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Cadmium
Kinds of Cadmium Terms modified by Cadmium Selected AbstractsSimultaneous Determination of Cadmium, Lead, Copper and Mercury Ions Using Organofunctionalized SBA-15 Nanostructured Silica Modified Graphite,Polyurethane Composite ElectrodeELECTROANALYSIS, Issue 1 2010Ivana Cesarino Abstract A new sensor has been developed for the simultaneous detection of cadmium, lead, copper and mercury, using differential pulse and square wave anodic stripping voltammetry (DPASV and SWASV) at a graphite,polyurethane composite electrode with SBA-15 silica organofunctionalized with 2-benzothiazolethiol as bulk modifier. The heavy metal ions were preconcentrated on the surface of the modified electrode at ,1.1,V vs. SCE where they complex with 2-benzothiazolethiol and are reduced to the metals, and are then reoxidized. Optimum SWASV conditions lead to nanomolar detection limits and simultaneous determination of Cd2+, Pb2+, Cu2+ and Hg2+ in natural waters was achieved. [source] Simultaneous Determination of Trace Zinc(II) and Cadmium(II) by Differential Pulse Anodic Stripping Voltammetry Using a MWCNTs,NaDBS Modified Stannum Film ElectrodeELECTROANALYSIS, Issue 23 2009Qing Tian Abstract A multiwalled carbon nanotubes,sodium dodecyl benzene sulfonate (MWCNTs,NaDBS) modified stannum film electrode was employed for the determination of cadmium(II) and zinc(II). The Sn/MWCNTs-NaDBS film electrode was prepared by applying MWCNTs,NaDBS suspension to the surface of the GCE, while the Sn film was plated in situ simultaneously with the target metal ions. Under optimal conditions, linear calibration curves were obtained in a range of 5.0 ,100.0,,g L,1 with detection limits of 0.9,,g L,1 for zinc(II) and 0.8,,g L,1 for cadmium(II), respectively. This film electrode was successfully applied to the determination of Zn(II) and Cd(II) in tap water sample. [source] Electroanalytical Determination of Cadmium(II) and Lead(II) Using an Antimony Nanoparticle Modified Boron-Doped Diamond ElectrodeELECTROANALYSIS, Issue 10 2009Kathryn Abstract We report the simultaneous electroanalytical determination of Pb2+ and Cd2+ by linear sweep anodic stripping voltammetry (LSASV) using an antimony nanoparticle modified boron doped diamond (Sb-BDD) electrode. Sb deposition was performed in situ with the analytes, from a solution of 1,mg L,1 SbCl3 in 0.1,M HCl (pH,1). Pb2+ inhibited the detection of Cd2+ during simultaneous additions at the bare BDD electrode, whereas in the presence of antimony, both peaks were readily discernable and quantifiable over the linear range 50,500,,g L,1. [source] Electrochemical Detection of Cadmium and Lead Complexes with Low Molecular Weight Organic AcidsELECTROANALYSIS, Issue 3-5 2009Jaklová Dytrtová Abstract The Cd and Pb complexes with oxalic (OA) and citric acid (CA) were detected in model and soil solutions using cyclic and stripping voltammetry. A mixed complex consisting of Cd, Pb, and OA was found; its peak potential varied from ,582.0 to ,542.5,mV (vs. Ag/AgCl/KCl(3,mol L,1)). For mixed complex formation, the presence of PbOH+ species and Cd2+ in oxalic acid solution was necessary. Only the ,simple' complexes of CA with Pb and Cd were found in the model solution. The existence of all investigated metal complexes is confined to neutral pH range. The mixed complex was also found in real soil solutions. [source] Simultaneous Quantitative Determination of Cadmium, Lead, and Copper on Carbon-Ink Screen-Printed Electrodes by Differential Pulse Anodic Stripping Voltammetry and Partial Least Squares RegressionELECTROANALYSIS, Issue 23 2008Michael Cauchi Abstract Water is a vital commodity for every living entity on the planet. However, water resources are threatened by various sources of contamination from pesticides, hydrocarbons and heavy metals. This has resulted in the development of concepts and technologies to create a basis for provision of safe and high quality drinking water. This paper focuses on the simultaneous quantitative determination of three common contaminants, the heavy metals cadmium, lead and copper. Multivariate calibration was applied to voltammograms acquired on in-house printed carbon-ink screen-printed electrodes by the highly sensitive electrochemical method of differential pulse anodic stripping voltammetry (DPASV). The statistically inspired modification of partial least squares (SIMPLS) algorithm was employed to effect the multivariate calibration. The application of data pretreatment techniques involving range-scaling, mean-centering, weighting of variables and the effects of peak realignment are also investigated. It was found that peak realignment in conjunction with weighting and SIMPLS led to the better overall root mean square error of prediction (RMSEP) value. This work represents significant progress in the development of multivariate calibration tools in conjunction with analytical techniques for water quality determination. It is the first time that multivariate calibration has been performed on DPASV voltammograms acquired on carbon-ink screen-printed electrodes. [source] A Study of Nafion-Coated Bismuth-Film Electrode for the Determination of Zinc, Lead, and Cadmium in Blood SamplesELECTROANALYSIS, Issue 21 2008Benzhi Liu Abstract In this article a sensitive differential pulse stripping voltammetry technique on Nafion-coated bismuth-film electrode (NCBFE) was studied for the simultaneous determination of zinc, cadmium, and lead ions