Heavy Metals (heavy + metal)

Distribution by Scientific Domains
Distribution within Life Sciences

Kinds of Heavy Metals

  • other heavy metal
  • toxic heavy metal

  • Terms modified by Heavy Metals

  • heavy metal accumulation
  • heavy metal concentration
  • heavy metal contamination
  • heavy metal exposure
  • heavy metal ion
  • heavy metal pollution
  • heavy metal toxicity

  • Selected Abstracts


    Heavy Metal, identity and the social negotiation of a community of practice

    JOURNAL OF COMMUNITY & APPLIED SOCIAL PSYCHOLOGY, Issue 6 2007
    Dave Snell
    Abstract Psychologists have raised concerns about Heavy Metal music and possible links with substance misuse and youth suicide. This paper moves beyond this traditional disciplinary focus on negative messages to document the media-related practices through which a Heavy Metal community is negotiated. Six participants contributed to ethnographic observations, interviews and photo-voice projects. Results illustrate how socio-material practices such as dressing a certain way, frequenting a bar and dancing are central to community maintenance and the reaffirmation of shared identities. Findings highlight the need for community psychology research to document the material and symbolic nature of contemporary communal life. Copyright © 2007 John Wiley & Sons, Ltd. [source]


    This Ain't the Summer of Love: Conflict and Crossover in Heavy Metal and Punk,by Steve Waksman

    JOURNAL OF POPULAR MUSIC STUDIES, Issue 1 2010
    Theo Cateforis
    First page of article [source]


    Simultaneous Quantification of Heavy Metals Using a Solid State Potentiometric Sensor Array

    ELECTROANALYSIS, Issue 8 2009
    Jesús Gismera
    Abstract A potentiometric sensor array of four nonspecific electrodes with solid-state membranes is developed and tested for simultaneous analysis of copper(II), mercury(II), and silver(I) ions. The cross-sensitivity responses of the sensors for these ions are evaluated. The array potentiometric signals are processed by partial least-squares regression (PLS) and back propagation artificial neural networks (ANN) to determinate analyte concentrations. The ANN configuration is optimized and two different training algorithms of the ANN are also evaluated. Best results are obtained when the potentiometric sensors are activated and the data are processed using ANN and the gradient descent adaptive algorithm. The system is used to quantify these heavy metals in synthetic samples and in dental amalgams with successful results. [source]


    Heavy Metals in Matrices of Food Interest: Sequential Voltammetric Determination at Trace and Ultratrace Level of Copper, Lead, Cadmium, Zinc, Arsenic, Selenium, Manganese and Iron in Meals

    ELECTROANALYSIS, Issue 18 2004
    Clinio Locatelli
    Abstract The voltammetric methods are very suitable and versatile techniques for the simultaneous metal determination in complex matrices. The present work, regarding the sequential determination of Cu(II), Pb(II), Cd(II), Zn(II) by square-wave anodic stripping voltammetry (SWASV), As(III), Se(IV) by square-wave cathodic stripping voltammetry (SWCSV) and Mn(II), Fe(III) by square-wave voltammetry (SWV) in matrices involved in foods and food chain as wholemeal, wheat and maize meal, are an interesting example of the possibility to sequentially determine each single element in real samples. Besides the set up of the analytical method, particular attention is aimed either at the problem of possible signal interference or to show that, using the peak area Ap as instrumental datum, it is possible to achieve lower limits of detection. The analytical procedure was verified by the analysis of the standard reference materials: Wholemeal BCR-CRM 189, Wheat Flour NIST-SRM 1567a and Rice Flour NIST-SRM 1568a. Precision, as repeatability, and accuracy, expressed as relative standard deviation and relative error, respectively, were lower than 6% in all cases. In the presence of reciprocal interference, the standard addition method considerably improved the resolution of the voltammetric technique. Once set up on the standard reference materials, the analytical procedure was transferred and applied to commercial meals sampled on market for sale. A critical comparison with spectroscopic measurements is also discussed. [source]


    Treatment of Process Water Containing Heavy Metals with a Two-Stage Electrolysis Procedure in a Membrane Electrolysis Cell

