Cadmium, copper, lead, and zinc contents of fish marketed in NW Mexico.
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ABSTRACT:
SUBMITTER: Frias-Espericueta MG
PROVIDER: S-EPMC3913528 | biostudies-other | 2014
REPOSITORIES: biostudies-other
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Project description:Farmland soil typical for the Polish rural environment was used in pot experiment to estimate the impact of cadmium and zinc on the manganese, lead and copper uptake by lemon balm (Melissa officinalis L). Bioavailable and total forms of investigated metals in soil and metal concentrations in plants were determined by atomic absorption spectrometry. The plant photosynthesis indicators were also examined. Intensification of photosynthesis upon the high zinc and cadmium soil supplementation was observed. This effect was not detected at low metal concentrations. ANOVA proved that cadmium and zinc treatments influenced manganese, lead and copper transfer from soil and their concentration in plants. Zinc uptake and accumulation in either roots or above-ground parts in plant was inversely proportional to cadmium concentration in soil. Manganese concentration in roots decreased upon the soil supplementation with either zinc or cadmium. It suggests that the latter ions are transported via symplastic pathways and compete with manganese for similar transporters. The opposite situation was observed for lead and copper. Soil supplementation with cadmium and zinc affects manganese, lead and copper concentrations and photosynthesis intensity in lemon balm plant. The following combined interactions in either normal or stress conditions are important indicators of the migration pathways.
| S-EPMC6997233 | biostudies-literature
Project description:Atmospheric deposition samples were collected over 15 mo at several locations near an operating smelter and an abandoned Pb smelter to investigate the contribution of Pb smelting to depositional fluxes and potential local air quality degradation. Samples were analyzed for As, Cd, Cu, Pb, and Zn and subjected to scanning electron microscopy (SEM)-energy dispersive spectroscopy (EDS). Concentrations of Cd and Pb at both sites were greater than at the control site (p < .05), and significant correlations existed between Cd and Pb concentrations at both sites (p < .05). Monthly depositional flux variations at both sites were similar, with greater deposition during cold and dry periods. Heavy metal(loid)s deposition during these periods was correlated with wind speed. Greater Cd depositional flux differences were found between the smelter and control sites compared with other elements. The SEM images suggested that some particles at the operating smelter site were from Pb smelting material. However, most particles at both sites had no characteristics of smelting, suggesting reactions occurred between the smelter-emitted particles and soil components. The EDS results indicated that atmospheric deposition from both sites had lower Pb concentrations than smelting material or ash. The main atmospheric deposition source at the operating and abandoned sites was likely from the resuspension of heavy metal(loid)-enriched soil particles. Greater risk of air pollution from historical Pb smelting facilities exists years after closing down. Reducing soil wind erosional losses may help reduce heavy metal(loid)s dispersion across environments.
| S-EPMC7963641 | biostudies-literature
Project description:BackgroundIn spite of the availability of substitutes for lead and cadmium compounds in paints, manufacturers continue to produce paints with high levels of these metals. As the population continues to grow and there is a continued shift from oil-based to water-based paints, the sales and use of these paints will increase the exposure of humans and the environment to these metals.ObjectivesWe measured the levels of lead (Pb) and cadmium (Cd) in 174 paint samples marketed in Lagos and Ibadan, Nigeria. Paint samples from different manufacturers registered with and without Standards Organization of Nigeria (SON) were considered.MethodsSamples were acid digested using a microwave digester and the levels of the elements were determined using inductively coupled plasma optical emission spectroscopy (ICP-OES).DiscussionThe levels of Cd and Pb (dry weight) in all samples ranged from 98-1999 μg/g and 170-3231 μg/g, respectively. All the samples were above the permissible limits of 90 ppm of the US Consumer Product Safety Commission and 100 ppm limit of the European Union (EU) for Pb and Cd in paint.ConclusionsWe concluded that water-based paints marketed in Nigeria still contain substantial amounts of lead and cadmium which are detrimental to human health and the entire ecosystem. These metals are among the EU priority metals due to the increased risk of occupational exposure to humans and vulnerable groups such as children.
| S-EPMC6221508 | biostudies-literature
Project description:BackgroundIn order to provide new knowledge on the storage of strontium (Sr), barium (Ba), cadmium (Cd), copper (Cu), zinc (Zn), manganese (Mn), chromium (Cr), antimony (Sb), selenium (Se) and lead (Pb) in the feline organism, we measured the concentrations of these elements in the liver, renal cortex and renal medulla, evaluating also the impact of age, sex or the occurrence of a chronic kidney disease (CKD). The element concentrations in the tissues of 47 cats (22 male; 25 female; aged between 2 months and 18 years) were measured using inductively coupled plasma mass spectrometry.ResultsCu, Zn and Mn were the highest in the liver, followed by the renal cortex and the renal medulla. The Cd concentrations were lower in the renal medulla compared to the renal cortex and the liver, and Sr was higher in the renal medulla compared to the liver. The Se concentrations in the cortex of the kidneys were higher than in the medulla of the kidneys and in the liver. Higher Cd concentrations were measured in the renal cortex of female cats, while no further gender-related differences were observed. Except for Cr, Sb and Se, age-dependencies were detected for the storage of all elements. The occurrence of a CKD also affected the storage of the elements, with lower concentrations of Ba (renal medulla), Zn (renal cortex; renal medulla) and Mn (liver; renal medulla), but higher Cd concentrations (liver; renal cortex) in diseased cats.ConclusionsIn conclusion, the present results provide new information on the accumulation of specific elements in the feline liver and kidneys, demonstrating a dependency on age and an impaired kidney function, but not on the sex of the animals.
