Enhancement of UV and chromate mutagenesis by nickel ions in the Chinese hamster HGPRT Assay †

1. The HGPRT (Hypoxanthine‐Guanine‐Phospho‐Ribosyl‐Transferase) assay with Chinese Hamster V79 cells was used to measure the mutagenic effects of UV irradiation, potassium dichromate and nickel chloride. The agents were tested separately and in the combinations of UV plus nickel and dichromate plus nickel.

2. UV, Cr(VI) and Ni(II) were confirmed to be mutagenic in the V79 cell assay. The combination of UV(5J/m²) and Ni(II) (0.5 mM) caused a mutation rate 11.2 times above that corresponding to the sum of the individual mutation rates of these agents. The combined action of Cr(VI) (0.1 mM) and Ni(II) (0.5 mM) produced a mutation rate 2.8 fold above that corresponding to the sum of the individual rates of the separate agents.

3. The enhancing effect of nickel chloride on the mutagenicity of UV or Cr(VI) is interpreted by an interference of Ni(II) with the repair of DNA lesions.     

羰基镍急性中毒对大鼠骨髓细胞的DNA损伤

通过动物实验观察不同剂量羰基镍对大鼠骨髓细胞DNA损伤程度。采用SD大鼠,以135 mg·m~(-3)和250 mg·m~(-3)羰基镍为染毒组,250 mg·m~(-3)氯气为阳性对照组,静态方式染毒30 min。未染毒组为正常对照组,大鼠染毒后1、2、3和7 d分别采集样本。采用单细胞凝胶电泳检测每组大鼠骨髓细胞DNA的损伤程度。彗星尾长和Olive尾矩2个指标的分析结果表明,大鼠骨髓细胞DNA损伤程度随着羰基镍染毒剂量的增加而增加,在4个时间点各剂量组间均有显著差异(P0.05)且随时间的变化有一定的规律,损伤程度在3 d时达到最大,而后缓慢下降。羰基镍急性中毒对大鼠骨髓细胞DNA有一定的损伤,且存在剂量-效应关系,各剂量组损伤程度有一定的时间效应规律。     

Effect of nickel exposure on serum amylase activity in nickel-plating workers

The objective of this study was to determine the effect of nickel (Ni) exposure on serum amylase activity in nickel-plating workers in Bangalore (India). Sixty-nine subjects using Ni during the electroplating process formed the exposed group. An equal number of age- and sex-matched subjects working in the administration section formed the control group. Urine Ni levels were determined using a flameless atomic absorption spectrophotometer. Serum amylase activity was determined using spectrophotometric method with 2-chloro-4-nitrophenyl-α-D-maltotrioside as substrate. A significant increase in urine Ni and serum amylase activity was noted in nickel platers as compared with the control group. The level of serum amylase activity was positively and significantly associated with Ni content in urine of nickel platers. Stepwise multiple regression analysis was used to assess the effects of Ni exposure, life style confounding factors and presence of gastrointestinal problems on serum amylase activity. The analysis showed that the subjects who had urine Ni levels beyond 10?µg?g^?1 of creatinine, nickel platers category, smoking and body mass index variables were significantly associated with serum amylase activity. The results of this study suggest that the increased serum amylase activity observed in nickel-exposed subjects could be used as a biomarker for investigating pancreatic function in Ni exposure.     

