A study on the effects of lead, cadmium and phosphorus on the lead and cadmium uptake efficacy of Viola baoshanensis inoculated with arbuscular mycorrhizal fungi

The effect of indigenous arbuscular mycorrhizal (AM) fungi on lead (Pb) and cadmium (Cd) uptake by the hyperaccumulator plant Viola baoshanensis was studied in greenhouse pot experiments. Seedlings of V. baoshanensis inoculated without or with indigenous AM fungi were grown in paddy soil with the addition of Pb at 0, 500, 1000 and 1500 mg kg(-1), or of Cd at 0, 50,100, 200 mg kg(-1), or in mine soil with the addition of phosphorus at 0, 50, 250, 500 mg kg(-1). AM colonization increased shoot biomass at low phosphorus levels, and this beneficial effect was diminished or reversed by high phosphorus availability. AM colonization decreased shoot Cd concentrations regardless of the availability of Cd and phosphorus, but the mechanisms involved varied with Cd availability. At low Cd bioavailability, reduced Cd uptake was due to decreased Cd translocation from the roots to the shoots, whereas that was attributed to reduced root uptake at high Cd bioavailability. In contrast, the effect of AM colonization on shoot Pb varied with the availability of phosphorous and Pb. Our results show that the interactions between V. baoshanensis and indigenous AM fungi were modified by the availability of Pb, Cd and phosphorus.     

Prediction of the solubility of zinc, copper, nickel, cadmium, and lead in metal-contaminated soils

Risk assessment of metal-contaminated soil depends on how precisely one can predict the solubility of metals in soils. Responses of plants and soil organisms to metal toxicity are explained by the variation in free metal ion activity in soil pore water. This study was undertaken to predict the free ion activity of Zn, Cu, Ni, Cd, and Pb in metal-contaminated soil as a function of pH, soil organic carbon, and extractable metal content. For this purpose, 21 surface soil samples (0–15 cm) were collected from agricultural lands of various locations receiving sewage sludge and industrial effluents for a long period. One soil sample was also collected from agricultural land which has been under intensive cropping and receiving irrigation through tube well water. Soil samples were varied widely in respect of physicochemical properties including metal content. Total Zn, Cu, Ni, Cd, and Pb in experimental soils were 2,015?±?3,373, 236?±?286, 103?±?192, 29.8?±?6.04, and 141?±?270 mg kg^?1, respectively. Free metal ion activity, viz., pZn²⁺, pCu²⁺, pNi²⁺, pCd²⁺, and pPb²⁺, as estimated by the Baker soil test was 9.37?±?1.89, 13.1?±?1.96, 12.8?±?1.89, 11.9?±?2.00, and 11.6?±?1.52, respectively. Free metal ion activity was predicted by pH-dependent Freundlich equation (solubility model) as a function of pH, organic carbon, and extractable metal. Results indicate that solubility model as a function of pH, Walkley–Black carbon (WBC), and ethylenediaminetetraacetic acid (EDTA)-extractable metals could explain the variation in pZn²⁺, pCu²⁺, pNi²⁺, pCd²⁺, and pPb²⁺ to the extent of 59, 56, 46, 52, and 51 %, respectively. Predictability of the solubility model based on pH, KMnO₄-oxidizable carbon, and diethylenetriaminepentaacetic acid-extractable or CaCl₂-extractable metal was inferior compared to that based on EDTA-extractable metals and WBC.     

Determination of lead, cadmium and copper in roadside soil and plants in Elazig, Turkey

The concentrations of lead, cadmium and copper in roadside soil and plants in Elazig, Turkey were investigated. Soil samples were collected at distances of 0, 25 and 50 m from the roadside. The concentrations of lead, cadmium and copper were measured by Flame Atomic Absorption Spectrophotometry (FAAS). A slotted tube atom trap (STAT) was used to increase the sensitivity of lead and cadmium in FAAS. Lead concentrations in soil samples varied from 1.3 to 45 mg kg⁻¹ while mean lead levels in plants ranged from120 ng g⁻¹ for grape in point-4 to 866 ng g⁻¹ for apple leaves in point-2. Lead analyses showed that there was a considerable contamination in both soil and plants affected from traffic intensity. Overall level of Cd in soil samples lies between 78 and 527 ng/g while cadmium concentration in different vegetations varied in the range of 0.8–98.0 ng g⁻¹. Concentrations of copper in soil and plant samples were found in the range of 11.1–27.9 mg kg⁻¹ for soil and 0.8–5.6 mg kg⁻¹ for plants. Standard reference material (SRM) was used to find the accuracy of the results of soil analyses.     

