.gov (United States)

    Antipov, E. V.

    2000-09-01

    Syntheses under high pressure and under controlled mercury and oxygen partial pressures of different members of the HgBa2Can-1CunO2n+2+δ series have been developed. There are two main parameters influencing Tc in this family: width of a perovskite slab (n) and concentration (δ) of the extra oxygen located in the Hg layer. The increase of Tc with n occurs until the third member, while after that it decreases. All the members of the series exhibit similar cupola shaped dependencies of Tc vs. δ. Strongly overdoped high members of the series with n = 3-5 were prepared only using high pressure technique and BaO2 as an internal oxidizer. Neutron powder diffraction experiments were carried out for monophase oxygenated HgBa2CuO4F4+δ and fluorinated HgBa2CuO4Fδ samples with different extra oxygen or fluorine content and Tc values. Fluorinated series also exhibits the cupola -like behavior for the Tc vs. δ dependence. NPD showed twice the amount of extra fluorine in comparison with those for the oxygenated Hg-1201 phases with close Tc's. The exchange of the extra oxygen by double amount of fluorine causes shortening of the apical Cu-O distances, while the in-plane ones, as well as Tc, do not vary. The influence of the external pressure on the structure and Tc of Hg-1201 strongly depends on the doping level. The increase of the extra oxygen content on going from underdoped to overdoped state results in the larger compression of the apical Cu-O and Ba-OHg distances while the HgO2 dumbbell as well as the distance between Ba and O from the (CuO2) layers becomes practically pressure independent. These results together with the data for fluorinated materials allow to elucidate the crucial structural features responsible for the Tc variation under high pressure.

  5. Relationship Between Soil Properties and Different Fractions of Soil Hg

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Correlation and path analysis methods were used to study the relationship between soil properties and the distribution of different soil Hg fractions with nine representative soils from Chongqing, China. Results showed that clay (< 2 m) could increase water-soluble Hg (r = 0.700*). Soil organic matter (OM) could enhance the increase of elemental Hg (r = 0.674*). The higher the base saturation percentage (BSP), the more the residual Hg (r = 0.684*). Organic Hg, the sum of acid-soluble organic Hg. and alkali-soluble Hg, was positively affected by silt (2~20μm) but negatively affected by pH, with the direct path coefficients amounting to 1.0487 and 0.5121, respectively. The positive effect of OM and negative effect of BSP on organic Hg were the most significant, with the direct path coefficients being 0.7614 and -0.8527, respectively. The indirect effect of clay (< 2 μm) via BSP (path coefficient = 0.4186) was the highest, showing that the real influencing factor in the effect of clay (< 2 μm) on acid-soluble organic Hg was BSP. Since the available Hg fraction, water-soluble Hg, was positively affected by soil clay content, and the quite immobile and not bioavailable residual Hg by soil BSP, suitable reduction of clay content and increase of BSP would be of much help to reduce the Hg availability and Hg activity in Hg-contaminated soils.

  6. Kinetics and mechanism of jack bean urease inhibition by Hg2+

    Directory of Open Access Journals (Sweden)

    Du Nana

    2012-12-01

    Full Text Available Abstract Background Jack bean urease (EC 3.5.1.5 is a metalloenzyme, which catalyzes the hydrolysis of urea to produce ammonia and carbon dioxide. The heavy metal ions are common inhibitors to control the rate of the enzymatic urea hydrolysis, which take the Hg2+ as the representative. Hg2+ affects the enzyme activity causing loss of the biological function of the enzyme, which threatens the survival of many microorganism and plants. However, inhibitory kinetics of urease by the low concentration Hg2+ has not been explored fully. In this study, the inhibitory effect of the low concentration Hg2+ on jack bean urease was investigated in order to elucidate the mechanism of Hg2+ inhibition. Results According to the kinetic parameters for the enzyme obtained from Lineweaver–Burk plot, it is shown that the Km is equal to 4.6±0.3 mM and Vm is equal to 29.8±1.7 μmol NH3/min mg. The results show that the inhibition of jack bean urease by Hg2+ at low concentration is a reversible reaction. Equilibrium constants have been determined for Hg2+ binding with the enzyme or the enzyme-substrate complexes (Ki =0.012 μM. The results show that the Hg2+ is a noncompetitive inhibitor. In addition, the kinetics of enzyme inhibition by the low concentration Hg2+ has been studied using the kinetic method of the substrate reaction. The results suggest that the enzyme first reversibly and quickly binds Hg2+ and then undergoes a slow reversible course to inactivation. Furthermore, the rate constant of the forward reactions (k+0 is much larger than the rate constant of the reverse reactions (k-0. By combining with the fact that the enzyme activity is almost completely lost at high concentration, the enzyme is completely inactivated when the Hg2+ concentration is high enough. Conclusions These results suggest that Hg2+ has great impacts on the urease activity and the established inhibition kinetics model is suitable.

  7. In Situ Behavioral Response of Common Loons Associated with Elevated Mercury (Hg Exposure

    Directory of Open Access Journals (Sweden)

    Joseph J. Nocera

    1998-12-01

    Full Text Available Common Loons (Gavia immer in Nova Scotia, Canada have the highest blood mercury (Hg concentrations of any loon population in North America. Previous studies have shown that exposure to varying levels of Hg in prey is associated with changes in pre-nesting adult behavior. We report here the first association of sublethal blood Hg contamination with changes in behavior of Common Loon young. As Hg levels in their blood rise, the amount of time that chicks spend brooding (by back-riding decreases (P = 0.004 and time spent preening increases (P = 0.003. The sum increase in energy expenditure is not being compensated for with expected increases in feeding rates or begging. We suggest that such altered time-activity budgets may disrupt the energetic balance of young. Our results show that variation in time spent back-riding is associated with changes in fledging rates. Adult behavior did not significantly vary with Hg, but results are suggestive that an association may exist. We also show that monitoring the time-activity budgets of very young chicks can serve to indicate the effects Hg concentrations in their blood. We confirm the hypothesis that loons and other upper trophic level predators could be at risk from elevated levels of bioavailable Hg. This may help to explain the chronically low productivity of such contaminated sites as Kejimkujik and allow for more focused management initiatives.

  8. Characterization of Hg-phytochelatins complexes in vines (Vitis vinifera cv Malbec) as defense mechanism against metal stress.

    Science.gov (United States)

    Spisso, Adrian A; Cerutti, Soledad; Silva, Fernanda; Pacheco, Pablo H; Martinez, Luis D

    2014-06-01

    An approach to understand vines (Vitis vinifera) defense mechanism against heavy metal stress by isolation and determination of Hg-phytochelatins (PCs) complexes was performed. PCs are important molecules involved in the control of metal concentration in plants. PCs complex toxic metals through -SH groups and stores them inside cells vacuole avoiding any toxic effect of free metals in the cytosol. The Hg-PCs identification was achieved by determination of Hg and S as hetero-tagged atoms. A method involving two-dimensional chromatographic analysis coupled to atomic spectrometry and confirmation by tandem mass spectrometry is proposed. An approach involving size exclusion chromatography coupled to inductively coupled plasma mass spectrometry on roots, stems, and leaves extracts describing Hg distribution according to molecular weight and sulfur associations is proposed for the first time. Medium-low molecular weight Hg-S associations of 29-100 kDa were found, suggesting PCs presence. A second approach employing reversed-phase chromatography coupled to atomic fluorescence spectrometry analysis allowed the determination of Hg-PCs complexes within the mentioned fractions. Chromatograms showed Hg-PC2, Hg-PC3 and Hg-PC4 presence only in roots. Hg-PCs presence in roots was confirmed by ESI-MS/MS analysis.

  9. Salt-marsh plants as potential sources of Hg0 into the atmosphere

    Science.gov (United States)

    Canário, João; Poissant, Laurier; Pilote, Martin; Caetano, Miguel; Hintelmann, Holger; O'Driscoll, Nelson J.

    2017-03-01

    To assess the role of salt-marsh plants on the vegetation-atmospheric Hg0 fluxes, three salt marsh plant species, Halimione portulacoides, Sarcocornia fruticosa and Spartina maritima were selected from a moderately contaminated site in the Tagus estuary during May 2012. Total mercury in stems and leaves for each plant as well as total gaseous mercury and vegetation-air Hg0 fluxes were measured over two continuous days. Mercury fluxes were estimated with a dynamic flux Tedlar® bag coupled to a high-resolution automated mercury analyzer (Tekran 2537A). Other environmental parameters such as air temperature, relative humidity and net solar radiation were also measured aside. H. portulacoides showed the highest total mercury concentrations in stems and leaves and the highest average vegetation-air Hg0 flux (0.48 ± 0.40 ng Hg m-2 h-1). The continuous measurements converged to a daily pattern for all plants, with enhanced fluxes during daylight and lower flux during the night. It is noteworthy that throughout the measurements a negative flux (air-vegetation) was never observed, suggesting the absence of net Hg0 deposition. Based on the above fluxes and the total area occupied by each species we have estimated the total amount of Hg0 emitted from this salt-marsh plants. A daily emission of 1.19 mg Hg d-1 was predicted for the Alcochete marsh and 175 mg Hg d-1 for the entire salt marsh area of the Tagus estuary.

  10. EDTA and urease effects on Hg accumulation by Lepidium sativum.

    Science.gov (United States)

    Smolińska, Beata; Cedzyńska, Krystyna

    2007-11-01

    The phytoextraction process was conducted under laboratory conditions with the use of garden cress plants (Lepidium sativum). The experiment was carried out in a model soil, which was characterized before conducting the process. Inorganic forms of mercury (HgCl(2), HgSO(4), Hg(NO(3))(2)) were used for contamination of the soil. The phytoextraction process was conducted after EDTA application to the soil and after urease application. Also the influence of simultaneous addition of ethylenediaminetetraacetic acid (EDTA) and urease into the soil on phytoextraction process was measured. In all variants of phytoextraction process the total mercury concentrations in roots, stems and leaves of garden cress were determined. The result showed that garden cress accumulated mercury from soil. The overall maximum concentration of mercury in its compounds was found in roots of the plant. In all cases, before addition of urease and EDTA, the translocation process and distribution of mercury in the plant tissues were limited. The addition of urease caused an increase of enzyme activity in the soil and at the same time caused an increase of mercury concentration in plant tissues. Application of EDTA increased solubility of mercury and caused an increase of metal accumulation by plants. After simultaneous addition of EDTA and urease into the soil garden cress accumulated about 20% of total mercury concentration in the soil. Most of mercury compounds were accumulated in leaves and stems of the plants (46.0-56.9% of total mercury concentration in the plant tissues).

  11. HgO-added YBa2Cu3O7- superconductors

    Indian Academy of Sciences (India)

    Mangalesh Dixit; Shovit Bhattacharya; Rajneesh Mohan; Kiran Singh; P S R Krishna; Vilas Shelke; N K Gaur; R K Singh

    2004-08-01

    The HgO-added YBa2Cu3O7- (YBCO) superconductor has been studied for its structural and superconducting properties. Polycrystalline YBCO samples were synthesized through solid-state reaction method by adding HgO in different concentrations without using oxygen annealing. All the samples showed a sharp superconducting transition temperature around 90 K. The X-ray diffraction patterns of all the samples revealed monophasic Y-123 nature. The structural studies were carried out by neutron scattering and Rietveld analysis. The neutron scattering revealed that Hg is not incorporated in the Y-123 system and has shown optimum oxygen concentration. The significant role played by the HgO is to provide oxygen ambient through its decomposition, thus changing the oxygen balance in favour of high Cu-valence state.

  12. Results Of Hg Speciation Testing On DWPF SMECT-1, SMECT-3, And SMECT-5 Samples

    Energy Technology Data Exchange (ETDEWEB)

    Bannochie, C. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

    2016-01-07

    The Savannah River National Laboratory (SRNL) was tasked with preparing and shipping samples for Hg speciation by Eurofins Frontier Global Sciences, Inc. in Seattle, WA on behalf of the Savannah River Remediation (SRR) Mercury Task Team. The thirteenth shipment of samples was designated to include Defense Waste Processing Facility (DWPF) Slurry Mix Evaporator Condensate Tank (SMECT) from Sludge Receipt and Adjustment Tank (SRAT) Batch 736 and 738 samples. Triplicate samples of each material were prepared for this shipment. Each replicate was analyzed for seven Hg species: total Hg, total soluble (dissolved) Hg, elemental Hg [Hg(0)], ionic (inorganic) Hg [Hg(I) and Hg(II)], methyl Hg [CH3Hg-X, where X is a counter anion], ethyl Hg [CH3CH2-Hg-X, where X is a counter anion], and dimethyl Hg [(CH3)2Hg]. The difference between the total Hg and total soluble Hg measurements gives the particulate Hg concentration, i.e. Hg adsorbed to the surface of particulate matter in the sample but without resolution of the specific adsorbed species. The average concentrations of Hg species in the aqueous samples derived from Eurofins reported data corrected for dilutions performed by SRNL are tabulated.

  13. The longitudinal translocation characters and the influencing factors of Hg, Cd in the soil

    Directory of Open Access Journals (Sweden)

    Zhang Yujuan

    2006-11-01

    Full Text Available Combining the methods of simulation test and field survey, the longitudinal distribution and the influencing factors of Hg and Cd in the profile in the typical sewage irrigation area were studied in this paper and the result shows: (1 the content distribution of Hg, Cd in the superficial soil profile was higher than that in the bottom and the content decreased with the increase of the depth, the translocation ability of the Hg, Cd in the garden mould and cinnamon soil were lower than that in the paddy soil and fluve-aquic soil, the longitudinal translocation ability of the Cd in the soil profile was stronger than that of Hg; (2 Hg was accumulated in the different soil and has the highest accumulation rate in the paddy soil and the lowest in the cinnamon soil; the translocation order of the Cd in the different was: garden mould > paddy soil > cinnamon soil > fluve-aquic soil; (3 the concentration of Hg, Cd in the soil leacheate increased with the concentration increase of Hg, Cd in the sewage, the migration rate increased with the roughness of the soil quality and decreased with the increase of pH and soil organic matter.

  14. Local probing of Hg neighboorhood in HgBa$_{2}$CuO$_{4+\\delta}$

    CERN Document Server

    Correia, J G; Loureiro, S M; Toulemonde, P; Le Floc'h, S; Bordet, P; Capponi, J J; Gatt, R; Tröger, W; Ctortecka, B; Butz, T; Haas, H; Marques, J G; Soares, J C

    2000-01-01

    Electric field gradients (EFG) on mercury sites of the Hg1201 high-TC superconductors were measured with the perturbed angular correlation (PAC) technique. In Hg1201 samples where PAC detects higher oxygen content the EFGs have decreased to lower values indicating an elongation of the Hg-apical oxygen dumb-bell. On the same samples the asymmetry parameter of the EFG becomes non-zero below 100 K, showing that the charge distribution near the Hg-apical oxygen chain becomes non-axially symmetric at low temperature.

  15. Complexation of Hg with phytochelatins is important for plant Hg tolerance.

    Science.gov (United States)

    Carrasco-Gil, Sandra; Alvarez-Fernández, Ana; Sobrino-Plata, Juan; Millán, Rocío; Carpena-Ruiz, Ramón O; Leduc, Danika L; Andrews, Joy C; Abadía, Javier; Hernández, Luís E

    2011-05-01

    Three-week-old alfalfa (Medicago sativa), barley (Hordeum vulgare) and maize (Zea mays) were exposed for 7 d to 30 µm of mercury (HgCl(2) ) to characterize the Hg speciation in root, with no symptoms of being poisoned. The largest pool (99%) was associated with the particulate fraction, whereas the soluble fraction (SF) accounted for a minor proportion (phytochelatins (PCs) in root SF, which was particularly varied in alfalfa (eight ligands and five stoichiometries), a species that also accumulated homophytochelatins. Spatial localization of Hg in alfalfa roots by microprobe synchrotron X-ray fluorescence spectroscopy showed that most of the Hg co-localized with sulphur in the vascular cylinder. Extended X-ray Absorption Fine Structure (EXAFS) fingerprint fitting revealed that Hg was bound in vivo to organic-S compounds, i.e. biomolecules containing cysteine. Albeit a minor proportion of total Hg, Hg-PCs complexes in the SF might be important for tolerance to Hg, as was found with Arabidopsis thaliana mutants cad2-1 (with low glutathione content) and cad1-3 (unable to synthesize PCs) in comparison with wild type plants. Interestingly, high-performance liquid chromatography-electrospray ionization-time of flight analysis showed that none of these mutants accumulated Hg-biothiol complexes.

  16. A millennial-scale record of Pb and Hg contamination in peatlands of the Sacramento-San Joaquin Delta of California, USA

    Science.gov (United States)

    Drexler, Judith; Alpers, Charles N.; Neymark, Leonid; Paces, James B.; Taylor, Howard E.; Fuller, Christopher C.

    2016-01-01

    In this paper, we provide the first record of millennial patterns of Pb and Hg concentrations on the west coast of the United States. Peat cores were collected from two micro-tidal marshes in the Sacramento-San Joaquin Delta of California. Core samples were analyzed for Pb, Hg, and Ti concentrations and dated using radiocarbon, 210Pb, and 137Cs. Pre-anthropogenic concentrations of Pb and Hg in peat ranged from 0.60 to 13.0 µg g-1and from 6.9 to 71 ng g-1, respectively. For much of the past 6000+ years, the Delta was free from anthropogenic pollution, however, beginning in ~1425 CE, Hg and Pb concentrations, Pb/Ti ratios, Pb enrichment factors (EFs), and HgEFs all increased. Pb isotope compositions of the peat suggest that this uptick was likely caused by smelting activities originating in Asia. The next increases in Pb and Hg contamination occurred during the California Gold Rush (beginning ~1850 CE), when concentrations reached their highest levels (74 µg g-1 Pb, 990 ng g-1 Hg; PbEF = 12 and HgEF = 28). Lead concentrations increased again beginning in the ~1920s with the incorporation of Pb additives in gasoline. The phase-out of lead additives in the late 1980s was reflected in Pb isotope ratios and reductions in Pb concentrations in the surface layers of the peat. The rise and fall of Hg contamination was also tracked by the peat archive, with the highest Hg concentrations occurring just before 1963 CE and then decreasing during the post-1963 period. Overall, the results show that the Delta was a pristine region for most of its ~6700-year existence; however, since ~1425 CE, it has received Pb and Hg contamination from both global and regional sources.

  17. A millennial-scale record of Pb and Hg contamination in peatlands of the Sacramento-San Joaquin Delta of California, USA.

    Science.gov (United States)

    Drexler, Judith Z; Alpers, Charles N; Neymark, Leonid A; Paces, James B; Taylor, Howard E; Fuller, Christopher C

    2016-05-01

    In this paper, we provide the first record of millennial patterns of Pb and Hg concentrations on the west coast of the United States. Peat cores were collected from two micro-tidal marshes in the Sacramento-San Joaquin Delta of California. Core samples were analyzed for Pb, Hg, and Ti concentrations and dated using radiocarbon and (210)Pb. Pre-anthropogenic concentrations of Pb and Hg in peat ranged from 0.60 to 13.0μgg(-1)and from 6.9 to 71ngg(-1), respectively. For much of the past 6000+ years, the Delta was free from anthropogenic pollution, however, beginning in ~1425CE, Hg and Pb concentrations, Pb/Ti ratios, Pb enrichment factors (EFs), and HgEFs all increased. Pb isotope compositions of the peat suggest that this uptick was likely caused by smelting activities originating in Asia. The next increases in Pb and Hg contamination occurred during the California Gold Rush (beginning ~1850CE), when concentrations reached their highest levels (74μgg(-1) Pb, 990ngg(-1) Hg; PbEF=12 and HgEF=28). Lead concentrations increased again beginning in the ~1920s with the incorporation of Pb additives in gasoline. The phase-out of lead additives in the late 1980s was reflected in changes in Pb isotope ratios and reductions in Pb concentrations in the surface layers of the peat. The rise and subsequent fall of Hg contamination was also tracked by the peat archive, with the highest Hg concentrations occurring just before 1963CE and then decreasing during the post-1963 period. Overall, the results show that the Delta was a pristine region for most of its ~6700-year existence; however, since ~1425CE, it has received Pb and Hg contamination from both global and regional sources.

  18. Responses of membrane protection enzyme system of tobacco leaves on Hg, Cd and Pb stresses in soil.

    Science.gov (United States)

    Yan, Chong Ling; Lin, Peng; Wang, Xiao Rong

    2002-09-01

    Pot experiment was used to study the responses of membrane protection enzyme system of tobacco leaves on Hg, Cd and Pb stresses in soil. The results showed that POD activity gradually increased with increasing concetrations of Hg, Cd and Pb. CAT and SOD activity gradually decreased under three heavy metals common existing and SOD variation curve showed unimodal curve under single or two elements existing with increase of concentration of Hg, Cd and Pb. The effects of Hg, Cd and Pb in soil: three elemets together > two elements together > single element only. The effects resulted in an imbalance--activated oxygen produce and scavenge and physiological biochemical process disorder. There was a synergistic action for the effect of Hg, Cd and Pb in soil on membrane protection enzyme system in tobacco leaves.

  19. Organ-specific accumulation, transportation, and elimination of methylmercury and inorganic mercury in a low Hg accumulating fish.

    Science.gov (United States)

    Peng, Xiaoyan; Liu, Fengjie; Wang, Wen-Xiong

    2016-08-01

    Low mercury (Hg) concentrations down to several nanograms Hg per gram of wet tissue are documented in certain fish species such as herbivorous fish, and the underlying mechanisms remain speculative. In the present study, bioaccumulation and depuration patterns of inorganic Hg(II) and methylmercury (MeHg) in a herbivorous rabbitfish Siganus canaliculatus were investigated at organ and subcellular levels following waterborne or dietary exposures. The results showed that the efflux rate constants of Hg(II) and MeHg were 0.104 d(-1) and 0.024 d(-1) , respectively, and are probably the highest rate constants recorded in fish thus far. The dietary MeHg assimilation efficiency (68%) was much lower than those in other fish species (∼90%). The predominant distribution of MeHg in fish muscle was attributable to negligible elimination of MeHg from muscle (rabbitfish was partly explained by its unique biokinetics. Environ Toxicol Chem 2016;35:2074-2083. © 2016 SETAC.

  20. Removal and recovery of Hg(II) from aqueous solution using chitosan-coated cotton fibers.

    Science.gov (United States)

    Qu, Rongjun; Sun, Changmei; Ma, Fang; Zhang, Ying; Ji, Chunnuan; Xu, Qiang; Wang, Chunhua; Chen, Hou

    2009-08-15

    Two types of chitosan-coated cotton fibers (SCCH and RCCH) were applied to remove and recover Hg(II) ions in aqueous solution. The adsorption kinetics and isotherms of the two fibers for Hg(II) were investigated at different temperatures. The results revealed that the adsorption kinetic processes of SCCH and RCCH fibers for Hg(II) followed the pseudo second-order model at lower temperatures and the pseudo first-order model at higher temperatures. Both the Langmuir and Freundlich models well described the adsorption isotherms of SCCH and RCCH fibers for Hg(II) in the temperature range studied. SCCH and RCCH fibers selectively adsorbed Hg(II) from binary ion systems in the presence of Pb(II), Cu(II), Ni(II), Cd(II), Zn(II), Co(II), Mn(II) and Ag(I). Increased temperature was beneficial to adsorption. The recovery of Hg(II) from aqueous solutions was also studied as a function of sample flow rate and volume, concentration and volume of eluent, elution rate, quantity of adsorbents added and concomitant ions. The results showed that the two fibers efficiently enriched and recovered Hg(II) in the presence of alkali and alkaline earth metals and some heavy metals under optimum conditions. The RCCH fiber exhibited better stability than the SCCH fiber following repeated use.

  1. Determination of As,Hg,Cd,Pb and Bi in gold concentrates by AFS%原子荧光光谱法测定金精矿中的砷汞镉铅铋

    Institute of Scientific and Technical Information of China (English)

    王菊; 陈永红; 苏广东; 孟宪伟; 王立臣

    2015-01-01

    研究建立了采用原子荧光光谱仪测定金精矿中砷、汞、镉、铅、铋的方法。通过对比实验选择了水浴溶样法作为砷、汞、铋的预处理方法,选择了盐酸、硝酸、高氯酸和氢氟酸混酸溶样法作为砷、铋、镉、铅的预处理方法。经过条件实验分别确定了两种预处理方法的最小称样量、试剂用量、水浴溶样法溶样时间、混酸溶样法定容介质酸度等最佳实验条件。该方法加入标准物质回收率为92.54%~125.10%,精密度(RSD,n=11)均小于10%,准确度小于8%。%The paper established a determination method of As,Hg,Cd,Pb and Bi in gold concentrates by AFS. Contrast test chose water bath dissolution as the pretreatment method of As,Hg and Bi,and the mixed acids dissolution with hydrochloric acid,nitric acid,perchloric acid and hydrofluoric acid for the pretreatment of As,Cd,Pb and Bi. Conditional experiments settled such optimal conditions as the minimum test portion weight,agent dosage,time for wa-ter bath dissolution and constant volume medium acidity respectively for the two pretreatment methods.The recovery rate with addition of standard substance is 92.54 % to 125.10 %,the precision rate(RSD,n=11) is less than 10%,and accuracy is less than 8 %.

  2. Uptake of HgCl{sub 2} and MeHgCl in an insect cell line (Aedes albopictus C6/36)

    Energy Technology Data Exchange (ETDEWEB)

    Braeckman, B.; Cornelis, R.; Rzeznik, U.; Raes, H. [Univ. of Ghent (Belgium)

    1998-10-01

    The authors studied the uptake mechanism of mercuric chloride (Hg) and methylmercuric chloride (MeHg) in Aedes albopictus C6/36 cells. The uptake kinetics, together with the effect of temperature and a metabolic inhibitor (2,4-dinitrophenol) on the mercury accumulation, were examined. Both amounts of internalized Hg and MeHg increased linearly with the extracellular concentration. Initially, the influx rate was high for both metal species but MeHg was found to accumulate seven times faster than Hg. At longer exposure times it leveled off for Hg, while for MeHg, the intracellular concentration decreased. Hg toxicity was not significantly influenced by elevated temperatures; in contrast there was a marked decrease of the LC{sub 50/24 h} value for MeHg. On the other hand, Hg accumulation was temperature dependent but MeHg was not. The different toxicity and uptake rate of both mercury compounds can be explained in terms of membrane permeability and target site. For Hg the main target seems to be the plasma membrane, while MeHg readily crosses this barrier and reacts with intracellular targets. 2,4-Dinitrophenol had no effect on the accumulation of Hg but that of MeHg was doubled.

  3. Persistent Hg contamination and occurrence of Hg-methylating transcript (hgcA) downstream of a chlor-alkali plant in the Olt River (Romania).

    Science.gov (United States)

    Bravo, Andrea G; Loizeau, Jean-Luc; Dranguet, Perrine; Makri, Stamatina; Björn, Erik; Ungureanu, Viorel Gh; Slaveykova, Vera I; Cosio, Claudia

    2016-06-01

    Chlor-alkali plants using mercury (Hg) cell technology are acute point sources of Hg pollution in the aquatic environment. While there have been recent efforts to reduce the use of Hg cells, some of the emitted Hg can be transformed to neurotoxic methylmercury (MeHg). Here, we aimed (i) to study the dispersion of Hg in four reservoirs located downstream of a chlor-alkali plant along the Olt River (Romania) and (ii) to track the activity of bacterial functional genes involved in Hg methylation. Total Hg (THg) concentrations in water and sediments decreased successively from the initial reservoir to downstream reservoirs. Suspended fine size particles and seston appeared to be responsible for the transport of THg into downstream reservoirs, while macrophytes reflected the local bioavailability of Hg. The concentration and proportion of MeHg were correlated with THg, but were not correlated with bacterial activity in sediments, while the abundance of hgcA transcript correlated with organic matter and Cl(-) concentration, indicating the importance of Hg bioavailability in sediments for Hg methylation. Our data clearly highlights the importance of considering Hg contamination as a legacy pollutant since there is a high risk of continued Hg accumulation in food webs long after Hg-cell phase out.

  4. HgZnTe-based detectors for LWIR NASA applications

    Science.gov (United States)

    Patten, Elizabeth A.; Kalisher, Murray H.

    1990-01-01

    The initial goal was to grow and characterize HgZnTe and determine if it indeed had the advantageous properties that were predicted. Researchers grew both bulk and liquid phase epitaxial HgZnTe. It was determined that HgZnTe had the following properties: (1) microhardness at least 50 percent greater than HgCdTe of equivalent bandgap; (2) Hg annealing rates of at least 2 to 4 times longer than HgCdTe; and (3) higher Hg vacancy formation energies. This early work did not focus on one specific composition (x-value) of HgZnTe since NASA was interested in HgZnTe's potential for a variety of applications. Since the beginning of 1989, researchers have been concentrating, however, on the liquid phase growth of very long wavelength infrared (VLWIR) HgZnTe (cutoff approx. equals 17 microns at 65K) to address the requirements of the Earth Observing System (EOS). Since there are no device models to predict the advantages in reliability one can gain with increased microhardness, surface stability, etc., one must fabricate HgZnTe detectors and assess their relative bake stability (accelerated life test behavior) compared with HgCdTe devices fabricated in the same manner. Researchers chose to fabricate HIT detectors as a development vehicle for this program because high performance in the VLWIR has been demonstrated with HgCdTe HIT detectors and the HgCdTe HIT process should be applicable to HgZnTe. HIT detectors have a significant advantage for satellite applications since these devices dissipate much less power than conventional photoconductors to achieve the same responsivity.

  5. Seasonal variations in metallic mercury (Hg0) vapor exchange over biannual wheat-corn rotation cropland in the North China Plain

    Science.gov (United States)

    Sommar, Jonas; Zhu, Wei; Shang, Lihai; Lin, Che-Jen; Feng, Xinbin

    2016-04-01

    Air-surface gas exchange of Hg0 was measured in five approximately bi-weekly campaigns (in total 87 days) over a wheat-corn rotation cropland located on the North China Plain (NCP) using the relaxed eddy accumulation (REA) technique. The campaigns were separated over the duration of a full-year period (2012-2013) aiming to capture the flux pattern over essential growing stages of the planting system with a low homogeneous topsoil Hg content ( ˜ 45 ng g-1). Contrasting pollution regimes influenced air masses at the site and corresponding Hg0 concentration means (3.3 in late summer to 6.2 ng m-3 in winter) were unanimously above the typical hemispheric background of 1.5-1.7 ng m-3 during the campaigns. Extreme values in bi-directional net Hg0 exchange were primarily observed during episodes of peaking Hg0 concentrations. In tandem with under-canopy chamber measurements, the above-canopy REA measurements provided evidence for a balance between Hg0 ground emissions and uptake of Hg0 by the developed canopies. During the wheat growing season covering ˜ 2 / 3 of the year at the site, net field-scale Hg0 emission prevailed for periods of active plant growth until canopy senescence (mean flux: 20.0 ng m-3), showing the dominance of Hg0 soil efflux during warmer seasons. In the final vegetative stage of corn and wheat, ground and above-canopy Hg0 flux displayed inversed daytime courses with a near mid-day maximum (emission) and minimum (deposition), respectively. In contrast to wheat, Hg0 uptake of the corn canopy at this stage offset ground Hg0 emissions with additional removal of Hg0 from the atmosphere. Differential uptake of Hg0 between wheat (C3 species) and corn (C4 species) foliage is discernible from estimated Hg0 flux (per leaf area) and Hg content in mature cereal leaves, being a factor of > 3 higher for wheat (at ˜ 120 ng g-1 dry weight). Furthermore, this study shows that intermittent flood irrigation of the air-dry field induced a short pulse of Hg0 emission

  6. Hg-Mask Coronagraph

    Science.gov (United States)

    Bourget, P.; Veiga, C. H.; Vieira Martins, R.; Assus, P.; Colas, F.

    In order to optimize the occulting process of a Lyot coronagraph and to provide a high dynamic range imaging, a new kind of occulting disk has been developed at the National Observatory of Rio de Janeiro. A mercury (Hg) drop glued onto an optical window by molecular cohesion and compressed by a pellicle film is used as the occulting disk. The minimum of the superficial tension potential function provides an optical precision (lambda/100) of the toric free surface of the mercury. This process provides a size control for the adaptation to the seeing conditions and to the apparent diameter of a resolved object, and in the case of adaptive optics, to the Airy diameter fraction needed. The occultation is a three dimensional process near the focal plane on the toric free surface that provides an apodization of the occultation. The Hg-Mask coronagraph has been projected for astrometric observations of faint satellites near to Jovian planets and works since 2000 at the 1.6 m telescope of the Pico dos Dias Observatory (OPD - Brazil).

  7. Bioindication of volcanic mercury (Hg) deposition around Mt Etna (Sicily)

    Science.gov (United States)

    Martin, R.; Witt, M. L.; Sawyer, G. M.; Watt, S.; Bagnato, E.; Calabrese, S.; Aiuppa, A.; Delmelle, P.; Pyle, D. M.; Mather, T. A.

    2012-12-01

    Mt. Etna is a major natural source of Hg to the Mediterranean region. Total mercury concentrations, [Hg]tot, in Castanea sativa (sweet chestnut) leaves sampled 7-13 km from Etna's vents (during six campaigns in 2005-2011) were determined using atomic absorption spectroscopy. [Hg]tot in C. sativa was greatest on Etna's SE flank reflecting Hg deposition from the typically overhead volcanic plume. When adjusted for leaf age, [Hg]tot in C. sativa also increased with recent eruptive activity. [Hg]tot in C. sativa was not controlled by [Hg]tot in soils, which instead was greatest on the (upwind) NW flank and correlated strongly with soil organic matter (% Org). Our results suggest that at least ~1% of Hg emitted from Etna is deposited proximally, supporting recent measurement and model results which indicate that GEM (Hg0; the dominant form of Hg in high temperature magmatic gases) is oxidised rapidly to RGM and Hgp in ambient temperature volcanic plumes. Samples of C. sativa and soils were also collected in July and September 2012 alongside SO2 and acid gas diffusion tube samples. These new samples will enable us to investigate Hg accumulation over a single growth season with reference to the exposure of vegetation to volcanic gases and particles.

  8. Factors affecting Hg (II adsorption in soils from the Rio Negro basin (Amazon

    Directory of Open Access Journals (Sweden)

    Patricia Miretzky

    2005-06-01

    Full Text Available Mercury (II adsorption studies in top soils (top 10 cm from the Rio Negro basin show this process depends strongly on some selected parameters of the aqueous phase in contact with the soils. Maximum adsorption occurred in the pH range 3.0-5.0 (>90%. Dissolved organic matter shows an inhibitory effect on the availability of Hg (II to be adsorbed by the soils, whereas a higher chloride content of the solution resulted in a lower adsorption of Hg (II at pH 5.0. Soils with higher organic matter content were less affected by changes in the salinity. An increase in the initial Hg (II concentration increased the amount of Hg (II adsorbed by the soil and decreased the time needed to reach equilibrium. A Freundlich isotherm provided a good model for Hg (II adsorption in the two types of soil studied. The kinetics of Hg (II adsorption on Amazonian soils showed to be very fast and followed pseudo-second order kinetics. An environmental implication of these results is discussed under the real scenario present in the Negro River basin, where acidic waters are in contact with a soil naturally rich in mercury.

  9. Screening of native plant species for phytoremediation potential at a Hg-contaminated mining site.

    Science.gov (United States)

    Marrugo-Negrete, José; Marrugo-Madrid, Siday; Pinedo-Hernández, José; Durango-Hernández, José; Díez, Sergi

    2016-01-15

    Artisanal and small-scale gold mining (ASGM) is the largest sector of demand for mercury (Hg), and therefore, one of the major sources of Hg pollution in the environment. This study was conducted in the Alacrán gold-mining site, one of the most important ASGM sites in Colombia, to identify native plant species growing in Hg-contaminated soils used for agricultural purposes, and to assess their potential as phytoremediation systems. Twenty-four native plant species were identified and analysed for total Hg (THg) in different tissues (roots, stems, and leaves) and in underlying soils. Accumulation factors (AF) in the shoots, translocation (TF) from roots to shoots, and bioconcentration (BCF) from soil-to-roots were determined. Different tissues from all plant species were classified in the order of decreasing accumulation of Hg as follows: roots > leaves > stems. THg concentrations in soil ranged from 230 to 6320 ng g(-1). TF values varied from 0.33 to 1.73, with high values in the lower Hg-contaminated soils. No correlation was found between soils with low concentrations of Hg and plant leaves, indicating that TF is not a very accurate indicator, since most of the Hg input to leaves at ASGM sites comes from the atmosphere. On the other hand, the BCF ranged from 0.28 to 0.99, with Jatropha curcas showing the highest value. Despite their low biomass production, several herbs and sub-shrubs are suitable for phytoremediation application in the field, due to their fast growth and high AF values in large and easily harvestable plant parts. Among these species, herbs such as Piper marginathum and Stecherus bifidus, and the sub-shrubs J. curcas and Capsicum annuum are promising native plants with the potential to be used in the phytoremediation of soils in tropical areas that are impacted by mining.

  10. Perturbed angular correlations studies in the HgBa$_2$CaCu$_2$O$_{6+\\delta}$ high-T$_c$ superconductor

    CERN Document Server

    Mendonca, Tania Melo; Haas, Heinz; Odier, Philippe; Tavares, Pedro; SIlva, Manuel Ribeiro; Lopes, Armandina; Darie, Celine; Araujo, Joao Pedro

    2011-01-01

    The electric field gradients at $^{199m}$Hg nuclei have been measured via the perturbed angular correlation (PAC) technique, allowing a full characterization of the Hg neighborhood charge distribution at high oxygen doping on the Hg planes. The PAC technique has been applied to investigate the effect of high oxygen pressure during the measurement. Polycrystalline HgBa$_2$CaCu$_2$O$_{6+\\delta}$ (Hg-1212) samples have been annealed at 152 bar pressurized oxygen. The influence of oxygen pressure during the experiment was then investigated by measuring the samples at atmospheric pressure and under 152 bar oxygen pressure. The present set of PAC experiments shows that at high oxygen concentrations there is a non-uniform oxygen distribution. Moreover, the Hg environment is not free from oxygen and the results hint to a new type of ordering.

  11. Hg/HgO electrode and hydrogen evolution potentials in aqueous sodium hydroxide

    Energy Technology Data Exchange (ETDEWEB)

    Nickell, Ryan A.; Zhu, Wenhua H.; Payne, Robert U.; Cahela, Donald R.; Tatarchuk, Bruce J. [Center for Microfibrous Materials Manufacturing, Department of Chemical Engineering, 230 Ross Hall, Auburn University, Auburn, AL 36849 (United States)

    2006-10-27

    The Hg/HgO electrode is usually utilized as a reference electrode in alkaline solution such as for development of an alkaline hydrogen electrode. The reference electrode provides a suitable reference point but is available from few commercial vendors and suffers from inadequate documentation on potential in varying electrolytes. A new numerical method uses activity, activity coefficients, and a few correlated empirical equations to determine the potential values in both dilute and concentrated sodium hydroxide solutions at temperatures of 0-90{sup o}C and at concentrations of 0.100-12.8mol kg{sub H{sub 2}O}{sup -1}. The computed potentials of the Hg/HgO electrodes versus a normal hydrogen electrode (NHE) at 25{sup o}C and 1atm are 0.1634V for 0.100m, 0.1077V for 1.00m, and 0.0976V for 1.45m NaOH solutions. The Hg/HgO reduction potential further changes to -0.0751V versus NHE and hydrogen evolution potential changes to -0.9916V versus NHE in a solution of 30.0wt.% NaOH at 80{sup o}C. The calculated values are compared with the measured data at 25 and 75{sup o}C. The experimental data agree well with the numerical values computed from the theoretical and empirical equations. (author)

  12. Hg/HgO electrode and hydrogen evolution potentials in aqueous sodium hydroxide

    Science.gov (United States)

    Nickell, Ryan A.; Zhu, Wenhua H.; Payne, Robert U.; Cahela, Donald R.; Tatarchuk, Bruce J.

    The Hg/HgO electrode is usually utilized as a reference electrode in alkaline solution such as for development of an alkaline hydrogen electrode. The reference electrode provides a suitable reference point but is available from few commercial vendors and suffers from inadequate documentation on potential in varying electrolytes. A new numerical method uses activity, activity coefficients, and a few correlated empirical equations to determine the potential values in both dilute and concentrated sodium hydroxide solutions at temperatures of 0-90 °C and at concentrations of 0.100-12.8 mol k gH2O-1 . The computed potentials of the Hg/HgO electrodes versus a normal hydrogen electrode (NHE) at 25 °C and 1 atm are 0.1634 V for 0.100m, 0.1077 V for 1.00m, and 0.0976 V for 1.45m NaOH solutions. The Hg/HgO reduction potential further changes to -0.0751 V versus NHE and hydrogen evolution potential changes to -0.9916 V versus NHE in a solution of 30.0 wt.% NaOH at 80 °C. The calculated values are compared with the measured data at 25 and 75 °C. The experimental data agree well with the numerical values computed from the theoretical and empirical equations.

  13. Changes in Sport Fish Mercury Concentrations from Food Web Shifts Suggest Partial Decoupling from Atmospheric Deposition in Two Colorado Reservoirs.

    Science.gov (United States)

    Wolff, Brian A; Johnson, Brett M; Lepak, Jesse M

    2017-02-01

    Partial decoupling of mercury (Hg) loading and observed Hg concentrations ([Hg]) in biotic and abiotic samples has been documented in aquatic systems. We studied two Colorado reservoirs to test whether shifts in prey for sport fish would lead to changes in [Hg] independent of external atmospheric Hg deposition. We compared sport fish total mercury concentrations ([T-Hg]) and macroinvertebrate (chironomids and crayfish) methylmercury concentrations ([MeHg]) before and after food web shifts occurred in both reservoirs. We also monitored wet atmospheric Hg deposition and sediment [T-Hg] and [MeHg] at each reservoir. We found rapid shifts in Hg bioaccumulation in each reservoir's sport fish, and these changes could not be attributed to atmospheric Hg deposition. Our study shows that trends in atmospheric deposition, environmental samples (e.g., sediments), and samples of species at the low trophic levels (e.g., chironomids and crayfish) may not accurately reflect conditions that result in fish consumption advisories for high trophic level sport fish. We suggest that in the short-term, monitoring fish [Hg] is necessary to adequately protect human health because natural and anthropogenic perturbations to aquatic food-webs that affect [Hg] in sport fish will continue regardless of trends in atmospheric deposition.

  14. A millennial-scale record of Pb and Hg contamination in peatlands of the Sacramento–San Joaquin Delta of California, USA

    Energy Technology Data Exchange (ETDEWEB)

    Drexler, Judith Z., E-mail: jdrexler@usgs.gov [U.S. Geological Survey, California Water Science Center, 6000 J Street, Placer Hall, Sacramento, CA 95819-6129 (United States); Alpers, Charles N., E-mail: cnalpers@usgs.gov [U.S. Geological Survey, California Water Science Center, 6000 J Street, Placer Hall, Sacramento, CA 95819-6129 (United States); Neymark, Leonid A., E-mail: lneymark@usgs.gov [U.S. Geological Survey, Box 25046, MS963, Denver Federal Center, Denver, CO 80225 (United States); Paces, James B., E-mail: jbpaces@usgs.gov [U.S. Geological Survey, Box 25046, MS963, Denver Federal Center, Denver, CO 80225 (United States); Taylor, Howard E., E-mail: hetaylor@usgs.gov [U.S. Geological Survey, 3215 Marine Street, Suite E-127, Boulder, CO 80303 (United States); Fuller, Christopher C., E-mail: ccfuller@usgs.gov [U.S. Geological Survey, 345 Middlefield Road, MS465, Menlo Park, CA 94025 (United States)

    2016-05-01

    In this paper, we provide the first record of millennial patterns of Pb and Hg concentrations on the west coast of the United States. Peat cores were collected from two micro-tidal marshes in the Sacramento–San Joaquin Delta of California. Core samples were analyzed for Pb, Hg, and Ti concentrations and dated using radiocarbon and {sup 210}Pb. Pre-anthropogenic concentrations of Pb and Hg in peat ranged from 0.60 to 13.0 μg g{sup −1}and from 6.9 to 71 ng g{sup −1}, respectively. For much of the past 6000 + years, the Delta was free from anthropogenic pollution, however, beginning in ~ 1425 CE, Hg and Pb concentrations, Pb/Ti ratios, Pb enrichment factors (EFs), and HgEFs all increased. Pb isotope compositions of the peat suggest that this uptick was likely caused by smelting activities originating in Asia. The next increases in Pb and Hg contamination occurred during the California Gold Rush (beginning ~ 1850 CE), when concentrations reached their highest levels (74 μg g{sup −1} Pb, 990 ng g{sup −1} Hg; PbEF = 12 and HgEF = 28). Lead concentrations increased again beginning in the ~ 1920s with the incorporation of Pb additives in gasoline. The phase-out of lead additives in the late 1980s was reflected in changes in Pb isotope ratios and reductions in Pb concentrations in the surface layers of the peat. The rise and subsequent fall of Hg contamination was also tracked by the peat archive, with the highest Hg concentrations occurring just before 1963 CE and then decreasing during the post-1963 period. Overall, the results show that the Delta was a pristine region for most of its ~ 6700-year existence; however, since ~ 1425 CE, it has received Pb and Hg contamination from both global and regional sources. - Highlights: • Micro-tidal peats were used to trace Pb and Hg contamination through the millennia. • Anthropogenic Pb and Hg were first evident in California in ~ 1425 CE. • Pb isotopes suggest early contamination may be from ore smelting in China

  15. Tracing anthropogenic Hg and Pb input using stable Hg and Pb isotope ratios in sediments of the central Portuguese Margin

    NARCIS (Netherlands)

    Mil-Holmens, M.; Blum, J.; Canário, J.; Caetano, M.; Costa, A.M.; Lebreiro, S.M.; Trancoso, M.; Richter, T.O.; de Stigter, H.; Johnson, M.; Branco, V.; Cesário, R.; Mouro, F.; Mateus, M.; Boer, W.; Melo, Z.

    2013-01-01

    Three short marine sediment cores from the Cascais Submarine Canyon (CSC; cores 252-32 and 252-35) and the Estremadura Spur (core 252-16) on the central Portuguese Margin were analysed for Hg, Pb, Al, and Mn concentrations, and both Pb and Hg stable isotope compositions, in order to reconstruct tren

  16. iUTAH Summer Research: Analyzing diel variations of MeHg in the Provo River, Utah

    Science.gov (United States)

    Hamilton, G. L.; Packer, B. N.; Carling, G. T.; Checketts, H. N.; Shepherd Barkdull, N.

    2016-12-01

    iUTAH is an interdisciplinary research program aimed at strengthening science for Utah's water future and funded by the National Science Foundation. iUTAH is comprised of three research areas with an overarching goal of understanding how Utah's water system operates as an integrated physical, chemical, biological, and social system. During the Summer of 2016, I participated in the iUTAH (Innovative Urban Transitions and Aridregion Hydro-sustainability) iFellows undergraduate research program. iUTAH provided the opportunity to conduct research at Brigham Young University with graduate students studying trace metal dynamics in the Provo River, Utah, USA. This report presents the chemical system evaluation of methylmercury (MeHg) during diurnal variations from snowmelt runoff. Water samples were collected during peak discharge from Soapstone Basin, a site along the Upper Provo River watershed, every hour over a 24-hour (diel) period. Sampling began at 1200 hours on June 1 and ended at 1100 hours on June 2, 2016. The results of the Provo River MeHg analysis showed dissolved MeHg had a concentration variance of 0.027 ng/L and particulate MeHg had a concentration variance of 0.056 ng/L. The variances during the diel cycle represent more than a two-fold change in concentration. The hourly MeHg concentration levels demonstrated an inverse relationship with gage height indicative of dilution. The purpose of the study is to develop a more thorough understanding of short-term variances over time and the potential affect on long-term interpretations of MeHg fluctuations in the river. The Provo River flows through Jordanelle Reservoir where there is a mercury advisory for two fish species. MeHg is a bioaccumulative neurotoxin that humans are primarily exposed to by the consumption of contaminated fish. The strong correlation between the levels of MeHg in water and fish make the river concentrations an important factor.

  17. Relationship Between Soil Properties and Different Fractions of Soil Hg

    Institute of Scientific and Technical Information of China (English)

    WUHONGTAO; YUGUIFEN; 等

    2001-01-01

    Correlation and path analysis methods were used to study the relationship between soil properties and the distribution of different soil Hg fractions with nine representative soils from Chongqing,China,Results showed that clay(<2m) could increase water-soluble Hg(r=0.700*).Soil organic matter (OM) could enhance the increase of elemental Hg(r=0.674*),The higher the base saturation percentage (BSP) ,the more the residual Hg(R=0.684*) .Organic Hg,the sum of said-soluble organic He and alkali-soluble Hg,was positively affected by silt(2-20μm)but negatively affected by pH,with the direct path coefficients amounting to 1.0487 and 0.5121,respectively .The positive effect of OM and negative effect of BSP on organic Hg were the most significant ,with the direct path coefficients being 0.7614 and -0.8527,respectively. The indirect effect of clay(<2μm) iva BSP (path coefficient=0.4186) was the highest,showing that the real influencing factor in the effect of clay(<2μm) via BSP (path coefficient=0.4186) was the highest,showing that the real influencing factor in the effect of clay(<2μm) on acid-soluble organic Hw was BSP.since the available Hg fraction,water-soluble Hg,was positively affected by soil clay content,and the quite immobile and not bioavailable residual Hg by soil BSP,suitable reduction of clay content and increase of BSP would be of much help to reduce the Hg availability and Hg activity in Hg-contaminated soils.

  18. Genome-Wide Association Study to Identify Genes Related to Renal Mercury Concentrations in Mice

    DEFF Research Database (Denmark)

    Alkaissi, Hammoudi; Ekstrand, Jimmy; Jawad, Aksa

    2016-01-01

    BACKGROUND: Following human mercury (Hg) exposure, the metal accumulates with considerable concentrations in kidney, liver, and brain. Although the toxicokinetics of Hg has been studied extensively, factors responsible for inter-individual variation in humans are largely unknown. Differences...... in accumulation of renal Hg between inbred mouse strains suggest a genetic inter-strain variation regulating retention or/and excretion of Hg. A.SW, DBA/2 and BALB/C mouse strains accumulate higher amounts of Hg than B10.S. OBJECTIVES: To find candidate genes associated with regulation of renal Hg concentrations...... enhanced by the Pprc1 (Nrf1 and Nrf2) were included for gene expression analysis. RESULTS: Renal Hg concentrations differed significantly between A.SW and B10.S mice and between males and females within each strain. QTL analysis showed a peak logarithm of odds ratio score 5.78 on chromosome 19 (p = 0...

  19. Maternal-fetal distribution of mercury ( sup 203 Hg) released from dental amalgam fillings

    Energy Technology Data Exchange (ETDEWEB)

    Vimy, M.J.; Takahashi, Y.; Lorscheider, F.L. (Univ. of Calgary, Alberta (Canada))

    1990-04-01

    In humans, the continuous release of Hg vapor from dental amalgam tooth restorations is markedly increased for prolonged periods after chewing. The present study establishes a time-course distribution for amalgam Hg in body tissues of adult and fetal sheep. Under general anesthesia, five pregnant ewes had twelve occlusal amalgam fillings containing radioactive 203Hg placed in teeth at 112 days gestation. Blood, amniotic fluid, feces, and urine specimens were collected at 1- to 3-day intervals for 16 days. From days 16-140 after amalgam placement (16-41 days for fetal lambs), tissue specimens were analyzed for radioactivity, and total Hg concentrations were calculated. Results demonstrate that Hg from dental amalgam will appear in maternal and fetal blood and amniotic fluid within 2 days after placement of amalgam tooth restorations. Excretion of some of this Hg will also commence within 2 days. All tissues examined displayed Hg accumulation. Highest concentrations of Hg from amalgam in the adult occurred in kidney and liver, whereas in the fetus the highest amalgam Hg concentrations appeared in liver and pituitary gland. The placenta progressively concentrated Hg as gestation advanced to term, and milk concentration of amalgam Hg postpartum provides a potential source of Hg exposure to the newborn. It is concluded that accumulation of amalgam Hg progresses in maternal and fetal tissues to a steady state with advancing gestation and is maintained. Dental amalgam usage as a tooth restorative material in pregnant women and children should be reconsidered.

  20. Factors affecting biotic mercury concentrations and biomagnification through lake food webs in the Canadian high Arctic

    Energy Technology Data Exchange (ETDEWEB)

    Lescord, Gretchen L., E-mail: glescord@gmail.com [University of New Brunswick/Canadian Rivers Institute, 100 Tucker Park Rd, Saint John, NB E2L 4A6 (Canada); Kidd, Karen A. [University of New Brunswick/Canadian Rivers Institute, 100 Tucker Park Rd, Saint John, NB E2L 4A6 (Canada); Kirk, Jane L. [Environment Canada, Aquatic Contaminants Research Division, 867 Lakeshore Rd, Burlington, ON L7S 1A1 (Canada); O' Driscoll, Nelson J. [Acadia University, 15 University Ave, Wolfville, NS B4P 2R6 (Canada); Wang, Xiaowa; Muir, Derek C.G. [Environment Canada, Aquatic Contaminants Research Division, 867 Lakeshore Rd, Burlington, ON L7S 1A1 (Canada)

    2015-03-15

    In temperate regions of Canada, mercury (Hg) concentrations in biota and the magnitude of Hg biomagnification through food webs vary between neighboring lakes and are related to water chemistry variables and physical lake features. However, few studies have examined factors affecting the variable Hg concentrations in landlocked Arctic char (Salvelinus alpinus) or the biomagnification of Hg through their food webs. We estimated the food web structure of six high Arctic lakes near Resolute Bay, Nunavut, Canada, using stable carbon (δ{sup 13}C) and nitrogen (δ{sup 15}N) isotopes and measured Hg (total Hg (THg) in char, the only fish species, and methylmercury (MeHg) in chironomids and zooplankton) concentrations in biota collected in 2010 and 2011. Across lakes, δ{sup 13}C showed that benthic carbon (chironomids) was the dominant food source for char. Regression models of log Hg versus δ{sup 15}N (of char and benthic invertebrates) showed positive and significant slopes, indicting Hg biomagnification in all lakes, and higher slopes in some lakes than others. However, no principal components (PC) generated using all water chemistry data and physical characteristics of the lakes predicted the different slopes. The PC dominated by aqueous ions was a negative predictor of MeHg concentrations in chironomids, suggesting that water chemistry affects Hg bioavailability and MeHg concentrations in these lower-trophic-level organisms. Furthermore, regression intercepts were predicted by the PCs dominated by catchment area, aqueous ions, and MeHg. Weaker relationships were also found between THg in small char or MeHg in pelagic invertebrates and the PCs dominated by catchment area, and aqueous nitrate and MeHg. Results from these high Arctic lakes suggest that Hg biomagnification differs between systems and that their physical and chemical characteristics affect Hg concentrations in lower-trophic-level biota. - Highlights: • Mercury (Hg) in Arctic char and invertebrates

  1. Quasiparticle excitations in superdeformed {sup 192}Hg

    Energy Technology Data Exchange (ETDEWEB)

    Lauritsen, T.; Carpenter, M.P.; Janssens, R.V.F. [and others

    1995-08-01

    The nucleus {sup 192}Hg plays a pivotal role for superdeformation in the mass 190 region, since calculations of single-particle levels show large shell-gaps for the superdeformed (SD) shape at N = 112 and Z = 80. As a result, {sup 192}Hg is referred to as the doubly magic SD nucleus for the A = 190 region. In previous studies, only one superdeformed band was observed in this nucleus, and this fact was cited as indirect evidence that large shell gaps do indeed exist at the proposed particle numbers.

  2. Oxygen ordering in the high-T$_c$ superconductor HgBa$_2$CaCu$_2$O$_{6+\\delta}$ as revealed by perturbed angular correlation

    CERN Document Server

    Mendonca, Tania Melo; Haas, Heinz; Odier, Philippe; Tavares, Pedro; Silva, Manuel Ribeiro; Lopes, Armandina; Pereira, Andre; Goncalves, Joao Nuno; Amaral, Joao; Darie, Celine; Araujo, Joao Pedro

    2011-01-01

    Lattice sites and collective ordering of oxygen atoms in HgBa$_2$CaCu$_2$O$_{6+\\delta}$ were studied using the perturbed angular correlation (PAC) technique at ISOLDE/CERN. The electric field gradients (EFG) at $^{199m}$Hg nuclei have been measured as functions of oxygen doping on the Hg planes, above and below T$_c$. In comparison with the results obtained for oxygen and fluorine doping in Hg-1201, the analysis shows a different oxygen ordering exhibited by Hg-1212. Moreover, for all studied cases, the experimental results show that at a local scale there is non-uniform oxygen distribution. A series of ab initio EFG calculations allowed to infer that at low concentrations, regions without oxygen coexist with regions where O$_{2\\delta}$ dumbbell molecules are located at the center of the Hg mesh. On the other side, at high concentrations, O$_{2\\delta}$ dumbbell molecules coexist with single O$_\\delta$ atoms occupying the center of the Hg mesh. The present results suggest that oxygen sits on the Hg planes in t...

  3. The lncRNA MIR31HG regulates p16(INK4A) expression to modulate senescence

    DEFF Research Database (Denmark)

    Montes Resano, Marta; Nielsen, Morten M; Maglieri, Giulia

    2015-01-01

    normal conditions, MIR31HG is found in both nucleus and cytoplasm, but following B-RAF expression MIR31HG is located mainly in the cytoplasm. We show that MIR31HG interacts with both INK4A and MIR31HG genomic regions and with Polycomb group (PcG) proteins, and that MIR31HG is required for Pc...

  4. Vapour pressure of components made by the presence of HgS(s,alpha) in an oil/gas reservoir and consequences for the produced gas

    Energy Technology Data Exchange (ETDEWEB)

    Oestvold, T.; Gustavsen, Oe.; Grande, K.; Aas, N.; Olsvik, Mimmi Kjetsaa

    2006-03-15

    A thermodynamic analysis is presented on how components made from HgS (s,alpha), existing in a oil/gas reservoir, will distribute themselves between gas, water, liquid and solid components as a function of temperature and pressure. The consequence of the formation of mercury containing components on gas injection and on gas quality is discussed. Since equilibrium is established in the model calculation, other gas components in the gas phase and components in condensed phases present will also influence the composition of the gas. Six cases are considered in the calculation: 1) HgS(s,alpha) - Ar(g), 2) HgS(s,alpha) - Ar (g) - water with 10-4 molal NaCl at pH = 7, 3) HgS(s,alpha) - CH{sub 4}(g), 4) HgS(s,alpha) - CH{sub 4} (g) - water with 10-4 molal NaCl at pH = 7 and 5) HgS(s,alpha) - natural gas - water with 10-4 molal NaCl at pH = 7, 6) HgS(s,alpha) - natural gas - water with 10-4 molal NaCl and 5*10-5 molal NO-3- at pH = 7. When HgS(s,alpha) is present in an oil reservoir at 170 deg C and 200 bar, these calculations show that the major components formed are: H{sub 2}(g), H{sub 2}S(g), Hg(l) and Hg(g) together with carbon. Mercury in the gas phase in the cases 1) is 4*10-7 bar and is determined by the evaporation and decomposition HgS(g) in the reservoir. In case 2) P{sub Hg} = 5.7*10-4 bar mainly determined by the formation of sulphate in the water phase. In the cases 3), 4) and 5) these calculations show that the major components formed are: H{sub 2}(g), H{sub 2}S(g), Hg(l) and Hg(g) together with carbon, and the gas phase is dominated by Hg(g) at approx. *10-3 bar. The water phase may contain Hg(CH{sub 3}NH{sub 2}){sub 2}2+ if NO{sub 3}- for some reasons is introduced into the formation water, and the very carcinogenic dimethyl mercury compound, C{sub 2}HgH{sub 6}, can be formed in the gas phase. Both compounds, however, in insignificant low concentration/partial pressure. (Author)

  5. Anti-aggregation-based spectrometric detection of Hg(II) at physiological pH using gold nanorods

    Energy Technology Data Exchange (ETDEWEB)

    Rajeshwari, A.; Karthiga, D.; Chandrasekaran, Natarajan; Mukherjee, Amitava, E-mail: amit.mookerjea@gmail.com

    2016-10-01

    An efficient detection method for Hg (II) ions at physiological pH (pH 7.4) was developed using tween 20-modified gold nanorods (NRs) in the presence of dithiothreitol (DTT). Thiol groups (-SH) at the end of DTT have a higher affinity towards gold atoms, and they can covalently interact with gold NRs and leads to their aggregation. The addition of Hg(II) ions prevents the aggregation of gold NRs due to the covalent bond formation between the -SH group of DTT and Hg(II) ions in the buffer system. The changes in the longitudinal surface plasmon resonance peak of gold NRs were characterized using a UV–visible spectrophotometer. The absorption intensity peak of gold NRs at 679 nm was observed to reduce after interaction with DTT, and the absorption intensity was noted to increase by increasing the concentration of Hg(II) ions. The TEM analysis confirms the morphological changes of gold NRs before and after addition of Hg(II) ions in the presence of DTT. Further, the aggregation and disaggregation of gold NRs were confirmed by particle size and zeta potential analysis. The developed method shows an excellent linearity (y = 0.001 x + 0.794) for the graph plotted between the absorption ratio and Hg(II) concentration (1 to 100 pM) under the optimized conditions. The limit of detection was noted to be 0.42 pM in the buffer system. The developed method was tested in simulated body fluid, and it was found to have a good recovery rate. - Highlights: • Tween-20 modified gold NRs used as a probe for Hg(II) at physiological pH. • TEM, particle size and surface charge analysis confirm the aggregation and • disaggregation of NRs • The sensitivity of the probe for Hg(II) ions detection was 0.42 pM. • Hg(II) estimation in simulated body fluids with good recovery.

  6. A Population Pharmacokinetic Modeling Approach Shows that Serum Penicillin G Concentrations Are Below Inhibitory Concentrations by Two Weeks after Benzathine Penicillin G Injection in the Majority of Young Adults

    Science.gov (United States)

    2014-11-01

    liter is the suggested minimum protective concentration of penicillin G against group A streptococcus . Note that the majority of measured concen- trations... pneumoniae , Streptococcus pyogenes and Haemophilus influenzae collected from patients across the USA, in 2001-2002, as part of the PROTEKT US study. J...Naval Health Research Center A Population Pharmacokinetic Modeling Approach Shows that Serum Penicillin G Concentrations Are Below Inhibitory

  7. Characterization of Electronic Materials HgZnSe and HgZnTe Using Innovative and Conventional Techniques

    Science.gov (United States)

    Tanton, George; Kesmodel, Roy; Burden, Judy; Su, Ching-Hua; Cobb, Sharon D.; Lehoczky, S. L.

    2000-01-01

    , obtained by combining results from conventional Hall measurements of the free carrier concentration with Faraday rotation measurements, will also be presented. One example of how this type of information was derived is illustrated in the following figure which shows Faraday rotation vs wavelength modeled for Hg(l-x)ZnxSe at a temperature of 300K and x=0.07. The plasma contribution, total Faraday rotation, and interband contribution to the Faraday rotation, are designated in the Figure as del(p), FR tot, and del(i) respectively. Experimentally measured values of FR tot, each indicated by + , agree acceptably well with the model at the probe wavelength of 10.6 microns. The model shows that at the probe wavelength, practically all the rotation is due to the plasma component, which can be expressed as delta(sub p)= 2pi(e(sup 3))NBL/c(sup 2)nm*(sup 2) omega(sup 2). In this equation, delta(sub p) is the rotation angle due to the free carrier plasma, N is the free carrier concentration, B the magnetic field strength, L the thickness of the sample, n the index of refraction, omega the probe radiation frequency, c the speed of light, e the electron charge, and m* the effective mass. A measurement of N by conventional techniques, combined with a measurement of the Faraday rotation angle allows m* to be accurately determined since it is an inverse square function.

  8. Magnetism, chemical spots, and stratification in the HgMn star phi Phoenicis

    CERN Document Server

    Makaganiuk, V; Piskunov, N; Jeffers, S V; Johns-Krull, C M; Keller, C U; Rodenhuis, M; Snik, F; Stempels, H C; Valenti, J A

    2011-01-01

    Mercury-manganese (HgMn) stars have been considered as non-magnetic and non-variable chemically peculiar (CP) stars for a long time. However, recent discoveries of the variability in spectral line profiles suggested an inhomogeneous surface distribution of chemical elements in some HgMn stars. From the studies of other CP stars it is known that magnetic field plays a key role in the formation of surface spots. All attempts to find magnetic fields in HgMn stars yielded negative results. In this study, we investigate a possible presence of the magnetic field in phi Phe (HD 11753) and reconstruct surface distribution of chemical elements that show variability in spectral lines. We also test a hypothesis that magnetic field is concentrated in chemical spots and look into the possibility that some chemical elements are stratified with depth in the stellar atmosphere.

  9. A Liquid Inorganic Electrolyte Showing an Unusually High Lithium Ion Transference Number: A Concentrated Solution of LiAlCl4 in Sulfur Dioxide

    Directory of Open Access Journals (Sweden)

    Martin Winter

    2013-08-01

    Full Text Available We report on studies of an inorganic electrolyte: LiAlCl4 in liquid sulfur dioxide. Concentrated solutions show a very high conductivity when compared with typical electrolytes for lithium ion batteries that are based on organic solvents. Our investigations include conductivity measurements and measurements of transference numbers via nuclear magnetic resonance (NMR and by a classical direct method, Hittorf’s method. For the use of Hittorf’s method, it is necessary to measure the concentration of the electrolyte in a selected cell compartment before and after electrochemical polarization very precisely. This task was finally performed by potentiometric titration after hydrolysis of the salt. The Haven ratio was determined to estimate the association behavior of this very concentrated electrolyte solution. The measured unusually high transference number of the lithium cation of the studied most concentrated solution, a molten solvate LiAlCl4 × 1.6SO2, makes this electrolyte a promising alternative for lithium ion cells with high power ability.

  10. Variations in stable isotope fractionation of Hg in food webs of Arctic lakes.

    Science.gov (United States)

    Gantner, Nikolaus; Hintelmann, Holger; Zheng, Wang; Muir, Derek C

    2009-12-15

    Biotic and abiotic fractionation of mercury (Hg) isotopes has recently been shown to occur in aquatic environments. We determined isotope ratios (IRs) of Hg in food webs (zooplankton, chironomids, Arctic char) and sediments of 10 Arctic lakes from four regions and investigated the extent of Hg isotope fractionation. Hg IRs were analyzed by multicollector inductively coupled plasma mass spectrometry (MC-ICP/MS). Hg mass independent fractionation (MIF; Delta(199)Hg) and mass dependent fractionation (MDF; delta(202)Hg) were calculated and compared among samples. IRs of Hg in sediment were characterized mainly by MDF and low MIF (Delta(199)Hg -0.37 to 0.74 per thousand). However, all biota showed evidence of MIF, most pronounced in zooplankton (Delta(199)Hg up to 3.40 per thousand) and char (Delta(199)Hg up to 4.87 per thousand). Zooplankton takes up highly fractionated MeHg directly from the water column, while benthic organisms are exposed to sedimentary Hg, which contains less fractionated Hg. As evidenced by delta(13)C measurements, benthic chironomids make up a large proportion of char diet, explaining in part why MIF(char) meteor impact crater lake (Pingualuk) reflects a "pure" atmospheric Hg signature, which is modified only by aqueous in-lake processes. All other lakes are also affected by terrestrial Hg inputs and sediment processes.