in blood samples at ultra trace levels. The measurement results were in excellent agreement with those obtained from atomic absorption spectroscopy. Various operational parameters were investigated and discussed in terms of their effect on the measurement signals. Under optimal conditions, calibration curves for the simultaneous determination of zinc, cadmium, and lead ions were achieved, based on three times the standard deviation of the baseline, the limits of detection were 0.09,,g L,1 for Cd(II), 0.13,,g L,1 for Pb(II), and 0.97,,g L,1 for Zn(II) respectively. [source] The Fabrication and Characterization of a Bismuth Nanoparticle Modified Boron Doped Diamond Electrode and Its Application to the Simultaneous Determination of Cadmium(II) And Lead(II)ELECTROANALYSIS, Issue 16 2008Kathryn Abstract We report the simultaneous electroanalytical determination of Pb2+ and Cd2+ by square-wave anodic stripping voltammetry (SWASV) using a bismuth nanoparticle modified boron doped diamond (Bi-BDD) electrode. Bi deposition was performed in situ with the analytes, from a solution of 0.1,mM Bi(NO3)3 in 0.1,M HClO4 (pH,1.2), and gave detection limits of 1.9,,g L,1 and 2.3,,g L,1 for Pb(II) and Cd(II) respectively. Pb2+ and Cd2+ could not be detected simultaneously at a bare BDD electrode, whilst on a bulk Bi macro electrode (BiBE) the limits of detection for the simultaneous determination of Pb2+ and Cd2+ were ca. ten times higher. [source] Simultaneous Determination of Nickel and Cadmium by Adsorptive Stripping VoltammetryELECTROANALYSIS, Issue 12 2008B. Gholivand Abstract A sensitive and fast method for the simultaneous determination of trace amounts of nickel and cadmium in real samples has been described using differential pulse adsorptive stripping voltammetry (DPASV) by adsorptive accumulation of the N,N,-bis(salicylaldehydo)4-carboxyphenylenediamine (BSCPDA),complex on the hanging mercury drop electrode (HMDE). As supporting electrolyte 0.02,mol L,1 ammonia buffers containing ligand has been used. Optimal analytical conditions were found to be: BSCPDA concentration of 42,,M, pH,9.6 and adsorption potential at ,50,mV versus Ag/AgCl. With an accumulation time of 20,s, the peaks current are proportional to the concentration of nickel and cadmium over the 1,180, and 0.5,200,ng mL,1 with detection limits of 0.06 and 0.03,ng mL,1 respectively. The sensitivity of method for determination of nickel and cadmium were obtained 0.54 and 0.98,nA mL ng,1, respectively. The procedure was applied to simultaneous determination of nickel and cadmium in some real and synthetic artificial samples with satisfactory results. [source] Determination of Lead and Cadmium at Silver Electrode by Subtractive Anodic Stripping Voltammetry in Plant Materials Containing TlELECTROANALYSIS, Issue 9 2005Beata Krasnod, bska-Ostr Abstract Lead and cadmium have been determined by the subtractive anodic stripping voltammetry using the square-wave mode at a silver electrode without removal of oxygen. The samples containing large amount of thallium were collected from a highly contaminated region. The presence of thallium strongly affects the peak shape of Cd. The plant material digestion was performed with HNO3/HClO4 mixture using pressurised microwave decomposition. The proposed method used for the lead determination was validated by the inter-method comparison (ICP-MS). The cadmium determination was validated using certified reference material. The results obtained, supported by statistical tests, demonstrated the usefulness of the method for the lead determination in samples containing large amounts of Cd and Tl. It is important to note that Cd can only be quantified when the thallium concentration is much lower than that of cadmium. [source] Asymmetrical Schiff Bases as Carriers in PVC Membrane Electrodes for Cadmium (II) IonsELECTROANALYSIS, Issue 8 2005Hossein Mashhadizadeh, Mohammad Abstract 5-[((4-Methyl phenyl) azo)- N -(6-amino-2-pyridin) salicylaldimine] (S1), and 5-[((4-methyl phenyl) azo)- N -(2-diamino-2-cyano-1-ethyl cyanide) salicylaldehyde] (S2) with N and O donor atoms are effective ionophores to make Cd2+ -selective membrane electrodes. The electrodes based on S1 and S2 exhibits a Nernstian or near-Nernstian response for cadmium ion over a wide concentration range 1.5×10,1,7.5×10,7 with a slope of 28 and 2.0×10,1,4.0×10,7 with a slope of 22, respectively. They have quick response and can be used for three or four months without any divergence in potential. The proposed sensors show fairly good selectivity over some alkali, alkaline earth, transition and heavy metal ions. The electrodes based on S1 and S2 can be used in the pH range 3.5,9. These electrodes were used as an indicator electrode in potentiometric titration of cadmium ion with EDTA and in the direct determination of cadmium ion in aqueous solutions. [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 MealsELECTROANALYSIS, Issue 18 2004Clinio 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] Electrochemical Detection of Trace Concentrations of Cadmium and Lead with a Boron-Doped Diamond Electrode: Effect of KCl and KNO3 Electrolytes, Interferences and Measurement in River WaterELECTROANALYSIS, Issue 3 2004Carol Babyak Abstract Parts-per-billion levels of cadmium and lead were detected using square-wave anodic stripping voltammetry with a boron-doped diamond electrode. Calibration plots (10-minute deposition time) in KCl and KNO3 were non-linear at low concentrations (1,5,ppb) due to the deposition mechanism of these metals. The preferred electrolyte for cadmium was KCl, while lead could be measured in either electrolyte. The lowest concentrations included in the linear portion of the calibration plot (5,minute deposition time) for cadmium were 10,ppb and 50,ppb in KCl and KNO3, respectively, and 10,ppb for lead in KNO3. The presence of either lead or copper suppressed the cadmium stripping peak, but the lead stripping peak was unaffected by cadmium, and enhanced by the addition of copper. A river water sample was analyzed for cadmium and lead, and the cadmium results were confirmed using ICP-AES spectrometry. It was determined electrochemically that a fraction of lead in the river sample was bound by complexing material in the sample. [source] Characteristics of Subtractive Anodic Stripping Voltammetry of Lead, Cadmium and Thallium at Silver-Gold Alloy ElectrodesELECTROANALYSIS, Issue 17 2003Y. Bonfil Abstract Silver-gold alloy electrodes have been studied for the purpose of the quantitative determination of heavy metals by subtractive anodic stripping voltammetry, (SASV). The results have been compared with those obtained with the silver and gold electrodes. The 50/50 a/o Ag/Au alloy electrode is the most suitable for quantifying thallium in the presence of lead and cadmium. The separation of its peak from those of lead and cadmium is 200,mV, which is about twice the separation obtained on the pure metal electrodes and is also better than on mercury. The silver electrode is suitable for the simultaneous determination of thallium, lead and cadmium. The peaks of lead and cadmium overlap on the 50/50 alloy. Pure silver or pure gold can be used for simultaneous quantification of these two metals. The use of gold for quantifying lead and cadmium is more limited because the peak potential of cadmium is shifted in the negative direction as its concentration increases and at [Cd2+]>200,nM, the two peaks merge. SASV enables correction for background currents and is of utmost importance for obtaining well-defined peaks. The peaks of lead, cadmium and thallium appear over a relatively narrow potential range (ca. 200,mV) on all the electrodes presented in this work. For this reason, the quantifying of a peak is based on the derivative at the inflection point of only one of its branches (ascending or descending). All SASV measurements were carried out without removal of oxygen. [source] Cadmium induced oxidative stress influence on glutathione metabolic genes of Camellia sinensis (L.) O. KuntzeENVIRONMENTAL TOXICOLOGY, Issue 4 2007Prashant Mohanpuria Abstract Glutathione, a tripeptide with sulfhydryl (-SH) group is a very crucial compound primarily involved in redox balance maintenance of the cellular environment. In this study, we monitored the influence of Cd exposure on the transcript levels of glutathione metabolic genes in bud tissues, the youngest leaf, of Camellia sinensis L. In addition, some physiochemical parameters were also studied. Cd exposure decreased chlorophyll and protein contents, while increase was observed in lipid peroxidation upon Cd treatments. These changes were found to be concentration and duration dependent, indicating the occurrence of oxidative stress upon Cd exposure. The transcript levels of glutathione biosynthetic genes viz. ,-glutamylcysteine synthetase (,-ECS) and glutathione synthetase (GSHS) increased upon Cd exposure. Furthermore, transcript levels of glutathione reductase (GR), an enzyme involved in reduction of oxidized glutathione (GSSG) to reduced glutathione (GSH), also showed upregulation on Cd exposure. However, the transcript levels of glutathione-S-transferase (GST), an enzyme involved in forming metal,GSH complex and help in sequestration of high levels of metal ions to vacuole, did not show any change on Cd treatment. This study document that Cd exposure induces oxidative stress in Camellia sinensis and the upregulation in transcript levels of glutathione metabolic genes except GST have suggested the role of these enzymes in the protection of plants from high level Cd exposure. © 2007 Wiley Periodicals, Inc. Environ Toxicol 22: 368,374, 2007. [source] Mechanism of DNA damage by cadmium and interplay of antioxidant enzymes and agentsENVIRONMENTAL TOXICOLOGY, Issue 2 2007Veera L. D. Badisa Abstract Cadmium is an environmental toxicant, which causes cancer in different organs. It was found that it damages DNA in the various tissues and cultured cell lines. To investigate the mechanism of DNA damage, we have studied the effect of cadmium-induced DNA damage in plasmid pBR322 DNA, and the possible ameliorative effects of antioxidative agents under in vitro conditions. It was observed that cadmium alone did not cause DNA damage. However, it caused DNA damage in the presence of hydrogen peroxide, in a dose dependent manner, because of production of hydroxyl radicals. Findings from this study show the conversion of covalently closed circular double-stranded pBR 322 DNA to the open circular and linear forms of DNA when treated with 10 ,M cadmium and various concentrations of H2O2. The conversion was due to nicking in DNA strands. The observed rate of DNA strand breakage was dependent on H2O2 concentration, temperature, and time. Metallothionein I failed to prevent cadmium-induced DNA nicking in the presence of H2O2. Of the two antioxidant enzymes (catalase and superoxide dismutase) studied, only catalase conferred significant (50,60%) protection. EDTA and