强酸型离子交换纤维富集-火焰原子吸收测定水中痕量铜、铅、镉、镍

通过强酸型离子交换纤维柱,在同一水样中同时富集和洗脱了铜、铅、镉、镍,采用火焰原子吸收光谱法测定,并对富集条件及洗脱条件、干扰因素进行了探讨。该方法简便易行,回收率在96.1%~105.5%之间,测定的相对标准偏差小于5.0%。     

WF-8型在线富集进样器应用于水中痕量CuPbCd测定的研究

用 WF 8型在线富集进样器与火焰原子吸收光度计联用 ,应用于水中痕量 Cu、Pb、Cd的测定 ,其富集倍数分别是 1 2 2、1 3 6和 94倍 ,测定的精密度分别是 3 7%、2 8%和 3 9% ,检出限分别是 0 4 7、1 3和 0 2 2μg L,在地表水样中的加标回收率分别为 94 2 %～ 1 0 0 %、98 8%～ 1 0 7%和 1 0 8%～ 1 2 0 % ,并对 WF 8型进样器与火焰原子吸收光度计的成功联用 ,提出了一种新操作程序。     

Environmental hazard of cadmium, copper, lead and zinc in metal-contaminated soils remediated by sulfosuccinamate formulation

Accumulation of metals in soil at elevated concentrations causes risks to the environmental quality and human health for more than one hundred million people globally. The rate of metal release and the alteration of metal distribution in soil phases after soil washing with a sulfosuccinamate surfactant solution (Aerosol 22) were evaluated for four contaminated soils. Furthermore, a sequential extraction scheme was carried out using selective extractants (HAcO, NH(2)OH·HCl, H(2)O(2) + NH(4)AcO) to evaluate which metal species are extracted by A22 and the alteration in metal distribution upon surfactant-washing. Efficiency of A22 to remove metals varied among soils. The washing treatment released up to 50% of Cd, 40% of Cu, 20% of Pb and 12% of Zn, mainly from the soluble and reducible soil fractions, therefore, greatly reducing the fraction of metals readily available in soil. Metal speciation analysis for the solutions collected upon soil washing with Aerosol 22 further confirmed these results. Copper and lead in solution were mostly present as soluble complexes, while Cd and Zn were present as free ions. Besides, redistribution of metals in soil was observed upon washing. The ratios of Zn strongly retained in the soil matrix and Cd complexed with organic ligands increased. Lead was mobilized to more weakly retained forms, which indicates a high bioavailability of the remaining Pb in soil after washing. Comprehensive knowledge on chemical forms of metals present in soil allows a feasible assessment of the environmental impact of metals for a given scenario, as well as possible alteration of environmental conditions, and a valuable prediction for potential leaching and groundwater contamination.     

Distribution and fractionation of cadmium, copper, lead, nickel, and zinc in a calcareous sandy soil receiving municipal solid waste

This study was conducted to evaluate the degree of mobility and fractionation of cadmium (Cd), copper (Cu), lead (Pb), nickel (Ni), and zinc (Zn) after the addition of municipal solid sewage sludge (MSS) in a sandy calcareous soil. Treatments were (1) soil application of MSS, (2) soil application of enriched municipal solid waste compost (EMSS), and (3) control soil. The MSS application represented a dose of 200 Mg dry weight per hectare. Soil columns were incubated at room temperature for 15 days and irrigated daily with deionized water to make a total of 505 mm. At the end of leaching experiments, soil samples from each column were divided into 14 layers, each being 1 cm down to 10 and 2.5 cm below that and analyzed for diethylenetriaminepentaacetic acid (DTPA)-extractable Cd, Cu, Pb, Ni, and Zn. The fractionation of the heavy metals in the top five layers of the surface soil samples was investigated by the sequential extraction method. All soil layers of the columns receiving MSS and EMSS had significantly higher concentrations of DTPA-extractable heavy metals than control soil. The maximum concentration of heavy metals in treated soil was in the surface layer and declined significantly with depth. Sequential extraction results showed that in the treated soil, a major proportion of Cd, Pb, and Ni was associated with organic matter (OM) and exchangeable (EXCH) fractions, and a major proportion of Cu and Zn was associated with residual (RES) and OM fractions. Based on relative percent, Pb, Cd, and Ni in the EXCH fraction was higher than Cu and Zn in soil leached with MSS and EMSS, suggesting that application of this MSS to a sandy calcareous soil, at the loading rate used here, may pose a risk in terms of groundwater contamination with Pb, Cd, and Ni.     