| S-EPMC4108249 | biostudies-literature
Project description:The concentrations of specific elements in the equine liver and kidneys are of practical relevance since horses are not only food-producing animals, but also partially serve as an indicator for the environmental pollution, as the basic feed includes plants like grass, grain and fruits. In this study, the concentrations of strontium (Sr), barium (Ba), cadmium (Cd), copper (Cu), zinc (Zn), manganese (Mn), chromium (Cr), antimony (Sb), selenium (Se) and lead (Pb) were measured in the liver, renal cortex and renal medulla of 21 horses (8 male; 13 female; aged between 5 months-28 years), using inductively coupled plasma mass spectrometry. Comparable Cu and Zn concentrations were detected in the liver and renal cortex, while approximately 50% lower concentrations were measured in the renal medulla. The lowest Sr, Cd and Se, but the highest Mn, Sb and Pb concentrations were measured in the liver. The Ba concentrations were comparable in the renal cortex and medulla, but lower in the liver of the horses. Gender-related differences were observed for Cd, Mn and Cr, with higher Cd concentrations in the liver, but lower Mn concentrations in the renal cortex and lower Cr concentrations in the renal medulla of female horses. Age-related differences were detected for most measured elements, however, the animal number per age-group was only low. In conclusion, the present study provides important reference data for the storage of Sr, Ba, Cd, Cu, Zn, Mn, Cr, Sb, Se and Pb in the liver and kidneys of horses, which are of practical relevance for an evaluation of the exposure of horses to these elements, either via feed or the environment.
| S-EPMC4108716 | biostudies-literature
Project description:The increase in photovoltaic panel installations in Europe will generate vast amounts of waste in the near future. Therefore, it is important to develop new technologies that allow the recycling of end-of-life photovoltaic panels. This material can serve as a secondary resource, not only for precious metals (e.g. silver), but also for base metals. In this work, the extraction and recovery of the base metals copper, zinc and lead from a copper-rich photovoltaic panel residue was investigated. The material was first leached at 80 °C under microwave irradiation with a mixture of hydrochloric acid, sodium chloride and hydrogen peroxide solutions. Based on the Box-Behnken factorial design optimization, it was possible to extract 81.2% of Cu, 96.4% of Zn and 77.6% of Pb, under the following leaching conditions: [HCl] = 0.5 mol L-1, [NaCl] = 200 g L-1, [H2O2] = 7.5 wt% and t = 60 min. Cementation with iron powder at a 1.2 iron-to-copper stoichiometric ratio allowed the recovery of copper nearly quantitatively (99.8%) as a copper-iron sediment. The gas-liquid separation technique of ion flotation was employed to separate lead and zinc from the dilute copper-free leachate. Cetyltrimethylammonium bromide (CTAB), a cationic surfactant, selectively recovered lead (99.4%) over zinc as lead(ii) tetrachloro cetyltrimethylammonium colloid, after eight ion flotation stages and [CTAB]total = 7.2 mmol L-1. The zinc that remained in the solution after the ion flotation step was recovered by precipitation and by adding sodium sulfide at 110% of the stoichiometric amount after removing iron as ferric hydroxide by slowly raising the pH to 3.7.
| S-EPMC8979222 | biostudies-literature
Project description:In this study, the preparation and electrochemical application of a chromium(III) oxide modified carbon paste electrode (Cr-CPE) and a screen printed electrode (SPE), made from the same material and optimized for the simple, cheap and sensitive simultaneous determination of zinc, cadmium, lead, copper and the detection of silver ions, is described. The limits of detection and quantification were 25 and 80 µg·L-1 for Zn(II), 3 and 10 µg·L-1 for Cd(II), 3 and 10 µg·L-1 for Pb(II), 3 and 10 µg·L-1 for Cu(II), and 3 and 10 µg·L-1 for Ag(I), respectively. Furthermore, this promising modification was transferred to the screen-printed electrode. The limits of detection for the simultaneous determination of zinc, cadmium, copper and lead on the screen printed electrodes were found to be 350 µg·L-1 for Zn(II), 25 µg·L-1 for Cd(II), 3 µg·L-1 for Pb(II) and 3 µg·L-1 for Cu(II). Practical usability for the simultaneous detection of these heavy metal ions by the Cr-CPE was also demonstrated in the analyses of wastewaters.