    ENGINEERING IN LIFE SCIENCES (ELECTRONIC), Issue 2 2005
    R. Fischer
    Abstract The capability of a two-stage electrochemical treatment for the regeneration of acidic heavy-metal containing process water was examined. The process water came from sediment bioleaching and was characterized by a wide spectrum of dissolved metals, a high sulfate content, and a pH of about 3. In the modular laboratory model cell used, the anode chamber and the cathode chamber were separated by a central chamber fitted with an ion exchanger membrane on either side. The experiments were carried out applying a platinum anode and a graphite cathode at a current density of 0.1,A/cm2. The circulation flow of the process water in the batch process amounted to 35,L/h, the electrolysis duration was 5.5,h at maximum and the total electrolysis current was about 1,A. In the first stage, the acidic process water containing metals passed through the cathode chamber. In the second stage, the cathodically pretreated process water was electrolyzed anodically. In the cathode chamber the main load of dissolved Cu, Zn, Cr and Pb was eliminated. The sulfuric acid surplus of 3,4,g/L decreased to about 1,g/L, the pH rose from initially 3.0 to 4,5, but the desired pH of 9,10 was not achieved. Precipitation in the proximity to the cathode evidently takes place at a higher pH than farther away. The dominant process in the anode chamber was the precipitation of amorphous MnO2 owing to the oxidation of dissolved Mn(II). The further depletion of the remaining heavy metals in the cathodically pretreated process water by subsequent anodic treatment was nearly exhaustive, more than 99,% of Cd, Cr, Cu, Mn, Ni, Pb, and Zn were removed from the leachate. The high depletion of heavy metals might be due to both the sorption on MnO2 precipitates and/or basic ferrous sulfate formed anodically, and the migration of metal ions through the cation exchanger membrane via the middle chamber into the cathode chamber. In the anode chamber, the sulfuric acid content increased to 6,7,g/L and the pH sank to 1.7. All heavy metals contained, with the exception of Zn, were removed to levels below the German limits for discharging industrial wastewaters into the receiving water. Moreover, the metal-depleted and acid-enriched process waters could be returned to the leaching process, hence reducing the output of wastewater. The results indicated that heavy metals could be removed from acidic process waters by two-stage electrochemical treatment to a large extent. However, to improve the efficiency of metal removal and to establish the electrochemical treatment in practice, further work is necessary to optimize the operation of the process with respect to current density, energy consumption, discharging of metal precipitates deposited in the electrode chambers and preventing membrane clogging. [source]


    Selim, H.M. & Kingery, W.L. (eds) Geochemical and Hydrological Reactivity of Heavy Metals in Soils.

    EUROPEAN JOURNAL OF SOIL SCIENCE, Issue 3 2004
    2003., Boca Raton, Lewis Publishers
    No abstract is available for this article. [source]


    Neutron Activation Analysis Applied to the Determination of Heavy Metals and Other Trace Elements in Sediments from Sepetiba Bay (RJ), Brazil

    GEOSTANDARDS & GEOANALYTICAL RESEARCH, Issue 2-3 2001
    Fŕbio Pellegatti
    analyse par activation neutronique; métaux lourds; éléments en traces; sédiments marins In this work, instrumental neutron activation analysis (INAA) was applied to the determination of the elements As, Ba, Br, Ce, Co, Cr, Cs, Eu, Fe, Hf, La, Lu, Nd, Rb, Sc, Sm, Ta, Tb, Th, U, Yb, Zn in twenty eight bottom sediment samples from Sepetiba Bay, Rio de Janeiro, Brazil. With the concentration data obtained, contour maps were prepared, by using Kriging method, to show the spatial distribution of the studied elements in the Bay. The elements Co, Cr, Cs, Fe, Sc, Ta and Zn showed similar behaviour in the sediments, with higher concentrations along the northern coast of the bay, where the fluvial water inputs are concentrated. The distribution of U, rare earth elements and Ba in the Bay indicates that these elements are not deposited as contaminants. Dans ce travail, les éléments suivants, As, Ba, Br, Ce, Co, Cr, Cs, Eu, Fe, Hf, La Lu, Nd, Rb, Sc, Sm, Ta, Tb, Th, U, Yb et Zn ont été analysés par activation neutronique instrumentale dans vingt huit sédiments de fond de la baie de Sepetiba, Rio de Janeiro, Brésil. Par krigeage et ŕ partir des concentrations obtenues, nous avons établi des cartes de la répartition spatiale des éléments étudiés dans la baie. Co, Cr, Cs, Fe, Sc, Ta et Zn ont des comportements similaires dans les sédiments, avec des concentrations plus importantes le long de la côte nord de la baie, oú les apports en eau fluviale sont concentrés. La distribution en U, Terres Rares et Ba indique que ces éléments ne sont pas déposés comme polluants dans la baie. [source]