DMSO exhibited protection similar to catalase, while mannitol showed only about 20% protection against DNA damage. Ethyl alcohol failed to ameliorate cadmium-induced DNA strands break. From this study, it is plausible to infer that cadmium in the presence of hydrogen peroxide causes DNA damage probably by the formation of hydroxyl ions. These results may indicate that cadmium in vivo could play a major role in the DNA damage induced by oxidative stress. © 2007 Wiley Periodicals, Inc. Environ Toxicol 22: 144,151, 2007. [source] Cadmium tolerance in the Nile tilapia (Oreochromis niloticus) following acute exposure: Assessment of some ionoregulatory parametersENVIRONMENTAL TOXICOLOGY, Issue 1 2006Sofia Garcia-Santos Abstract The Nile tilapia (Oreochromis niloticus) can tolerate very high levels of waterborne cadmium. It has one of the highest 96 h LC50 recorded for a freshwater teleost fish (14.8 mg/L Cd; hardness 50 mg/L CaCO3). Cadmium is known to perturb ion balance in teleost fishes. However, in an acute time course experiment, plasma Na+ concentrations were unaffected, and plasma Ca2+ values only decreased after 96 h exposure in a dose-independent manner. Branchial Na+/K+ -ATPase activity and ,-subunit protein level expression in crude gill homogenates were not affected by Cd exposure during this period. Branchial chloride cell numbers, identified as Na+/K+ -ATPase immunoreactive cells using immunohistochemistry, decreased 24 h after exposure but recovered thereafter. Histopathological changes did not follow a consistent pattern of variation with exposure time, and the alterations noted in gill epithelium were basically nonspecific to cadmium. Because of its tolerance, it can be concluded that the tilapia O. niloticus would not be a suitable test organism to evaluate sublethal toxicity of cadmium and the realistic impact of this pollutant in the environment. However, it certainly could contribute significantly to our understanding of the toxic mechanism of cadmium exposure in aquatic organisms. This is the first work to investigate the effect of waterborne pollutants on Na+/K+ -ATPase ,-subunit protein expression in fish gills. © 2006 Wiley Periodicals, Inc. Environ Toxicol 21: 33,46, 2006. [source] Histopathological alterations in the edible snail, Babylonia areolata (spotted babylon), in acute and subchronic cadmium poisoningENVIRONMENTAL TOXICOLOGY, Issue 2 2005P. Tanhan Abstract Histopathological alterations in 6- to 8-month-old juvenile spotted babylon, Babylonia areolata, from acute and subchronic cadmium exposure were studied by light microscopy. The 96-h LC50 value of cadmium for B. areolata was found to be 3.35 mg/L, and the maximum acceptable toxicant concentration (MATC) was 1.6 mg/L. Snails were exposed to 3.35 and 0.08 mg/L (5% of MATC) of cadmium for 96 h and 90 days, respectively. After exposure the gill, the organs of the digestive system (proboscis, esophagus, stomach, digestive gland, and rectum), and the foot were analyzed for cadmium accumulation. The results showed that most digestive organs had a high affinity for cadmium. The main target organ was the stomach, which could accumulate on average 1192.18 ,g/g dry weight of cadmium. Cadmium was shown to accumulate to a lesser extent in the digestive gland, gill, rectum, esophagus, proboscis, and foot. Histopathological alterations were observed in the gill and digestive organs (proboscis, esophagus, stomach, and rectum). The study showed that the stomach and gill were the primary target organs of both acute and subchronic exposure. Gill alterations included increased size of mucous vacuoles, reduced length of cilia, dilation and pyknosis of nuclei, thickening of basal lamina, and accumulation of hemocytes. The epithelial lining of the digestive tract showed similar alterations such as increased size of mucous vacuoles, reduced length of cilia, and dilation of nuclei. In addition, fragmentation of the muscle sheath was observed. © 2005 Wiley Periodicals, Inc. Environ Toxicol 20: 142,149, 2005. [source] Uptake kinetics and subcellular compartmentalization of cadmium in acclimated and unacclimated earthworms (Eisenia andrei)ENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 7 2010Shuo Yu Abstract Acclimation to cadmium (Cd) levels exceeding background concentrations may influence the ability of earthworms to accumulate Cd with minimum adverse effects. In the present study, earthworms (Eisenia andrei) were acclimated by exposure to 20,mg/kg Cd (dry wt) in Webster soil for 28 d. A 224-d bioaccumulation test was subsequently conducted with both acclimated and unacclimated worms exposed in Webster soils spiked with 20,mg/kg and 100,mg/kg Cd (dry wt). Uptake kinetics and subcellular compartmentalization of Cd were examined. Results suggest that acclimated earthworms accumulated more Cd and required a longer time to reach steady state than unacclimated worms. Most of the Cd was present in the metallothionein (MT) fraction. Cadmium in the MT fraction increased approximately linearly with time and required a relatively longer time to reach steady state than Cd in cell debris and granule fractions, which quickly reached steady state. Cadmium in the cell debris fraction is considered potentially toxic, but low steady state concentrations observed in the present study would not suggest the potential for adverse effects. Future use of earthworms in ecological risk assessment should take into consideration pre-exposure histories of the test organisms. A