  11. Imobilisasi TiO2 ke dalam Resin Penukar Kation dan Aplikasinya sebagai Fotokatalis dalam Proses Fotoreduksi Ion Hg2+

    Directory of Open Access Journals (Sweden)

    Rosyid Ridho

    2017-03-01

    kenaikan fotoreduksi pada ion Hg(II, akan tetapi pada pH yang lebih tinggi dari 4 menyebabkan terjadinya penurunan efektivitas fotoreduksi terhadap ion Hg(II.   Kata kunci : Fotokatalis, TiO2-resin, Ion Hg(II   Abstract To develop TiO2 photoreduction photocatalyst in order to decrease the Hg(II ion concentrate, in this research, it has been done the TiO2-Resin photocatalyst preparation with the characterization and application to Hg(II ion photoreduction process. This preparation was done with ion exchange method which followed by studied calcinations at certain temperature. The preparation has been studied the influence of titanium isopropoxide concentrate toward TiO2-Resin which has been characterized by using X-Ray Diffraction(XRD and Thermografimetry (TGA. In Hg(II ion photoreduction process, it has been studied the influence of photocatalyst mass, the content of TiO2 which immobilized into sulfonated polystyrene (resin, the ion Hg(II concentrate, and the pH influence. The photoreduction process has been done in the closed reactor that equipped by UV lamp, and uses the irradiating a mixture which contents of Hg(II ion solution and TiO2-Resin photocatalyst powder, with the stirring at certain time. The result of photoreduction was calculated based on the difference between the earlier Hg(II ion concentrate and unreduced Hg(II ion. The determining of unreduced Hg(II ion concentrate was done by using cold vapor atomic absorption spectrophotometry (CV-AAS. The preparation result showed that the higher isopropoxide titanium that was added into sulfonated polystyrene, the higher the content of TiO2 that was formed in TiO2-Resin. the result of photocatalyst test showed that the using using of TiO2-Resin photocatalyst can increase the result of Hg(II ion photoreduction  which the increase is higher than TiO2 powder. The added of photocatalyst by the higher mass, adds the photoreduction effectiveness toward the Hg(II ion. The higher the Hg(II concentrate that added, the

  12. Hg(II) removal from aqueous solution by bayberry tannin-immobilized collagen fiber.

    Science.gov (United States)

    Huang, Xin; Liao, Xuepin; Shi, Bi

    2009-10-30

    A novel adsorbent was prepared by immobilizing barberry tannin (BT) onto collagen fiber, which was found effective to remove Hg(II) from aqueous solution. The bayberry tannin-immobilized collagen fiber (BTICF) shows high adsorption capacity to Hg(II) in a wide pH range of 4.0-9.0, and a maximum adsorption capacity (198.49 mg/g) was reached at pH 7.0 and 303 K when the initial concentration of Hg(II) was 200.0 mg/L. The adsorption isothermal and kinetic data were well fitted by the Langmuir equation and the pseudo-first-order rate equation, respectively. The adsorption mechanism of BTICF to Hg(II) was proved to follow a chelating reaction. The BTICF can be easily regenerated with 0.1M lactic acid after adsorption process and recycled at least 4 times without the loss of adsorption capacity. These facts indicate that BTICF can be used as a low-cost adsorbent for effective removal of Hg(II) from aqueous solutions.

  13. The Upside to Hg-DOM Associations for Water Quality: Removal of Hg from Solution Using Coagulaion with Metal-Based Salts

    Science.gov (United States)

    Henneberry, Y.; Kraus, T. E.; Fleck, J.; Krabbenhoft, D. P.; Horwath, W. R.

    2011-12-01

    This study assessed the potential use of metal-based coagulants to remove dissolved mercury (Hg) from natural waters and provides information regarding the importance of Hg associations with the dissolved organic matter (DOM) fraction and metal hydroxides. Previous research indicated coagulants were not effective at removing Hg from solution; however those studies used high concentrations of Hg, which did not reflect naturally occurring concentrations of Hg. Filtered water collected from an agricultural drain in the Sacramento-San Joaquin Delta (Delta) was treated with three industrial-grade coagulants (ferric chloride, ferric sulfate, and polyaluminum chloride) to determine their efficacy in removing both inroganic (IHg) and methylmercury (MeHg) from the water column. The Delta suffers from elevated surface water Hg concentrations and as a result is listed as an imparied water body. Coagulants removed up to 85% of DOM from solution. In the absence of DOM, all three coagulants released IHg into solution, however in the presence of DOM the coagulants removed up to 97% of IHg and 80% of MeHg. Results suggest that the removal of Hg is mediated by DOM-coagulant interactions. There was a preferential association of IHg with the more aromatic, higher molecular weight fraction of DOM but no such relationship was found for MeHg. This study offers new fundamental insights regarding large-scale removal of Hg at environmentally relevant concentrations. Research using isotopically labeled Hg is providing insight into whether coagulation can remove recently added Hg (e.g. atmospheric deposition) from solution and whether once formed, the floc can remove additional Hg from the water column.

  14. Possible link between Hg and Cd accumulation in the brain of long-finned pilot whales (Globicephala melas)

    Energy Technology Data Exchange (ETDEWEB)

    Gajdosechova, Zuzana [Trace Element Speciation Laboratory, Department of Chemistry, Meston Walk, University of Aberdeen, Aberdeen AB24 3UE (United Kingdom); Brownlow, Andrew [SAC Wildlife Unit, Inverness (United Kingdom); Cottin, Nicolas T.; Fernandes, Mariana [Trace Element Speciation Laboratory, Department of Chemistry, Meston Walk, University of Aberdeen, Aberdeen AB24 3UE (United Kingdom); Read, Fiona L. [Oceanlab, University of Aberdeen, Main Street, Newburgh AB41 6AA (United Kingdom); Urgast, Dagmar S.; Raab, Andrea; Feldmann, Jörg; Krupp, Eva M. [Trace Element Speciation Laboratory, Department of Chemistry, Meston Walk, University of Aberdeen, Aberdeen AB24 3UE (United Kingdom)

    2016-03-01

    The bioaccumulation of metals was investigated by analysis of liver, kidney, muscle and brain tissue of a pod of 21 long-finned pilot whales (Globicephala melas) of all ages stranded in Scotland, UK. The results are the first to report cadmium (Cd) passage through the blood–brain barrier of pilot whales and provide a comprehensive study of the long-term (up to 35 years) mammalian exposure to the environmental pollutants. Additionally, linear accumulation of mercury (Hg) was observed in all studied tissues, whereas for Cd this was only observed in the liver. Total Hg concentration above the upper neurochemical threshold was found in the sub-adult and adult brains and methylmercury (MeHg) of 2.2 mg/kg was found in the brain of one individual. Inter-elemental analysis showed significant positive correlations of Hg with selenium (Se) and Cd with Se in all studied tissues. Furthermore, differences in the elemental concentrations in the liver and brain tissues were found between juvenile, sub-adult and adult groups. The highest concentrations of manganese, iron, zinc, Se, Hg and MeHg were noted in the livers, whereas Cd predominantly accumulated in the kidneys. High concentrations of Hg and Cd in the tissues of pilot whales presented in this study reflect ever increasing toxic stress on marine mammals. - Highlights: • Trace elements were measured in a pod of 21 pilot whales stranded in Scotland. • Bioaccumulation of mercury and methyl mercury was found in all studied tissues. • Cadmium age related accumulation was observed in the liver and brain tissues. • Cadmium-selenium correlations suggest formation of cadmium-selenium complexes.

  15. Mercury Concentrations in Pacific Angel Sharks (Squatina californica) and Prey Fishes from Southern Gulf of California, Mexico.

    Science.gov (United States)

    Escobar-Sánchez, O; Ruelas-Inzunza, J; Moreno-Sánchez, X G; Romo-Piñera, A K; Frías-Espericueta, M G

    2016-01-01

    Concentrations of mercury (Hg) were quantified in muscle tissues of the Pacific angel shark, Squatina californica sampled from Southern Gulf of California, Mexico, considering total length, sex, diet and the dietary risk assessment. High Hg levels are typically associated with carnivorous fishes, however S. californica showed low Hg concentrations (shark (p > 0.05). Hg concentrations were highest in the darkedge mishipman: Porichthys analis (0.14 ± 0.08 µg g(-1)) and red-eye round herring Etrumeus teres (0.13 ± 0.05 µg g(-1)) relative to other prey species, which could suggest that Hg concentrations in S. californica were influenced by these species. Given the relatively low concentration of Hg across age-classes and sex, consumption of S. californica's muscle tissue poses limited risk to humans.

  16. Assessment of Hg contamination and exposure to miners and schoolchildren at a small-scale gold mining and recovery operation in Thailand.

    Science.gov (United States)

    Umbangtalad, S; Parkpian, P; Visvanathan, C; Delaune, R D; Jugsujinda, A

    2007-12-01

    Hg urine concentration was detected in group I and group II (involved and not involved in gold recovery) at average levels of 15.82 and 9.95 microg/g creatinine, respectively. The average Hg values for both groups were below the established levels indicating no risk from Hg intake. Average Hg hair level in all schoolchildren (0.93 microg/g) was not significantly higher than reference group. There were two variables (gender and personal hygiene) which affected the concentration of Hg in urine of schoolchildren (P < 0.05). The result (HQ) also suggested that schoolchildren were not at risk (< 1). Schoolchildren involved in gold mining activities showed some indirect exposure to Hg from the adults working in mining area.

  17. Incorporation of inorganic mercury (Hg{sup 2+}) in pelagic food webs of ultraoligotrophic and oligotrophic lakes: The role of different plankton size fractions and species assemblages

    Energy Technology Data Exchange (ETDEWEB)

    Soto Cárdenas, Carolina, E-mail: sotocardenascaro@gmail.com [Laboratorio de Fotobiología, Instituto de Investigaciones en Biodiversidad y Medioambiente (INIBIOMA, UNComahue-CONICET), Quintral 1250, 8400 San Carlos de Bariloche, Río Negro (Argentina); Diéguez, Maria C. [Laboratorio de Fotobiología, Instituto de Investigaciones en Biodiversidad y Medioambiente (INIBIOMA, UNComahue-CONICET), Quintral 1250, 8400 San Carlos de Bariloche, Río Negro (Argentina); Ribeiro Guevara, Sergio [Laboratorio de Análisis por Activación Neutrónica, CAB, CNEA, Av. Bustillo Km 9.5, 8400, San Carlos de Bariloche, Río Negro (Argentina); Marvin-DiPasquale, Mark [United States Geological Survey, 345 Middlefield Rd./MS 480, Menlo Park, CA 94025 (United States); Queimaliños, Claudia P. [Laboratorio de Fotobiología, Instituto de Investigaciones en Biodiversidad y Medioambiente (INIBIOMA, UNComahue-CONICET), Quintral 1250, 8400 San Carlos de Bariloche, Río Negro (Argentina)

    2014-10-01

    In lake food webs, pelagic basal organisms such as bacteria and phytoplankton incorporate mercury (Hg{sup 2+}) from the dissolved phase and pass the adsorbed and internalized Hg to higher trophic levels. This experimental investigation addresses the incorporation of dissolved Hg{sup 2+} by four plankton fractions (picoplankton: 0.2–2.7 μm; pico + nanoplankton: 0.2–20 μm; microplankton: 20–50 μm; and mesoplankton: 50–200 μm) obtained from four Andean Patagonian lakes, using the radioisotope {sup 197}Hg{sup 2+}. Species composition and abundance were determined in each plankton fraction. In addition, morphometric parameters such as surface and biovolume were calculated using standard geometric models. The incorporation of Hg{sup 2+} in each plankton fraction was analyzed through three concentration factors: BCF (bioconcentration factor) as a function of cell or individual abundance, SCF (surface concentration factor) and VCF (volume concentration factor) as functions of individual exposed surface and biovolume, respectively. Overall, this investigation showed that through adsorption and internalization, pico + nanoplankton play a central role leading the incorporation of Hg{sup 2+} in pelagic food webs of Andean lakes. Larger planktonic organisms included in the micro- and mesoplankton fractions incorporate Hg{sup 2+} by surface adsorption, although at a lesser extent. Mixotrophic bacterivorous organisms dominate the different plankton fractions of the lakes connecting trophic levels through microbial loops (e.g., bacteria–nanoflagellates–crustaceans; bacteria–ciliates–crustaceans; endosymbiotic algae–ciliates). These bacterivorous organisms, which incorporate Hg from the dissolved phase and through their prey, appear to explain the high incorporation of Hg{sup 2+} observed in all the plankton fractions. - Highlights: • Hg{sup 2+} incorporation in lake plankton fractions was studied using the isotope {sup 197}Hg{sup 2+}. • Hg{sup 2

  18. Dissolved gaseous Hg (DGM in the Mediterranean surface and deep waters

    Directory of Open Access Journals (Sweden)

    Kotnik J.

    2013-04-01

    Full Text Available Dissolved gaseous mercury (DGM was studied in surface and deep waters of the Mediterranean Sea for last 12 years during several oceanographic cruises on board the Italian research vessel Urania and covered both Western and Eastern Mediterranean Basins as well as Adriatic Sea. DGM was measured together with other mercury species (RHg - reactive Hg, THg - total Hg, MeHg - monomethyl Hg and DMeHg - dimethylmercury, and with some water quality parameters in coastal and open sea deep water profiles, however only DGM will be discussed here. DGM represents a considerable portion of THg (average of about 20 % in Mediterranean waters. Spatial and seasonal variations of measured DGM concentrations were observed in different indentified water masses as well as iwere observed. DGM was the highest in the northern Adriatic, most polluted part of the Mediterranean Sea as the consequence of Hg mining in Idrija and heavy industry of northern Italy.Generally, average DGM concentration was higher in W and E Mediteranean Deep Waters (WMDW and EMDW and Leavantine Intermediate Water (LIW than overlaying Modified Atlantic Water (MAW, however it was the highest in N Adriatic Surface waters and consequently in out flowing Adriatic Deep Waters (ADW. In deep water profiles the portion of DGM typically increased at depths with oxygen minimum and then towards the bottom, especially in areas with strong tectonic activity (Alboran Sea, Strait of Sicily, Tyrrhenian Sea, indicating its bacterial and/or geotectonic origin. A comparison of the results obtained in this study to others performed in the Mediterranean shows no significant differences. Results were also compared to the results obtained in the Pacific and Atlantic Oceans. During last oceanographic cruise in 2011 covering area between Livorno and Lipari Islands a novel method for continuous DGM determination in surface waters (Wangberg and Gardfeldt, 2011 was applied and compared to standard method.

  19. Study of atomic structure of liquid Hg-In alloys using ab-initio molecular dynamics

    Energy Technology Data Exchange (ETDEWEB)

    Sharma, Nalini; Ahluwalia, P. K. [Department of Physics, Himachal Pradesh University, Shimla(HP)-171005 (India); Thakur, Anil [Department of Physics, Govt. P. G. College Solan (HP)-173212 (India)

    2015-05-15

    Ab-initio molecular dynamics simulations are performed to study the structural properties of liquid Hg-In alloys. The interatomic interactions are described by ab-initio pseudopotentials given by Troullier and Martins. Five liquid Hg-In mixtures (Hg{sub 10}In{sub 90}, Hg{sub 30}In{sub 70}, Hg{sub 50}In{sub 50}, Hg{sub 70}In{sub 30} and Hg{sub 90}In{sub 10}) at 299K are considered. The radial distribution function g(r) and structure factor S(q) of considered alloys are compared with respective experimental results for liquid Hg (l-Hg) and (l-In). The radial distribution function g(r) shows the presence of short range order in the systems considered. Smooth curves of Bhatia-Thornton partial structure factors factor shows the presence of liquid state in the considered alloys.

  20. Formation of PdHg by reaction of palladium thin film contacts deposited onto mercuric iodide ({alpha}-HgI{sub 2}) radiation detector crystals

    Energy Technology Data Exchange (ETDEWEB)

    Medlin, D.L. [Sandia National Labs., Livermore, CA (United States); Van Scyoc, J.M. [Carnegie-Mellon Univ., Pittsburgh, PA (United States). Dept. of Electrical and Computer Engineering; Gilbert, T.S. [Carnegie-Mellon Univ., Pittsburgh, PA (United States). Dept. of Electrical and Computer Engineering; Schlesinger, T.E. [Carnegie-Mellon Univ., Pittsburgh, PA (United States). Dept. of Electrical and Computer Engineering; Boehme, D. [Sandia National Labs., Livermore, CA (United States); Schieber, M. [Sandia National Labs., Livermore, CA (United States); Natarajan, M. [TN Technologies, Inc., Round Rock, TX (United States); James, R.B. [Sandia National Labs., Livermore, CA (United States)

    1996-10-01

    The microstructure and phase distribution of palladium thin films sputter deposited onto {alpha}-HgI{sub 2} for use as electrical contacts in radiation detectors are investigated using electron microscopy. Our results show a limited reaction to form palladium mercuride (PdHg). It is shown that the formation of PdHg via several reaction pathways is thermodynamically feasible. (orig.).

  1. Comparison of the characteristics and mechanisms of Hg(II) sorption by biochars and activated carbon.

    Science.gov (United States)

    Xu, Xiaoyun; Schierz, Ariette; Xu, Nan; Cao, Xinde

    2016-02-01

    Two biochars were produced from bagasse and hickory chips (referred to as BB and HCB, respectively) and evaluated for their sorption ability of Hg(II) in aqueous solution. A commercial activated carbon (AC) which is commonly used for Hg(II) removal was included for comparison. Both biochars showed higher sorption capacities than AC, following the trend of BB>HCB>AC. The sorption of Hg(II) by BB and AC was mainly attributed to the formation of (COO)2Hg(II) and (O)2Hg(II). As a result, the adsorption capacity of Hg(II) by BB decreased 17.6% and 37.6% after COOH and OH were blocked, respectively and that of Hg(II) by AC decreased 6.63% and 62.2% for COOH and OH hindered, respectively. However, blocking the function groups had little effect on the Hg removal by HCB since sorption of Hg(II) by HCB was mainly resulted from the π electrons of CC and CO induced Hg-π binding. Further X-ray photoelectron spectroscopy analysis indicated the possibility of reduction of the Hg(II) to Hg(I) by phenol groups or π electrons during the removal of Hg(II) by both biochars. In conclusion, biochar is more effective than activated carbon in removing Hg(II) and there exists a high potential that biochar can be a substitute of activated carbon for removal of Hg(II) from wastewater.

  2. [Influence of inorganic ions and humic acid on the removal of Pb(II) and Hg(II) in water by zero-valent iron].

    Science.gov (United States)

    Shi, Qiu-Ling; Zhou, Xin; Zhang, Jin-Zhong; Qiu, Xin-Kai

    2014-08-01

    The effects of Ca2+, Cl- and humic acid (HA) on the removal rates of Pb(II) and Hg(II) in water by zero-valent (ZVI) and the kinetic characteristics were studied, and the removal mechanism of Pb(II) and Hg(II) by ZVI were preliminarily investigated using X-ray diffraction (XRD). The results indicated that the removal mechanism of Pb(II) might mainly be attributed to the adsorption and co-precipitation of ZVI, while that of Hg(II) might mainly be attributed to the oxidation-reduction of ZVI. With the increase of Ca2+ concentration, the removal rates of Hg(II) and Pb(II) showed the trends of gradual increase and slight decrease, respectively. The Hg(II) removal increased with increasing Cl- concentration, whereas no obvious increase in Pb(II) removal was observed. The removal rates of Hg(II) and Pb(II) showed the trends of slow increase and slow decrease with increasing HA concentration, respectively. When Ca2+, Cl- and HA coexisted, the removal rates of Hg(II) and Pb(II) reached 99.71% and 97.95%, respectively. The removal processes of Pb(II) and Hg(II) could be described by pseudo first-order reaction kinetic equations when Ca2+, Cl- and HA existed alone and in combination. The removal rate constant of Pb(II) was the maxinum (0.024 0 min(-1)) when 5 mg x L(-1) HA existed alone, whereas that of Hg(II) was the maximum (0.0169 min(-1)) when 0.80 mmol x L(-1) Ca2+ existed alone.

  3. RESPONSES OF MEMBRANE PROTECTION ENZYME SYSTEM OF TOBACCO LEAVES ON Hg, Cd AND Pb STRESSES IN SOIL%烟草叶片膜保护酶系统对土壤Hg,Cd,Pb胁迫的响应

    Institute of Scientific and Technical Information of China (English)

    严重玲; 林鹏; 王晓蓉

    2002-01-01

    采用盆栽实验,就烟草膜保护酶系统对土壤Hg,Cd,Pb胁迫的响应进行研究.结果表明:随着Hg,Cd,Pb浓度的增加,POD活性逐渐增加,CAT活性逐渐减小,SOD活性在三种元素共同作用时逐渐下降,在元素单一或两两作用时,SOD活性呈单峰曲线,但总体水平仍较低.土壤Hg,Cd,Pb的这种影响表现出三元素共同作用>两两元素作用>单一元素作用.影响的结果造成活性氧产生与清除之间的不平衡,致使相关生理生化过程紊乱.三种重金属对烟草活性氧清除系统的影响表现出明显地协同作用.%Pot experiment was used to study the responses of membrane protection enzyme system of tobac-co loves on Hg, Cd and Pb stresses in soil. The results showed that POD activity gradually increased with in-creasing concetrations of Hg, Cd and Pb. CAT and SOD activity gradually decreased under three heavy metalscommon existing and SOD variation curve showed unimodal curve under single or two elements existing withincrease of concentration of Hg, Cd and Pb. The effects of Hg, Cd and Pb in soil: three elemets together>twoelements together>single element only. The effects resulted in an imbalance -- activated oxygen produce andscavenge and physiological biochemical process disorder. There was a synergistic action for the effect of Hg, Cdand Pb in soil on membrane protection enzyme system in tobacco leaves.

  4. GNAQPMS-Hg v1.0, a global nested atmospheric mercury transport model: model description, evaluation and application to trans-boundary transport of Chinese anthropogenic emissions

    Directory of Open Access Journals (Sweden)

    H. S. Chen

    2014-10-01

    Full Text Available Atmospheric mercury (Hg is a toxic pollutant and can be transported over the whole globe due to its long lifetime in the atmosphere. For the purpose of assessing Hg hemispheric transport and better characterizing regional Hg pollution, a global nested atmospheric Hg transport model (GNAQPMS-Hg has been developed. In GNAQPMS-Hg, the gas and aqueous phase Hg chemistry representing the transformation among three forms of Hg: elemental mercury (Hg(0, divalent mercury (Hg(II, and primary particulate mercury (Hg(P are calculated. A detailed description of the model, including mercury emissions, gas and aqueous phase chemistry, and dry and wet deposition is given in this study. Worldwide observations including extensive data in China have been collected for model evaluation. Comparison results show that the model reasonably simulates the global mercury budget and the spatial–temporal variation of surface mercury concentrations and deposition. Overall, model predictions of annual total gaseous mercury (TGM and wet deposition agree with observations within a factor of two, and within a factor of five for oxidized mercury and dry deposition. The model performs significantly better in North America and Europe than in East Asia. This can probably be attributed to the large uncertainties in emission inventories, coarse model resolution and to the inconsistency between the simulation and observation periods in East Asia. Compared to the global simulation, the nested simulation shows improved skill at capturing the high spatial variability of Hg concentrations and deposition over East Asia. In particular, the root mean square error (RMSE of simulated Hg wet deposition over East Asia is reduced by 24% in the nested simulation. Model sensitivity studies indicate that Chinese primary anthropogenic emissions account for 30 and 62% of surface mercury concentrations and deposition over China, respectively. Along the rim of the western Pacific, the contributions

  5. Concentration, distribution, and translocation of mercury and methylmercury in mine-waste, sediment, soil, water, and fish collected near the Abbadia San Salvatore mercury mine, Monte Amiata district, Italy.

    Science.gov (United States)

    Rimondi, Valentina; Gray, John E; Costagliola, Pilario; Vaselli, Orlando; Lattanzi, Pierfranco

    2012-01-01

    The distribution and translocation of mercury (Hg) was studied in the Paglia River ecosystem, located downstream from the inactive Abbadia San Salvatore mine (ASSM). The ASSM is part of the Monte Amiata Hg district, Southern Tuscany, Italy, which was one of the world's largest Hg districts. Concentrations of Hg and methyl-Hg were determined in mine-waste calcine (retorted ore), sediment, water, soil, and freshwater fish collected from the ASSM and the downstream Paglia River. Concentrations of Hg in calcine samples ranged from 25 to 1500 μg/g, all of which exceeded the industrial soil contamination level for Hg of 5 μg/g used in Italy. Stream and lake sediment samples collected downstream from the ASSM ranged in Hg concentration from 0.26 to 15 μg/g, of which more than 50% exceeded the probable effect concentration for Hg of 1.06 μg/g, the concentration above which harmful effects are likely to be observed in sediment-dwelling organisms. Stream and lake sediment methyl-Hg concentrations showed a significant correlation with TOC indicating considerable methylation and potential bioavailability of Hg. Stream water contained Hg as high as 1400 ng/L, but only one water sample exceeded the 1000 ng/L drinking water Hg standard used in Italy. Concentrations of Hg were elevated in freshwater fish muscle samples and ranged from 0.16 to 1.2 μg/g (wet weight), averaged 0.84 μg/g, and 96% of these exceeded the 0.3 μg/g (methyl-Hg, wet weight) USEPA fish muscle standard recommended to protect human health. Analysis of fish muscle for methyl-Hg confirmed that >90% of the Hg in these fish is methyl-Hg. Such highly elevated Hg concentrations in fish indicated active methylation, significant bioavailability, and uptake of Hg by fish in the Paglia River ecosystem. Methyl-Hg is highly toxic and the high Hg concentrations in these fish represent a potential pathway of Hg to the human food chain.

  6. Concentration, distribution, and translocation of mercury and methylmercury in mine-waste, sediment, soil, water, and fish collected near the Abbadia San Salvatore mercury mine, Monte Amiata district, Italy

    Science.gov (United States)

    Rimondi, V.; Gray, J.E.; Costagliola, P.; Vaselli, O.; Lattanzi, P.

    2012-01-01

    The distribution and translocation of mercury (Hg) was studied in the Paglia River ecosystem, located downstream from the inactive Abbadia San Salvatore mine (ASSM). The ASSM is part of the Monte Amiata Hg district, Southern Tuscany, Italy, which was one of the world’s largest Hg districts. Concentrations of Hg and methyl-Hg were determined in mine-waste calcine (retorted ore), sediment, water, soil, and freshwater fish collected from the ASSM and the downstream Paglia River. Concentrations of Hg in calcine samples ranged from 25 to 1500 μg/g, all of which exceeded the industrial soil contamination level for Hg of 5 μg/g used in Italy. Stream and lake sediment samples collected downstream from the ASSM ranged in Hg concentration from 0.26 to 15 μg/g, of which more than 50% exceeded the probable effect concentration for Hg of 1.06 μg/g, the concentration above which harmful effects are likely to be observed in sediment-dwelling organisms. Stream and lake sediment methyl-Hg concentrations showed a significant correlation with TOC indicating considerable methylation and potential bioavailability of Hg. Stream water contained Hg as high as 1400 ng/L, but only one water sample exceeded the 1000 ng/L drinking water Hg standard used in Italy. Concentrations of Hg were elevated in freshwater fish muscle samples and ranged from 0.16 to 1.2 μg/g (wet weight), averaged 0.84 μg/g, and 96% of these exceeded the 0.3 μg/g (methyl-Hg, wet weight) USEPA fish muscle standard recommended to protect human health. Analysis of fish muscle for methyl-Hg confirmed that > 90% of the Hg in these fish is methyl-Hg. Such highly elevated Hg concentrations in fish indicated active methylation, significant bioavailability, and uptake of Hg by fish in the Paglia River ecosystem. Methyl-Hg is highly toxic and the high Hg concentrations in these fish represent a potential pathway of Hg to the human food chain.

  7. 40 CFR 75.38 - Standard missing data procedures for Hg CEMS.

    Science.gov (United States)

    2010-07-01

    ... reduces the concentration of Hg emitted to the atmosphere (including circulating fluidized bed units that... concentration data have been obtained following initial certification, the owner or operator shall provide substitute data for Hg concentration in accordance with the procedures in ( 75.33(b)(1) through (b)(4...

  8. Differential influences of Cu and Zn chronic exposure on Cd and Hg bioaccumulation in an estuarine oyster.

    Science.gov (United States)

    Liu, Fengjie; Wang, Wen-Xiong

    2014-03-01

    In this study, the effects of Cu and Zn exposure, alone and in combination, on the bioaccumulation of Cd and Hg were investigated in an estuarine oyster Crassostrea hongkongensis under different salinity gradients. We showed that Zn, but not Cu, exposure significantly enhanced the Cd bioaccumulation. In contrast, both Cu and Zn exposure significantly enhanced the Hg bioaccumulation. Combined exposure and salinity did not affect the metal interactions in oysters. The increased tissue concentrations of Cd or Hg were associated with their increased storage in inducible metal-binding ligands (e.g. metallothionein-like proteins, MTLP) by Cu/Zn exposure. The differential roles of Cu and Zn exposure in Cd and Hg bioaccumulation resulted from their contrasting ligand induction and affinities. Analysis of field collected oysters indicated that Cu/Zn exposure was a significant contributor to tissue concentrations of Cd, Cu and Hg. Overall, biochemical/physiological changes of the animals chronically exposed to metal stressors played a key role in affecting tissue concentrations of other metals. One metal's ability to enhance the bioaccumulation of other metals depended upon the relative affinities of the metals for MTLP.

  9. SO2/Hg removal from flue gas by dry FGD

    Institute of Scientific and Technical Information of China (English)

    Wang Fan; Wang Hongmei; Zhang Fan; Zhu Jinwei; Tian Gang; Liu Yu; Mao Jixian

    2012-01-01

    To study the mechanism of SO2 and Hg removal from flue gas,an experimental packed bed reactor was designed to simulate the dry FGD,where a mixture of lime and fly ash in ratio 1∶3 w/w was used as the SO2 and Hg sorbent,and steam at temperature of 100 ℃ was applied for activation of the sorbent,while the activation time set to 20 min.The experimental factors including the SO2/Hg sorbent characteristics,50% breakthrough time for SO2/Hg removal,sorbent packed bed depth and reaction temperature were investigated.The experimental results show that after steam activation,the BET specific surface area and specific pore volume increased from 37.8 to 45.5 m2/g and from 0.42 to 0.51 cm3/g,respectively.With activation of the sorbent by steam,the 50% breakthrough times of SO2 and Hg removal increased from 34 to 42 min and from 23 to 45 min,respectively.When the packed bed depth was increased from 5 to 25 mm,the 50% breakthrough times for Hg and SO2 removal increased from 12 to 52 min and from 6 to 47 min,respectively.With the increase of the reaction temperature,the 50% breakthrough of SO2/Hg removal decreased accordingly.Steam activation can efficiently improve SO2/Hg removal simultaneously.

  10. concentration

    Directory of Open Access Journals (Sweden)

    Seth F. Oppenheimer

    1999-01-01

    Full Text Available We consider a model for biochemical oxygen demand (BOD in a semi-infinite river where the BOD is prescribed by a time varying function at the left endpoint. That is, we study the problem with a time varying boundary loading. We obtain the well-posedness for the model when the boundary loading is smooth in time. We also obtain various qualitative results such as ordering, positivity, and boundedness. Of greatest interest, we show that a periodic loading function admits a unique asymptotically attracting periodic solution. For non-smooth loading functions, we obtain weak solutions. Finally, for certain special cases, we show how to obtain explicit solutions in the form of infinite series.

  11. Removal of Hg{sup 0} from flue gases in wet FGD by catalytic oxidation with air - An experimental study

    Energy Technology Data Exchange (ETDEWEB)

    Andrej Stergarsek; Milena Horvat; Peter Frkal; Jost Stergarsek [' Jozef Stefan' Institute, Ljubljana (Slovenia)

    2010-11-15

    Research efforts are being focused on the development of mercury removal technologies, mainly directed to two alternative approaches: (I) the enhancement of homogeneous oxidation in the flue gases of Hg{sup 0} to water soluble Hg{sup 2+} by the addition of chlorides or bromides to the boiler or; (ii) the adsorption of Hg{sup 2+} and Hg{sup 0} on impregnated activated carbon (AC). A third option gaining more attention lately is based on the oxidation and retention of dissolved Hg{sup 0} in the wet flue gas desulphurisation (FGD) system. The experimental evidence of the present work showed that Hg{sup 0} present in the gaseous phase can be dissolved and oxidized to a high degree (70-90%) by air together with SO{sub 3}{sup 2-} in wet FGD solutions. Transition metals such as Fe{sup 2+} and Mn{sup 2+} act as catalysts, chloride enhances the reaction, while some oxosulphur compounds, e.g. tetrathionate, inhibit the oxidation. A combination of several catalysts at a concentration of sulphite (SO{sub 3}{sup 2-}) below 100 mg L{sup -1} and an adequate redox potential of the solution can assure reasonable mercury removal even in the presence of oxidation inhibiting compounds. The main competitive reactions that govern final Hg{sup 0} removal in the FGD are as follows: (1) oxidation of Hg{sup 0} together with SO{sub 2} with air, enhanced by catalysts; (2) removal of catalysts by precipitation in the form of Fe(OH){sub 3} and eventually as MnO{sub 2} (to overcome this problem continuous addition of catalysts to the solution is required); (3) reduction of Fe{sup 3+} by tetrathionate to Fe{sup 2+} which (4) may reduce Hg{sup 2+} to Hg{sup 0} and probably (5) the complexation of Hg{sup 2+} by anions present which may play an important role in the mechanism by complexing the product(s) of the Hg{sup 0} oxidation reaction. 35 refs., 10 figs., 7 tabs.

  12. Hg localisation in Tillandsia usneoides L. (Bromeliaceae), an atmospheric biomonitor

    Energy Technology Data Exchange (ETDEWEB)

    Filho, G.M.A. [Instituto de Pesquisas Jardim Botanico do Rio de Janeiro (Brazil). Programa Zona Costeira; Andrade, L.R.; Farina, M. [Cidade Universitaria, Rio de Janeiro (Brazil). Instituto de Ciencias Biomedicas, Departamento de Anatomia; Malm, O. [Cidade Universitaria, Rio de Janeiro (Brazil). Instituto de Biofisica Carlos Chagas Filho, Laboratorio de Radioisotopos Eduardo Penna Franca

    2002-07-01

    The Spanish moss, Tillandsia usneoides, has been applied as an atmospheric biomonitor of Hg contamination, although the mechanism of metal plant accumulation has not been understood until now. In the present work, analytical scanning electron microscopy (SEM) was used to localize Hg in T. usneoides exposed to a Hg-air-contaminated area during 15 days. After this period, Hg was determined by the flow injection mercury system, and plants were prepared for SEM observation and energy-dispersive X-ray analysis. A concentration of 2702{+-}318{mu}g Hgg{sup -1} was determined in exposed plants. The presented microanalytical results demonstrated that Hg was partly associated with atmospheric particles deposited upon the plant surface, but it was highly absorbed by the scales, stem and leaves surfaces and less absorbed by epidermal cells of T. usneoides. No Hg was detected in mesophyll parenchyma or in vascular system cells. The great surface adsorption area provided by the scales, in addition to the characteristics of T. usneoides morphology, especially of the node region, are suggested to confer the great capability of T. usneoides in Hg holding. (author)

  13. Mechanistic understanding of MeHg-Se antagonism in soil-rice systems: the key role of antagonism in soil

    Science.gov (United States)

    Wang, Yongjie; Dang, Fei; Evans, R. Douglas; Zhong, Huan; Zhao, Jiating; Zhou, Dongmei

    2016-01-01

    Methylmercury (MeHg) accumulation in rice has great implications for human health. Here, effects of selenium (Se) on MeHg availability to rice are explored by growing rice under soil or foliar fertilization with Se. Results indicate that soil amendment with Se could reduce MeHg levels in soil and grain (maximally 73%). In contrast, foliar fertilization with Se enhanced plant Se levels (3-12 folds) without affecting grain MeHg concentrations. This evidence, along with the distinct distribution of MeHg and Se within the plant, demonstrate for the first time that Se-induced reduction in soil MeHg levels (i.e., MeHg-Se antagonism in soil) rather than MeHg-Se interactions within the plant might be the key process triggering the decreased grain MeHg levels under Se amendment. The reduction in soil MeHg concentrations could be mainly attributed to the formation of Hg-Se complexes (detected by TEM-EDX and XANES) and thus reduced microbial MeHg production. Moreover, selenite and selenate were equally effective in reducing soil MeHg concentrations, possibly because of rapid changes in Se speciation. The dominant role of Se-induced reduction in soil MeHg levels, which has been largely underestimated previously, together with the possible mechanisms advance our mechanistic understanding about MeHg dynamics in soil-rice systems.

  14. Mercury concentrations and pools in four Sierra Nevada forest sites, and relationships to organic carbon and nitrogen

    Directory of Open Access Journals (Sweden)

    D. Obrist

    2009-05-01

    Full Text Available This study presents data on mercury (Hg concentrations, stochiometric relations to carbon (C and nitrogen (N, and Hg pool sizes in four Sierra Nevada forest sites of similar exposure and precipitation regimes, and hence similar atmospheric deposition, to evaluate how ecosystem parameters control Hg retention in ecosystems. In all four sites, the largest amounts of Hg reside in soils which account for 94–98% of ecosystem pools. Hg concentrations and Hg/C ratios increase in the following order: Green Needles/Leavesshow negative correlations between Hg and C (r2=0.58 and N and C (r2=0.64 in decomposing litter, but a positive correlation between litter Hg and N (r2=0.70. These inverse relations may reflect preferential retention of N and Hg over C during decomposition, or may be due to older age of decomposed litter layers which are exposed to longer-term atmospheric Hg deposition in the field. The results indicate that litter Hg levels depend on decomposition stage and may not follow generally observed positive relationships between Hg and organic C.

    Mineral soil layers show strong positive correlations of Hg to C across all sites and soil horizons (r2=0.83, but Hg concentrations are even more closely related to N with a similar slope to that observed in litter (r2=0.92. Soil N levels alone explain over 90% of Hg pool sizes across the four Sierra Nevada forest sites. This suggests that soil organic N and C groups provide sorption sites for Hg to retain atmospheric deposition. However, the patterns could be due to indirect relationships where high soil N and C levels reflect high ecosystem productivity which leads to corresponding high atmospheric Hg deposition inputs via leaf litterfall and plant senescence. Our results also show that two of the sites previously affected by

  15. Mercury concentrations and pools in four Sierra Nevada forest sites, and relationships to organic carbon and nitrogen

    Directory of Open Access Journals (Sweden)

    D. Obrist

    2009-02-01

    Full Text Available This study presents data on Hg concentrations, stochiometric relations to carbon (C and nitrogen (N, and Hg pool sizes in four Sierra Nevada forest sites of similar exposure and precipitation regimes, and hence similar atmospheric deposition, to evaluate how ecosystem parameters control Hg retention in ecosystems. In all four sites, the largest amounts of Hg reside in soils which account for 94–98% of ecosystem pools. Hg concentrations and Hg/C ratios increase in the following order: Green Needles/Leaves < Dry Needles/Leaves < Oi litter < Oe litter < Oa litter. Stochiometric relations show negative correlations between Hg and C (r2=0.58 and N and C (r2=0.64 in decomposing litter, but a positive correlation between litter Hg and N (r2=0.70. These inverse relations may reflect preferential retention of N and Hg over C during decomposition, or may be due to older age of decomposed litter layers which are exposed to longer-term atmospheric Hg deposition in the field. The results indicate that litter Hg levels depend on decomposition stage and may not follow generally observed positive relationships between Hg and organic C.

    Mineral soil layers show strong positive correlations of Hg to C across all sites and soil horizons (r2=0.83, but Hg concentrations are even more closely related to N with a similar slope to that observed in litter (r2=92%. Soil N levels alone explain over 90% of Hg pool sizes across the four Sierra Nevada forest sites. This suggest that soil organic N and C groups provide sorption sites for Hg to retain atmospheric deposition. However, the patterns could be due indirect relationships where high soil N and C levels reflect high ecosystem productivity which leads to corresponding high atmospheric Hg deposition inputs via leaf litterfall and plant senescence. Our results also show that two of the sites previously affected by

  16. Influence of humic acid on adsorption of Hg(II) by vermiculite.

    Science.gov (United States)

    do Nascimento, Fernando Henrique; Masini, Jorge Cesar

    2014-10-01

    Geochemical mobility of Hg(II) species is strongly affected by the interactions of these compounds with naturally occurring adsorbents such as humic acids, clay minerals, oxides, etc. Interactions among these sorbents affect their affinity for Hg(II) and a full understanding of these processes is still lacking. The present work describes the influence of a humic acid (HA) sample on the adsorption of Hg(II) by vermiculite (VT). Adsorption isotherms were constructed to evaluate the affinity of Hg(II) by VT, HA, VT modified with humic acid (VT-HA), and VT-HA in presence of soluble humic acid (VT-HA + HA). All experiments were made at pH 6.0 ± 0.1 in 0.02 M NaNO3 and 25.0 ± 0.5 °C for initial Hg(II) concentrations from 1.0 to 100 μM. Determinations of Hg(II) were made by square wave voltammetry automated by sequential injection analysis, an approach that enables the determination of the free plus labile fractions of Hg(II) in HA suspensions without the need for laborious separation steps. The adsorption isotherms were fitted to Langmuir and Freundlich equations, showing that HA was the material with the higher adsorption capacity (537 ± 30 μmol g(-1)) in comparison with VT and VT-HA (44 ± 3 and 51 ± 11 μmol g(-1), respectively). Adsorption order was HA > VT-HA + HA > VT = VT-HA. At pH 6.0 the interaction of HA with VT is weak and only 14% of C initially added to the suspension was effectively retained by the mineral. Desorption of Hg(II) in acidic medium (0.05 M HCl) was higher in binary (VT-HA) and ternary (VT-HA + HA) systems in comparison with that of VT and HA alone, suggesting that interactions between VT and HA are facilitated in acidic medium, weakening the binding to Hg(II).

  17. Incorporation of inorganic mercury (Hg2+) in pelagic food webs of ultraoligotrophic and oligotrophic lakes: the role of different plankton size fractions and species assemblages

    Science.gov (United States)

    Soto Cárdenas, Carolina; Diéguez, Maria C.; Ribeiro Guevara, Sergio; Marvin-DiPasquale, Mark; Queimaliños, Claudia P.

    2014-01-01

    In lake food webs, pelagic basal organisms such as bacteria and phytoplankton incorporate mercury (Hg2+) from the dissolved phase and pass the adsorbed and internalized Hg to higher trophic levels. This experimental investigation addresses the incorporation of dissolved Hg2+ by four plankton fractions (picoplankton: 0.2–2.7 μm; pico + nanoplankton: 0.2–20 μm; microplankton: 20–50 μm; and mesoplankton: 50–200 μm) obtained from four Andean Patagonian lakes, using the radioisotope 197Hg2+. Species composition and abundance were determined in each plankton fraction. In addition, morphometric parameters such as surface and biovolume were calculated using standard geometric models. The incorporation of Hg2+ in each plankton fraction was analyzed through three concentration factors: BCF (bioconcentration factor) as a function of cell or individual abundance, SCF (surface concentration factor) and VCF (volume concentration factor) as functions of individual exposed surface and biovolume, respectively. Overall, this investigation showed that through adsorption and internalization, pico + nanoplankton play a central role leading the incorporation of Hg2+ in pelagic food webs of Andean lakes. Larger planktonic organisms included in the micro- and mesoplankton fractions incorporate Hg2+ by surface adsorption, although at a lesser extent. Mixotrophic bacterivorous organisms dominate the different plankton fractions of the lakes connecting trophic levels through microbial loops (e.g., bacteria–nanoflagellates–crustaceans; bacteria–ciliates–crustaceans; endosymbiotic algae–ciliates). These bacterivorous organisms, which incorporate Hg from the dissolved phase and through their prey, appear to explain the high incorporation of Hg2+ observed in all the plankton fractions.

  18. Phytoextraction of HG by parsley (Petroselinum crispum) and its growth responses.

    Science.gov (United States)

    Bibi, Asma; Farooq, Umar; Naz, Sadia; Khan, Afsar; Khan, Sara; Sarwar, Rizwana; Mahmood, Qaisar; Alam, Arif; Mirza, Nosheen

    2016-01-01

    The effect of mercury (Hg) on the growth and survival of parsley (Petroselinum crispum) was explored at various treatments. The plants were grown in pots having Hoagland's solution to which various Hg treatments were applied and placed under greenhouse conditions. The treatments were: no metal applied (control) and six doses of Hg as mercuric chloride for 15 days. Linear trend of Hg accumulation was noted in roots, stems, and leaves with increasing Hg treatments. The maximum Hg concentration in root, stem and leaf was 8.92, 8.27, and 7.88 at Hg treatments of 25 mg l(-1), respectively. On the whole, Hg accumulation in different plant parts was in the following order: leaves > stem > roots. Linear trend was also observed for Bioaccumulation Factor (BF) and Translocation Factor (TF) with increasing Hg concentrations in the growth medium. The highest respective BFHg and TFHg values were 9.32 and 2.02 for the Hg treatments of 25 and 50 mg l(-1). In spite of the reduced growth in the presence of Hg, the plant has phytoremediation potential. It is recommended that parsley should not be cultivated in Hg contaminated sites in order to avoid dietary toxicity.

  19. Mercury and methylmercury concentrations in high altitude lakes and fish (Arctic charr) from the French Alps related to watershed characteristics.

    Science.gov (United States)

    Marusczak, Nicolas; Larose, Catherine; Dommergue, Aurélien; Paquet, Serge; Beaulne, Jean-Sébastien; Maury-Brachet, Régine; Lucotte, Marc; Nedjai, Rachid; Ferrari, Christophe P

    2011-04-15

    Total mercury (THg) and methylmercury (MeHg) concentrations were measured in the muscle of Arctic charr (Salvelinus alpinus) and in the water column of 4 lakes that are located in the French Alps. Watershed characteristics were determined (6 coverage classes) for each lake in order to evaluate the influence of watershed composition on mercury and methylmercury concentrations in fish muscle and in the water column. THg and MeHg concentrations in surface water were relatively low and similar among lakes and watershed characteristics play a major role in determining water column Hg and MeHg levels. THg muscle concentrations for fish with either a standardized length of 220mm, a standardized age of 5 years or for individualuals did not exceed the 0.5mg kg(-1) fish consumption advisory limit established for Hg by the World Health Organization (WHO, 1990). These relatively low THg concentrations can be explained by watershed characteristics, which lead to short Hg residence time in the water column, and also by the short trophic chain that is characteristic of mountain lakes. Growth rate did not seem to influence THg concentrations in fish muscles of these lakes and we observed no relationship between fish Hg concentrations and altitude. This study shows that in the French Alps, high altitude lakes have relatively low THg and MeHg concentrations in both the water column and in Arctic charr populations. Therefore, Hg does not appear to present a danger for local populations and the fishermen of these lakes.

  20. Sexual difference in mercury concentrations of lake trout (Salvelinus namaycush) from Lake Ontario

    Science.gov (United States)

    Madenjian, C.P.; Keir, M.J.; Whittle, D.M.

    2011-01-01

    We determined total mercury (Hg) concentrations in 50 female lake trout (Salvelinus namaycush) and 69 male lake trout from Lake Ontario (Ontario, Canada and New York, United States). Results showed that, on average, males were 8% higher in Hg concentration than females in Lake Ontario. We also used bioenergetics modeling to determine whether a sexual difference in gross growth efficiency (GGE) could explain the observed sexual difference in Hg concentrations. According to the bioenergetics modeling results, male GGE was about 3% higher than female GGE, on average. Although the bioenergetics modeling could not explain the higher Hg concentrations exhibited by the males, a sexual difference in GGE remained a plausible explanation for the sexual difference in Hg concentrations of the lake trout. In an earlier study, male lake trout from Lake Ontario were found to be 22% higher in polychlorinated biphenyl (PCB) concentration than females from Lake Ontario. Thus, although males were higher in both Hg and PCB concentrations, the degree of the sexual difference in concentration varied between the two contaminants. Further research on sexual differences in Hg excretion rates and Hg direct uptake rates may be needed to resolve the disparity in results between the two contaminants.

  1. Lupinus albus plants acquire mercury tolerance when inoculated with an Hg-resistant Bradyrhizobium strain.

    Science.gov (United States)

    Quiñones, Miguel A; Ruiz-Díez, Beatriz; Fajardo, Susana; López-Berdonces, Miguel A; Higueras, Pablo L; Fernández-Pascual, Mercedes

    2013-12-01

    One strain of Bradyrhizobium canariense (L-7AH) was selected for its metal-resistance and ability to nodulate white lupin (Lupinus albus L.) plants, from a collection of rhizobial strains previously created from soils of the Almadén mining district (Spain) with varying levels of Hg contamination. Plants were inoculated with either strain L-7AH (Hg-tolerant) or L-3 (Hg-sensitive, used as control), and watered with nutrient solutions supplemented with various concentrations (0-200 μM) of HgCl2 in a growth chamber. L. albus inoculated with L-7AH were able to nodulate even at the highest concentration of Hg while those inoculated with L-3 had virtually no nodules at Hg concentrations above 25 μM. Plants inoculated with L-7AH, but not those with the control strain, were able to accumulate large amounts of Hg in their roots and nodules. Nodulation with L-7AH allowed plants to maintain constant levels of both chlorophylls and carotenoids in their leaves and a high photosynthetic efficiency, whereas in those inoculated with L-3 both pigment content and photosynthetic efficiency decreased significantly as Hg concentration increased. Nitrogenase activity of plants nodulated with L-7AH remained fairly constant at all concentrations of Hg used. Results suggest that this symbiotic pair may be used for rhizoremediation of Hg-contaminated soils. Copyright © 2013 Elsevier Masson SAS. All rights reserved.

  2. Ultrasound-induced gelation of fluorenyl-9-methoxycarbonyl-l-lysine(fluorenyl-9-methoxycarbonyl)-OH and its dipeptide derivatives showing very low minimum gelation concentrations.

    Science.gov (United States)

    Geng, Huimin; Ye, Lin; Zhang, Ai-Ying; Shao, Ziqiang; Feng, Zeng-Guo

    2017-03-15

    Four l-Lysine(Lys)-l-glutamic acid(Glu) dipeptide derivatives (1-4) and their precursor-a single fluorenyl-9-methoxycarbonyl(Fmoc)-l-Lys(Fmoc)-OH amino acid (5) were demonstrated as gelators to gelate a variety of alcohols and aromatic solvents under the sonication conditions. Compared to the routine heating-cooling protocol, the ultrasound substantially brought down the minimum gelation concentrations (MGCs) of the resulting organogels. The Fourier transform infrared spectroscopy (FT-IR) and fluorescence studies revealed that the π-π stacking and hydrogen bonding act as major driving forces for the self-assembly of these lysine-based gelators into supramolecular fibrous three dimensional (3D) network, where the more the Fmoc protecting groups, the gelators are more responsive to ultrasound-stimulus and more conducive to an ordered molecular arrangement reinforcing the intermolecular forces. Moreover, the ultrasound-triggered organogels of 5 exhibited the thixotropic property. Upon imposing a mechanical shear, its gels with the fibrous 3D network structure were unraveled into sols. However, after standing quiescently over time, these sols returned to the gels showing a more ordered lamella-like packing structure as evidenced by scanning electron microscopy (SEM) and X-ray diffraction (XRD) analyses.

  3. Observations of atmospheric Hg species and depositions in remote areas of China

    Directory of Open Access Journals (Sweden)

    Feng X.

    2013-04-01

    Full Text Available From September 2007, we conducted continuous measurements of speciated atmospheric mercury (Hg and atmospheric mercury depositions at five remote sites in China. Four of these sites were involved in the Global Mercury Observation System (GMOS as ground-based stations. These stations were located in the northwest, southwest, northeast, and east part of China, respectively, which represent the regional atmospheric Hg budgets in different areas of China. The preliminary results showed that mean TGM concentrations were in the range of 1.60 – 2.88 ng m-3, with relatively higher levels observed at sites in Eastern China and Southwestern China and lower levels at sites in Northeastern and Northwestern China. TGM concentrations at remote sites of China were also higher than those reported from background sites in North America and Europe, and this is corresponding very well with the Chinese great anthropogenic Hg emissions. Gaseous oxidized mercury (GOM and particulate bounded mercury (PBM were in the ranges of 3.2 – 7.4 pg m−3 and 19.4 – 43.5 pg m-3, respectively. The preliminary result on precipitation showed mean precipitation THg concentrations were in the range of 2.7 – 18.0 ng L-1.

  4. Resonance Scattering Detection of Trace Hg2+ Using Aptamer-modified AuPd Nanoalloy Probe as Catalyst

    Institute of Scientific and Technical Information of China (English)

    刘庆业; 范燕燕; 梁爱惠; 蒋治良

    2011-01-01

    The 5 nm AuPd nanoalloy in mole ratio of Au:Pd=32 : 1 was prepared, using sodium citrate as the stabilizing agent and NaBH4 as the reductant. The AuPd nanoalloy was modified by the aptamer to prepare an aptamer- AuPd (AptAuPd) probe for resonance scattering (RS) detection of 5.(Y-1250 nmol/L Hg2+. The AptAuPd-Hg2+ aptamer reaction solution was filtrated by membrane, and the AptAuPd in the filtrate exhibited strong catalytic ef- fect on the slow NiP particle reaction between NiCI2 and NaHzPO2, and the NiP particles showed a RS peak at 508 nm. The RS intensity decreased when Hg2+ concentration increased. The decreased RS intensity was linear to Hg2+ concentration in the range of 0.5--1250 nmol/L. The RS assays were used to determine Hg2+ in real samples, with good results.

  5. Assessment of Cu, Pb and Hg Contamination in Bottom Sediments Of Surface Water in XuZhou

    Institute of Scientific and Technical Information of China (English)

    王晓; 韩宝平; 朱雪强

    2004-01-01

    Pollution of heavy metals Cu,Pb and Hg is assessed using geo-accumulation index in this paper. The result shows that the bottom sediments of surface water in Xuzhou is polluted by these heavy metals to deferent degrees, of which the Jinma River is the most serious, and then the Kuihe River, the abandoned Yellow River, and the Jinghang Canal. The Yunlong Lake has also been polluted by Hg. The three kinds of heavy metals in the order of concentration is Hg>Cu>Pb. The pollution degree and the type of element is closely related with industrial structure in Xuzhou.

  6. A simultaneous multiple species acute toxicity test comparing relative sensitivities of six aquatic organisms to HgCl{sub 2}

    Energy Technology Data Exchange (ETDEWEB)

    McCrary, J.E.; Heagler, M.G. [McNeese State Univ., Lake Charles, LA (United States). Dept. of Biological and Environmental Science

    1995-12-31

    In the last few years there has been concern in the scientific community about observed declines in some amphibian species. These population declines could be reflecting a global phenomenon due to a general class sensitivity or may be part of a natural cycle. The suggestion of an overall greater sensitivity of amphibians is not supported. Studies show that amphibians, as a class, are neither more or less susceptible than fish to environmental conditions. Mercury has been found to be one of the most toxic of the heavy metals introduced into amphibian breeding waters. Six aquatic species were simultaneously exposed in a comparative acute toxicity test with mercury chloride: three amphibians, Rana catesbeiana (bullfrog), R. clamitans (green frog), and R. sphenocephala (southern leopard frog, formally classified as R. utricularia); two fish, Gambusia affinis (mosquitofish) and Notemigonus crysoleucas (golden shiner); one aquatic aligochaete, Lumbriculus variegatus (aquatic earthworm). The five test concentrations used were 1.4, 3.9, 12.0, 110.0, and 487.0 {micro}g Hg/L respectively. Ten organisms per species were randomly placed into the six test tanks (control and five concentrations), each species in a separate chamber. The resultant LC50-96hr values produced the following rank order: R. sphenocephala, 6.59 {micro}g Hg/L; R. clamitans, 14.7 {micro}g Hg/L; N. crysoleucas, 16.75 {micro}g Hg/L; L. variegatus, 43.72,ug Hg/L; G. affinis, 52.62 {micro}g Hg/L; R. catesbeiana, 63.36 {micro}g Hg/L. No general organism class sensitivity trend, for amphibians, was developed from this data, contrary to the implicit suggestions of some researchers.

  7. Impacts of TCDD and MeHg on DNA methylation in zebrafish (Danio rerio) across two generations.

    Science.gov (United States)

    Olsvik, Pål A; Williams, Timothy D; Tung, Hui-shan; Mirbahai, Leda; Sanden, Monica; Skjaerven, Kaja H; Ellingsen, Ståle

    2014-09-01

    This study aimed to investigate whether dioxin (TCDD) and methylmercury (MeHg) pose a threat to offspring of fish exposed to elevated concentrations of these chemicals via epigenetic-based mechanisms. Adult female zebrafish were fed diets added either 20 μg/kg 2,3,7,8 TCDD or 10 mg/kg MeHg for 47 days, or 10 mg/kg 5-aza-2'-deoxycytidine (5-AZA), a hypomethylating agent, for 32 days, and bred with unexposed males in clean water to produce F1 and F2 offspring. Global DNA methylation, promoter CpG island methylation and target gene transcription in liver of adult females and in 3 days post fertilization (dpf) F1 and F2 embryos were determined with HPLC, a novel CpG island tiling array containing 54,933 different probes and RT-qPCR, respectively. The results showed that chemical treatment had no significant effect on global DNA methylation levels in F1 (MeHg and TCDD) and F2 (MeHg) embryos and only a limited number of genes were identified with altered methylation levels at their promoter regions. CYP1A1 transcription, an established marker of TCDD exposure, was elevated 27-fold in F1 embryos compared to the controls, matching the high levels of CYP1A1 expression observed in F0 TCDD-treated females. This suggests that maternal transfer of TCDD is a significant route of exposure for the F1 offspring. In conclusion, the selected doses of TCDD and MeHg, two chemicals often found in high concentrations in fish, appear to have only modest effects on DNA methylation in F1 (MeHg and TCDD) and F2 (MeHg) embryos of treated F0 females.

  8. Bioaccumulation of Hg in the mushroom Pleurotus ostreatus

    Energy Technology Data Exchange (ETDEWEB)

    Bressa, G.; Cima, L.; Costa, P.

    1988-10-01

    The possibility of utilizing industrial, urban, and other wastes for the growth of a product which is directly edible by humans is fascinating. However, it is possible that many wastes containing toxic substances, for example, heavy metals, could reach the food chain and produce adverse effects on human health. To this end, we studied the possibility of bioaccumulation of Hg by a mushroom, Pleurotus ostreatus, grown on an artificial compost containing this element. Concentrations of 0.05, 0.1, and 0.2 mg/kg of Hg as Hg(NO/sub 3/)/sub 2/.H/sub 2/O were added to three groups of the same compost, successively inoculated with the mycelia of the mushroom. Higher concentrations strongly reduced the growth of the mycelia and therefore were not utilized. The concentrations of Hg in the substrate and in the mushroom were evaluated by AAS. The range of the accumulation factor was found to be 65-140, i.e., very marked. This finding suggests that the cultivation of P. ostreatus on substrates containing Hg from industrial and urban wastes could involve possible risks to human health.

  9. Spatial distribution and accumulation of Hg in soil surrounding a Zn/Pb smelter.

    Science.gov (United States)

    Wu, Qingru; Wang, Shuxiao; Wang, Long; Liu, Fang; Lin, Che-Jen; Zhang, Lei; Wang, Fengyang

    2014-10-15

    Nonferrous metal smelting is an important atmospheric mercury (Hg) emission source that has significant local and global impacts. To quantify the impact of Hg emission from non-ferrous metal smelter on the surrounding soil, an integrated model parameterizing the processes of smelter emission, air dispersion, atmospheric deposition and Hg accumulation in soil was developed. The concentrations of gaseous elemental Hg (GEM) around the smelter and the spatial distribution of Hg in the surrounding soil were measured and compared with the model results. Atmospheric deposition of Hg emitted from the smelter was identified as the main source of Hg accumulation in the surrounding soil. From 1960 to 2011, the smelter emitted approximately 105 t of Hg into the atmosphere, of which 15 t deposited locally and resulted in an increase of Hg concentration in soil from 0.12 to 1.77 mg kg(-1). A detailed examination of wind rose and model data suggested that the area within 1.0-1.5 km northwest and southeast of the smelter was most severely impacted. It was estimated that the smelter operation from 1969 to 1990, when large scale emission controls were not implemented, resulted in 6450 μg m(-2)yr(-1) of Hg net deposition and a model simulated increase of 0.40 mg kg(-1) of Hg accumulation in the soil. During the period from 1991 to 2011, atmospheric Hg emission from the smelter alone increased the average concentration in soil from 0.41 mg kg(-1) to 0.45 mg kg(-1). In the past 50 years, over 86% of Hg emitted from this smelter went into the global pool, indicating the importance of controlling Hg emissions from non-ferrous metal smelters.

  10. Maps showing anomalous concentrations of zinc, silver, antimony, manganese, barium and strontium in stream sediment and heavy-mineral concentrate from parts of the Ajo and Lukeville 1 degree by 2 degrees quadrangles, Arizona

    Science.gov (United States)

    Theobald, P.K.; Barton, H.N.

    1988-01-01

    This map is part of a folio of maps of the Ajo and Lukeville 1 degree x 2 degrees quadrangles, Arizona, prepared under the Conterminous United States Mineral Assessment Program. Other publications in this folio include U.S. Geological Survey Open-File Reports 82-419 (Barton and others, 1982), 82-599 (Klein, 1982), and 830734 (Theobald and Barton, 1983), and Miscellaneous Field Studies Maps MF-1834-A (Peterson and Tosdal, 1986), MF-1834-B (Peterson and others, 1987), MF-1834-C (Theobald and Barton, 1987), and MF-1834-D (Theobald and Barton, 1988). Open-File Reports 82-419 and 83-734 constitute the basic data and initial interpretation on which this discussion is predicated. MF-1834-C and D show the distributions of anomalous concentrations of copper, lead, molybdenum, bismuth, and tungsten.

  11. A double-stage tube furnace--acid-trapping protocol for the pre-concentration of mercury from solid samples for isotopic analysis.

    Science.gov (United States)

    Sun, Ruoyu; Enrico, Maxime; Heimbürger, Lars-Eric; Scott, Clint; Sonke, Jeroen E

    2013-08-01

    High-precision mercury (Hg) stable isotopic analysis requires relatively large amounts of Hg (>10 ng). Consequently, the extraction of Hg from natural samples with low Hg concentrations (CO2, SO2, etc. The O2 carrier gas, including combustion products and elemental Hg, is then purged into a 40% (v/v) acid-trapping solution. The method was optimized by assessing the variations of Hg pre-concentration efficiency and Hg isotopic compositions as a function of acid ratio, gas flow rate, and temperature ramp rate for two certified reference materials of bituminous coals. Acid ratios of 2HNO3/1HCl (v/v), 25 mL/min O2 flow rate, and a dynamic temperature ramp rate (15 °C/min for 25-150 and 600-900 °C; 2.5 °C/min for 150-600 °C) were found to give optimal results. Hg step-release experiments indicated that significant Hg isotopic fractionation occurred during sample combustion. However, no systematic dependence of Hg isotopic compositions on Hg recovery (81-102%) was observed. The tested 340 samples including coal, coal-associated rocks, fly ash, bottom ash, peat, and black shale sediments with Hg concentrations varying from <5 ng/g to 10 μg/g showed that most Hg recoveries were within the acceptable range of 80-120%. This protocol has the advantages of a short sample processing time (∼3.5 h) and limited transfer of residual sample matrix into the Hg trapping solution. This in turn limits matrix interferences on the Hg reduction efficiency of the cold vapor generator used for Hg isotopic analysis.

  12. Capability of Catfish (Clarias gariepinus to Accumulate Hg2+ From Water

    Directory of Open Access Journals (Sweden)

    Heny Suseno

    2015-12-01

    Full Text Available Mercury is hazardous contaminant that can be accumulated by aquatic organisms such as fishes, mussels etc. Catfish is one of source of animal protein but it also can accumulate Hg2+ from water that used in aquaculture. Due to less information about capability of catfish to accumulate Hg2+, therefore we studied bioaccumulation of Hg2+ that used biokinetic approach (aqueous uptake-rate, and elimination-rate.  Nuclear application technique was applied in this study by using radiotracer of 203Hg.  A simple kinetic model was then constructed to predict the bioaccumulation capability of   by catfish. The result of experiments were shown that the uptake rate of difference Hg2+ concentration were 79.90 to 101.22 ml.g-1.d-1. Strong correlation between uptake rates with increasing Hg2+concentration. In addition, the elimination rates were range 0.080 – 0.081 day-1. The biology half time (t1/2b of Hg2+ in whole body catfish were 8.50 – 8.63 days.  However, no clear correlation  between elimination rate with increasing concentration of Hg2+. The calculation of Bio Concentration Factor (BCF shown catfish have capability to accumulated Hg maximum 1242.69 time than its concentration in water

  13. An analytical protocol for the determination of total mercury concentrations in solid peat samples.

    Science.gov (United States)

    Roos-Barraclough, F; Givelet, N; Martinez-Cortizas, A; Goodsite, M E; Biester, H; Shotyk, W

    2002-06-20

    Traditional peat sample preparation methods such as drying at high temperatures and milling may be unsuitable for Hg concentration determination in peats due to the possible presence of volatile Hg species, which could be lost during drying. Here, the effects of sample preparation and natural variation on measured Hg concentrations are investigated. Slight increases in mercury concentrations were observed in samples dried at room temperature and at 30 degrees C (6.7 and 2.48 ng kg(-1) h(-1), respectively), and slight decreases were observed in samples dried at 60, 90 and 105 degrees C (2.36, 3.12 and 8.52 ng kg(-1) h(-1), respectively). Fertilising the peat slightly increased Hg loss (3.08 ng kg(-1) h(-1) in NPK-fertilised peat compared to 0.28 ng kg(-1) h(-1) in unfertilised peat, when averaged over all temperatures used). Homogenising samples by grinding in a machine also caused a loss of Hg. A comparison of two Hg profiles from an Arctic peat core, measured in frozen samples and in air-dried samples, revealed that no Hg losses occurred upon air-drying. A comparison of Hg concentrations in several plant species that make up peat, showed that some species (Pinus mugo, Sphagnum recurvum and Pseudevernia furfuracea) are particularly efficient Hg retainers. The disproportionally high Hg concentrations in these species can cause considerable variation in Hg concentrations within a peat slice. The variation of water content (1.6% throughout 17-cm core, 0.97% in a 10 x 10 cm slice), bulk density (40% throughout 17-cm core, 15.6% in a 10 x 10 cm slice) and Hg concentration (20% in a 10 x 10 cm slice) in ombrotrophic peat were quantified in order to determine their relative importance as sources of analytical error. Experiments were carried out to determine a suitable peat analysis program using the Leco AMA 254, capable of determining mercury concentrations in solid samples. Finally, an analytical protocol for the determination of Hg concentrations in solid peat samples

  14. Synthesis of undoped and manganese-doped hgte nanoparticles using [Hg(TeCH2CH2NMe2)2] as a single source precursor.

    Science.gov (United States)

    Kedarnath, Gotluru; Dey, Sandip; Jain, Vimal K; Dey, Gautam K; Kadam, Ramakant M

    2008-09-01

    The Reaction of [HgCl2(tmeda)] with NaTeCH2CH2NMe2 gave a mercury tellurolate, [Hg(TeCH2CH2. NMe2)2] (1) as a yellow crystalline solid, which was characterized by elemental analysis, UV-vis, mass and NMR (1H, 13C, 125Te, 199Hg) spectroscopy. Thermolysis of 1 in hexadecylamine (HDA) at 90 degrees C in the absence and presence of Mn(OAc)2.4H2O gave undoped and Mn-doped HgTe nanoparticles which were characterized by XRD, EDAX, TEM, EPR and magnetic measurements. These particles could be synthesized with mean particle size of 6-7 nm (from TEM). Manganese substitution at Hg site in HgTe lead to a linear decrease in lattice parameter with increasing concentration of Mn. Magnetization measurements showed ferromagnetic ordering at room temperature with very small coercive field (Hc, 50 Oe) for Hg0.973 Mn0.027 Te sample. This sample also exhibited distinct ferromagnetic resonance (FMR) in the EPR spectrum.