    Sequestration of Heavy Metals from Water with Layered Metal Sulfides

    CHEMISTRY - A EUROPEAN JOURNAL, Issue 19 2009
    Manolis
    Abstract Extraordinarily effective heavy metal ion scavenger: We show here that the material K2xMnxSn3,xS6 (x=0.5,0.95) (KMS-1) overcomes the limitations of the known heavy metal ion sorbents, showing the capability to rapidly reduce the concentrations of Cd, Hg, and Pb ions well-below the legally acceptable levels for drinking water. KMS-1 is inexpensive, easily prepared in large quantities, and may play a role in addressing the global problem of water contamination with heavy metal ions. The paradigm of heavy metal ion absorption of KMS-1 is the ability to form very strong MS bonds. [source]


    Impacts of heavy metals, polyaromatic hydrocarbons, and pesticides on freeze tolerance of the earthworm Dendrobaena octaedra

    ENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 11 2009
    Anne-Mette Bindesbřl
    Abstract Previous studies have shown that the interactions between chemicals and climatic stressors can lead to synergistically increased mortality. In the present study, we investigated the effect of seven common environmental contaminants on survival at ,6 and 15°C as well as on reproduction at 15°C in the earthworm Dendrobaena octaedra. Three classes of chemicals were considered: Heavy metals (nickel, lead, and mercury), polycyclic aromatic hydrocarbons (pyrene and phenanthrene), and pesticides (abamectin and carbendazim). Phenanthrene interacted antagonistically with freezing temperatures, whereas no interaction was observed with any of the tested pesticides. Two of the three tested metals (nickel and mercury) reduced the freeze tolerance synergistically (mercury was especially potent). This suggests that traditional laboratory studies, in which organisms are exposed to increasing concentrations of a single compound under otherwise optimal conditions, may underestimate the toxicity of some metals to field populations living in cold areas. [source]


    Influence of heavy metals on microbial growth kinetics including lag time: Mathematical modeling and experimental verification,

    ENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 10 2009
    S. Sevinç, engör
    Abstract Heavy metals can significantly affect the kinetics of substrate biodegradation and microbial growth, including lag times and specific growth rates. A model to describe microbial metabolic lag as a function of the history of substrate concentration has been previously described by Wood et al. (Water Resour Res 31:553,563) and Ginn (Water Resour Res 35:1395,1408). In the present study, this model is extended by including the effect of heavy metals on metabolic lag by developing an inhibitor-dependent functional to account for the metabolic state of the microorganisms. The concentration of the inhibiting metal is explicitly incorporated into the functional. The validity of the model is tested against experimental data on the effects of zinc on Pseudomonas species isolated from Lake Coeur d'Alene sediments, Idaho, USA, as well as the effects of nickel or cobalt on a mixed microbial culture collected from the aeration tank of a wastewater treatment plant in Athens, Greece. The simulations demonstrate the ability to incorporate the effect of metals on metabolism through lag, yield coefficient, and specific growth rates. The model includes growth limitation due to insufficient transfer of oxygen into the growth medium. [source]


    Heavy metals in traditional medicines

    FOCUS ON ALTERNATIVE AND COMPLEMENTARY THERAPIES AN EVIDENCE-BASED APPROACH, Issue 2 2008
    Article first published online: 3 JUN 2010
    [source]


    Effect of metal cations on the conformation and inactivation of recombinant human factor VIII

    JOURNAL OF PHARMACEUTICAL SCIENCES, Issue 10 2004
    Tiffany S. Derrick
    Abstract Heavy metals have been implicated in the aggregation of proteins and the pathophysiology of several neurodegenerative diseases. Herein, we describe the interaction of recombinant human factor VIII (rhFVIII) with Al+3, Tb+3, Co+2, and Fe+3 using a combination of intrinsic fluorescence, circular dichroism, and high-resolution fourth-derivative absorbance analysis. rhFVIII in solution was titrated with the metal cations and the properties of the resulting complexes were examined. rhFVIII has a tendency to aggregate and inactivate slowly over time under physiological conditions, but this aggregation process is greatly accelerated in the presence of metals with Al+3 being the most efficient. This leads to a complete loss of activity of the protein. Al+3 -induced conformational changes in the protein were small but detectable with limited changes seen in secondary and tertiary structure. Because rhFVIII is a multidomain protein with subunits linked through divalent metal cations, the small intramolecular changes seen may be attributed to rearrangements of the subunits to an aggregation-competent conformer that is very similar to that of the native form. © 2004 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 93:2549,2557, 2004 [source]


    Heavy-metal displacement in chelate-treated soil with sludge during phytoremediation