prolonged test period may be required for a comprehensive understanding of Cd uptake kinetics and compartmentalization. Environ. Toxicol. Chem. 2010;29:1568,1574. © 2010 SETAC [source] Critical period of sensitivity for effects of cadmium on frog growth and development,ENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 6 2009Jackson A. Gross Abstract Cadmium is a ubiquitous pollutant in aquatic environments that can alter organismal physiology and ecology. Previous experiments found that ecological Cd exposures increased the growth and development of two North American anurans. However, the generality of these effects among species, the time period over which they occur, and the mechanisms responsible remain conjectural. The goal of the present study was to determine the critical period of sensitivity of Rana pipiens exposed to ecologically relevant levels of Cd. We exposed tadpoles to Cd (0 [control], 1.0, and 10.0 ,g/L) from Gosner stage (GS) 25 to metamorphic climax. We assessed effects of Cd on amphibian length, survival, and development during premetamorphosis (GS 25,30) and prometamorphosis (GS 31,42). After 14 d of exposure, we staged tadpoles and recorded snout-vent length. Tadpoles were then pooled according to treatment and stage (GS , 29 or GS , 30) and allowed to undergo metamorphic development. Tadpoles exposed to 10 ,g/L were significantly larger and more advanced in development by 14 d. Survival to forelimb emergence exceeded 90% in all treatments, and time to metamorphic climax was not different from that in controls. Body burdens of Cd were positively correlated with increasing treatment. Early amphibian development (premetamorphosis) was shown to be the critical period of sensitivity for growth and development. Whereas the freshwater criterion for Cd appears to be protective for survival, a lack of knowledge remains about the sublethal effects of chronic exposures of metal pollutants, especially as they relate to tissue concentrations at various stages of amphibian life history. [source] Trout density and health in a stream with variable water temperatures and trace element concentrations: Does a cold-water source attract trout to increased metal exposure?ENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 4 2009David D. Harper Abstract A history of hard-rock mining has resulted in elevated concentrations of heavy metals in Prickly Pear Creek (MT, USA). Remediation has improved water quality; however, dissolved zinc and cadmium concentrations still exceed U.S. Environmental Protection Agency water-quality criteria. Physical habitat, salmonid density, fish health, and water quality were assessed, and metal concentrations in fish tissues, biofilm, and macroinvertebrates were determined to evaluate the existing condition in the watershed. Cadmium, zinc, and lead concentrations in fish tissues, biofilm, and invertebrates were significantly greater than those at the upstream reference site and an experimental site farther downstream of the confluence. Fish densities were greatest, and habitat quality for trout was better, downstream of the confluence, where water temperatures were relatively cool (16°C). Measures of fish health (tissue metal residues, histology, metallothionein concentrations, and necropsies), however, indicate that the health of trout at this site was negatively affected. Trout were in colder but more contaminated water and were subjected to increased trace element exposures and associated health effects. Maximum water temperatures in Prickly Pear Creek were significantly lower directly below Spring Creek (16°C) compared to those at an experimental site 10 km downstream (26°C). Trout will avoid dissolved metals at concentrations below those measured in Prickly Pear Creek; however, our results suggest that the preference of trout to use cool water temperatures may supersede behaviors to avoid heavy metals. [source] Influence of in-stream diel concentration cycles of dissolved trace metals on acute toxicity to one-year-old cutthroat trout (Oncorhynchus clarki lewisi)ENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 12 2007David A. Nimick Abstract Extrapolating results of laboratory bioassays to streams is difficult, because conditions such as temperature and dissolved metal concentrations can change substantially on diel time scales. Field bioassays conducted for 96 h in two mining-affected streams compared the survival of hatchery-raised, metal-näive westslope cutthroat trout (Oncorhynchus clarki lewisi) exposed to dissolved (0.1-,m filtration) metal concentrations that either exhibited the diel variation observed in streams or were controlled at a constant value. Cadmium and Zn concentrations in these streams increased each night by as much as 61 and 125%, respectively, and decreased a corresponding amount the next day, whereas Cu did not display a diel concentration cycle. In High Ore Creek (40 km south of Helena, MT, USA), survival (33%) after exposure to natural diel-fluctuating Zn concentrations (range, 214,634 ,g/L; mean, 428 ,g/L) was significantly (p = 0.008) higher than survival (14%) after exposure to a controlled, constant Zn concentration (422 ,g/L). Similarly, in Dry Fork Belt Creek (70 km southeast of Great Falls, MT, USA), survival (75%) after exposure to diel-fluctuating Zn concentrations (range, 266,522 ,g/L; mean, 399 ,g/L) was significantly (p = 0.022) higher than survival (50%) in the constant-concentration treatment (392 ,g/L). Survival likely was