| S-EPMC5580028 | biostudies-literature
Project description:Synthesis, characterization, reactivity, and sensing properties of 4-formylbenzoate complexes of copper(II), zinc(II), and cadmium(II) possessing the 1,10-phenanthroline ancillary ligand are studied. The crystal structures of the (1,10-phenanthroline)bis(4-formylbenzoate)(aqua)copper(II) and (1,10-phenanthroline)bis(4-formylbenzo-ate)zinc(II) and a novel molecular complex comprising an assembly of mononuclear and dinuclear species of (1,10-phenanthroline)bis(4-formylbenzoate)cadmium(II) are reported. These zinc and cadmium complexes are fluorescent; they show differentiable sensitivity to detect three positional isomers of nitroaniline. The mechanism of sensing of nitroanilines by 1,10-phenanthroline and the complexes are studied by fluorescence titrations, photoluminescence decay, and dynamic light scattering. A plausible mechanism showing that 1,10-phenanthroline ligand-based emission quenched by electron transfer from the excited state of 1,10-phenanthroline to nitroaniline is supported by density functional theory calculations. In an anticipation to generate a fluorescent d10-copper(I) formylbenzoate complex by a mild reducing agent such as hydroxylamine hydrochloride for similar sensing of nitroaromatics as that of the d10-zinc and cadmium 4-formylbenzoate complexes, reactivity of d9-copper(II) with hydroxylamine hydrochloride in the presence of 4-formylbenzoic acid and 1,10-phenanthroline is studied. It did not provide the expected copper(I) complex but resulted in stoichiometry-dependent reactions of 4-formylbenzoic acid with hydroxylamine hydrochloride in the presence of copper(II) acetate and 1,10-phenanthroline. Depending on the stoichiometry of reactants, an inclusion complex of bis(1,10-phenanthroline)(chloro)copper(II) chloride with in situ-formed 4-((hydroxyimino)methyl)benzoic acid or copper(II) 4-(hydroxycarbamoyl)benzoate complex was formed. The self-assembly of the inclusion complex has the bis(1,10-phenanthroline)(chloro)copper(II) cation encapsulated in hydrogen-bonded chloride-hydrate assembly with 4-((hydroxyimino)methyl)benzoic acid.
| S-EPMC6844117 | biostudies-literature
Project description:BACKGROUND:This study is focused on the measurement of trace elements (zinc, copper, cadmium, lead and selenium) in the saliva of pigs in order to study their levels on different porcine pathological conditions in the field. The experiment involved 15 pigs without clinical signs of disease and 42 diseased pigs (suffering from lameness, rectal prolapse, fatigue or growth rate retardation). Individual saliva samples were collected, allowing the pigs to chew a sponge each for trace element quantifications through atomic absorption spectrometry (AAS). Since this is the first report on the measurements of trace elements in porcine saliva, a routine analytical validation study was performed for the quantification of all the studied elements. Moreover, the acute phase proteins C-reactive protein (CRP) and haptoblobin (Hp), the total antioxidant capacity (TAC) and adenosine deaminase (ADA) were quantified in the saliva samples for the animal's health status assessment. RESULTS:Modifications in the levels of acute phase proteins or ADA were only recorded in animals with lameness and rectal prolapse and those with fatigue respectively. Moreover, TAC level changes were observed in pigs with growth-rate retardation. However, alterations in the levels of two or more trace elements were reported for all the different groups of diseased pigs with evident variations within pathologies. CONCLUSIONS:The salivary quantification of trace elements could be considered as a complementary tool to acute phase proteins, TAC and ADA determinations for disease detection and differentiation in the pig and should be explored in greater depth.
| S-EPMC6993390 | biostudies-literature
Project description:Lead-zinc deposits are often difficult to classify because clear criteria are lacking. In recent years, new tools, such as Cd and Zn isotopes, have been used to better understand the ore-formation processes and to classify Pb-Zn deposits. Herein, we investigate Cd concentrations, Cd isotope systematics and Zn/Cd ratios in sphalerite from nine Pb-Zn deposits divided into high-temperature systems (e.g., porphyry), low-temperature systems (e.g., Mississippi Valley type [MVT]) and exhalative systems (e.g., sedimentary exhalative [SEDEX]). Our results showed little evidence of fractionation in the high-temperature systems. In the low-temperature systems, Cd concentrations were the highest, but were also highly variable, a result consistent with the higher fractionation of Cd at low temperatures. The ?(114/110)Cd values in low-temperature systems were enriched in heavier isotopes (mean of 0.32?±?0.31‰). Exhalative systems had the lowest Cd concentrations, with a mean ?(114/110)Cd value of 0.12?±?0.50‰. We thus conclude that different ore-formation systems result in different characteristic Cd concentrations and fraction levels and that low-temperature processes lead to the most significant fractionation of Cd. Therefore, Cd distribution and isotopic studies can support better understanding of the geochemistry of ore-formation processes and the classification of Pb-Zn deposits.
| S-EPMC4848528 | biostudies-literature