Calcareous electrochemical precipitation,a new method to trap nickel in seawater

There are few efficient, rapid and cheap methods to remove toxic metals from contaminated waters. Here we hypothesised that cathodic protection, an existing method used to control the corrosion of metallic structures, may trap toxic metals. Indeed, in seawater, the application of a cathodic current on a metallic structure induces the precipitation of limestone (CaCO₃) and magnesium dihydroxyde (Mg(OH)₂), thus forming a calcareous deposit on the metal surface. We therefore presumed that such calcareous deposit may trap metals dissolved in waters. Actually calcareous deposit formation has never been studied in the presence of dissolved metallic contaminants such as nickel. Here we tested ionic nickel (Ni²⁺) precipitation in calcareous deposit with a galvanized steel electrode by spiking artificial seawater with a NiCl₂ salt during 7 days of applied current. We analysed deposit surface and cross section by µ-Raman spectroscopy and scanning electron microscopy (SEM) with X-ray microanalysis. Ni concentration in the deposit was quantified by inductively coupled plasma analysis, after deposit dissolution in 60% HNO₃. Results show that in 7 days up to 24% of nickel can be trapped in the calcareous deposit. Scanning electron microscopy reveals that Ni is trapped under a pure CaCO₃ layer of aragonite. Raman spectra show that nickel is incorporated as nickel dihydroxyde (Ni(OH)₂), as evidence by vibration bands at 446 and 510 cm^?1. Overall our findings disclose a new and efficient method, calcareous electrochemical precipitation, which has potential applications to remove toxic metals from contaminated waters.     

Entfernung von Schwermetallen aus einem Boden mit hohem Schluffanteil

A soil, containing 2.8% organic carbon and a high concentration (76.4%) of small particles (<63 μm), and which had been contaminated over a long period of time by galvanic waste waters (Ni, Cu) and lead wastes, was subjected to detailed analysis and subsequently treated with various extracting solutions in order to remove the heavy metals. For this purpose, representative samples containing 114 mg kg^?1 Cu, 1151 mg kg^?1 Ni and 366 mg kg^?1 Pb were treated with amino acids and solutions containing other complexing agents, as well as with diluted acids, in order to compare the relative effectiveness of these solutions. Satisfactory metal extractions were only achieved by the use of diluted mineral acids, notably hydrochloric acid, which released more than 90% of the nickel and approximately 80% of the copper and lead from the soil. The results obtained with weak complexing agents such as tartaric acid (0.07–2.9%, 24 h) and amino acids (0.01–36%, 24h) were worse. For reprocessing of the hydrochloric acid solutions, a direct precipitation of the heavy metals in their hydroxide forms and selective separation with N-acylthiourea modified polysiloxanes were carried out.     

Nickel in the muscle tissues of freshwater fish from north eastern Poland should not cause human health concerns

Excessive intake of nickel (Ni) is known to produce adverse health effects in humans, including carcinogenicity and allergenicity. The main route of exposure for humans is diet, including fish. There is, however, little information concerning Ni content in freshwater fish in Poland. The aim of the study was to determine the concentrations of Ni in meat tissues of three fish species from north eastern Poland and assess toxic potential to healthy and susceptible sub-groups of individuals. The settings for the study lakes span a range of anthropogenic influence from protected areas to a basin with a town and several villages and another one influenced by a pesticide tomb leakage. Fish were netted and kept frozen until analysis. After defrosting, the fish were filleted and minced. The ashed samples were dissolved in nitric acid and analyzed for Ni by flame atomic absorption spectrometry. Roach meat contained 6.6–23 µg kg^?1 Ni, bream 9.5–178 µg kg^?1, and carp 16.5–139 µg kg^?1. These concentrations are low, indicating that the fish were not excessively contaminated with the metal. Consuming a 250 g portion of fish would result in an average nickel intake of 4 µg for roach, <10 µg for bream, and <20 µg for carp. These values represent only 0.4–2% of the maximum level that is likely to pose a risk of adverse effects as established in the USA. Consumption of fish from the study region need not necessarily pose a health threat.     