  15. Highly enhanced adsorption for the removal of Hg(II) from aqueous solution by Mercaptoethylamine/Mercaptopropyltrimethoxysilane functionalized vermiculites.

    Science.gov (United States)

    Tran, Lytuong; Wu, Pingxiao; Zhu, Yajie; Yang, Lin; Zhu, Nengwu

    2015-05-01

    Vermiculites modified with Mercaptoethylamine (MEA) and 3-Mercaptopropyltrimethoxysilane (MPTMS) were used as effective adsorbents for the removal of Hg(II) from aqueous solution. The physicochemical characteristics of the pristine and functionalized vermiculites were analyzed by XRD, BET, FTIR, SEM, TEM and Zeta potentials, confirming that the vermiculite was successfully functionalized by the organic ligands containing the thiol (SH) metal-chelating groups. Batch adsorption experiments demonstrated that the factors such as initial pH, contact time, temperature, coexisting cations and initial Hg(II) concentration could significantly influence the adsorption behaviors typically for VER and MEA-VER, whereas the adsorption capacity of MPTMS-VER showed negligible dependence on such factors. The maximum adsorption capacity of Hg(II) ions was greatly improved after functionalization, which was in the order of MPTMS-VER>MEA-VER>VER (286.29 μg g(-1), 176.33 μg g(-1), 99.95 μg g(-1), respectively). The adsorption isotherm could be well described with Langmuir model and the kinetic studies indicated that the adsorption process fitted well with the pseudo-second-order model. The calculated thermodynamic parameters suggested that the adsorption process was feasible and spontaneous. The adsorption mechanism of Hg(II) on thiol groups was studied through XPS analysis. Considering the favorable adsorption capacities, thiol-functionalized vermiculites show a promising application in the removal of Hg(II) from wastewater.

  16. Process of [sup 196]Hg enrichment

    Science.gov (United States)

    Grossman, M.W.; Mellor, C.E.

    1993-04-27

    A simple rate equation model shows that by increasing the length of the photochemical reactor and/or by increasing the photon intensity in said reactor, the feedstock utilization of [sup 196]Hg will be increased. Two preferred embodiments of the present invention are described, namely (1) long reactors using long photochemical lamps and vapor filters; and (2) quartz reactors with external UV reflecting films. These embodiments have each been constructed and operated, demonstrating the enhanced utilization process dictated by the mathematical model (also provided).

  17. Process of .sup.196 Hg enrichment

    Science.gov (United States)

    Grossman, Mark W.; Mellor, Charles E.

    1993-01-01

    A simple rate equation model shows that by increasing the length of the photochemical reactor and/or by increasing the photon intensity in said reactor, the feedstock utilization of .sup.196 Hg will be increased. Two preferred embodiments of the present invention are described, namely (1) long reactors using long photochemical lamps and vapor filters; and (2) quartz reactors with external UV reflecting films. These embodiments have each been constructed and operated, demonstrating the enhanced utilization process dictated by the mathematical model (also provided).

  18. Identifying the sources and processes of mercury in subtropical estuarine and ocean sediments using Hg isotopic composition.

    Science.gov (United States)

    Yin, Runsheng; Feng, Xinbin; Chen, Baowei; Zhang, Junjun; Wang, Wenxiong; Li, Xiangdong

    2015-02-03

    The concentrations and isotopic compositions of mercury (Hg) in surface sediments of the Pearl River Estuary (PRE) and the South China Sea (SCS) were analyzed. The data revealed significant differences between the total Hg (THg) in fine-grained sediments collected from the PRE (8-251 μg kg(-1)) and those collected from the SCS (12-83 μg kg(-1)). Large spatial variations in Hg isotopic compositions were observed in the SCS (δ(202)Hg, from -2.82 to -2.10‰; Δ(199)Hg, from +0.21 to +0.45‰) and PRE (δ(202)Hg, from -2.80 to -0.68‰; Δ(199)Hg, from -0.15 to +0.16‰). The large positive Δ(199)Hg in the SCS indicated that a fraction of Hg has undergone Hg(2+) photoreduction processes prior to incorporation into the sediments. The relatively negative Δ(199)Hg values in the PRE indicated that photoreduction of Hg is not the primary route for the removal of Hg from the water column. The riverine input of fine particles played an important role in transporting Hg to the PRE sediments. In the deep ocean bed of the SCS, source-related signatures of Hg isotopes may have been altered by natural geochemical processes (e.g., Hg(2+) photoreduction and preferential adsorption processes). Using Hg isotope compositions, we estimate that river deliveries of Hg from industrial and urban sources and natural soils could be the main inputs of Hg to the PRE. However, the use of Hg isotopes as tracers in source attribution could be limited because of the isotope fractionation by natural processes in the SCS.

  19. Prevention of La3+ on DNA Damage Caused by Hg2+ from Fish Intestines

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    The aim of this study was to investigate the effects of rare earth elements (REEs) in preventing Hg2+ pollution, using fish intestinal DNA in vitro and study the mechanism of the interactions between Hg2+, La3+, the mixture of La3+ and Hg2+ and DNA by spectroscopy. The interactions between Hg2+, La3+, the mixture of La3+ and Hg2+ and DNA from fish intestine in vitro was investigate by using absorption spectrum and fluorescence emission spectrum. Ultraviolet absorption spectra indicated that the addition of Hg2+, La3+, and the mixture of La3+ and Hg2+ to DNA generated obvious hypochromic effect. Meanwhile, the 205.2 nm peak of DNA blue and the 258.2 nm peak of DNA red shifted. The hypochromic effect and peak shift was caused by these ions in an order of Hg2+>Hg2++La3+>La3+. The fluorescence emission spectra showed that as the addition of Hg2+, La3+, and the mixture of La3+ and Hg2+, the emission peak at about 416.2 nm of DNA did not obviously change, but the fluorescence intensity reduced gradually with the order in treatment was Hg2+>Hg2+ + La3+>La3+. Hg2+, La3+, and the mixture of La3+ and Hg2+ had 1.12, 0.58, and 0.81 binding sites to DNA, the fluorescence quenching of DNA caused by them all attributed to static quenching. The binding constants KA of binding sites were 3.82×104 and 4.22×102 L·mol-1;2.50×104 and 2.95×103 L·mol-1;3.05×104 and 1.00×103 L·mol-1. The results showed that La3+ could relieve destruction caused by Hg2+ on the DNA structure.

  20. Enhanced Hg{sup 2+} removal and Hg{sup 0} re-emission control from wet fuel gas desulfurization liquors with additives

    Energy Technology Data Exchange (ETDEWEB)

    Tingmei Tang; Jiang Xu; Rongjie Lu; Jingjing Wo; Xinhua Xu [Zhejiang University, Hangzhou (China). Department of Environmental Engineering

    2010-12-15

    Secondary atmospheric pollutions may result from wet flue gas desulfurization (FGD) systems caused by the reduction of Hg{sup 2+} to Hg{sup 0}. The present study employed three agents: Na{sub 2}S, 2,4,6-trimercaptotiazine, trisodium salt nonahydrate (TMT) and sodium dithiocarbamate (DTCR) to precipitate aqueous Hg{sup 2+} in simulated desulfurization solutions. The effects of the precipitator's dosing quantity, the initial pH value, the reaction temperature, the concentrations of Cl{sup -} and other metal ions (e.g. Cu{sup 2+} and Pb{sup 2+}) on Hg{sup 2+} removal were studied. A linear relationship was observed between Hg{sup 2+} removal efficiency and the increasing precipitator's doses along with initial pH. The addition of chloride and metal ions impaired the Hg{sup 2+} removal from solutions due to the complexation of Cl{sup -} and Hg{sup 2+} as well as the chelating competition between Hg{sup 2+} and other metal ions. Based on a comprehensive comparison of the treatment effects, DTCR was found to be the most effective precipitating agent. Moreover, all the precipitating agents were potent enough to inhibit Hg{sup 2+} reduction as well as Hg{sup 0} re-emission from FGD liquors. More than 90% Hg{sup 2+} was captured by precipitating agents while Hg{sup 2+} reduction efficiency decreased from 54% to just less than 3%. The additives could efficiently control the secondary Hg{sup 0} pollution from FGD liquors. 21 refs., 6 figs.

  1. X-ray Absorption Spectroscopy of Zinc in Airborne Particulate Matter Shows Tire Debris Concentrated in > 0.5 μm Fraction

    Science.gov (United States)

    Pingitore, N. E.; Clague, J. W.; Gill, T. E.; Amaya, M. A.; Cahill, T. A.

    2009-12-01

    Using X-ray absorption spectroscopy (XAS), we speciated Zn in size-resolved fractions of particulate matter (PM) from El Paso, Texas. Spectral patterns indicated that Zn in tire debris is the dominant form of Zn in PM coarser than 0.5 μm in aerodynamic diameter. Although concentrated in the > 0.5 μm fraction, a large portion of the tire debris in PM is small enough to penetrate and deposit in the lower respiratory tract. We collected 3 sets of size-resolved samples of airborne particulate matter (PM) over periods of several days to several weeks in November 2008, and April and May 2009. Local PM compositions typically are dominated by anthropogenic input in November and geologic sources in April, and a mixture in May. The collection site is in the urban core of El Paso, TX, contiguous to the University of Texas at El Paso, 0.6 km from Interstate Highway 10, 0.4 km from State Highway 20, and 1 km from Cd. Juarez, Chihuahua, Mexico. The DRUM sampler (Davis Rotating Uniform size-cut Monitor) employs a rotating Lundgren-type impactor, draws 10 l per minute, and deposits PM on plastic strips mounted on rotating drums. The sampler collected and segregated ambient PM into 8 size cuts: 12-5 μm, 5-2.5, 2.5-1.15, 1.15-0.75, 0.75-0.56, 0.56-0.34, 0.34-0.26, and 0.26-0.09. We conducted the X-ray absorption spectroscopy (XAS) experiments at the Stanford Synchrotron Radiation Lightsource on beam line 7-3. Spectra of the 24 samples of PM and numerous model compounds were collected at the Zn K absorption edge in fluorescence mode using a 30-element Ge solid-state detector. The overall spectral patterns from the 3 seasons were similar to one another. But strikingly, each set of 8 XAS spectra displayed an obvious change in the Zn speciation at the 0.56-0.75 μm size cut. We compared the PM spectra to those of our suite of known model compounds and materials. The spectral pattern of the coarser size cuts was quite similar to those of the tires we tested. The Zn in the tires

  2. Mercury (Hg2+) effect on enzyme activities and hepatopancreas histostructures of juvenile Chinese mitten crab Eriocheir sinensis

    Science.gov (United States)

    Zhao, Yanmin; Wang, Xinhua; Qin, Yanwen; Zheng, Binghui

    2010-05-01

    We studied the effects of mercury (Hg2+) on antioxidant and digestive enzyme activities in terms of LC50 value and on hepatopancreas histostructures of juvenile Chinese mitten crabs Eriocheir sinensis in 40-day exposure to various concentrations of Hg2+ (0, 0.01, 0.05, 0.10, 0.20, and 0.30 mg/L). The results show that the activities of superoxide dismutase (SOD), glutathione peroxidase (GPX) and catalase (CAT) significantly increased in the concentrations of 0.01 and 0.05 mg/L, while that of enzyme decreased in 0.10, 0.20 and 0.30 mg/L treatments. Meanwhile, Hg2+ disrupted the histostructures of the hepatopancreas, causing decreases in activities of pepsin, tryptase, amylase, and cellulose, which are synthesized in the hepatopancreas. Moreover, as the Hg2+ concentration increased, the survival rate of the crabs decreased, worst at 56.57% in 0.30 mg/L. Therefore, although crabs are able to tolerate low levels of mercury pollution, high levels lead to cellular injury and tissue damage in hepatopancreas, which then loses some of its vital physiological functions such as absorption, storage, and secretion.

  3. Competitive adsorption of Cd, Cu, Hg and Pb by agricultural soils of the Changjiang and Zhujiang deltas in China

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Soils can often be contaminated simultaneously by more than one heavy metal. The sorption-desorption behavior of a metal in a soil will be affected by the presence of other metals. Therefore, selective retention and competitive adsorption of the soils to heavy metals can affect their availability and movement through the soils. In this study, the simultaneous competitive adsorption of four heavy metals (Cd, Cu, Hg, and Pb) on ten agricultural soils collected from the Changjiang and Zhujiang deltas,China was assessed. The results showed that the competition affected the behavior of heavy metal cations in such a way that the soils adsorbed less Cd and Hg, and more Pb and Cu with increasing total metal concentrations, regardless of the molar concentration applied. As the applied concentrations increased, Pb and Cu adsorption increased, while Cd and Hg adsorption decreased.The adsorption sequence most found was Pb>Cu>Hg>Cd. The maximum adsorption capacity for the heavy metal cations was calculated, and affected markedly by soil properties. The results suggest that Hg and Cd have higher mobility associated to the lower adsorption and that Pb and Cu present the opposite behavior. Significant correlations were found between the maximum adsorption capacity of the metals and pH value and exchangeable acid, suggesting that soil pH and exchangeable acid were key factors controlling the solubility and mobility of the metals in the agricultural soils.

  4. Concentrations of alprazolam in blood from impaired drivers and forensic autopsies were not much different but showed a high prevalence of co-ingested illicit drugs.

    Science.gov (United States)

    Jones, Alan Wayne; Holmgren, Anita

    2013-03-01

    Alprazolam is a benzodiazepine anxiolytic widely prescribed for treatment of panic-disorder and social phobias, although this medication is also subject to abuse. In this paper, the concentrations of alprazolam in venous blood samples from impaired drivers were compared with femoral blood samples from forensic autopsies classified as intoxication or other causes of death (e.g. natural, trauma). After liquid-liquid extraction (n-butyl acetate) alprazolam was determined in blood by capillary gas chromatography with a nitrogen-phosphorous detector. The mean (median) and range of alprazolam concentrations in blood from impaired drivers (n = 773) were 0.08 mg/L (0.05 mg/L) and 0.02-3.9 mg/L, respectively. Many traffic offenders had co-ingested ethanol (13%), amphetamine (46%), cannabis (32%), or heroin (14%), as well as other drugs. In deaths attributed to drug intoxication, the mean (median) and range of alprazolam concentrations in blood (n = 438) were 0.10 mg/L (0.06 mg/L) and 0.02-1.6 mg/L, respectively, which were not much different from other causes of death (n = 278); 0.08 mg/L (0.05 mg/L) and 0.02-0.9 mg/L. Median concentrations of alprazolam in blood from living and deceased persons did not seem to depend on the number of co-ingested substances. The result of this pharmacoepidemiological study suggests that alprazolam is a fairly innocent drug when used as monotherapy, but toxicity problems arise when co-ingested with illicit drugs and/or psychoactive medication.

  5. Preparation and Hg~(2+) Adsorption of N-thioacyl Thioglycolic Acid Functionalized Triethylenetetramine Crosslinked PVC Resin%N-硫代酰基硫乙酸功能化三乙撑四胺交联PVC树脂的制备及对Hg~(2+)的吸附

    Institute of Scientific and Technical Information of China (English)

    刘春萍; 纪春暖; 蒙延峰; 吕菊波; 孙琳

    2009-01-01

    A novel acidic N-thioacyl thioglycolic acid functionalized triethylentetramine crosslinked PVC resin was preparated from PVC, triethylenetetramine, CS_2 and ClCH_2COONa and characterized by FTIR and elemental analysis. Adsorption properties of the resin for Hg~(2+) were investigated under different conditions such as pH, temperature, contact time and the initial concentration of Hg~(2+). The results show that the adsorption of the resin for Hg~(2+) could rapidly reach balance, and it displayed a higher capacity when pH was about 2.0. The adsorption capacity of the resin for Hg~(2+) reached 3.330 mmol/g at 35 ℃ and 17.66 mmol/L Hg~(2+). The adsorption process was fitted to Langmuir and Freundlich isotherms in the studied concentration range. The loaded resin with Hg~(2+) was regenerated in an efficiency of 99.2% via 0.2 mol/L HNO_3-10% thiourea.%以聚氯乙烯为原料依次与四乙烯五胺、CS_2和ClCH_2COONa反应合成了一种新的含N、O、S的N-硫代酰基硫乙酸功能化三乙撑四胺交联聚氯乙烯螯合树脂,树脂结构经红外分析和元素分析表征. 探讨了在不同pH值、Hg~(2+)初始浓度、吸附温度和时间等条件下合成树脂对Hg~(2+)的吸附性能. 结果表明,螯合树脂对Hg~(2+)有较快的吸附速率,pH值约为2.0时,树脂对Hg~(2+)的吸附效果最好,随温度升高吸附量逐渐增大. 温度在35 ℃、Hg~(2+)起始浓度为17.66 mmol/L时,树脂对Hg~(2+)的吸附量可达3.330 mmol/g. 树脂对Hg~(2+)的吸附符合Langmuir和Freundlich等温式. 用0.2 mol/L HNO3-10%硫脲对吸附后的树脂进行洗脱,脱附率达99.20%.

  6. New technique for quantification of elemental Hg in mine wastes and its implications for mercury evasion into the atmosphere.

    Science.gov (United States)

    Jew, Adam D; Kim, Christopher S; Rytuba, James J; Gustin, Mae S; Brown, Gordon E

    2011-01-15

    Mercury in the environment is of prime concern to both ecosystem and human health. Determination of the molecular-level speciation of Hg in soils and mine wastes is important for understanding its sequestration, mobility, and availability for methylation. Extended X-ray absorption fine structure (EXAFS) spectroscopy carried out under ambient P-T conditions has been used in a number of past studies to determine Hg speciation in complex mine wastes and associated soils. However, this approach cannot detect elemental (liquid) mercury in Hg-polluted soils and sediments due to the significant structural disorder of liquid Hg at ambient-temperature. A new sample preparation protocol involving slow cooling through the crystallization temperature of Hg(0) (234 K) results in its transformation to crystalline α-Hg(0). The presence and proportion of Hg(0), relative to other crystalline Hg-bearing phases, in samples prepared in this way can be quantified by low-temperature (77 K) EXAFS spectroscopy. Using this approach, we have determined the relative concentrations of liquid Hg(0) in Hg mine wastes from several sites in the California Coast Range and have found that they correlate well with measured fluxes of gaseous Hg released during light and dark exposure of the same samples, with higher evasion ratios from samples containing higher concentrations of liquid Hg(0). Two different linear relationships are observed in plots of the ratio of Hg emission under light and dark conditions vs % Hg(0), corresponding to silica-carbonate- and hot springs-type Hg deposits, with the hot springs-type samples exhibiting higher evasion fluxes than silica-carbonate type samples at similar Hg(0) concentrations. Our findings help explain significant differences in Hg evasion data for different mine sites in the California Coast Range.

  7. New technique for quantification of elemental hg in mine wastes and its implications for mercury evasion into the atmosphere

    Science.gov (United States)

    Jew, A.D.; Kim, C.S.; Rytuba, J.J.; Gustin, M.S.; Brown, Gordon E.

    2011-01-01

    Mercury in the environment is of prime concern to both ecosystem and human health. Determination of the molecular-level speciation of Hg in soils and mine wastes is important for understanding its sequestration, mobility, and availability for methylation. Extended X-ray absorption fine structure (EXAFS) spectroscopy carried out under ambient P-T conditions has been used in a number of past studies to determine Hg speciation in complex mine wastes and associated soils. However, this approach cannot detect elemental (liquid) mercury in Hg-polluted soils and sediments due to the significant structural disorder of liquid Hg at ambient-temperature. A new sample preparation protocol involving slow cooling through the crystallization temperature of Hg(0) (234 K) results in its transformation to crystalline ??-Hg(0). The presence and proportion of Hg(0), relative to other crystalline Hg-bearing phases, in samples prepared in this way can be quantified by low-temperature (77 K) EXAFS spectroscopy. Using this approach, we have determined the relative concentrations of liquid Hg(0) in Hg mine wastes from several sites in the California Coast Range and have found that they correlate well with measured fluxes of gaseous Hg released during light and dark exposure of the same samples, with higher evasion ratios from samples containing higher concentrations of liquid Hg(0). Two different linear relationships are observed in plots of the ratio of Hg emission under light and dark conditions vs % Hg(0), corresponding to silica-carbonate- and hot springs-type Hg deposits, with the hot springs-type samples exhibiting higher evasion fluxes than silica-carbonate type samples at similar Hg(0) concentrations. Our findings help explain significant differences in Hg evasion data for different mine sites in the California Coast Range. ?? 2011 American Chemical Society.

  8. Gold nanoparticles generated through "green route" bind Hg2+ with a concomitant blue shift in plasmon absorption peak.

    Science.gov (United States)

    Radhakumary, C; Sreenivasan, K

    2011-07-21

    We discuss here a quick, simple, economic and ecofriendly method through a completely green route for the selective detection of Hg(2+) in aqueous samples. Here we exploited the ability of chitosan to generate gold nanoparticles and subsequently to act as a stabilizer for the formed nanoparticles. When chitosan stabilized gold nanoparticles (CH-Au NPs) are interacted with Hg(2+) a blue shift for its localized surface plasmon resonance absorbance (LSPR) band is observed. The blue shift is reasoned to be due to the formation of a thin layer of mercury over gold. A concentration as low as 0.01 ppm to a maximum of 100 ppm Hg(2+) can be detected based on this blue shift of the CH-Au NPs. While all other reported methods demand complex reaction steps and costly chemicals, the method we reported here is a simple, rapid and selective approach for the detection of Hg(2+). Our results also show that the CH-Au NPs have excellent selectivity to Hg(2+) over common cations namely, Pb(2+), Cd(2+), Mn(2+), Fe(2+), Ag(1+), Ce(4+), Ni(2+), and Cu(2+).

  9. Self-powered sensor for trace Hg2+ detection.

    Science.gov (United States)

    Wen, Dan; Deng, Liu; Guo, Shaojun; Dong, Shaojun

    2011-05-15

    A self-powered electrochemical sensor has been facilely designed for sensitive detection of Hg(2+) based on the inhibition of biocatalysis process of enzymatic biofuel cell (BFC) for the first time. The as-prepared one-compartment BFC, which was consisted of alcohol dehydrogenase supported on single-walled carbon nanohorns-based mediator system as the anode and bilirubin oxidase as the cathodic biocatalyst, generated an open circuit potential (V(oc)) of 636 mV and a maximum power density of 137 μW cm(-2). It was interestingly found that the presence of Hg(2+) would affect the performance of the constructed BFC (e.g., V(oc)). Taking advantage of the inhibitive effect of Hg(2+), a novel self-powered Hg(2+) sensor has been developed, which showed a linear range of 1-500 nM (R(2) = 0.999) with a detection limit of 1 nM at room temperature. In addition, this BFC-type sensor exhibited good selectivity for Hg(2+) against other common environmental metal ions, and the feasibility of the method for Hg(2+) detection in actual water samples (i.e., tap, ground, and lake water) was demonstrated with satisfactory results.

  10. Concentrations of mercury in tissues of striped dolphins suggest decline of pollution in Mediterranean open waters.

    Science.gov (United States)

    Borrell, A; Aguilar, A; Tornero, V; Drago, M

    2014-07-01

    The Mediterranean is a semi-enclosed sea subject to high mercury (Hg) pollution from both natural and anthropogenic sources. With the objective of discerning temporal changes in marine Hg pollution in the oceanic waters of the northwestern Mediterranean Sea, we analysed liver and kidney from striped dolphins (Stenella coeruleoalba) collected during 2007-2009 and compared them with previous results from a similar sample from 1990-1993. The effect of body length and sex on tissue Hg concentrations was investigated to ensure an unbiased comparison between the periods. The Hg concentrations did not show significant sex-related differences in any tissue or period but were correlated positively with body length. Using body length as a covariate, Hg concentrations in liver and kidney were higher in 1990-1993 than in 2007-2009. This result suggests that measures to reduce emissions in Western European countries have been effective in reducing mercury pollution in Mediterranean open waters.

  11. Mercury in stream water at five Czech catchments across a Hg and S deposition gradient

    Science.gov (United States)

    Navrátil, Tomáš; Shanley, James B.; Rohovec, Jan; Oulehle, Filip; Krám, Pavel; Matoušková, Šárka; Tesař, Miroslav; Hojdová, Maria

    2015-01-01

    The Czech Republic was heavily industrialized in the second half of the 20th century but the associated emissions of Hg and S from coal burning were significantly reduced since the 1990s. We studied dissolved (filtered) stream water mercury (Hg) and dissolved organic carbon (DOC) concentrations at five catchments with contrasting Hg and S deposition histories in the Bohemian part of the Czech Republic. The median filtered Hg concentrations of stream water samples collected in hydrological years 2012 and 2013 from the five sites varied by an order of magnitude from 1.3 to 18.0 ng L− 1. The Hg concentrations at individual catchments were strongly correlated with DOC concentrations r from 0.64 to 0.93 and with discharge r from 0.48 to 0.75. Annual export fluxes of filtered Hg from individual catchments ranged from 0.11 to 13.3 μg m− 2 yr− 1 and were highest at sites with the highest DOC export fluxes. However, the amount of Hg exported per unit DOC varied widely; the mean Hg/DOC ratio in stream water at the individual sites ranged from 0.28 to 0.90 ng mg− 1. The highest stream Hg/DOC ratios occurred at sites Pluhův Bor and Jezeří which both are in the heavily polluted Black Triangle area. Stream Hg/DOC was inversely related to mineral and total soil pool Hg/C across the five sites. We explain this pattern by greater soil Hg retention due to inhibition of soil organic matter decomposition at the sites with low stream Hg/DOC and/or by precipitation of a metacinnabar (HgS) phase. Thus mobilization of Hg into streams from forest soils likely depends on combined effects of organic matter decomposition dynamics and HgS-like phase precipitation, which were both affected by Hg and S deposition histories.

  12. 生物质材料山核桃壳对水中汞离子的吸附研究%Study on Adsorption of Hg( Ⅱ ) by Chinese Walnut (Juglans mandshurica Maxim.) of Biomass Material

    Institute of Scientific and Technical Information of China (English)

    于春光; 杜茂安; 孟召辉; 查金苗

    2012-01-01

    [Objective] The aim of the study was to make research on adsorption of Chinese walnut (Juglans mandshurica Maxim. ) Shell (CWS) to Hg( II ) in water. [Method] Shells of Juglans mandshurica Maxim were used as biosorption to remove Hg( II ) in water solution to explore the influence to adsorption of Hg( Ⅱ ) under different conditions, like pH solution, adsorption time, and Hg( II ). [Result] The experimental results show that when absorptivity of Hg( II ) by CWS reached the highest, pH ranged within 5.0-6. 0. The adsorptivity decreased as initial Hg( II ) concentrations increased. Fourier Transform Infrared Spectroscopy (FTIR) spectrum revealed some chemical groups of CWS may affect the adsorption of Hg( II ), such as hydroxyl groups, methyl groups, aromatic methoxyl groups, unconjugated carbonyl , and typical aromatic ring , etc. Adsorption equation can be concluded considering the biosorption process relationship with Langmuir and Fren-drich isotherm. [Conclusion] The study found that CW could be employed as a promising biosorption to remove Hg( II ) from aqueous environments.%[目的]对生物质材料山核桃(Juglans mandshurica Maxim.)壳(CWS)对水中汞离子的吸附效果进行研究.[方法]利用山核桃壳作为生物吸附剂去除水溶液中Hg(Ⅱ)离子,探讨不同条件即溶液pH、吸附时间、Hg(Ⅱ)初始浓度对Hg(Ⅱ)离子吸附效率的影响.[结果] CWS对Hg(Ⅱ)离子吸附率最大时的pH范围为5.0~6.0;随着初始Hg(Ⅱ)浓度的增加吸附率逐渐减小;FTIR分析显示CWS的一些化学基团如羟基、甲基、芳香环甲氧基、羰基可能与吸附Hg(Ⅱ)离子有关;CWS对Hg(Ⅱ)离子的吸附过程与Langmuir和Frendrich吸附等温线相关性较高,从而拟合出吸附方程.[结论]山核桃壳可以作为一种很有前景的生物吸附剂来去除水中Hg(Ⅱ)离子.

  13. Overcoming phytoremediation limitations. A case study of Hg contaminated soil

    Science.gov (United States)

    Barbafieri, Meri

    2013-04-01

    Phytoremediation is a broad term that comprises several technologies to clean up water and soil. Despite the numerous articles appearing in scientific journals, very few field applications of phytoextraction have been successfully realized. The research here reported on Phytoextraction, the use the plant to "extract" metals from contaminated soil, is focused on implementations to overcome two main drawbacks: the survival of plants in unfavorable environmental conditions (contaminant toxicity, low fertility, etc.) and the often lengthy time it takes to reduce contaminants to the requested level. Moreover, to overcome the imbalance between the technology's potential and its drawbacks, there is growing interest in the use of plants to reduce only the fraction that is the most hazardous to the environment and human health, that is to target the bioavailable fractions of metals in soil. Bioavailable Contaminant Stripping (BCS) would be a remediation approach focused to remove the bioavailable metal fractions. BCS have been used in a mercury contaminated soil from Italian industrial site. Bioavailable fractions were determined by sequential extraction with H2O and NH4Cl.Combined treatments of plant hormone and thioligand to strength Hg uptake by crop plants (Brassica juncea and Helianthus annuus) were tested. Plant biomass, evapotranspiration, Hg uptake and distribution following treatments were compared. Results indicate the plant hormone, cytokinine (CK) foliar treatment, increased evapotranspiration rate in both tested plants. The Hg uptake and translocation in both tested plants increased with simultaneous addition of CK and TS treatments. B. juncea was the most effective in Hg uptake. Application of CK to plants grown in TS-treated soil lead to an increase in Hg concentration of 232% in shoots and 39% in roots with respect to control. While H. annuus gave a better response in plant biomass production, the application of CK to plants grown in TS-treated soil lead to

  14. Earthworm casts as a sampling medium – a case study from highly contaminated Hg roasting site Pšenk (Idrija area, Slovenia

    Directory of Open Access Journals (Sweden)

    Tamara Teršič

    2013-12-01

    Full Text Available In this study an interesting sampling medium - earthworm casts was examined in a highly Hg contaminated area. Enrichment factor (EF has been applied to assess elevated concentrations of analyzed elements in earthworm casts and to determine elevated concentrations of these elements in soils and casts with regard to European average concentrations in topsoil. In a previous study (Teršič & Gosar, 2012 it was shown that Hg contents and dispersion in casts from studied roasting site are comparable to those in soil, which indicates that soil contamination is substantially reflected in contamination of earthworm casts. Therefore the comparison between elemental concentrations in earthworm casts and soil was investigated with the intention to assess the reflection of possible soil contamination in casts. Besides Hg contamination, elevated concentrations of As, Ca, Cd, Mo, Pb and U were also determined in earthworm casts. The calculated EFs show moderate enrichment of casts with Ca, Sr and P and minimal enrichment with Mg, Zn and Cu. Cast, SOM (surface organic matter rich soil layer and soil enrichments with regard to the European averages show extreme enrichment of all studied media with Hg, followed by significant enrichment with Mo and Cd and moderate enrichment with As. Spatial distributions of analyzed elements in casts mostly show similar pattern as in soil, however, because of the different nature of different earthworm species and specific properties of different elements, the data about cast contamination can only serve as an approximate prediction about the dispersion and distribution of contaminant in soil.

  15. Identification of host transcriptional networks showing concentration-dependent regulation by HPV16 E6 and E7 proteins in basal cervical squamous epithelial cells.

    Science.gov (United States)

    Smith, Stephen P; Scarpini, Cinzia G; Groves, Ian J; Odle, Richard I; Coleman, Nicholas

    2016-07-26

    Development of cervical squamous cell carcinoma requires increased expression of the major high-risk human-papillomavirus (HPV) oncogenes E6 and E7 in basal cervical epithelial cells. We used a systems biology approach to identify host transcriptional networks in such cells and study the concentration-dependent changes produced by HPV16-E6 and -E7 oncoproteins. We investigated sample sets derived from the W12 model of cervical neoplastic progression, for which high quality phenotype/genotype data were available. We defined a gene co-expression matrix containing a small number of highly-connected hub nodes that controlled large numbers of downstream genes (regulons), indicating the scale-free nature of host gene co-expression in W12. We identified a small number of 'master regulators' for which downstream effector genes were significantly associated with protein levels of HPV16 E6 (n = 7) or HPV16 E7 (n = 5). We validated our data by depleting E6/E7 in relevant cells and by functional analysis of selected genes in vitro. We conclude that the network of transcriptional interactions in HPV16-infected basal-type cervical epithelium is regulated in a concentration-dependent manner by E6/E7, via a limited number of central master-regulators. These effects are likely to be significant in cervical carcinogenesis, where there is competitive selection of cells with elevated expression of virus oncoproteins.

  16. Anti-aggregation-based spectrometric detection of Hg(II) at physiological pH using gold nanorods.

    Science.gov (United States)

    Rajeshwari, A; Karthiga, D; Chandrasekaran, Natarajan; Mukherjee, Amitava

    2016-10-01

    An efficient detection method for Hg (II) ions at physiological pH (pH7.4) was developed using tween 20-modified gold nanorods (NRs) in the presence of dithiothreitol (DTT). Thiol groups (-SH) at the end of DTT have a higher affinity towards gold atoms, and they can covalently interact with gold NRs and leads to their aggregation. The addition of Hg(II) ions prevents the aggregation of gold NRs due to the covalent bond formation between the -SH group of DTT and Hg(II) ions in the buffer system. The changes in the longitudinal surface plasmon resonance peak of gold NRs were characterized using a UV-visible spectrophotometer. The absorption intensity peak of gold NRs at 679nm was observed to reduce after interaction with DTT, and the absorption intensity was noted to increase by increasing the concentration of Hg(II) ions. The TEM analysis confirms the morphological changes of gold NRs before and after addition of Hg(II) ions in the presence of DTT. Further, the aggregation and disaggregation of gold NRs were confirmed by particle size and zeta potential analysis. The developed method shows an excellent linearity (y=0.001x+0.794) for the graph plotted between the absorption ratio and Hg(II) concentration (1 to 100pM) under the optimized conditions. The limit of detection was noted to be 0.42pM in the buffer system. The developed method was tested in simulated body fluid, and it was found to have a good recovery rate. Copyright © 2016 Elsevier B.V. All rights reserved.

  17. 活性染料染色用高浓液体有机固色剂HG的开发和应用%Development and Application on High-concentrated Organic Fixing Agent HG Used in Reactive Dyeing

    Institute of Scientific and Technical Information of China (English)

    徐蔚; 魏巍; 陆海英; 庄永祥; 杨军浩

    2012-01-01

    The passage introduces a high-concentrated organic fixing agent HC~ which was applicable to all kinds of reactive dyes, including Dyeing at Low Liquor Ratio. Perfect tinctorial yield and reproducibility were achieved when used on different structured reactive dyes. It was act as fixing agent when dyeing in the reactive dyes. It consumes only 1/8~1/10 compared with Sodium carbonate and shortened 20-30 minutes with excellent leveling effect and low dyeing disadvantages. Furthermore, owing to the less consumption, the textile is easier to wash, cutting down the washing times, eliminating acid wash and saving great: amount on energy as well as working hours. It only consumes half of the water compared with Sodium carbonate techniques and 1/3 of gas consumption. This can greatly reduce amount of waste water and alkali content. Different from the Substitution alkali which was sold in the market, it is a high concentrated and organic liquid. In its molecular structure, the carbon chain of hydrophobic groups is shorter, water-soluble groups and hydrophilic group are included, which plays important role in the buffer solution system regarding fluxing, penetrating, dispersing, retarding and migrating.%该文介绍了一种自主研发的高浓液体有机固着剂HG,它适用于各种类型的活性染料的染色,也适用于小浴比染色新工艺。对各种结构的活性染料能得到较高的给色量和良好的重现性。它在活性染料染色时用作固色剂,其用量仅为纯碱的1/8~1/10,加碱时间缩短为20~30min,匀染效果佳,可大幅降低染色疵病率。同时,由于用量少,染色后的织物易于洗涤,可以减少水洗道数,省去酸洗,节约了大量的水和汽及工时,用水量仅为纯碱工艺的1/2,蒸汽用量仅是纯碱工艺的1/3,减少了污水和污水中碱剂含量。它和已进入市场的代碱剂有所不同,它是高浓液体的、有机的,它的分子结构中疏抽№

  18. Show Time

    Institute of Scientific and Technical Information of China (English)

    2004-01-01

    <正> Story: Show Time!The whole class presents the story"Under the Sea".Everyone is so excited and happy.Both Leo and Kathy show their parentsthe characters of the play."Who’s he?"asks Kathy’s mom."He’s the prince."Kathy replies."Who’s she?"asks Leo’s dad."She’s the queen."Leo replieswith a smile.

  19. Snobbish Show

    Institute of Scientific and Technical Information of China (English)

    YIN PUMIN

    2010-01-01

    @@ The State Administration of Radio,Film and Television (SARFT),China's media watchdog,issued a new set of mles on June 9 that strictly regulate TV match-making shows,which have been sweeping the country's primetime programming. "Improper social and love values such as money worship should not be presented in these shows.Humiliation,verbal attacks and sex-implied vulgar content are not allowed" the new roles said.

  20. Mother-embryo isotope (δ 15 N, δ 13 C) fractionation and mercury (Hg) transfer in aplacental deep-sea sharks : aplacental shark isotope fractionation and hg

    OpenAIRE

    Le Bourg, B.; Kiszka, J.; Bustamante, P.

    2014-01-01

    Stable carbon (δ13C) and nitrogen (δ15N) isotopic values and total mercury (Hg) concentrations were analysed in muscle and liver of mothers and embryos of two aplacental shark species, Squalus megalops and Centrophorus moluccensis. Embryos of the two species had similar or lower isotopic values than their respective mothers, the only exception being for δ13C, which was higher in the liver of C. moluccensis embryos than in their mothers. Hg concentrations were systematically lower in embryos c...

  1. Linkage between community diversity of sulfate-reducing microorganisms and methylmercury concentration in paddy soil.

    Science.gov (United States)

    Liu, Yu-Rong; Zheng, Yuan-Ming; Zhang, Li-Mei; He, Ji-Zheng

    2014-01-01

    Sulfate-reducing microorganisms (SRM) have been thought to play a key role in mercury (Hg) methylation in anoxic environments. The current study examined the linkage between SRM abundance and diversity and contents of methylmercury (MeHg) in paddy soils collected from a historical Hg mining area in China. Soil profile samples were collected from four sites over a distance gradient downstream the Hg mining operation. Results showed that MeHg content in the soil of each site significantly decreased with the extending distance away from Hg mine. Soil MeHg content was correlated positively with abundance of SRM and the contents of organic matter (OM), NH4(+), SO4(2-), and Hg. The abundances of SRM based on dissimilatory (bi) sulfite reductase (dsrAB) gene at 0-40 cm depths were higher than those at 40-80 cm depth at all sites. The SRM community composition varied in the soils of different sampling sites following terminal restriction fragment length polymorphism (T-RFLP) and phylogenetic analyses, which appeared to be correlated with contents of MeHg, OM, NH4(+), and SO4(2-) through canonical correspondence analysis. The dominant groups of SRM in the soils examined belonged to Deltaproteobacteria and some unknown SRM clusters that could have potential for Hg methylation. These results advance our understanding of the relationship between SRM and methylmercury concentration in paddy soil.

  2. Local chemical composition of HgBaCaCuO high-temperature superconductors

    Science.gov (United States)

    Alméras, P.; Dell'Orto, T.; Coluzza, C.; Almeida, J.; Margaritondo, G.; Xue, Y. Y.; Meng, R. L.; Chu, C. W.

    1994-07-01

    The microchemical composition and the electronic structure of the two superconductors HgBa2Ca2Cu3O8+δ (Hg-1223) and HgBa2Ca1Cu2O6+δ (Hg-1212) were analyzed with the technique of photoemission with high spatial resolution. This enabled primary spectral peaks to be separated from their satellites due to local charging induced by the primary photon beam. Each sample contains superconducting and impurity phases with inhomogeneous spatial distributions. The oxygenation-induced increase in the critical temperature is related to a increase in the Cu-O plane carrier concentration.

  3. Mercury concentrations in fish-eating birds from the Pinchi Lake area in relation to productivity and reproductive success

    Energy Technology Data Exchange (ETDEWEB)

    Weech, S.A. [Minnow Environmental Inc., Victoria, BC (Canada); Scheuhammer, T.M. [Environment Canada, Ottawa, ON (Canada)]|[Carleton Univ., Ottawa, ON (Canada). National Wildlife Research Centre

    2006-07-01

    A known bird breeding area along the Pinchi fault in central British Columbia is a source of geologic mercury (Hg) in the form of cinnabar. Lakes with a range of sediment Hg concentrations are also present. This study examined the extent to which inorganic Hg from local geologic sources is methylated and incorporated into the food chain of birds feeding on fishes. The possible toxic effects of natural and mining-related Hg releases on local piscivorous breeding bird populations were also studied. Bald eagles and red-necked grebes were monitored from 2000 to 2002 in an effort to determine if increased Hg concentrations were affecting reproductive success and productivity. Fish tissues were collected from rainbow trout and northern pike minnow to determine if Hg levels were elevated. Eagles breeding on 5 lakes were sampled for blood- and feather-Hg concentrations. Red-necked grebe eggs were also collected. All samples were analyzed for total Hg. It was shown that Hg does not appear to have any obvious adverse effects on reproduction. Concentrations of Hg in all grebe eggs were below 0.5 {mu}g.g wet weight, the lowest observed adverse effect level (LOAEL) for Hg developmental toxicity in birds. Although the level of Hg in tissues of Pinchi Lake birds was elevated, the birds were in excellent condition and showed similar reproductive success and productivity to reference populations. This study showed that concurrent tissue sampling and population monitoring can provide a helpful way to prove or refute findings that may indicate a potential contaminant effect on local wildlife. 27 refs., 1 tab., 4 figs.

  4. Subcellular localization of several heavy metals of Hg,Cd and Pb in human liver

    Institute of Scientific and Technical Information of China (English)

    CHEN Chunying; ZHANG Peiqun; CHAI Zhifang

    2005-01-01

    Liver, as an important metabolic and detoxicological organ of human body, can be used as a good bioindicator for evaluating body burden of environmental pollutants. Its elemental contents and their chemical forms are closely related to the status of human health and disease. In this paper, the liver samples collected from normal subjects were separated to different subcellular fractions of nuclei, mitochondria, lysosome, microsome and cytosol by differential centrifugation. Then their concentrations of heavy metals of As, Pb, Cd, and Hg were determined by atomic absorption and atomic fluorescent spectroscopy. Our results show no significant difference with literature ones when comparing their gross concentrations. In the case of their subcellular distribution, the Hg concentrations are higher in mitochondrial, microsomal and cytosolic fractions; the Cd concentrations are higher in cytosolic and mitochondrial fractions, while As highest in nuclear fraction. The highest concentration of Pb is found in microsomal fraction with similarity to Fe. Mercury in liver is mainly in the form of inorganic, and methylmercury ranged from 9% to 50% with the average value of 20.9%(13.3%. These results indicate that the cellular distribution and the accumulated target organelles are quite different among these heavy metals, which suggest their various pathways and toxic mechanism in vivo.

  5. EROBATIC SHOW

    Institute of Scientific and Technical Information of China (English)

    2016-01-01

    Visitors look at plane models of the Commercial Aircraft Corp. of China, developer of the count,s first homegrown large passenger jet C919, during the Singapore Airshow on February 16. The biennial event is the largest airshow in Asia and one of the most important aviation and defense shows worldwide. A number of Chinese companies took part in the event during which Okay Airways, the first privately owned aidine in China, signed a deal to acquire 12 Boeing 737 jets.

  6. Food preferences and Hg distribution in Chelonia mydas assessed by stable isotopes.

    Science.gov (United States)

    Bezerra, M F; Lacerda, L D; Rezende, C E; Franco, M A L; Almeida, M G; Macêdo, G R; Pires, T T; Rostán, G; Lopez, G G

    2015-11-01

    Mercury (Hg) is a highly toxic pollutant that poses in risk several marine animals, including green turtles (Chelonia mydas). Green turtles are globally endangered sea turtle species that occurs in Brazilian coastal waters as a number of life stage classes (i.e., foraging juveniles and nesting adults). We assessed total Hg concentrations and isotopic signatures ((13)C and (15)N) in muscle, kidney, liver and scute of juvenile green turtles and their food items from two foraging grounds with different urban and industrial development. We found similar food preferences in specimens from both areas but variable Hg levels in tissues reflecting the influence of local Hg backgrounds in food items. Some juvenile green turtles from the highly industrialized foraging ground presented liver Hg levels among the highest ever reported for this species. Our results suggest that juvenile foraging green turtles are exposed to Hg burdens from locally anthropogenic activities in coastal areas.

  7. Taguchi optimization approach for Pb(II) and Hg(II) removal from aqueous solutions using modified mesoporous carbon.

    Science.gov (United States)

    Zolfaghari, Ghasem; Esmaili-Sari, Abbas; Anbia, Mansoor; Younesi, Habibollah; Amirmahmoodi, Shahram; Ghafari-Nazari, Ali

    2011-09-15

    Using the Taguchi method, this study presents a systematic optimization approach for removal of lead (Pb) and mercury (Hg) by a nanostructure, zinc oxide-modified mesoporous carbon CMK-3 denoted as Zn-OCMK-3. CMK-3 was synthesized by using SBA-15 and then oxidized by nitric acid. The zinc oxide was loaded to the modified CMK-3 by the equilibrium adsorption of Zn(II) ions from aqueous solution followed by calcination to convert zinc nitrate to zinc oxide. The CMK-3 had porous structure and high specific surface area which can accommodate zinc oxide in a spreading manner, the zinc oxide connects to the carbon surface via oxygen atoms. The controllable factors such as agitation time, initial concentration, temperature, dose and pH of solution have been optimized. Under optimum conditions, the pollutant removal efficiency (PRE) was 97.25% for Pb(II) and 99% for Hg(II). The percentage contribution of each controllable factor was also determined. The initial concentration of pollutant is the most influential factor, and its value of percentage contribution is up to 31% and 43% for Pb and Hg, respectively. Our results show that the Zn-OCMK-3 is an effective nanoadsorbent for lead and mercury pollution remediation. Langmuir and Freundlich adsorption isotherms were used to model the equilibrium adsorption data for Pb(II) and Hg(II).

  8. Hg removal and the effects of coexisting metals in forward osmosis and membrane distillation.

    Science.gov (United States)

    Wu, Chia-Yu; Chen, Shiao-Shing; Zhang, Dai-Zhou; Kobayashi, Jun

    2017-06-01

    In this study, we investigate the rejection of Hg, Cd, and Pb and the effect of coexisting metals on Hg removal through forward osmosis (FO) and membrane distillation (MD) in order to establish a more effective water treatment process. The results of our laboratory experiment indicate that more than 97% of the rejection for each metal is achieved through the FO system, and this rejection is the highest among previous studies using membrane filtrations. Moreover, we examine the matrix effect of the coexisting Cd and Pb on the rejection of Hg in the FO system. Hg(2+) rejection increases with increase in the concentration of the coexisting metals. Furthermore, we study the effect of the Hg concentration and the water temperature on rejection of Hg(2+). Indeed, the rejection of Hg(2+) is achieved above 95% under any condition. However, approximately 1-10 ppb Hg from the feed solution remains in the draw solution due to permeation. Therefore, we use a FO-MD hybrid system. Approximately 100% rejection of Hg(2+) and a stable water flux are achieved. Thus, the FO-MD hybrid system is considered an important alternative to previous studies using membrane filtration for heavy metals removal.

  9. 通过简单微波法使用新型硫化剂制备HgS纳米颗粒的结构与光谱表征%Structural and spectroscopic characterization of HgS nanoparticles prepared via simple microwave approach in presence of novel sulfuring agent

    Institute of Scientific and Technical Information of China (English)

    Hossein SAFARDOUST-HOJAGHAN; Maryam SHAKOURI-ARANI; Masoud SALAVATI-NIASARI

    2016-01-01

    Mercury sulfide (HgS) crystals with different morphologies and particle sizes, were obtained via a simple microwave reaction by a new precursor complex, [bis ((2-suphanylphenyl)imino]methylphenol) Hg(II)] ([Hg(C13H11NSO)2]2+). The products were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), ultraviolet–visible (UV−Vis) spectroscopy. Mercury sulfide nanostructures with different sizes were prepared. The effects of precursor concentration, type of solvent, microwave time, and power on the particle size and morphology were investigated. The results show that the type of solvent and microwave power play key roles in the final size of HgS. Ethylene glycol is the best solvent for the synthesis of very fine particles of HgS, and the best power for the preparation of HgS nanoparticles with uniform size distribution is 900 W. The band gap for HgS nanoparticles calculated by UV–Vis spectrum was 3.2 eV which had about 1.2 eV blue shift in comparison with the band gap of 2 eV for bulk sample.%通过简单的微波反应,使用一种新型的前驱体复合物[Hg(C13H11NSO)2]2+,制备具有不同形貌和颗粒尺寸的晶体汞硫化物(HgS)。通过X射线、扫描电镜、紫外−可见光谱对产物进行表征,获得了具有不同尺寸的汞硫化物纳米结构。研究前驱体浓度、溶剂种类、微波时间和功率对产物尺寸和形貌的影响。结果表明:溶剂种类和微波功率极大地影响HgS的最终尺寸。乙二醇是合成细小颗粒HgS的最佳溶剂,制备具有尺寸分布均匀的HgS纳米颗粒的最佳功率是900 W。通过紫外−可见光谱计算出HgS纳米颗粒的带隙是3.2 eV,这相对于块体样品2 eV的带隙蓝移了1.2 eV。

  10. Using Simple Science to Influence Corporate Responsibility—A Lesson from Mercury (Hg)

    Science.gov (United States)

    Filippelli, G. M.

    2016-12-01

    Mercury (Hg) is a powerful neurotoxin with wide environmental distribution. Typical population exposure to Hg comes from fish consumption, with fish being the final ecological endpoint of Hg magnification after a series of biogeochemical processes. The emission of Hg from coal-fired power plants has been strongly implicated as a key source of environmental Hg, and thus the target for various public policy initiatives in the US and abroad. We conducted a study of Hg distribution in surface soils over a broad area of central Indiana (US) to understand the major sources of Hg to local fish, and to assess the potential role of policy compliance in reducing Hg. We found a plume-like distribution pattern for soil Hg, with values exceeding 400 ppb Hg in the heart of the plume, and reducing to background concentration of about 30 ppb outside of the plume. The plume covered hundreds of square kilometers, was centered directly over the downtown area of Indianapolis (a city of roughly 1 million inhabitants), and could be roughly backtracked to a source in the southwest corner of the city, coincident with a large coal-fired utility plant that has the highest reported emissions of Hg in the area. Evidence of this link between a local source of Hg and net Hg deposition, with related implications for Hg runoff to local stream, biomagnification to fish, and fish consumption advisories was reported in regional newspapers and eventually published in scientific journals. But importantly, these findings were used by an NGO (the Beyond Coal campaign by Indiana branch of the Sierra Club) at a critical time to influence a decision by the owner of the power plant of whether to comply with the Hg policy rule by either adding higher technology scrubbing technologies to the plant or simply to convert the plant over to natural gas as the fuel source (a costlier choice upfront). The utility chose the latter option, and with the permanent elimination of Hg emissions, the net measurable effects

  11. Stability studies of Hg implanted YBa$_{2}$Cu$_{3}$O$_{6+x}$

    CERN Document Server

    Araújo, J P; Wahl, U; Marques, J G; Alves, E; Amaral, V S; Lourenço, A A; Galindo, V; Von Papen, T; Senateur, J P; Weiss, F; Vantomme, A; Langouche, G; Melo, A A; Da Silva, M F A; Soares, J C; Sousa, J B

    1999-01-01

    High quality YBa$_{2}$Cu$_{3}$O$_{6+x}$ (YBCO) superconducting thin films were implanted with the radioactive $^{197m}$Hg (T$_{1/2}$ = 24 h) isotope to low fluences of 10$^{13}$ atoms/cm$^{2}$ and 60 keV energy. The lattice location and stability of the implanted Hg were studied combining the Perturbed Angular Correlation (PAC) and Emission Channeling (EC) techniques. We show that Hg can be introduced into the YBCO lattice by ion implantation into unique regular sites. The EC data show that Hg is located on a highly symmetric site on the YBCO lattice, while the PAC data suggests that Hg occupies the Cu(1) site. Annealing studies were performed under vacuum and O$_{2}$ atmosphere and show that Hg starts to diffuse only above 653 K.

  12. The redox processes in Hg-contaminated soils from Descoberto (Minas Gerais, Brazil): implications for the mercury cycle.

    Science.gov (United States)

    Windmöller, Cláudia C; Durão Júnior, Walter A; de Oliveira, Aline; do Valle, Cláudia M

    2015-02-01

    Investigations of the redox process and chemical speciation of Hg(II) lead to a better understanding of biogeochemical processes controlling the transformation of Hg(II) into toxic and bioaccumulative monomethyl mercury, mainly in areas contaminated with Hg(0). This study investigates the speciation and redox processes of Hg in soil samples from a small area contaminated with Hg(0) as a result of gold mining activities in the rural municipality of Descoberto (Minas Gerais, Brazil). Soil samples were prepared by adding Hg(0) and HgCl2 separately to dry soil, and the Hg redox process was monitored using thermodesorption coupled to atomic absorption spectrometry. A portion of the Hg(0) added was volatilized (up to 37.4±2.0%) or oxidized (from 36±7% to 88±16%). A correlation with Mn suggests that this oxidation is favored, but many other factors must be evaluated, such as the presence of microorganisms and the types of organic matter present. The interaction of Hg with the matrix is suggested to involve Hg(II)-complexes formed with inorganic and organic sulfur ligands and/or nonspecific adsorption onto oxides of Fe, Al and/or Mn. The kinetics of the oxidation reaction was approximated for two first-order reactions; the faster reaction was attributed to the oxidation of Hg(0)/Hg(I), and the slower reaction corresponded to Hg(I)/Hg(II). The second stage was 43-139 times slower than the first. The samples spiked with Hg(II) showed low volatilization and a shifting of the signal of Hg(II) to lower temperatures. These results show that the extent, rate and type of redox process can be adverse in soils. Descoberto can serve as an example for areas contaminated with Hg(0).

  13. Taguchi optimization approach for Pb(II) and Hg(II) removal from aqueous solutions using modified mesoporous carbon

    Energy Technology Data Exchange (ETDEWEB)

    Zolfaghari, Ghasem; Esmaili-Sari, Abbas [Department of Environment, Faculty of Natural Resources and Marine Sciences, Tarbiat Modares University, Noor, Mazandaran, P.O. Box: 46414-356 (Iran, Islamic Republic of); Anbia, Mansoor, E-mail: anbia@iust.ac.ir [Research Laboratory of Nanoporous Materials, Faculty of Chemistry, Iran University of Science and Technology, Farjam Street, Narmak, Tehran 16846 (Iran, Islamic Republic of); Younesi, Habibollah [Department of Environment, Faculty of Natural Resources and Marine Sciences, Tarbiat Modares University, Noor, Mazandaran, P.O. Box: 46414-356 (Iran, Islamic Republic of); Amirmahmoodi, Shahram [Research Laboratory of Nanoporous Materials, Faculty of Chemistry, Iran University of Science and Technology, Farjam Street, Narmak, Tehran 16846 (Iran, Islamic Republic of); Ghafari-Nazari, Ali [Loabiran Company, Research and Development Group, Shiraz (Iran, Islamic Republic of)

    2011-09-15

    Graphical abstract: The effect of agitation time (min) (A), initial concentration (mg/l) (B), dose of adsorbent (g/l) (C), temperature ({sup o}C) (D), and pH of solution (E), on the S/N ratio in the removal of lead (II) (left) and mercury (II) (right) by zinc oxide-modified mesoporous carbon CMK-3. Circles on figures indicate optimum conditions for adsorption process. Highlights: {yields} Using the Taguchi method, the removal of Pb(II) and Hg(II) by zinc oxide-modified CMK-3(Zn-OCMK-3) was optimized. {yields} The CMK-3 had high surface area which can accommodate ZnO in a spreading manner. {yields} The results suggest that Zn-OCMK-3 can be effectively used for remediation of Pb (97.25%) and Hg (99%). {yields} Removal of Pb(II) and Hg(II) were highly concentration dependent. - Abstract: Using the Taguchi method, this study presents a systematic optimization approach for removal of lead (Pb) and mercury (Hg) by a nanostructure, zinc oxide-modified mesoporous carbon CMK-3 denoted as Zn-OCMK-3. CMK-3 was synthesized by using SBA-15 and then oxidized by nitric acid. The zinc oxide was loaded to the modified CMK-3 by the equilibrium adsorption of Zn(II) ions from aqueous solution followed by calcination to convert zinc nitrate to zinc oxide. The CMK-3 had porous structure and high specific surface area which can accommodate zinc oxide in a spreading manner, the zinc oxide connects to the carbon surface via oxygen atoms. The controllable factors such as agitation time, initial concentration, temperature, dose and pH of solution have been optimized. Under optimum conditions, the pollutant removal efficiency (PRE) was 97.25% for Pb(II) and 99% for Hg(II). The percentage contribution of each controllable factor was also determined. The initial concentration of pollutant is the most influential factor, and its value of percentage contribution is up to 31% and 43% for Pb and Hg, respectively. Our results show that the Zn-OCMK-3 is an effective nanoadsorbent for lead and mercury

  14. Fractionation, distribution and transport of total mercury and Methylmercury in rivers and tributaries around Wanshan Hg mining district, Guizhou Province, Southwestern China

    Science.gov (United States)

    Feng, X.; Zhang, H.; Larssen, T.; Vogt, R.; Rothenberg, S. E.

    2009-12-01

    The Wanshan mercury (Hg) mining area in Guizhou, China, was one of the world's largest Hg producing regions. Numerous tailings containing mine quarry or calcines still remain, leaching Hg to local rivers and streams and potentially impacting the local population. This study focuses on the regional distribution and temporal variation of aqueous Hg fractions in the 5 main watercourses draining the Wanshan Hg mining and smelting area, covering more than 700 square kilometers. Highly elevated concentrations of total Hg in water samples were found slightly downstream from the Hg mine and smelter tailings, while concentrations decreased sharply to a level well below 50 ng L-1 (US EPA Hg concentration standard for protection of fresh water), within 6-8 km. Total Hg concentrations ranged from extremely high (up to 12 492 ng L-1) just below the calcine tailings, to near the detection level (1.9 ng L-1) in tributary streams. Total Hg levels were correlated with particulate Hg (R2 = 0.996-0.999, Pmethylmercury (MeHg) were inversely related to distance from Hg mine tailings (mine waste calcines), suggesting that mine waste calcines were an important source of both inorganic and MeHg to the downstream environment.

  15. Mercury (Hg) burden in children: The impact of dental amalgam

    Energy Technology Data Exchange (ETDEWEB)

    Al-Saleh, Iman, E-mail: iman@kfshrc.edu.sa [Biological and Medical Research Department, King Faisal Specialist Hospital and Research Centre, PO Box: 3354, Riyadh 11211 (Saudi Arabia); Al-Sedairi, Al anoud [Department of Zoology, College of Science, King Saud University, PO Box: 24452, Riyadh 11495 (Saudi Arabia)

    2011-07-15

    The risks and benefits of using mercury (Hg) in dental amalgam have long been debated. This study was designed to estimate Hg body burden and its association with dental amalgam fillings in 182 children (ages: 5-15 years) living in Taif City. Hg was measured in urine (UHg), hair (HHg) and toenails (NHg) by the Atomic Absorption Spectrophotometer with Vapor Generator Accessory system. Urinary Hg levels were calculated as both micrograms per gram creatinine ({mu}g/g creatinine) and micrograms per liter ({mu}g/L). We found that children with amalgam fillings (N = 106) had significantly higher UHg-C levels than children without (N = 76), with means of 3.763 {mu}g/g creatinine versus 3.457 {mu}g/g creatinine, respectively (P = 0.019). The results were similar for UHg (P = 0.01). A similar pattern was also seen for HHg, with means of 0.614 {mu}g/g (N = 97) for children with amalgam versus 0.242 {mu}g/g (N = 74) for those without amalgam fillings (P = 0). Although the mean NHg was higher in children without amalgam (0.222 {mu}g/g, N = 61) versus those with (0.163 {mu}g/g, N = 101), the relationship was not significant (P = 0.069). After adjusting for many confounders, the multiple logistic regression model revealed that the levels of UHg-C and HHg were 2.047 and 5.396 times higher, respectively, in children with dental amalgam compared to those without (P < 0.01). In contrast, a significant inverse relationship was seen between NHg levels and dental amalgam fillings (P = 0.003). Despite the controversy surrounding the health impact of dental amalgam, this study showed some evidence that amalgam-associated Hg exposure might be related with symptoms of oral health, such as aphthous ulcer, white patches, and a burning-mouth sensation. Further studies are needed to reproduce these findings. The present study showed that significant numbers of children with or without amalgam had Hg levels exceeding the acceptable reference limits. The detrimental neurobehavioral and

  16. Mass Dependent Fractionation of Hg Isotopes in Source Rocks, Mineral Deposits and Spring Waters of the California Coast Ranges, USA

    Science.gov (United States)

    Smith, C. N.; Kesler, S. E.; Blum, J. D.; Rytuba, J. J.

    2007-12-01

    We present here the first study of the isotopic composition of Hg in rocks, ore deposits, and active hydrothermal systems from the California Coast Ranges, one of Earth's largest Hg-depositing systems. The Franciscan Complex and Great Valley Sequence, which form the bedrock in the California Coast Ranges, are intruded and overlain by Tertiary volcanic rocks including the Clear Lake Volcanic Sequence. These rocks contain two types of Hg deposits, hot-spring deposits that form at shallow depths (geothermal systems that release Hg to the present surface. The Franciscan Complex and Great Valley Sequence contain clastic sedimentary rocks with higher concentrations of Hg than volcanic rocks of the Clear Lake Volcanic Field. Mean Hg isotope compositions for all three rock units are similar, although the range of values in Franciscan Complex rocks is greater than in either Great Valley or Clear Lake rocks. Hot spring and silica-carbonate Hg deposits have similar average isotopic compositions that are indistinguishable from averages for the three rock units, although δ202Hg values for the Hg deposits have a greater variance than the country rocks. Precipitates from dilute spring and saline thermal waters in the area have similarly large variance and a mean δ202Hg value that is significantly lower than the ore deposits and rocks. These observations indicate there is little or no isotopic fractionation during release of Hg from its source rocks into hydrothermal solutions. Isotopic fractionation does appear to take place during transport and concentration of Hg in deposits, especially in their uppermost parts. Boiling of hydrothermal fluids is likely the most important process causing of the observed Hg isotope fractionation. This should result in the release of Hg with low δ202Hg values into the atmosphere from the top of these hydrothermal systems and a consequent enrichment in heavy Hg isotopes in the upper crust through time.

  17. Isatin functionalized nanoporous SBA-15 as a selective fluorescent probe for the detection of Hg(II) in water.

    Science.gov (United States)

    Lashgari, Negar; Badiei, Alireza; Mohammadi Ziarani, Ghodsi; Faridbod, Farnoush

    2017-03-07

    A highly ordered mesoporous silica material functionalized with isatin (SBA-Pr-IS) was designed and synthesized. Characterization techniques including XRD, TGA, BET, SEM, and FT-IR were employed to characterize the pore structure, textural properties, microscopic morphology, and molecular composition of grafted organic moieties of SBA-Pr-IS. The successful attachment of the organic moiety (0.34 mmol g(-1)) without the SBA-15 structure collapsing after the modification steps was confirmed. Fluorescence characterization of SBA-Pr-IS was examined upon addition of a wide variety of cations in aqueous medium and it showed high sensitivity toward Hg(2+) ions. During testing in an ion competition experiment, it was observed that the fluorescence changes of the probe were remarkably specific for Hg(2+) ions. Furthermore, a good linearity between the fluorescence intensity of this material and the concentration of Hg(2+) ions was constructed with a suitable detection limit of 3.7 × 10(-6) M. Finally, the applicability of the proposed method was successfully evaluated for the determination of Hg(2+) ions in real samples. Therefore, SBA-Pr-IS can be used as an efficient fluorescence probe for Hg(2+) ions. Graphical Abstract A novel organic-inorganic hybrid material was designed and synthesized by functionalization of SBA-15 mesoporous silica material with isatin. The evaluation of the sensing ability of SBA-Pr-IS using fluorescence spectroscopy revealed that the SBA-Pr-IS was a selective fluorescent probe for Hg(2+) ion in water in the presence of a wide range of metal cations.

  18. Tail-end Hg capture on Au/carbon-monolith regenerable sorbents.

    Science.gov (United States)

    Izquierdo, M Teresa; Ballestero, Diego; Juan, Roberto; García-Díez, Enrique; Rubio, Begoña; Ruiz, Carmen; Pino, M Rosa

    2011-10-15

    In this work, a regenerable sorbent for Hg retention based on carbon supported Au nanoparticles has been developed and tested. Honeycomb structures were chosen in order to avoid pressure drop and particle entrainment in a fixed bed. Carbon-based supports were selected in order to easily modify the surface chemistry to favour the Au dispersion. Results of Hg retention and regeneration were obtained in a bench scale experimental installation working at high space velocities (for sorbent, 53,000 h(-1); for active phase, 2.6 × 10(8) h(-1)), 120 °C for retention temperature and Hg inlet concentration of 23 ppbv. Gold nanoparticles were shown to be the active phase for mercury capture through an amalgamating mechanism. The mercury captured by the spent sorbent can be easily released to be disposed or reused. Mercury evolution from spent sorbents was followed by TPD experiments showing that the sorbent can be regenerated at temperatures as low as 220 °C.

  19. Graphene field-effect transistors with tunable sensitivity for high performance Hg (II) sensing

    Science.gov (United States)

    Li, Peng; Liu, Baijun; Zhang, Dongzhi; Sun, Yan'e.; Liu, Jingjing

    2016-10-01

    Graphene field-effect transistors (FETs) capped with ionophore were fabricated to demonstrate the highly sensitive and selective detection of Hg (II) ions in solution. We systematically investigated the ion detection performances and sensing mechanism of this 2D material. Due to its ambipolar nature, graphene can work as either an n-type or a p-type sensor when a gate voltage is applied to switch its carrier characteristic, resulting in completely different sensing performances. The strong dependence of sensitivity on gate voltage was also investigated. Graphene FETs in optimal regimes were able to detect Hg2+ down to 0.1 ppb, one-fold lower than the World Health Organization tolerance level. Hg2+ ions can be effectively detected over a wide range of concentration (from 0.1 ppb to 1000 ppb) with graphene conductance change following the Langmuir isotherm for molecules adsorption on surface, and the time constant for ion adsorption extracted was only 3.5 s, approximately. The transfer characteristics of graphene FETs capped with mercury ionophore did not show obvious change by the existence of arsenite ions, demonstrating good selectivity. Our results illustrate the potential utility of ionophore integrated graphene FETs for monitoring heavy metal ions in solution.