greater in these diel treatments, both because the periods of lower metal concentrations provided some relief for the fish and because toxicity during periods of higher metal concentrations was lessened by the simultaneous occurrence each night of lower water temperatures, which reduce the rate of metal uptake. Based on the present study, current water-quality criteria appear to be protective for streams with diel concentration cycles of Zn (and, perhaps, Cd) for the hydrologic conditions tested. [source] Biological significance of metals partitioned to subcellular fractions within earthworms (Aporrectodea caliginosa),ENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 3 2006Martina G. Vijver Abstract Metal ions in excess of metabolic requirements are potentially toxic and must be removed from the vicinity of important biological molecules to protect organisms from adverse effects. Correspondingly, metals are sequestrated in various forms, defining the accumulation pattern and the magnitude of steady-state levels reached. To investigate the subcellular fractions over which Ca, Mg, Fe, Cu, Zn, Cd, Pb, Ni, and As are distributed, earthworms (Aporrectodea caliginosa) collected from the field were analyzed by isolating metal-rich granules and tissue fragments from intracellular microsomal and cytosolic fractions (i.e., heat-stable proteins and heat-denatured proteins). The fractions showed metal-specific binding capacity. Cadmium was mainly retrieved from the protein fractions. Copper was equally distributed over the protein fraction and the fraction comprising tissue fragments, cell membranes, and intact cells. Zinc, Ca, Mg, and As were mainly found in this fraction as well. Lead, Fe, and Ni were mainly isolated from the granular fraction. To study accumulation kinetics in the different fractions, three experiments were conducted in which earthworms were exposed to metal-spiked soil and a soil contaminated by anthropogenic inputs and, indigenous earthworms were exposed to field soils. Although kinetics showed variation, linear uptake and steady-state types of accumulation patterns could be understood according to subcellular compartmentalization. For risk assessment purposes, subcellular distribution of metals might allow for a more precise estimate of effects than total body burden. Identification of subcellular partitioning appears useful in determining the biological significance of steady-state levels reached in animals. [source] Kinetic uptake of bioavailable cadmium, selenium, and zinc by Daphnia magnaENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 11 2002Ri-Qing Yu Abstract Kinetic uptake of Cd, Se(IV), and Zn by Daphnia magna from the dissolved phase was determined using radiotracer techniques in moderately hard water. The metal influx rate and distribution in the soft tissue and the exoskeleton of the daphnids as influenced by metal concentration, inorganic ligands including pH, Ca2+ and SO42,, and body size were quantified. When the metal concentrations were <180 nM for Cd and <769 nM for Zn, the concentration factor in daphnids increased linearly within the 12 h of exposure. At a higher concentration, apparent steady state was reached after 3 h of exposure. Cadmium and Zn distribution in the soft tissues was not affected by the total ambient concentrations, whereas Se distribution in the soft tissue decreased by 7 to 10% with increasing Se concentration from 16 to 643 nM. A linear positive power relationship was found between the influx rates of the metals and the ambient concentrations. The concentration factor for Se, however, decreased significantly with increasing Se concentration in water. The influx rate of metals was inversely related to the body size in a power function. When the pH in ambient water increased from 5.0 to 7.0, the influx rate of Cd, Se, and Zn increased by 2.9, 16.6, and 4.1 times, respectively. The influx rates of Cd, Se, and Zn decreased by 6.9, 8.7, and 4.4 times, respectively, with an increase in Ca2+ concentration from 0.6 to 5.1 mM. In contrast, the uptake rates of all three metals were not significantly affected by the SO42, concentration. The majority of accumulated Se was distributed in the soft tissues after 12 h of exposure, whereas Cd and Zn were about evenly distributed in the soft tissue and exoskeleton. Any changes in pH, Ca2+, and SO42, concentrations did not apparently affect their distributions in the daphnids. Our study provides important kinetic data necessary for delineating the exposure routes and for further development of the biotic ligand model in Daphnia. Using a bioenergetic-based kinetic model, we showed that the dissolved uptake is dominant for Zn accumulation (>50%). For Cd and Se, dietary exposure is dominant when the bioconcentration factors of these metals in phytoplankton are at the high end. [source] Cellular and molecular basis of cadmium-induced deformities in zebrafish embryosENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 12 2000Shuk Han Cheng Abstract Cadmium is known to cause developmental defects in a varietyof vertebrate species, but relatively little is known about the underlying molecular mechanisms. In this study, we used zebrafish (Danio rerio) embryos as a model system to investigate cadmium-induced toxicities. Fertilized embryos collected at 5-h after fertilization were incubated for 18 h in culture media containing 1 to 1, 000 ,M CdCl2. The median embryolethal concentration (LC50) was 168 ,M, whereas the median