Concentrations of Heavy Metals in Hair and Nails of Young Pakistanis: Correlation with Dietary Elements

Hair and nail samples from young Pakistani adults were separately analyzed for quantification of Cd, Cr, Cu, Ni, Pb, and Zn concentrations. The concentrations of these metals were also analyzed in commonly consumed local foods to evaluate potential correlation of hair and nail concentrations with diet. Pearson correlation coefficients ranged from 0.349 to 0.999, demonstrating diet to be a significant contributor for accumulation of heavy metals in humans.     

Assessment of heavy metals in water,sediment, Anabas testudineus and Eichhornia crassipes in a former mining pond in Perak,Malaysia

The concentrations of Al, As, Cd, Cr, Cu, Fe, Hg, Mn, Ni, Pb, Sn and Zn were analysed in water, sediment, muscle of climbing perch fish (Anabas testudineus), and tissue of water hyacinth plants (Eichhornia crassipes) collected from a former tin-mining pond in Perak, Malaysia. The monitoring was performed during the minimum and maximum rainfall periods. The concentrations of As, Cr, Fe, Ni, Pb and Zn in water exceeded the permissible limits set by the Interim National Water Quality Standards for Malaysia (INWQS). The risk index (RI) values determined for As, Cd, Cr, Cu, Hg, Pb and Zn in sediment presented a low degree of ecological risk. The order of the top three heavy metals measured in fish muscle was Zn?>?Fe?>?Al. The estimated daily intake (EDI) of As and Cr exceeded the allowable limits in both rainfall periods. The bioconcentration factor (BCF) and translocation factor (TF) values of Zn in water hyacinth were 24.865 and 3.214, respectively. The concentrations of Cu and Zn in the plant tissue were significantly correlated (p?<?.05) with the concentrations of heavy metals in water. Overall, climbing perch and water hyacinth are excellent bioindicators of environmental impacts on water bodies.     

Bacillus safensis with plant-derived smoke stimulates rice growth under saline conditions

Environmental Science and Pollution Research - Salinity is a worldwide environmental problem of agricultural lands. Smoke and plant growth-promoting bacteria (PGPR) are individually used to improve...     

Nature and prevalence of non-additive toxic effects in industrially relevant mixtures of organic chemicals

The concentration addition (CA) and the independent action (IA) models are widely used for predicting mixture toxicity based on its composition and individual component dose–response profiles. However, the prediction based on these models may be inaccurate due to interaction among mixture components. In this work, the nature and prevalence of non-additive effects were explored for binary, ternary and quaternary mixtures composed of hydrophobic organic compounds (HOCs). The toxicity of each individual component and mixture was determined using the Vibrio fischeri bioluminescence inhibition assay. For each combination of chemicals specified by the 2ⁿ factorial design, the percent deviation of the predicted toxic effect from the measured value was used to characterize mixtures as synergistic (positive deviation) and antagonistic (negative deviation). An arbitrary classification scheme was proposed based on the magnitude of deviation (d) as: additive (10%, class-I) and moderately (10 < d  30%, class-II), highly (30 < d  50%, class-III) and very highly (>50%, class-IV) antagonistic/synergistic. Naphthalene, n-butanol, o-xylene, catechol and p-cresol led to synergism in mixtures while 1, 2, 4-trimethylbenzene and 1, 3-dimethylnaphthalene contributed to antagonism. Most of the mixtures depicted additive or antagonistic effect. Synergism was prominent in some of the mixtures, such as, pulp and paper, textile dyes, and a mixture composed of polynuclear aromatic hydrocarbons. The organic chemical industry mixture depicted the highest abundance of antagonism and least synergism. Mixture toxicity was found to depend on partition coefficient, molecular connectivity index and relative concentration of the components.     