  20. Variation in fish mercury concentrations in streams of the Adirondack region, New York: A simplified screening approach using chemical metrics

    Science.gov (United States)

    Burns, Douglas A.; Riva-Murray, Karen

    2018-01-01

    Simple screening approaches for the neurotoxicant methylmercury (MeHg) in aquatic ecosystems may be helpful in risk assessments of natural resources. We explored the development of such an approach in the Adirondack Mountains of New York, USA, a region with high levels of MeHg bioaccumulation. Thirty-six perennial streams broadly representative of 1st and 2nd order streams in the region were sampled during summer low flow and analyzed for several solutes and for Hg concentrations in fish. Several landscape and chemical metrics that are typically strongly related to MeHg concentrations in aquatic biota were explored for strength of association with fish Hg concentrations. Data analyses were based on site mean length-normalized and standardized Hg concentrations (assumed to be dominantly MeHg) in whole juvenile and adult Brook Trout Salvelinus fontinalis, Creek Chub Semotilus atromaculatus, Blacknose Dace Rhinichthys atratulus, and Central Mudminnow Umbra limi, as well as on multi-species z-scores. Surprisingly, none of the landscape metrics was related significantly to regional variation in fish Hg concentrations or to z-scores across the study streams. In contrast, several chemical metrics including dissolved organic carbon (DOC) concentrations, sulfate concentrations (SO42−), pH, ultra-violet absorbance (UV254), and specific ultra-violet absorbance were significantly related to regional variation in fish Hg concentrations. A cluster analysis based on DOC, SO42−, and pH identified three distinct groups of streams: (1) high DOC, acidic streams, (2) moderate DOC, slightly acidic streams, and (3) low DOC circum-neutral streams with relatively high SO42−. Preliminary analysis indicated no significant difference in fish Hg z-scores between the moderate and high DOC groups, so these were combined for further analysis. The resulting two groups showed strong differences (p 6.9 mg/L, SO42− 0.31 cm−1 were tested as thresholds to identify Adirondack

  1. Functionalized CMK-3 mesoporous carbon with 2-amino-5-mercapto-1,3,4-thiadiazole for Hg(II) removal from aqueous media.

    Science.gov (United States)

    Anbia, Mansoor; Dehghan, Roghaye

    2014-07-01

    Ordered mesoporous carbon (CMK-3) was synthesized and functionalized with 2-amino-5-mercapto-1,3,4-thiadiazole groups (AMT-OCMK-3) for Hg(II) removal from aqueous solution. The modified CMK-3 was characterized by X-ray diffraction, N2 adsorption-desorption isotherm, scanning electron microscopy and Fourier transform infrared spectroscopy. The effects of solution pH, contact time, initial Hg(II) concentration and matrix effect were studied. The adsorption data were successfully fitted with the Langmuir model, exhibiting high adsorption capacity of 450.45 mg/g of AMT-OCMK-3. In the solid-phase extraction system a series of experimental parameters such as sample flow rate, sample volume, eluent volume and concentration of the eluent solution have been investigated and established for preconcentration of Hg(II) in aqueous solution. The results showed that the enrichment factor for Hg(II) was 250, the precision (relative standard deviation (RSD), %) for six replicate measurements was 2.05% and the limit of detection for Hg(II) was achieved at 0.17 μg/L.

  2. Hypotension is 100 mm Hg on the Battlefield

    Science.gov (United States)

    2011-10-01

    corroborate the predictive value of admission metabolic acidosis on patient survival. We also were able to show that an SBP of 110 mm Hg after injury was... metabolic acidosis , complications, length of stay, intensive care unit days, and ventilator days all increased. The implication of our result suggested

  3. Experimental study of 199Hg spin anti-relaxation coatings

    CERN Document Server

    Chowdhuri, Z; Horras, M; Kirch, K; Krempel, J; Lauss, B; Mtchedlishvili, A; Rebreyend, D; Roccia, S; Schmidt-Wellenburg, P; Zsigmond, G

    2013-01-01

    We report on a comparison of spin relaxation rates in a $^{199}$Hg magnetometer using different wall coatings. A compact mercury magnetometer was built for this purpose. Glass cells coated with fluorinated materials show longer spin coherence times than if coated with their hydrogenated homologues. The longest spin relaxation time of the mercury vapor was measured with a fluorinated paraffin wall coating.

  4. In vivo formation of natural HgSe nanoparticles in the liver and brain of pilot whales

    Science.gov (United States)

    To understand the biochemistry of methylmercury (MeHg) that leads to the formation of mercury-selenium (Hg-Se) clusters is a long outstanding challenge that promises to deepen our knowledge of MeHg detoxification and the role SE plays in this process. Here, we show that mercury ...

  5. In vivo formation of natural HgSe nanoparticles in the liver and brain of pilot whales

    Science.gov (United States)

    To understand the biochemistry of methylmercury (MeHg) that leads to the formation of mercury-selenium (Hg-Se) clusters is a long outstanding challenge that promises to deepen our knowledge of MeHg detoxification and the role SE plays in this process. Here, we show that mercury ...

  6. Linking diurnal trends in methylmercury concentration and organic matter photo-reactivity in wetlands of the Yolo Bypass, California

    Science.gov (United States)

    Fleck, J. A.; Downing, B. D.; Saraceno, J.; Gill, G.; Stephenson, M.; Bergamaschi, B. A.

    2008-12-01

    Aqueous concentrations of methylmercury (MeHg) are known to vary temporally and spatially due to multiple concurrent production and loss mechanisms, and due to variations in the hydrologic connectivity between the methylating substrate (most commonly the benthos) and the overlying water compartments. Diurnal trends in MeHg production, bacterial demethylation, photo-demethylation, diffusion and advection transport processes have been identified and investigated; however, the magnitude and relative importance of each process in mediating overlying water MeHg concentrations, is not well known in natural wetland systems. Temporal variations in aqueous MeHg concentrations may impact the biological accumulation of MeHg into the base of the aquatic food chain, and may challenge regulatory efforts designed to mitigate MeHg exports from point and non-point sources. To identify the possible "hot moments" during the diurnal cycle, surface water MeHg concentrations were monitored in two agricultural wetland settings (wild rice and white rice fields) over a 24- hour period within the Yolo Bypass Wildlife Area, California using a combination of in situ optical sensors and traditional surface-water grab samples. In the wild rice field, MeHg concentrations doubled from 1 ng/L to 2 ng/L over the nighttime hours and returned to 1 ng/L during the daylight hours, whereas the white rice field showed no significant variation in MeHg concentration (0.73 +/- 0.08 ng/L) throughout the diurnal cycle. Similar trends were observed when MeHg data was expressed as a percentage of total Hg, with both wetland habitats exhibiting similar levels (20% MeHg) following the nighttime period and the wild rice field declining to 10% in the early evening. Field parameters measured in situ (including: solar radiation, pH, dissolved oxygen, and temperature) exhibited large diurnal trends in both wetlands, whereas optical proxies for dissolved organic matter (DOM) composition mirrored the fluctuations in MeHg

  7. Genetic Polymorphisms in Glutathione (GSH- Related Genes Affect the Plasmatic Hg/Whole Blood Hg Partitioning and the Distribution between Inorganic and Methylmercury Levels in Plasma Collected from a Fish-Eating Population

    Directory of Open Access Journals (Sweden)

    Andréia Ávila Soares de Oliveira

    2014-01-01

    Full Text Available This study aims to evaluate the effects of polymorphisms in glutathione (GSH- related genes (GSTM1, GSTT1, GSTP1, GCLM, and GCLC in the distribution of Hg in the blood compartments in humans exposed to methylmercury (MeHg. Subjects (n=88, exposed to MeHg from fish consumption, were enrolled in the study. Hg species in the plasma compartment were determined by LC-ICP-MS, whereas genotyping was performed by PCR assays. Mean total Hg levels in plasma (THgP and whole blood (THgB were 10±4.2 and 37±21, whereas mean evels of plasmatic MeHg (MeHgP, inorganic Hg (IHgP, and HgP/HgB were 4.3±2.9, 5.8±2.3 µg/L, and 0.33±0.15, respectively. GSTM1 and GCLC polymorphisms influence THgP and MeHgP (multivariate analyses, P<0.050. Null homozygotes for GSTM1 showed higher THgP and MeHgP levels compared to subjects with GSTM1 (THgP β=0.22, P=0.035; MeHgP β=0.30, P=0.050 and persons carrying at least one T allele for GCLC had significant higher MeHgP (β=0.59, P=0.046. Also, polymorphic GCLM subjects had lower THgP/THgB than those with the nonvariant genotype. Taken together, data of this study suggest that GSH-related polymorphisms may change the metabolism of MeHg by modifying the distribution of mercury species iin plasma compartment and the HgP/HgB partitioning.

  8. Effect of bimetal Hg2+ and Cu2+on activity and conformation of papain%双金属Hg2+和Cu2+对木瓜蛋白酶活性与构象的影响

    Institute of Scientific and Technical Information of China (English)

    张存滢; 曾虹燕; 熊龙斌; 刘学英; Gohi A; 蔡西玲; 陈泽新

    2013-01-01

    The effect of the bimetal Hg2+ and Cu2+ on activity and conformation of papain was studied.The secondary structures of the papain treated by the bimetal ions were investigated by characterization using FT-IR,fluorescence emitting and ultraviolet-absorption spectra.The results show that there exists the dosage-response relationship between the metals and papain activity,which indicates that the bimetal ions have Hormesis effect on the activity known as “a low dose stimulation,high dose inhibition”.Under low concentration,the bimetal ions exhibit synergistic activation effect on papain activity,and Cu2+ shields Hg2+ inhibition on the activity at high concentration.On the one hand,when the concentrations of Hg2+ and Cu2+ are 10-6 and 10-8 mol/L respectively,the strongest activity effect of the bimetal ions on papain is obtained.The content of the nonrandom secondary structures (α-helix and β-sheet) of the treated papain is the highest with the secondary structures of papain being most stable,and enzymatic affinity strongest and papain activity being best.When the concentrations of Hg2+ and Cu2+ are 10-4mol/L,the ordered structure content and papain activity are the lowest.The bimetal ions unfold the enzymic protein and cause the destruction of the secondary structures.The order degree ofpapain conformation is correlated positively with the activity.%研究双金属Hg2+和Cu2+对木瓜蛋白酶活性与构象的影响.利用FT-IR、荧光发射以及紫外吸收光谱探讨Hg2+和Cu2+处理与木瓜蛋白酶二级结构变化的关系.研究结果表明:金属离子与木瓜蛋白酶活性之间存在剂量-效应关系,表现出低剂量促进,高剂量抑制的Hormesis现象.低浓度下,双金属Hg2+和Cu2+表现出协同激活效应;高浓度下,Cu2+的添加屏蔽了Hg2+的抑制作用.双金属离子浓度为10-6 mol/L Hg2+和10-8 mol/L Cu2+时,对酶的激活效应最大,其处理的木瓜蛋白酶的有序结构(α-螺旋和β-折叠)含量最高,二

  9. High-value utilization of lignin to synthesize Ag nanoparticles with detection capacity for Hg²⁺.

    Science.gov (United States)

    Shen, Zuguang; Luo, Yuqiong; Wang, Qun; Wang, Xiaoying; Sun, Runcang

    2014-09-24

    This study reports the rapid preparation of silver nanoparticles (AgNPs) from Tollens' reagent under microwave irradiation. In the synthesis, lignin with reducing groups and spatial three-dimensional structure was used as reducing and stabilizing agents without other chemical reagents, and the effects of the ratio of lignin to Ag(+), reaction temperature, and heating time on the synthesis of AgNPs were investigated. The obtained AgNPs were further characterized by UV-vis, Malvern particle size, TEM, XRD, and XPS analyses. The structural changes of lignin before and after reaction were also studied by FT-IR, (1)H NMR, (13)C NMR, and GC-MS. The results revealed that the obtained AgNPs were mostly spherical with diameters of around 24 nm. The optimum reaction conditions were a ratio 50 mg of lignin to 0.3 mM of Ag(+), a microwave irradiation temperature of 60 °C, and a heating time of 10 min. Moreover, AgNPs redispersed well in water and ethanol after centrifugation for the removal of lignin. During the formation of AgNPs, lignin was oxidized, and the side chains of lignin were partly disrupted into small molecules, such as hydrocarbon and alcohol. The resultant lignin-AgNPs showed highly selective sensing detection for Hg(2+), and the color of the lignin-AgNP solution containing Hg(2+) decreased gradually with increasing amounts of Hg(2+) within seconds, but the other 19 metal ions had little effect on the color and surface plasmon absorption band of the lignin-AgNPs. Also, there was a linear relationship between the absorbance and Hg(2+) concentration, with a limit of detection concentration of 23 nM. This study provides not only a new way to take advantage of agricultural and forestry residues, but also a green and rapid method for the synthesis of AgNPs to detect the toxic ion Hg(2+) selectively and sensitively.

  10. Mercury (Hg) burden in children: the impact of dental amalgam.

    Science.gov (United States)

    Al-Saleh, Iman; Al-Sedairi, Al Anoud

    2011-07-15

    The risks and benefits of using mercury (Hg) in dental amalgam have long been debated. This study was designed to estimate Hg body burden and its association with dental amalgam fillings in 182 children (ages: 5-15 years) living in Taif City. Hg was measured in urine (UHg), hair (HHg) and toenails (NHg) by the Atomic Absorption Spectrophotometer with Vapor Generator Accessory system. Urinary Hg levels were calculated as both micrograms per gram creatinine (μg/g creatinine) and micrograms per liter (μg/L). We found that children with amalgam fillings (N=106) had significantly higher UHg-C levels than children without (N=76), with means of 3.763 μg/g creatinine versus 3.457 μg/g creatinine, respectively (P=0.019). The results were similar for UHg (P=0.01). A similar pattern was also seen for HHg, with means of 0.614 μg/g (N=97) for children with amalgam versus 0.242 μg/g (N=74) for those without amalgam fillings (P=0). Although the mean NHg was higher in children without amalgam (0.222 μg/g, N=61) versus those with (0.163 μg/g, N=101), the relationship was not significant (P=0.069). After adjusting for many confounders, the multiple logistic regression model revealed that the levels of UHg-C and HHg were 2.047 and 5.396 times higher, respectively, in children with dental amalgam compared to those without (Pdental amalgam fillings (P=0.003). Despite the controversy surrounding the health impact of dental amalgam, this study showed some evidence that amalgam-associated Hg exposure might be related with symptoms of oral health, such as aphthous ulcer, white patches, and a burning-mouth sensation. Further studies are needed to reproduce these findings. The present study showed that significant numbers of children with or without amalgam had Hg levels exceeding the acceptable reference limits. The detrimental neurobehavioral and/or nephrotoxic effects of such an increased Hg on children should be a cause of concern, and further investigation is warranted. Our

  11. Evaluation and development of soil values for the pathway 'soil to plant'. Significance of mercury evaporation for the burden of plants; Ueberpruefung und Fortentwicklung der Bodenwerte fuer den Boden-Pflanze-Pfad. Teilbericht 2: Evaporation von Quecksilber aus kontaminierten Boeden und deren Bedeutung fuer die Hg-Aufnahme von Kulturpflanzen

    Energy Technology Data Exchange (ETDEWEB)

    Schlueter, K.; Gaeth, S.

    2001-10-01

    In cooperation with the Ad-hoc working group 'Transfer of heavy metals from soil to plant' of the Laenderarbeitsgemeinschaft Bodenschutz (LABO) the significance of mercury evaporation for the deduction of threshold values in respect of the impact via the pathway soil to plant was investigated. Mercury contamination of food- and feeding stuff plants was examined with special emphasis. For these purposes a lab experiment including three different soils with varying initial mercury load (background level, geogenic and anthropogenic contamination) and two different plant species (parsley and spinach) was carried out under defined conditions in closed lysimeters. Mercury uptake via the roots was minimised since the plants grew in isolated customary substrate which showed a low concentration of mercury. Thus, only the surrounding soil evaporated mercury. The concentrations of mercury in the plants in the background level treatment (0.1 mg Hg/kg dry soil) were 0.15 mg/kg dry matter (spinach). The treatment with anthropogenic contaminated soil (111 mg Hg/kg dry soil) resulted in concentrations in the two plants of 2.0 and 2.6 mg/kg dry matter, respectively. A comparable order of magnitude was achieved in the geogenic contaminated treatment (34 mg Hg/kg dry soil) with 2.1 mg/kg dry matter (spinach) and 0.44 mg/kg dry matter (parsley). Experiments conducted with radioactive {sup 203}Hg showed in each case Hg-tracer in the leaves, in the stem and in the roots, indicating a translocation within the plant from leaf to root. By means of a comprehensive literature study the state of the art for Hg-evaporation and Hg-uptake of plants was compiled. Comparing the experimental results with data derived from literature, the Hg-concentrations found are confirmed by results of other authors. (orig.) [German] In fachlicher Zusammenarbeit mit der Ad-hoc-Arbeitsgruppe 'Schwermetalltransfer Boden/Pflanze' der Laenderarbeitsgemeinschaft Bodenschutz (LABO) wurde fuer die

  12. Development of a novel fluorimetric bulk optode membrane based on meso-tetrakis(2-hydroxynaphthyl) porphyrin (MTHNP) for highly sensitive and selective monitoring of trace amounts of Hg2+ ions.

    Science.gov (United States)

    Shamsipur, Mojtaba; Sadeghi, Marzieh; Beyzavi, Mohammad Hassan; Sharghi, Hashem

    2015-03-01

    The fluorescence spectra and response characteristics of two porphyrin compounds meso-tetrakis(2-hydroxynaphthyl) porphyrin and meso-tetra (2-thiophene) porphyrin (MTHNP) to Hg(2+) were investigated. MTHNP showed preferable fluorescence response to Hg(2+). Thereby, an efficient and selective fluorimetric optode membrane based on the fluorescence quenching of MTHNP for Hg(2+) ion determination at low concentration levels has been developed. The sensing membrane containing MTHNP reversibly responded to Hg(2+) with a working concentration range covering from 5.0×10(-9) to 1.25×10(-5)M with a relatively fast response time less than 3min. In addition to high stability, reversibility and reproducibility, the sensor showed extremely high selectivity toward Hg(2+) ion with respect to some alkali, alkaline earth and heavy metal ions. The limit of detection for Hg(2+) was 5.0×10(-9)M. The proposed fluorescent sensor was successfully applied to the direct determination of mercury content of biofenac eye drop, hair and different water samples. Copyright © 2014 Elsevier B.V. All rights reserved.

  13. A Comparative Study on the Sorption Characteristics of Pb(II and Hg(II onto Activated Carbon

    Directory of Open Access Journals (Sweden)

    N. Muthulakshmi Andal

    2010-01-01

    Full Text Available Biosorption equilibrium and kinetics of Pb(II and Hg(II on coconut shell carbon (CSC were investigated by batch equilibration method. The effects of pH, adsorbent dosage, contact time, temperature and initial concentration of Pb(II and Hg(II on the activated carbon of coconut shell wastes were studied. Maximum adsorption of Pb(II occurred at pH 4.5 and Hg(II at pH 6. The sorptive mechanism followed the pseudo second order kinetics. The equilibrium data were analysed by Langmuir, Freundlich and Dubinin-Radushkevich isotherm models. The equilibration data fitted well with both Langmuir and Freundlich isotherm model. The Langmuir adsorption capacity for Pb(II was greater than Hg(II. The mean free energy of adsorption calculated from Dubinin-Radushkevich (D-R isotherm model indicated that the adsorption of metal ions was found to be by chemical ion exchange. Thermodynamic parameter showed that the sorption process of Pb(II onto SDC was feasible, spontaneous and endothermic under studied conditions. A comparison was evaluated for the two metals.

  14. Growth, properties and applications of HgCdTe

    Science.gov (United States)

    Schmit, J. L.

    1983-12-01

    This paper provides primarily a review of the methods used to grow HgCdTe with a summary of some of its basic properties and applications. Methods of crystal growth fall generally into three classes: growth from the melt, from solution and from the vapor phase. All three methods have been and are being used to grow HgCdTe. The high vapor pressure of HgCdTe at the melting point, combined with a large segregation coefficient, have effectively limited the use of Czochralski or zone melting techniques, but two melt growth techniques have survived: (1) a variation of Bridgman growth called quench-anneal wherein a dendritic crystal is formed by quenching the melt and is homogenized by solid state recrystallization below the melting point, (2) a variation of freezing from a large volume called slush-growth wherein a melt is held in a temperature gradient for several weeks while a crystal grows. Growth from solution has taken the form of liquid phase epitaxy (LPE) on CdTe with the LPE systems including growth from Hg-rich, HgTe-rich and Te-rich solutions and using tipping, vertical dipping, vertical sliding and horizontal sliding. Vapor phase growth is very promising but is not yet in production. Techniques include growth by isothermal close spaced epitaxy in which HgTe is transported isothermally by chemical potential onto CdTe, molecular beam epitaxy (MBE) in which elements are evaporated in a high vacuum, and metal organic chemical vapor deposition (MOCVD) in which some of the metal atoms are carried to the substrate bound to organic radicals before being freed by pyrolysis. In all these methods, control of Hg pressure is a major concern. The fundamental properties discussed briefly are those of prime interest to detector manufacturers: energy gap ( Eg), intrinsic carrier concentration ( ni), and electrical activity of dopants. A reasonable fit to the Eg data from ˜ 20 papers is given by Eg = -0.302+1.93x+5.35×10 -4T(1-2x)-0.810x 2+0.832x 3. This gap, combined with k

  15. Folic acid functionalized silver nanoparticles with sensitivity and selectivity colorimetric and fluorescent detection for Hg2+ and efficient catalysis

    Science.gov (United States)

    Su, Dongyue; Yang, Xin; Xia, Qingdong; Zhang, Qi; Chai, Fang; Wang, Chungang; Qu, Fengyu

    2014-09-01

    In this research, folic acid functionalized silver nanoparticles (FA-AgNPs) were selected as a colorimetric and a ‘turn on’ fluorescent sensor for detecting Hg2+. After being added into Hg2+, AgNPs can emit stable fluorescence at 440 nm when the excitation wavelength is selected at 275 nm. The absorbance and fluorescence of the FA-AgNPs could reflect the concentration of the Hg2+ ions. Thus, we developed a simple, sensitive analytical method to detect Hg2+ based on the colorimetric and fluorescence enhancement of FA-AgNPs. The sensor exhibits two linear response ranges between absorbance and fluorescence intensity with Hg2+ concentration, respectively. Meanwhile, a detection limit of 1 nM is estimated based on the linear relationship between responses with a concentration of Hg2+. The high specificity of Hg2+ with FA-AgNPs interactions provided the excellent selectivity towards detecting Hg2+ over other metal ions (Pb2+, Mg2+, Zn2+, Ni2+, Cu2+, Co2+, Ca2+, Mn2+, Fe2+, Cd2+, Ba2+, Cr6+ and Cr3+). This will provide a simple, effective and multifunctional colorimetric and fluorescent sensor for on-site and real-time Hg2+ ion detection. The proposed method can be applied to the analysis of trace Hg2+ in lake water. Additionally, the FA-AgNPs can be used as efficient catalyst for the reduction of 4-nitrophenol and potassium hexacyanoferrate (III).

  16. Identification of contamination in a lake sediment core using Hg and Pb isotopic compositions, Lake Ballinger, Washington, USA

    Science.gov (United States)

    Gray, John E.; Pribil, Michael J.; Van Metre, Peter C.; Borrok, David M.; Thapalia, Anita

    2013-01-01

    Concentrations and isotopic compositions of Hg and Pb were measured in a sediment core collected from Lake Ballinger, near Seattle, Washington, USA. Lake Ballinger has been affected by input of metal contaminants emitted from the Tacoma smelter, which operated from 1887 to 1986 and was located about 53 km south of the lake. Concentrations and loadings of Hg and Pb in Lake Ballinger increased by as much as three orders of magnitude during the period of smelting as compared to the pre-smelting period. Concentrations and loadings of Hg and Pb then decreased by about 55% and 75%, respectively, after smelting ended. Isotopic compositions of Hg changed considerably during the period of smelting (δ202Hg = −2.29‰ to −0.38‰, mean −1.23‰, n = 9) compared to the pre-smelting period (δ202Hg = −2.91‰ to −2.50‰, mean −2.75‰, n = 4). Variations were also observed in 206Pb/207Pb and 208Pb/207Pb isotopic compositions during these periods. Data for Δ199Hg and Δ201Hg indicate mass independent fractionation (MIF) of Hg isotopes in Lake Ballinger sediment during the smelting and post-smelting period and suggest MIF in the ore smelted, during the smelting process, or chemical modification at some point in the past. Negative values for Δ199Hg and Δ201Hg for the pre-smelting period are similar to those previously reported for soil, peat, and lichen, likely suggesting some component of atmospheric Hg. Variations in the concentrations and isotopic compositions of Hg and Pb were useful in tracing contaminant sources and the understanding of the depositional history of sedimentation in Lake Ballinger.

  17. MBE - growth of capped, strained HgTe, a 3D topological insulator

    Energy Technology Data Exchange (ETDEWEB)

    Ames, Christopher; Leubner, Philipp; Bruene, Christoph; Buhmann, Hartmut; Molenkamp, Laurens [Universitaet Wuerzburg, D-97074 Wuerzburg (Germany)

    2013-07-01

    The discovery of two (2D) and three dimensional (3D) topological insulator (TI) behavior in HgTe - systems opens a large field for studying magneto transport properties of both. We grow HgTe as a 3D topological insulator by molecular beam epitaxy. Unstrained bulk HgTe is a semimetal but opens a gap of roughly 22 meV when grown fully strained on <001> CdTe substrate due to 0.3 % lattice mismatch and shows magnetotransport properties of a 3D TI. Hall measurements show electron mobilities of around 50.000 cm{sup 2}(V s){sup -1}. To increase electron mobilities, various growth optimizations have been carried out. Firstly we grew an HgCdTe buffer layer between the substrate and bulk HgTe. Different buffer thicknesses were analyzed ex-situ by HRXRD, AFM and standard Hall measurements. Secondly, we added a cap-layer of HgCdTe on top of the bulk HgTe. Doing so, we were able to raise the electron mobility of the bulk HgTe up to one order of magnitude. Time-dependent XPS measurements allowed us to hold the suppressed oxidization of the surface responsible for this effect. Through the advanced material quality we have now more prospects for better understanding of the transport properties in strained HgTe.

  18. Multi-elemental concentrations in the tissues of the oceanic squid Todarodes filippovae from Tasmania and the southern Indian Ocean.

    Science.gov (United States)

    Kojadinovic, Jessica; Jackson, Christine H; Cherel, Yves; Jackson, George D; Bustamante, Paco

    2011-07-01

    This study investigates 14 elements (Ag, As, Cd, Co, Cr, Cu, Fe, Hg, Mn, Ni, Pb, Se, V and Zn) in the tissues of the oceanic ommastrephid squid Todarodes filippovae from waters surrounding Île Amsterdam (southern Indian Ocean) and Tasmania (Australia). As for other cephalopod species, the digestive gland and branchial hearts showed the highest concentrations of many elements (Ag, Cd, Se, V and Zn, and Cr and Ni, respectively) highlighting their role in bioaccumulation and detoxification processes. With the exception of As and Hg, the muscles showed relatively low trace element concentrations. Squid size was positively correlated to Ag, As, Cd, Hg and Zn concentrations in Tasmanian squid and negatively correlated to all but Hg and Zn concentrations in Île Amsterdam squid. Furthermore, no differences in elemental concentrations were noted between sexes. There were, however, some differences between mated and non-mated females from Tasmania. Comparing elemental concentrations in squid from both islands, higher concentrations of Cd, Co, Cr, Ni, Pb and V in squid sampled in Île Amsterdam reflect different exposure conditions. When considering T. filippovae as a dietary resource for humans it should be noted that, given their Hg content, squids from Île Amsterdam are not recommended for consumption on a regular basis. Moreover, regardless of the squid's origin, digestive glands should be avoided as Cd and Hg concentrations were above the European Union authorized limits in these organs.

  19. Emission Spectra of Working Mixtures of a HgBr/HgCl Excimer Lamp

    Science.gov (United States)

    Malinin, A. N.; Guĭvan, N. N.; Shimon, L. L.

    2000-12-01

    A study of emission spectra of a gas-discharge plasma produced in a HgBr/HgCl excimer lamp, which is filled with multicomponent working mixtures at atmospheric pressure (HgBr2 and HgCl2 with additions of molecular nitrogen and xenon), are reported. A gas-discharge plasma was produced by high-frequency (pulses ˜100 ns long with a repetition rate of up to 2000 Hz) barrier and surface discharges, which took place simultaneously. Emission of HgBr* and HgCl* excimer molecules, the second positive system of molecular oxygen, and helium and xenon lines in the UV, visible, and IR spectral regions was observed. The strongest emission of HgBr* and HgCl* molecules (the emission intensities were in the ratio 10:1) was observed in the HgBr2: HgCl2: N2: He mixture. Regularities in spectral and integrated characteristics of gas-discharge plasma emission are discussed.

  20. HgTe-CdTe SUPERLATTICES

    OpenAIRE

    Smith, D; Mcgill, T.

    1984-01-01

    We report on a theoretical study of the electronic properties of HgTe-CdTe superlattices. The band gap as a function of layer thickness, effective masses normal to the layer plane and tunneling length are compared to the corresponding (Hg, Cd)Te alloys. We find that the superlattice possesses a number of properties that may make it superior to the corresponding alloy as an infrared material.

  1. Synthesis of current data for Hg in areas of geologic resource extraction contamination and aquatic systems in China.

    Science.gov (United States)

    Qiu, Guangle; Feng, Xinbin; Jiang, Guibin

    2012-04-01

    China has become the largest contributor of anthropogenic atmospheric mercury (Hg) in the world owing to its fast growing economy and the largest of populations. Over the last two decades, Hg has become of increasing environmental concern in China and much has been published on its distribution, transportation, methylation, and bioaccumulation in aquatic systems and areas of geologic resource extraction contaminated sites, such as coal-fired power plants, non-ferrous smelters, Hg mining and retorting sites, Au amalgam, landfills, chemical plants, etc.. Environmental compartments, like soil, water, air, and crop from areas of geologic resource extraction contamination, especially from Hg mining regions, exhibit elevated values of total-Hg and MMHg. Risk assessments indicate that the consumption of rice, which has a high bioaccumulation of MMHg, has become the dominant pathway of MMHg exposure of inhabitants living in Hg mining areas. Low concentrations less than 5ngl(-1) in total-Hg can be observed in rivers from remote areas, however, high concentrations that reached 1600ngl(-1) in total-Hg can be found in rivers from industrial and urban areas. The studies of hydropower reservoirs of southwest China indicated the old reservoirs act as net sinks for total-Hg and net sources of MMHg, while newly established ones act as net sinks for both total-Hg and MMHg, which is in sharp contrast to the evolution of biomethylation in reservoirs established in the boreal belt of North America and Eurasia. Fish from those reservoirs have relatively low levels of total-Hg, which do not exceed the maximum total-Hg limit of 0.5mgkg(-1) recommended by WHO. Currently, however, there is still a large data gap regarding Hg even in the areas mentioned above in China, which results in poor understanding of its environmental biogeochemistry. Moreover, for a better understanding of human and environmental health effects caused by the fast growing economy, long-term Hg monitoring campaigns are

  2. Novel methodology for the study of mercury methylation and reduction in sediments and water using 197Hg radiotracer.

    Science.gov (United States)

    Ribeiro Guevara, Sergio; Zizek, Suzana; Repinc, Urska; Pérez Catán, Soledad; Jaćimović, Radojko; Horvat, Milena

    2007-03-01

    Mercury tracers are powerful tools that can be used to study mercury transformations in environmental systems, particularly mercury methylation, demethylation and reduction in sediments and water. However, mercury transformation studies using tracers can be subject to error, especially when used to assess methylation potential. The organic mercury extracted can be as low as 0.01% of the endogenous labeled mercury, and artefacts and contamination present during methylmercury (MeHg) extraction processes can cause interference. Solvent extraction methods based on the use of either KBr/H2SO4 or HCl were evaluated in freshwater sediments using 197Hg radiotracer. Values obtained for the 197Hg tracer in the organic phase were up to 25-fold higher when HCl was used, which is due to the coextraction of 197Hg2+ into the organic phase during MeHg extraction. Evaluations of the production of MeHg gave similar results with both MeHg extraction procedures, but due to the higher Hg2+ contamination of the controls, the uncertainty in the determination was higher when HCl was used. The Hg2+ contamination of controls in the HCl extraction method showed a nonlinear correlation with the humic acid content of sediment pore water. Therefore, use of the KBr/H2SO4 method is recommended, since it is free from these interferences. 197Hg radiotracer (T1/2=2.673 d) has a production rate that is about 50 times higher than that of 203Hg (T1/2=46.595 d), the most frequently used mercury radiotracer. Hence it is possible to obtain a similar level of performance to 203Hg when it is used it in short-term experiments and produced by the irradiation of 196Hg with thermal neutrons, using mercury targets with the natural isotopic composition. However, if the 0.15% natural abundance of the 196Hg isotope is increased, the specific activity of the 197Hg tracer can be significantly improved. In the present work, 197Hg tracer was produced from mercury 51.58% enriched in the 196Hg isotope, and a 340-fold

  3. Hg-contaminated terrestrial spiders pose a potential risk to songbirds at Caddo Lake (Texas/Louisiana, USA).

    Science.gov (United States)

    Gann, Gretchen L; Powell, Cleveland H; Chumchal, Matthew M; Drenner, Ray W

    2015-02-01

    Methylmercury (MeHg) is an environmental contaminant that can have adverse effects on wildlife. Because MeHg is produced by bacteria in aquatic ecosystems, studies of MeHg contamination of food webs historically have focused on aquatic organisms. However, recent studies have shown that terrestrial organisms such as songbirds can be contaminated with MeHg by feeding on MeHg-contaminated spiders. In the present study, the authors examined the risk that MeHg-contaminated terrestrial long-jawed orb weaver spiders (Tetragnatha sp.) pose to songbirds at Caddo Lake (Texas/Louisiana, USA). Methylmercury concentrations in spiders were significantly different in river, wetland, and open-water habitats. The authors calculated spider-based wildlife values (the minimum spider MeHg concentrations causing physiologically significant doses in consumers) to assess exposure risks for arachnivorous birds. Methylmercury concentrations in spiders exceeded wildlife values for Carolina chickadee (Poecile carolinensis) nestlings, with the highest risk in the river habitat. The present study indicates that MeHg concentrations in terrestrial spiders vary with habitat and can pose a threat to small-bodied nestling birds that consume large amounts of spiders at Caddo Lake. This MeHg threat to songbirds may not be unique to Caddo Lake and may extend throughout the southeastern United States. © 2014 SETAC.

  4. 46 CFR 53.05-1 - Safety valve requirements for steam boilers (modifies HG-400 and HG-401).

    Science.gov (United States)

    2010-10-01

    ... 46 Shipping 2 2010-10-01 2010-10-01 false Safety valve requirements for steam boilers (modifies HG... requirements for steam boilers (modifies HG-400 and HG-401). (a) The pressure relief valve requirements and the safety valve requirements for steam boilers must be as indicated in HG-400 and HG-401 of section IV...

  5. Investigation of Hg uptake and transport between paddy soil and rice seeds combining Hg isotopic composition and speciation

    Directory of Open Access Journals (Sweden)

    C. Feng

    2016-02-01

    Full Text Available Abstract Human consumption of rice constitutes a potential toxicological risk in mercury (Hg polluted areas such as Hg mining regions in China. It is recognized to be an important source of Hg for the local human diet considering the efficient bioaccumulation of methylmercury (MeHg in rice seed. To assess Hg sources and uptake pathways to the rice plants, Hg speciation and isotopic composition were investigated in rice seeds and their corresponding paddy soils from different locations within the Wanshan Hg mining area (Guizhou Province, China. A large variation of Hg speciation is observed in rice seeds and paddy soils irrespective of the sampling location. Mass dependent fractionation (MDF of Hg in rice seeds differs by up to ∼4.0 ‰ in δ202Hg values, while mass independent fractionation (MIF of Hg isotopes remains constant (Δ199Hg ∼ 0‰. Hg isotopic composition in rice seeds covaries with that of paddy soils but exhibits lighter isotopic signature (δ202Hg. Such isotopic offset is mainly attributed to plant uptake and translocation processes. Also, seeds containing higher MeHg (MeHg/total Hg > 50% have significantly heavier Hg isotopes suggesting that MeHg uptake and transport to the seed in such rice plants is facilitated compared to inorganic Hg.

  6. Effects of salinity and humic acid on the sorption of Hg on Fe and Mn hydroxides.

    Science.gov (United States)

    Liang, Peng; Li, Yi-Chun; Zhang, Chan; Wu, Sheng-Chun; Cui, Hao-Jie; Yu, Shen; Wong, Ming H

    2013-01-15

    The objective of this study was to investigate the influence of humic acid (HA) and salinity on adsorption of Hg on the amorphous and crystalline of iron and manganese hydroxides. The results show that the adsorption of Hg(2+) on Fe and Mn hydroxides was inhibited in marine system due to the formation of stable, nonsorbing aqueous HgCl(2) complexes in solution. Moreover, Cl(-) inhibited the Hg(2+) adsorption more severely on amorphous than crystalline hydroxides. The addition of HA inhibited Hg(2+) adsorption on Fe and Mn hydroxides in freshwater system might be attributed to the competition between Hg(2+) and HA on adsorption to Fe and Mn hydroxides. In contrast, the addition of HA promoted Hg(2+) adsorption on Fe and Mn hydroxides in the marine system, which might be due to the addition of humic acid resulted in the reaction between Cl(-) and HA, and therefore the reducing of Cl(-) promoted more Hg(2+) on Fe and Mn hydroxides. In addition, the influence of HA on Hg(2+) adsorption on Fe and Mn hydroxides are more visible for crystalline than amorphous hydroxides.

  7. Long-term Hg pollution induced Hg tolerance in the terrestrial isopod Porcellio scaber (Isopoda, Crustacea).

    Science.gov (United States)

    Lapanje, A; Drobne, D; Nolde, N; Valant, J; Muscet, B; Leser, V; Rupnik, M

    2008-06-01

    The aim of our work was to assess the pollution-induced community tolerance (PICT) of isopod gut microbiota and pollution-induced isopod population tolerance (PIPT). Animals collected from a chronically Hg polluted and an unpolluted location were exposed for 14 days to 10microg Hg/g dry food under laboratory conditions. The lysosomal membrane stability, hepatopancreas epithelium thickness, feeding activity and animal bacterial gut microbiota composition were determined. The results confirm the hypothesis that the response to short-term Hg exposure differs for animals from the Hg polluted and the unpolluted field locations. The animals and their gut microbiota from the Hg polluted location were less affected by Hg in a short-term feeding experiment than those from the unpolluted environment. We discuss the pollution-induced population tolerance of isopods and their gut microbiota as a measure of effects of long-term environmental pollution. The ecological consequences of such phenomena are also discussed.

  8. Zuotai and HgS differ from HgCl2 and methyl mercury in Hg accumulation and toxicity in weanling and aged rats.

    Science.gov (United States)

    Zhang, Bin-Bin; Li, Wen-Kai; Hou, Wei-Yu; Luo, Ya; Shi, Jing-Zhen; Li, Cen; Wei, Li-Xin; Liu, Jie

    2017-09-15

    Mercury sulfides are used in Ayurvedic medicines, Tibetan medicines, and Chinese medicines for thousands of years and are still used today. Cinnabar (α-HgS) and metacinnabar (β-HgS) are different from mercury chloride (HgCl2) and methylmercury (MeHg) in their disposition and toxicity. Whether such scenario applies to weanling and aged animals is not known. To address this question, weanling (21d) and aged (450d) rats were orally given Zuotai (54% β-HgS, 30mg/kg), HgS (α-HgS, 30mg/kg), HgCl2 (34.6mg/kg), or MeHg (MeHgCl, 3.2mg/kg) for 7days. Accumulation of Hg in kidney and liver, and the toxicity-sensitive gene expressions were examined. Animal body weight gain was decreased by HgCl2 and to a lesser extent by MeHg, but unaltered after Zuotai and HgS. HgCl2 and MeHg produced dramatic tissue Hg accumulation, increased kidney (kim-1 and Ngal) and liver (Ho-1) injury-sensitive gene expressions, but such changes are absent or mild after Zuotai and HgS. Aged rats were more susceptible than weanling rats to Hg toxicity. To examine roles of transporters in Hg accumulation, transporter gene expressions were examined. The expression of renal uptake transporters Oat1, Oct2, and Oatp4c1 and hepatic Oatp2 was decreased, while the expression of renal efflux transporter Mrp2, Mrp4 and Mdr1b was increased following HgCl2 and MeHg, but unaffected by Zuotai and HgS. Thus, Zuotai and HgS differ from HgCl2 and MeHg in producing tissue Hg accumulation and toxicity, and aged rats are more susceptible than weanling rats. Transporter expression could be adaptive means to reduce tissue Hg burden. Copyright © 2017 Elsevier Inc. All rights reserved.

  9. Significant interaction effects from sulfate deposition and climate on sulfur concentrations constitute major controls on methylmercury production in peatlands

    Science.gov (United States)

    Åkerblom, Staffan; Bishop, Kevin; Björn, Erik; Lambertsson, Lars; Eriksson, Tobias; Nilsson, Mats B.

    2013-02-01

    Transformation of inorganic mercury (Hg) to methyl mercury (MeHg) in peatlands is a key process in making boreal catchments a source of MeHg to freshwater ecosystems. Due to the importance of sulfur-reducing bacteria (SRB) for this process, past atmospheric deposition of sulfate (SO42-) may have increased net terrestrial Hg methylation. A long-term (14-year) factorial design field experiment was used to investigate the effect of enhanced SO42- deposition and raised temperature using a greenhouse (GH) treatment (air temperature˜+4 °C; soil temperature 20 cm below mire surface ˜+2 °C) on sulfur (S) turnover, net Hg methylation, MeHg and total Hg concentrations in a boreal mire in northern Sweden. Of the SO42--S added during 14 years, 50% was retained in the plots without GH treatment while the combination of SO42- addition and GH treatment resulted in 15% S retention. The addition of SO42- (7-fold ambient SO42--deposition) increased (p important than the concentration of Hg for the production of MeHg in this boreal landscape. These results also show that long-term chronic SO42- deposition at rates similar to those found in polluted areas of Europe and North America increase the capacity of wetlands to methylate Hg and store MeHg, which can ultimately be released to streams and lakes. This study also, for the first time, indicates that the enhancing effect of SO42- on the production of MeHg might be counteracted by increased temperature.

  10. In situ bioavailability of DDT and Hg in sediments of the Toce River (Lake Maggiore basin, Northern Italy): accumulation in benthic invertebrates and passive samplers.

    Science.gov (United States)

    Pisanello, Francesca; Marziali, Laura; Rosignoli, Federica; Poma, Giulia; Roscioli, Claudio; Pozzoni, Fiorenzo; Guzzella, Licia

    2016-06-01

    DDT and mercury (Hg) contamination in the Toce River (Northern Italy) was caused by a factory producing technical DDT and using a mercury-cell chlor-alkali plant. In this study, DDT and Hg contamination and bioavailability were assessed by using different approaches: (1) direct evaluation of sediment contamination, (2) assessment of bioaccumulation in native benthic invertebrates belonging to different taxonomic/functional groups, and (3) evaluation of the in situ bioavailability of DDT and Hg using passive samplers. Sampling sites were selected upstream and downstream the industrial plant along the river axis. Benthic invertebrates (Gammaridae, Heptageniidae, and Diptera) and sediments were collected in three seasons and analyzed for DDT and Hg content and the results were used to calculate the biota sediment accumulation factor (BSAF). Polyethylene passive samplers (PEs) for DDT and diffusive gradients in thin films (DGTs) for Hg were deployed in sediments to estimate the concentration of the toxicants in pore water. Analysis for (DDx) were performed using GC-MS. Accuracy was within ±30 % of the certified values and precision was >20 % relative standard deviation (RSD). Total mercury concentrations were determined using an automated Hg mercury analyzer. Precision was >5 % and accuracy was within ±10 % of certified values. The results of all the approaches (analysis of sediment, biota, and passive samplers) showed an increasing contamination from upstream to downstream sites. BSAF values revealed the bioavailability of both contaminants in the study sites, with values up to 49 for DDx and up to 3.1 for Hg. No correlation was found between values in sediments and the organisms. Concentrations calculated using passive samplers were correlated with values in benthic invertebrates, while no correlation was found with concentrations in sediments. Thus, direct analysis of toxicant in sediments does not provide a measurement of bioavailability. On the contrary

  11. Sources and cycling of mercury in the paleo Arctic Ocean from Hg stable isotope variations in Eocene and Quaternary sediments

    Science.gov (United States)

    Gleason, J. D.; Blum, J. D.; Moore, T. C.; Polyak, L.; Jakobsson, M.; Meyers, P. A.; Biswas, A.

    2017-01-01

    Mercury stable isotopic compositions were determined for marine sediments from eight locations in the Arctic Ocean Basin. Mass dependent fractionation (MDF) and mass independent fractionation (MIF) of Hg stable isotopes were recorded across a variety of depositional environments, water depths, and stratigraphic ages. δ202Hg (MDF) ranges from -2.34‰ to -0.78‰; Δ199Hg (MIF) from -0.18‰ to +0.12‰; and Δ201Hg (MIF) from -0.29‰ to +0.05‰ for the complete data set (n = 33). Holocene sediments from the Chukchi Sea and Morris Jesup Rise record the most negative Δ199Hg values, while Pleistocene sediments from the Central Arctic Ocean record the most positive Δ199Hg values. The most negative δ202Hg values are recorded in Pleistocene sediments. Eocene sediments (Lomonosov Ridge) show some overlap in their Hg isotopic compositions with Quaternary sediments, with a sample of the Arctic Ocean PETM (56 Ma) most closely matching the average Hg isotopic composition of Holocene Arctic marine sediments. Collectively, these data support a terrestrially-dominated Hg source input for Arctic Ocean sediment through time, although other sources, as well as influences of sea ice, atmospheric mercury depletion events (AMDEs), and anthropogenic Hg (in core top samples) on Hg isotopic signatures must also be considered.

  12. Effects of properties of manganese oxide-impregnated catalysts and flue gas condition on multipollutant control of Hg{sup 0} and NO

    Energy Technology Data Exchange (ETDEWEB)

    Chiu, Chun-Hsiang [Institute of Environmental Engineering and Management, National Taipei University of Technology, No. 1, Sec. 3, Chung-Hsiao E. Rd., Taipei 106, Taiwan (China); Hsi, Hsing-Cheng, E-mail: hchsi@ntu.edu.tw [Graduate Institute of Environmental Engineering, National Taiwan University, No. 71, Chou-Shan Rd., Taipei 106, Taiwan (China); Lin, Hong-Ping [Department of Chemistry, National Cheng-Kung University, No. 1, University Rd., Tainan 701, Taiwan (China); Chang, Tien-Chin [Institute of Environmental Engineering and Management, National Taipei University of Technology, No. 1, Sec. 3, Chung-Hsiao E. Rd., Taipei 106, Taiwan (China)

    2015-06-30

    Highlights: • MnO{sub x} impregnation caused changes in physical/chemical properties of catalyst. • Mn{sup 4+} was the main valence state of impregnated MnO{sub x}. • MnO{sub x} impregnation enhanced the removal of Hg{sup 0}/NO/SO{sub 2} with SCR catalyst. • HCl, O{sub 2}, and SO{sub 2} at ≤200 ppm and elevating temperature promoted Hg{sup 0} oxidation. • Increasing NO and NH{sub 3} concentrations reduced Hg{sup 0} oxidation. - Abstract: This research investigated the effects of manganese oxide (MnO{sub x}) impregnation on the physical/chemical properties and multi pollutant control effectiveness of Hg{sup 0} and NO using a V{sub 2}O{sub 5}–WO{sub 3}/TiO{sub 2}–SiO{sub 2} selective catalytic reduction (SCR) catalyst. Raw and MnO{sub x}-treated SCR samples were bean-shaped nanoparticles with sizes within 10–30 nm. Impregnating MnO{sub x} of ≤5 wt% caused limited changes in physical properties of the catalyst. The decrease in surface area when the impregnated MnO{sub x} amount was 10 wt% may stem from the pore blockage and particle growth or aggregation of the catalyst. Mn{sup 4+} was the main valence state of impregnated MnO{sub x}. Apparent crystallinity of MnO{sub x} was not observed based on X-ray diffraction. MnO{sub x} impregnation enhanced the Hg{sup 0} oxidation and NO/SO{sub 2} removal of SCR catalyst. The 5 and 10% MnO{sub x}-impregnated samples had the greatest multi pollutant control potentials for Hg{sup 0} oxidation and NO removal; however, the increasing SO{sub 2} removal that may be mainly due to SO{sub 2}–SO{sub 3} conversion should be cautioned. HCl and O{sub 2} greatly promoted Hg{sup 0} oxidation. SO{sub 2} enhanced Hg{sup 0} oxidation at ≤200 ppm while NO and NH{sub 3} consistently inhibited Hg{sup 0} oxidation. Elevating flue gas temperature enhanced Hg{sup 0} oxidation. Overall, MnO{sub x}-impregnated catalysts show stable and consistent multi pollutant removal effectiveness under the test conditions.

  13. Hg(II) removal from aqueous solutions by bacillus subtilis biomass

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Xue Song; Li, Fei Yan; He, Wen; Miao, Hua Hua [Department of Chemical Engineering, Huaihai Institute of Technology, Lianyungang (China)

    2010-01-15

    The biosorption of Hg(II) from aqueous solutions using Bacillus subtilis biomass was investigated in this study. The adsorbent was characterized by FTIR. Various factors including solution pH, initial concentration of Hg(II), contact time, reaction temperature and ionic strength were taken into account and promising results were obtained. An initial solution pH of 5.0 was most favorable for Hg(II) removal. The kinetic data was also analyzed using pseudo first order and pseudo second order equations. The results suggested that Hg(II) bioadsorption was best represented by the pseudo second order equation. Freundlich, Langmuir and Langmuir-Freundlich isotherms for the present systems were analyzed. The most satisfactory interpretation for the equilibrium data at different temperatures was given by the Langmuir-Freundlich isotherm. The effect of ionic strength on bioadsorption was significant. Bacillus subtilis biomass could serve as low cost adsorbent to remove Hg(II) from aqueous solutions, especially at lower concentrations of Hg(II) (<20 mg Hg/L). (Abstract Copyright [2010], Wiley Periodicals, Inc.)

  14. Beer Law Constants and Vapor Pressures of HgI2 over HgI2(s,l)

    Science.gov (United States)

    Su, Ching-Hua; Zhu, Shen; Ramachandran, N.; Burger, A.

    2002-01-01

    Optical absorption spectra of the vapor phase over HgI2(s,l) were measured at sample temperatures between 349 and 610 K for wavelengths between 200 and 600 nm. The spectra show the samples sublimed congruently into HGI2 without any observed Hg or I2 absorption spectra. The Beer's Law constants for 15 wavelengths between 200 and 440 nm were derived. From these constants the vapor pressure of HgI2, P, was found to be a function of temperature for the liquid and the solid beta-phases: ln P(atm) = -7700/T(K) + 12.462 (liquid phase) and ln P(atm) = -10150/T(K) + 17.026 (beta-phase). The expressions match the enthalpies of vaporization and sublimation of 15.30 and 20.17 kcal/mole respectively, for the liquid and the beta-phase HgI2. The difference in the enthalpies gives an enthalpy of fusion of 4.87 kcal/mole, and the intersection of the two expressions gives a melting point of 537 K.

  15. Hg(0) Removal Using Se(0)-doped Montmorillonite from Selenite(IV)

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Jooyoup [Univ. of Cincinnati, Ohio (United States); Kim, Yongjin [Korea Institute of Industrial Technology, Chonan (Korea, Republic of)

    2013-12-15

    Potassium methylselenite (KSeO{sub 2}(OCH{sub 3})) was reduced to elemental selenium, Se(0), and then doped onto montmorillonite K 10 (MK10) clay to examine the interaction between elemental mercury (Hg(0)) vapor and Se(0) in an effort to understand the possible heterogeneous reaction of Hg(0) vapor and Se(0) solid. The clay was used as a cost-effective support material for uniform dispersion of Se(0). The Se(0)-doped MK10 showed an excellent reaction performance with Hg(0) under an inert nitrogen gas at 70 and 140 .deg. C in our lab-scale fixed-bed system. However, the precursor, KSeO{sub 2}(OCH{sub 3})-doped MK10 showed a negligible reaction performance with Hg(0), suggesting that the oxidation state of selenium plays a key role in the reaction of Hg(0) vapor and selenium compounds.

  16. Growth and characterization of HgI2, PbI2 and PbI2:HgI2 layered semiconductors

    Directory of Open Access Journals (Sweden)

    Manoel E.R.

    1999-01-01

    Full Text Available This paper presents a methodology for the preparation of a-HgI2 by Physical Vapor Transport and of PbI2 crystals using the Bridgman technique. The results of the growth of HgI2 diluted in PbI2 by the Bridgman technique are shown for the first time, its limit of solubility having been determined at 600 ppm of HgI2 in the PbI2 matrix. Optical absorption, photoluminescence and electrical conductivity measurements show that the crystals prepared are of good crystalline quality.

  17. Pencemaran air raksa (Hg sebagai dampak pengolahan bijih emas di Sungai Ciliunggunung, Waluran, Kabupaten Sukabumi

    Directory of Open Access Journals (Sweden)

    Widodo Widodo

    2014-06-01

    Full Text Available http://dx.doi.org/10.17014/ijog.vol3no3.20083Gold ore mining at Waluran Subregency, Sukabumi Regency was carried out by an underground mining method, and only rock that contains high enough gold ore would be taken (selective mining. The gold ore from the mining was processed with a direct amalgamation method, so it produced low gold concentrate, but the concentrate of mercury discarded to the river was high enough. Monitoring result of water and sedimentation in Ciliunggunung River in 2004, showed that the river was contamined by mercury (Hg, and the contamination was above the value limit. This happened especially in August 2005 where the Hg content was about 0.218 mg/l on the Ciliunggunung River in CLG.07. The chemical analysis result of heavy metals for the water of the Ciliunggunung River in CLG.07 was known to contain Fe above the standard drinking water criteria, meanwhile Mn, Cu, Pb, and As were still under the maximum drinking water criteria value. To decrease the mercury contamination, it is suggested the process of gold ore from the amalgamation direct method to be changed to the amalgamation indirect method. The indirect gold ore amalgamation process consists of: removing fine particles by washing, grinding ore, and the amalgamation phase. The total impact of the indirect amalgamation method will increase the tying of gold by mercury, so the losing of mercury will be decreased and the gain of gold will be optimum.  

  18. Magnetic fields of HgMn stars

    CERN Document Server

    Hubrig, S; Ilyin, I; Korhonen, H; Schoeller, M; Savanov, I; Arlt, R; Castelli, F; Curto, G Lo; Briquet, M; Dall, T H

    2012-01-01

    The frequent presence of weak magnetic fields on the surface of spotted late-B stars with HgMn peculiarity in binary systems has been controversial during the two last decades. We re-analyse available spectropolarimetric material by applying the moment technique on spectral lines of inhomogeneously distributed elements separately. Furthermore, we present new determinations of the mean longitudinal magnetic field for the HgMn star HD65949 and the hotter analog of HgMn stars, the PGa star HD19400, using FORS2 installed at the VLT. We also give new measurements of the eclipsing system AR Aur with a primary star of HgMn peculiarity which were obtained with the SOFIN spectropolarimeter installed at the Nordic Optical Telescope. We downloaded from the ESO archive the publically available HARPS spectra for eight HgMn stars and one normal and one superficially normal B-type star obtained in 2010. The application of the moment technique to the HARPS and SOFIN spectra allowed us to study the presence of the longitudina...

  19. HgCdTe barrier infrared detectors

    Science.gov (United States)

    Kopytko, M.; Rogalski, A.

    2016-05-01

    In the last decade, new strategies to achieve high-operating temperature (HOT) detectors have been proposed, including barrier structures such as nBn devices, unipolar barrier photodiodes, and multistage (cascade) infrared detectors. The ability to tune the positions of the conduction and valence band edges independently in a broken-gap type-II superlattices is especially helpful in the design of unipolar barriers. This idea has been also implemented in HgCdTe ternary material system. However, the implementation of this detector structure in HgCdTe material system is not straightforward due to the existence of a valence band discontinuity (barrier) at the absorber-barrier interface. In this paper we present status of HgCdTe barrier detectors with emphasis on technological progress in fabrication of MOCVD-grown HgCdTe barrier detectors achieved recently at the Institute of Applied Physics, Military University of Technology. Their performance is comparable with state-of-the-art of HgCdTe photodiodes. From the perspective of device fabrication their important technological advantage results from less stringent surface passivation requirements and tolerance to threading dislocations.

  20. Spatial-temporal dynamics and sources of total Hg in a hydroelectric reservoir in the Western Amazon, Brazil.

    Science.gov (United States)

    Pestana, I A; Bastos, W R; Almeida, M G; de Carvalho, D P; Rezende, C E; Souza, C M M

    2016-05-01

    Damming rivers to construct hydroelectric reservoirs results in a series of impacts on the biogeochemical Hg cycle. For example, modifying the hydrodynamics of a natural watercourse can result in the suspension and transport of Hg deposits in the water column, which represents an exposure risk for biota. The objective of this study was to evaluate the influences of seasonality on the dispersion of total Hg in the Hydroelectric Power Plant (HPP)-Samuel Reservoir (Porto Velho/Brazil). Sampling campaigns were performed during the three following hydrological periods characteristic of the region: low (Oct/2011), ebbing (May/2012), and high (Feb/2013) water. Sediment profiles, suspended particulate matter (SPM), and aquatic macrophytes (Eicchornia crassipes and Oryza spp.) were collected, and their Hg concentrations and isotopic and elemental C and N signatures were determined. The drainage basin significantly influenced the SPM compositions during all the periods, with a small autochthonous influence from the reservoir during the low water. The highest SPM Hg concentrations inside the reservoir were observed during the high water period, suggesting that the hydrodynamics of this environment favor the suspension of fine SPM, which has a higher Hg adsorption capacity. The Hg concentrations in the sediment profiles were ten times lower than those in the SPM, indicating that large particles with low Hg concentrations were deposited to form the bottom sediment. Hg concentrations were higher in aquatic macrophyte roots than in their leaves and appeared to contribute to the formation of SPM during the low water period. In this environment, Hg transport mainly occurs in SPM from the Jamari River drainage basin, which is the primary source of Hg in this environment.

  1. "Reactive" optical sensor for Hg(2+) and its application in environmental aqueous media and biological systems.

    Science.gov (United States)

    Chen, Zhi; Chen, Jiayun; Pan, Dong; Li, Hongwei; Yao, Yunhui; Lyu, Zu; Yang, Liting; Ma, Li-Jun

    2017-03-01

    A new rhodamine B-based "reactive" optical sensor (1) for Hg(2+) was synthesized. Sensor 1 shows a unique colorimetric and fluorescent "turn-on" selectivity to Hg(2+) over 14 other metal ions with a hypersensitivity (detection limits are 27.6 nM (5.5 ppb) and 6.9 nM (1.4 ppb), respectively) in neutral buffer solution. To test its applicability in the environment, sensor 1 was applied to quantify and visualize low levels of Hg(2+) in tap water and river water samples. The results indicate sensor 1 is a highly sensitive fluorescent sensor for Hg(2+) with a detection limit of 1.7 ppb in tap water and river water. Moreover, sensor 1 is a convenient visualizing sensor for low levels of Hg(2+) (0.1 ppm) in water environment (from colorless to light pink). In addition, sensor 1 shows good potential as a fluorescent visualizing sensor for Hg(2+) in fetal bovine serum and living 293T cells. The results indicate that sensor 1 shows good potential as a highly sensitive sensor for the detection of Hg(2+) in environmental and biological samples. Graphical Abstract A new rhodamine B-based "reactive" optical sensor (1) for Hg(2+) was synthesized. 1 shows a unique colorimetric and fluorescent "turn-on" selectivity to Hg(2+) over 14 other metal ions with a hypersensitivity in water environment. And it is a convenient visualizing probe for low levels of Hg(2+) in environment aqueous media, fetal bovine serum and living 293T cells.

  2. Magnetic properties of fluorinated Pb-doped Hg-1223 high Tc superconductors

    Energy Technology Data Exchange (ETDEWEB)

    Hamdan, N.M.; Sastry, P.V.P.S.S.; Schwartz, J.

    2001-09-23

    Fluorination of Pb-doped HgBa{sub 2}Ca{sub 2}Cu{sub 3}O{sub y} (Hg-1223) system was investigated. Structural and magnetic measurements reveal that fluorine addition promotes the phase formation, optimize the charge carrier concentration, and enhance flux pinning. We report an increase in both the transition temperature and the critical current density through controlled fluorine incorporation. Even a possible change in the pinning mechanism in this technologically important system is suggested.

  3. Mercury methylation and reduction potentials in marine water: An improved methodology using {sup 197}Hg radiotracer

    Energy Technology Data Exchange (ETDEWEB)

    Koron, Neza [National Institute of Biology, Marine Biology Station, Fornace 41, 6330 Piran (Slovenia); Bratkic, Arne [Department of Environmental Sciences, ' Jozef Stefan' Institute, Jamova 39, 1000 Ljubljana (Slovenia); Ribeiro Guevara, Sergio, E-mail: ribeiro@cab.cnea.gov.ar [Laboratorio de Analisis por Activacion Neutronica, Centro Atomico Bariloche, Av. Bustillo km 9.5, 8400 Bariloche (Argentina); Vahcic, Mitja; Horvat, Milena [Department of Environmental Sciences, ' Jozef Stefan' Institute, Jamova 39, 1000 Ljubljana (Slovenia)

    2012-01-15

    A highly sensitive laboratory methodology for simultaneous determination of methylation and reduction of spiked inorganic mercury (Hg{sup 2+}) in marine water labelled with high specific activity radiotracer ({sup 197}Hg prepared from enriched {sup 196}Hg stable isotope) was developed. A conventional extraction protocol for methylmercury (CH{sub 3}Hg{sup +}) was modified in order to significantly reduce the partitioning of interfering labelled Hg{sup 2+} into the final extract, thus allowing the detection of as little as 0.1% of the Hg{sup 2+} spike transformed to labelled CH{sub 3}Hg{sup +}. The efficiency of the modified CH{sub 3}Hg{sup +} extraction procedure was assessed by radiolabelled CH{sub 3}Hg{sup +} spikes corresponding to concentrations of methylmercury between 0.05 and 4 ng L{sup -1}. The recoveries were 73.0{+-}6.0% and 77.5{+-}3.9% for marine and MilliQ water, respectively. The reduction potential was assessed by purging and trapping the radiolabelled elemental Hg in a permanganate solution. The method allows detection of the reduction of as little as 0.001% of labelled Hg{sup 2+} spiked to natural waters. To our knowledge, the optimised methodology is among the most sensitive available to study the Hg methylation and reduction potential, therefore allowing experiments to be done at spikes close to natural levels (1-10 ng L{sup -1}). - Highlights: Black-Right-Pointing-Pointer Inorganic mercury methylation and reduction in marine water were studied. Black-Right-Pointing-Pointer High specific activity {sup 197}Hg was used to label Hg{sup 2+} spikes at natural levels. Black-Right-Pointing-Pointer Methylmercury extraction had 73% efficiency for 0.05-4 ng L{sup -1} levels. Black-Right-Pointing-Pointer High sensibility to assess methylation potentials, below 0.1% of the spike. Black-Right-Pointing-Pointer High sensibility also for reduction potentials, as low as 0.001% of the spike.

  4. In vivo formation of natural HgSe nanoparticles in the liver and ...

    Science.gov (United States)

    To understand the biochemistry of methylmercury (MeHg) that leads to the formation of mercury-selenium (Hg-Se) clusters is a long outstanding challenge that promises to deepen our knowledge of MeHg detoxification and the role SE plays in this process. Here, we show that mercury selenide (HgSe) nanoparticles in the liver and brain of long-finned pilot whales are attached to Se-rich structures and possibly act as a nucleation point for the formation of large Se-Hg clusters, which can grow with age to over 5 µm in size. The detoxification mechanism is fully developed from the early age of the animals, with particulate Hg found already in juvenile tissues. As a consequence of MeHg detoxification, Se-methionine, the selenium pool in the system is depleted in the efforts to maintain essential levels of Se-cysteine. This study provides evidence of so far unreported depletion of bioavailable Se pool, a plausible driving mechanism of demonstrated neurotoxic effects of MeHg in the organism affected by its high dietary intake. We investigated in vivo formation of natural HgSe particles in a pod of stranded long-finned pilot whales (Globicephala melas), with age of the animal and the potency of the environmentally relevant dose of dietary MeHg to disrupt the Se-proteins synthesis. This has been previously investigated despite the substantial indications of the interaction between Hg and Se, and therefore we conducted a multi-method analytical approach on brain and liv

  5. Microsolvation of methylmercury: structures, energies, bonding and NMR constants ((199)Hg, (13)C and (17)O).

    Science.gov (United States)

    Flórez, Edison; Maldonado, Alejandro F; Aucar, Gustavo A; David, Jorge; Restrepo, Albeiro

    2016-01-21

    Hartree-Fock (HF) and second order perturbation theory (MP2) calculations within the scalar and full relativistic frames were carried out in order to determine the equilibrium geometries and interaction energies between cationic methylmercury (CH3Hg(+)) and up to three water molecules. A total of nine structures were obtained. Bonding properties were analyzed using the Quantum Theory of Atoms In Molecules (QTAIM). The analyses of the topology of electron densities reveal that all structures exhibit a partially covalent HgO interaction between methylmercury and one water molecule. Consideration of additional water molecules suggests that they solvate the (CH3HgOH2)(+) unit. Nuclear magnetic shielding constants σ((199)Hg), σ((13)C) and σ((17)O), as well as indirect spin-spin coupling constants J((199)Hg-(13)C), J((199)Hg-(17)O) and J((13)C-(17)O), were calculated for each one of the geometries. Thermodynamic stability and the values of NMR constants correlate with the ability of the system to directly coordinate oxygen atoms of water molecules to the mercury atom in methylmercury and with the formation of hydrogen bonds among solvating water molecules. Relativistic effects account for 11% on σ((13)C) and 14% on σ((17)O), which is due to the presence of Hg (heavy atom on light atom, HALA effect), while the relativistic effects on σ((199)Hg) are close to 50% (heavy atom on heavy atom itself, HAHA effect). J-coupling constants are highly influenced by relativity when mercury is involved as in J((199)Hg-(13)C) and J((199)Hg-(17)O). On the other hand, our results show that the values of NMR constants for carbon and oxygen, atoms which are connected through mercury (C-HgO), are highly correlated and are greatly influenced by the presence of water molecules. Water molecules introduce additional electronic effects to the relativistic effects due to the mercury atom.

  6. Effects of Hg~(2+) on the Reproductive Capacity and Longevity and Esterase Isozyme of Drosophila Melanogast%Hg~(2+)对果蝇寿命和生育力及酯酶同工酶的影响

    Institute of Scientific and Technical Information of China (English)

    叶文斌; 王昱; 何九军; 杨小录

    2012-01-01

    This paper using discontinuous polyacrylamide gel electrophoresis method,with different concentrations of Hg2+ on Drosophila melanogaster reproductive capacity,longevity and esterase activity and its isozyme expression.The results showed that,different concentrations of Hg2 + on Drosophila melanogaster reproductive capacity and longevity are affected,produce different zymogram,change as the enzyme bands,coloring degree and different relative activity.With the Hg2 + concentration increasing the Drosophila melanogaster of reproductive capacity is reduce,life expectancy decurtation;Drosophila melanogaster larvae EST relative activity changes,isozyme expression have been significantly affected.%采用不连续聚丙烯酰胺垂直板凝胶电泳方法,对不同浓度Hg2+对果蝇生育力、寿命和酯酶活性及其同工酶表达的影响.结果表明:不同浓度的Hg2+对果蝇的生育力和寿命均有影响,产生出不同酶谱,其变化为酶带数、着色度、酶相对活性的不同.说明随着Hg2+浓度的升高,果蝇的生育力降低、寿命缩短;果蝇幼虫体内的EST酶相对活性发生变化,同工酶表达受到显著的影响.

  7. Complexation of Hg with phytochelatins is important for plant Hg tolerance

    National Research Council Canada - National Science Library

    CARRASCO‐GIL, SANDRA; ÁLVAREZ‐FERNÁNDEZ, ANA; SOBRINO‐PLATA, JUAN; MILLÁN, ROCÍO; CARPENA‐RUIZ, RAMÓN O; LEDUC, DANIKA L; ANDREWS, JOY C; ABADÍA, JAVIER; HERNÁNDEZ, LUÍS E

    2011-01-01

    Three‐week‐old alfalfa ( Medicago sativa ), barley ( Hordeum vulgare ) and maize ( Zea mays ) were exposed for 7 d to 30  µ m of mercury (HgCl 2 ) to characterize the Hg speciation in root, with no symptoms of being poisoned...