Delimiting soil chemistry thresholds for nickel hyperaccumulator plants in Sabah (Malaysia)

Nickel hyperaccumulator plants have been the focus of considerable research because of their unique ecophysiological characteristics that can be exploited in phytomining technology. Comparatively little research has focussed on the soil chemistry of tropical nickel hyperaccumulator plants to date. This study aimed to elucidate whether the soil chemistry associated with nickel hyperaccumulator plants has distinctive characteristics that could be indicative of specific edaphic requirements. The soil chemistry associated with 18 different nickel hyperaccumulator plant species occurring in Sabah (Malaysia) was compared with local ultramafic soils where nickel hyperaccumulator plants were absent. The results showed that nickel hyperaccumulators in the study area were restricted to circum-neutral soils with relatively high phytoavailable calcium, magnesium and nickel concentrations. There appeared to be a ‘threshold response’ for the presence of nickel hyperaccumulator plants at >20 μg g^?1 carboxylic-extractable nickel or >630 μg g^?1 total nickel, and >pH 6.3 thereby delimiting their edaphic range. Two (not mutually exclusive) hypotheses were proposed to explain nickel hyperaccumulation on these soils: (1) hyperaccumulators excrete large amounts of root exudates thereby increasing nickel phytoavailability through intense rhizosphere mineral weathering; and (2) hyperaccumulators have extremely high nickel uptake efficiency thereby severely depleting nickel and stimulating re-supply of Ni from diffusion from labile Ni pools. It was concluded that since there was an association with soils with highly labile nickel pools, the available evidence primarily supports hypothesis (2).     

Toxicity of metals to tadpoles of the common Sunda toad,Duttaphrynus melanostictus

Tadpoles of the common freshwater Sunda toad, Duttaphrynus melanostictus (Amphibia, Bufonidae), were exposed for a 4-day period under laboratory conditions to copper (Cu), cadmium (Cd), zinc (Zn), lead (Pb), nickel (Ni), iron (Fe), aluminum (Al), and manganese (Mn) at various concentrations. Mortality was assessed and median times of death (LT₅₀) and lethal concentrations (LC₅₀) were calculated. LT₅₀ and LC₅₀ increased with the decrease in mean exposure times and concentrations for all metals. LC₅₀ (96?h) for Cu, Cd, Zn, Pb, Ni, Fe, Al, and Mn were 0.03, 0.3, 4.2, 1.5, 8.8, 0.4, 1.9, and 39?mg?L^?1, respectively. Cu was the most toxic to D. melanostictus, followed by Cd, Fe, Al, Pb, Zn, Ni, and Mn (Cu?>?Cd?>?Fe?>?Al?>?Pb?>?Zn?>?Ni?>?Mn). Duttaphrynus melanostictus is similarly sensitive to these metals as other amphibian tadpoles.     

Recovery of Ni(II) from real electroplating wastewater using fixed-bed resin adsorption and subsequent electrodeposition

Resin adsorption and subsequent electrodeposition were used for nickel recovery. Treated wastewater can meet the Electroplating Pollutant Discharge Standard. The spent resin is completely regenerated by 3 BV of 4% HCl solution. 95.6% of nickel in concentrated eluent was recovered by electrodeposition. Effective recovery of high-value heavy metals from electroplating wastewater is of great significance, but recovering nickel ions from real electroplating wastewater as nickel sheet has not been reported. In this study, the pilot-scale fixed-bed resin adsorption was conducted to recover Ni(II) ions from real nickel plating wastewater, and then the concentrated Ni(II) ions in the regenerated solution were reduced to nickel sheet via electrodeposition. A commercial cation-exchange resin was selected and the optimal resin adsorption and regeneration conditions were investigated. The resin exhibited an adsorption capacity of 63 mg/g for Ni(II) ions, and the average amount of treated water was 84.6 bed volumes (BV) in the pilot-scale experiments. After the adsorption by two ion-exchange resin columns in series and one chelating resin column, the concentrations of Ni(II) in the treated wastewater were below 0.1 mg/L. After the regeneration of the spent resin using 3 BV of 4% (w/w) HCl solution, 1.5 BV of concentrated neutral nickel solution (>30 g/L) was obtained and used in the subsequent electrodeposition process. Using the aeration method, alkali and water required in resin activation process were greatly reduced to 2 BV and 3 BV, respectively. Under the optimal electrodeposition conditions, 95.6% of Ni(II) in desorption eluent could be recovered as the elemental nickel on the cathode. The total treatment cost for the resin adsorption and regeneration as well as the electrodeposition was calculated.     