    JOURNAL OF PLANT NUTRITION AND SOIL SCIENCE, Issue 6 2006
    Stanley Liphadzi
    Abstract Heavy metals (HMs) in domestic sewage sludge, applied to land, contaminate soils. Phytoremediation is the use of plants to clean-up toxic HMs from soil. Chelating agents are added to soil to solubilize the metals for enhanced uptake. Yet no studies report the displacement of HMs in soil with sludge following solubilization with chelates. The objective of this work was to determine the uptake or leaching of HMs due to a chelate added to a soil from a sludge farm that had received sludge for 25 y. The soil was placed in long columns (105,cm long; , 39,cm) in a greenhouse. Columns either had a plant (hybrid poplar; Populus deltoides Marsh. × P. nigra L.) or no plant. After the poplar seedlings had grown for 144 d, the tetrasodium salt of the chelating agent EDTA was irrigated onto the surface of the soil at a rate of 1 g per,kg of soil. Drainage water, soil, and plants were analyzed for three toxic HMs (Cd, Ni, Pb) and four essential HMs (Cu, Fe, Mn, Zn). At harvest, extractable and total concentrations of each HM in the soil with EDTA were similar to those in soil without EDTA. The chelate did not affect the concentrations of HMs in the roots or leaves. With or without plants, EDTA mobilized all seven HMs and increased their concentrations in drainage water. Lower concentrations of Cd, Cu, Fe, Ni, and Zn in leachate from columns with EDTA and plants compared to columns with EDTA and no plants showed that poplars can reduce groundwater contamination by intercepting these HMs in the soil. But the poplar plants did not reduce Pb and Mn in the leachate from columns with EDTA. Concentrations of Cd and Pb in the leachate mobilized by EDTA remained above drinking-water standards with or without plants. The results showed that a chelate (EDTA) should not be added to a soil at a sludge farm to enhance phytoremediation. The chelate mobilized HMs that leached to drainage water and contaminated it. [source]


    Heavy metals and plants , model systems and hyperaccumulators

    NEW PHYTOLOGIST, Issue 2 2003
    Christopher Cobbett
    First page of article [source]


    Simultaneous detection of cyanide and heavy metals for environmental analysis by means of µISEs

    PHYSICA STATUS SOLIDI (A) APPLICATIONS AND MATERIALS SCIENCE, Issue 4 2010
    Monika Turek
    Abstract In environmental analysis, cyanide and heavy metals play an important role, because these substances are highly toxic for biological systems. They can lead to chronic and acute diseases. Due to the chemical properties of cyanide it is frequently used for industrial processes such as extraction of silver and gold. Heavy metals can be found as trace elements in nature and are often applied in industries e.g., galvanization processes. Up to now, cyanide and heavy metals can be detected by several sensors separately and their detection is often limited to laboratory investigations. In this publication, with regard to an in situ analysis, a new miniaturized silicon-based sensor system for the simultaneous detection of cyanide and heavy metals in aqueous solutions is presented that is based on chalcogenide glass-based micro ion-selective electrodes (µISEs). The µISEs are incorporated into a specially designed measuring system for the simultaneous detection of heavy metals and cyanide in solutions and validated by simultaneous measurements of Cu2+ - and CN, -ions, Cd2+ - and CN, - ions and Pb2+ - and CN, -ions. The particular sensor system has shown good sensor properties in the µ-molar ion-concentration range. For simultaneous measurements in complex heavy metal and cyanide solutions an intelligent software using fuzzy logic is discussed. [source]


    Green Approaches to Field Nitrate Analysis: An Electroanalytical Perspective

    ELECTROANALYSIS, Issue 7 2009
    Radha Desai
    Abstract The different approaches that have been taken in the development of analytical methods for the determination of nitrate within the field are reviewed. The emphasis has been placed on providing a critical appraisal of the chemistry that underpins current commercial systems and the need to remove the dependence on heavy metal and concentrated acid components. The search for more environmentally acceptable and user friendly systems has long been pursued and the present communication seeks to explore the recent development in portable testing technologies and how they might evolve in the future. In particular, the role of electrochemical techniques in the latter are investigated and their potential application compared and contrasted with the more traditional wet chemical detection strategies. [source]


    Protein-Based Capacitive Biosensors: a New Tool for Structure-Activity Relationship Studies

    ELECTROANALYSIS, Issue 24 2008
    Alessia Mortari
    Abstract The present work reports a new application of a protein-based capacitive biosensor as an in vitro assay for the selectivity study of the bacterial periplasmic protein MerP and four MerP variants. The modified MerP proteins were produced by site-directed mutagenesis of the heavy metal associated motif (HMA). The MerP and modified MerPs selectivity for copper, zinc, cadmium and mercury bivalent ions were investigated and compared. The variations in the proteins affinity were related to the primary structure of the HMA motifs. Key amino acids for copper coordination of metalloproteins that contain the metal binding sequence Gly-Met-Thr-Cys-xxx-xxx-Cys were identified. The results brought insights valid for Menkes and Wilson ATPases. The protein-based capacitive biosensors were a simple and useful tool for studying structure-activity relationships of proteins. [source]


    Shell disease in crustaceans , just chitin recycling gone wrong?