effect concentration (EC50) for total adverse effect (mortality and developmental defects) was 138 ,M. Six major types of deformities were observed: head and eye hypoplasia, hypopigmentation, cardiac edema, yolk sac abnormalities, altered axial curvature, and tail malformations. The frequency of malformations increased with cadmium concentration. Somites of embryos with altered axial curvature were investigated using the antimyosin antibody MF-20. This study demonstrated, to our knowledge for the first time, reduced myotome formation in cadmium-induced spinal deformity. Embryos with head and eye hypoplasia were studied using the anti-neural tissue antibody zns-2, and a poorly developed central nervous system was revealed. Head and eye hypoplasia were associated with lack of expression of the sonic hedgehog gene, which controls the patterning of the neural tube and somites. Genes involved in tail formations, such as evenskipped 1 and no tail, were ectopically expressed in embryos with tail malformations. Our data support the hypothesis that fish embryonic malformations induced by cadmium might be mediated through ectopic expression of developmental regulatory genes. [source] Metal Ion Complementarity: Effect of Ring-Size Variation on the Conformation and Stability of Lead(II) and Cadmium(II) Complexes with Pendant-Armed CrownsEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 15 2007Martín Regueiro-Figueroa Abstract The binding tendencies of the pendant-armed crown ethers L1,L3 [L1 = N,N, -bis(benzimidazol-2-ylmethyl)-1,7-diaza-12-crown-4, L2 = N,N, -bis(benzimidazol-2-ylmethyl)-1,10-diaza-15-crown-5) and L3 = N,N, -bis(benzimidazol-2-ylmethyl)-4,13-diaza-18-crown-6] towards PbII and CdII have been investigated. The X-ray crystal structure of [Cd(L3)](ClO4)2·EtOH shows that, in the solid state, the CdII ion is eight-coordinate and fits quite well into the crown hole, favouring an anti arrangement of the organic receptor. NMR measurements recorded in acetonitrile solution indicate that increasing the crown size induces a conformational change in the series of CdII complexes. The conformation goes from a syn arrangement for L1 to an anti arrangement for L3, passing through a syn [lrarr2] anti equilibrium in the complex derived from L2. On the contrary, no conformational change was observed for the corresponding PbII complexes, which have a syn conformation in all cases. These results have been confirmed by means of density functional theory (DFT) calculations performed by using the B3LYP model. The binding constants obtained from UV/Vis titration experiments in DMSO solution demonstrate that a decrease in the crown size provokes a 102 -fold enhancement of the stability for this series of CdII complexes, whereas for PbII a gradual decrease of the binding constants is observed. Receptor L1 shows a certain degree of selectivity for CdII over PbII, with a selectivity factor > 102. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007) [source] Novel Cadmium(II) Adipate Coordination Polymers with Structural Transformation via Oxalate Ligand: Syntheses, Structures and Fluorescence PropertiesEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 20 2004Na Hao Abstract Two novel cadmium adipate coordination polymers [Cd{O2C(CH2)4CO2}{1,10-phen}]n (1) and [Cd2(C2O4){O2C(CH2)4CO2(OH2)2}{2,2,-bipy}]·H2O (2) [adipic acid = HO2C(CH2)4CO2H] have been hydrothermally synthesized and characterized by elemental analyses, IR spectroscopy, thermogravimetric analysis and single-crystal X-ray diffraction. Crystallographic data for 1: monoclinic, C2/c, a = 16.186(3) Ĺ, b = 15.487(3) Ĺ, c = 14.052(3) Ĺ, , = 112.73(3)°, Z = 8. Crystal data for 2: monoclinic, Cc, a = 23.448(5) Ĺ, b = 11.826(2) Ĺ, c = 8.3163(17) Ĺ, , = 99.08(3)°, Z = 4. The structural analysis reveals that 1 forms a novel one-dimensional chain in which the binuclear Cd centers are linked by adipate anions. Compound 2 is the first example in which both a 2,2,-bipy ligand and an oxalate group are found in the {M/adipate} system. Compound 2 possesses one-dimensional sine- or cosine-type chains, which are alternately connected together by the oxalate group to form a three-dimensional framework. The structural determination reveals that the introduction of the oxalate ligand causes the dimensional transformation of the compounds. Compounds 1 and 2 show strong fluorescent properties at room temperature. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004) [source] Trace element distributions in soils developed in loess deposits from northern FranceEUROPEAN JOURNAL OF SOIL SCIENCE, Issue 3 2006T. Sterckeman Summary A pedo-geochemical survey was carried out in the Nord-Pas de Calais region (France) on soils developed in loess deposits. Total concentrations of Al, Fe and 18 trace elements, as well as common soil characteristics, were determined in samples from 52 surface and 97 deep horizons developed in these loess deposits. The Pb isotopic composition was determined in two sola. The composition of deep horizons, compared with that of the upper continental crust, with that of horizons developed from 21 other sedimentary rocks from the region and with that of loess from various parts of the world, confirms that loess from the Nord-Pas de Calais region derives from multi-recycled and well-mixed ancient sedimentary rocks. Correlation analysis shows that least mobile (i.e. ionic potential (Z/r) is between 3 and 7) geogenic elements (Bi, Co, Cr, Cu, In, Ni, Pb, Sn, Tl, V, Zn) are