Distribution of heavy metals in sediment and water of river Gomti

Gomti river receives industrial as well as domestic wastes from various drains of Lucknow city. In the process the water and sediment of the river Gomti get contaminated with heavy metals and other pollutants. In the present study, impacts of domestic/industrial wastes on the water and sediment chemistry of river Gomti with special reference to heavy metals have been investigated in different seasons (summer, winter and rainy). For this, seven sampling sites: Gaughat, Mohan Meakin, Martyrs Memorial, Hanuman Setu, Nishatganj bridge, Pipraghat and Malhaur, in the river Gomti in Lucknow region were identified and samples of water and sediments were collected in all the three seasons. In the collected water and sediment samples, six metals (Cd, Cr, Cu, Ni, Pb, and Zn) were analyzed on ICP-AES (Inductively coupled plasma emission spectroscopy) Labtam Plasmalab 8440. High concentrations of all the metals were noticed in water and sediment in rainy season compared to summer and winter. Because in rainy season runoff from open contaminated sites, agricultural field and industries, directly comes into the river without any treatment. In both the cases, the concentration of zinc was maximum (0.091 g/ml in water and 182.13 g/g in sediment) and the concentration of cadmium (0.001 g/ml in water and 17.26 g/g in sediment) was minimum. Higher concentration of metal in water and sediment during rainy season could be due to the industrial/agricultural/domestic runoff coming into the river.     

A probabilistic water quality index for river water quality assessment: a case study

Available water quality indices have some limitations such as incorporating a limited number of water quality variables and providing deterministic outputs. This paper presents a hybrid probabilistic water quality index by utilizing fuzzy inference systems (FIS), Bayesian networks (BNs), and probabilistic neural networks (PNNs). The outputs of two traditional water quality indices, namely the indices proposed by the National Sanitation Foundation and the Canadian Council of Ministers of the Environment, are selected as inputs of the FIS. The FIS is trained based on the opinions of several water quality experts. Then the trained FIS is used in a Monte Carlo analysis to provide the required input-output data for training both the BN and PNN. The trained BN and PNN can be used for probabilistic water quality assessment using water quality monitoring data. The efficiency and applicability of the proposed methodology is evaluated using water quality data obtained from water quality monitoring system of the Jajrood River in Iran.     

Sources and distribution of hexabromocyclododecanes (HBCDs) in Japanese river sediment

The distribution of hexabromocyclododecane (HBCD) in the sediment of three Japanese rivers with different characteristics (i.e., population and potential source in the catchment) was investigated and compared with the results estimated using a multimedia fate model (ChemCAN). High concentrations of HBCD in sediments in the range of 134-2060 ng g(-1) were found in a river receiving textile wastewater. This contrasted with the much lower concentrations (0.8-4.8 ng g(-1)) observed for an urban river (with a surrounding population of 1.8 million). The medians of observed HBCD concentrations in each river were close to those estimated based on the assumed input source (e.g., 1810 ng g(-1) for the observed median concentration, and 1436 ng g(-1) for the estimation, in the Kuzuryu River). These results demonstrated the importance of considering source contributions of HBCD, including both industrial and consumer sources, to aquatic environments, for reliable risk management.     