Heavy metal pollution in soil and plants at bone char site

This study determined the heavy metal concentration in soil and plants at a bone char site in Umuahia, Nigeria. Soil and plant samples collected in a randomized complete block design (RCBD) were analyzed for zinc (Zn), lead (Pb), cadmium (Cd), nickel (Ni), and arsenic (As). The concentration of metals in soil and plants in the vicinity of the bone char site are as follows: Zn (172?mg?kg^?1) and Ni (0.62?mg?kg^?1) in soil were highest at site P₃, Pb (2.37?mg?kg^?1) and As (0.08?mg?kg^?1) at site P₁, and Cd (18.30?mg?kg^?1) at site P₂. In plants, the concentrations of Zn (41.17?mg?kg^?1) and Cd (3?mg?kg^?1) were highest in Albizia ferruginea, Ni in Dialium guineense (0.09?mg?kg^?1), while Pb was in D. guineense (0.08?mg?kg^?1) and Spathodea companulata (0.06?mg?kg^?1). The levels of Zn, Cd, Pb, Ni, and As in soil ranged from 11.2 to 172, 2.68 to 18.2, 0.026 to 2.37, 0.33 to 0.62, and 0.02 to 0.08?mg?kg^?1, respectively. In plants, the concentration of Zn, Cd, Pb, and Ni ranged from 2.01 to 41.17, 0.12 to 3, 0.02 to 0.08, and 0.03 to 0.09?mg?kg^?1, respectively. There were significant correlations between Zn and Cd, and Pb and As in soil. The high concentration of Cd in soil might affect soil productivity.     

铜和镍对大麦根伸长的联合毒性研究

重金属的复合污染在环境污染中普遍存在,所以复合污染的联合毒性研究对于准确评价重金属污染有着重要的意义.本论文以大麦根伸长为研究对象,探索了铜(Cu)和镍(Ni)对大麦根伸长的联合毒性.基于Cu-Ni混合物的剂量-效应曲线,运用扩展的浓度加和(CA)与独立作用(RA)两个模型对不同浓度组合的Cu-Ni混合物的交互作用及联合毒性进行预测.结果表明,扩展的CA和RA模型均能较好地预测Cu-Ni混合物对大麦根伸长的联合毒性,低剂量的Ni能缓解Cu对大麦根伸长的毒性作用,但是低剂量的Cu对Ni的生物毒性没有显著影响.研究阐明了Cu、Ni复合作用对大麦根伸长联合毒性的效应机理.     

Bioleaching of cadmium and nickel from synthetic sediments by Acidithiobacillus ferrooxidans

The microbial leaching process was evaluated for the treatment of synthetic sediments contaminated with cadmium and nickel sulfides. A series of batch leaching experiments was conducted to compare metal solubilization in sediment inoculated with Acidithiobacillus ferrooxidans -inoculated sediments to that in sterile control sediment. The rate and extent of metal solubilization were significantly higher in A. ferrooxidans -inoculated reactors than in acidified sterile reactors. The efficiency of cadmium (Cd) solubilization (80) in the bioleaching process was higher than that of nickel (Ni) solubilization (60). The performance of leaching reactors containing only culture supernatants was comparable to that of A. ferrooxidans -inoculated reactors, indicating that indirect non-contact leaching by the products of microbial metabolism is the predominant mechanism for metal solubilization rather than direct microbial sulfide oxidation. Moreover, the similar (60–75%) extents of Cd²⁺ leaching with A. ferrooxidans , cell-free filtrate, and Fe³⁺ suggest that abiotic oxidation of CdS by Fe³⁺ controls the overall leaching rate, and the role of A.␣ferrooxidans is most likely not to oxidize CdS mineral directly but to regenerate Fe³⁺ as an oxidant.     