    ENVIRONMENTAL MICROBIOLOGY, Issue 4 2008
    Claire L. Vogan
    Summary The exoskeletons of aquatic crustaceans and other arthropods contain chitin, a biopolymer of ,-(1,4)-linked N -acetylglucosamine together with associated proteins. Despite the vast amounts of chitin within such animals little is found in sediments and open water because microorganisms rapidly degrade this following its loss after moulting or upon the animals' death. Shell disease syndrome is a worldwide disease condition that affects a wide range of crustaceans. It comes about as a result of bacterial degradation of the exoskeleton leading to unsightly lesions and even death if the underlying tissues become infected. There are at least two potential forms of the disease; one that appears to centre around chitin degradation and an additional form termed ,epizootic' shell disease, in which chitin degradation is of less significance. This account reviews our current understanding of the causative agents of this syndrome, assesses the potential economic consequences of the disease, and critically examines whether it is associated with anthropogenic disturbances including pollution. Overall, despite extensive studies during the last few decades, the potential links between faecal, heavy metal and insecticide pollution and shell disease are still unclear. [source]


    Structural diversity of bacterial communities in a heavy metal mineralized granite outcrop

    ENVIRONMENTAL MICROBIOLOGY, Issue 3 2006
    Deirdre Gleeson
    Summary This laboratory study of a variably mineralized and hydrothermally altered granite outcrop investigated the influences of rock-surface chemistry and heavy metal content on resident bacterial populations. Results indicated that elevated heavy metal concentrations had a profound impact on bacterial community structure, with strong relationships found between certain ribotypes and particular chemical/heavy metal elements. Automated ribosomal intergenic sequence analysis (ARISA) was used to assess the nature and extent of bacterial diversity, and this was combined with chemical analysis and multivariate statistics to identify the main geochemical factors influencing bacterial community structure. A randomization test revealed significant changes in bacterial structure between samples, while canonical correspondence analysis (CCA) related each individual ARISA profile to linear combinations of the chemical variables (mineralogy, major element and heavy metal concentrations) revealing the geochemical factors that correlated with changes in the ARISA data. anova was performed to further explore interactions between individual ribotypes and chemical/heavy metal composition, and revealed that a high proportion of ribotypes correlated significantly with heavy metals. [source]


    A study of copper recovery from copper-contaminated sludge with ferrite and selective leaching processes

    ENVIRONMENTAL PROGRESS & SUSTAINABLE ENERGY, Issue 1 2007
    S.H. Hu
    Abstract The purpose of this study was to develop an effective resource recovery and leached residue stabilization process for copper-contaminated sludge. To this end, a treatment procedure utilizing ferrite and selective leaching processes was developed. The XRD examination of ferrite complex revealed the crystalline phases to be mainly Fe3O4, CuO, and 6CuO·Cu2O. A selective leaching process was followed to recover the copper content of the ferrite complex. To promote the dissolution percentage of copper and repress that of iron, additional 0.5 N sulfuric acid was added at intervals to the suspension in the second step of the selective leaching process. The purpose of this operation was to return the suspension pH back to 3 to promote the dissolution of copper oxide and repress the dissolution of iron. Finally, the heavy metal (i.e., Cu, Pb, Cr, and Cd) dissolution of the above residue was examined with toxicity characteristic leaching procedure (TCLP) testing and all met the regulatory standard. © 2007 American Institute of Chemical Engineers Environ Prog 26:104,112, 2007 [source]


    Response of the charophyte Nitellopsis obtusa to heavy metals at the cellular, cell membrane, and enzyme levels