  8. Temporal Characteristics of Emission of Working Mixtures of a HgBr/HgCl Excimer Lamp

    Science.gov (United States)

    Malinin, A. N.; Guĭvan, N. N.; Shimon, L. L.; Polyak, A. V.; Zubrilin, N. G.; Shchedrin, A. I.

    2001-12-01

    Results of a study of temporal characteristics of the emission of gas-discharge plasma of atmospheric pressure in multicomponent mixtures (mercury dibromide and dichloride with helium and additions of molecular nitrogen and xenon) of working media of HgBr/HgCl excimer lamps are presented. Gas-discharge plasma was produced and components of the working mixture were excited by high-frequency barrier and surface discharges occurring simultaneously. The repetition rate of the pumping pulse and its duration are 1000 Hz and ˜100 ns, respectively. It is found that the amplitude and the length of emission pulses and their trailing edge are modified in HgBr2: HgCl2: Xe: He and HgBr2: HgCl2: N2: He mixtures when xenon and molecular nitrogen are added, as compared to a HgBr2: HgCl2: He mixture. Regularities observed in temporal characteristics of gas-discharge plasma emission are discussed.

  9. Ground-state potential energy curves of LiHg, NaHg, and KHg revisited

    Science.gov (United States)

    Thiel, Linda; Hotop, Hartmut; Meyer, Wilfried

    2003-11-01

    We present the results of large-scale CCSD(T) calculations on the potential energy curves for the ground states of LiHg, NaHg, and KHg. In these calculations, the Hg20+ core is simulated by a pseudopotential which has been adjusted to reproduce experimental excitation and ionization energies of the Hg atom at the coupled-cluster level. Moreover, we apply a weighted multiproperty fitting procedure to determine reliable potentials for LiHg, NaHg, and KHg which reproduce the available experimental results. In the case of LiHg, this best-fit potential is based solely on experimental data and its agreement with our calculated potential supports our computational procedure. For NaHg and KHg the experimental data had to be complemented by theoretical results in order to fix a best-fit potential. Our potentials and those proposed previously are evaluated by comparing calculated scattering cross sections and vibrational energy levels with the available experimental data.

  10. Valve movement response of the mussel mytilus galloprovincialis to metals (Cu, Hg, Cd and Zn) and phosphate industry effluents from Moroccan Atlantic coast.

    Science.gov (United States)

    Fdil, Mohamed Ait; Mouabad, Abdelfattah; Outzourhit, Abdelkader; Benhra, Ali; Maarouf, Abdelmalek; Pihan, Jean Claude

    2006-07-01

    Valve activity was measured in the Mediterranean mussel Mytilus galloprovincialis in response to sublethal concentrations of four metals (Hg, Cu, Zn and Cd) and two phosphate industry effluents from the Atlantic coast of Morocco. Valve movements were monitored using a proximity inductive sensor which could display all activity figures from full closure to wide opening of the shell valves. In a 1 h exposure experiments, all metals induced a decrease in the time of normal opening and the appearance of sequences of stress behaviour, including enhanced valve adductions and complete closure at high concentrations. Mercury (tested from 5 to 75 microg Hg l(-1)) was the most toxic to the valve activity, with a threshold effective concentration at 10 microg Hg l(-1) and full valve closure occurring at 50 microg Hg l(-1). Copper (15-150 microg Cu l(-1)) showed a toxic effect starting at threshold concentration of 20 microg Cu l(-1) and induced full valve closure at 150 microg Cu l(-1). Zinc (100-500 microg Zn l(-1)) was effective in reducing the time of normal opening (threshold concentration at 100 microg Zn I(-1)) but no complete closure was recorded in any of the tested concentrations. For cadmium (1000-5000 microg Cd l(-1)), the valve activity was insensitive for exposures under 2000 microg Cd l(-1). Results for the testing of several samplings of the phosphate industry effluents (Safi and Jorf Lasfar) showed that their toxicity varied over the time. The effluent of the Jorf Lasfar plant (2-9.4%) was, however, more toxic than that of Safi (1-25%). In the light of these results, the sensitivity of the valve activity of Mytilus galloprovincialis to pollutants and its usefulness for in situ monitoring of coastal pollution in Morocco are discussed.

  11. Sensing Hg(II) in vitro and in vivo using a benzimidazole substituted BODIPY.

    Science.gov (United States)

    Madhu, Sheri; Sharma, Dharmendar Kumar; Basu, Santanu Kumar; Jadhav, Sameer; Chowdhury, Arindam; Ravikanth, Mangalampalli

    2013-10-07

    A multisignaling Hg(II) sensor based on a benzimidazole substituted BODIPY framework was designed, which displays excellent selectively toward Hg(II) in vitro and in vivo. Optical and fluorogenic measurements in solution reveal that the sensor can detect mercury ions at submicromolar concentrations, with high specificity. The detection of Hg(II) is associated with a blue-shift in optical spectra and a simultaneous increase in the fluorescence quantum yield of the sensor, which is attributed to a decrease in charge delocalization and inhibition of photoinduced electron transfer upon binding to Hg(II). Using several spectroscopic measurements, it is shown that the binding mechanism involves two sensor molecules, where lone pairs of the benzimidazole nitrogen coordinate to a single mercury ion. The utility of this BODIPY sensor to detect Hg(II) in vivo was demonstrated by fluorescence imaging and spectroscopy of labeled human breast adenocarcinoma cells. While average emission intensity of the sensor over a large number of cells increases with incubated mercury concentrations, spatially resolved fluorescence spectroscopy performed on individual cells reveals clear spectral blue-shifts from a subensemble of sensors, corroborating the detection of Hg(II). Interestingly, the emission spectra at various submicrometer locations within cells exhibited considerable inhomogeneity in the extent of blue-shift, which demonstrates the potential of this sensor to monitor the local (effective) concentration of mercury ions within various subcellular environments.

  12. Electric field gradients in Hg compounds

    DEFF Research Database (Denmark)

    Arcisauskaité, Vaida; Knecht, Stefan; Sauer, Stephan P. A.

    2012-01-01

    We examine the performance of Density Functional Theory (DFT) approaches based on the Zeroth-Order Regular Approximation (ZORA) Hamiltonian (with and without inclusion of spinorbit coupling) for predictions of electric ¿eld gradients (EFGs) at the heavy atom Hg nucleus. This is achieved by compar......We examine the performance of Density Functional Theory (DFT) approaches based on the Zeroth-Order Regular Approximation (ZORA) Hamiltonian (with and without inclusion of spinorbit coupling) for predictions of electric ¿eld gradients (EFGs) at the heavy atom Hg nucleus. This is achieved...

  13. Soil and Plant Mercury Concentrations and Pools in the Arctic Tundra of Northern Alaska by Hedge Christine, Obrist Daniel, Agnan Yannick, Moore Christopher, Biester Harald, Helmig Detlev

    Science.gov (United States)

    Hedge, C.; Agnan, Y.

    2015-12-01

    We present vegetation, soil and runoff mercury (Hg) concentrations and pool sizes in vegetation and soils at several arctic tundra sites, an area that represents <7 x 106 km2 of land surface globally. The primary measurement location is at Toolik Field Station (TFS, 68° 38' N) in northern Alaska, with additional samples collected along a transect from TFS to the Arctic Ocean, and in Noatak National Preserve to be collected in August 2015. Soil and vegetation samples from all sites will be analyzed for total Hg concentration, pH, soil texture, bulk density, soil moisture content, organic and total carbon (C), nitrogen, along with major and trace elements. Initial results already obtained from TFS (characterized as moist to wet tundra with Typic Aquiturbel soils) show Hg concentrations in tundra vegetation (112±15 μg kg-1) and organic soil (140±8 μg kg-1) similar to those found in temperate sites. Calculation of plant-based Hg deposition rates by litterfall of 17.3 μg kg-1 yr-1 were surprisingly high, exceeding all other Hg deposition fluxes at this site. Hg concentrations in mineral soils (95±3 μg kg-1) were 2-3 times higher than those found at temperate sites. Hg concentrations showed weak relationships to organic C concentrations contrasting patterns from temperate soils where concentrations typically decline with depth following lower organic carbon contents. In fact, vertical mass profiles of Hg showed a strong increase with depth, with mineral layers storing over 90% (200-500 g ha-1) of Hg within these soils. A principle component analysis including major and trace elements indicated that soil Hg was not of lithogenic origin but from atmospheric sources, possibly by long-range transport. Carbon-14 dating results showed over 7,000 years old organic carbon in mineral soils of the active layer where highest concentrations of soil Hg were observed, suggesting long term retention of atmospheric Hg. These patterns suggest vertical translocation of Hg from the

  14. Studies on photoinduced effects in pulse-electrodeposited Ag/Hg-1212/CdSe hetero-nanostructures

    Indian Academy of Sciences (India)

    D D Shivagan; P M Shirage; S H Pawar

    2002-05-01

    Metal/superconductor/semiconductor (Ag/Hg-1212/CdSe) hetero-nanostructures have been fabricated using pulse-electrodeposition technique and are characterized by X-ray diffraction (XRD), full-width at half-maximum (FWHM) and scanning electron microscopy (SEM) studies. The junction capacitance of Ag/Hg-1212, Hg-1212/CdSe and Ag/Hg-1212/CdSe heterojunctions is measured in dark and under laser irradiation at room temperature. The nature of the junction formed and built-in-junction potentials were determined. The increase in carrier concentration across the junction due to photo-irradiation has been observed.

  15. Magnetically recoverable fluorescence chemosensor for the adsorption and selective detection of Hg2+ in water.

    Science.gov (United States)

    Lv, Qiang; Li, Gang; Cheng, Zhuhong; Lu, Hong; Gao, Xiaoxia

    2014-01-01

    In order to conveniently and effectively detect the heavy metal ion Hg(2+) existing in water, a magnetic fluorescence chemosensor has been strategically prepared by immobilizing a Rhodamine B derivative RhB-tris(2-aminoethyl)amine on Fe3O4@SiO2-Au@PSiO2 composites via gold particles. The adsorption and detection for Hg(2+) ions were investigated with fluorophotometry. This chemosensor shows high sensitivity and high selectivity for Hg(2+) over other metal cations owing to the ring opening of the rhodamine fluorophore selectively induced by Hg(2+). In addition, the presence of Fe3O4 in the sensor also facilitates the magnetic separation of the Fe3O4@SiO2-Au-Hg(2+)@PSiO2 from the solution.

  16. Antioxidative response of Lepidium sativum L. during assisted phytoremediation of Hg contaminated soil.

    Science.gov (United States)

    Smolinska, Beata; Szczodrowska, Agnieszka

    2017-09-25

    In this study, Lepidium sativum L. was used in repeated phytoextraction processes to remove Hg from contaminated soil, assisted by combined use of compost and iodide (KI). L. sativum L. is sensitive to changes in environmental conditions and has been used in environmental tests. Its short vegetation period and ability to accumulate heavy metals make it suitable for use in repeated phytoextraction. The antioxidant enzymatic system of the plant (catalase (CAT), ascorbate peroxidase (APX), superoxide dismutase (SOD) and glutathione S-transferase (GST)) was analysed, to understand the effects of increasing Hg accumulation and translocation. Phytoextraction was repeated six times to decrease Hg contamination in soil, and the efficiency of each step was assessed. The results indicate that L. sativum L. is able to take up and accumulate Hg from contaminated soil. A corresponding increase in enzymatic antioxidants shows that the plant defence system is activated in response to Hg stress. Using compost and KI increases total Hg accumulation and translocation to the above-ground parts of L. sativum L. Repeating the process decreases Hg contamination in pot experiments in all variants of the process. The combined use of compost and KI during repeated phytoextraction increases the efficiency of Hg removal from contaminated soil. Copyright © 2016 Elsevier B.V. All rights reserved.

  17. Influence of Ga and Hg on microstructure and electrochemical corrosion behavior of Mg alloy anode materials

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    The effects of Hg and Ga on the electrochemical corrosion behavior of Mg-5%Hg (molar fraction) alloys were investigated by the measurement of polarization curves and galvanostatic test. The microstructure of the alloys and the corroded surface of the specimens were investigated by scanning electron microscopy, X-ray diffractometry and emission spectrum analysis. It can be concluded that the addition of 1%Ga (molar fraction) reduces corrosion current density from 26.98 mA/cm2 to 2.34 mA/cm2;while the addition of 1%Hg (molar fraction) increases corrosion current density. The addition of Ga and Hg both promotes the electrochemical activity of the alloys and the influence of Ga is more effective than Hg. Mg-5%Hg-1%Ga alloy has the best electrochemical activity, showing mean potential of-1.992 V. The activation mechanism of the magnesium alloy produced by Hg and Ga was put forward. Magnesium atoms are dissolved in liquid Hg and Ga to form amalgam and undergo severe oxidation at the amalgam/electrolyte interface.

  18. Growing rice aerobically markedly decreases mercury accumulation by reducing both Hg bioavailability and the production of MeHg.

    Science.gov (United States)

    Wang, Xun; Ye, Zhihong; Li, Bing; Huang, Linan; Meng, Mei; Shi, Jianbo; Jiang, Guibin

    2014-01-01

    Rice consumption represents a major route of mercury (Hg) and methylmercury (MeHg) exposure for those living in certain areas of inland China. In this study we investigated the effects of water management on bioavailable Hg, MeHg, and sulfate-reducing bacteria (SRB, abundance and community composition) in rhizosphere soil, and total Hg (THg) and MeHg in rice plants grown under glasshouse and paddy field conditions. Aerobic conditions greatly decreased the amount of THg and MeHg taken up by rice plants and affected their distribution in different plant tissues. There were positive correlations between bioavailable Hg and THg in brown rice and roots and between numbers of SRB and MeHg in brown rice, roots, and rhizosphere soil. Furthermore, the community composition of SRB was dramatically influenced by the water management regimes. Our results demonstrate that the greatly reduced bioavailability of Hg and production of MeHg are due to decreased SRB numbers and proportion of Hg methylators in the rhizosphere under aerobic conditions. These are the main reasons for the reduced Hg and MeHg accumulation in aerobically grown rice. Water management is indicated as an effective measure that can be used to reduce Hg and MeHg uptake by rice plants from Hg-contaminated paddy fields.

  19. Application of Neutron Activation Analysis for Determination of As, Cr, Hg, and Se in Mosses in the Metropolitan Area of the Valley of Toluca, Mexico

    Directory of Open Access Journals (Sweden)

    R. Mejía-Cuero

    2015-01-01

    Full Text Available This research presents a study of environmental monitoring at different sampling sites from the Metropolitan Area of the Valley of Toluca (MAVT, Mexico, using mosses (Leskea angustata (Tayl. and Fabronia ciliaris (Brid. and soil samples. The epiphytic mosses and soils were sampled in two campaigns within two periods of the year, a rainy and dry-cold season. The selected sampling sites included urban regions (UR, transitional regions (TR, and protected natural areas (PA. The samples were analyzed by the Instrumental Neutron Activation Analysis (INAA to determine As, Cr, Hg, and Se principally. However, due to the versatility of the analytic technique used, other elements including Cs, Co, Sc, Sb, Rb, Ce, La, Eu, and Yb were also detected. Statistical analysis (As, Cr, Hg, and Se was carried out with principal components and cluster analysis methods; this revealed that a good correlation exists between metal content in mosses and the degree of pollution in the areas sampled. The obtained results in mosses showed that the concentrations of As, Cr, Co, Cs, Rb, Ce, La, and Yb increased with respect to the concentrations obtained during the first sampling, whereas Se, Sc, Sb and Eu, concentrations were decreased. For As and Hg, the concentrations were similar in both sampling periods. The soil samples present the most significant concentration.

  20. 40 CFR 60.45Da - Standard for mercury (Hg).

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standard for mercury (Hg). 60.45Da... for mercury (Hg). (a) For each coal-fired electric utility steam generating unit other than an IGCC... gases that contain mercury (Hg) emissions in excess of each Hg emissions limit in paragraphs...

  1. MBE Growth and Characterization of Hg Based Compounds and Heterostructures

    Science.gov (United States)

    2002-06-03

    The molecular beam epitaxy ( MBE ) growth of Mercury Cadmium Telluride (Hg(1-x)Cd(x)Te) alloys and type III HgTe/Hg(1-x)Cd(x)Te heterostructures has...been discussed, including similarities and differences between the (0 0 1) and (1 1 2)Beta orientations. Furthermore, the MBE growth of HgTe-based

  2. Bioaccumulation of Hg, Cd and Pb by Fucus vesiculosus in single and multi-metal contamination scenarios and its effect on growth rate.

    Science.gov (United States)

    Henriques, Bruno; Lopes, Cláudia B; Figueira, Paula; Rocha, Luciana S; Duarte, Armando C; Vale, Carlos; Pardal, Miguel A; Pereira, Eduarda

    2017-03-01

    Results of 7-days exposure to metals, using environmentally realistic conditions, evidenced the high potential of living Fucus vesiculosus to remove Pb, Hg and Cd from contaminated salt waters. For different contamination scenarios (single- and multi-contamination), ca 450 mg L(-1) (dry weight), enable to reduce the concentrations of Pb in 65%, of Hg in 95% and of Cd between 25 and 76%. Overall, bioconcentration factors ranged from 600 to 2300. Elovich kinetic model described very well the bioaccumulation of Pb and Cd over time, while pseudo-second-order model adjusted better to experimental data regarding Hg. F. vesiculosus showed different affinity toward studied metals, following the sequence order: Hg > Pb > Cd. Analysis of metal content in the macroalgae after bioaccumulation, proved that all metal removed from solution was bound to the biomass. Depuration experiments reveled no significant loss of metal back to solution. Exposure to contaminants only adversely affected the organism's growth for the highest concentrations of Cd and Pb. Findings are an important contribute for the development of remediation biotechnologies for confined saline waters contaminated with trace metal contaminants, more efficient and with lower costs than the traditional treatment methods.

  3. Kinetics of Hg(II) adsorption and desorption in calcined mussel shells.

    Science.gov (United States)

    Peña-Rodríguez, Susana; Fernández-Calviño, David; Nóvoa-Muñoz, Juan Carlos; Arias-Estévez, Manuel; Núñez-Delgado, Avelino; Fernández-Sanjurjo, María José; Alvarez-Rodríguez, Esperanza

    2010-08-15

    The potential use of calcined mussel shells to purify water contaminated with mercury was evaluated. The Hg(II) adsorption and desorption kinetics were studied in batch-type and stirred-flow chamber experiments. The adsorption/desorption experiments revealed some differences between the batches of shells used. The batch of shells that displayed the greatest capacity to adsorb Hg(II), via a highly irreversible reaction, also contained more Fe and Al than the other batches. The results of the stirred-flow chamber experiments indicated a high degree of irreversibility in the process of Hg(II) adsorption in the mussel shell, and that Hg(II) was rapidly retained. The results of these experiments also revealed that the efficiency of depuration differed depending on the length of time that the system was used: when the system was operated for 55 min, depurating 162 mL of inflowing water g(-1) mussel shell, a 90% reduction in the initial concentration of Hg(II) was obtained; use of the system for 90 min, depurating 265 mL water g(-1) mussel shell, produced a 75% reduction in the initial Hg(II), and use of the system for 162.5 min, depurating 487 mL of water g(-1) mussel shell, resulted in a 50% reduction in the initial Hg(II).

  4. Phytochelatin synthesis in response to Hg uptake in aquatic plants near a chlor-alkali factory.

    Science.gov (United States)

    Turull, Marta; Grmanova, Gabriela; Dago, Àngela; Ariño, Cristina; Díez, Sergi; Díaz-Cruz, José Manuel; Esteban, Miquel

    2017-06-01

    The effects of mercury (Hg) released from a chlor-alkali factory in aquatic plants along the Ebro River basin (NE Spain) were analysed considering the phytochelatins (PCn) and their isoforms content in these plants. These compounds were analyzed using HPLC with amperometric detection, and the macrophytes species Ceratophyllum demersum and Myriopyllum spicatum were collected in two sampling campaigns, autumn and spring, respectively. To correlate the PCn content in macrophytes with the Hg contamination, analysis of total Hg (THg) content in plants and suspended particulate matter, as well as the dissolved-bioavailable fraction of Hg in water measured by the diffusive gradient in thin film (DGT) technique were done. The results confirm the presence of PC2-Ala in extracts of C. demersum and PC2-desGly in M. spicatum, and the concentration of these thiol compounds depends clearly on the distance between the hot spot and the downstream sites: the higher the levels are, the closer the hot spot is. Since most of the Hg is hypothesized to be associated with SPM and transported downstream, our results of the DGT suggest that trace amounts of Hg in water can be released as free metal ions yielding a certain accumulation in plants (reaching the ppb level) that are enough for activation of induction of PCs. A few PCs species have been determined, at different seasons, indicating that they can be used as good indicators of the presence of bioavailable Hg in aquatic media throughout the year.

  5. Phenylselenolate Mercury Alkyl Compounds, PhSeHgMe and PhSeHgEt: Molecular Structures, Protolytic Hg-C Bond Cleavage and Phenylselenolate Exchange.

    Science.gov (United States)

    Yurkerwich, Kevin; Quinlivan, Patrick J; Rong, Yi; Parkin, Gerard

    2016-01-08

    The phenylselenolate mercury alkyl compounds, PhSeHgMe and PhSeHgEt, have been structurally characterized by X-ray diffraction, thereby demonstrating that both compounds are monomeric with approximately linear coordination geometries; the mercury centers do, nevertheless, exhibit secondary Hg•••Se intermolecular interactions that serve to increase the coordination number in the solid state. The ethyl derivative, PhSeHgEt, undergoes facile protolytic cleavage of the Hg-C bond to release ethane at room temperature, whereas PhSeHgMe exhibits little reactivity under similar conditions. Interestingly, the cleavage of the Hg-C bond of PhSeHgEt is also more facile than that of the thiolate analogue, PhSHgEt, which demonstrates that coordination by selenium promotes protolytic cleavage of the mercury-carbon bond. The phenylselenolate compounds PhSeHgR (R = Me, Et) also undergo degenerate exchange reactions with, for example, PhSHgR and RHgCl. In each case, the alkyl groups preserve coupling to the (199)Hg nuclei, thereby indicating that the exchange process involves metathesis of the Hg-SePh/Hg-X groups rather than metathesis of the Hg-R/Hg-R groups.

  6. The application of 199Hg NMR and 199mHg perturbed angular correlation (PAC) spectroscopy to define the biological chemistry of HgII

    DEFF Research Database (Denmark)

    Iranzo, Olga; Thulstrup, Peter Waaben; Ryu, Seung-baek;

    2007-01-01

    H values and at peptide/HgII ratios of 3:1 with an unusual trigonal thiolate coordination mode. The resulting HgII complexes are good water-soluble models for HgII binding to the protein MerR. We have carried out a parallel study using 199Hg NMR and 199mHg perturbed angular correlation (PAC) spectroscopy...... to characterize the distinct species that are generated under different pH conditions and peptide TRI L9C/HgII ratios. These studies prove for the first time the formation of [Hg{(TRI L9C)2-(TRI L9C H)}], a dithiolate-HgII complex in the hydrophobic interior of the three-stranded coiled coil (TRI L9C)3. 199Hg NMR...... and 199mHg PAC data demonstrate that this dithiolate-HgII complex is different from the dithiolate [Hg(TRI L9C)2], and that the presence of third -helix, containing a protonated cysteine, breaks the symmetry of the coordination environment present in the complex [Hg(TRI L9C)2]. As the pH is raised...

  7. Magnetic fields of HgMn stars

    DEFF Research Database (Denmark)

    Hubrig, S.; Gonzalez, J. F.; Ilyin, I.

    2012-01-01

    Context. The frequent presence of weak magnetic fields on the surface of spotted late-B stars with HgMn peculiarity in binary systems has been controversial during the two last decades. Recent studies of magnetic fields in these stars using the least-squares deconvolution (LSD) technique have fai...

  8. Temporal Trends and Future Predictions of Mercury Concentrations in Northwest Greenland Polar Bear (Ursus maritimus) Hair

    DEFF Research Database (Denmark)

    Dietz, Rune; Born, E.W.; Riget, Frank Farsø

    2011-01-01

    Hair samples from 117 Northwest Greenland polar bears (Ursus maritimus) were taken during 1892-2008 and analyzed for total mercury (hereafterHg). The sample represented 28 independent years and the aim of the study was to analyze for temporal Hg trends. Mercury concentrations showed yearly...... significant increases of 1.6-1.7% (p bear......-2008 concentrations ofHg in Northwest Greenland polar bear hair exceeded the general guideline values of 20-30 μg/g dry weight for terrestrial wildlife, whereas the neurochemical effect level of 5.4 μg Hg/g dry weight proposed for East Greenland polar bears was exceeded in 93.5% of the cases. These results call...

  9. Excitation spectra and ground-state properties from density functional theory for the inverted band-structure systems $\\beta$-HgS, HgSe, and HgTe

    CERN Document Server

    Delin, A

    2002-01-01

    We have performed a systematic density-functional study of the mercury chalcogenide compounds $\\beta$-HgS, HgSe, and HgTe using an all-electron full-potential linear muffin-tin orbital (FP-LMTO) method. We find that, in the zinc-blende structure, both HgSe and HgTe are semimetals whereas $\\beta$-HgS has a small spin-orbit induced band gap. Our calculated relativistic photoemission and inverse photoemission spectra (PES and IPES, respectively) reproduce very well the most recently measured spectra, as do also our theoretical optical spectra. In contrast to the normal situation, we find that the local density approximation (LDA) to the density functional gives calculated equilibrium volumes in much better agreement with experiment than does the generalized gradient corrected functional (GGA). We also address the problem of treating relativistic $p$ electrons with methods based on a scalar-relativistic basis set, and show that the effect is rather small for the present systems.

  10. Seasonal and diurnal variations of Hg° over New England

    Directory of Open Access Journals (Sweden)

    J. D. Hegarty

    2007-11-01

    Full Text Available Factors influencing diurnal to interannual variability in Hg° over New England were investigated using multi-year measurements conducted by the AIRMAP program at the Thompson Farm (TF coastal site, an inland elevated site at Pac Monadnock (PM, and one summer of measurements on Appledore Island (AI in the Gulf of Maine. Mixing ratios of Hg° at TF showed distinct seasonality with maxima in March and minima in October. In comparison, Hg° at AI tracked the trend at TF but with higher minima, while at PM the diurnal and annual cycles were dampened. In winter, Hg° was correlated most strongly with CO and NOy, indicative of anthropogenic emissions as their primary source. Our analysis indicates that Hg° had a regional background level of ~160 fmol/mol, a summertime dry deposition velocity of ~0.20 cm s−1, and a ~16 day lifetime in the coastal boundary layer. The influence of oceanic emissions on ambient Hg° levels was identified using the Hg°-CHBr3 correlation at both TF and AI. Moreover, the lower Hg° levels and steeper decreasing warm season trend at TF (0.5–0.6 fmol/mol d−1 compared to PM (0.2–0.3 fmol/mol d−1 likely reflected the impact of marine halogen chemistry. Large interannual variability in warm season Hg° levels in 2004 versus 2005/2006 may be due to the role of precipitation patterns in influencing surface evasion of Hg°. In contrast, changes in wintertime maximum levels of Hg° were small compared to drastic reductions in CO, CO2, NOy, and SO2 from 2004/2005 to 2006/2007. These trends could be explained by a homogeneous surface distribution of Hg° over the North American continent in winter and/or rapid removal of mercury released from anthropogenic sources. We caution that during warmer winters, the Hg°-CO slope possibly reflects the ratio of Hg° loss relative to changes in CO more than their emission ratio.

  11. Seasonal and diurnal variations of Hg° over New England

    Directory of Open Access Journals (Sweden)

    J. D. Hegarty

    2008-03-01

    Full Text Available Factors influencing diurnal to interannual variability in Hg° over New England were investigated using multi-year measurements conducted by AIRMAP at the Thompson Farm (TF coastal site, an inland elevated site at Pac Monadnock (PM, and two month measurements on Appledore Island (AI in the Gulf of Maine. Mixing ratios of Hg° at TF showed distinct seasonality with maxima in March and minima in October. Hg° at AI tracked the trend at TF but with higher minima, while at PM the diurnal and annual cycles were dampened. In winter, Hg° was correlated most strongly with CO and NOy, indicative of anthropogenic emissions as their primary source. Our analysis indicates that Hg° had a regional background level of ~160 fmol/mol in winter, a dry deposition velocity of ~0.20 cm s−1 with a ~16 day lifetime in the coastal boundary layer in summer. The influence of oceanic emissions on ambient Hg° levels was identified using the Hg°-CHBr3 correlation at both TF and AI. Moreover, the lower Hg° levels and steeper decreasing warm season trend at TF (0.5–0.6 fmol/mol d−1 compared to PM (0.2–0.3 fmol/mol d−1 likely reflected the impact of marine halogen chemistry. Large interannual variability in warm season Hg° levels in 2004 versus 2005/2006 may be due to the role of precipitation patterns in influencing surface evasion of Hg°. In contrast, changes in wintertime maximum levels of Hg° were small compared to drastic reductions in CO, CO2, NOy, and SO2 from 2004/2005 to 2006/2007. These trends could be explained by a homogeneous distribution of Hg° over North American in winter due to its long lifetime and/or rapid removal of reactive mercury from anthropogenic sources. We caution that during warmer winters, the Hg°-CO slope possibly reflects Hg° loss relative to changes in CO more than their emission ratio.

  12. Acumulación de mercurio (Hg por caña flecha (Gynerium sagittatum (Aubl Beauv. in vitro

    Directory of Open Access Journals (Sweden)

    Rafael Esteban Ortega-Ortega

    2011-04-01

    (p ≤ 0.05 to establish significant differences between the treatments, tests of normality (Kolmogorov-Smirnov and homogeneity test Bartlett variance. The mercury analyses were performed on atomic absorption spectrophotometer Thermo Electron S4, a cell equipped with quartz windows, by the method of atomic absorption spectrometry with cold steam. The results show that the plant part that presents the greatest accumulation is the root with 55.98 mg g-1 HgT, followed by the stems, leaves 14.84 g g-1 HgT and these values ​​are related to the degree of metal concentration in the culture medium. Furthermore, the accumulation of mercury in roots and stems increased with time. In conclusion, in vitro this plant accumulates due to the high Hg concentrations in their tissues without affecting the viability of plants.Key words: Phytoremediation, removal, heavy metals.

  13. Beaver Ponds Increase Methylmercury and Nutrients Concentrations in Canadian Shield Streams

    Science.gov (United States)

    Roy, V.; Amyot, M.; Carignan, R.

    2007-12-01

    Beaver populations and the number of beaver dams are currently increasing in many Canadian regions. Since natural and anthropogenic impoundments have historically been identified as sources of the potent neurotoxin methylmercury (MeHg), beaver dams could also increase MeHg levels in streams. During summer 2006, we collected water samples upstream and downstream from twenty beaver dams of the Laurentians, located on the Canadian Shield. Samples were analysed for total Hg, MeHg and other chemical variables including DOC, TP, TDP, TN, and major ions. Significant increases of nutrients (DOC, TP, TDP, TN) and ammonium concentrations and depletions of oxygen, nitrate and sulphate concentrations between inlet and outlet show that beaver ponds provide environmental conditions that can favour methylation of inorganic mercury. Heterogeneity of the ratio MeHg/THg at the outlet among our sites was well explained by the estimated age of the impoundment, with methylation capacity of beaver ponds decreasing with age. Further, the geographic location of beaver ponds influenced water chemistry at the outlet, as we observed a dichotomy between northern and southern sites; these differences were based mainly on forest composition. On average, beaver impoundments increased MeHg concentrations by 5.7 fold, total Hg concentrations by 1.6 fold and nutrients concentrations by 2-3 fold. Overall, our results suggest that beaver dams may considerably increase MeHg and nutrients levels in downstream ecosystems. The impact of beavers on the cycling of contaminants and nutrients in boreal watersheds should therefore be considered in the management of their populations.

  14. Phase diagrams and microscopic structures of (Hg,Cd)Te, (Hg,Zn)Te, and (Cd,Zn)Te alloys

    Science.gov (United States)

    Patrick, R. S.; Chen, A.-B.; Sher, A.; Berding, M. A.

    1988-01-01

    A cluster theory based on the quasi-chemical approximation has been applied to study the local correlation bond-length distribution, and phase diagrams of the II-VI pseudobinary alloys Hg(1 - x)Cd(x)Te, Hg(1 - x)Zn(x)Te, and Cd(1 - x)Zn(x)Te. The cluster energy is calculated by letting it relax in some effective alloy medium and then considering the contributions from the strain and chemical energies. Two different models are presented to simulate the alloy medium. While both models show that all three alloys have nearly random distributions, the signs of the local correlation prove to be sensitive to the alloy medium chosen for the energy calculation. Good agreement is found between experiment and the bond lengths and phase diagrams in both models.

  15. The lncRNA MIR31HG regulates p16(INK4A) expression to modulate senescence.

    Science.gov (United States)

    Montes, Marta; Nielsen, Morten M; Maglieri, Giulia; Jacobsen, Anders; Højfeldt, Jonas; Agrawal-Singh, Shuchi; Hansen, Klaus; Helin, Kristian; van de Werken, Harmen J G; Pedersen, Jakob S; Lund, Anders H

    2015-04-24

    Oncogene-induced senescence (OIS) can occur in response to oncogenic insults and is considered an important tumour suppressor mechanism. Here we identify the lncRNA MIR31HG as upregulated in OIS and find that knockdown of MIR31HG promotes a strong p16(INK4A)-dependent senescence phenotype. Under normal conditions, MIR31HG is found in both nucleus and cytoplasm, but following B-RAF expression MIR31HG is located mainly in the cytoplasm. We show that MIR31HG interacts with both INK4A and MIR31HG genomic regions and with Polycomb group (PcG) proteins, and that MIR31HG is required for PcG-mediated repression of the INK4A locus. We further identify a functional enhancer, located between MIR31HG and INK4A, which becomes activated during OIS and interacts with the MIR31HG promoter. Data from melanoma patients show a negative correlation between MIR31HG and p16(INK4A) expression levels, suggesting a role for this transcript in cancer. Hence, our data provide a new lncRNA-mediated regulatory mechanism for the tumour suppressor p16(INK4A).

  16. Can Nassarius reticulatus be used as a bioindicator for Hg contamination? Results from a longitudinal study of the Portuguese coastline.

    Science.gov (United States)

    Coelho, J P; Pimenta, J; Gomes, R; Barroso, C M; Pereira, M E; Pardal, M A; Duarte, A

    2006-06-01

    The focus of this work is to explore the use of the netted whelk, Nassarius reticulatus (L.), as an indicator of mercury (Hg) contamination, by assessing the concentration of Hg in the sediments and in the whelk along the entire Portuguese coast. Total Hg concentrations ranged from below the detection limit (0.01 ng absolute mercury) up to 0.87 mg kg(-1) dry weight (dwt) in sediments and between 0.06 and 1.02 mg kg(-1) (dwt) for organisms, with no significant differences between males and females. Although organic mercury was not detected in the sediments, it represented, on average, 52% of the total Hg in the whelk tissues, and as high as 88% in some cases, suggesting mercury accumulation from dietary intake. Significant negative correlations were found between the total Hg concentrations in the sediments and the log(10) of Hg concentrations in whelk tissues males (r=-0.64; P<0.01) and females (r=-0.52; P<0.01) indicating that the species is a poor indicator of Hg contamination. Nevertheless, since the highest concentrations of organic mercury in the whelk tissues were found in the least contaminated areas, this species must be highly relevant in the trophic web, namely on the possible biomagnification of mercury. The high dietary mercury accumulation from feeding on carrion and the low bioavailability of mercury to whelks in estuarine sediments may be the basis of the mercury accumulation pattern in N. reticulatus.

  17. Determination of Trace Germanium in Marine Sediments by Hydride Generation-Atomic Fluorescence Spectrometry (HG-AFS)

    Institute of Scientific and Technical Information of China (English)

    LI Jing; ZHAO Shilan; ZHANG Zhaohui; ZENG Xianjie

    2004-01-01

    A method for the analysis of trace germanium in marine sediments by HG-AFS has been investigated. The experimental conditions such as the acidity of reduction reaction, the amount of sodium boro-hydride, the carrier gas flow rate, etc., were tested and optimized by using a kind of orthogonal design. The detection limit of the presented method is 0.95 μg L-1 for germanium. The calibration curve shows a satisfactory line in the concentration range 0-320 μg L-1 Ge with a variation coefficient of ±2.1%.

  18. Hg, Bi, Cu and Zn distribution in human teeth treated by dental amalgam measured by synchrotron microprobe

    Science.gov (United States)

    Carvalho, M. L.; Marques, J. P.; Brito, J.; Casaca, C.; Cunha, A. S.

    2002-11-01

    Human teeth restored with dental amalgam were analysed by a synchrotron microprobe to evaluate the diffusion of its major constituents, Cu, Zn and Hg, throughout the tooth structures. We measured the elemental distribution inside the tooth from the root to the enamel, specially the region around the amalgam, after its total removal. Hg is present only in restored teeth and concentration profiles show strongly increased levels of this element close to the amalgam region, reaching 500 μg g -1 in one or two cases, decreasing strongly to the inner part of the tooth. Pb concentration profiles do not seem to be affected by metallic amalgam. Very high concentrations of Bi were found in one of the restored teeth, reaching more than 2000 μg g -1, decreasing sharply to the outer regions. The distribution of Mn, Fe, Cu and Zn was also determined in order to evaluate elemental influences by amalgam components. No significant changes in elemental concentrations were detected for Mn and Fe between healthy and restored teeth. However, the levels of Zn and Cu are increased in restored teeth. An X-ray fluorescence set-up with microprobe capabilities, 100 μm of spatial resolution and an energy of 18 keV, installed at LURE synchrotron (France) was used.

  19. Hg, Bi, Cu and Zn distribution in human teeth treated by dental amalgam measured by synchrotron microprobe

    Energy Technology Data Exchange (ETDEWEB)

    Carvalho, M.L. E-mail: luisa@cii.fc.ul.pt; Marques, J.P.; Brito, J.; Casaca, C.; Cunha, A.S

    2002-11-01

    Human teeth restored with dental amalgam were analysed by a synchrotron microprobe to evaluate the diffusion of its major constituents, Cu, Zn and Hg, throughout the tooth structures. We measured the elemental distribution inside the tooth from the root to the enamel, specially the region around the amalgam, after its total removal. Hg is present only in restored teeth and concentration profiles show strongly increased levels of this element close to the amalgam region, reaching 500 {mu}g g{sup -1} in one or two cases, decreasing strongly to the inner part of the tooth. Pb concentration profiles do not seem to be affected by metallic amalgam. Very high concentrations of Bi were found in one of the restored teeth, reaching more than 2000 {mu}g g{sup -1}, decreasing sharply to the outer regions. The distribution of Mn, Fe, Cu and Zn was also determined in order to evaluate elemental influences by amalgam components. No significant changes in elemental concentrations were detected for Mn and Fe between healthy and restored teeth. However, the levels of Zn and Cu are increased in restored teeth. An X-ray fluorescence set-up with microprobe capabilities, 100 {mu}m of spatial resolution and an energy of 18 keV, installed at LURE synchrotron (France) was used.

  20. Polymorphisms in MIR137HG and microRNA-137-regulated genes influence gray matter structure in schizophrenia.

    Science.gov (United States)

    Wright, C; Gupta, C N; Chen, J; Patel, V; Calhoun, V D; Ehrlich, S; Wang, L; Bustillo, J R; Perrone-Bizzozero, N I; Turner, J A

    2016-02-02

    Evidence suggests that microRNA-137 (miR-137) is involved in the genetic basis of schizophrenia. Risk variants within the miR-137 host gene (MIR137HG) influence structural and functional brain-imaging measures, and miR-137 itself is predicted to regulate hundreds of genes. We evaluated the influence of a MIR137HG risk variant (rs1625579) in combination with variants in miR-137-regulated genes TCF4, PTGS2, MAPK1 and MAPK3 on gray matter concentration (GMC). These genes were selected based on our previous work assessing schizophrenia risk within possible miR-137-regulated gene sets using the same cohort of subjects. A genetic risk score (GRS) was determined based on genotypes of these four schizophrenia risk-associated genes in 221 Caucasian subjects (89 schizophrenia patients and 132 controls). The effects of the rs1625579 genotype with the GRS of miR-137-regulated genes in a three-way interaction with diagnosis on GMC patterns were assessed using a multivariate analysis. We found that schizophrenia subjects homozygous for the MIR137HG risk allele show significant decreases in occipital, parietal and temporal lobe GMC with increasing miR-137-regulated GRS, whereas those carrying the protective minor allele show significant increases in GMC with GRS. No correlations of GMC and GRS were found in control subjects. Variants within or upstream of genes regulated by miR-137 in combination with the MIR137HG risk variant may influence GMC in schizophrenia-related regions in patients. Given that the genes evaluated here are involved in protein kinase A signaling, dysregulation of this pathway through alterations in miR-137 biogenesis may underlie the gray matter loss seen in the disease.

  1. Barrier formation at graded HgTe/CdTe heterojunctions

    Science.gov (United States)

    Goren, D.; Asa, G.; Nemirovsky, Y.

    1996-11-01

    Numerical calculations of graded HgTe/CdTe heterojunction (HJ) band diagrams at equilibrium are presented and discussed. The calculations are performed in the entire compositional range (0HJs are examined as a function of the graded region width and the graded region doping profiles. The graded region width and doping profiles were found to be the two main factors that determine whether barriers are formed as well as their shape and magnitude. The calculated results indicate that epitaxial ohmic HgTe contacts to extrinsic CdTe are possible, provided that the graded region is wider than one micron, and that it has the same doping type as the doping of the substrate with equal or higher absolute value. Further numerical calculations take into consideration the possible existence of distributed interface charges in the graded region of the HJ. It is shown that by assuming a classical transport over the potential barrier, the effective graded interface charge can be determined from the zero bias differential resistance of the HJ. Experimental transport measurements of metalorganic chemical vapor deposition (MOCVD) grown HgTe/p-CdTe graded HJs show a varying degree of rectification, indicating variations in the graded interface charge distributions which result from different MOCVD growth conditions.

  2. Effects of metals doping on the removal of Hg and H2S over ceria

    Science.gov (United States)

    Ling, Lixia; Zhao, Zhongbei; Zhao, Senpeng; Wang, Qiang; Wang, Baojun; Zhang, Riguang; Li, Debao

    2017-05-01

    The effects of Mn and Fe doping into the CeO2(111) surface on the simultaneous removal of Hg and H2S was investigated, a density functional theory calculation with the on-site Coulomb interaction taken into account was adopted. The adsorptions of Hg-containing species on perfect CeO2(111), Mn/CeO2(111) and Fe/CeO2(111) surfaces were studied, the results showed that Mn and Fe dopants facilitated Hg adsorption, and more charge transferred from Hg atom to the metal doped surfaces; HgS preferred to adsorb on the perfect surface with the dissociated mode, while with the molecular mode on Mn/CeO2(111) and Fe/CeO2(111) surfaces. The reaction mechanism show that the dissociated S by H2S can easily react with Hg leading to the formation of HgS on Mn/CeO2(111) and Fe/CeO2(111) surfaces, which is crucial to capture mercury.

  3. Adsorption of Ag, Cu and Hg from aqueous solutions using expanded perlite.

    Science.gov (United States)

    Ghassabzadeh, Hamid; Mohadespour, Ahmad; Torab-Mostaedi, Meisam; Zaheri, Parisa; Maragheh, Mohammad Ghannadi; Taheri, Hossein

    2010-05-15

    The aim of the present work was to investigate the ability of expanded perlite (EP) to remove of silver, copper and mercury ions from aqueous solutions. Batch adsorption experiments were carried out and the effect of pH, adsorbent dosage, contact time and temperature of solution on the removal process has been investigated. The optimum pH for the adsorption was found to be 6.5. Adsorption of these metal ions reached their equilibrium concentration in 120, 240 and 180 min for Ag (I), Cu (II) and Hg (II) ions, respectively. Experimental data were also evaluated in terms of kinetic characteristics of adsorption and it was found that adsorption process for these metal ions followed well pseudo-second-order kinetics. Using Langmuir isotherm model, maximum adsorption capacity of EP was found to be 8.46, 1.95 and 0.35 mg/g for Ag (I), Cu (II) and Hg (II) ions, respectively. Finally, the thermodynamic parameters including, the change of free energy (DeltaG degrees ), enthalpy (DeltaH degrees ) and entropy (DeltaS degrees ) of adsorption were calculated for each metal ion. The results showed that the adsorption of these metal ions on EP was feasible and exothermic at 20-50 degrees C.

  4. [Study on Kinetic of Hg2+ from Wastewater Absorbed by Lemon Residues].

    Science.gov (United States)

    Shen, Wang-qing; Wang, Miao; Yang, Ting

    2016-03-01

    With low price and its superior adsorption performance after modification, currently agricultural waste is used as adsorbent of heavy metals in wastewater, which has become a hot research topic. To study on Hg2+ from wastewater absorbed by lemon residues that has been modified by 15% concentration of sulphuric acid. The pore volume, pore size and other properties of the adsorbent were test. The samples were characterized by differential thermal analysis, IR, electron microscopy and spectroscopy. The result showed that the adsorption rate was controlled by membrane diffusion kinetics that was viewed as the first order kinetics equation of the Lagergren, which was physically absorbed. The adsorption properties of modified lemon residues were improved greatly, and the pore size distribution mainly was medium. There were three losses-weight process. There was a endothermic peak around 66 degrees C and two exotherm near 316 degrees C and 494 degrees C. Basic framework of Lemon residues was not changed and structure of Lemon residues was amorphous; the surface of modified lemon residues loosen and many pores formed, and Hg2+ have been adsorbed effectively.

  5. The construction, characterization, Hg(II)-sensing and removal behavior of magnetic core-shell nanospheres loaded with fluorescence "Off-On" probe.

    Science.gov (United States)

    Tan, Jun; Wei, Xiaoyan; Chen, Jie; Sun, Ping; Ouyang, Yuxia; Fan, Juhong; Liu, Rui

    2014-12-10

    The present paper constructed and discussed core-shell structured nanospheres grafted with rhodamine based probe for Hg(II) sensing and removal. Electron microscopy images, XRD curves, thermogravimetric analysis and N2 adsorption/desorption isotherms were used to identify the core-shell structure. The inner core consisted of superparamagnetic Fe3O4 nanoparticles, which made the nanocomposite magnetically removable. The outer shell was constructed with silica molecular sieve which provided large surface area and ordered tunnels for the sensing probe, accelerating analyte adsorption and transportation. The rhodamine based sensing probe emission increased with the increasing Hg(II) concentration, showing emission "Off-On" effect, which could be explained by the structural transformation from a non-emissive one to a highly emissive one. The influence from various metal ions and pH values was also investigated, which suggested this structural transformation could only be triggered by Hg(II), showing high selectivity and linear response. The Hg(II) sensing nanocomposite could be regenerated after usage. The response time was slightly compromised and could be further improved.

  6. Mercury (Hg) emissions from domestic biomass combustion for space heating.

    Science.gov (United States)

    Huang, Jiaoyan; Hopke, Philip K; Choi, Hyun-Deok; Laing, James R; Cui, Huailue; Zananski, Tiffany J; Chandrasekaran, Sriraam Ramanathan; Rattigan, Oliver V; Holsen, Thomas M

    2011-09-01

    Three mercury (Hg) species (gaseous elemental mercury (GEM), gaseous oxidized mercury (GOM), and fine particulate-bound mercury (PBM(2.5))) were measured in the stack of a small scale wood combustion chamber at 400°C, in the stack of an advanced wood boiler, and in two areas influenced by wood combustion. The low temperature process (lab-scale) emitted mostly GEM (∼99% when burning wood pellets and ∼95% when burning unprocessed wood). The high temperature wood boiler emitted a greater proportion of oxidized Hg (approximately 65%) than the low temperature system. In field measurements, mean PBM(2.5) concentrations at the rural and urban sites in winter were statistically significantly higher than in warmer seasons and were well correlated with Delta-C concentrations, a wood combustion indictor measured by an aethalometer (UV-absorbable carbon minus black carbon). Overall the results suggest that wood combustion may be an important source of oxidized mercury (mostly in the particulate phase) in northern climates in winter.

  7. TOTAL MERCURY (HgT BIOACCUMULATION AND FISH FOOD HABITS IN NEGRO RIVER BASIN, AMAZON, BRAZIL

    Directory of Open Access Journals (Sweden)

    Jean Louchard Ferreira Soares

    2016-03-01

    Full Text Available In the Amazon, the fish is the main nutritional source for the riverine. Thus, fish have been commonly used in environmental monitoring work to be good biomonitors. This study analyzed the total mercury concentration (THg in fish of different species and feeding habits in order to investigate the existence of bioaccumulation in species in the basin of the Negro river and verify that the THg levels found are in accordance with the stipulated limit for consumption human. Sampling points were distributed in the basin of the Negro river during the period of high water. After the fisheries specimens were identified, measured and weighed. Then muscle samples were taken and subjected to acid digestion and analyzed by Cold Vapor Atomic Fluorescence Spectrophotometer - CVAFS. To research data was used analysis of variance and linear regression. A total of 264 specimens distributed into 10 species were analyzed, and the THg of the concentrations ranged from 0.030 for 1,670 mg.kg-1. The species Hoplias malabaricus, Serrasalmus rhombeus, Hemiodus immaculatus and Cichla temensis showed bioaccumulation. High concentrations of THg were found in carnivorous, piscivorous, planctívos and omnivores fish. No specimen showed mean concentrations of THg in violation to ANVISA, but this occurred in relation to FAO and WHO. keywords: Brazilian Amazon; biomonitoring; high waters; Hg.

  8. Immobilization of Hg(II) in water with polysulfide-rubber (PSR) polymer-coated activated carbon.

    Science.gov (United States)

    Kim, Eun-Ah; Seyfferth, Angelia L; Fendorf, Scott; Luthy, Richard G

    2011-01-01

    An effective mercury removal method using polymer-coated activated carbon was studied for possible use in water treatment. In order to increase the affinity of activated carbon for mercury, a sulfur-rich compound, polysulfide-rubber (PSR) polymer, was effectively coated onto the activated carbon. The polymer was synthesized by condensation polymerization between sodium tetrasulfide and 1,2-dichloroethane in water. PSR-mercury interactions and Hg-S bonding were elucidated from x-ray photoelectron spectroscopy, and Fourier transform infra-red spectroscopy analyses. The sulfur loading levels were controlled by the polymer dose during the coating process and the total surface area of the activated carbon was maintained for the sulfur loading less than 2 wt%. Sorption kinetic studies showed that PSR-coated activated carbon facilitates fast reaction by providing a greater reactive surface area than PSR alone. High sulfur loading on activated carbon enhanced mercury adsorption contributing to a three orders of magnitude reduction in mercury concentration. μ-X-ray absorption near edge spectroscopic analyses of the mercury bound to activated carbon and to PSR on activated carbon suggests the chemical bond with mercury on the surface is a combination of Hg-Cl and Hg-S interaction. The pH effect on mercury removal and adsorption isotherm results indicate competition between protons and mercury for binding to sulfur at low pH.

  9. Studies on efficiency of guava (Psidium guajava) bark as bioadsorbent for removal of Hg (II) from aqueous solutions

    Energy Technology Data Exchange (ETDEWEB)

    Lohani, Minaxi B. [Integral University, Kursi Road, Lucknow 226026, UP (India)], E-mail: minaxi_lohani@sify.com; Singh, Amarika; Rupainwar, D.C. [Institute of Engineering and Technology Sitapur Road, Lucknow 226021, UP (India); Dhar, D.N. [IIT Kanpur (India)

    2008-11-30

    Biosorption of Hg (II) was investigated in this study by using guava bark powder (GBP). In the batch system, effects of various parameters like contact time, initial concentration, pH and temperature were investigated. Removal of Hg (II) was pH dependent and was found maximum at pH 9.0. Based on this study, the thermodynamic parameters like change in standard Gibb's free energy ({delta}G{sup 0}), standard enthalpy ({delta}H{sup 0}) and standard entropy ({delta}S{sup 0}) were evaluated. The rate kinetic study was found to follow second-order. The applicability of Freundlich adsorption isotherm model was tested. The value of regression coefficient was greater than 0.99. This indicated that the isotherm model adequately described the experimental data of the biosorption of Hg (II). Maximum adsorption of 3.364 mg g{sup -1} was reached at 80 min. The results of the study showed that guava bark powder can be efficiently used as a low-cost alternative for the removal of divalent mercury from aqueous solutions.

  10. Concentration, distribution, and bioavailability of mercury and methylmercury in sediments of Baltimore Harbor and Chesapeake Bay, Maryland, USA

    Energy Technology Data Exchange (ETDEWEB)

    Mason, R.P.; Lawrence, A.L.

    1999-11-01

    For the Chesapeake Bay, sediments in regions such as Baltimore Harbor have total mercury (Hg) concentrations that exceed environmental effects guidelines. However, fish concentrations do not appear elevated. Indeed, the factors controlling the transfer of sedimentary Hg, especially as monomethylmercury (MMHg), the most bioaccumulative form of Hg, to these aquatic organisms are poorly understood. To examine this, the authors have investigated the distribution and bioavailability of Hg and MMHg to benthic organisms in Baltimore harbor and the Chesapeake Bay, in Maryland, USA. The results discussed here show that sediment concentration for both total Hg and MMHg covaries with sediment organic content and that this parameter is a better predictor, for surface sediments, of concentration than iron content, acid volatile sulfide (AVS), or other factors. Furthermore, correlations between inorganic Hg and MMHg in benthic biota with sediment levels suggest that variation in the bioaccumulation factor (SBAF) for invertebrates is best explained in terms of sediment organic content. thus, the results from this study emphasize the importance of organic matter in regions removed from point source input in controlling both the concentration and bioavailability of MMHg to organisms. Because of the exponential nature of the SBAF/organic content relationship, there is a nonlinear organism response to MMHg in sediments that must be considered in any estimation of the toxic effect of sediment MMHg. Also, as a result of the decoupling between total Hg and MMHg concentration and bioavailability in surface sediments, any remediation evaluation of bioavailability and/or toxicity that is based only on total Hg concentration is unlikely to provide a reliable prediction.

  11. Long-term Hg pollution induced Hg tolerance in the terrestrial isopod Porcellio scaber (Isopoda, Crustacea)

    Energy Technology Data Exchange (ETDEWEB)

    Lapanje, A. [University of Ljubljana, Biotechnical Faculty, Department of Biology, Vecna pot 111, 1000 Ljubljana (Slovenia); Institute of Physical Biology, Veliko Mlacevo 59, 1290 Grosuplje (Slovenia)], E-mail: ales.lapanje@bf.uni-lj.si; Drobne, D. [University of Ljubljana, Biotechnical Faculty, Department of Biology, Vecna pot 111, 1000 Ljubljana (Slovenia); Nolde, N. [Institute Jozef Stefan, Department of Environmental Sciences, Jamova 39, 1000 Ljubljana (Slovenia); Valant, J. [University of Ljubljana, Biotechnical Faculty, Department of Biology, Vecna pot 111, 1000 Ljubljana (Slovenia); Muscet, B. [Institute of Physical Biology, Veliko Mlacevo 59, 1290 Grosuplje (Slovenia); Leser, V. [University of Ljubljana, Biotechnical Faculty, Department of Biology, Vecna pot 111, 1000 Ljubljana (Slovenia); Rupnik, M. [Institute of Public Health, Prvomajska 1, 2000 Maribor (Slovenia); Faculty of Medicine, University of Maribor, Slomskov trg 15, 2000 Maribor (Slovenia)

    2008-06-15

    The aim of our work was to assess the pollution-induced community tolerance (PICT) of isopod gut microbiota and pollution-induced isopod population tolerance (PIPT). Animals collected from a chronically Hg polluted and an unpolluted location were exposed for 14 days to 10 {mu}g Hg/g dry food under laboratory conditions. The lysosomal membrane stability, hepatopancreas epithelium thickness, feeding activity and animal bacterial gut microbiota composition were determined. The results confirm the hypothesis that the response to short-term Hg exposure differs for animals from the Hg polluted and the unpolluted field locations. The animals and their gut microbiota from the Hg polluted location were less affected by Hg in a short-term feeding experiment than those from the unpolluted environment. We discuss the pollution-induced population tolerance of isopods and their gut microbiota as a measure of effects of long-term environmental pollution. The ecological consequences of such phenomena are also discussed. - Isopods (Porcellio scaber) as well as their bacterial gut community from a mercury-polluted site are mercury tolerant.

  12. Hg(2+) mediated quinazoline ensemble for highly selective recognition of Cysteine.

    Science.gov (United States)

    Anand, Thangaraj; Sivaraman, Gandhi; Chellappa, Duraisamy

    2014-04-05

    A fluorimetric sensor for Hg(2+) ion and Cysteine based on quinazoline platform was designed and synthesized by one step reaction and characterized by using common spectroscopic methods. Time Dependent Density Functional Theory calculations shows that probe behaves as "ON-OFF" fluorescent quenching sensor via electron transfer/heavy atom effect. Receptor was found to exhibit selective fluorescence quenching behavior over the other competitive metal ions, and also the receptor-Hg(2+) ensemble act as an efficient "OFF-ON" sensor for Cysteine. Moreover this sensor has also been successfully applied to detection of Hg(2+) in natural water samples with good recovery.

  13. [AuHg(o-C6H4PPh22I]: A Dinuclear Heterometallic Blue Emitter

    Directory of Open Access Journals (Sweden)

    José M. López-de-Luzuriaga

    2015-02-01

    Full Text Available The heteronuclear AuI/HgII complex [AuHg(o-C6H4PPh22I] (1 was prepared by reacting of [Hg(2-C6H4PPh22] with [Au(tht2]ClO4 (1:1 and NaI in excess. The heterometallic compound 1 has been structurally characterized and shows an unusual blue luminescent emission in the solid state. Theoretical calculations suggest that that the origin of the emission arises from the iodide ligand arriving at metal-based orbitals in a Ligand to Metal-Metal Charge Transfer transition.

  14. Abundancias químicas de dos binarias de HgMn

    Science.gov (United States)

    Gonzalez, E. J.; González, J. F.; Collado, A. E.

    We present the results of the abundance analysis of two HgMn single-line binary systems: NGC 2287-106 and NGC 6025-14. The spectroscopic ob- servations have been carried out at the Complejo Astronómico el Leon-cito (CASLEO) with the REOSC spectrograph in cross-dispersion mode, cov- ering the spectral range 3800-5800 ≈. Compared to the Sun, NGC 6025-14 shows great overabundances of Hg, Mn, P, Ga and Xe, while Hg, Mn, Sr, Pt and Zr are overabundant in NGC 2287-106. FULL TEXT IN SPANISH

  15. Induced superconductivity in the surface state of mercury telluride (HgTe)

    Energy Technology Data Exchange (ETDEWEB)

    Maier, Luis; Knott, Daniel; Ames, Christopher; Bruene, Christoph; Leubner, Philipp; Oostinga, Jeroen; Buhmann, Hartmut; Molenkamp, Laurens W. [Physikalisches Institut (EP3), Universitaet Wuerzburg, 97074 Wuerzburg (Germany)

    2012-07-01

    It has been recently shown that the strained epitaxial growth of bulk HgTe layers opens a band gap in the normally semi-metallic material. This means that strained HgTe meets all prerequisites of a topological insulator, i.e. surface states and an insulating bulk, which does not contribute to transport measurements. The interfaces between topological insulators and superconductors are especially interesting due to the possibility of creation and detection of majorana fermions. Our current work is focussing on investigating contacts between strained HgTe and Nb as a superconducting material. First results show proximity effect and multiple sub gap features which are discussed in detail.

  16. Toxic metal dispersion in mining areas: from point source to diffusion pollution. The case of the Mt. Amiata Hg mining district (Southern Tuscany - Italy): new results.

    Science.gov (United States)

    Colica, Antonella; Chiarantini, Laura; Rimondi, Valentina; Benvenuti, Marco; Costagliola, Pilario; Lattanzi, Pierfranco; Paolieri, Mario; Rinaldi, Massimo

    2016-04-01

    Rivers draining mining areas may contribute to the diffusion of contaminants through their dispersion and accumulation into different morphological river units. The Paglia River's catchment (southern Tuscany) hosts the SE portion of the Mt. Amiata mercury district, the third most important worldwide (exploited from 1880 to 1980 with a total production of 100,000 tonnes Hg) before becoming a tributary of the Tiber River, which directly flows into Mediterranean Sea. The goals of this study are: 1) to recognize and distinguish different morphological units along the Paglia River watercourse, 2) to determine spatial/temporal distribution and concentration of Hg (and other toxic elements, particularly As) in different units. The analysis of morphological units was made by mapping their evolution from the beginning of mining activity (1883) to present day along 43 km of the Paglia watercourse defining eleven morphological sections across this river, and one across one of its tributaries, the Siele Creek, which drains various Hg mines located upstream. Four fundamental morphological/sedimentary unit types have been distinguished: stream sediments, bar, floodplain, and terraces. The latter occur in various orders and age: Pleistocenic, pre-mining (i.e., dating before 1880), and coeval to the mining activity. A total of 100 samples were taken from the various units in the selected transects, georeferenced and then analyzed for their Hg and As contents by ICP-OES. Arsenic contents generally never exceed 10 mg/kg. The observed ranges are: stream sediments 4.1÷8.2 mg/kg; bars 4.1÷6.6 mg/kg; floodplains 3.8÷6.6 mg/kg; terrace coeval with mining activity 3.2÷10.1 mg/kg. Hg contents in present-day stream sediments and bars are extremely variable (0.2÷27.5 and 1.4÷22.4 mg/kg respectively), and show a sharp increase at the confluence with Siele Creek. Floodplain sediments may reach up to 98 mg/kg. Terraces coeval with mining activity also show variable Hg contents (0.1÷66

  17. Mercury concentration trend as a possible result of changes in cod population demography.

    Science.gov (United States)

    Ruus, Anders; Hjermann, Dag Ø; Beylich, Bjørnar; Schøyen, Merete; Øxnevad, Sigurd; Green, Norman W

    2017-07-20

    Mercury (Hg) in Atlantic cod (Gadus morhua) is one of many parameters that are monitored through OSPAR's Joint Assessment and Monitoring Programme. Time series for cod in the Inner Oslofjord (Norway) go back to 1984. Until 2014, annual median Hg-concentrations in cod from the Inner Oslofjord showed both significant upward long-term (whole time series) and short-term (recent 10 years) trends (when 2015 was included, the short-term trend was not significant). However, the median length of the cod sampled also showed upward trends. This may have been caused by low cod recruitment in the area since the start of the 2000s, as indicated by beach seine surveys. To investigate how length would impact the trend analysis, the Hg-concentrations in the cod were normalised to 50 cm. No significant short-term trend in Hg-concentrations could be detected for length-normalised concentrations. The results indicated that most of the upward trend in Hg-concentrations could be attributed to the sampling of larger fish. The reasons for the apparent change in the cod population demography are not conclusive, however, sampling bias must also be considered. Copyright © 2017 Elsevier Ltd. All rights reserved.

  18. Induction by mercury compounds of brain metallothionein in rats: Hg{sup 0} exposure induces long-lived brain metallothionein

    Energy Technology Data Exchange (ETDEWEB)

    Yasutake, Akira; Nakano, Atsuhiro [Biochemistry Section, National Institute for Minamata Disease, Kumamoto (Japan); Hirayama, Kimiko [Kumamoto University, College of Medical Science (Japan)

    1998-03-01

    Metallothionein (MT) is one of the stress proteins which can easily be induced by various kind of heavy metals. However, MT in the brain is difficult to induce because of blood-brain barrier impermeability to most heavy metals. In this paper, we have attempted to induce brain MT in rats by exposure to methylmercury (MeHg) or metallic mercury vapor, both of which are known to penetrate the blood-brain barrier and cause neurological damage. Rats treated with MeHg (40 {mu}mol/kg per day x 5 days, p.o.) showed brain Hg levels as high as 18 {mu}g/g with slight neurological signs 10 days after final administration, but brain MT levels remained unchanged. However, rats exposed to Hg vapor for 7 days showed 7-8 {mu}g Hg/g brain tissue 24 h after cessation of exposure. At that time brain MT levels were about twice the control levels. Although brain Hg levels fell gradually with a half-life of 26 days, MT levels induced by Hg exposure remained unchanged for >2 weeks. Gel fractionation revealed that most Hg was in the brain cytosol fraction and thus bound to MT. Hybridization analysis showed that, despite a significant increase in MT-I and -II mRNA in brain, MT-III mRNA was less affected. Although significant Hg accumulation and MT induction were observed also in kidney and liver of Hg vapor-exposed rats, these decreased more quickly than in brain. The long-lived MT in brain might at least partly be accounted for by longer half-life of Hg accumulated there. The present results showed that exposure to Hg vapor might be a suitable procedure to provide an in vivo model with enhanced brain MT. (orig.) With 4 figs., 1 tab., 27 refs.

  19. MBE HgCdTe heterostructure detectors

    Science.gov (United States)

    Schulman, Joel N.; Wu, Owen K.

    1990-01-01

    HgCdTe has been the mainstay for medium (3 to 5 micron) and long (10 to 14 micron) wavelength infrared detectors in recent years. Conventional growth and processing techniques are continuing to improve the material. However, the additional ability to tailor composition and placement of doped layers on the tens of angstroms scale using molecular beam epitaxy (MBE) provides the opportunity for new device physics and concepts to be utilized. MBE-based device structures to be discussed here can be grouped into two categories: tailored conventional structures and quantum structures. The tailored conventional structures are improvements on familiar devices, but make use of the ability to create layers of varying composition, and thus band gap, at will. The heterostructure junction can be positioned independently of doping p-n junctions. This allows the small band gap region in which the absorption occurs to be separated from a larger band gap region in which the electric field is large and where unwanted tunneling can occur. Data from hybrid MBE/liquid phase epitaxy (LPE)/bulk structures are given. Quantum structures include the HgTe-CdTe superlattice, in which the band gap and transport can be controlled by alternating thin layers (tens of angstroms thick) of HgTe and CdTe. The superlattice has been shown to exhibit behavior which is non-alloy like, including very high hole mobilities, two-dimensional structure in the absorption coefficient, resonant tunneling, and anisotropic transport.