Analysis of heavy metals in ecstasy tablets by electrochemical methods

Trace amounts of heavy metals have been analysed by electrochemical techniques in ecstasy tablets obtained from different police seizures in Spain. Lead, cadmium, copper and zinc were determined by differential-pulse anodic stripping voltammetry at a hanging mercury drop electrode, whereas nickel and cobalt were determined by adsorptive differential-pulse cathodic stripping voltammetry from their dimethylglyoxime complexes, M(DMG)₂. The performance of the procedure was compared with electrothermal atomic absorption spectrometry. The procedure was applied to the determination of these elements in nine ecstasy samples, finding that Zn is the element present in the highest concentration, ranging from 0.3 to 200?mg?kg^?1, Ni, Cu appear below 15?mg?kg^?1 and Pb below 8?mg?kg^?1, while Cd and Co levels were always lower than 0.51?mg?kg^?1.     

Cadmium and nickel determinations in some food and water samples by the combination of carrier element-free coprecipitation and flame atomic absorption spectrometry

A procedure for separation and enrichment of Cd(II) and Ni(II) ions based upon carrier element-free coprecipitation by using an organic coprecipitant, 2-{4-[2-(1H-Indol-3-yl)ethyl]-3-(4-methylbenzyl)-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl}-N′-(3-fluoro-phenylmethyliden) acetohydrazide, prior to their flame atomic absorption spectrometric detections has been developed. The effects of varied experimental conditions on the performance of the developed method such as pH, sample volume, amount of coprecipitating agent, etc. were evaluated in detail on the recovery of analyte ions, and the influences of some anions and cations were investigated. The limits of detection for Cd(II) and Ni(II) ions based on three times the standard deviation of the blanks (N: 10) were obtained as 0.70 μg L^?1 and 1.21 μg L^?1, respectively. The accuracy of the method was tested by analyzing a certified reference material and by spike tests. The method was applied to determine the levels of cadmium and nickel in stream and sea water, rice, red lentil, and wheat samples.     

Toxicity and bioaccumulation of heavy metals in mullet fish Liza klunzingeri (Mugilidae: Perciformes)

The mullet fish, Liza klunzingeri, commercially important and widely relished by Kuwaiti residents, and the stressed ecosystem in Kuwait Bay instigated us to conduct toxicity and bioaccumulation tests on heavy metals (Pb, Ni, V, Cu and Fe). Among five metals, Pb had the lowest observed effect concentration (LOEC) at 1 μg?l ^?1. Using multi-factor Probit analysis, toxicity tests (72 h) on L. klunzingeri reared in filtered sea water in the laboratory showed Pb with maximum effect at median lethal concentration (LC₅₀) followed by V, Ni, Cu and Fe. Their bioaccumulation factor (BAF) was in the sequence Pb>V>Fe>Cu and Ni. For fish exposed for 30 d, bioaccumulation exhibited increasing metal levels in liver followed by gills and muscles. These results suggest the potential use of L. klunzingeri as a bioindicator of metal pollution in the future.     

Biosorption of cadmium and nickel ions using marine macrophyte,Cymodocea nodosa

ABSTRACT

Seagrass (Cymodocea nodosa) ability to remove cadmium and nickel ions from single metal solutions was investigated in the present study. Metal ions were measured in the solution using an atomic absorption spectrophotometer. Various operational parameters (initial pH, biomass dose, metal ion concentration, and contact time) were tested and found to affect the uptake capacity of Cd (II) and Ni (II). More than 70% of biosorption capacity occurred in the first few minutes for both metal ions. The pseudo-second-order kinetic model and the Langmuir model were found to best fit the experimental data of Cd (II) and Ni (II) biosorption. The maximum uptake capacity (q_max) was 11.6 and 16.7?mg.g^?1 for Cd (II) and Ni (II), respectively. The biosorbent was characterised using Fourier transform infrared spectrometry (FTIR), scanning electron microscope (SEM), and energy-dispersive X-ray spectroscopy (EDX). The infrared spectrum demonstrated that hydroxyl, carboxyl, and phenolic functional groups are the major binding sites for Cd (II) and Ni (II) metals. The ion exchange mechanism plays an important role during biosorption process as shown in EDX analysis. Our results conclude that marine macrophyte C. nodosa can be used as a low-cost biosorbent for the removal of Cd (II) and Ni (II) in wastewater.     