    ENVIRONMENTAL TOXICOLOGY, Issue 3 2002
    Levonas Manusad, ianas
    Abstract The responses of the freshwater macroalga Nitellopsis obtusa to heavy metal (HM) salts of Hg, Cd, Co, Cu, Cr, and Ni were assessed at different levels: whole-cell mortality (96-h LC50), in vivo cell membrane (45-min depolarization of resting potential, EC50), and enzyme in plasma membrane preparations (K+, Mg2+ -specific H+ -ATPase inhibition, IC50). To measure ATPase activity, a novel procedure for isolation of plasma membrane,enriched vesicles from charophyte cells was developed. The short-term ATPase inhibition assay (IC50 from 6.0 × 10,7 to 4.6 × 10,4 M) was slightly more sensitive than the cell mortality test (LC50 from 1.1 × 10,6 to 2.6 × 10,3 M), and the electrophysiological test with the end point of 45-min depolarization of resting potential was characterized by less sensitivity for HMs (EC50 from 1.1 × 10,4 to 2.2 × 10,2 M). The variability of IC50 values assessed for HMs in the ATPase assays was close to that of LC50 values in the mortality tests (CVs from 33.5 to 83.5 and from 12.4% to 57.7%, respectively), whereas the EC50 values in the electrophysiological tests were characterized by CVs generally below 30%. All three end points identified two separate HM groups according to their toxicity to N. obtusa: Co, Ni, and Cr comprised a group of less toxic metals, whereas Hg, Cu, and Cd comprised a group of more toxic metals. However, the adverse effects within each group were discriminated differently. For example, the maximum difference between the highest and lowest LC50 for the group of less toxic metals in the long-term mortality test was approximately 60% of the response range, whereas the corresponding difference in IC50 values in the ATPase assay was 30%. In contrast, the LC50 values of the more toxic metals occupied only 10% of the response range, whereas the IC50 values were spread over 70%. Further investigation should be done of the underlying mechanism or mechanisms responsible for the observed differences in the dynamic range of a particular end point of the groups of toxicants of varying strength. © 2002 Wiley Periodicals, Inc. Environ Toxicol 17: 275,283, 2002; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/tox.10058 [source]


    Influence of complexation with chloride on the responses of a lux-marked bacteria bioassay to cadmium, copper, lead, and mercury

    ENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 2 2000
    Charoon Sarin
    Abstract The toxicity of a heavy metal in solution to a microorganism depends not only on its concentration but also on pH and the concentrations of any aqueous complexing ligands in the microorganism's environment. This paper reports on the use of different inorganic resuscitation media and effect of the chloride ion, Cl,, on the bioluminescence response of a bacterial biosensor, Escherichia coli HB101 (pUCD607), to four metals: Cd, Cu, Hg, and Pb. The toxicity tests were conducted at pH 4, using 0.1 M KNO3 as resuscitation medium and adding KCl to investigate effect of Cl, concentration. The species distributions of metals as a function of Cl, concentration were calculated using GeoChem-PC. Resuscitation in 0.1 M KC1 gave significantly higher light output than that in 0.1 M KNO3, demonstrating that Cl, in the resuscitation medium has a direct effect on the bioluminescence response of the E. coli biosensor. Increasing concentrations of Cl, ions increased the toxicity of Hg, apparently because of the formation of HgCl,3, and increased the toxicity of Pb because of PbCl+ formation. The toxicity of Cu decreased at high Cl, concentrations as free Cu2+ decreased, in accordance with the free ion model. Concentrations of Cl, had no significant effect on the toxicity of Cd. This study clearly demonstrates that the chloro-complexes of some heavy metals can be toxic and, for Pb and Hg, more toxic than the free ion. [source]


    Effects of chromium on the immune system

    FEMS IMMUNOLOGY & MEDICAL MICROBIOLOGY, Issue 1 2002
    Richa Shrivastava
    Abstract Chromium is a naturally occurring heavy metal found commonly in the environment in trivalent, Cr(III), and hexavalent, Cr(VI), forms. Cr(VI) compounds have been declared as a potent occupational carcinogen among workers in chrome plating, stainless steel, and pigment industries. The reduction of Cr(VI) to Cr(III) results in the formation of reactive intermediates that together with oxidative stress oxidative tissue damage and a cascade of cellular events including modulation of apoptosis regulatory gene p53, contribute to the cytotoxicity, genotoxicity and carcinogenicity of Cr(VI)-containing compounds. On the other hand, chromium is an essential nutrient required to promote the action of insulin in body tissues so that the body can use sugars, proteins and fats. Chromium is of significant importance in altering the immune response by immunostimulatory or immunosuppressive processes as shown by its effects on T and B lymphocytes, macrophages, cytokine production and the immune response that may induce hypersensitivity reactions. This review gives an overview of the effects of chromium on the immune system of the body. [source]


    Aquifer vulnerability assessment to heavy metals using ordinal logistic regression