Lead,cadmium, arsenic and zinc in the ecosystem surrounding a lead smelter

A lead smelter has been operating at Belledune in the province of New Brunswick, in eastern Canada, since 1966. This paper presents data on the concentrations of the four primary metals emitted from the smelter — lead, cadmium, arsenic and zinc — which were measured in the terrestrial environment near the smelter and the concentrate transport route. Deposition of these metals to the snowpack and the uptake by grass forage are discussed in relation to non-regulatory guidelines, toxicity and atmospheric emissions. A 1992 snowpack transect survey extending 0.5–40 km northwest, southeast and south of the smelter revealed lead concentrations of 2–3193 ppb, cadmium <0.10–49.7 ppb, arsenic <3.0–72.0 ppb, and zinc 3–401 ppb. Deposition estimates within this zone for lead were between 0.046 and 20.1 kg/ha/yr, cadmium <0.007 and 313 g/ha/yr, arsenic <0.016 and 453 g/ha/yr and zinc 0.020 and 2.52 kg/ha/yr. Concentrations of these metals in the snowpack were highest within 3 km of the smelter and were detectable at greater distances SE of the smelter. Lead was dispersed greater distances from the smelter than cadmium or arsenic. Snowpack samples collected within 5–20 m of the railway contained 140–7270 ppb of lead, 0.4–36.9 ppb of cadmium, <3.0–72.0 ppb of arsenic and 41–13100 ppb of zinc. Grass forage sampled within 0.6–16 km of the smelter contained lead 5–152 ppm, cadmium 0.10–4.1 ppm, and zinc 22–154 ppm. Highest concentrations of lead, cadmium and zinc in grass forage were found were found within 2.2 km of the smelter. Grass forage collected within 10–70 m of the railway contained lead 13–288 ppm, cadmium 0.4–1.3 ppm and zinc 98–831 ppm.     

Permeability of hair to cadmium,copper and lead in five species of terrestrial mammals and implications in biomonitoring

The capacity of mammal hair to absorb toxic metals and its utility in biomonitoring has been broadly studied. Though these metal-binding properties has generally been attributed to the sulphur contained in cysteine, an amino acid that forms part of keratin, there are not many experimental studies that analyze the role of sulphur in the external deposition of potentially toxic metallic elements in order to better understand the potential of hair in biomonitoring and generate better tools for differentiating between internal and external deposition of contaminants. In this study, an experimental analysis is carried out using a scanning electron microscope on hairs of five terrestrial mammal species (Peromyscus furvus, P. maniculatus, Glossophaga soricina, Artibeus jamaicensis and Marmosa mexicana) treated with cadmium, copper and lead salts. We quantified absorbed metals as well as natural elements of the hair by energy dispersive X-ray spectroscopy (EDS) to analyze using simple statistics the role of sulphur in the absorption Cd, Cu and Pb. Given the lack of studies comparing the mechanisms of deposition of metal elements among different orders of Class Mammalia, external morphology was considered to be an important factor in the deposition of metallic particles of Cd, Cu and Pb. Bat species (Glossophaga soricina, Artibeus jamaicensis) showed a high concentration of particles in their scales, however, no between-species differences in metal absorption were observed, and during the exogenous deposition metal particles do not permeate the medulla. These results suggest that the sulphur in hair itself cannot bind metals to hair cuticle and that hair absorption capacity depends on a variety of factors such as aspects of hair morphology.     

Distribution patterns of nitroaromatic compounds in the water, suspended particle and sediment of the river in a long-term industrial zone (China)

Nitroaromatic compounds are known to be hazardous to ecological and human health. To assess the status of nitroaromatic compounds contamination in the main rivers in the important industrial bases of the northeastern China, we collected water, suspended particulate matter (SPM) and sediment samples from 28 sites in the Daliao River watershed and analysed them for eight nitroaromatic compounds by gas chromatography. The total concentrations of eight nitrobenzenes in the water column including aqueous and SPM phases ranged from 740 to 15,828 ng L^???1, with a mean concentration of 3,460 ng L^???1. The total concentrations of eight nitrobenzenes in the sediment were 7.47 to 8,185.76 ng g^???1, with a mean concentration of 921.98 ng g^???1, and several times higher than those found from the Yellow River in China. 4-Nitrotoluene was the predominant contaminant in the water and sediment of the three rivers of the Daliao River watershed. 2,6-Dichloro-4-nitroaniline was generally dominant in the SPM. The levels of nitroaromatic compounds were different among different sites in the Daliao River watershed, mainly caused by the distribution of pollution sources. No obvious correlation was found between the total concentrations of eight nitrobenzenes concentrations and TOC or the slit-clay content of the sediments.     