Enhanced degradation of trichloroethylene using bentonite-supported nanoscale Fe/Ni and humic acids

Nanoscale zero-valent iron, named nano-Fe⁰, is a reagent used to degrade trichloroethylene in groundwater. However, the efficiency of nano-Fe⁰ is moderate due to issues of dispersion and reactivity. As an alternative we synthesized bentonite-supported nanoscale Fe/Ni bimetals, named bentonite-Fe/Ni, to test the degradation of trichloroethylene in the presence of Suwannee River humic acids, as a representative of natural organic matter. 0.1 mmol/L trichloroethylene was reacted with 0.5 g/L of nano-Fe⁰, bentonite-Fe, Fe/Ni, and bentonite-Fe/Ni nanoparticles. Results show first that without humic acids the reaction rate constants k _obs were 0.0036/h for nano-Fe⁰, 0.0101/h for bentonite-Fe, 0.0984/h for Fe/Ni, and 0.181/h for bentonite-Fe/Ni. These findings show that bentonite-Fe/Ni is the most efficient reagent. Second, the addition of humic acids increased the rate constant from 0.178/h for 10 mg/L humic acids to 0.652/h for 40 mg/L humic acids, using the bentonite-Fe/Ni catalyst. This finding is explained by accelerated dechlorination by faster electron transfer induced by humic quinone moieties. Indeed, the use of 9, 10-anthraquinone-2, 6-disulfonate as a humic analogue gave similar results.     

A comparison of two methods to observe the effects of dual metal exposure to the chironomus larvae

A study was conducted to investigate the effects of metal mixtures on the Chironomus plumosus. Two methods of preparing the mixtures were used, the Toxic Unit (TU) method and the parts per million (PPM) + PPM method. A comparison was undertaken between the two methods to observe the ease with which (1) experiment could be conducted and (2) whether LC₅₀ values could be obtained. In this study, it was noted that the PPM + PPM method was an easier method to conduct metal mixture experiments as the LC₅₀ values could be easily calculated for individual metals and compared with the LC₅₀ values of metals obtained from single metal experiments. The findings showed that the LC₅₀ value for zinc (Zn) was more toxic for chromium (Cr) when it was reduced from 9.6 to 0.3 mg L^?1, with silver the LC₅₀ value became 3.6 mg L^?1, 4.5 mg L^?1 with nickel (Ni). In the PPM + PPM method, the LC₅₀ value for Zn was observed to be 10.2 mg L^?1 when in mixture with chromium, 23.8 mg L^?1 with silver, and 13.4 mg L^?1 with Ni. Changes in the 96 h LC₅₀ value were found to be significant for all metals.     

Cytogenetic and epigenetic alterations by cobalt and nickel on Zea mays L

Changes in DNA methylation in Zea mays plantlets in response to cobalt and nickel (5, 10, 20, and 40 mmol L^?1) evaluated by the coupled restriction enzyme digestion-random amplification technique revealed dose-related increases in hypermethylation. The effects on mitotic index and phytohormone levels were also determined. Co and Ni caused a decrease in mitotic index and an attenuation in the growth-promoting hormones gibberellic acid, zeatin, and indole acetic acid, while abscisic acid levels rose. These findings have shown that the increase in abscisic acid levels and DNA methylation depend on the concentrations of Co and Ni.