    GROUND WATER, Issue 2 2005
    Navin K.C. Twarakavi
    A methodology using ordinal logistic regression is proposed to predict the probability of occurrence of heavy metals in ground water. The predicted probabilities are defined with reference to the background concentration and the maximum contaminant level. The model is able to predict the occurrence due to different influencing variables such as the land use, soil hydrologic group (SHG), and surface elevation. The methodology was applied to the Sumas-Blaine Aquifer located in Washington State to predict the occurrence of five heavy metals. The influencing variables considered were (1) SHG; (2) land use; (3) elevation; (4) clay content; (5) hydraulic conductivity; and (6) well depth. The predicted probabilities were in agreement with the observed probabilities under existing conditions. The results showed that aquifer vulnerability to each heavy metal was related to different sets of influencing variables. However, all heavy metals had a strong influence from land use and SHG. The model results also provided good insight into the influence of various hydrogeochemical factors and land uses on the presence of each heavy metal. A simple economic analysis was proposed and demonstrated to evaluate the cost effects of changing the land use on heavy metal occurrence. [source]


    Competitive coordination between lead and oligoelements with respect to some therapeutic heavy-metal chelators

    INTERNATIONAL JOURNAL OF QUANTUM CHEMISTRY, Issue 11 2008
    C. Gourlaouen
    Abstract The competitive complexation of Ca2+, Fe2+, Cu2+, Zn2+, and Pb2+ toward ethylene diamine tetraacetate (EDTA), dimercaprol and D -penicillamine, three liganding agents commonly used in chelation therapy against heavy metal, especially lead, poisonings is examined by means of B3LYP calculations, natural population analyses, and the topological analysis of the electron localization function. It is shown that Pb2+ can displace any of Ca2+, Fe2+, Cu2+, or Zn2+ chelated by any of dimercaprol or D -penicillamine, but can only displace Ca2+ if EDTA is concerned. The first two chelators thus appear as better entities than EDTA to be used in chelation therapy, where in vivo selective complexation is essential. Moreover, the comparison of the bonding characteristics of Pb2+ with those of the other cations allows deriving three features to be taken into account in designing new chelators expecting to have an increased selectivity toward this cation. © 2008 Wiley Periodicals, Inc. Int J Quantum Chem, 2008 [source]


    Efficient removal of hexavalent chromium by a tolerant Streptomyces sp. affected by the toxic effect of metal exposure

    JOURNAL OF APPLIED MICROBIOLOGY, Issue 6 2007
    D.K. Morales
    Abstract Aims:, To isolate and analyse chromium-resistant micro-organisms suitable for bioremediation. Methods and Results:, Strain CG252, with a minimal inhibitory concentration of 500 ,g ml,1, was isolated from contaminated soils and identified as a Streptomyces sp. by 16S rDNA sequence analysis. Assays carried out at various Cr(VI) concentrations indicated that chromium removal was more efficient at lower concentrations and that this activity resulted in accumulation of Cr(III). Atomic adsorption analysis indicated that the chromium removed was not associated with cell mass and activity assays showed that the capacity to reduce Cr(VI) was most probably due to a soluble cytosolic enzyme. Cells grown as biofilms showed enhanced removal of Cr(VI) with respect to planktonic cells, while analysis of growth and colony morphology indicated that Cr(VI) had a toxic effect on this strain. Conclusions:,Streptomyces sp. CG252 tolerated heavy metals and elevated levels of chromium, despite its negative effect on growth and development, and was efficient at removing Cr(VI) by promoting reduction to Cr(III). Significance and Impact of the Study:, Strain CG252's capacity to tolerate heavy metals and to reduce Cr(VI) to the less toxic Cr(III), especially when forming biofilms, makes it a promising candidate for detoxification of sites containing this heavy metal. [source]


    Binding of several heavy metal ions by polyaspartyl polymers and their application to some Chinese herbal medicines

    JOURNAL OF APPLIED POLYMER SCIENCE, Issue 4 2007
    Bo Sun
    Abstract Water-insoluble polyaspartyl polymers were synthesized by using water as medium instead of organic medium. Taking Ca2+ as a reference, the binding of several heavy-metal ions, including Pb2+, Cd2+, Hg2+, Cr3+, Cu2+, and Mn2+, by polyaspartyl polymers was studied. The experimental results revealed that polyaspartate is an excellent binding agent for the investigated heavy-metal ions. These cation ions were bound to polyaspartate polymer by the same mechanism as Pb2+, which can be explained by ion exchange model. Since polyaspartate has a protein-resembling structure that is sensitive to trace heavy metal, it was used to remove some trace heavy-metal elements in Chinese herbal medicines. It was found that polyaspartate material was an effective agent for the removal of Pb2+, Cd2+, and Hg2+ ions from glycyrrhizin, angelica, and gynostemma pentaphyllum. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007 [source]