  20. Mechanism of Hg(II) Immobilization in Sediments by Sulfate-Cement Amendment.

    Science.gov (United States)

    Serrano, Susana; Vlassopoulos, Dimitri; O'Day, Peggy A

    2016-04-01

    Reactive amendments such as Portland and super-sulfate cements offer a promising technology for immobilizing metalloid contaminants such as mercury (Hg) in soils and sediments through sequestration in less bioavailable solid forms. Tidal marsh sediments were reacted with dissolved Hg(II) in synthetic seawater and fresh water solutions, treated with Portland cement and FeSO4 amendment, and aged for up to 90 days. Reacted solids were analyzed with bulk sequential extraction methods and characterized by powder X-ray diffraction (XRD), electron microscopy, and synchrotron X-ray absorption spectroscopy at the Hg LIII- and S K-edge. In amended sediments, XRD, SEM and sulfur K-edge XANES indicated formation of gypsum in seawater experiments or ettringite-type (Ca6Al2(SO4)3(OH)12(.)26H2O) phases in fresh water experiments, depending on the final solution pH (seawater ∼8.5; freshwater ∼10.5). Analysis of Hg EXAFS spectra showed Cl and Hg ligands in the first- and second-coordination shells at distances characteristic of a polynuclear chloromercury(II) salt, perhaps as a nanoparticulate phase, in both seawater and fresh water experiments. In addition to the chloromercury species, a smaller fraction (∼20-25%) of Hg was bonded to O atoms in fresh water sample spectra, suggesting the presence of a minor sorbed Hg fraction. In the absence of amendment treatment, Hg sorption and resistance to extraction can be accounted for by relatively strong binding by reduced S species present in the marsh sediment detected by S XANES. Thermodynamic calculations predict stable aqueous Hg-Cl species at seawater final pH, but higher final pH in fresh water favors aqueous Hg-hydroxide species. The difference in Hg coordination between aqueous and solid phases suggests that the initial Hg-Cl coordination was stabilized in the cement hydration products and did not re-equilibrate with the bulk solution with aging. Collectively, results suggest physical encapsulation of Hg as a polynuclear

  1. A SERS biosensor with magnetic substrate CoFe2O4@Ag for sensitive detection of Hg2+

    Science.gov (United States)

    Yang, Xia; He, Yi; Wang, Xueling; Yuan, Ruo

    2017-09-01

    Mercuric ion (Hg2+) is one toxic metal ion existed in aquatic ecosystems which would seriously damage human central nervous system and other organs. So developing an approach to sensitively detect Hg2+ in our living environment is urgent and important. In this work, a novel surface enhancement Raman spectrum(SERS) sensor is fabricated for high selective and ultrasensitive detection of Hg2+ in aqueous solution, based on a stable thymine-Hg2+-thymine (T-Hg2+-T) structure and the π-π interaction between single-stranded DNA (ssDNA) and single walled carbon nanotubes (SWCNTs). Herein, SWCNTs act as Raman labels to produce characteristic Raman peaks which can be a beacon to quantitative detect Hg2+. In the presence of Hg2+, the ssDNA can capture Hg2+ forming T-Hg2+-T structure, which makes SWCNTs leave the hot spots of the SERS-based biosensor. With this design, the Raman intensity of SWCNTs decreased with the increasing concentration of Hg2+. At the same time, CoFe2O4@Ag as active SERS substrates can effectively enhance sensitivity and uniformity of the biosensor through aggregation by magnet. Under optimal conditions, this proposed biosensor can detect Hg2+ at a range from 1 pM to 100 nM with a detection limit of 0.84 pM. With the advantages of good sensitivity, selectivity, simplicity and rapidity, the biosensor is potentially suitable for monitoring of Hg2+ in environmental applications.

  2. Transition state kinetics of Hg(II) adsorption at gibbsite-water interface.

    Science.gov (United States)

    Weerasooriya, Rohan; Tobschall, Heinz J; Seneviratne, Wasana; Bandara, Atula

    2007-08-25

    Kinetics of adsorption plays a pivotal factor in determining the bio-availability and mobility of Hg(II) in the environment. The kinetics of Hg(II) adsorption on gibbsite was examined as a function of pH, temperature and electrolyte type. Adsorption of Hg(II) was highly non-linear where the rate of Hg(II) retention was rapid initially and was followed by gradual or somewhat slow retention behavior with increasing contact time. The respective rate constants designated as k(1) (S-1: fast step) and k(2) (S-2: slow step). Always k(1) follows the order: k(1)(CIO)(4) >/= k(1)(NO3)(4) > k(1)(Cl). Such a relationship was not observed for the S-2 route. A two-step reaction model with pseudo-first order kinetics successfully described the adsorption rates of Hg(II) on gibbsite. Arrhenius and Erying models determined the thermodynamic parameters at activation states, which correspond to S-1 and S-2 routes. In a given system, always the activation energies showed a decrease with the pH. Gibbs free energy (DeltaG(#)), enthalpy (DeltaH(#)), and entropy (DeltaS(#)) values of activation states were almost similar both in NaClO(4) and NaNO(3) which signal a similar Hg(II) adsorptive mechanism on gibbsite. The configurations of different Hg(II)-surface complexes were elucidated by transmission vibration spectroscopy.

  3. [Dissolution, absorption and bioaccumulation in gastrointestinal tract of mercury in HgS-containing traditional medicines Cinnabar and Zuotai].

    Science.gov (United States)

    Zheng, Zhi-yuan; Li, Cen; Zhang, Ming; Yang, Hong-xia; Geng, Lu-jing; Li, Lin-shuai; Du, Yu-zhi; Wei, Li-xin

    2015-06-01

    α-HgS is the main component of traditional Chinese medicine cinnabar, while β-HgS is the main component of Tibetan medicine Zuotai. However, there was no comparative study on the dissolution and absorption in gastrointestinal tract and bioaccumulation in organs of mercury in Cinnabar, Zuotai, α-HgS and β-HgS. In this study, the dissolution process of the four compounds in the human gastrointestinal tract was simulated to determine the mercury dissolutions and compare the mercury dissolution of different medicines and the dissolution-promoting capacity of different solutions. To explore the absorption and bioaccumulation of cinnabar and Zuotai in organisms, mice were orally administered with clinical equivalent doses cinnabar and Zuotai. Meanwhile, a group of mice was given α-HgS and β-HgS with the equivalent mercury with cinnabar, while another group was given β-HgS and HgCl2 with the equivalent mercury with Zuotai. The mercury absorption and bioaccumulation capacities of different medicines in mice and their mercury bioaccumulation in different tissues and organs were compared. The experimental results showed a high mercury dissolutions of Zuotai in artificial gastrointestinal fluid, which was followed by β-HgS, cinnabar and α-HgS. As for the mercury absorption and bioaccumulation in mice, HgCl2 was the highest, β-HgS was the next, and a-HgS was slightly higher than cinnabar. The organs with the mercury bioaccumulation from high to low were kidney, liver and brain. This study is close to clinical practices and can provide reference for the clinical safe medication as well as a study model for the safety evaluation on heavy metal-containing medicines by observing the mercury dissolution, absorption, distribution and accumulation of mercury-containing medicines cinnabar and zuotai.

  4. Low-Roughness Plasma Etching of HgCdTe Masked with Patterned Silicon Dioxide

    Science.gov (United States)

    Ye, Z. H.; Hu, W. D.; Yin, W. T.; Huang, J.; Lin, C.; Hu, X. N.; Ding, R. J.; Chen, X. S.; Lu, W.; He, L.

    2011-08-01

    A novel mask technique utilizing patterned silicon dioxide films has been exploited to perform mesa etching for device delineation and electrical isolation of HgCdTe third-generation infrared focal-plane arrays (IRFPAs). High-density silicon dioxide films were deposited at temperature of 80°C, and a procedure for patterning and etching of HgCdTe was developed by standard photolithography and wet chemical etching. Scanning electron microscopy (SEM) showed that the surfaces of inductively coupled plasma (ICP) etched samples were quite clean and smooth. Root-mean-square (RMS) roughness characterized by atomic force microscopy (AFM) was less than 1.5 nm. The etching selectivity between a silicon dioxide film and HgCdTe in the samples masked with patterned silicon dioxide films was greater than 30:1. These results show that the new masking technique is readily available and promising for HgCdTe mesa etching.

  5. Total mercury concentrations in fish from Urrá reservoir (Sinú river, Colombia. Six years of monitoring

    Directory of Open Access Journals (Sweden)

    José Marrugo-Negrete

    2015-09-01

    Full Text Available Objective. The aim of this study was to monitor the total mercury (T-Hg concentrations in fish from the Urrá reservoir, after impoundment. Materials and methods. Five fish species at different trophic levels were sampled from 2004 to 2009 and analyzed by cold-vapor atomic absorption spectroscopy for T-Hg concentrations in muscle tissue. Water quality parameters were evaluated. Results. The highest (1.39±0.69 μg/g ww and lowest (0.15±0.02 μg/g ww T-Hg concentrations were detected in Hoplias malabaricus (piscivorous and Cyphocharax magdalenae (iliophagous/detritivorous respectively, whereas Leporinus muyscorum (omnivorous had an intermediate level (0.40±0.11 μg/g ww. The organic matter content in the water increased with time and depth, whereas dissolved oxygen and pH decreased. A covariance analysis (with fish length as a covariate shows a steady increase of T-Hg levels in all the studied species after impoundment. Conclusions. The T-Hg concentrations in the evaluated fish species, increased after impoundment. The water quality variables showed conditions favoring Hg methylation and its biomagnification, this last was evident in the fish food chain of the reservoir.

  6. Temporal trends in mercury concentrations in raptor flight feathers stored in an environmental specimen bank in Galicia (NW Spain) between 2000 and 2013.

    Science.gov (United States)

    García-Seoane, Rita; Varela, Zulema; Carballeira, Alejo; Aboal, Jesús R; Fernández, J Ángel

    2017-03-01

    Temporal trends in Hg concentrations were investigated in primary flight feathers from 319 specimens of three birds of prey: P7 in the northern goshawk (Accipiter gentilis), P6 in the common buzzard (Buteo buteo) and P5 in the tawny owl (Strix aluco). The samples were stored in a regional environmental specimen bank and belonged to specimens which died between 2000 and 2013 in Galicia (NW Spain). We would expect to see a decline in Hg concentrations across the study period, as data of atmospheric emissions show a gradual reduction of this pollutant in Europe in the last two decades. The study did not reveal any temporal pattern in Hg concentrations of feathers in any of the three species for the study period, may be due to the persistence of Hg in the environment, but showed a low level of contamination by this metal in the study area. In addition, the results show high intra-specific, as well as, inter-annual and inter-specific variability in data, mainly attributed to the level of exposure of the raptors to this pollutant and to the biomagnification process of Hg through food chains. These findings indicate that the high variability can be a limiting factor in the use of raptors for biomonitoring temporal patterns of Hg, but nevertheless, the technique provides qualitative information about the amount of Hg that reach the top of the terrestrial food chains.

  7. Hg Vetical Transference in Soil—Water System

    Institute of Scientific and Technical Information of China (English)

    GUOYIJUN; MOUSUSEN; 等

    1998-01-01

    Hg vertial transference in soil-water system was studied by analyzing Hg vertical ditribution in soil column after adding Hg and one of the two leacheates,deionzied water or acid rain,into soil column.The results indicated that Hg was hardly transferable in puple soil.About 86%-88% of the total soil Hg was distributed in the top layer (0-2cm) and to Hg was detected in the leakage when the purple soil column was leached by deionized water and simulated acid rain.But Hg was more movalbe in yellow soil with only about 20%-22% of the total soil Hg distributed in the top layer (0-2cm),and about 17%-25% washed out from the soil column by deionized water and simulted acid rain,Incremant in soil bulk density colud reduce Hg leaching,thus the more the Hg kept in soil,the less the Hg leached into underground water,Deionized water and acid rain almost played the same role in leaching Hg.Bentioint was most effecient in preventing Hg from vertcal transferring in the soil coulumn.

  8. Dynamic and static adsorption and desorption of Hg(II) ions on chitosan membranes and spheres.

    Science.gov (United States)

    Vieira, Rodrigo S; Beppu, Marisa M

    2006-05-01

    The adsorption and desorption of Hg(II) ions was studied using static and dynamic methods, employing membranes and spheres of chitosan as the adsorbent. The quantity of adsorption was influenced by chitosan crosslinking and by the adsorbent shape. The Langmuir model was applied to fit the experimental equilibrium data. Glutaraldehyde-crosslinked membranes presented a lower desorption capacity, when compared to natural membranes, but could be regenerated for use in successive cycles. Dynamic adsorption experiments suggested that the adsorption capacity depended mainly on adsorbent geometry, due to differences between surface area to mass ratio and initial concentration of Hg(II) ions. The adsorption capacity determined by the dynamic method was 65% and 77% for membranes and spheres, respectively of the value obtained static method results. A process combining dynamic adsorption and static desorption can be used to concentrate the Hg(II) ions by a factor of nearly seven (7x), when compared to the initially treated volume.

  9. KONTAMINASI LOGAM BERAT MERKURI (Hg DAN TIMBAL (Pb PADA AIR, SEDIMEN DAN IKAN SELAR TETENGKEK (Megalaspis cordyla L DI TELUK PALU, SULAWESI TENGAH

    Directory of Open Access Journals (Sweden)

    Matius Paundanan

    2015-09-01

    Full Text Available Palu bay waters is susceptible to heavy metal pollution due to the inclusion of the waste product of Palu city, and such as agriculture, and traditional mining. The objective of this research was to determine the contamination of heavy metals mercury (Hg and lead (Pb in water, sediment, and torpedo scad fish (Megalaspis cordyla. Sampling was done purposively at 10 sampling points. Parameters of water quality measurements were done in the field for temperature, pH, brightness, turbidity, and dissolved oxygen (DO, and at laboratory analysis for salinity, chemical oxygen demand (COD, ammonia, and nitrates. Heavy metals were analized by following APHA, and Indonesian National Standard (SNI methods. The results showed that Hg consentrations in water, sediment, gill, meat, liver, and spleen were 0.0008-0.0042 mg/l, 0.017-0.287 mg/kg, 0.007-0.145 mg/kg, 0.014-0.046 mg/kg, 0.052-0.106 mg/kg, and 0.043-0.414 mg/kg, respectively. Pb concentrations in water, sediments, gill, meat, liver, and spleen were 0.0130-0.0392 mg/l, 2.647-8.987 mg/kg, 0.132-0.775 mg/kg, 0.005-0.734 mg/kg, 0.295-1.871 mg/kg, and 1.654-12.92 mg/kg, respectively. The average of Hg and Pb concentrations in the water had exceeded the specified quality standards, while in the sediment were still below the quality standards. The average of Hg and Pb concentrations in all observed fish organs were below the quality standards, except for Pb concentrations in gill, liver, and spleen.Keywords: heavy metals, water, sediment, Megalaspis cordyla, Palu Bay

  10. Ultrasensitive detection of Hg{sup 2+} using oligonucleotide-functionalized AlGaN/GaN high electron mobility transistor

    Energy Technology Data Exchange (ETDEWEB)

    Cheng, Junjie [Key Laboratory of Ion Beam Bioengineering, Hefei Institutes of Physical Science, Chinese Academy of Sciences, Hefei 230031 (China); Division of Nanobiomedicine, Key Laboratory for Nano-Bio Interface Research, Suzhou Institute of Nano-Tech and Nano-Bionics, Chinese Academy of Sciences, Suzhou 215123 (China); Li, Jiadong; Miao, Bin; Wu, Dongmin, E-mail: dmwu2008@sinano.ac.cn [i-Lab, Suzhou Institute of Nano-Tech and Nano-Bionics, Chinese Academy of Sciences, Suzhou 215125 (China); Key Laboratory of Nanodevices and Applications, Suzhou Institute of Nano-Tech and Nano-Bionics, Chinese Academy of Sciences, Suzhou 215123 (China); Wang, Jine; Pei, Renjun, E-mail: rjpei2011@sinano.ac.cn [Division of Nanobiomedicine, Key Laboratory for Nano-Bio Interface Research, Suzhou Institute of Nano-Tech and Nano-Bionics, Chinese Academy of Sciences, Suzhou 215123 (China); Wu, Zhengyan, E-mail: zywu@ipp.ac.cn [Key Laboratory of Ion Beam Bioengineering, Hefei Institutes of Physical Science, Chinese Academy of Sciences, Hefei 230031 (China)

    2014-08-25

    An oligonucleotide-functionalized ion sensitive AlGaN/GaN high electron mobility transistor (HEMT) was fabricated to detect trace amounts of Hg{sup 2+}. The advantages of ion sensitive AlGaN/GaN HEMT and highly specific binding interaction between Hg{sup 2+} and thymines were combined. The current response of this Hg{sup 2+} ultrasensitive transistor was characterized. The current increased due to the accumulation of Hg{sup 2+} ions on the surface by the highly specific thymine-Hg{sup 2+}-thymine recognition. The dynamic linear range for Hg{sup 2+} detection has been determined in the concentrations from 10{sup −14} to 10{sup −8} M and a detection limit below 10{sup −14} M level was estimated, which is the best result of AlGaN/GaN HEMT biosensors for Hg{sup 2+} detection till now.

  11. A Highly Sensitive and Selective Competition Assay for the Detection of Cysteine Using Mercury-Specific DNA, Hg2+ and Sybr Green I

    Directory of Open Access Journals (Sweden)

    Gang Liu

    2011-10-01

    Full Text Available We here report a rapid, sensitive, selective and label-free fluorescence detection method for cysteine (Cys. The conformation of mercury-specific DNA (MSD changes from a random coil form to a hairpin structure in the presence of Hg2+ due to the formation of a thymine-Hg2+-thymine (T-Hg2+-T complex. Cys can selectively coordinate with Hg2+ and extract it from the thymine-Hg2+-thymine complex. The hairpin structure dehybridizes and the fluorescence intensity of Sybr Green I (SG decreases upon addition of Cys because SG efficiently discriminates mercury-specific DNA and mercury-specific DNA/Hg2+ complex. The detection can be finished within 5 min with high sensitivity and selectivity. In addition, we can obtain variable dynamic ranges for Cys by changing the concentration of MSD/Hg2+.

  12. A highly sensitive and selective competition assay for the detection of cysteine using mercury-specific DNA, Hg and Sybr Green I.

    Science.gov (United States)

    Xu, Hui; Gao, Shuli; Liu, Quanwen; Pan, Dun; Wang, Lihua; Ren, Shuzhen; Ding, Min; Chen, Jingwen; Liu, Gang

    2011-01-01

    We here report a rapid, sensitive, selective and label-free fluorescence detection method for cysteine (Cys). The conformation of mercury-specific DNA (MSD) changes from a random coil form to a hairpin structure in the presence of Hg2+ due to the formation of a thymine-Hg2+ -thymine (T-Hg2+ -T) complex. Cys can selectively coordinate with Hg2+ and extract it from the thymine-Hg2+ -thymine complex. The hairpin structure dehybridizes and the fluorescence intensity of Sybr Green I (SG) decreases upon addition of Cys because SG efficiently discriminates mercury-specific DNA and mercury-specific DNA/Hg2+ complex. The detection can be finished within 5 min with high sensitivity and selectivity. In addition, we can obtain variable dynamic ranges for Cys by changing the concentration of MSD/Hg2+.

  13. Manila clams from Hg polluted sediments of Marano and Grado lagoons (Italy) harbor detoxifying Hg resistant bacteria in soft tissues

    Energy Technology Data Exchange (ETDEWEB)

    Baldi, Franco, E-mail: baldi@unive.it [Dipartimento di Scienze Molecolari e Nanosistemi, Cà Foscari University of Venice, Dorsoduro 2137, 30123 Venice (Italy); Gallo, Michele; Marchetto, Davide [Dipartimento di Scienze Molecolari e Nanosistemi, Cà Foscari University of Venice, Dorsoduro 2137, 30123 Venice (Italy); Faleri, Claudia [Department of Environmental Science ‘G. Sarfatti’, University of Siena, 53100 Siena (Italy); Maida, Isabel; Fani, Renato [Dipartimento di Biologia Evoluzionistica, Via Romana, 17, University of Florence, 50125 Florence (Italy)

    2013-08-15

    A mechanism of mercury detoxification has been suggested by a previous study on Hg bioaccumulation in Manila clams (Ruditapes philippinarum) in the polluted Marano and Grado lagoons and in this study we demonstrate that this event could be partly related to the detoxifying activities of Hg-resistant bacteria (MRB) harbored in clam soft tissues. Therefore, natural clams were collected in six stations during two different periods (winter and spring) from Marano and Grado Lagoons. Siphons, gills and hepatopancreas from acclimatized clams were sterile dissected to isolate MRB. These anatomical parts were glass homogenized or used for whole, and they were lying on a solid medium containing 5 mg l{sup −1} HgCl{sub 2} and incubated at 30 °C. A total of fourteen bacterial strains were isolated and were identified by 16S rDNA sequencing and analysis, revealing that strains were representative of eight bacterial genera, four of which were Gram-positive (Enterococcus, Bacillus, Jeotgalicoccus and Staphylococcus) and other four were Gram-negative (Stenotrophomonas, Vibrio, Raoultella and Enterobacter). Plasmids and merA genes were found and their sequences determined. Fluorescence in situ hybridization (FISH) technique shows the presence of Firmicutes, Actinobacteria and Gammaproteobacteria by using different molecular probes in siphon and gills. Bacterial clumps inside clam flesh were observed and even a Gram-negative endosymbiont was disclosed by transmission electronic microscope inside clam cells. Bacteria harbored in cavities of soft tissue have mercury detoxifying activity. This feature was confirmed by the determination of mercuric reductase in glass-homogenized siphons and gills. -- Highlights: ► We isolated Gram-positive and Gram-negative Hg resistant strains from soft tissues of Ruditapes philippinarum. ► We identify 14 mercury resistant strains by 16S rRNA gene sequences. ► Bacteria in siphon and gill tissues of clams were observed by TEM and identified

  14. Measuring Hg and MeHg fluxes from dynamic systems using high resolution in situ monitoring - case study: the Sacramento-San Joaquin Delta

    Science.gov (United States)

    Fleck, J. A.; Bergamaschi, B. A.; Downing, B. D.; Lionberger, M. A.; Schoellhamer, D.; Boss, E.; Heim, W.; Stephenson, M.

    2006-12-01

    Quantifying net loads in tidal systems is difficult, time consuming, and often very expensive. Owing to the relatively rapid nature of tidal exchange, numerous measurements are required in a brief amount of time to accurately quantify constituent fluxes between a tidal wetland and its surrounding waters. Further complicating matters, the differences in chemical concentrations of a constituent between the flood and ebb tides are often small, so that the net export of the constituent is orders of magnitude smaller than the bulk exchange in either direction over the tidal cycle. Thus, high-resolution sampling coupled with high-sensitivity instruments over an adequate amount of time is required to accurately determine a net flux. These complications are exacerbated for mercury species because of the difficulties related to clean sampling and trace-level analysis. The USGS currently is collecting data to determine the fluxes of total mercury (Hg) and methyl-Hg (MeHg) in dissolved and particulate phases at Browns Island in the San Francisco Bay-Delta, a tidally influenced estuarine system. Our field deployment package consists of an upward-looking current profiler to quantify water flux, and an array of other instruments measuring the following parameters: UV absorption, DO, pH, salinity, temperature, water depth, optical backscatter, fluorescence, and spectral attenuation. Measurements are collected at 30-minute intervals for seasonal, month-long deployments in the main slough of Brown's Island. We infer Hg and MeHg concentrations by using multivariate analysis of spectral absorbance and fluorescence properties of the continuous measurements, and comparing them to those of discrete samples taken hourly over a 25-hour tidal cycle for each deployment. Preliminary results indicate that in situ measurements can be used to predict MeHg concentrations in a tidal wetland slough in both the filtered (r2=0.96) and unfiltered (r2=0.95) fractions. Despite seasonal differences in

  15. Superconductivity in Hg-Substituted BaPb0.75Bi0.25O3

    Institute of Scientific and Technical Information of China (English)

    Yong-Liang Chen; Ya-Jing Cui; Yong Zhang; Cui-Hua Cheng; Yong Zhao

    2008-01-01

    A series of Hg-doped BaPb0.75Bi0.25O3 with a nominal composition of BaPb0.75-xHgxBi0.25O3 (x=0 to 0.40 with 0.05 intervals) have been synthesized by solid-state reaction. These compounds exhibit a cubic perovskite-related structure with the lattice parameter being expanded by Hg doping. Superconducting transition temperature Tc and superconducting volume fraction are suppressed by Hg doping in the low doping level region (0≤ x ≤0.25). However, further increasing Hg content makes the superconductivity recovered at x>0.3. The superconductivity suppression in Hg-doped BaPb0.75Bi0.25O3 can be explained by the decrease of electron carrier concentration as well as the band- narrowing-induced electron localization.

  16. Magnetic fields of HgMn stars

    DEFF Research Database (Denmark)

    Hubrig, S.; González, J. F.; Ilyin, I.

    2012-01-01

    Context. The frequent presence of weak magnetic fields on the surface of spotted late-B stars with HgMn peculiarity in binary systems has been controversial during the two last decades. Recent studies of magnetic fields in these stars using the least-squares deconvolution (LSD) technique have...... failed to detect magnetic fields, indicating an upper limit on the longitudinal field between 8 and 15G. In these LSD studies, assumptions were made that all spectral lines are identical in shape and can be described by a scaled mean profile. Aims. We re-analyse the available spectropolarimetric material...

  17. Of Variability, or its Absence, in HgMn Stars

    CERN Document Server

    Turcotte, S

    2003-01-01

    Current models and observations of variability in HgMn stars disagree. We present here the models that argue for pulsating HgMn stars with properties similar to those of Slowly Pulsating B Stars. The lack of observed variable HgMn stars suggests that some physical process is missing from the models. Some possibilities are discussed.

  18. Bonding and Moessbauer Isomer Shifts in (Hg,Pb)—1223 Cuprate

    Institute of Scientific and Technical Information of China (English)

    高发明; 田永君; 谌岩; 李东春; 董海峰; 张思远

    2003-01-01

    By using the chemical bond theory of dielectric description,the chemical bond parameters of(Hg,Pb)-1223 were calculated.The results show that the(Ba,Sr)-O and Ca-0 types of bond have higher ionic character,while the Cu-O and(Hg,Pb)-0 types of bond have more covalent character.Moessbauer isomer shifts of 57Fe and 119Sn doped in(Hg,Pb)-1223 were calculated by using the chemical environmental factor,he,defined by covalency and electronic polarizability.Four valence state tin and three valence iron sites were identified in 57Fe and 119Sn doped(Hg,Pb)-1223 superconductor.It can be concluded that all of the Fe atoms substitute the Cu at square planar Cu(1) site,Whereas Sn prefers to substitute the square pyramidal Cu(2) site.

  19. A benzothiazole-based fluorescent probe for distinguishing and bioimaging of Hg(2+) and Cu(2).

    Science.gov (United States)

    Gu, Biao; Huang, Liyan; Su, Wei; Duan, Xiaoli; Li, Haitao; Yao, Shouzhuo

    2017-02-15

    A new benzothiazole-based fluorescent probe 2-(benzo[d]thiazol-2-yl)-4-(1,3- dithian-2-yl)phenol (BT) with two different reaction sites, a thioacetal group (site 1 for Hg(2+)), and O and N atoms of the benzothiazole dye (site 2 for Cu(2+)), was designed and synthesized. The probe BT showed ratiometric fluorescent response to Hg(2+) and fluorescence quenching behavior to Cu(2+), which induces naked-eye fluorescent color changes from green to blue and colorless, respectively. Moreover, it displayed highly sensitivity and selectivity toward Hg(2+) and Cu(2+) without interference from other metal ions. The sensing mechanisms were also confirmed by (1)H NMR titration, mass spectrum and Job's plot analyses. Finally, probe BT was successfully used for fluorescent imaging of Hg(2+) and Cu(2+) in living cells, demonstrating its potential applications in biological science.

  20. Photodegradation of petroleum under Na and Hg lamps by EPR

    Energy Technology Data Exchange (ETDEWEB)

    Mauro, Eduardo di; Melo, Fernando Alves de; Turini, Marilene; Campos, Ariana de [Universidade Estadual de Londrina (UEL), PR (Brazil). Dept. of Physics; Guedes, Carmen Luisa Barbosa [Universidade Estadual de Londrina (UEL), PR (Brazil). Dept. of Chemistry; Mangrich, Antonio Salvio [Universidade Federal do Parana (UFPR), PR (Brazil). Dept. of Chemistry

    2002-07-01

    Full text: The environment has become frequent victim of the action of pollutants. This situation has been stimulating several scientific works in the attempt to monitor the self-defence of the environment and minimise the effects caused by these pollutants. The petroleum and its derived, among the several substances that attack the environment, occupy a distinction place in the pollution picture. In the present work, we studied the photodegradation of the Arabian Light and Brazilian (Campos Basin- RJ) oils. Sample of theses oils were irradiated by different time periods in a reactor equipped with Na and Hg vapour lamps, whose emission spectra have different features. The irradiated and non-irradiated samples were subjected to Electron Paramagnetic Resonance (EPR) analysis in a BRUKER (ESP-300) equipment, which operates in the X band (9 GHz) at room temperature. The EPR spectra showed similar features to the two oils. The EPR spectra are composed of a intense signal (one line) with g (spectroscopic factor) about two relative to free radicals and groups of eight lines correspondent to vanadyl porphyrinic compounds (VO{sup 2+}). The parameters of spin Hamiltonian were determined to the two detected paramagnetic species. The two oils irradiated by Na and Hg lamps showed variations in the values of g and {delta}H (linewidth) of the paramagnetic species. The changes in the parameters are the most significant in Brazilian petroleum samples irradiated by Hg lamp. The modifications in the linewidth of free radicals of the Arabian Light petroleum have the same tendency to the two utilised lamps. (author)

  1. Effects of Hg and Cu on the activities of soil acid phosphatase

    Institute of Scientific and Technical Information of China (English)

    XU Dong-mei; CHEN Bo; LIU Wen-li; LIU Guang-shen; LIU Wei-ping

    2007-01-01

    Comparative study on the activity and kinectic properties of acid phosphatase (ACPase) of three soils amended with Hg and Cu at constant temperature and humidity was carried out. The results indicated that the inhibition on ACPase of the three sample soils by Hg and Cu varied with the content of soil organic matter and pH, where, Soil 1 was the most seriously contaminated due to its lowest content of organic matter and the lowest pH among three samples, Soil 2 took the second place, and Soil 3was the least contaminated. Except Soil 3, the activity of soil ACPase tended to increase along with the contact time under the same type and the same concentration of heavy metal. In particular the Vmax values of ACPase in all three samples decreased with increasing Hg and Cu concentration, whereas the Km values were affected weakly. According to the change of Vmax and Km values,Cu and Hg had the same inhibition effect on soil ACPase. Both of them may be a type of compound of non-competitive and anti-competitive inhibition. Statistic analyses indicated that activities of soil ACPase and Vmax values could serve as bioindicator to partially denote the heavy metal Hg and Cu contamination degree.

  2. Experimental study on mercury removal by Taixi activated coke under complex atmosphere of flue gases%复杂烟气条件下太西活性焦脱除Hg0的实验研究

    Institute of Scientific and Technical Information of China (English)

    张海茹; 刘浩; 王萌; 吴昊; 杨宏旻

    2012-01-01

    为了解复杂烟气条件下活性焦吸附剂的脱汞特性,利用汞渗透管和主要气体成分模拟复杂烟气,在实验室规模的固态吸附剂汞吸附效能测定系统上,进行了太西活性焦吸附单质汞的实验研究,并采用FT-IR对活性焦表面进行了光谱表征.结果表明,在活性焦表面存在各种含氧官能团;在CO2/N2/O2/SO2/Hg0烟气体系中,当SO2加入量为400、855、1 520 mL/m3时,出口汞浓度分别为36、43、48 μg/m3,SO2对系统吸附Hg0的能力有抑制作用;在CO2/N2/O2/NO/Hg0烟气体系中,较低浓度的NO对Hg0脱除有抑制作用,而高浓度值的NO抑制作用减弱;在CO2/N2/O2/NO/SO2/Hg0烟气体系下,提高NO浓度对Hg2脱除有一定的促进作用,而提高SO2浓度初期促进汞的脱除,后期则表现为抑制作用.%In order to clarify the adsorption characteristic of activated coke under complex atmosphere of flue gases, a series of tests were conducted with a bench-scale fixed bed reactor. The simulated flue gas was prepared by mixing main composition of flue gas with mercury vapors generated through permeation tube. The surface properties were characterized by FT-IR. The results show that the performance of mercury removal is related to the surface chemistry of activated coke, and the oxygen-containing functional groups are the important factor affecting the adsorption and catalysis of Hg°. The adsorption performance of Hg° with activated coke is influenced by SO2 obviously and inhibition is observed in the removal process. With increasing concentration of SO2, from 400, 855 to 1 520 mL/m3, the concentration of Hg° at the outlet of the reactor increased from 36, 43 to 48 μg/m3. The complex impact of NO on the adsorptive capacity of Hg° is found that NO with lower concentration promotes the adsorption of elemental mercury while inhibits it at higher value in CO2/N2/O2/NO/ Hg° system. The increasing concentration of NO with the stationary concentration of SO2 has a

  3. Toxicity Effect of Hg2+ and Cr(Ⅵ)on Alga Growth in Eutrophic Water%Hg2+与Cr(Ⅵ)对富营养化水体中藻类生长的毒性效应

    Institute of Scientific and Technical Information of China (English)

    毕东苏; 钱春龙

    2007-01-01

    [Objective]The toxicity effect of Hg2+ and Cr(Ⅵ)on alga growth in eutrophic water was studied to provide reference for biomonitoring and bioremediation of eutrophic water.[Method]The mother liquid of alga,which was separated from the eutrophic water,were put into the solutions of Hg2+and Cr(Ⅵ)with different concentrations and their mixture solution,respectively.And the toxicity effect of Hg2+ and Cr(Ⅵ)on the growth and propagation of alga in eutrophic water was observed.[Result]The alga in eutrophic water performed rather sensitive to Cr(Ⅵ)and when its concentration Was over 1 ms/L,threre was obvious effect on alga growth.The alga Was not very sensitive to Hg2+ when its concentration was lower, but its toxicity became stronger and stronger when its concentration increased to some extent and the toxicity effect of Cr(Ⅵ)on alga growth was inst on the centrary. When the ion concentration was lower than 10 ms/L,the toxicity of Hg2+ on alga was lower than that of Cr(Ⅵ).When the concentration was over 10 ms/L,the toxieity of Hg2+ exceeded that of Cr(Ⅵ).The toxicity of ion mixture solution of Hg2+ and Cr(Ⅵ)had synergism inhibition on alga,which could be performed only when the concentration was over4 mg/L.[Conclusion]The toxicity of heavy metal on alga not only related to the alga cell,but also related to the concentration of heavy metal ion.

  4. [Absorption of Hg in typical farmland soils in the Linglong gold mining area].

    Science.gov (United States)

    Wang, Fei; Wang, Ming; Tang, Jing-Chun; Zhang, Lei

    2011-09-01

    This study focused on the adsorption properties of Hg in 2 typical farmland soils in the Linglong gold mining area in Yantai area of China. The adsorption-desorption of Hg(II) research result showed higher adsorption of Hg in neutral soil with the value of 201.38 microg/g than that in acid soil with the value of 156.9 microg/g. The desorption of Hg in both soils was low with neutral soil showing a higher desorption ratio (13%) than acid soil (12%). Hg(II) adsorption isotherms were well fitted by Langmuir and Freundlich equation in the acid soil, with the correlation coefficient r value of 0.995 6 and 0.982 6, respectively. Langmuir equation can best describe Hg(II) adsorption isotherm in the neutral soil and acid soil, with the r value of 0.995 6 and 0.955 9, respectively. The adsorption was a bi-phasic process which started with a fast-adsorption phase and a slow-adsorption phase. The adsorption amount and rate of Hg in the fast reaction phase were much larger than that in the slow one. The adsorption kinetic can be better fitted by Elovich equation with correlation coefficient of 0.971 4 and 0.967 2, respectively. At pH 3.0 - 5.5, the equilibrium adsorption amount of Hg(II) increased with higher pH, and then decreased when the pH reached 6.5.

  5. Gaseous elemental mercury concentration in atmosphere at urban and remote sites in China

    Institute of Scientific and Technical Information of China (English)

    WANG Zhang-wei; CHEN Zuo-shuai; DUAN Ning; ZHANG Xiao-shan

    2007-01-01

    An investigation of gaseous elemental mercury concentration in atmosphere was conducted at Beijing and Guangzhou urban, Yangtze Delta regional sites and China Global Atmosphere Watch Baseline Observatory (CGAWBO) in Mt. Waliguan of remote continental area of China. High temporal resolved data were obtained using automated mercury analyzer RA-915+. Results showed that the overall hourly mean Hg0 concentrations in Mt. Waliguan were 1.7± 1.1 ng/m3 in summer and 0.6±0.08 ng/m3 in winter. The concentration in Yangtze Delta regional site was 5.4±4.1 ng/m3, which was much higher than those in Waliguan continental background area and also higher than that found in North America and Europe rural areas. In Beijing urban area the overall hourly mean Hg0 concentrations were 8.3±3.6 ng/m3 in winter, 6.5±5.2 ng/m3 in spring, 4.9±3.3 ng/m3 in summer, and 6.7±3.5 ng/m3 in autumn, respectively, and the concentration was 13.5±7.1 ng/m3 in Guangzhou site. The mean concentration reached the lowest value at 14:00 and the highest at 02:00 or 20:00 in all monitoring campaigns in Beijing and Guangzhou urban areas, which contrasted with the results measured in Yangtze Delta regional site and Mt. Waliguan. The features of concentration and diurnal variation of Hg0 in Beijing and Guangzhou implied the importance of local anthropogenic sources in contributing to the high Hg0 concentration in urban areas of China. Contrary seasonal variation patterns of Hg0 concentration were found between urban and remote sites. In Beijing the highest Hg0concentration was in winter and the lowest in summer, while in Mt. Waliguan the Hg0 concentration in summer was higher than that in winter. These indicated that different processes and factors controlled Hg0 concentration in urban, regional and remote areas.

  6. Long-term Hg pollution-induced structural shifts of bacterial community in the terrestrial isopod (Porcellio scaber) gut

    Energy Technology Data Exchange (ETDEWEB)

    Lapanje, Ales, E-mail: ales@ifb.s [Institute of Physical Biology, Ljubljana (Slovenia); Zrimec, Alexis [Institute of Physical Biology, Ljubljana (Slovenia); Drobne, Damjana [Department of Biology, Biotechnical Faculty, University of Ljubljana, Ljubljana (Slovenia); Rupnik, Maja [Institute of Public Health Maribor, Maribor (Slovenia)

    2010-10-15

    In previous studies we detected lower species richness and lower Hg sensitivity of the bacteria present in egested guts of Porcellio scaber (Crustacea, Isopoda) from chronically Hg polluted than from unpolluted environment. Basis for such results were further investigated by sequencing of 16S rRNA genes of mercury-resistant (Hg{sup r}) isolates and clone libraries. We observed up to 385 times higher numbers of Hg{sup r} bacteria in guts of animals from polluted than from unpolluted environment. The majority of Hg{sup r} strains contained merA genes. Sequencing of 16S rRNA clones from egested guts of animals from Hg-polluted environments showed elevated number of bacteria from Pseudomonas, Listeria and Bacteroidetes relatives groups. In animals from pristine environment number of bacteria from Achromobacter relatives, Alcaligenes, Paracoccus, Ochrobactrum relatives, Rhizobium/Agrobacterium, Bacillus and Microbacterium groups were elevated. Such bacterial community shifts in guts of animals from Hg-polluted environment could significantly contribute to P. scaber Hg tolerance. - Chronic environmental mercury pollution induces bacterial community shifts and presence of elevated number as well as increased diversity of Hg-resistant bacteria in guts of isopods.

  7. Cytotoxicity of dental composite (co)monomers and the amalgam component Hg(2+) in human gingival fibroblasts.

    Science.gov (United States)

    Reichl, Franz-Xaver; Simon, Sabine; Esters, Magalie; Seiss, Mario; Kehe, Kai; Kleinsasser, Norbert; Hickel, Reinhard

    2006-08-01

    Unpolymerized resin (co)monomers or mercury (Hg) can be released from restorative dental materials (e.g. composites and amalgam). They can diffuse into the tooth pulp or the gingiva. They can also reach the gingiva and organs by the circulating blood after the uptake from swallowed saliva. The cytotoxicity of dental composite components hydroxyethylmethacrylate (HEMA), triethyleneglycoldimethacrylate (TEGDMA), urethanedimethacrylate (UDMA), and bisglycidylmethacrylate (Bis-GMA) as well as the amalgam component Hg(2+) (as HgCl(2)) and methyl mercury chloride (MeHgCl) was investigated on human gingival fibroblasts (HGFs) at two time intervals. To test the cytotoxicity of substances, the bromodeoxyuridine (BrdU) assay and the lactate dehydrogenase (LDH) assay were used. The test substances were added in various concentrations and cells were incubated for 24 or 48 h. The EC(50) values were obtained as half-maximum-effect concentrations from fitted curves. Following EC(50) values were found [BrdU: mean (mmol/l); SEM in parentheses; n=12]: (24 h/48 h) HEMA 8.860 (0.440)/6.600(0.630), TEGDMA 1.810(0.130)/1.220(0.130), UDMA 0.120(0.010)/0.140(0.010), BisGMA 0.060(0.004)/0.040(0.002), HgCl(2) 0.015(0.001)/0.050(0.006), and MeHgCl 0.004(0.001)/0.005(0.001). Following EC(50) values were found [LDH: mean (mmol/l); SEM in parentheses; n=12]: (24 h/48 h) HEMA 9.490(0.300)/7.890(1.230), TEGDMA 2.300(0.470)/1.950(0.310), UDMA 0.200(0.007)/0.100(0.007), BisGMA 0.070(0.005)/0.100(0.002), and MeHgCl 0.014(0.006)/0.010(0.003). In both assays, the following range of increased toxicity was found for composite components (24 and 48 h): HEMA < TEGDMA < UDMA < BisGMA. In both assays, MeHgCl was the most toxic substance. In the BrdU assay, Hg(2+) was about fourfold less toxic than MeHgCl but Hg(2+) was about fourfold more toxic than BisGMA. In the BrdU test, a significantly (P<0.05) decreased toxicity was observed for Hg(2+) at 48 h, compared to the 24 h Hg(2+)-exposure. A time depending

  8. Fully relativistic coupled cluster and DFT study of electric field gradients at Hg in 199Hg compounds

    DEFF Research Database (Denmark)

    Arcisauskaité, Vaida; Knecht, Stefan; Sauer, Stephan P. A.

    2012-01-01

    We investigate the magnitude and interplay of relativistic and electron correlation effects on the electric field gradient (EFG) at the position of Hg in linear and bent HgL2 (L=CH3, Cl, Br, I) and trigonal planar [HgCl3]- complexes using four-component relativistic Dirac-Coulomb (DC) and non...

  9. A laboratory-incubated redox oscillation experiment to investigate Hg fluxes from highly contaminated coastal marine sediments (Gulf of Trieste, Northern Adriatic Sea).

    Science.gov (United States)

    Emili, A; Carrasco, L; Acquavita, A; Covelli, S

    2014-03-01

    Mercury (Hg) mobility at the sediment-water interface was investigated during a laboratory incubation experiment conducted with highly contaminated sediments (13 μg g(-1)) of the Gulf of Trieste. Undisturbed sediment was collected in front of the Isonzo River mouth, which inflows Hg-rich suspended material originating from the Idrija (NW Slovenia) mining district. Since hypoxic and anoxic conditions at the bottom are frequently observed and can influence the Hg biogeochemical behavior, a redox oscillation was simulated in the laboratory, at in situ temperature, using a dark flux chamber. Temporal variations of several parameters were monitored simultaneously: dissolved Hg (DHg) and methylmercury (MeHg), O2, NH4 (+), NO3 (-) + NO2 (-), PO4 (3-), H2S, dissolved Mn(2+), dissolved inorganic and organic carbon (DIC and DOC). Under anoxic conditions, both Hg (665 ng m(2) day(-1)) and MeHg (550 ng m(2) day(-1)) fluxed from sediments into the water column, whereas re-oxygenation caused concentrations of MeHg and Hg to rapidly drop, probably due to re-adsorption onto Fe/Mn-oxyhydroxides and enhanced demethylation processes. Hence, during anoxic events, sediments of the Gulf of Trieste may be considered as an important source of DHg species for the water column. On the contrary, re-oxygenation of the bottom compartment mitigates Hg and MeHg release from the sediment, thus acting as a natural "defence" from possible interaction between the metal and the aquatic organisms.

  10. The Chevrel phase HgMo6S8

    Directory of Open Access Journals (Sweden)

    Michel Potel

    2009-05-01

    Full Text Available The crystal structure of HgMo6S8, mercury(II hexamolybdenum octasulfide, is based on (Mo6S8S6 cluster units (overline{3} symmetry interconnected through interunit Mo—S bonds. The Hg2+ cations occupy large voids between the different cluster units and are covalently bonded to two S atoms. The Hg atoms and one S atom lie on sites with crystallographic overline{3} and 3 symmetry, respectively. Refinement of the occupancy factor of the Hg atom led to the composition Hg0.973 (3Mo6S8.

  11. The concentrations and distribution of mercury in aquatic ecosystem of Baihua Reservoir

    Institute of Scientific and Technical Information of China (English)

    YAN Haiyu; FENG Xinbin; JIANG Hongmei; QIU Guangle; LI Guanghui; Shang Lihai

    2005-01-01

    Mercury species in water column, sediment and fish from the Hg-contaminated Baihua Reservoir were measured by trap pre-concentration and CVAFS and CVAAS detection methods. The results showed that the highest average total Hg concentration is up to 73.36 ng/L in the water column, 186.7 ng/L in pore water of surface sediment in the Baihua Reservoir. The total mercury concentrations in the sediments range from 0.87 to 33.74 mg/kg. This suggests that sediment re-suspending and Hg input from the upstream organochemical plant are the main mercury sources of water body for this reservoir. In addition, the possible reason why mercury is low in fish is that the low DOC and high pH are infavarable to methylmercury formation or absorption by fish.

  12. A selective colorimetric Hg2+ probe featuring a styryl dithiaazacrown containing platinum (II) terpyridine complex through modulation of the relative strength of ICT and MLCT transitions.

    Science.gov (United States)

    Chung, Sung-Kuang; Tseng, Yong-Ren; Chen, Chan-Yu; Sun, Shih-Sheng

    2011-04-04

    A series of platinum(II) terpyridine complexes featuring an aminostilbene donor-acceptor framework was synthesized. The complex with a dithiaazacrown moiety exhibits a highly sensitive and selective colorimetric response to a Hg(2+) cation through modulation of the relative strength of ICT and MLCT transitions. The results from (1)H NMR titration suggest the existence of a weak Pt(II)···Hg(II) metallophilic interaction at low Hg(2+) concentration.

  13. Development and validation of an SPE HG-AAS method for determination of inorganic arsenic in samples of marine origin

    Energy Technology Data Exchange (ETDEWEB)

    Rasmussen, Rie R.; Larsen, Erik H.; Sloth, Jens J. [Technical University of Denmark, National Food Institute, Division of Food Chemistry, Soeborg (Denmark); Hedegaard, Rikke V. [Technical University of Denmark, National Food Institute, Division of Food Chemistry, Soeborg (Denmark); University of Copenhagen, Faculty of Life Sciences, Department of Food Science, Frederiksberg (Denmark)

    2012-07-15

    The present paper describes a novel method for the quantitative determination of inorganic arsenic (iAs) in food and feed of marine origin. The samples were subjected to microwave-assisted extraction using diluted hydrochloric acid and hydrogen peroxide, which solubilised the analytes and oxidised arsenite (As{sup III}) to arsenate (As{sup V}). Subsequently, a pH buffering of the sample extract at pH 6 enabled selective elution of As{sup V} from a strong anion exchange solid-phase extraction (SPE) cartridge. Hydride generation atomic absorption spectrometry (HG-AAS) was applied to quantify the concentration of iAs (sum of As{sup III} and As{sup V}) as the total arsenic (As) in the SPE eluate. The results of the in-house validation showed that mean recoveries of 101-104% were achieved for samples spiked with iAs at 0.5, 1.0 and 1.5 mg.kg{sup -1}, respectively. The limit of detection was 0.08 mg kg{sup -1}, and the repeatability (RSD{sub r}) and intra-laboratory reproducibility (RSD{sub IR}) were less than 8% and 13%, respectively, for samples containing 0.2 to 1.5 mg kg{sup -1} iAs. The trueness of the SPE HG-AAS method was verified by confirming results obtained by parallel analysis using high-performance liquid chromatography coupled to inductively coupled plasma mass spectrometry. It was demonstrated that the two sets of results were not significantly different (P < 0.05). The SPE HG-AAS method was applied to 20 marine food and feed samples, and concentrations of up to 0.14 mg kg{sup -1} of iAs were detected. (orig.)

  14. Local structure and site occupancy of Cd and Hg substitutions in CeTIn_5 (T=Co, Rh, Ir)

    Energy Technology Data Exchange (ETDEWEB)

    Booth, Corwin H.; Bauer, Eric. D.; Bianchi, Andrea D.; Ronning, Fillip; Thompson, Joe D.; Sarrao, John L.; Cho, Jung Young; Chan, Julia Y.; Capan, Cigdem; Fisk, Zachary

    2009-04-22

    The CeTIn_5 superconductors (T=Co, Rh, or Ir) have generated great interest due to their relatively high transition temperatures, non-Fermi liquid behavior, and their proximity to antiferromagnetic order and quantum critical points. In contrast to small changes with the T-species, electron doping in CeT(In_1-x M_x)_5 with $M$=Sn and hole doping with Cd or Hg have a dramatic effect on the electronic properties at very low concentrations. The present work reports local structure measurements usingthe extended x-ray absorption fine-structure (EXAFS) technique that address the substituent atom distribution as a function of T, M, and x, in the vicinity of the superconducting phase. Together with previous measurements for M=Sn, the proportion of the $M$ atom residing on the In(1) site, f_\\textrm In(1), increases in the order M=Cd, Sn, and Hg, ranging from about 40\\percent to 70percent, showing a strong preference for each of these substituents to occupy the In(1) site (random occupation = 20percent). In addition, f_In(1) ranges from 70percent to 100percent for M=Hg in the order T=Co,Rh, and Ir. These fractions track the changes in the atomic radii of the various species, and help explain the sharp dependence of $T_c$ on substituting into the In site. However, it is difficult to reconcile the small concentrations of M with the dramatic changes in the ground state in the hole-doped materials with only an impurity scattering model. These results therefore indicate that while such substitutions have interesting local atomic structures with important electronic and magnetic consequences, other local changes in the electronic and magnetic structure are equally important in determining the bulk properties of these materials.

  15. Local structure and site occupancy of Cd and Hg substitutions in CeTIn5 (T=Co, Rh, Ir)

    Energy Technology Data Exchange (ETDEWEB)

    Bauer, Eric D [Los Alamos National Laboratory; Ronning, Filip [Los Alamos National Laboratory; Thompson, J D [Los Alamos National Laboratory; Sarrao, J L [Los Alamos National Laboratory; Booth, C H [LBNL; Bianchi, A D [UC, IRVINE; Cho, J Y [LSU; Chan, J Y [LSU; Capan, C [UC-IRVINE; Fisk, Z [UC-IRVINE

    2009-01-01

    The CeTIn{sub 5} superconductors (T = Co, Rh, or Ir) have generated great interest due to their relatively high transition temperatures, non-Fermi liquid behavior, and their proximity to antiferromagnetic order and quantum critical points. In contrast to small changes with the T-species, electron doping in CeT(In{sub 1-x}M{sub x}){sub 5} with M = Sn and hole doping with Cd or Hg have a dramatic effect on the electronic properties at very low concentrations. The present work reports local structure measurements using the extended x-ray absorption fine-structure (EXAFS) technique that address the substituent atom distribution as a function of T, M, and x, in the vicinity of the superconducting phase. Together with previous measurements for M = Sn, the proportion of the M atom residing on the In(1) site, f{sub 1n(1)}, increases in the order M = Cd, Sn, and Hg, ranging from about 40% to 70%, showing a strong preference for each of these substituents to occupy the In(1) site (random occupation = 20%). In addition, f{sub In(1)} ranges from 70% to 100% for M = Hg in the order T = Co, Rh, and Ir. These fractions track the changes in the atomic radii of the various species, and help explain the sharp dependence of T{sub c} on substituting into the In site. However, it is difficult to reconcile the small concentrations of M with the dramatic changes in the ground state in the hole-doped materials with only an impurity scattering model. These results therefore indicate that while such substitutions have interesting local atomic structures with important electronic and magnetic consequences, other local changes in the electronic and magnetic structure are equally important in determining the bulk properties of these materials.

  16. Fluvial geomorphology and aquatic-to-terrestrial Hg export are weakly coupled in small urban streams of Columbus, Ohio

    Science.gov (United States)

    Sullivan, S. Mažeika P.; Boaz, Lindsey E.; Hossler, Katie

    2016-04-01

    Although mercury (Hg) contamination is common in stream ecosystems, mechanisms governing bioavailability and bioaccumulation in fluvial systems remain poorly resolved as compared to lentic systems. In particular, streams in urbanized catchments are subject to fluvial geomorphic alterations that may contribute to Hg distribution, bioaccumulation, and export across the aquatic-to-terrestrial boundary. In 12 streams of urban Columbus, Ohio, we investigated the influence of fluvial geomorphic characteristics related to channel geometry, streamflow, and sediment size and distribution on (1) Hg concentrations in sediment and body burdens in benthic larval and adult emergent aquatic insects and (2) aquatic-to-terrestrial contaminant transfer to common riparian spiders of the families Pisauridae and Tetragnathidae via changes in aquatic insect Hg body burdens as well as in aquatic insect density and community composition. Hydrogeomorphic characteristics were weakly related to Hg body burdens in emergent insects (channel geometry) and tetragnathid spiders (streamflow), but not to Hg concentrations in sediment or benthic insects. Streamflow characteristics were also related to emergent insect density, while wider channels were associated with benthic insect community shifts toward smaller-bodied and more tolerant taxa (e.g., Chironomidae). Thus, our results provide initial evidence that fluvial geomorphology may influence aquatic-to-terrestrial contaminant Hg transfer through the collective effects on emergent insect body burdens as well as on aquatic insect community composition and abundance.

  17. Protective Effects of Quercetin Against HgCl₂-Induced Nephrotoxicity in Sprague-Dawley Rats.

    Science.gov (United States)

    Shin, Yu Jin; Kim, Jeong Jun; Kim, Ye Ji; Kim, Won Hee; Park, Eun Young; Kim, In Young; Shin, Han-Seung; Kim, Kyeong Seok; Lee, Eui-Kyung; Chung, Kyu Hyuck; Lee, Byung Mu; Kim, Hyung Sik

    2015-05-01

    Mercury is a well-known environmental pollutant that can cause nephropathic diseases, including acute kidney injury (AKI). Although quercetin (QC), a natural flavonoid, has been reported to have medicinal properties, its potential protective effects against mercury-induced AKI have not been evaluated. In this study, the protective effect of QC against mercury-induced AKI was investigated using biochemical parameters, new protein-based urinary biomarkers, and a histopathological approach. A 250 mg/kg dose of QC was administered orally to Sprague-Dawley male rats for 3 days before administration of mercury chloride (HgCl2). All animals were sacrificed at 24 h after HgCl2 treatment, and biomarkers associated with nephrotoxicity were measured. Our data showed that QC absolutely prevented HgCl2-induced AKI, as indicated by biochemical parameters such as blood urea nitrogen (BUN) and serum creatinine (sCr). In particular, QC markedly decreased the accumulation of Hg in the kidney. Urinary excretion of protein-based biomarkers, including clusterin, kidney injury molecule-1 (KIM-1), neutrophil gelatinase-associated lipocalin (NGAL), monocyte chemoattractant protein-1 (MCP-1), tissue inhibitor of metalloproteinases 1 (TIMP-1), and vascular endothelial growth factor (VEGF) in response to HgCl2 administration were significantly decreased by QC pretreatment relative to that in the HgCl2-treated group. Furthermore, urinary excretion of metallothionein and Hg were significantly elevated by QC pretreatment. Histopathological examination indicated that QC protected against HgCl2-induced proximal tubular damage in the kidney. A TUNEL assay indicated that QC pretreatment significantly reduced apoptotic cell death in the kidney. The administration of QC provided significant protective effects against mercury-induced AKI.

  18. Efficient removal and highly selective adsorption of Hg2+ by polydopamine nanospheres with total recycle capacity

    Science.gov (United States)

    Zhang, Xiulan; Jia, Xin; Zhang, Guoxiang; Hu, Jiamei; Sheng, Wenbo; Ma, Zhiyuan; Lu, Jianjiang; Liu, Zhiyong

    2014-09-01

    This study reported a new method for efficient removal of Hg2+ from contaminated water using highly selective adsorptive polydopamine (PDA) nanospheres, which were uniform and had a small diameter (150-200 nm). The adsorption isotherms, kinetics, thermodynamics were investigated. Also, the effects of ionic strength, co-existing ions on removing ability of PDA nanospheres for Hg2+ were studied. Adsorption of Hg2+ was very fast and efficient as adsorption equilibrium was completed within 4 h and the maximum adsorption capacities were 1861.72 mg/g, 2037.22 mg/g, and 2076.81 mg/g at 298 K, 313 K, and 328 K respectively, increasing with increasing of temperature. The PDA nanospheres exhibited highly selective adsorption of Hg2+ and had a total desorption capacity of 100% in hydrochloric acid solution, pH 1. The results showed that the structure of PDA nanospheres remained almost unchanged after recycling five times. Furthermore, X-ray photoelectron spectroscopy (XPS) was employed to determine the elements of PDA nanospheres before and after Hg2+ adsorption. Considering their efficient and highly Hg2+ selective adsorption, total recycle capacity, and high stability, PDA nanospheres will be feasible in a number of practical applications.

  19. [Heavy metals contents and Hg adsorption characteristics of mosses in virgin forest of Gongga Mountain].

    Science.gov (United States)

    Liang, Peng; Yang, Yong-Kui; He, Lei; Wang, Ding-Yong

    2008-06-01

    Seven main moss species in the Hailuogou virgin forest of Gongga Mountain were sampled to determine their heavy metals (Hg, Cr, Cd, Ni, Pb, Cu, Mn, Zn and Fe) content, and two widely distributed species, Pleurozium schreberi (Brid.) Mitt. and Racomitrium laetum Besch., were selected to study their Hg adsorption characteristics. The results showed that the heavy metals contents in the mosses were lower than the background values in Europe and America, except that the Cd had a comparable value, which indicated that the atmosphere in study area was not polluted by heavy metals and good in quality. The Hg adsorption by P. schreberi and R. laetum was an initiative and rapid process, with the equilibrium reached in about two hours, and could be well fitted by Freundlich and Langmuir equations. Based on Langmuir equation, the maximum Hg adsorption capacities of P. schreberi and R. laetum were 15.24 and 8.19 mg x g(-1), respectively, suggesting that the two mosses had a good capacity of Hg adsorption, and could be used as the bio-monitors of atmospheric Hg pollution.

  20. Rhubarb Anthraquinones Protect Rats against Mercuric Chloride (HgCl2-Induced Acute Renal Failure

    Directory of Open Access Journals (Sweden)

    Dan Gao

    2016-03-01

    Full Text Available Mercury (Hg causes severe nephrotoxicity in subjects with excess exposure. This work attempted to identify whether a natural medicine—rhubarb—has protective effects against mercuric chloride (HgCl2-induced acute renal failure (ARF, and which of its components contributed most to the treatment. Total rhubarb extract (TR were separated to the total anthraquinones (TA, the total tannins (TT and remaining component extract (RC. Each extract was orally pre-administered to rats for five successive days followed by HgCl2 injection to induce kidney injury. Subsequently, renal histopathology and biochemical examinations were performed in vitro to evaluate the protective effects. Pharmacological studies showed that TR and TA, but not TT or RC manifested significant protection activity against HgCl2-induced ARF. There were also significant declines of serum creatine, urea nitrogen values and increases of total protein albumin levels in TR and TA treated groups compared to HgCl2 alone (p < 0.05. At last, the major components in TA extract were further identified as anthraquinones by liquid chromatography coupled mass spectroscopy. This study thus provides observational evidences that rhubarb could ameliorate HgCl2-induced ARF and its anthraquinones in particular are the effective components responsible for this activity in rhubarb extract.

  1. Mass Independent Fractionation of Hg Isotopes Preserved in the Precambrian

    Science.gov (United States)

    Thibodeau, A. M.; Bergquist, B. A.; Kah, L. C.; Ono, S.; Ghosh, S.; Hazen, R. M.

    2013-12-01

    Mercury (Hg) is a photochemically active, redox-sensitive, chalcophilic metal with complex biogeochemistry that displays a wide range of mass-dependent (MDF) and mass-independent (MIF) stable isotopic fractionation. In the past decade, Hg isotopes have emerged as important tracers of both the sources and cycling of Hg in the modern environment. However, their utility as environmental proxies in ancient rocks remains largely unexplored. The potential of Hg isotopes to inform Precambrian environments derives from the observation that Hg isotopes with odd atomic mass numbers (199Hg and 201Hg) undergo large MIF by the magnetic isotope effect (MIE) and smaller MIF through the nuclear volume effect (NVE). Small MIF produced via NVE has been observed for numerous transformations and is characterized by MIF ratios (Δ199Hg/Δ201Hg) of about 1.6. Large Hg-MIF driven by MIE has been observed during photochemical transformations and is characterized by Δ199Hg/Δ201Hg ratios between 1 and 1.3. This MIF signal is sensitive to a range of environmental conditions, including the amount and type of solar radiation, the presence and type of complexing organic ligands, and the Hg/dissolved organic carbon (DOC) ratio. Thus, it is hoped that Hg-MIF signals may indirectly record changes in atmospheric composition or seawater chemistry if preserved in marine sedimentary records. Previous work has clearly demonstrated that Hg-MIF signals are preserved in Archean and Paleoproterozoic marine shales and massive sulfide deposits. Here, we present evidence that such signals are also preserved in marine shales of mid-Proterozoic age, including the ~1.3 Ga Sulky formation (Dismal Lakes Group, NW Arctic), the ~1.45 Ga Greyson Shale (Belt Basin, Montana), and the ~1.5 Ga Katalsy formation (Kypry Group, Eastern European Platform). We observe that the Greyson shale and shales within the Sulky formation yield negative Hg-MIF with Δ199Hg/Δ201Hg ratios close to 1 and that Kaltasy group sediments

  2. Seasonal mercury concentrations and {delta}{sup 15}N and {delta}{sup 13}C values of benthic macroinvertebrates and sediments from a historically polluted estuary in south central Chile

    Energy Technology Data Exchange (ETDEWEB)

    Diaz-Jaramillo, Mauricio, E-mail: mdiazjaramillo@conicet.gov.ar [Aquatic Systems Research Unit, EULA Chile Environmental Sciences Centre, Universidad de Concepcion (Chile); Munoz, Claudia; Rudolph, Ignacio [Aquatic Systems Research Unit, EULA Chile Environmental Sciences Centre, Universidad de Concepcion (Chile); Servos, Mark [Department of Biology, University of Waterloo, ON (Canada); Barra, Ricardo [Aquatic Systems Research Unit, EULA Chile Environmental Sciences Centre, Universidad de Concepcion (Chile)

    2013-01-01

    The Lenga Estuary is one of the most industrialized sites in south central Chile where the historic operation of chlor-alkali plants resulted in large quantities of mercury (Hg) being deposited into the estuary. This historical contamination may still represent a risk to the biota in the estuary. To investigate this four macroinvertebrates, Neotrypaea uncinata (ghostshrimp), Elminius kingii (barnacle), Hemigrapsus crenulatus (shore crab) and Perinereis gualpensis (ragworm) were collected seasonally from three different sites in the Lenga Estuary and one in a reference estuary (Tubul Estuary), and analyzed for Hg and stable isotopes ({delta}{sup 15}N and {delta}{sup 13}C). Mercury concentrations in Lenga sediments ranged from 0.4 {+-} 0.1 to 13 {+-} 3 mg/kg, while those in Tubul sediments ranged from 0.02 {+-} 0.01 to 0.07 {+-} 0.09 mg/kg. Total Hg concentrations of invertebrates were significantly different between estuaries (p < 0.05), but not by species or season for each estuary (p > 0.05). In contrast, organic Hg concentrations were different by species and season with shore crab muscle tissues exhibiting the greatest percent difference. Site-specific relationships demonstrated that total Hg concentrations in ragworm best reflected the total Hg sediment mercury concentrations. Signatures of {delta}{sup 13}C were correlated to the organic Hg % rather than total Hg. This suggests that organic Hg concentrations in these species were related to the carbon sources. -- Highlights: Black-Right-Pointing-Pointer Hg in sediments and biota from Lenga Estuary were elevated compared to nearby estuary. Black-Right-Pointing-Pointer Invertebrates showed interspecific and seasonal differences in terms of organic Hg %. Black-Right-Pointing-Pointer Total Hg levels in the ragworm best reflect Hg sediment gradient in Lenga Estuary. Black-Right-Pointing-Pointer Interspecific variation in {delta}{sup 13}C signatures indicated different feeding modes. Black

  3. Superdeformation studies in {sup 191}Hg

    Energy Technology Data Exchange (ETDEWEB)

    Carpenter, M.P.; Janssens, R.V.F.; Crowell, B. [and others

    1995-08-01

    Superdeformation in the A {approximately} 190 region was first observed in {sup 191}Hg from an experiment performed at ATLAS using the Argonne Notre Dame {gamma}-ray facility. We recently revisited the study of superdeformation in this nucleus using Gammasphere and the {sup 160}Gd({sup 36}S,5n) and {sup 174}Yb({sup 22}Ne,5n) reactions at 172 and 120 MeV in order to populate and measure states in the second well. The goal of the experiment was to identify new bands in the data, and thus allow us to gain understanding on the relative placement of single particle orbitals near the N = 112 SD shell gap. From an analysis of the data, the three previously identified SD bands were extended, and their feeding into the yrast states delineated. Two new SD bands were observed and preliminary evidence for a third new band was obtained as well.

  4. Diffusion Mechanism for Arsenic in Intrinsic and Extrinsic Conditions in HgCdTe

    Science.gov (United States)

    Grenouilloux, T.; Ferron, A.; Péré-Laperne, N.; Mathiot, D.

    2017-09-01

    Due to its low diffusivity and high activation rate, arsenic has become the dopant of choice in p/n HgCdTe high operating temperature technology. Its diffusion mechanism, however, remains imprecise. In this work, arsenic diffusion was studied in molecular beam epitaxy HgCdTe structures consisting of alternatively As-doped and intrinsic layers grown on a CdZnTe substrate. The diffusion coefficient of As was extracted from secondary ion mass spectroscopy concentration profiles. Annealings were performed for different temperatures, mercury partial pressures ( P Hg), annealing times and cadmium atomic fractions. Fermi-level effect on diffusion was observed, indicating extrinsic conditions for diffusion at high As concentration. Based on the variation of As diffusivity with P Hg and As concentration, we propose that As diffusion occurs on both II and VI sublattices. Our results are consistent with the fact that AsVI diffusion is assisted by the Te interstitial, introducing donor levels in the bandgap, while AsII diffusion is assisted by the cation vacancy.

  5. Hydrogen sensor based on Au and YSZ/HgO/Hg electrode for in situ measurement of dissolved H2 in high-temperature and -pressure fluids.

    Science.gov (United States)

    Zhang, R H; Hu, S M; Zhang, X T; Wang, Y

    2008-11-15

    Gold as a hydrogen-sensing electrode for in situ measurement of dissolved H2 in aqueous solutions under extreme conditions is reported. The dissolved H2 sensor, constructed with a Au-based sensing element and coupled with a YSZ/HgO/Hg electrode, is well suited for determining dissolved H2 concentrations of aqueous fluids at elevated temperatures and pressures. The Au electrode is made of Au wire mounted in a quartz bar, which can be pressurized and heated in the high-pressure and -temperature conditions. The Au-YSZ sensor has been tested for its potential response to the concentrations of dissolved H2 in fluids by using a flow-through reactor at high temperatures up to 400 degrees C and pressures to 38 MPa. Good sensitivity and linear response between the hydrogen concentrations in the fluids and the H2 sensor potentials are reported for hydrogen gas in the concentration range of 0.1-0.001 M H2 in aqueous fluids at temperatures up to 340 degrees C and 30 MPa. Nernstian response of the cell potential to dissolved H2 in fluids was determined at 340 degrees C and 30 MPa, described as follows: DeltaE = 0.9444 + 0. 0603 log m H2 The experimental results indicate that the Au-YSZ/HgO/Hg cell can be used to measure the solubility of H2 in aqueous fluid at temperatures and pressures near to the critical state of water. Thus, this type of Au hydrogen sensor could be easily used for in situ measurement of H2 in hydrothermal fluids in a high-pressure vessel, or at midocean ridge, due to its structure of compression resistance.