Bioaccumulation of zinc,lead, copper,and cadmium from contaminated sediments by native plant species and Acrida cinerea in South China

This research was conducted to search and identify spontaneously growing heavy metal-tolerant plant species that are potentially useful for phytoremediation in contaminated sediment. Five sites were selected for collection of plants growing on polluted shore (river bank) sediment of the Xiang River, China. The concentrations of Zn, Pb, Cu and Cd in plants, sediments, and grasshoppers were determined using flame atomic absorption spectrophotometer (AAS700, Perkin-Elmer, USA). Considering translocation factor and bioaccumulation factor, Rumex crispus (Polygonaceae), Rumex dentatus (Polygonaceae), and Lagopsis supina (Labiatae) could be potentially useful for phytostabilization of metals. R. crispus can be considered potentially useful for phytoextraction of Cd. In light of the biomagnification factors, grasshoppers are deconcentrators for Pb and Cd, microconcentrators for Zn and macroconcentrators for Cu to the plants, respectively. To the best of our knowledge, the present study is the first report on Zn, Pb, Cu and Cd accumulation in R. crispus and L. supina, providing a pioneer contribution to the very small volume of data available on the potential use of native plant species from contaminated sediments in phytostabilization and phytoremediation technologies.     

A risk assessment study of water quality,biota, and legacy sediment prior to small dam removal in a tributary to the Delaware River

The proposed removal of three run-of-river dams (all ≤5-m height) in eastern Pennsylvania along lower Bushkill Creek, a tributary of the Delaware River, has provided a valuable opportunity for multidisciplinary research involving the collection of more than 5 years of pre-removal monitoring data, analysis of heavy metals in legacy sediment cores, and associated toxicity assays to determine the singular and interactive effects of lead, copper, and cadmium on survival and behavior of a common macroinvertebrate found in Bushkill Creek. Monitoring data were collected from sites approximately 35 m upstream and downstream of dams and reference sites located approximately 5 km upstream of all dams. Results indicate that oxygen levels, macroinvertebrate diversity, and proportion of sensitive taxa were significantly lower upstream and downstream of dams in comparison with upstream reference reaches. The strong correlation between water quality and macroinvertebrates in this system implies that removal of the lower three dams would lead to improvements in water quality, biotic integrity, and resilience in lower Bushkill Creek. Sediment analyses and toxicity assays suggest that dam removal and sediment mobilization may route contaminated sediments downstream at concentrations that may harm more sensitive biota. However, macroinvertebrate mortality and behavior were not significantly different from clean water controls for the large majority of toxicity assays. All together, these results suggest that dams 1–3 are good candidates for successful stream restoration but that the removals would best be planned in a way that mitigates potential impacts of contaminated legacy sediment.     

Correlation between soil characteristics and lead and cadmium content in the aboveground biomass of Virginia tobacco

The study was conducted on alluvial-meadow, maroon-forest soils and vertisols with Virginia tobacco. The total content of lead and cadmium is measured through decomposition by HF, HClO₄, and HNO₃ acids. A solution of 0.005 M diethylentriaminepentaacetic acid + 0.1 M triethanolamine, pH 7.3 was used for extraction of the elements’ mobile forms from soils. The preparation of plant samples was made by means of dry ashing and dissolution in 3 M HCl. An atomic absorption spectrometer “Spektra AA 220” of the Australian company Varian was used for determination of Pb and Cd content in the soil and plant samples. Certified reference materials (three soils and tobacco leaves) were also analyzed for the verification of the accuracy of Pb and Cd determination. A correlation/regression analysis was conducted between pH, humus content, total and mobile forms of lead and cadmium in the soil, and the concentration of these elements in the aboveground biomass of Virginia tobacco. It was established that there are no statistically significant dependencies determined between soil pH and lead concentration in the plant organs of Virginia tobacco. Regressional dependencies of great significance were determined between the humus content, total and mobile lead and cadmium in the soil, and the element concentration in the leaves of the three harvesting zones.     