    Depleted uranium,the growing concern

    JOURNAL OF APPLIED TOXICOLOGY, Issue 3 2002
    Aqel W. Abu-Qare
    Abstract Recently, several studies have reported on the health and environmental consequences of the use of depleted uranium. Depleted uranium is a heavy metal that is also radioactive. It is commonly used in missiles as a counterweight because of its very high density (1.6 times more than lead). Immediate health risks associated with exposure to depleted uranium include kidney and respiratory problems, with conditions such as kidney stones, chronic cough and severe dermatitis. Long-term risks include lung and bone cancer. Several published reports implicated exposure to depleted uranium in kidney damage, mutagenicity, cancer, inhibition of bone, neurological deficits, significant decrease in the pregnancy rate in mice and adverse effects on the reproductive and central nervous systems. Acute poisoning with depleted uranium elicited renal failure that could lead to death. The environmental consequences of its residue will be felt for thousands of years. It is inhaled and passed through the skin and eyes, transferred through the placenta into the fetus, distributed into tissues and eliminated in urine. The use of depleted uranium during the Gulf and Kosovo Wars and the crash of a Boeing airplane carrying depleted uranium in Amsterdam in 1992 were implicated in a health concern related to exposure to depleted uranium. Copyright © 2002 John Wiley & Sons, Ltd. [source]


    Diphenyl diselenide protects against hematological and immunological alterations induced by mercury in mice

    JOURNAL OF BIOCHEMICAL AND MOLECULAR TOXICOLOGY, Issue 5 2008
    Ricardo Brandăo
    Abstract Mercury is a heavy metal that can cause a variety of toxic effects on the organism, such as hematological and immunological alterations. In the present investigation, deleterious effects of mercury-intoxication in mice and a possible protective effect of diphenyl diselenide (PhSe)2 were studied. Male adult Swiss albino mice received daily a pretreatment with (PhSe)2 (15.6 mg/kg, orally) for 1 week. After this week, mice received daily mercuric chloride (1 mg/kg, subcutaneously) for 2 weeks. A number of hematological (erythrocytes, leukocytes, platelets, hemoglobin, hematocrit, reticulocytes, and leukocytes differential) and immunological (immunoglobulin G and M plasma concentration) parameters were evaluated. Another biomarker of tissue damage, lactate dehydrogenase (LDH), was also determined. The results demonstrated that mercury exposure caused a reduction in the erythrocyte, hematocrit, hemoglobin, leukocyte, and platelet counts and an increase in the reticulocyte percentages. (PhSe)2 was effective in protecting against the reduction in hematocrit, hemoglobin, and leukocyte levels. (PhSe)2 ameliorated reticulocyte percentages increased by mercury. However, (PhSe)2 was partially effective in preventing against the decrease in erythrocyte and platelet counts. Immunoglobulin G and M concentrations and LDH activity were increased by mercury exposure, and (PhSe)2 was effective in protecting against these effects. In conclusion, (PhSe)2 was effective in protecting against hematological and immunological alterations induced by mercury in mice. © 2008 Wiley Periodicals, Inc. J Biochem Mol Toxicol 22:311,319, 2008; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/jbt.20242 [source]


    Effectiveness test of alginate-derived polymeric surfactants

    JOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 2 2002
    Hyun-Ah Kang
    Abstract A series of alginate-derived polymeric surfactants (APSs) with a linear alkyl group (C8, C12, C16) was synthesized by oxidation followed by reductive amination of 2,3-dialdehydic alginate. The products were characterized by measuring IR spectra, NMR spectra, surface tension and critical micelle concentration (cmc). They were also tested for the solubilization of azobenzene and adsorption of heavy metal. In the case of 40% CHO-C8 APSs, the lowest interfacial tension value (31.5,m Nm,1) was obtained at the cmc value of 1.35,g,dm,3. The dissolving capacity of 40% CHO-C8 APS towards azobenzene was 27 times greater than that of alginate. The overall cobalt (Co2+) removal efficiency by adsorption using APSs was high compared with that of sodium alginate at pH 3, 5 and 7. Equilibrium aspects of cobalt adsorption onto 10% CHO-APSs were studied, and the results show that APSs had high equilibrium capacities for cobalt uptake, 115.5,mgg,1. © 2002 Society of Chemical Industry [source]