associated with the fraction <2 µm (which we define as ,lutum'). More mobile elements (As, Cd, Hg, Mn, Mo, Sb, Se) are less associated with this fraction. Cadmium is particularly linked to Mn. The distribution of [trace element]/([Al] or [Fe]) in the French loess gives the background content for soils developed from most sedimentary materials in northwestern Europe. Topsoils are enriched with all the trace elements examined, except Co, Cr and Ni. Enrichments with Cd, Cu, Mn and Zn are greater in cultivated soils than in forest soils. Enrichments with Pb and with Cu, Hg, Mo, Sb, Se and Sn are mainly due to human contamination through atmospheric fallout. Organic matter seems to act as a sink for all the exogenous trace elements. [source] Cadmium leaching from some New Zealand pasture soilsEUROPEAN JOURNAL OF SOIL SCIENCE, Issue 1 2003C. W. Gray Summary Cadmium (Cd) inputs and losses from agricultural soils are of great importance because of the potential adverse effects Cd can pose to food quality, soil health and the environment in general. One important pathway for Cd losses from soil systems is by leaching. We investigated loss of Cd from a range of contrasting New Zealand pasture soils that had received Cd predominantly from repeated applications of phosphate fertilizer. Annual leaching losses of Cd ranged between 0.27 and 0.86 g ha,l, which are less than most losses recorded elsewhere. These losses equate to between 5 and 15% of the Cd added to soil through a typical annual application of single superphosphate, which in New Zealand contains on average 280 mg Cd kg,1 P. It appears that Cd added to soil from phosphate fertilizer is fairly immobile and Cd tends to accumulate in the topsoil. The pH of the leachate and the total volume of drainage to some extent control the amount of Cd leached. Additional factors, such as the soil sorption capacity, are also important in controlling Cd movement in these pasture soils. The prediction of the amount of Cd leached using the measured concentrations of Cd in the soil solution and rainfall data resulted in an overestimation of Cd losses. Cadmium concentrations in drainage water are substantially less than the current maximum acceptable value of 3 µg l,1 for drinking water in New Zealand set by the Ministry of Health. [source] Cadmium blocks hypoxia-inducible factor (HIF)-1-mediated response to hypoxia by stimulating the proteasome-dependent degradation of HIF-1,FEBS JOURNAL, Issue 13 2000Yang-Sook Chun Cadmium is a substantial industrial and environmental pollutant which seriously impairs erythropoiesis. Cd has been demonstrated to aggravate anemia by suppressing erythropoietin gene expression in anemic patients. As hypoxic induction of erythropoietin mRNA depends on a transcription factor, hypoxia-inducible factor 1 (HIF-1), we hypothesized that Cd suppresses the hypoxic activation of HIF-1. In hypoxic Hep3B cells, all mRNAs of various genes, which are known to be upregulated by HIF-1 activation under hypoxia, were suppressed by Cd in a dose-dependent manner. Cd inhibited the hypoxia-induced activity of luciferase in 293 cells which was transfected with a reporter plasmid carrying a hypoxia response element. By electrophoretic mobility gel shift assay, Cd inhibited the DNA-binding activity of HIF-1 in hypoxic Hep3B cells. Cd reduced the amount of HIF-1, protein in hypoxia, whereas it didn't affect HIF-1 , mRNA levels. Moreover, Cd inhibited HIF-1, accumulation induced by cobalt and desferrioxamine. Antioxidants and a proteasome inhibitor prevented the HIF-1, degradation caused by Cd. The possibility that oxidative stress mediates this action of Cd was examined. Cd didn't affect protein oxidation and reduced glutathione levels in hypoxic cells. These results indicate that Cd triggers a redox/proteasome-dependent degradation of HIF-1, protein, reducing HIF-1 activity and in turn suppressing the hypoxic induction of hypoxia-inducible genes. [source] Effects of a toxicant on population growth rates: sublethal and delayed responses in blowfly populationsFUNCTIONAL ECOLOGY, Issue 6 2001S. J. MOE Summary 1,Previous studies have shown that cadmium exposure of blowfly populations (Lucilia sericata[Meigen 1826]) results in reduced population growth rate, but also in higher individual mass, because of reduced competition for food. In this study, the discrepancy between the positive effect on individual growth and the negative effect on population growth is investigated, by measuring direct and delayed effects of cadmium in the adult stage. 2,Blowfly populations were exposed to cadmium through the diet in four treatment combinations: larval stage, adult stage, both stages or neither stage. The effects on accumulation of cadmium, survival, development time, mass and reproductive rate were measured. 3,Cadmium was accumulated from both stages. 4,Individuals exposed to cadmium in the larval stage had higher mean pupal and adult mass (because of reduced densities), but also reduced adult longevity and fecundity. 5,Adult longevity and fecundity were also reduced by cadmium exposure in the adult stage. 6,In stage-structured populations, the link between individual-level and population-level responses to a toxicant may be complicated by stage-specific sensitivities to the toxicant, by delayed responses in the adult stage to sublethal effects in the juvenile stage, and by density-dependent compensatory responses to toxicant-induced mortality. [source] | ||||||||||||||||||||||||||||||||||||||||