Regional monitoring of lead and cadmium contamination in a tropical grazing land site,Thailand

An investigation was carried out to monitor Pb and Cd contamination in grazing land located near a highway. Environmental media at different distances fromhighway (soil, grass, water, cow's forage, fertilizer,manure and milk samples) were collected from three samplinglocations. Soil and grass were characterized by high metalmobility (soil with Pb: 5.25±0.71–14.59±1.17 mgkg^-1, dry mass and Cd: 0.038–0.33±0.04 mg kg^-1, dry mass and grass with Pb: 0.76±0.05–6.62±0.18 mg kg^-1, dry mass and Cd: 0.17±0.01–0.73±0.09 mg kg^-1, dry mass). One-way analysis of variane (ANOVA) was applied to find out the correlation between metal (total and bioavailable) concentrationsin the soil and the distance from roadside. In most cases, the finding showed that plants growing nearer to the highway are usually exposed to more heavy metal accumulations than those awayfrom the highway. In addition, a correlation was established between plant available metal concentrations and plant metaluptake concentrations.Analysis of fertilizer and manure showed considerable amountof metals (fertilizer with Pb: 1.53±0.06 mg kg^-1 andCd: 0.038 mg kg^-1 and manure with Pb: 2.55–3.34 mgkg^-1 and Cd: 0.14–0.31 mg kg^-1). Long termsimultaneous application of fertilizer and manure on thecommercial farm showed higher metal accumulation in the soiland plants than those of co-operative farm Considerableconcentrations of metals (Pb: 1.60–2.94 mg kg^-1 andCd: 0.025–0.19 mg kg^-1) were observed in fodder. The finding clearly demonstrated that there are seasonalvariation in total daily metal intake by individual cow (Pb:109.37 mg day^-1 (dry), 273.47 mg day^-1 (rainy) andCd: 2.02 mg day^-1 (dry), 19.62 mg day^-1 (rainy)).The provisional tolerable weekly intake of heavy metals incows is 390 g Pb and 28 g Cd per kg bodyweight in the rainy season and 156 g Pb and 2 gCd per kg body weight in the dry season. The levels of metals (Pb: 0.014 mg L^-1 and Cd: not detectable) and bio-transferfactor (10^-5–10^-4) in raw milk were found to be well below the Codex Alimentarius Commissions Draft (1997). Ouranalysis revealed that improvements on farm management give significant reduction in elevated levels of Pb and Cdin soil and plants, and however leads to minimize the amountof Pb and Cd in consumed milk.     

Impacts of climate-induced changes on the distribution of pesticides residues in water and sediment of Lake Naivasha, Kenya

This study reports evidence of increased chlorpyrifos contamination in sediment and water in Lake Naivasha following its intensive application in the horticultural farms in the catchment area. Analytical results show that levels of chlorpyrifos residues were influenced by climate-induced rainfall pattern with higher levels reported during period of heavy precipitation with significant decrease during low rainfall. On average, the levels ranged between 14.8 and 32.8 ng g^?1 in sediment during rainy season compared to a range of 8.5–16.6 ng g^?1 in the dry season. Additionally, the mean concentration of chlorpyrifos in water ranged between 8.61 and 22.4 μg L^?1 during rainy season and below detection limit (bdl) ?13.6 μg L^?1 in dry season as quantified by enzyme-linked immunosorbent assay. Meanwhile, independent t test analysis indicated that there was significant difference in concentration at p?≤?0.05 between the seasons with respect to sediment and water samples. This demonstrated that climate-induced variations had considerable influence on contamination. While diazinon and carbofuran were equally applied intensively, their levels were below the detection limit in the all the samples analyzed. ELISA results were validated by the capillary-HPLC photodiode-array detector instrument analysis, and statistical comparison showed no significant difference between them. It was evident that chlorpyrifos residues determination in water and sediment by ELISA can be a useful strategy in environmental management and monitoring program, and a complimentary analytical tool to high performance liquid chromatography. Levels of chlorpyrifos detected in sediment and water were found to exceed recommended criteria for protection of aquatic life and preservation of water quality and may be hazardous if not regularly monitored.