TiO2/Ag modified penta-bismuth hepta-oxide nitrate and its adsorption performance for azo dye removal

A modified hydrophilic penta-bismuth hepta-oxide nitrate (Bi₅O₇NO₃) surface was synthesized via a precipitation method using TiO₂ and Ag as modified agents. The synthesized product was characterized by different analytical techniques. The removal efficiency was evaluated using mono-and di-sulphonated azo dyes as model pollutants. Different kinetic, isotherm and diffusion models were chosen to describe the adsorption process. X-ray photoelectron spectroscopy (XPS) results revealed no noticeable differences in the chemical states of modified adsorbent when compared to pure Bi₅O₇NO₃;however, the presence of hydrophilic centres such as TiO₂ and Ag developed positively charged surface groups and improved its adsorption performance to a wide range of azo dyes. Dyes removal was found to be a function of adsorbent dosage, initial dye concentration, solution pH and temperature. The reduction of Langmuir 1,2-mixed order kinetics to the second or first-order kinetics could be successfully used to describe the adsorption of dyes onto the modified adsorbent. Mass transfer can be described by intra-particle diffusion at a certain stage, but it was not the rate limiting step that controlled the adsorption process. Homogenous behavior of adsorbent surface can be explored by applying Langmuir isotherm to fit the adsorption data.     

Comparison of a plant based natural surfactant with SDS for washing of As(Ⅴ) from Fe rich soil

This study explores the possible application of a biodegradable plant based surfactant, obtained from Sapindus mukorossi, for washing low levels of arsenic （As） from an iron （Fe） rich soil. Natural association of As（Ⅴ） with Fe（Ⅲ） makes the process difficult. Soapnut solution was compared to anionic surfactant sodium dodecyl sulfate （SDS） in down-flow and a newly introduced suction mode for soil column washing. It was observed that soapnut attained up to 86% efficiency with respect to SDS in removing As. Full factorial design of experiment revealed a very good fit of data. The suction mode generated up to 83 kPa pressure inside column whilst down-flow mode generated a much higher pressure of 214 kPa, thus making the suction mode more efficient. Micellar solubilisation was found to be responsible for As desorption from the soil and it followed 1st order kinetics. Desorption rate coefficient of suction mode was found to be in the range of 0.005 to 0.01, much higher than down-flow mode values. Analysis of the PT-IR data suggested that the soapnut solution did not interact chemically with As, offering an option for reusing the surfactant. Soapnut can be considered as a soil washing agent for removing As even from soil with high Fe content.     

Polycyclic aromatic hydrocarbons in crude oil-contaminated soil: A two-step method for the isolation and characterization of PAHs

A two-step analytical method is developed for the isolation and characterization of polycyclic aromatic hydrocarbons (PAHs) in crude oil contaminated soil. In the first step, those crude oil components were isolated which are easily mobilized with water from the contaminated soil (determination of groundwater pollution potential). In the second step, the fraction containing the remaining crude oil compounds was extracted using toluene. After the cleanup of the fractions, both fractions were analyzed using high-performance liquid chromatography (HPLC). The HPLC of the toluene extracted fraction shows that along with the sixteen priority pollutants from the US-EPA list, many other polycyclic aromatic hydrocarbons (PAHs) are present as well. It is evident from the chromatograms that a significant amount of PAHs are present as is also the case in the fractions eluted by water. The described method allows the determination of total organic pollutants from crude oil, some of them being potential groundwater contaminants. The major part of the total pollutants could not be mobilized by water and therefore remains in the soil, which was extracted in the second step.     

Determination of total hydrocarbon concentration in coastal waters and sediments off the east coast of Peninsular Malaysia

To determine the level of total hydrocarbon concentrations (THCs) along the eastern coastal regions of Peninsular Malaysia, samples of subsurface seawater (1 m) and surface sediments were collected from several sampling stations between June and August 1993. THCs in seawater and sediments as determined by fluorescence spectroscopy ranged from 1.4 to 21.8 µg L-1 (Seligi crude oil equivalents) and from 0.79 to 20.0 mg kg-1 (dry weight Seligi crude oil equivalents) respectively. In comparison to results obtained in similar surveys in Malaysian waters, the levels of THCs found in the present study were significantly lower indicating lower hydrocarbon contamination in the area studied.     

Phosphate-arsenate relations to affect arsenic concentration in plant tissues,growth, and antioxidant efficiency of sunflower (Helianthus annuus L.) under arsenic stress

Environmental Science and Pollution Research - Relations between phosphate and arsenate are important but inconsistent to influence arsenic (As) phytotoxicity depending on many plant and soil...