  6. Mercury concentrations in eggs of red-winged blackbirds and tree swallows breeding in Voyageurs National Park, Minnesota

    Science.gov (United States)

    Robin W. Tyser,; Kristofer R. Rolfhus,; James G. Wiener,; Steve K. Windels,; Custer, Thomas W.; Dummer, Paul

    2016-01-01

    Most investigations of the environmental effects of mercury (Hg) have focused on aquatic food webs that include piscivorous fish or wildlife. However, recent investigations have shown that other species, including passerine songbirds, may also be at risk from exposure to methylmercury (MeHg). We quantified Hg concentrations in eggs of two species of songbirds, red-winged blackbirds (Agelaius phoeniceus) and tree swallows (Tachycineta bicolor), nesting in Voyageurs National Park, Minnesota, USA. Geometric mean concentrations of total Hg (THg) were lower in red-winged blackbird eggs [218 and 107 ng/g dry weight (dw) for 2012 and 2013, respectively] than in tree swallow eggs (228 and 300 ng/g dw for 2012 and 2013, respectively), presumably reflecting differences in the trophic positions of these two species. Concentrations of MeHg averaged 98.4 % of THg in red-winged blackbird eggs. Levels of THg observed in this study were well below critical toxicological benchmarks commonly applied to eggs of avian species, suggesting these breeding populations were not adversely affected by exposure to MeHg. In red-winged blackbirds, concentrations of THg in eggs collected in 2012 were twice those in eggs collected in 2013. Hg levels in eggs of both species increased with date of clutch initiation. In red-winged blackbirds, for example, temporal patterns showed that a 3-week delay in clutch initiation increased egg THg by 60 %. These observations indicate that in ovo exposure of wetland birds to MeHg can vary significantly within nesting season as well as between years.

  7. [Resonance scattering detection of trace Hg2+ using aptamer modified AuSe nanoalloy].

    Science.gov (United States)

    Jiang, Zhi-liang; Zhang, Yi; Qin, Hui-min; Zhou, Lian-ping; Liang, Ai-hui; Wang, Peng-fei; Ouyang, Hui-xiang

    2011-05-01

    Under the condition of sodium citrate as stabilizer, the gold-selenium (AuSe) nano-alloy was prepared by sodium borohydride reduction procedure, and was modified by single-strand aptamer to obtain an aptamer nano-alloy probe (apta-AuSe) for Hg(II). In pH 6.8 Na2HPO4-NaH2PO4 buffer solution and in the presence of NaCl of 33 mmol L(-1), the Apta-AuSe probe is not aggregation. The apta-AuSe interacts with Hg2+ to form stable double-strand T-Hg(II)-T mismatches and to release AuSe nano-alloy particles from the probe. The released AuSe nano-alloy particles (20:1) aggregated to form bigger clusters that resulted in the resonance scattering (RS) intensity (I590 nm) increasing at 590 nm. The increased intensity delta I590 nm was proportional to the Hg2+ concentration from 1.3 to 1466 nmol L(-1), with a detection limit of 0.74 nmol L(-1). The regress equation was delta I590 nm = 0.603c + 2.0. Thus, a new resonance scattering (RS) spectroscopy of apta-AuSe was applied to the analysis of trace mercury ion. This simple, rapid, selective and sensitive aptamer AuSe nano-alloy RS assay was applied to the determination of Hg2+ in wastewater, with satisfactory results.

  8. Concentrations of trace elements in muscle of sturgeons in the Caspian Sea.

    Science.gov (United States)

    Agusa, Tetsuro; Kunito, Takashi; Tanabe, Shinsuke; Pourkazemi, Mohammad; Aubrey, David G

    2004-11-01

    Concentrations of 21 trace elements were determined in muscle of beluga (Huso huso), Persian sturgeon (Acipenser persicus), Russian sturgeon (Acipenser gueldenstaedtii), ship sturgeon (Acipenser nudiventris) and stellate sturgeon (Acipenser stellatus) collected from coastal regions of Azerbaijan, Iran, Kazakhstan and Turkmenistan, surrounding the Caspian Sea during 2000-2001. Concentrations of Mn, Co, Cu, Mo, Sn, Hg, Pb and Bi in the muscle were apparently different among the five species of sturgeons. Especially, beluga showed the highest concentrations of Hg, Pb and Mn in all the five species. In addition, more than half of the individuals of beluga exceeded the guideline level (0.3 microg/g wet wt.) of Hg for food in UK. However, V, Cr, Zn, Ga, Rb, Sr and Ba concentrations were similar among five sturgeons. Growth-dependent increase in Hg in beluga, Cu in Persian sturgeon, and Zn in Russian sturgeon were observed, whereas V, Mn, Co, Cu, Ga, Sr, Mo, Sn, Hg and Bi concentrations in Persian sturgeon, Pb in ship sturgeon, and Cr, Mn, and Rb in stellate sturgeon were negatively correlated with body length. All species of sturgeon in Azerbaijan showed the highest concentration of Sr and the lowest concentration of Rb, while the five sturgeons from Iran showed opposite trends. Concentration of V, which is present in oil, in sturgeons in the Caspian Sea was considerably lower than that of fish from Kuwait, but was comparable to that of Cambodia and the Gulf and Gulf of Oman. To our knowledge, this study provides the first extensive data on multielemental accumulation in sturgeons of the Caspian Sea.

  9. Search for improved surface treatment procedures in fabrication of HgI/sub 2/ X-ray spectrometers

    Energy Technology Data Exchange (ETDEWEB)

    Levi, A.; Burger, A.; Nissenbaum, J. (Hebrew Univ., Jerusalem (Israel). School of Applied Science and Technology); Schieber, M. (Hebrew Univ., Jerusalem (Israel). School of Applied Science and Technology; EG and G, Inc., Santa Barbara, CA (USA)); Burshtein, Z. (Israel Atomic Energy Commission, Beersheba. Nuclear Research Center-Negev)

    1983-07-15

    The influence of various fabrication parameters on the surface quality of HgI/sub 2/ X-ray spectrometers has been studied in detail. Exposure of etched HgI/sub 2/ to ambient atmosphere for proportional 24 h may reduce the electron surface recombination velocity by almost an order of magnitude. Reduction of the etching solution temperature (KI in water) to about 0/sup 0/C and an increase of the KI concentration to proportional 20 wt.% are also important.

  10. Search for improved surface treatment procedures in fabrication of HgI/sub 2/ x-ray spectrometers

    Energy Technology Data Exchange (ETDEWEB)

    Levi, A.; Burger, A.; Nissenbaum, J.; Schieber, M.; Burshtein, Z.

    1980-01-01

    The influence of various fabrication parameters on the surface quality of HgI/sub 2/ x-ray spectrometers was studied in detail. Exposure of etched HgI/sub 2/ to ambient atmosphere for approx. 24 hours may reduce the electron surface recombination velocity by almost an order of magnitude. Reduction of the etching solution temperature (KI in water) to about 0/sup 0/C and an increase of the KI concentration to approx. 20 wt % are also important.

  11. Impacts of Mercury Pollution Controls on Atmospheric Mercury Concentration and Occupational Mercury Exposure in a Hospital.

    Science.gov (United States)

    Li, Ping; Yang, Yan; Xiong, Wuyan

    2015-12-01

    Mercury (Hg) and Hg-containing products are used in a wide range of settings in hospitals. Hg pollution control measures were carried out in the pediatric ward of a hospital to decrease the possibility of Hg pollution occurring and to decrease occupational Hg exposure. Total gaseous Hg (TGM) concentrations in the pediatric ward and hair and urine Hg concentrations for the pediatric staff were determined before and after the Hg pollution control measures had been implemented. A questionnaire survey performed indicated that the pediatric staff had little understanding of Hg pollution and that appropriate disposal techniques were not always used after Hg leakage. TGM concentrations in the pediatric ward and urine Hg (UHg) concentrations for the pediatric staff were 25.7 and 22.2% lower, respectively, after the Hg pollution control measures had been implemented than before, which indicated that the control measures were effective. However, TGM concentrations in the pediatric ward remained significantly higher than background concentrations and UHg concentrations for the pediatric staff were remained significantly higher than the concentrations in control group, indicating continued existence of certain Hg pollution.

  12. Synthesis and Crystal Structure of New Coordination Compound Mn2Hg4(SCN)12%新型配合物Mn2Hg4(SCN)12的合成与晶体结构分析

    Institute of Scientific and Technical Information of China (English)

    李广慧; 方奇; 薛刚; 于文涛

    2005-01-01

    A new inorganic coordination compound Mn2Hg4(SCN)12 was synthesized. The grown crystals were characterized by elemental analysis, infrared spectroscopic analysis and powder crystal X-ray diffraction in detail. The crystal structure of Mn2Hg4(SCN)12 was determined by single-crystal X-ray diffraction. It belongs to monoclinic system, P21/c space group. The cell dimensions are: a=1.171 6 nm, b=1.431 05 nm, c=2.105 1 nm,β=100.738°,and Z=4. In the structure of it, half of Mn2+ cations have five-coordinate number, and other half of Mn2+ cations have six-coordinate number; 3/4 of Hg2+ cations are coordinated by four SCN-, 1/4 of Hg2+ cations are coordinated by three SCN- and one NCS-, all the coordination geometry of Hg2+ show slightly distorted tetrahedrons. CCDC:244939.

  13. Aqueous solvation of Hg(OH)2: energetic and dynamical density functional theory studies of the Hg(OH)2-(H2O)n (n = 1-24) structures.

    Science.gov (United States)

    Amaro-Estrada, J I; Maron, L; Ramírez-Solís, A

    2013-09-19

    A systematic study of the hydration of Hg(OH)2 by the stepwise solvation approach is reported. The optimized structures, solvation energies, and incremental free energies of 1-24 water molecules interacting with the solute have been computed at the B3PW91 level using 6-31G(d,p) basis sets for the O and H atoms. The mercury atom was treated with the Stuttgart-Köln relativistic core potential in combination with an extended optimized valence basis set. One to three direct Hg-water interactions appear along the solvation process. The first solvation shell is fully formed with 24 water molecules. A stable pentacoordinated Hg trigonal bipyramid structure appears for n > 15. Density functional theory (DFT) Born-Oppenheimer molecular dynamics simulations showed the thermal stability of the Hg(OH)2-(H2O)24 structure at room temperature and the persistence of the trigonal bipyramid coordination around Hg. The Gibbs free energy for the first solvation shell is significantly larger for the fully solvated Hg(OH)2 than the one previously obtained for the HgCl2 case, due to σ-acceptor and π-donor properties involving the hydroxyl groups of the solute. This suggests that the transmembrane passage of Hg(OH)2 into the cell via simple diffusion is less favorable compared to the case when the metal is coordinated with two Cl groups.

  14. [HG-AFS determination of selenium in Moringa oleifera].

    Science.gov (United States)

    Huang, Guo-qing; Xiao, Zi-jun

    2007-02-01

    The Se content in Moringa oleifera was studied by hydride generation atom fluorescence spectrometry (HG-AFS) with wet digestion. The effects of the way of digestion, the work condition of apparatus, the reaction medium and acidity, and the reducing agent and masking agent on the determination of Se were investigated. And the operating condition of apparatus was optimized. The results showed that the detection limit of Se in this method was 0.42 ng x mL(-1) in the linear ranger of 0-120 ng x mL(-1), the relative standard deviation was 3.53% (n = 11), and the recovery of the method was 95.2%-104.6%. It was showed that the method was very sensitive, simple, rapid and accurate.

  15. Environmental impact of CO2, Rn, Hg degassing from the rupture zones produced by Wenchuan M s 8.0 earthquake in western Sichuan, China.

    Science.gov (United States)

    Zhou, Xiaocheng; Chen, Zhi; Cui, Yueju

    2016-10-01

    The concentrations and flux of CO2, (222)Radon (Rn), and gaseous elemental mercury (Hg) in soil gas were investigated based on the field measurements in June 2010 at ten sites along the seismic rupture zones produced by the May 12, 2008, Wenchuan M s 8.0 earthquake in order to assess the environmental impact of degassing of CO2, Rn and Hg. Soil gas concentrations of 344 sampling points were obtained. Seventy measurements of CO2, Rn and Hg flux by the static accumulation chamber method were performed. The results of risk assessment of CO2, Rn and Hg concentration in soil gas showed that (1) the concentration of CO2 in the epicenter of Wenchuan M s 8.0 earthquake and north end of seismic ruptures had low risk of asphyxia; (2) the concentrations of Rn in the north segment of seismic ruptures had high levels of radon, Maximum was up to level 4, according to Chinese code (GB 50325-2001); (3) the average geoaccumulation index I geo of soil Hg denoted the lack of soil contamination, and maximum values classified the soil gas as moderately to strongly polluted in the epicenter. The investigation of soil gas CO2, Rn and Hg degassing rate indicated that (1) the CO2 in soil gas was characterized by a mean [Formula: see text] of -20.4 ‰ and by a mean CO2 flux of 88.1 g m(-2) day(-1), which were in the range of the typical values for biologic CO2 degassing. The maximum of soil CO2 flux reached values of 399 g m(-2) day(-1) in the epicenter; (2) the soil Rn had higher exhalation in the north segment of seismic ruptures, the maximum reached value of 1976 m Bq m(-2) s(-1); (3) the soil Hg flux was lower, ranging from -2.5 to 18.7 n g m(-2) h(-1) and increased from south to north. The mean flux over the all profiles was 4.2 n g m(-2) h(-1). The total output of CO2 and Hg degassing estimated along seismic ruptures for a survey area of 18.17 km(2) were approximately 0.57 Mt year(-1) and 688.19 g year(-1). It is recommended that land-use planners should

  16. A Comparison of Mathematical Models of Fish Mercury Concentration as a Function of Atmospheric Mercury Deposition Rate and Watershed Characteristics

    Science.gov (United States)

    Smith, R. A.; Moore, R. B.; Shanley, J. B.; Miller, E. K.; Kamman, N. C.; Nacci, D.

    2009-12-01

    Mercury (Hg) concentrations in fish and aquatic wildlife are complex functions of atmospheric Hg deposition rate, terrestrial and aquatic watershed characteristics that influence Hg methylation and export, and food chain characteristics determining Hg bioaccumulation. Because of the complexity and incomplete understanding of these processes, regional-scale models of fish tissue Hg concentration are necessarily empirical in nature, typically constructed through regression analysis of fish tissue Hg concentration data from many sampling locations on a set of potential explanatory variables. Unless the data sets are unusually long and show clear time trends, the empirical basis for model building must be based solely on spatial correlation. Predictive regional scale models are highly useful for improving understanding of the relevant biogeochemical processes, as well as for practical fish and wildlife management and human health protection. Mechanistically, the logical arrangement of explanatory variables is to multiply each of the individual Hg source terms (e.g. dry, wet, and gaseous deposition rates, and residual watershed Hg) for a given fish sampling location by source-specific terms pertaining to methylation, watershed transport, and biological uptake for that location (e.g. SO4 availability, hill slope, lake size). This mathematical form has the desirable property that predicted tissue concentration will approach zero as all individual source terms approach zero. One complication with this form, however, is that it is inconsistent with the standard linear multiple regression equation in which all terms (including those for sources and physical conditions) are additive. An important practical disadvantage of a model in which the Hg source terms are additive (rather than multiplicative) with their modifying factors is that predicted concentration is not zero when all sources are zero, making it unreliable for predicting the effects of large future reductions in

  17. First principle study of the interaction of elemental Hg with small neutral, anionic and cationic Pd ( = 1-6) clusters

    Indian Academy of Sciences (India)

    Shamoon Ahmad Siddiqui; Nadir Bouarissa

    2013-11-01

    Density functional theory (DFT)-based calculations have been performed so as to study the interaction of elemental mercury (Hg) with small neutral, cationic and anionic palladium clusters (Pd, = 1-6). Results of these calculations clearly indicate that frontier molecular orbital (FMO) theory is a useful method to predict the selectivity of Hg adsorption. Binding energies of Hg on cationic Pd clusters are generally found to be greater than those on neutral and anionic clusters. Results of natural bond orbital (NBO) analysis show that the flow of electrons in the neutral and charged complexes is mainly due to s orbitals of Hg. NBO analysis also indicates that, in most of the cases, the binding energies of Hg with Pdn clusters are directly proportional to charge transfer, i.e., greater the charge transfer, higher is the binding energy.

  18. Long-term Hg pollution-induced structural shifts of bacterial community in the terrestrial isopod (Porcellio scaber) gut.

    Science.gov (United States)

    Lapanje, Ales; Zrimec, Alexis; Drobne, Damjana; Rupnik, Maja

    2010-10-01

    In previous studies we detected lower species richness and lower Hg sensitivity of the bacteria present in egested guts of Porcellio scaber (Crustacea, Isopoda) from chronically Hg polluted than from unpolluted environment. Basis for such results were further investigated by sequencing of 16S rRNA genes of mercury-resistant (Hgr) isolates and clone libraries. We observed up to 385 times higher numbers of Hgr bacteria in guts of animals from polluted than from unpolluted environment. The majority of Hgr strains contained merA genes. Sequencing of 16S rRNA clones from egested guts of animals from Hg-polluted environments showed elevated number of bacteria from Pseudomonas, Listeria and Bacteroidetes relatives groups. In animals from pristine environment number of bacteria from Achromobacter relatives, Alcaligenes, Paracoccus, Ochrobactrum relatives, Rhizobium/Agrobacterium, Bacillus and Microbacterium groups were elevated. Such bacterial community shifts in guts of animals from Hg-polluted environment could significantly contribute to P. scaber Hg tolerance.

  19. A fluorescent probe based upon anthrancene-dopamine thioether for imaging Hg(2+) ions in living cells.

    Science.gov (United States)

    Feng, Wenjie; Xia, Qing; Zhou, Haiyan; Ni, Yun; Wang, Liulin; Jing, Su; Li, Lin; Ji, Wei

    2017-05-15

    A novel anthrancene-dopamine thioether L compound was designed as fluorescent probe for detecting Hg(2+) in living cells sample. L exhibits a good sensitive and selective recognition towards Hg(2+) ions in the presence of other important relevant metal ions and amino acids in HEPES solution. The addition of Hg(2+) causes a marked enhancement in the fluorescence emission intensity with the detection limit as low as 1.1×10(-6)M, combining with obvious colormetric change from colorless to pale brown. Mechanistic studies show that catechol group and sulfur atom in L all participate in the coordination with Hg(2+), though catechol group contributes mainly to chelation-enhanced fluorescence enhancement and sulfur atom to selectivity. Furthermore, L demonstrates good cell permeability and compatibility for sensitive fluorescent detection of Hg(2+) in HepG2 cells. This present probe will have broad applications in biological imaging. Copyright © 2017 Elsevier B.V. All rights reserved.

  20. In vivo formation of natural HgSe nanoparticles in the liver and brain of pilot whales

    Science.gov (United States)

    Gajdosechova, Zuzana; Lawan, Mohammed M.; Urgast, Dagmar S.; Raab, Andrea; Scheckel, Kirk G.; Lombi, Enzo; Kopittke, Peter M.; Loeschner, Katrin; Larsen, Erik H.; Woods, Glenn; Brownlow, Andrew; Read, Fiona L.; Feldmann, Jörg; Krupp, Eva M.

    2016-01-01

    To understand the biochemistry of methylmercury (MeHg) that leads to the formation of mercury-selenium (Hg-Se) clusters is a long outstanding challenge that promises to deepen our knowledge of MeHg detoxification and the role Se plays in this process. Here, we show that mercury selenide (HgSe) nanoparticles in the liver and brain of long-finned pilot whales are attached to Se-rich structures and possibly act as a nucleation point for the formation of large Se-Hg clusters, which can grow with age to over 5 μm in size. The detoxification mechanism is fully developed from the early age of the animals, with particulate Hg found already in juvenile tissues. As a consequence of MeHg detoxification, Se-methionine, the selenium pool in the system is depleted in the efforts to maintain essential levels of Se-cysteine. This study provides evidence of so far unreported depletion of the bioavailable Se pool, a plausible driving mechanism of demonstrated neurotoxic effects of MeHg in the organism affected by its high dietary intake. PMID:27678068

  1. In vivo formation of natural HgSe nanoparticles in the liver and brain of pilot whales

    Science.gov (United States)

    Gajdosechova, Zuzana; Lawan, Mohammed M.; Urgast, Dagmar S.; Raab, Andrea; Scheckel, Kirk G.; Lombi, Enzo; Kopittke, Peter M.; Loeschner, Katrin; Larsen, Erik H.; Woods, Glenn; Brownlow, Andrew; Read, Fiona L.; Feldmann, Jörg; Krupp, Eva M.

    2016-09-01

    To understand the biochemistry of methylmercury (MeHg) that leads to the formation of mercury-selenium (Hg-Se) clusters is a long outstanding challenge that promises to deepen our knowledge of MeHg detoxification and the role Se plays in this process. Here, we show that mercury selenide (HgSe) nanoparticles in the liver and brain of long-finned pilot whales are attached to Se-rich structures and possibly act as a nucleation point for the formation of large Se-Hg clusters, which can grow with age to over 5 μm in size. The detoxification mechanism is fully developed from the early age of the animals, with particulate Hg found already in juvenile tissues. As a consequence of MeHg detoxification, Se-methionine, the selenium pool in the system is depleted in the efforts to maintain essential levels of Se-cysteine. This study provides evidence of so far unreported depletion of the bioavailable Se pool, a plausible driving mechanism of demonstrated neurotoxic effects of MeHg in the organism affected by its high dietary intake.

  2. Toward real-time measurement of atmospheric mercury concentrations using cavity ring-down spectroscopy

    Directory of Open Access Journals (Sweden)

    X. Faïn

    2010-03-01

    Full Text Available Cavity ring-down spectroscopy (CRDS is a direct absorption technique that utilizes path lengths up to multiple kilometers in a compact absorption cell and has a significantly higher sensitivity than conventional absorption spectroscopy. This tool opens new prospects for study of gaseous elemental mercury (Hg0 because of its high temporal resolution and reduced sample volume requirements (<0.5 l of sample air. We developed a new sensor based on CRDS for measurement of (Hg0 mass concentration. Sensor characteristics include sub-ng m−3 detection limit and high temporal resolution using a frequency-doubled, tuneable dye laser emitting pulses at ~253.65 nm with a pulse repetition frequency of 50 Hz. The dye laser incorporates a unique piezo element attached to its tuning grating allowing it to tune the laser on and off the Hg0 absorption line on a pulse-to-pulse basis to facilitate differential absorption measurements. Hg0 absorption measurements with this CRDS laboratory prototype are highly linearly related to Hg0 concentrations determined by a Tekran 2537B analyzer over an Hg0 concentration range from 0.2 ng m−3 to 573 ng m−3, implying excellent linearity of both instruments. The current CRDS instrument has a sensitivity of 0.10 ng Hg0 m−3 at 10-s time resolution. Ambient-air tests showed that background Hg0 levels can be detected at low temporal resolution (i.e., 1 s, but also highlight a need for high-frequency (i.e., pulse-to-pulse differential on/off-line tuning of the laser wavelength to account for instabilities of the CRDS system and variable background absorption interferences. Future applications may include ambient Hg0 flux measurements with eddy covariance techniques, which require measurements of Hg0 concentrations with sub-ng m−3 sensitivity and sub-second time

  3. Preparation and characterization of a novel nano-absorbent based on multi-cyanoguanidine modified magnetic chitosan and its highly effective recovery for Hg(II) in aqueous phase

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Yang; Qi, Yongxin; Li, Yanfeng, E-mail: liyf@lzu.edu.cn; Wu, Jianjun; Ma, Xiaojie; Yu, Cui; Ji, Lei

    2013-09-15

    Highlights: • The multi-cyanoguanidine modified magnetic chitosan was firstly synthesized. • Introduce more functional group by modification of cross-linking agent. •The absorbent showed the prominent adsorption capacity and strong removal ability. • The absorbent shows excellent selectively separate for Hg(II). -- Abstract: A new kind of nano-absorbent with the entirely novel structure, nano-absorbent of multi-cyanogunidine modified magnetic chitosan (CG-MCS nano-absorbent), has been firstly synthesized by using the functionalized chitosan and cross-linking agent with cyanoguanidine group simultaneously. The resulting nano-absorbent was characterized by means of the Fourier transform infrared spectra (FT-IR), transmission electron microscope (TEM), X-ray diffraction (XRD), elemental analysis and vibrating sample magnetometer (VSM). The resulting nano-absorbent basen on multi-cyanoguanidine modified magnetic chitosan has been demonstrated holding highly effective recovery for mercury ions, in other words, it showed both the extraordinary adsorption capacity for Hg(II) at high initial concentration and the strong removal ability for it at low concentration, the maximum adsorption capacity was up to 285 mg g{sup −1} and the removal percentage could reach 96% at low concentration. Meanwhile, the resulting CG-MCS nano-absorbent also showed a high selectivity adsorption for Hg(II) among coexisting heavy metals and the good regeneration performance.

  4. Oxidative stress in MeHg-induced neurotoxicity

    Energy Technology Data Exchange (ETDEWEB)

    Farina, Marcelo, E-mail: farina@ccb.ufsc.br [Departamento de Bioquimica, Centro de Ciencias Biologicas, Universidade Federal de Santa Catarina, Florianopolis, SC (Brazil); Aschner, Michael [Department of Pediatrics, Vanderbilt University Medical Center, Nashville, TN (United States); Department of Pharmacology, Vanderbilt University Medical Center, Nashville, TN (United States); Rocha, Joao B.T., E-mail: jbtrocha@yahoo.com.br [Departamento de Quimica, Centro de Ciencias Naturais e Exatas, Universidade Federal de Santa Maria, Santa Maria, RS (Brazil)

    2011-11-15

    Methylmercury (MeHg) is an environmental toxicant that leads to long-lasting neurological and developmental deficits in animals and humans. Although the molecular mechanisms mediating MeHg-induced neurotoxicity are not completely understood, several lines of evidence indicate that oxidative stress represents a critical event related to the neurotoxic effects elicited by this toxicant. The objective of this review is to summarize and discuss data from experimental and epidemiological studies that have been important in clarifying the molecular events which mediate MeHg-induced oxidative damage and, consequently, toxicity. Although unanswered questions remain, the electrophilic properties of MeHg and its ability to oxidize thiols have been reported to play decisive roles to the oxidative consequences observed after MeHg exposure. However, a close examination of the relationship between low levels of MeHg necessary to induce oxidative stress and the high amounts of sulfhydryl-containing antioxidants in mammalian cells (e.g., glutathione) have led to the hypothesis that nucleophilic groups with extremely high affinities for MeHg (e.g., selenols) might represent primary targets in MeHg-induced oxidative stress. Indeed, the inhibition of antioxidant selenoproteins during MeHg poisoning in experimental animals has corroborated this hypothesis. The levels of different reactive species (superoxide anion, hydrogen peroxide and nitric oxide) have been reported to be increased in MeHg-exposed systems, and the mechanisms concerning these increments seem to involve a complex sequence of cascading molecular events, such as mitochondrial dysfunction, excitotoxicity, intracellular calcium dyshomeostasis and decreased antioxidant capacity. This review also discusses potential therapeutic strategies to counteract MeHg-induced toxicity and oxidative stress, emphasizing the use of organic selenocompounds, which generally present higher affinity for MeHg when compared to the classically

  5. Lithography process for patterning HgI2 photonic devices

    Science.gov (United States)

    Mescher, Mark J.; James, Ralph B.; Hermon, Haim

    2004-11-23

    A photolithographic process forms patterns on HgI.sub.2 surfaces and defines metal sublimation masks and electrodes to substantially improve device performance by increasing the realizable design space. Techniques for smoothing HgI.sub.2 surfaces and for producing trenches in HgI.sub.2 are provided. A sublimation process is described which produces etched-trench devices with enhanced electron-transport-only behavior.

  6. Epitaxial growth of HgTe by a MOVPE process

    Energy Technology Data Exchange (ETDEWEB)

    Irvine, S.J.C.; Mullin, J.B.; Royle, A. (Royal Signals and Radar Establishment, Malvern (UK))

    1982-03-01

    Epitaxial layers of HgTe have been grown onto insulating CdTe substrates by the pyrolysis of (C/sub 2/H/sub 5/)/sub 2/Te in the presence of Hg vapour using a H/sub 2/ flow system. Temperature-dependent Hall effect and conductivity measurements have shown that the electrical properties of the layers are comparable with good quality bulk HgTe.

  7. Concentrations and isotope ratios of mercury in sediments from shelf and continental slope at Campos Basin near Rio de Janeiro, Brazil.

    Science.gov (United States)

    Araujo, Beatriz Ferreira; Hintelmann, Holger; Dimock, Brian; Almeida, Marcelo Gomes; Rezende, Carlos Eduardo

    2017-07-01

    Mercury (Hg) may originate from both anthropogenic and natural sources. The measurement of spatial and temporal variations of Hg isotope ratios in sediments may enable source identification and tracking of environmental processes. In this study we establish the distribution of mercury concentrations and mercury isotope ratios in surface sediments of three transects along the continental shelf and slope in Campos Basin-RJ-Brazil. The shelf showed on average lower total Hg concentrations (9.2 ± 5.3 ng g(-1)) than the slope (24.6 ± 8.8 ng g(-1)). MMHg average concentrations of shelf 0.15 ± 0.12 ng g(-1) and slope 0.13 ± 0.06 ng g(-1) were not significantly different. Distinct differences in Hg isotope ratio signatures were observed, suggesting that the two regions were impacted by different sources of Hg. The shelf showed more negative δ(202)Hg and Δ(199)Hg values ranging from -0.59 to -2.19‰ and from -0.76 to 0.08‰, respectively. In contrast, the slope exhibited δ(202)Hg values from -0.29 to -1.82‰ and Δ(199)Hg values from -0.23 to 0.09‰. Mercury found on the shelf, especially along the "D" and "I" transects, is depleted in heavy isotopes resulting in more negative δ(202)Hg compared to the slope. Isotope ratios observed in the "D" and "I" shelf region are similar to Hg ratios commonly associated with plants and vegetation and very comparable to those detected in the estuary and adjoining mangrove forest, which suggests that Hg exported from rivers may be the dominating source of Hg in near coastal regions along the northern part of the shelf. Copyright © 2017 Elsevier Ltd. All rights reserved.

  8. A fluorescent chemodosimeter for Hg2+ based on a spirolactam ring-opening strategy and its application towards mercury determination in aqueous and cellular media.

    Science.gov (United States)

    Kumar, Kempahanumakkagaari Suresh; Ramakrishnappa, Thippeswamy; Balakrishna, R Geetha; Pandurangappa, Mallingappagari

    2014-01-01

    A novel fluorescent chemosensor rhodamine B phenyl hydrazide (RBPH) for Hg(2+) was designed and synthesized. This probe is highly sensitive, selective, and irreversible for Hg(2+) and exhibits fluorescent response at 580 nm. RBPH also displayed detectable color change from colorless to pink upon treatment with Hg(2+). This property has been utilized as naked eye detection for Hg(2+) in various industrial samples. Fluorescence microscopic experiments demonstrated that this chemosensor is cell permeable and can be used for fluorescence imaging of Hg(2+) in cellular media. This probe can detect Hg(2+) with good linear relationships from 1 to 100 nM with r = 0.99983 and the limit of detection were found to be 0.019 nM with ± 0.91 % RSD at 10 nM concentrations.

  9. Electrical resistivity and thermoelectric power of a quasi-one-dimensional Nb{sub 3}Te{sub 4} single crystal inserted with mercury: Hg{sub x}Nb{sub 3}Te{sub 4}

    Energy Technology Data Exchange (ETDEWEB)

    Kagohashi, Takanori; Takarada, Tukasa; Hasegawa, Hitoshi; Katumata, Yuriko; Kuga, Masanori; Okamoto, Hiroyuki; Kaneko, Hiroshi; Ishihara, Yutaka [Department of Physics, Faculty of Science, Kanazawa University, Kanazawa 920-1192 (Japan)

    1999-08-23

    The electrical resistivity and the thermoelectric power of Nb{sub 3}Te{sub 4} inserted with mercury have been measured in the temperature range from 1.4 to 300 K. The magnitude of the resistivity and the residual-resistivity ratio are not greatly affected by addition of Hg. The magnitude of the resistive anomaly at 90 K increases when adding a small amount of Hg but begins to decrease at about x=0.03 and is no longer visible at about x=0.15. Similarly, the magnitude of the resistive anomaly at 30 K decreases with increasing Hg concentration and disappears at about x=0.26. The thermoelectric power S also shows two anomalies at about 90 and 30 K. The anomaly of S at 90 K becomes smeared by addition of Hg and disappears at about x=0.3. The anomaly of S at 30 K becomes clear by addition of Hg and is still present at an amount of x=0.8. The sign of S is negative at all measured temperatures for x<0.3 and is positive at temperatures below 7 K for x>0.3. The superconducting transition temperature is enhanced from 1.9 to 5.4 K by addition of Hg. The upper critical fields parallel (H{sub c2parallel}) and perpendicular (H{sub c2} perpendicular) to the c axis have been measured near T{sub C}. The critical fields show large anisotropy for x{>=}0.3: the ratio H{sub c2parallel}/H{sub c2} perpendicular is about 5 for x<0.3 and 40 for x{>=}0.3. These results are discussed on the basis of the multiband model with electron-like and hole-like carriers and with phonon drag. (author)

  10. A NIR fluorescent probe for the rapid detection of Hg2+ in living cells and in vivo mice imaging

    Science.gov (United States)

    Wang, Jiaoliang; Long, Liping; Xia, Li; Fang, Fang

    2017-06-01

    A near-infrared fluorescent probe NIR-Hg, for the detection of Hg2+ ion, has been synthesized directly by condensing Changsha dye with 4-Phenyl-3-thiosemicarbazide and the structure has fully characterized by 1HNMR, 13CNMR, and ESI-MS. The probe has been designed on the basis of the reaction that Hg2+ ion promotes thiosemicarbazide to oxazole in aqueous media and had been induced to produce turn-on fluorescence via an irreversible spirolactam ring-opening process. The probe NIR-Hg has exhibited fast response (1 min), high sensitivity with 44-fold fluorescence intensity enhancement under six equivalent amounts of Hg2+ added, high selectivity over other related metal ions and a low detection limit of 5.8 × 10-8 M in the phosphate buffer. The linear response range covers the concentration of Hg2+ from 5 × 10-7 to 5 × 10-6 M. In addition, the probe has good cell-membrane permeability, which is suitable for fluorescence imaging for Hg2+ in living cells and in vivo mice.

  11. Electrochemical DNA probe for Hg(2+) detection based on a triple-helix DNA and Multistage Signal Amplification Strategy.

    Science.gov (United States)

    Wang, Huan; Zhang, Yihe; Ma, Hongmin; Ren, Xiang; Wang, Yaoguang; Zhang, Yong; Wei, Qin

    2016-12-15

    In this work, an ultrasensitive electrochemical sensor was developed for detection of Hg(2+). Gold nanoparticles decorated bovine serum albumin reduction of graphene oxide (AuNP-BSA-rGO) were used as subsurface material for the immobilization of triple-helix DNA. The triple-helix DNA containing a thiol labelled single-stranded DNA (sDNA) and a thymine-rich DNA (T-rich DNA), which could be unwinded in the present of Hg(2+) to form more stable thymine-Hg(2+)-thymine (T-Hg(2+)-T) complex. T-Hg(2+)-T complex was then removed and the sDNA was left on the electrode. At this time, gold nanoparticle carrying thiol labelled cytosine-rich complementary DNA (cDNA-AuNP) could bind with the free sDNA. Meanwhile, the other free cDNA on AuNP could bind with each other in the present of Ag(+) to form the stable cytosine-Ag(+)-cytosine (C-Ag(+)-C) complex and circle amplification. Plenty of C-Ag(+)-C could form silver nanoclusters by electrochemical reduction and the striping signal of Ag could be measured for purpose of the final electrochemical detection of Hg(2+). This sensor could detect Hg(2+) over a wide concentration range from 0.1 to 130nM with a detection limit of 0.03nM.

  12. Chemical substitution of Cd ions by Hg in CdSe nanorods and nanodots: Spectroscopic and structural examination

    Energy Technology Data Exchange (ETDEWEB)

    Prudnikau, Anatol [Institute for Physico-Chemical Problems, Belarussian State University, 220030 Minsk (Belarus); Artemyev, Mikhail, E-mail: m_artemyev@yahoo.com [Institute for Physico-Chemical Problems, Belarussian State University, 220030 Minsk (Belarus); Laboratory of Nano-Bioengineering, Moscow Engineering Physics Institute, 31 Kashirskoe sh., 115409 Moscow (Russian Federation); Molinari, Michael; Troyon, Michel [Universite de Reims Champagne-Ardenne, 51100 Reims (France); Sukhanova, Alyona; Nabiev, Igor [Universite de Reims Champagne-Ardenne, 51100 Reims (France); Laboratory of Nano-Bioengineering, Moscow Engineering Physics Institute, 31 Kashirskoe sh., 115409 Moscow (Russian Federation); Baranov, Alexandr V.; Cherevkov, Sergey A.; Fedorov, Anatoly V. [Saint-Petersburg State University of Information Technologies, Mechanics and Optics, St.-Petersburg 197101 (Russian Federation)

    2012-06-05

    Highlights: Black-Right-Pointing-Pointer We studied cadmium-by-mercury chemical substitution in CdSe nanocrystals. Black-Right-Pointing-Pointer Zinc blende CdSe quantum dots can be easily converted to isostructural Cd{sub x}Hg{sub 1-x}Se. Black-Right-Pointing-Pointer Wurtzite CdSe QDs require longer time to convert to a zinc blende Cd{sub x}Hg{sub 1-x}Se. Black-Right-Pointing-Pointer Wurtzite CdSe nanorods transform to nanoheterogeneous luminescent Cd{sub x}Hg{sub 1-x}Se rods. - Abstract: The chemical substitution of cadmium by mercury in colloidal CdSe quantum dots (QDs) and nanorods has been examined by absorption, photoluminescence and Raman spectroscopy. The crystalline structure of original CdSe QDs used for Cd/Hg substitution (zinc blende versus wurtzite) shows a strong impact on the optical and structural properties of resultant Cd{sub x}Hg{sub 1-x}Se nanocrystals. Substitution of Cd by Hg in isostructural zinc blende CdSe QDs converts them to ternary Cd{sub x}Hg{sub 1-x}Se zinc blende nanocrystals with significant NIR emission. Whereas, the wurtzite CdSe QDs transformed first to ternary nanocrystals with almost no emission followed by slow structural reorganization to a NIR-emitting zinc blende Cd{sub x}Hg{sub 1-x}Se QDs. CdSe nanorods with intrinsic wurtzite structure show unexpectedly intense NIR emission even at early Cd/Hg substitution stage with PL active zinc blende Cd{sub x}Hg{sub 1-x}Se regions.

  13. Experiments with a New 201Hg+ Ion Clock

    Science.gov (United States)

    Burt, E. A.; Taghavi-Larigani, S.; Lea, S. N.; Prestage, J. D.; Tjoelker, R. L.

    2009-04-01

    In this paper we describe a new clock based on 201Hg+. All previous mercury ion clocks have been based on 199Hg+. We have recently completed construction of the 201Hg+ clock and will describe modifications to the design of our existing 199Hg+ clocks to accommodate the new isotope. We will also describe initial spectroscopic measurements of the hyperfine manifold, and possible future experiments. One experiment could place a limit on variations in the strong interaction fundamental constant ratio mq/ΛQCD.REFID="9789812838223_0043FN001">

  14. Novel methodology for the study of mercury methylation and reduction in sediments and water using {sup 197}Hg radiotracer

    Energy Technology Data Exchange (ETDEWEB)

    Ribeiro Guevara, Sergio; Perez Catan, Soledad [Centro Atomico Bariloche, Laboratorio de Analisis por Activacion Neutronica, Bariloche (Argentina); Zizek, Suzana; Repinc, Urska; Jacimovic, Radojko; Horvat, Milena [Jozef Stefan Institute, Department of Environmental Sciences, Ljubljana (Slovenia)

    2007-03-15

    Mercury tracers are powerful tools that can be used to study mercury transformations in environmental systems, particularly mercury methylation, demethylation and reduction in sediments and water. However, mercury transformation studies using tracers can be subject to error, especially when used to assess methylation potential. The organic mercury extracted can be as low as 0.01% of the endogenous labeled mercury, and artefacts and contamination present during methylmercury (MeHg) extraction processes can cause interference. Solvent extraction methods based on the use of either KBr/H{sub 2}SO{sub 4} or HCl were evaluated in freshwater sediments using {sup 197}Hg radiotracer. Values obtained for the {sup 197}Hg tracer in the organic phase were up to 25-fold higher when HCl was used, which is due to the coextraction of {sup 197}Hg{sup 2+} into the organic phase during MeHg extraction. Evaluations of the production of MeHg gave similar results with both MeHg extraction procedures, but due to the higher Hg{sup 2+} contamination of the controls, the uncertainty in the determination was higher when HCl was used. The Hg{sup 2+} contamination of controls in the HCl extraction method showed a nonlinear correlation with the humic acid content of sediment pore water. Therefore, use of the KBr/H{sub 2}SO{sub 4} method is recommended, since it is free from these interferences. {sup 197}Hg radiotracer (T{sub 1/2} = 2.673 d) has a production rate that is about 50 times higher than that of {sup 203}Hg (T{sub 1/2} = 46.595 d), the most frequently used mercury radiotracer. Hence it is possible to obtain a similar level of performance to {sup 203}Hg when it is used it in short-term experiments and produced by the irradiation of {sup 196}Hg with thermal neutrons, using mercury targets with the natural isotopic composition. However, if the 0.15% natural abundance of the {sup 196}Hg isotope is increased, the specific activity of the {sup 197}Hg tracer can be significantly improved. In

  15. Photoelectric properties of defect chalcogenide HgGa2X4 (x=S, Se, Te)

    Science.gov (United States)

    Sharma, Ramesh; Dwivedi, Shalini; Sharma, Yamini

    2016-05-01

    We present results of ab initio study of ordered vacancy compounds of mercury. The electronic structure, charge density, optical and transport properties of the semiconductor family HgGa2X4 (X=S, Se, Te) are calculated using the full potential linearized augmented plane wave method which is based on the density functional theory. A direct bandgap is observed in these compounds, which reduces in the order S>Se>Te. From the density of states it is observed that there is strong hybridization of Hg-d, Ga-d and X-p states. The optical properties show a red shift with increasing size and atomic no. of the chalcogenide atoms. We have also reported the transport properties of mercury thiogallates for the first time. The selenide compound exhibits n-type nature whereas HgGa2S4 and HgGa2Te4 show p-type behavior. The power factor and ZT for the HGS increases at low temperatures, the figure of merit is highest for HgGa2Se4 (1.17) at 19 K.

  16. The characterization of HG10MNN and an evaluation of suitability for use in naval applications

    Energy Technology Data Exchange (ETDEWEB)

    Hawxhurst, K.L.; Westerberg, J.M., E-mail: m166918@usna.edu; Woertz, J.C., E-mail: woertz@usna.edu

    2016-06-15

    Highlights: • HG10MNN alloy showed good strength, hardness and ductility compared to NAB. • In air, four point bending fatigue tests suggest an endurance limit between 8 and 10 ksi. • As compared to NAB, HG10MNN has excellent casting and corrosion behavior. - Abstract: An initial mechanical evaluation and standard material characterization were conducted for the stainless steel alloy HG10MNN in order to evaluate its use in naval and marine applications. HG10MNN is a newly developed stainless steel designed for improved resistance to mechanical and thermal fatigue. This material could eventually replace the Nickel–Aluminum–Bronze (NAB) currently used in many naval propulsion systems, however, additional testing is required to validate the alloy's performance characteristics. Although stainless steels are commonly used in marine applications, there is insufficient HG10MNN documentation to permit its use in naval ship design. This investigation also involved an evaluation of castability and machinability to determine whether the material could be formed into the complex shapes required in a modern naval construction. Initial results showed that the alloy exhibits a fully austenitic microstructure in the as-cast condition, while maintaining acceptable mechanical properties and superior castability as compared to NAB.

  17. Dissecting the effect of anions on Hg2+ detection using a FRET based DNA probe.

    Science.gov (United States)

    Kiy, Mehmet Murat; Zaki, Ahmed; Menhaj, Arsalsan Beg; Samadi, Azadeh; Liu, Juewen

    2012-08-07

    Many biosensors have been developed to detect Hg(2+) using thymine-rich DNA. While sensor response to various cations is often studied to demonstrate selectivity, the effect of anions has been largely overlooked. Anions may compete with DNA for metal binding and thus produce a false negative result. Anions cannot be added alone; the cation part of a salt may cause DNA compaction and other effects, obscuring the role of anions. We find that the sensitivity of a FRET-based Hg(2+) probe is independent of Na(+) concentration. Therefore, by using various sodium salts, any change in sensitivity can be attributed solely to the effect of anions. Halide salts, sulfides, and amines are strong inhibitors; anions containing oxo or hydroxyl groups (e.g. nitrate, sulfate, phosphate, carbonate, acetate, and citrate) do not interfere with Hg(2+) detection even at 100 mM concentration. Mercury hydrolysis and its diffusion into polypropylene containers can also strongly affect the detection results. We conclude that thymine-rich DNA should be useful for Hg(2+) detection in many environmental water samples.

  18. Temperature-driven massless Kane fermions in HgCdTe crystals

    Science.gov (United States)

    Teppe, F.; Marcinkiewicz, M.; Krishtopenko, S. S.; Ruffenach, S.; Consejo, C.; Kadykov, A. M.; Desrat, W.; But, D.; Knap, W.; Ludwig, J.; Moon, S.; Smirnov, D.; Orlita, M.; Jiang, Z.; Morozov, S. V.; Gavrilenko, V. I.; Mikhailov, N. N.; Dvoretskii, S. A.

    2016-08-01

    It has recently been shown that electronic states in bulk gapless HgCdTe offer another realization of pseudo-relativistic three-dimensional particles in condensed matter systems. These single valley relativistic states, massless Kane fermions, cannot be described by any other relativistic particles. Furthermore, the HgCdTe band structure can be continuously tailored by modifying cadmium content or temperature. At critical concentration or temperature, the bandgap collapses as the system undergoes a semimetal-to-semiconductor topological phase transition between the inverted and normal alignments. Here, using far-infrared magneto-spectroscopy we explore the continuous evolution of band structure of bulk HgCdTe as temperature is tuned across the topological phase transition. We demonstrate that the rest mass of Kane fermions changes sign at critical temperature, whereas their velocity remains constant. The velocity universal value of (1.07+/-0.05) × 106 m s-1 remains valid in a broad range of temperatures and Cd concentrations, indicating a striking universality of the pseudo-relativistic description of the Kane fermions in HgCdTe.

  19. Removal of Cd (II and Hg(II by chelating resin Chelex-100

    Directory of Open Access Journals (Sweden)

    Afaf Amara-Rekkab

    2015-03-01

    Full Text Available A sensitive, simple method for the determination of amounts of mixture of Hg2+and Cd2+ by spectrophotometry was described based on the formation of the Hg2+- Cd2+- PAN complex in water media. Optimal conditions such as reagent amounts, and pH for the Hg2+- Cd2+ determination were reported. It was found that the 2:1 PAN- Hg2+- Cd2+ complex dominate at pH 13.0. In another hand, the sorption of mixture mercury (II and cadmium (II from aqueous medium on a chelating resin Chelex 100 was studied in batch mode. Since the extraction kinetic was obtained, with a mixture of 0.1 g of resin and 5 mL of mixture at 1 mmol/L of initial concentration, extraction equilibrium was reached within 20 min of mixing. The influence of some parameters such as initial mixture ions concentrations, initial pH of aqueous solution, ion strength and the amounts of resin have been studied at fixed temperature (20±1°C. The optimum pH value level for quantitative sorption was up to 2.6. The best performance obtained was 97.1% of extraction yield equivalent to 15.65 mg/g of resin. The pseudo-first- order, pseudo-second-order models and the intra-particle diffusion model were used to describe the kinetic data and rate constants were evaluated.

  20. Determination of Hg and diet identification in otter (Lontra longicaudis) feces

    Energy Technology Data Exchange (ETDEWEB)

    Ferreira Josef, Carla [Centro de Energia Nuclear na Agricultura - CENA-USP, Universidade de Sao Paulo, Av. Centenario 303, 13400-970 Piracicaba, Sao Paulo (Brazil)], E-mail: carlajosef@hotmail.com; Ramos Adriano, Leonardo; Franca, Elvis Joacir de; Gustinelli Arantes de Carvalho, Gabriel [Centro de Energia Nuclear na Agricultura - CENA-USP, Universidade de Sao Paulo, Av. Centenario 303, 13400-970 Piracicaba, Sao Paulo (Brazil); Ferreira, Jose Roberto [Centro de Energia Nuclear na Agricultura - CENA-USP, Universidade de Sao Paulo, Av. Centenario 303, 13400-970 Piracicaba, Sao Paulo (Brazil); Polo de Pesquisa e Desenvolvimento Regional do Centro Sul - APTA, Agencia Paulista de Tecnologia dos Agronegocios. Rua Alberto Coral 1500, 13400-000 Piracicaba, Sao Paulo (Brazil)

    2008-04-15

    An analytical procedure for the determination of Hg in otter (Lontra longicaudis) feces was developed, to separate fish scales for the identification of the animal diet. Samples were washed with ultra-pure water and the suspension was sampled and transferred for digestion. The solubilization was performed with nitric-perchloric acid mixture, and detection carried out by the atomic fluorescence spectrometry (AFS). The quality of the analytical procedure was assessed by analyzing in-house standard solutions and certified reference materials. Total Hg concentrations were in the range of 7.6-156 ng g{sup -1} (July 2004), 25.6-277 ng g{sup -1} (January 2005) and 14.6-744 ng g{sup -1} (May 2005) that is approximately the same order of magnitude for all samples collected in two reservoirs at the Tiete River, Brazil. Although Hg concentrations varied with sampling periods and diet, high levels were correlated to the percentage of carnivorous fish scales present in the otter feces. - The importance of otter feces preparation for Hg analysis, focusing the food web.

  1. PENCEMARAN LOGAM BERAT MERKURI (Hg PADA AIRTANAH

    Directory of Open Access Journals (Sweden)

    Thomas Triadi Putranto

    2012-02-01

    Full Text Available The earth consists largely of water because the land area is smaller than the ocean. Human beings on this earthcan not escape the need for water. Water is the main requirement for the process of life on the earth.Relatively clean water that is coveted by men, whether for purposes of daily life, for industrial purposes, for thecleanliness of city sanitation, as well as for agricultural purposes and so forth. Heavy metal pollution is a veryserious issue to be handled, because of adverse environmental and ecosystem in general. Heavy metallic elementis the element which has a density of more than 5 gr/cm3. Hg has a density of 13.55 gr/cm3. Disaster is anoutbreak of Minamata mercury poisoning in people who eat fish contaminated by mercury in Minamata Japan,and this event is known as Minamata Disease. Efforts to tackle the heavy metal pollution can actually be doneusing a chemical process or by microorganism such as microbes and bacteria.

  2. Hg-coordination studies of oligopeptides containing cysteine, histidine and tyrosine by $^{199m}$Hg-TDPAC

    CERN Document Server

    Ctortecka, B; Mallion, S; Butz, T; Hoffmann, R

    1999-01-01

    In order to study the interaction of histidine- and tyrosine- containing peptide chains with Hg(II), the nuclear quadrupole interaction (NQI) of /sup 199m/Hg in the Hg complexes of the oligopeptides alanyl-alanyl-histidyl-alanyl-alanine-amid (AAHAA-NH /sub 2/) and alanyl-alanyl-tyrosyl-alanyl-alanine-amid (AAYAA-NH/sub 2/) was determined by time differential perturbed angular correlation and is compared with previous data on alanyl-alanyl-cysteyl-alanyl- alanyl (AACAA-OH). The /sup 199m/Hg-NQIs depend on the oligopeptide to Hg(II) stoichiometry and indicate that two-fold and four-fold coordinations occur for the bound Hg(II). (12 refs).

  3. Mechanism of Hg-C Protonolysis in the Organomercurial Lyase MerB

    Energy Technology Data Exchange (ETDEWEB)

    Parks, Jerry M [ORNL; Guo, Hong [ORNL; Liang, Liyuan [ORNL; Miller, Susan M [ORNL; Summers, Anne O [ORNL; Smith, Jeremy C [ORNL

    2009-01-01

    Demethylation is a key reaction in global mercury cycling. The bacterial organomercurial lyase, MerB, catalyzes the demethylation of a wide range of organomercurials via Hg-C protonolysis. Two strictly conserved cysteine residues in the active site are required for catalysis, but the source of the catalytic proton and the detailed reaction mechanism have not been determined. Here, the two major proposed reaction mechanisms of MerB are investigated and compared using hybrid density functional theory calculations. A model of the active site was constructed from an X-ray crystal structure of the Hg(II)-bound MerB product complex. Stationary point structures and energies characterized for the Hg-C protonolysis of methylmercury rule out the direct protonation mechanism in which a cysteine residue delivers the catalytic proton directly to the organic leaving group. Instead, the calculations support a two-step mechanism in which Cys96 or Cys159 first donates a proton to Asp99, enabling coordination of two thiolates with R-Hg(II). At the rate-limiting transition state, Asp99 protonates the nascent carbanion in a trigonal planar, bis thiol-ligated R-Hg(II) species to cleave the Hg-C bond and release the hydrocarbon product. Reactions with two other substrates, vinylmercury and cis-2-butenyl-2-mercury, were also modeled, and the computed activation barriers for all three organomercurial substrates reproduce the trend in the experimentally observed enzymatic reaction rates. Analysis of atomic charges in the rate-limiting transition state structure using Natural Population Analysis shows that MerB lowers the activation free energy in the Hg-C protonolysis reaction by redistributing electron density into the leaving group and away from the catalytic proton.

  4. Hg(II Coordination Polymers Based on N,N’-bis(pyridine-4-ylformamidine

    Directory of Open Access Journals (Sweden)

    Wayne Hsu

    2016-04-01

    Full Text Available Reactions of N,N’-bis(pyridine-4-ylformamidine (4-Hpyf with HgX2 (X = Cl, Br, and I afforded the formamidinate complex {[Hg(4-pyf2]·(THF}n, 1, and the formamidine complexes {[HgX2(4-Hpyf]·(MeCN}n (X = Br, 2; I, 3, which have been structurally characterized by X-ray crystallography. Complex 1 is a 2D layer with the {44·62}-sql topology and complexes 2 and 3 are helical chains. While the helical chains of 2 are linked through N–H···Br hydrogen bonds, those of 3 are linked through self-complementary double N–H···N hydrogen bonds, resulting in 2D supramolecular structures. The 4-pyf- ligands of 1 coordinate to the Hg(II ions through one pyridyl and one adjacent amine nitrogen atoms and the 4-Hpyf ligands of 2 and 3 coordinate to the Hg(II ions through two pyridyl nitrogen atoms, resulting in new bidentate binding modes. Complexes 1–3 provide a unique opportunity to envisage the effect of the halide anions of the starting Hg(II salts on folding and unfolding the Hg(II coordination polymers. Density function theory (DFT calculation indicates that the emission of 1 is due to intraligand π→π * charge transfer between two different 4-pyf- ligands, whereas those of 2 and 3 can be ascribed to the charge transfer from non-bonding p-type orbitals of the halide anions to π * orbitals of the 4-pyf- ligands (n→π *. The gas sorption properties of the desolvated product of 1 are compared with the Cu analogues to show that the nature of the counteranion and the solvent-accessible volume are important in determining their adsorption capability.

  5. 40 CFR 75.81 - Monitoring of Hg mass emissions and heat input at the unit level.

    Science.gov (United States)

    2010-07-01

    ... cubic meter (µg/scm); and (2) A flow monitoring system; and (3) A continuous moisture monitoring system... Hg concentration monitoring system (as defined in § 72.2 of this chapter) or a sorbent trap monitoring system (as defined in § 72.2 of this chapter), to measure the mass concentration of total...

  6. Mercury concentrations and pools in four adjacent coniferous and deciduous upland forests in Beijing, China

    Science.gov (United States)

    Zhou, Jun; Wang, Zhangwei; Zhang, Xiaoshan; Gao, Yu

    2017-05-01

    Understanding of forest mercury (Hg) pools is important for quantifying the global atmospheric Hg removal. We studied gaseous elemental Hg (GEM) concentrations, litterfall Hg depositions, and pool sizes in four adjacent stands at Mount Dongling to assess Hg dynamics in the forested catchment and the potential of Hg release during wildfires. The average GEM concentration was 2.5 ± 0.5 ng m-3, about 1.5 times of the background levels in the Northern Hemisphere. In all four stands, Hg concentrations increase in the following order: bole wood < branch/twig < bark < mineral soil < needles/leaves < litterfall < Oi litter < Oe soil < Oa organic soil. The Hg pools of aboveground biomass were comparable in the forests of larch, oak, and Chinese pine, which were much greater than that of mixed broadleaf stands due to lower biomass. The total Hg pools in ecosystems were similar in the four stands, because of the comparable Hg pool in the soil horizons (0-40 cm), which accounted for over 97% of the total ecosystem Hg storage in the four stands. Although Hg pools of the forest ecosystem in north China were comparable to North America and North Europe, Hg storage in forests constituted a high threat for large Hg emission pulses to the atmosphere by wildfires. The potential Hg emissions from the combustion at the four stands were ranged from 0.675 to 1.696 mg m-2.

  7. Cobalamin Concentrations in Fetal Liver Show Gender Differences: A Result from Using a High-Pressure Liquid Chromatography-Inductively Coupled Plasma Mass Spectrometry as an Ultratrace Cobalt Speciation Method.

    Science.gov (United States)

    Bosle, Janine; Goetz, Sven; Raab, Andrea; Krupp, Eva M; Scheckel, Kirk G; Lombi, Enzo; Meharg, Andrew A; Fowler, Paul A; Feldmann, Jörg

    2016-12-20

    Maternal diet and lifestyle choices may affect placental transfer of cobalamin (Cbl) to the fetus. Fetal liver concentration of Cbl reflects nutritional status with regards to vitamin B12, but at these low concentration current Cbl measurement methods lack robustness. An analytical method based on enzymatic extraction with subsequent reversed-phase-high-pressure liquid chromatography (RP-HPLC) separation and parallel ICPMS and electrospray ionization (ESI)-Orbitrap-MS to determine specifically Cbl species in liver samples of only 10-50 mg was developed using 14 pig livers. Subsequently 55 human fetal livers were analyzed. HPLC-ICPMS analysis for cobalt (Co) and Cbl gave detection limits of 0.18 ng/g and 0.88 ng/g d.m. in liver samples, respectively, with a recovery of >95%. Total Co (Cot) concentration did not reflect the amount of Cbl or vitamin B12 in the liver. Cbl bound Co contributes only 45 ± 15% to Cot. XRF mapping and μXANES analysis confirmed the occurrence of non-Cbl cobalt in pig liver hot spots indicating particular Co. No correlations of total cobalt nor Cbl with fetal weight or weeks of gestation were found for the human fetal livers. Although no gender difference could be identified for total Co concentration, female livers were significantly higher in Cbl concentration (24.1 ± 7.8 ng/g) than those from male fetuses (19.8 ± 7.1 ng/g) (p = 0.04). This HPLC-ICPMS method was able to quantify total Cot and Cbl in fetus liver, and it was sensitive and precise enough to identify this gender difference.

  8. Oriented functionalization of natural hollow kapok fiber for highly efficient removal of toxic Hg(II from aqueous solution

    Directory of Open Access Journals (Sweden)

    Feng eWang

    2016-02-01

    Full Text Available Due to hollow and tubular structure, a natural kapok fiber (KF was used as the support and orientation matrix to control the polymerization of ethyleneglycol dimethacrylate (EGDMA and N-vinylimidazole (VIM along its inherent axial surface via a facile in situ rapid polymerization reaction in air atmosphere. The as-formed KF@VIM/EGDMA composite is featured with porous surface and rich N-containing functional groups for potential application as a highly efficient adsorbent for removal of toxic Hg(II from aqueous solution. The variables affecting the adsorption capacity were studied, including monomer ratio, external pH values, contact time, and initial Hg(II concentration. The pseudo-second-order equation and two adsorption isotherms including Langmuir and Freundlich equations were applied to determine the adsorption kinetics and adsorption capacity. The results show that the as-prepared KF@VIM/EGDMA composite has a maximum adsorption capacity of 697 mg/g to Hg(II, while no appreciable adsorption capacity can be found for KF itself. Given its intrinsic large lumen, faster adsorption kinetics (45 min are also expected and observed for KF@VIM/EGDMA. After a simple filtration, this adsorbent can be directly separated from the aqueous solution and then be regenerated for multi-cyclable utilization. During the adsorption process, the chemical complexing represents the main adsorption mechanism. As a naturally renewable KF, such a simple preparation method opens a new avenue to develop highly efficient and economically viable adsorbent for removal of toxic heavy metal from aqueous solution.

  9. Synthesis of silica gel supported salicylaldehyde modified PAMAM dendrimers for the effective removal of Hg(II) from aqueous solution.

    Science.gov (United States)

    Niu, Yuzhong; Qu, Rongjun; Chen, Hou; Mu, Lei; Liu, Xiguang; Wang, Ting; Zhang, Yue; Sun, Changmei

    2014-08-15

    A series of silica gel supported salicylaldehyde modified PAMAM dendrimers (SiO2-G0-SA ∼ SiO2-G2.0-SA) were synthesized and their structures were characterized by FTIR, XRD, SEM, TGA, and porous structure analysis. The feasibility of these adsorbents for the removal of Hg(II) from aqueous solution was first described and the adsorption mechanism was proposed. The adsorption was found to depend on solution pH, the generation number of salicylaldehyde modified PAMAM dendrimers, contact time, temperature, and initial concentration. Results showed that the optimal pH was about 6 and the adsorption capacity increased with the increasing of generation number. Density functional theory (DFT) method was used to investigate the coordination geometries and the chelating mechanism. Adsorption kinetics was found to follow the pseudo-second-order model with film diffusion process as rate controlling step. Adsorption isotherms revealed that adsorption capacities increased with the increasing of temperature. Langmuir, Freundlich and Dubinin-Radushkevich (D-R) isotherm models were employed to analyze the equilibrium data. The adsorption can be well described by Langmuir isotherm model and took place by chemical mechanism. The thermodynamics properties indicated the adsorption processes were spontaneous and endothermic nature. The maximum adsorption capacity of SiO2-G0-SA, SiO2-G1.0-SA, and SiO2-G2.0-SA were 0.91, 1.52, and 1.81 mmol g(-1), respectively. The considerable higher adsorption capacity compared with other adsorbents indicates SiO2-G0-SA ∼ SiO2-G2.0-SA are favorable and useful for the uptake of Hg (II), and can be potentially used as promising adsorbents for the effective removal of Hg(II) from aqueous solution.

  10. Detoxification of Hg(II) from aqueous and enzyme media: Pristine vs. tailored calcium alginate hydrogels.

    Science.gov (United States)

    Sarkar, Kangkana; Ansari, Zarina; Sen, Kamalika

    2016-10-01

    Calcium alginate (CA) hydrogels were tailored using phenolic compounds (PC) like, thymol, morin, catechin, hesperidin, during their preparation. The PC incorporated gels show modified surface features as indicated by scanning electron microscopic images (SEM). The rheological studies show that excepting the hesperidin incorporated gels all the other kinds including calcium alginate pristine have similar mechanical strength. The hesperidine incorporated CA gels had the maximum capacity to adsorb Hg. The Freundlich adsorption isotherms show higher values of adsorption capacity for all PC incorporated CA beads than the pristine CA (PCA). The hesperidin incorporated CA gels were found to show the best adsorption condition at neutral pH and an optimum contact time of 2.5h at 25°C. Considering the possibility of ingested Hg detoxification from human alimentary tract, the hesperidin and morin incorporated CA beads were further modified through incorporation of cod liver oil as the digestion time of fat in stomach is higher. In vitro uptake capacities of Hg in pepsin and pancreatin containing enzyme media were studied with hesperidin and morin incorporated beads and their corresponding fat incorporated beads also. In the pepsin medium, there was no uptake by hesperidin and fat-hesperidin incorporated beads, which is possibly due to the higher acidity of the medium. But in pancreatin medium Hg was taken up by both kinds of beads. Morin and morin-fat incorporated beads were efficient to uptake Hg from both the pepsin and pancreatin medium. The tailored CA beads may therefore serve as efficient scaffolds to rescue Hg ingested individuals.

  11. Graphene-Rhodamine Nanoprobe for Colorimetric and Fluorimetric Hg(2+) Ion Assay.

    Science.gov (United States)

    Mohan, Anju; Neeroli Kizhakayil, Renuka

    2016-06-08

    This article reveals the first ever prospective application of Graphene-Rhodamine array (GRH) as a colorimetric and fluorimetric sensor for Hg(2+) ions. The duality of Graphene to undergo π-π and dispersive interactions with Rhodamine as well as to act as a selective adsorbent for Hg(2+) is conceptualized in this study. These interactions lead to decrease in absorbance of the dye in the presence of graphene, which is restored when kept in contact with Hg(2+) ions. The feasibility of the mechanism has been proved using EDTA as the coordinating ligand. It is noteworthy that all the optical variations occurred in the visible scale of the electromagnetic spectrum. The GRH array exhibited higher sensitivity toward the target ion with a limit of detection of 2 ppb. A perfect linear variation of absorbance at 554 nm with Hg(2+) concentration was observed in 0-1000 nM range, enabling the use of the system as a quantitative sensor for the test ion. The commendable selectivity of the array toward Hg(2+) ion has been investigated by observing the optical response in the presence of other environmentally relevant metal ions. A reversible turn off and turn on INHIBIT logic gate has been proposed which extends the scope of the designed array for the development of automated chemical systems. The fluorescence resonance energy transfer (FRET) ability of graphene paves the backbone for the fluorimetric detection. Fluorimetric strategy yielded a much lower limit of detection of 380 ppt using this probe, which makes a significant advance in trace detection of Hg(2+) ions.

  12. Elucidation of the defence mechanism in microalgae Chlorella sorokiniana under mercury exposure. Identification of Hg-phytochelatins.

    Science.gov (United States)

    Gómez-Jacinto, Verónica; García-Barrera, Tamara; Gómez-Ariza, José Luis; Garbayo-Nores, Inés; Vílchez-Lobato, Carlos

    2015-08-01

    Algae and aquatic macrophytes are capable of accumulating heavy metals up to concentrations several orders of magnitude higher than those existing in their surrounding environment. Investigation of mercury toxicology in microalgae is of great interest from ecological point of view, since they could be used as bioindicator to evaluate aquatic ecosystems affected by Hg pollution. In this study, we have performed an exposure experiment focused on the biological response of microalgae Chlorella sorokiniana, a unicellular model organism, to Hg-induced toxicity. The culture was exposed to different concentrations of this element for nine days, namely 0.5, 1, 5 and 10mg L(-1) of HgCl2 (as Hg). To achieve a better understanding of the biological mechanisms triggered by Hg-induced toxicity in this alga a metallomic approach based on SEC-ICP-ORS-MS was applied to survey biomarkers of biological response to mercury contamination in surface water. In addition, the combination of RP-HPLC-ICP-ORS-MS and RP-HPLC-ESI-QqQ-TOF-MS was applied to identify, for the first time, two Hg-binding phytochelatins in this aquatic organism, using cell extracts from microalgae exposed to inorganic mercury.

  13. Highly Selective Hg (II Ion Detection Based on Linear Blue-Shift of the Maximum Absorption Wavelength of Silver Nanoparticles

    Directory of Open Access Journals (Sweden)

    Li Ping Wu

    2012-01-01

    Full Text Available A new method of detecting Hg (II ion with silver nanoparticles (AgNPs is developed in this contribution. When Hg (II ions were added into AgNPs solution, the solution displayed rapid color change and blue shift of the maximum absorption wavelength (Δλ, which was in proportion to the Hg (II ion concentration over the range of 2.0 × 10−7–6.0 × 10−6 mol/L, with detection limit (3σ of 6.6 × 10−9 mol/L. Under the same experimental conditions, other metal ions did not interfere. Thus, we propose a rapid, simple and highly selective method for detecting Hg (II ion.

  14. Study of the analytic quality in the determinations of Cr, Fe, Mn, Cu, Zn, Pb and Hg through conventional and nuclear analytical techniques in mosses of the MATV; Estudio de la calidad analitica en las determinaciones de Cr, Fe, Mn, Cu, Zn, Pb y Hg a traves de tecnicas analiticas nucleares y convencionales en musgos de la ZMVT

    Energy Technology Data Exchange (ETDEWEB)

    Caballero S, B.

    2013-07-01

    To evaluate the environmental risks of air pollution and to facilitate the decision-making for control, is necessary to have the capacity to generate data with analytical quality. A comparison between nuclear (Neutron activation analysis and total reflection X-ray fluorescence spectrometry) and no nuclear analytical techniques (atomic absorption spectrometry and inductively coupled plasma optical emission spectrometry) for simultaneous determination of metal content (Cr, Cu, Fe, Hg, Mn, Pb and Zn) in mosses from Metropolitan Area of the Toluca Valley (MATV) was performed. Epiphytic mosses (Fabriona ciliaris and Leskea angustata) were sampled in two campaigns, 16 sites (urban, transition and natural) and were prepared for each technique. The biological certified reference materials were used for the quality control and to evaluate accuracy, precision, linearity, detection and quantification limits. Results show that nuclear analytical techniques and no nuclear applied in chemical analysis of Cr, Cu, Fe, Hg, Mn, Pb and Zn in moss from MATV are comparable and therefore all of these can potentially be used for this purpose. However, if its considered both, the performance parameters and economic/operational characteristics is widely recommended inductively coupled plasma optical emission spectrometry, conventional analytical technique, which showed the highest analytical grade quality. Also were observed spatial and temporal variations in the concentrations of Cr, Cu, Fe, Hg, Mn, Pb and Zn in mosses from MATV and was discussed its potential origin. The urban sites had the highest concentration of anthropogenic elements as Cr, Cu, Fe, Hg, Pb and Zn because are strongly impacted by roads with high vehicle traffic. (Author)

  15. Quantitative imaging of D-2-hydroxyglutarate (D2HG in selected histological tissue areas by a novel bioluminescence technique

    Directory of Open Access Journals (Sweden)

    Nadine Fabienne Voelxen

    2016-03-01

    Full Text Available AbstractPatients with malignant gliomas have a poor prognosis with average survival of less than one year. Whereas in other tumor entities the characteristics of tumor metabolism are successfully used for therapeutic approaches, such developments are very rare in brain tumors, notably in gliomas. One metabolic feature characteristic of gliomas, in particular diffuse astrocytomas and oligodendroglial tumors, is the variable content of D-2-hydroxyglutarate (D2HG, a metabolite, which was discovered first in this tumor entity. D2HG is generated in large amounts due to various gain-of–function mutations in the isocitrate dehydrogenases IDH-1 and IDH-2. Meanwhile, D2HG has been detected in several other tumor entities including intrahepatic bile-duct cancer, chondrosarcoma, acute myeloid leukemia, and angioimmunoblastic T-cell lymphoma. D2HG is barely detectable in healthy tissue (< 0.1 mM, but its concentration increases up to 35 mM in malignant tumor tissues. Consequently, the oncometabolite D2HG has gained increasing interest in the field of tumor metabolism. To facilitate its quantitative measurement without loss of spatial resolution at a microscopical level, we have developed a novel bioluminescence assay for determining D2HG in sections of snap-frozen tissue. The assay was verified independently by photometric tests and liquid chromatography / mass spectrometry (LC/MS. The novel technique allows the microscopically resolved determination of D2HG in a concentration range of 0 – 10 µmol/g tissue (wet weight. In combination with the already established bioluminescence imaging techniques for ATP, glucose, pyruvate, and lactate, the novel D2HG assay enables a comparative characterization of the metabolic profile of individual tumors in a further dimension.

  16. MicroCT vs. Hg porosimetry: microporosity in commercial stones

    Science.gov (United States)

    Fusi, N.; Martinez-Martinez, J.; Barberini, V.; Galimberti, L.

    2009-04-01

    Decay of rocks, due both to extrinsic and intrinsic factors, can show up in several different forms, such as neoformation of minerals, decohesion of grains and/or crystals, magnification of previous defects, new discontinuities, etc. Intrinsic factors include the type of material, its properties and microstructure, in particular porosity and microporosity. Extrinsic factors relate to atmosphere and usage of the material itself. Rock degradation has several heavy consequences for commercial stones, such as increase of permeability, loss of material, loss of mechanical strength; these consequences are of crucial importance for conservation of historical buildings. Aim of this study is to compare microporosity of some massive commercial stones by means of X ray microtomography, a non destructive technique, and Hg porosimetry. Nine of the most used Spanish limestones and dolostones have been analysed. The lithotypes have been chosen for their homogeneous mineralogical composition (calcitic or dolomitic) and for their low porosity; some of them have been widely used in Spain for historical buildings. Different lithotypes have been described in thin section: Ambarino (A) and Beige Serpiente (BS): brecciated dolostone, composed by microcrystalline dolomitic clasts, in a dolomitic and/or calcitic microcrystalline matrix. Amarillo Triana (AT): yellow dolomitic marble, with fissures filled up by calcite and Fe oxides. Blanco Alconera (BA): a white-pink homogeneous limestone, with veins. Blanco Tranco (BT): a homogeneous white calcitic marble, without any fissures and/or fractures. Crema Valencia (CV): a pinkish limestone, characterized by abundant stilolythes, filled mainly by quartz (80%) and kaolin (11%). Gris Macael (GM): a calcitic marble wiht darker and lighter beds, conferring a strong anisotropy. Rojo Cehegin (RC): a red fossiliferous limestone with white calcitic veins. Travertino Blanco (TB): a massive white calcitic travertine. Prismatic samples of about 2x1x1 cm

  17. Development of High-Performance eSWIR HgCdTe-Based Focal-Plane Arrays on Silicon Substrates

    Science.gov (United States)

    Park, J. H.; Pepping, J.; Mukhortova, A.; Ketharanathan, S.; Kodama, R.; Zhao, J.; Hansel, D.; Velicu, S.; Aqariden, F.

    2016-09-01

    We report the development of high-performance and low-cost extended short-wavelength infrared (eSWIR) focal-plane arrays (FPAs) fabricated from molecular beam epitaxial (MBE)-grown HgCdTe on Si-based substrates. High-quality n-type eSWIR HgCdTe (cutoff wavelength ˜2.68 μm at 77 K, electron carrier concentration 5.82 × 1015 cm-3) layers were grown on CdTe/Si substrates by MBE. High degrees of uniformity in composition and thickness were demonstrated over three-inch areas, and low surface defect densities (voids 9.56 × 101 cm-2, micro-defects 1.67 × 103 cm-2) were measured. This material was used to fabricate 320 × 256 format, 30 μm pitch FPAs with a planar device architecture using arsenic implantation to achieve p-type doping. The dark current density of test devices showed good uniformity between 190 K and room temperature, and high-quality eSWIR imaging from hybridized FPAs was obtained with a median dark current density of 2.63 × 10-7 A/cm2 at 193 K with a standard deviation of 1.67 × 10-7 A/cm2.

  18. Direct contamination of barley with 51Cr, 59Fe, 58Co, 65Zn, 203Hg, and 210Pb

    DEFF Research Database (Denmark)

    Aarkrog, Asker; Lippert, Jørgen Emil

    1971-01-01

    . The field loss depended on the growing rate and the development of the plants and thus varied throughout the growing period. The field loss coefficient λ was 0·054 days−1 in the first part of the period and 0·017 days−1 in the second part. If the whole growing season is considered, the loss of activity......A study of barley sprayed at six different stages of development with radionuclides of Cr, Fe, Co, Zn, Hg and Pb. The initial retention followed the equation: IR= 1—e−0·31 g.cmstaggered−1, where g is the dry weight of the herbage in a plot in grammes, and cm the height of the plants at spraying...... in per cent is about equal to the time in days from the spraying to harvest. Zn and Co showed the highest concentrations in the grain. The translocation of Cr, Pb and Hg within the plant was small. Fe was translocated to the grain as was Zn, but to a far less extent....

  19. Background concentrations of heavy metals in benthos from transboundary rivers of the Transbaikalia region, Russia.

    Science.gov (United States)

    Kuklin, Aleksei Petrovich; Matafonov, Petr Viktorovich

    2014-02-01

    The concentrations (mg/kg dry weight) of Cu, Zn, As, Cd, Hg, and Pb were measured in benthic macroalgae and invertebrates collected in the upper transboundary tributaries of the Onon River, Transbaikalia, Russia. The background concentration ranges in Cladophora fracta, Ulothrix zonata and Zygnemataceae were: 6.4-9.1 for Cu, 27.2-73.1 for Zn, 0.4-0.9 for Cd, 6.7-35.3 for As, 0.01-0.02 for Hg, and 1.9-4.3 for Pb. In Brachycentrus americanus and Lymnaea media the concentration ranges were: 9.0-25.5 for Cu, 21.4-96.0 for Zn, 0.1-0.3 for Cd, 1.7-5.6 for As, 0.004-0.02 for Hg, and 0.4-2.2 for Pb. The concentrations of Cu, Zn, Pb, and Hg were consistent with data for uncontaminated areas. Under contamination conditions the concentrations in C. fracta were: 938 for Zn, 513 for Pb, and 9.5 for Cd; in Lymnaea media were: 46.8 for Cu, 176 for Zn, 52.3 for Pb, and 3.0 for Cd. All the organisms showed a common response to contamination, and consequently can be used as biomonitors of contamination by heavy metals.

  20. Simultaneous removal of Hg0 and HCN from the yellow phosphorus tail gas

    Science.gov (United States)

    Li, Yanan; Wang, Xueqian

    2017-08-01

    Transition metal oxides supported on TiO2 were synthesized by a sol-gel method and implied to simultaneous removal of Hg0 and HCN under low temperature and micro-oxygen conditions. The results show that catalysts that modified by manganese oxide have superior catalytic oxidation activity for both the removal of elemental mercury (Hg0) and HCN. Furthermore, the O2 can promote in the removal reaction process. The fresh and used catalysts were characterized by BET and XPS. The catalyst characterization indicated that the catalyst possessed a large specific surface area and the chemisorbed oxygen participated in the catalytic oxidation reaction. The MnOx/TiO2 catalyst was demonstrated to a good catalytic oxidant for simultaneous removal of elemental mercury (Hg0) and HCN under micro-oxygen conditions.

  1. Turn-On Fluorescent Chemosensor for Hg2+ Based on Multivalent Rhodamine Ligands

    Directory of Open Access Journals (Sweden)

    Xuemei Wang

    2012-12-01

    Full Text Available Rhodamine-based fluorescent chemosensors 1 and 2 exhibit selective fluorescence enhancement to Fe3+ and Hg2+ over other metal ions at 580 nm in CH3CN/H2O (3/1, v/v solution. Bis(rhodamine chemosensor 1, under optimized conditions (CH3CN/HEPES buffer (0.02 M, pH = 7.0 (95/5, v/v, shows a high selectivity and sensitivity to Hg2+, with a linear working range of 0–50 μM, a wide pH span of 4–10, and a detection limit of 0.4 μM Hg2+.

  2. Textured α-HgI2 ceramics for sensitive X-ray detection

    Science.gov (United States)

    Rault, Mathieu; Binet, Laurent; Gourier, Didier; Wallez, Gilles; Ponpon, Jean-Pierre; Biava, Dominique; Inglese, Jean-Marc; Barboux, Philippe

    2016-02-01

    In the prospect of manufacturing ionizing radiation detectors, dense ceramics of α-HgI2 with a strong preferred orientation were elaborated. X-ray diffraction showed that most crystallites exhibited their crystal c-axis perpendicular to the ceramic plane, which should be favorable for optimum electrical transport properties. Dark current densities about 2 nA mm-2 (under 0.2 V μm-1 bias) were measured and were shown to arise mostly from the release of carriers from trap defects (Poole-Frenkel emission). The X-ray sensitivity ≈1600 nC mGy-1 cm-2 and the μτ value ≈ 3 × 10-5 cm2 V-1 were comparable to those of other forms of polycrystalline HgI2. The HgI2 ceramics also exhibited a perfectly linear response as a function of the X-ray dose.

  3. Highly Sensitive Fluorescence Probe Based on Functional SBA-15 for Selective Detection of Hg2+

    Directory of Open Access Journals (Sweden)

    Wang Xiaoyu

    2010-01-01

    Full Text Available Abstract An inorganic–organic hybrid fluorescence chemosensor (DA/SBA-15 was prepared by covalent immobilization of a dansylamide derivative into the channels of mesoporous silica material SBA-15 via (3-aminopropyltriethoxysilane (APTES groups. The primary hexagonally ordered mesoporous structure of SBA-15 was preserved after the grafting procedure. Fluorescence characterization shows that the obtained inorganic–organic hybrid composite is highly selective and sensitive to Hg2+ detection, suggesting the possibility for real-time qualitative or quantitative detection of Hg2+ and the convenience for potential application in toxicology and environmental science.

  4. Thymine rich-DNA sensing probe for Hg2+detection%富含胸腺嘧啶DNA传感探针对水体中Hg2+的检测

    Institute of Scientific and Technical Information of China (English)

    肖慧; 杨婵; 赵珍; 家意; 刘凤; 周银香徐思嘉; 许庭琦; 何婧琳; 曹忠

    2015-01-01

    Mercury is one of the most toxic heavy metals that present in environment. Therefore, a sensitive and se-lective sensing system for mercury detection is highly demanded. This paper described a fluorescent sensor using a label free Hg2+specific DNA probe(43mer-T18Stem) and an intercalation dye SYBR Green I(SG). As is known to all, Hg2+can specifically interact with thymine base to form strong and stable thymine-Hg2+-thymine (T-Hg2+-T) com-plexes. This specific T-Hg2+-T formation affected the hybridization of the Hg2+specific probe and the intercalation of SG. The proposed sensor showed a linear response in the range of 4.000×10-7~2.000×10-6 mol/L of Hg2+with a detec-tion limit of 3.900×10-8 mol/L. The sensor revealed good recovery rates from 98.72%to 102.8%, indicating that the sensing system can be utilized for the determination of Hg2+in real samples.%该工作以富含大量胸腺嘧啶(Thymine,T)核酸单链为识别分子,SYBR Green I (SG)为荧光基团,建立了一种简单、灵敏的荧光增强法检测Hg2+。由于T-Hg2+-T键的形成,富T单链自我折叠或者两两配对形成双链DNA结构,当溶液中的SG嵌入DNA双链中时,SG荧光强度显著增强。实验结果表明,SG荧光强度随着Hg2+浓度的增加而增加。在最优实验条件下,SG的荧光强度与Hg2+的浓度在4.000×10-7~2.000×10-6 mol/L范围内呈线性关系,检出限为3.900×10-8 mol/L。该方法在含5.0%湘江水实际样品中获得的回收率为98.72%~104.5%,因此该传感器可用于实际湘江水样品中Hg2+的测量。

  5. Toxicity and Traces of Hg, Pb and Cd in the Hepatopancreas, Gills and Muscles of Perna viridis from Jakarta Bay, Indonesia.

    Science.gov (United States)

    Irnidayanti, Y

    2015-02-01

    Heavy metals contamination on the coast of Jakarta Bay has led to the level of pollution and can cause toxicity to organisms living in the sea, i.e., green mussels. Green mussels have the ability to detoxify metals entering their bodies. Their ability to accumulate metals is higher than other aquatic animals. This is due to their sedentary life which prevents them from avoiding the effects of pollution and their high tolerance to certain metals. The high concentration of metal content would be toxic to the cell because metal ions can act as oxidants and bind to organic and protein molecules. The results of the study showed that traces of heavy metals were detected in the hepatopancreas, gills, muscles and gonads organs of the mussels living in the waters of Muara Angke. Lead (Pb) and cadmium (Cd) were found in all four organs, while mercury (Hg) was not detected in the muscles. Traces of Hg and Cd were not detected in hepatopancreas, gills, muscles and gonads of green mussels in Panimbang, while Pb was detected by 0.00 1 in the male gonads and 0.01 in hepatopancreas. The concentration of Pb in the male gonads are still below the acceptable limit and concentration of Pb in the hepatopancreas is relatively equivalent to the acceptable limit. Metal detection in the organs above shows that the Muara Angke waters tend to be polluted and have an impact on the mussels weight loss as a result of heavy metal toxicity.

  6. Biogeochemical factors affecting the distribution, speciation, and transport of Hg species in the Deûle and Lys Rivers (Northern France).

    Science.gov (United States)

    Daye, Mirna; Kadlecova, Milada; Ouddane, Baghdad

    2015-02-01

    The Deûle River is a highly polluted River by heavy metals caused by the historical discharges of ore minerals from the former ore smelter "Metaleurop." The potential mercury (Hg) pollution in the Deûle River implicates the importance of Hg distribution study in the river. As well as to configure the different biogeochemical factors that control the distribution and the potential transport of Hg to distant places. Four different sites were studied as follows: D-A (Deûle River, a site located upstream the river), D-B (Deûle River, a site located near a Zn, Pb, Cu, and Ni smelter that closed in 2003), L-C (Lys River, a site located upstream the confluence of the Deûle River with Lys River), and L-D (downstream the rivers confluence). Different Hg analyses were performed including total mercury in sediment (HgTS), methylmercury (MeHg) in sediment, total mercury in pore water (HgTPW), total mercury in surface water (HgTD), and total suspended particulate Hg in water (HgTP). HgTS decreases downstream from the Deûle River sites with a mean value of 11 ± 0.34 mg/kg to Lys River site (L-D) with a mean value of 0.53 ± 0.02 mg/kg at the confluence. The unaffected side of the Lys River, localized before the confluence (L-C), is characterized by low HgTS of an average value of 0.042 ± 0.003 mg/kg and high % MeHg reaching 4.2 %. Whereas, the highly contaminated Deûle sites are designated by low % MeHg with an average value of 0.053 %. Low pristine environments like that found in L-C site with more favorable biogeochemical conditions of lower concentrations of HgTS, sulfides, and Corg host more active biotic methylation than that of the highly polluted Deûle sites with high concentrations of HgTS and sulfides concentrations. Methylation in D-B (the closet site to Metaleurop smelter) is an old and recent methylation activity that has contributed to MeHg accumulation in the sediments as opposed to the exclusive recent events of methylation in Lys sites. MeHg

  7. Thermodynamics of the complexation of Hg(II) by cysteinyl peptide ligands using isothermal titration calorimetry

    Energy Technology Data Exchange (ETDEWEB)

    Ngu-Schwemlein, Maria, E-mail: Schwemleinmn@wssu.edu [Department of Chemistry, Winston-Salem State University, Winston-Salem, NC 27110 (United States); Merle, John K.; Healy, Patrick; Schwemlein, Stefanie; Rhodes, Sade [Department of Chemistry, Winston-Salem State University, Winston-Salem, NC 27110 (United States)

    2009-12-10

    The present study was undertaken to better understand the complexation of mercury (II) by cysteine, histidine, tryptophan, and their di- and tri-peptides. Their mercury (II) binding affinities and associated thermodynamic parameters are evaluated by isothermal titration calorimetry. Cysteine S-donor atoms form the strongest complexes, which can be attributed to a more exothermic Hg-S soft acid and soft base interaction. These thiol S-donor peptide ligands show two sequential binding for mercury (II). Their stability constants for the first binding (10{sup 8} M{sup -1} to >10{sup 10} M{sup -1}) are largely due to favorable contribution of the enthalpy term to the free energy of complexation. As more mercury (II) ions are added, this enthalpy contribution decreases and the free energy of the second binding (10{sup 5} M{sup -1} to 10{sup 6} M{sup -1}) is partially compensated by the entropy term. The dependency of the fluorescence intensity for these peptides on mercury (II) concentration shows two different Stern-Volmer plots, which corroborates the calorimetric data and supports the formation of two types of stable complexes.

  8. Concentrations of 17 elements, including mercury, in the tissues, food and abiotic environment of Arctic shorebirds

    Energy Technology Data Exchange (ETDEWEB)

    Hargreaves, Anna L., E-mail: alhargreaves@gmail.com [Calgary Zoo, Centre for Conservation Research, 1300 Zoo Rd NE, Calgary, AB, T2E 7V6 (Canada); Whiteside, Douglas P. [Calgary Zoo, Animal Health Centre, 1300 Zoo Rd NE, Calgary, AB, T2E 7V6 (Canada); University of Calgary, Department of Ecosystem and Public Health, Faculty of Veterinary Medicine, 2500 University Dr. NW, Calgary, AB, T2N 1N4 (Canada); Gilchrist, Grant [Carleton University, National Wildlife Research Centre, Ottawa, ON, KIA OH3 (Canada)

    2011-09-01

    Exposure to contaminants is one hypothesis proposed to explain the global decline in shorebirds, and is also an increasing concern in the Arctic. We assessed potential contaminants (As, Be, Cd, Co, Cr, Cu, Fe, Hg, Mn, Mo, Ni, Pb, Sb, Se, Tl, V, and Zn) at a shorebird breeding site in Nunavut, Canada. We compared element levels in soil, invertebrates and shorebird blood to assess evidence for bioconcentration and biomagnification within the Arctic-based food chain. We tested whether elements in blood, feathers and eggs of six shorebird species (Pluvialis squatarola, Calidris alpina, C. fuscicollis, Phalaropus fulicarius, Charadrius semipalmatus, and Arenaria interpres) were related to fitness endpoints: adult body condition, blood-parasite load, egg size, eggshell thickness, nest duration, and hatching success. To facilitate comparison to other sites, we summarise the published data on toxic metals in shorebird blood and egg contents. Element concentrations and invertebrate composition differed strongly among habitats, and habitat use and element concentrations differed among shorebird species. Hg, Se, Cd, Cu, and Zn bioconcentrated from soil to invertebrates, and Hg, Se and Fe biomagnified from invertebrates to shorebird blood. As, Ni, Pb, Co and Mn showed significant biodilution from soil to invertebrates to shorebirds. Soil element levels were within Canadian guidelines, and invertebrate Hg levels were below dietary levels suggested for the protection of wildlife. However, maximum Hg in blood and eggs approached levels associated with toxicological effects and Hg-pollution in other bird species. Parental blood-Hg was negatively related to egg volume, although the relationship varied among species. No other elements approached established toxicological thresholds. In conclusion, whereas we found little evidence that exposure to elements at this site is leading to the declines of the species studied, Hg, as found elsewhere in the Canadian Arctic, is of potential

  9. 以葡萄糖为碳源的荧光碳点构建 Hg 2+的检测方法%On Novel Fluorescent Method for Detections of Hg2+ Based on Carbon Dots

    Institute of Scientific and Technical Information of China (English)

    杨文雨; 罗凡雨; 朱姗姗; 廖洪波; 杨晓明

    2014-01-01

    首次以葡萄糖为碳源制得一种新型碳点,其具有较高的荧光强度.在此碳点中加入 Hg2+后,碳点荧光强度显著降低,同时对其他金属离子无响应.为使Hg2+对碳点荧光的猝灭作用效果最佳,对检测过程的各个条件进行优化,在优化的最佳条件下,Hg2+与碳点荧光强度的变化呈良好的线性关系:ΔF=919.04+130.41 log CQ ,线性回归相关系数 R2=0.9888,检出限为1.010-7 mol/L .基于新型碳点成功建立了一种快速、有效检测 Hg2+的新方法.%Glucose ,as carbon source ,has first been successfully employed to synthesize carbon dots ,w hich implies high fluorescence .Subsequently ,the introduction of mercury ions rather than other metal ions ob-viously leads to the fluorescence quenching of carbon dots .To further explore the optimized conditions to-wards determining mercury ions ,kinds of experiments have been performed .Under the optimized condi-tions ,the relative fluorescence intensity of carbon dots and the concentration of mercury ions show a satis-factory linear relationship :F=919 .04+130 .41log CQ ,with a correlation coefficient (R2 ) of 0 .9888 and a detection limit of 1 .0 10-7 mol/L ,suggesting the practicability of this proposed method .Finally ,a fast , novel method for assaying mercury ions has been well established in this study .

  10. Effects of an Applied Magnetic Field on the Directional Solidification of Hg(1-x)Zn(x)Se Alloys

    Science.gov (United States)

    Cobb, S. D.; Lehoczky, S. L.; Szofran, F. R.; Jones, K. S.

    1999-01-01

    Directionally solidified Hg(0.9)Zn(0.1)Se alloys were studied as an alternative to HgCdTe for the detection of electromagnetic radiation because of predicted improvements in lattice stability. Several boules were grown using a modified Bridgman-Stockbarger method and in an applied magnetic field. Axial compositional profiles showed mass transfer was primarily diffusion controlled. Radial compositional variations were greatly reduced when solidification occurred in an applied magnetic field. Microstructural characteristics and dislocation etch pit densities were greatly improved over HgTe based alloys. The extreme importance of processing conditions on defect generation was illustrated by comparing ampoule configurations and thermal profiles.

  11. Inorganic arsenic - SPE HG-AAS method for RICE tested in-house and collaboratively

    DEFF Research Database (Denmark)

    Rasmussen, Rie Romme; Qian, Yiting; Sloth, Jens Jørgen

    As) and the methylated species monomethylarsonic acid (MA) and dimethylarsinic acid (DMA). Dietary intake of iAs is of special concern due to its carcinogenicity to humans, whereas DMA and MA are considered of less toxicological importance. Rice grains and rice-based products are staple foods in many countries...... spectrometry (ICP-MS) analysis. The SPE separation step was tested collaboratively, where the laboratories (N=10) used either HG-AAS or ICPMS for iAs determination in a wholemeal rice powder. The trial gave satisfactory results (HorRat value of 1.6) and did not reveal significant difference (t test, p>0.......05) between HG-AAS and ICP-MS quantification. The iAs concentration in 36 rice samples purchased on the Danish retail market varied (0.03–0.60 mg/kg), with the highest concentration found in a red rice sample....

  12. Synthesis and characterization of La11+xHg45-x and RE11Hg44.5 (RE = Nd, Sm) as hettotypes of the Sm11Cd45 structure type

    Science.gov (United States)

    Tambornino, Frank; Schwärzer, Kuno; Hoch, Constantin

    2016-10-01

    The mercury-rich amalgams La11+xHg45-x and RE11Hg44.5 (space group F4bar3m (No. 216), La11+xHg45-x : a = 21.9342(19) Å, RE = Nd: a = 21.7384(14) Å; RE = Sm: a = 21.6555(4) Å), were synthesized by dissolving the respective rare earth metals in a mercury surplus and subsequently distilling off the excess. The compounds were characterized by single crystal and powder X-ray methods together with ab-initio band structure calculations. Both crystal structures deviate significantly and in different ways from their common aristotype, the Sm11Cd45 structure type. In La11+xHg45-x (x = 0.7(1)) two crystallographic sites show mixed occupancy, whereas in RE11Hg44.5 one of the Hg positions is fully unoccupied. Their band structures exhibit typical broad Hg d states at low energies, and a strong mixing of s and p states indicates a mercury sublattice with high connectivity.

  13. The effects of sediment and mercury mobilization in the South Yuba River and Humbug Creek Confluence Area, Nevada County, California: Concentrations, speciation, and environmental fate-Part 1: Field characterization

    Science.gov (United States)

    Fleck, Jacob A.; Alpers, Charles N.; Marvin-DiPasquale, Mark; Hothem, Roger L.; Wright, Scott A.; Ellett, Kevin; Beaulieu, Elizabeth; Agee, Jennifer L.; Kakouros, Evangelos; Kieu, Le H.; Eberl, Dennis D.; Blum, Alex E.; May, Jason T.

    2011-01-01

    size distribution, Hg speciation, and mineralogy of bed and suspended sediment; 3) a determination of the past and current sources of sediment in the study area; 4) an assessment of Hg bioaccumulation in the local invertebrate population; and 5) a comparison of potential Hg transport caused 2 by natural storm disturbances with potential Hg mobilization caused by suction dredging as a method of Hg removal at the study site. The laboratory component of the study assessed the potential influenc of the disturbance of Hg-contaminated sediment through experiments designed to simulate in-stream transport, deposition, and potential methylation of Hg, described in a companion report (see Marvin-DiPasquale and others, 2010). Results of the field studies indicate that the fine-grained fraction (silt-clay, less than 0.063 millimeters) contains the greatest concentration of Hg in contaminated sediment. Because the fine-grained fraction is the most susceptible to long-range fluvial transport, disturbance of Hg-contaminated sediment is likely to increase the concentration and load of Hg in downstream waters. The preliminary, small-scale dredge test showed an increase in the concentration of fine particles and Hg in the water column caused by the dredge activity, despite relatively low concentrations of fine particles and Hg (about 300 nanograms per gram) at the dredge site. Characterization of sediment from two test pits and other sites in the vicinity of the confluence of the South Yuba River and Humbug Creek revealed a highly variable distribution of fine- and coarse-grained sediment. The highest levels of Hg contamination (up to 14,000 ng/g) were associated with the fine-grained fraction of sediment from the bedrock contact zone of Pit 2, a horizon which also yielded grains of gold and gold-Hg amalgam. A closed-circuit tank experiment with a venturi dredge at the base of Pit 1, in a gravel bar within the South Yuba River, resulted in fine-grained suspended sediment remaining in

  14. Heavy metal tolerance (Cr, Ag and Hg in bacteria isolated from sewage

    Directory of Open Access Journals (Sweden)

    Agostinho A. de Lima e Silva

    2012-12-01

    Full Text Available Samples of sewage from a university hospital and a chemistry technical school were analysed for the percentage of bacterial tolerance to chromium (Cr, silver (Ag and mercury (Hg. Additionally, we investigated the effect of these metals on pigmentation and on some enzymatic activities of the metal tolerant strains isolated, as well as antimicrobial resistance in some metal tolerant Enterobacteriaceae strains. Tolerance to Cr was observed mainly in Gram positive bacteria while in the case of Ag and Hg the tolerant bacteria were predominately Gram negative. Hg was the metal for which the percentage of tolerance was significantly higher, especially in samples from the hospital sewage (4.1%. Mercury also had the most discernible effect on color of the colonies. Considering the effect of metals on the respiratory enzymes, one strain of Ag-tolerantBacillus sp. and one of Hg-tolerant P. aeruginosa were unable to produce oxidase in the presence of Ag and Hg, respectively, while the expression of gelatinase was largely inhibited in various Gram negative strains (66% by Cr. Drug resistance in Hg-tolerant Enterobacteriaceae strains isolated from the university hospital sewage was greater than 80%, with prevalence of multiple resistance, while the Ag-tolerant strains from the same source showed about 34% of resistance, with the predominance of mono-resistance. Our results showed that, despite the ability of metal tolerant strains to survive and grow in the presence of these elements, the interactions with these metals may result in metabolic or phisiological changes in this group of bacteria.

  15. Heavy metal tolerance (Cr, Ag AND Hg) in bacteria isolated from sewage

    Science.gov (United States)

    Lima de Silva, Agostinho A.; de Carvalho, Márcia A. Ribeiro; de Souza, Sérgio A. L; Dias, Patrícia M. Teixeira; da Silva Filho, Renato G.; de Meirelles Saramago, Carmen S.; de Melo Bento, Cleonice A.; Hofer, Ernesto

    2012-01-01

    Samples of sewage from a university hospital and a chemistry technical school were analysed for the percentage of bacterial tolerance to chromium (Cr), silver (Ag) and mercury (Hg). Additionally, we investigated the effect of these metals on pigmentation and on some enzymatic activities of the metal tolerant strains isolated, as well as antimicrobial resistance in some metal tolerant Enterobacteriaceae strains. Tolerance to Cr was observed mainly in Gram positive bacteria while in the case of Ag and Hg the tolerant bacteria were predominately Gram negative. Hg was the metal for which the percentage of tolerance was significantly higher, especially in samples from the hospital sewage (4.1%). Mercury also had the most discernible effect on color of the colonies. Considering the effect of metals on the respiratory enzymes, one strain of Ag-tolerant Bacillus sp. and one of Hg-tolerant P. aeruginosa were unable to produce oxidase in the presence of Ag and Hg, respectively, while the expression of gelatinase was largely inhibited in various Gram negative strains (66% by Cr). Drug resistance in Hg-tolerant Enterobacteriaceae strains isolated from the university hospital sewage was greater than 80%, with prevalence of multiple resistance, while the Ag-tolerant strains from the same source showed about 34% of resistance, with the predominance of mono-resistance. Our results showed that, despite the ability of metal tolerant strains to survive and grow in the presence of these elements, the interactions with these metals may result in metabolic or phisiological changes in this group of bacteria. PMID:24031994

  16. Determination of MeHg sources to fish in the St. Louis River, MN, USA, using Hg stable isotopes

    Science.gov (United States)

    Mercury contamination in the Great Lakes region has become a prevalent concern due to elevated methylmercury (MeHg) levels in fish. While atmospheric deposition of Hg is ubiquitous, releases from legacy point-sources give rise to numerous Areas of Concern (AOCs) across the Great ...

  17. Catalytic oxidation of Hg(0) by MnOx-CeO2/γ-Al2O3 catalyst at low temperatures.

    Science.gov (United States)

    Wang, Pengying; Su, Sheng; Xiang, Jun; You, Huawei; Cao, Fan; Sun, Lushi; Hu, Song; Zhang, Yun

    2014-04-01

    MnOx-CeO2/γ-Al2O3 (MnCe) selective catalytic reduction (SCR) catalysts prepared by sol-gel method were employed for low-temperature Hg(0) oxidation on a fixed-bed experimental setup. BET, XRD and XPS were used to characterize the catalysts. MnCe catalysts exhibited high Hg(0) oxidation activity at low temperatures (100-250 °C) under the simulated flue gas (O2, CO2, NO, SO2, HCl, H2O and balanced with N2). Only a small decrease in mercury oxidation was observed in the presence of 1200 ppm SO2, which proved that the addition of Ce helped resist SO2 poisoning. An enhancing effect of NO was observed due to the formation of multi-activity NOx species. The presence of HCl alone had excellent Hg(0) oxidation ability, while 10 ppm HCl plus 5% O2 further increased Hg(0) oxidation efficiency to 100%. Hg(0) oxidation on the MnCe catalyst surface followed the Langmiur-Hinshelwood mechanism, where reactions took place between the adsorbed active species and adsorbed Hg(0) to form Hg(2+). NH3 competed with Hg(0) for active sites on the catalyst surface, hence inhibiting Hg(0) oxidation. This study shows the feasibility of a single-step process integrating low-temperature SCR and Hg(0) oxidation from the coal combustion flue gas.

  18. Thermal Cycle Annealing and its Application to Arsenic-Ion Implanted HgCdTe

    Science.gov (United States)

    2014-06-26

    doping profile, as shown in Figure 3. The TCA treatment on the unimplanted epilayers showed an exponential defect reduction proportional to the...Chamonal, P. Castelein, J. Zanatta, M. Tchagaspanian, A. Papon, J. Barnes, F. Henry, S. Gout , G. Bourgeois, C. Pautet and P. Fougeres, "HgCdTe FPAs

  19. The accumulation of heavy metals (Cd, Pb, Hg, Cr) and their state in ...

    African Journals Online (AJOL)

    ONOS

    2010-01-25

    Jan 25, 2010 ... metals (Cd, Pb, Hg and Cr) in the water and plankton of Beysehir and ... In addition, heavy metals show harmful effects ... in laboratory for a period of time for evaporation of water. ...... biochemical effects in an estuarine teleost.

  20. Ni^2+、Hg^2+对果蝇生长发育的影响%The Effects of Ni2+ and Hg2+ on the Growth and Development of Drosophila Melanogaster

    Institute of Scientific and Technical Information of China (English)

    曾秀存

    2012-01-01

    Drosophila melanogasters were cultured in the media with the different concentrations of nickelous nitrate and the mercuric chloride (0.5μg/mL, 5μ/mL, 151μg/mL, 301a, g/mL). The effect of nickelous nitrate and the mercuric chloride on its Male-female sex ratio of adults insect, survival rate of adult insect, the weight of adult insect. The results showed that with nickel, mercury concentration and generation of extended treatment, nickel ions on the Drosophila male and female sex ratio, survival rate and weight were less than mercury ions; High concentrations of mercury ions significantly reduce the development of male Drosophila melanogaster, reduce the survival rate of Drosophila, and restrain weight gain of Drosophila; Mercury ions cause severer injury on compared with nickel ions. Drosophila,%以黑体红眼长翅果蝇(Drosophilamelanogaster)为材料,培养基用硝酸镍和氯化汞染毒(浓度为0.5μg/mL、51MmL、151a,g/mL、30μg/mL)后对果蝇后代的雌雄性比、存活率,体重的影响进行研究.结果表明:随着镍、汞浓度的增加和处理世代的增加,Ni^2+对果蝇雌雄性比、存活率和体重的毒害较Hg^2+轻;高浓度的Hg^2+严重抑制雄果蝇的发育;降低果蝇的存活率,抑制果蝇体重的增加.这表明Hg^2+对果蝇的毒害要比Ni“重.

  1. Comparative proteomic study and functional analysis of translationally controlled tumor protein in rice roots under Hg2+ stress

    Institute of Scientific and Technical Information of China (English)

    Feijuan Wang; Yongshen Shang; Ling Yang; Cheng Zhu

    2012-01-01

    So far,very little is known about mercury stress-induced intercellular metabolic changes in rice roots at the proteome level.To investigate the response of rice roots to mercury stress,changes in protein expression in rice roots were analyzed using a comparative proteomics approach.Six-leaf stage rice seedlings were treated with 50 μmol/L HgCl2 for 3 hr; 29 protein spots showed a significant changes in abundance under stress when compared with the Hg2+-tolerant rice mutant and wild type (Zhonghua 11).Furthermore,all these protein spots were identified by mass spectrometry to match 27 diverse protein species.The identified proteins were involved in several processes,including stress response,redox homeostasis,signal transduction,regulation and metabolism; some were found to be cellular structure proteins and a few were unknown.Among the up-regulated proteins,OsTCTP (translationally controlled tumor protein) was chosen to perform hetereologous expression in yeast which was presumed to participate in the Hg2+ tolerance of rice,providing evidence for its role in alleviating Hg2+ damage.Among the many tests,we found that OsTCTP-overexpressed yeast strains were more resistant to Hg2+ than wild-type yeast.Thus,we propose that OsTCTP contributes to Hg2+ resistance.Here we present,for the first time,the functional characterization of OsTCTP in connection with Hg2+ stress in plants.

  2. Evaluation on the stability of Hg in ABS disk CRM during measurements by wavelength dispersive X-ray fluorescence spectrometry.

    Science.gov (United States)

    Ohata, Masaki; Kidokoro, Toshihiro; Hioki, Akiharu

    2012-01-01

    The stability of Hg in an acrylonitrile-butadiene-styrene disk certified reference material (ABS disk CRM, NMIJ CRM 8116-a) during measurements by wavelength dispersion X-ray fluorescence (WD-XRF) analysis was evaluated in this study. The XRF intensities of Hg (L(α)) and Pb (L(α)) as well as the XRF intensity ratios of Hg (L(α))/Pb (L(α)) observed under different X-ray tube current conditions as well as their irradiation time were examined to evaluate the stability of Hg in the ABS disk CRM. The observed XRF intensities and the XRF intensity ratios for up to 32 h of measurements under 80 mA of X-ray tube current condition were constant, even though the surface of the ABS disk CRM was charred by the X-ray irradiation with high current for a long time. Moreover, the measurements on Hg and Pb in the charred disks by an energy dispersive XRF (ED-XRF) spectrometer showed constant XRF intensity ratios of Hg (L(α))/Pb (L(α)). From these results, Hg in the ABS disk CRM was evaluated to be sufficiently stable for XRF analysis.

  3. Papillary thyroid carcinoma shows elevated levels of 2-hydroxyglutarate.

    Science.gov (United States)

    Rakheja, Dinesh; Boriack, Richard L; Mitui, Midori; Khokhar, Shama; Holt, Shelby A; Kapur, Payal

    2011-04-01

    Elevated levels of D: -2-hydroxyglutarate (D: -2-HG) occur in gliomas and myeloid leukemias associated with mutations of IDH1 and IDH2. L: -2-Hydroxyglutaric aciduria, an inherited metabolic disorder, predisposes to brain tumors. Therefore, we asked whether sporadic cancers, without IDH1 or IDH2 hot-spot mutations, show elevated 2-hydroxyglutarate levels. We retrieved 15 pairs of frozen papillary thyroid carcinoma (PTC) and adjacent non-neoplastic thyroid, and 14 pairs of hyperplastic nodule (HN) and adjacent non-hyperplastic thyroid. In all lesions, exon 4 sequencing confirmed the absence of known mutations of IDH1 and IDH2. We measured 2-hydroxyglutarate by liquid chromatography-tandem mass spectrometry. Compared to normal thyroid, PTCs had significantly higher D: -2-HG and L: -2-hydroxyglutarate (L: -2-HG) levels, and compared to HNs, PTCs had significantly higher D: -2-HG levels. D: -2-HG/L: -2-HG levels were not significantly different between HNs and normal thyroid. Further studies should clarify if elevated 2-hydroxyglutarate in PTC may be useful as cancer biomarker and evaluate the role of 2-hydroxyglutarate in cancer biology.

  4. Lower than expected mercury concentration in piscivorous African sharptooth catfish Clarias gariepinus (Burchell)

    Energy Technology Data Exchange (ETDEWEB)

    Desta, Zerihun [Norwegian University of Life Sciences, Department of Ecology and Natural Resource Management, P.O. Box 5003, N-1432, As (Norway) and Awassa University, Faculty of Natural Sciences, Department of Applied Biology, P.O. Box 5, Awassa (Ethiopia)]. E-mail: zerihun.desta@gmail.com; Borgstrom, Reidar [Norwegian University of Life Sciences, Department of Ecology and Natural Resource Management, P.O. Box 5003, N-1432, As (Norway); Rosseland, Bjorn Olav [Norwegian University of Life Sciences, Department of Ecology and Natural Resource Management, P.O. Box 5003, N-1432, As (Norway); Dadebo, Elias [Awassa University, Faculty of Natural Sciences, Department of Applied Biology, P.O. Box 5, Awassa (Ethiopia)

    2007-04-15

    The concentrations of total mercury (THg), stable isotopes of nitrogen ({delta}{sup 15}N) and carbon ({delta}{sup 13}C), and the diet of the African sharptooth catfish Clarias gariepinus in Lake Awassa, Ethiopia, were studied from January 2003 to February 2004. Values of the {delta}{sup 15}N were used as an index of trophic position in four length groups and compared to actual stomach contents. The diet of C. gariepinus within the length range of 201-600 mm L {sub T} mainly consisted of the small barb Barbus paludinosus, aquatic insects, and mollusks. The proportion of fish prey in the diet was 60% by volume, irrespective of fish size. The differences in {delta}{sup 15}N values of individuals within and between length classes were less than 3 per mille , and were not significantly related to total length, showing the similarity in trophic niche of the different sizes, which corresponded to recorded stomach contents. Mercury concentrations were in the range of 0.002-0.154 mg kg{sup -1} ww, and had no significant relationship to total length. Hence, even large specimens of C. gariepinus have Hg values below the WHO threshold of 0.2 mg kg{sup -1} ww. The slope of the regression line between log [Hg] and {delta}{sup 15}N was small, 0.06, indicating the absence of trophic shifts and biomagnification of Hg in larger specimens in our samples. The low Hg concentrations in C. gariepinus compared to the Hg concentrations in other piscivorous fish species in Lake Awassa, such as Barbus intermedius and B. paludinosus, may be due to its dependence on invertebrate preys at small size, diet switching towards low Hg prey fish at larger size, and growth biodilution owing to higher growth rate.

  5. Mother-embryo isotope (δ15N, δ13C) fractionation and mercury (Hg) transfer in aplacental deep-water sharks

    OpenAIRE

    Le Bourg, Baptiste; Kiszka, Jeremy; Bustamante, Paco

    2014-01-01

    International audience; Stable carbon (δ13C) and nitrogen (δ15N) isotopic values and total mercury (Hg) concentrations were analysed in muscle and liver of mothers and embryos of two aplacental shark species, Squalus megalops and Centrophorus moluccensis. Embryos of the two species had similar or lower isotopic values than their respective mothers, the only exception being for δ13C, which was higher in the liver of C. moluccensis embryos than in their mothers. Hg concentrations were systemati...

  6. Comparative assessment of Azolla pinnata and Vallisneria spiralis in Hg removal from G.B. Pant Sagar of Singrauli Industrial region, India.

    Science.gov (United States)

    Rai, Prabhat Kumar; Tripathi, B D

    2009-01-01

    The aim of the present work was to monitor the Hg pollution in water and sediments of G.B. Pant Sagar located in Singrauli Industrial Region, India and to suggest the efficient aquatic plants for its phytoremediation. The study assessed the comparative potential of a free floating water fern Azolla pinnata and submerged aquatic macrophyte Vallisneria spiralis to purify waters polluted by Hg. Six days laboratory experiments have been conducted to mark the percentage removal of Hg at initial concentration of 0.1, 0.5, 1.0 and 3.0 mg L(-1). The percentage removal of Hg was higher for A. pinnata (80-94%) than V. spiralis (70-84%). Likewise, the Hg accumulated in dry mass was much higher for A. pinnata and a high correlation (R(2) = 0.91 for A. pinnata and 0.99 for V. spiralis) was obtained between applied Hg doses and accumulated amounts in biomass. A concentration dependent decrease in chlorophyll a, protein, RNA, DNA and nutrients (NO(3-) and PO(4)(3-)) uptake was detected in A. pinnata and V. spiralis due to Hg toxicity. The decrease was more prominent in Azolla than Vallisneria. The results recommended the use of A. pinnata and V. spiralis to ameliorate the industrial effluents (thermal power, chlor-alkali and coal mine effluent) contaminated with Hg.

  7. Colorimetric and fluorescent sensor for selective sensing of Hg{sup 2+} ions in semi aqueous medium

    Energy Technology Data Exchange (ETDEWEB)

    Udhayakumari, Duraisamy [Organic and Polymer Synthesis Laboratory, Department of Chemistry, National Institute of Technology, Tiruchirappalli 620 015 (India); Velmathi, Sivan, E-mail: velmathis@nitt.edu [Organic and Polymer Synthesis Laboratory, Department of Chemistry, National Institute of Technology, Tiruchirappalli 620 015 (India)

    2013-04-15

    A highly sensitive and selective detection of Hg{sup 2+} ion with simple salophen probe was developed. In DMSO: water (40:60, v/v) solution, Hg{sup 2+} ions coordinate with imine and shows color turn-off from yellow to colorless. Receptor 1 showed its ability for sensing Hg{sup 2+} cations sensitively through three channels: colorimetric, UV–vis and fluorescence spectroscopy. Hg{sup 2+} ions coordinate to the imine (Receptor 1) through NONO binding site forming 1:1 complex. It exhibits fluorescent 'Turn-on' behavior based on solvent polarity. The detection limit of our receptor with mercury is 1 μg L{sup −1}. -- Graphical abstract: A highly sensitive and rapid detection of Hg{sup 2+} with simple salophen probe was developed. In DMSO: water (40:60, v/v) solution, Hg{sup 2+} ions coordinate with imine and shows color turn-off from yellow to colorless. Receptor 1 showed its ability for sensing Hg{sup 2+} cations sensitively through three channels: colorimetric, UV–vis and Fluorescence Spectroscopy. Hg{sup 2+} ions coordinate to the imine (Receptor 1) through the NONO binding site forming 1:1 complex. It exhibits fluorescent 'Turn-on' behavior based on solvent polarity. The detection limit of our receptor with mercury is 1 μg L{sup −1}. Highlights: ► Hg{sup 2+} ions coordinate with imine and shows color turn-off from yellow to colorless. ► The binding constant of the receptor 1 (DMSO) with Hg{sup 2+} ion (DMSO) is 1.35×10{sup 5}. ► Hg{sup 2+} ions coordinate to the imine through NONO binding site forming 1:1 complex. ► The receptor 1 shows fluorescent 'Turn-on' behavior based on solvent polarity. ► The detection limit of receptor 1 with mercury is 1 μg L{sup −1}.

  8. Viscosity Relaxation in Molten HgZnTe

    Science.gov (United States)

    Baird, James K.

    2002-01-01

    Because of its narrow electronic band-gap, HgZnTe solid solutions have been proposed as effective detectors for infrared radiation. To produce the best single crystals of these materials for this application, knowledge of the phase diagram that governs the freezing of the liquid is essential. Besides the phase diagram, however, some information concerning the thermophysical properties of the melt, such as viscosity, density, specific heat, and enthalpy of mixing, can also be useful. Of these thermophysical properties, the viscosity is perhaps of the most interest scientifically. Measurements using the oscillating cup method have shown that the isothermal melt requires tens of hours of equilibration time before a steady value of the viscosity can be achieved. Over this equilibration time, which depends upon temperature, the viscosity can increase by as much as a factor of two before reaching a steady state. We suggest that this relaxation phenomenon may be due to a slight polymerization of Te atoms in the melt. To account for the time dependence of the viscosity in the HgZnTe melt, we propose that the liquid acts as a solvent that favors the formation of Te atom chains. We suggest that as the melt is cooled from a high temperature to the temperature for measurement of the viscosity, a free radical polymerization of Te atoms begins. To estimate this average molecular weight, we use a simple free radical polymerization mechanism, including a depolymerization step, to calculate the time dependence to the concentration of each Te polymer molecular weight fraction. From these molecular weight fractions, we compute the weight average molecular weight of the distribution. Using the semi-empirical relation between average molecular weight and viscosity, we obtain a formula for the time dependence of the viscosity of the melt. Upon examining this formula, we find that the viscosity achieves a steady value when a balance is achieved between the rate of formation of the chains

  9. Biokinetics of Hg and Pb accumulation in the encapsulated egg of the common cuttlefish Sepia officinalis: Radiotracer experiments

    Energy Technology Data Exchange (ETDEWEB)

    Lacoue-Labarthe, T., E-mail: tlacouel@gmail.com [Littoral, Environnement et Societes (LIENSs), UMR 6250, CNRS-Universite de La Rochelle, 2 rue Olympe de Gouges, F-17042 La Rochelle Cedex 01 (France); Warnau, M., E-mail: warnaumichel@yahoo.com [International Atomic Energy Agency - Marine Environment Laboratories, 4 Quai Antoine Ier, MC-98000 (Monaco); Metian, M. [Littoral, Environnement et Societes (LIENSs), UMR 6250, CNRS-Universite de La Rochelle, 2 rue Olympe de Gouges, F-17042 La Rochelle Cedex 01 (France); International Atomic Energy Agency - Marine Environment Laboratories, 4 Quai Antoine Ier, MC-98000 (Monaco); Oberhaensli, F. [International Atomic Energy Agency - Marine Environment Laboratories, 4 Quai Antoine Ier, MC-98000 (Monaco); Rouleau, C. [Institut Maurice-Lamontagne, 850 Route de la Mer, C.P. 1000, Mont-Joli, Quebec (Canada); Bustamante, P., E-mail: pbustama@univ-lr.fr [Littoral, Environnement et Societes (LIENSs), UMR 6250, CNRS-Universite de La Rochelle, 2 rue Olympe de Gouges, F-17042 La Rochelle Cedex 01 (France)

    2009-12-01

    Uptake and depuration kinetics of dissolved {sup 203}Hg and {sup 210}Pb were determined during the entire embryonic development of the eggs of the cuttlefish, Sepia officinalis (50 d at 17 {sup o}C). {sup 203}Hg and {sup 210}Pb were accumulated continuously by the eggs all along the development time reaching load/concentration ratio (LCR) of 467 {+-} 43 and 1301 {+-} 126 g, respectively. During the first month, most of the {sup 203}Hg and {sup 210}Pb remained associated with the eggshell indicating that the latter acted as an efficient shield against metal penetration. From this time onwards, {sup 203}Hg accumulated in the embryo, indicating that it passed through the eggshell, whereas {sup 210}Pb did not cross the chorion during the whole exposure time. It also demonstrated that translocation of Hg associated with the inner layers of the eggshell is a significant source of exposure for the embryo. This study highlighted that the maturing embryo could be subjected to the toxic effects of Hg in the coastal waters where the embryonic development is taking place.

  10. 实验室条件下Hg2+胁迫对集球藻生理生化特性的影响%Study on the physiological and biochemical properties of Palmellococcus sp. subjected to Hg2 + stress in laboratory condition

    Institute of Scientific and Technical Information of China (English)

    王文欣; 饶本强

    2012-01-01

    重金属污染是当今世界最为关注的生态环境问题之~。在实验室条件下,以一种从荒漠土壤中分离的单细胞绿藻——集球藻(Palmellococcussp.)为试验材料,研究Hg2+胁迫对集球藻生理生化特性的影响。结果表明:与对照相比,Hg2+胁迫明显抑制了集球藻的生长和光合活性,表现为藻体生物量(叶绿素a)和叶绿素荧光参数(Fv/Fm)均发生显著性下降。随Hg2+胁迫剂量加大,集球藻细胞内可溶性糖出现一定程度的积累,而HS2+胁迫明显抑制细胞内可溶性蛋白质的合成。集球藻细胞抗氧化活性的测定结果表明,Hg2+胁迫导致集球藻细胞MDA含量明显升高,SOD和CAT活性亦呈现增大的变化趋势。研究结果对于更好地理解荒漠土壤绿藻对重金属胁迫的耐受性及其适应机制提供了有意义的参考。%Heavy metal pollution is one of the most common ecological and environmental problems faced in current world. In this study, we selected one species of single cellular green alga, Palmelloeoccus sp. , separated from desert soil, as experimental material to investigate the effect of Hg2 + stress on its physiological and biochemical properties in laboratory condition. Our results showed that Hg2 + stress obviously inhibited the growth and photosynthetic activity of Palmelloeoccus sp. There were evident decreases in biomass (chlorophyll a) and chlorophyll fluorescence parameter (Fv/Fm) of the treated cells compared to the control cells. It also indicated that the soluble saccharide content of the treated algal cells present accumulation to some extent along with Hg2 + concentration addition, while Hg2 + stress evi- dently restrained the synthesis of cellular soluble protein of Palmelloeoecus sp. The results from examination of antioxidant activities of Palmellococcus sp. subjected to Hg2 + treatments validated that Hg2 + stress had a significantly deleterious effect on

  11. An investigation for the HgCdTe cleaning process

    Science.gov (United States)

    Lan, Tian-Yi; Wang, Nili; Zhao, Shuiping; Liu, Shi-Jia; Li, Xiang-Yang

    2014-11-01

    A new cleaning process for HgCdTe was designed - which used the improved SC-1,SC-2 and Br2- C2H5OH solutions as the main cleaning fluid and applied mega sound waves in the cleaning process. By analyzing the test results carried out on the HgCdTe surface, it was found that the material of HgCdTe for the application of new cleaning process was better than the one for the application of conventional cleaning process in the minority carrier lifetime, residual organic contamination, responsivity and specific detectivity.

  12. Doping and Diffusion in HgCdTe

    Science.gov (United States)

    1991-01-28

    In’i, -InT. Te - 1.8 ( - 3 .5 )h ( + 2.9 - 6/) TeT1’- Tej . 4 Hg rich HgCdTe Hg - 1.8 + 1.2 + 1.4 - 2p H - ’g, - H g j.. ’TI - tetrahedral position...A. Anderson, Appl. Phys. Lett. 53, 11.81 (1988). B. D. Patterson, Rev. Mod. Phys. 60, 69 (1988). 60 V. A. Singh , C. Weigel, J. W. Corbett, and L. M

  13. MeHg Developing Exposure Causes DNA Double-Strand Breaks and Elicits Cell Cycle Arrest in Spinal Cord Cells

    Directory of Open Access Journals (Sweden)

    Fabiana F. Ferreira

    2015-01-01

    Full Text Available The neurotoxicity caused by methylmercury (MeHg is well documented; however, the developmental neurotoxicity in spinal cord is still not fully understood. Here we investigated whether MeHg affects the spinal cord layers development. Chicken embryos at E3 were treated in ovo with 0.1 μg MeHg/50 μL saline solution and analyzed at E10. Thus, we performed immunostaining using anti-γ-H2A.X to recognize DNA double-strand breaks and antiphosphohistone H3, anti-p21, and anti-cyclin E to identify cells in proliferation and cell cycle proteins. Also, to identify neuronal cells, we used anti-NeuN and anti-βIII-tubulin antibodies. After the MeHg treatment, we observed the increase on γ-H2A.X in response to DNA damage. MeHg caused a decrease in the proliferating cells and in the thickness of spinal cord layers. Moreover, we verified that MeHg induced an increase in the number of p21-positive cells but did not change the cyclin E-positive cells. A significantly high number of TUNEL-positive cells indicating DNA fragmentation were observed in MeHg-treated embryos. Regarding the neuronal differentiation, MeHg induced a decrease in NeuN expression and did not change the expression of βIII-tubulin. These results showed that in ovo MeHg exposure alters spinal cord development by disturbing the cell proliferation and death, also interfering in early neuronal differentiation.

  14. MeHg Developing Exposure Causes DNA Double-Strand Breaks and Elicits Cell Cycle Arrest in Spinal Cord Cells

    Science.gov (United States)

    Ferreira, Fabiana F.; Ammar, Dib; Bourckhardt, Gilian F.; Kobus-Bianchini, Karoline; Müller, Yara M. R.; Nazari, Evelise M.

    2015-01-01

    The neurotoxicity caused by methylmercury (MeHg) is well documented; however, the developmental neurotoxicity in spinal cord is still not fully understood. Here we investigated whether MeHg affects the spinal cord layers development. Chicken embryos at E3 were treated in ovo with 0.1 μg MeHg/50 μL saline solution and analyzed at E10. Thus, we performed immunostaining using anti-γ-H2A.X to recognize DNA double-strand breaks and antiphosphohistone H3, anti-p21, and anti-cyclin E to identify cells in proliferation and cell cycle proteins. Also, to identify neuronal cells, we used anti-NeuN and anti-βIII-tubulin antibodies. After the MeHg treatment, we observed the increase on γ-H2A.X in response to DNA damage. MeHg caused a decrease in the proliferating cells and in the thickness of spinal cord layers. Moreover, we verified that MeHg induced an increase in the number of p21-positive cells but did not change the cyclin E-positive cells. A significantly high number of TUNEL-positive cells indicating DNA fragmentation were observed in MeHg-treated embryos. Regarding the neuronal differentiation, MeHg induced a decrease in NeuN expression and did not change the expression of βIII-tubulin. These results showed that in ovo MeHg exposure alters spinal cord development by disturbing the cell proliferation and death, also interfering in early neuronal differentiation. PMID:26793240

  15. Mexico City normal weight children exposed to high concentrations of ambient PM2.5 show high blood leptin and endothelin-1, vitamin D deficiency, and food reward hormone dysregulation versus low pollution controls. Relevance for obesity and Alzheimer disease.

    Science.gov (United States)

    Calderón-Garcidueñas, Lilian; Franco-Lira, Maricela; D'Angiulli, Amedeo; Rodríguez-Díaz, Joel; Blaurock-Busch, Eleonore; Busch, Yvette; Chao, Chih-kai; Thompson, Charles; Mukherjee, Partha S; Torres-Jardón, Ricardo; Perry, George

    2015-07-01

    Millions of Mexico, US and across the world children are overweight and obese. Exposure to fossil-fuel combustion sources increases the risk for obesity and diabetes, while long-term exposure to fine particulate matter (PM2.5) and ozone (O3) above US EPA standards is associated with increased risk of Alzheimer's disease (AD). Mexico City Metropolitan Area children are chronically exposed to PM2.5 and O3 concentrations above the standards and exhibit systemic, brain and intrathecal inflammation, cognitive deficits, and Alzheimer disease neuropathology. We investigated adipokines, food reward hormones, endothelial dysfunction, vitamin D and apolipoprotein E (APOE) relationships in 80 healthy, normal weight 11.1±3.2 year olds matched by age, gender, BMI and SES, low (n: 26) versus high (n:54) PM2.5 exposures. Mexico City children had higher leptin and endothelin-1 (pchildren. Mexico City APOE 4 versus 3 children had higher glucose (p=0.009). Serum 25-hydroxyvitamin DMexico City children. Leptin is strongly positively associated to PM 2.5 cumulative exposures. Residing in a high PM2.5 and O3 environment is associated with 12h fasting hyperleptinemia, altered appetite-regulating peptides, vitamin D deficiency, and increases in ET-1 in clinically healthy children. These changes could signal the future trajectory of urban children towards the development of insulin resistance, obesity, type II diabetes, premature cardiovascular disease, addiction-like behavior, cognitive impairment and Alzheimer's disease. Increased efforts should be made to decrease pediatric PM2.5 exposures, to deliver health interventions prior to the development of obesity and to identify and mitigate environmental factors influencing obesity and Alzheimer disease.

  16. Multi-decadal decline of mercury in the North Atlantic atmosphere explained by changing subsurface seawater concentrations

    Science.gov (United States)

    Soerensen, Anne L.; Jacob, Daniel J.; Streets, David G.; Witt, Melanie L. I.; Ebinghaus, Ralf; Mason, Robert P.; Andersson, Maria; Sunderland, Elsie M.

    2012-11-01

    We analyze 1977-2010 trends in atmospheric mercury (Hg) from 21 ship cruises over the North Atlantic (NA) and 15 over the South Atlantic (SA). We find a steep 1990-2009 decline of -0.046 ± 0.010 ng m-3 a-1 (-2.5% a-1) over the NA (steeper than at Northern Hemispheric land sites) but no significant decline over the SA. Surface water Hg0 measurements in the NA show a decline of -5.7% a-1 since 1999, and limited subsurface ocean data show an ˜80% decline from 1980 to present. We use a coupled global atmosphere-ocean model to show that the decline in NA atmospheric concentrations can be explained by decreasing oceanic evasion from the NA driven by declining subsurface water Hg concentrations. We speculate that this large historical decline of Hg in the NA Ocean could have been caused by decreasing Hg inputs from rivers and wastewater and by changes in the oxidant chemistry of the atmospheric marine boundary layer.

  17. Future trends in environmental mercury concentrations: implications for prevention strategies

    Directory of Open Access Journals (Sweden)

    Sunderland Elsie M

    2013-01-01

    Full Text Available Abstract In their new paper, Bellanger and coauthors show substantial economic impacts to the EU from neurocognitive impairment associated with methylmercury (MeHg exposures. The main source of MeHg exposure is seafood consumption, including many marine species harvested from the global oceans. Fish, birds and other wildlife are also susceptible to the impacts of MeHg and already exceed toxicological thresholds in vulnerable regions like the Arctic. Most future emissions scenarios project a growth or stabilization of anthropogenic mercury releases relative to present-day levels. At these emissions levels, inputs of mercury to ecosystems are expected to increase substantially in the future, in part due to growth in the legacy reservoirs of mercury in oceanic and terrestrial ecosystems. Seawater mercury concentration trajectories in areas such as the North Pacific Ocean that supply large quantities of marine fish to the global seafood market are projected to increase by more than 50% by 2050. Fish mercury levels and subsequent human and biological exposures are likely to also increase because production of MeHg in ocean ecosystems is driven by the supply of available inorganic mercury, among other factors. Analyses that only consider changes in primary anthropogenic emissions are likely to underestimate the severity of future deposition and concentration increases associated with growth in mercury reservoirs in the land and ocean. We therefore recommend that future policy analyses consider the fully coupled interactions among short and long-lived reservoirs of mercury in the atmosphere, ocean, and terrestrial ecosystems. Aggressive anthropogenic emission reductions are needed to reduce MeHg exposures and associated health impacts on humans and wildlife and protect the integrity of one of the last wild-food sources globally. In the near-term, public health advice on safe fish consumption choices such as smaller species, younger fish, and harvests

  18. Estudio de la cinética de adsorción de Cu y Hg a partir de soluciones binarias usando quitosano

    Directory of Open Access Journals (Sweden)

    Martha Benavente

    2011-06-01

    Full Text Available In this work, the adsorption kinetic of Cu(II and Hg(II onto chitosan was studied from a binary solution at different initial concentration of metallic ions, at different particle sizes and agitation rate. Chitosan was obtained from shrimp shells. Solutions of 1 L of Cu(II and Hg(II were placed in contact with 2 g of chitosan and the mixture was agitated by 8 h. Afterwards, the samples were analysed by atomic absorption. The experimental data were tested by application of kinetic models of pseudo-first order and pseudo-second order. The results of adsorption process showed that in the most cases, both ions were effectively adsorbed by chitosan. The percentage of adsorption was 43-100 % and 94-100 % for Cu(II and Hg(II, respectively. The results also showed that at low concentrations, experimental data were better adjusted by pseudo-first order models; meanwhile, at high concentration, the data were well described by the pseudo-second model. Therefore, the rate-limiting step is the adsorption reaction and not mass transfer. Keywords: Adsorption kinetics; Binary solution; Chitosan; Kinetic models; Shrimp shell En este trabajo se estudió la cinética de adsorción de Cu(II y Hg(II en quitosano a partir de una solución binaria, a diferentes concentraciones iniciales de los iones metálicos, tamaño de partículas del adsorbente y velocidad de agitación. El quitosano fue extraído por métodos químicos de caparazón de camarón. Soluciones de 1 L de Cu(II y Hg(II fueron puestas en contacto con 2 g de quitosano y se agitaron por un período de 8 h. Al final del proceso, las muestras fueron analizadas en un espectrómetro de absorción atómica. Los datos experimentales fueron evaluados aplicando los modelos cinéticos de pseudo-primer orden y pseudo-segundo orden. Los resultados del proceso de adsorción de los iones metálicos Cu(II y Hg(II con quitosano, mostraron que en la mayoría de los casos, ambos iones fueron eficazmente adsorbidos por la

  19. Pd(II)-catalysed and Hg(II)-co-catalysed oxidation of D-glucose and D-fructose by N-bromoacetamide in the presence of perchloric acid: a kinetic and mechanistic study.

    Science.gov (United States)

    Singh, Ashok Kumar; Srivastava, Jaya; Rahmani, Shahla; Singh, Vineeta

    2006-02-27

    The kinetics of Pd(II)-catalysed and Hg(II)-co-catalysed oxidation of D-glucose (Glc) and D-fructose (Fru) by N-bromoacetamide (NBA) in the presence of perchloric acid using mercury(II) acetate as a scavenger for Br- ions have been studied. The results show first-order kinetics with respect to NBA at low concentrations, tending to zero order at high concentrations. First-order kinetics with respect to Pd(II) and inverse fractional order in Cl- ions throughout their variation have also been noted. The observed direct proportionality between the first-order rate constant (k1) and the reducing sugar concentration shows departure from the straight line only at very higher concentration of sugar. Addition of acetamide (NHA) decreases the first-order rate constant while the oxidation rate is not influenced by the change in the ionic strength (mu) of the medium. Variation of [Hg(OAc)2] shows a positive effect on the rate of reaction. The observed negative effect in H+ at lower concentrations tends to an insignificant effect at its higher concentrations. The first-order rate constant decreases with an increase in the dielectric constant of the medium. The various activation parameters have also been evaluated. The products of the reactions were identified as arabinonic acid and formic acid for both the hexoses. A plausible mechanism involving HOBr as the reactive oxidising species, Hg(II) as co-catalyst, and [PdCl3.S]-1 as the reactive Pd(II)-sugar complex in the rate-controlling step is proposed.

  20. The Copper concentration variation to physical properties of high copper amalgam alloy

    Directory of Open Access Journals (Sweden)

    Aminatun Aminatun

    2006-09-01

    Full Text Available The function of copper (Cu inside amalgam is to increase hardness and impact force and to decrease thermal expansion coefficient. In general, amalgam which is used in dentistry and available in the market is contain Cu 22%, while the maximum Cu concentration is 30%. It is necessary to determine the concentration Cu does generate the best physical properties to be used as dental restorative agent. Amalgam is made by mixing blended-metal Ag-Sn-Cu (with Cu concentration of 13%, 21%, 22%, and 29% and Hg, stirred manually in a bowl for 15 minutes,leave it in temperature 27°C for 24 hours to become hardened. The result of X-Ray Diffractometer (XRD, analyzed by Rietveld method and Rietica program,