Organochlorine pesticide and polychlorinated biphenyl residues in feathers of birds from different trophic levels of South-West Iran

Persistent organochlorine pesticides (OCPs), such as dichlorodiphenyltrichloroethane (DDT) and its metabolites, hexachlorobenzene (HCB), alpha, beta and gamma-hexachlorocyclohexane (HCH) isomers, together with polychlorinated biphenyl (PCB) congeners (IUPAC Nos. 28, 52, 101, 138, 153 and 180), were determined in tail feathers from 37 birds belonging to 18 species, all originating from the South-West of Iran (Khuzestan, coast of the Persian Gulf). This is the first report on organochlorine contaminants in feathers from museum collections and it is an indication of the concentrations of OCPs and PCBs in the past (1991-1996). Median concentrations of HCHs, DDTs, PCBs and HCB were 22, 14, 11 and 10 ng/g feather, respectively. Significant correlations (p<0.05) were calculated between OCPs (except HCB) and PCBs in the bird feathers. p,p'-DDE and gamma-HCH were the most abundant OCPs, while CB 180, CB 138 and CB 101 were the predominant PCB congeners in almost all species. Significant differences (p<0.05) in the mean concentrations of DDTs and PCBs were detected among species grouped according to their feeding habits. Levels of DDTs and PCBs were highest in the carnivorous species and lowest in the herbivorous species. Levels of OCPs and PCBs in feathers of bids in the 1990s were generally below the thresholds reported to affect reproduction.     

Parametric uncertainty analysis on hydrodynamic coefficients in groundwater numerical models using Monte Carlo method and RPEM

Groundwater resources are the only source of water in many arid and semi-arid regions. It is important to manage these resources to have a sustainable development. However, there are many factors influencing the accuracy of the results in groundwater modeling. In this research, the uncertainty of two important groundwater model parameters (hydraulic conductivity and specific yield) were considered as the main sources of uncertainty in estimating water level in an unconfined aquifer, in Iran. For this purpose, a simple method called Rosenblueth Point Estimate Method (RPEM) was used to assess groundwater modeling parametric uncertainty, and its performance was compared with Monte Carlo method as a very complicated and time-consuming method. According to calibrated values of hydraulic conductivity and specific yield, several uncertainty intervals were considered to analyze uncertainty. The results showed that the optimum interval for hydraulic conductivity was 40% increase–30% decrease of the calibrated values in both Monte Carlo and RPEM methods. This interval for specific yield was 200% increase–90% decrease of the calibrated values. RPEM showed better performance using the evaluating indices in comparison with Monte Carlo method for both hydraulic conductivity and specific yield with 43% and 17% higher index values, respectively. These results can be used in groundwater management and future prediction of groundwater level.

     

Chromium retention potential of two contrasting Solanum lycopersicum Mill. cultivars as deciphered by altered pH dynamics,growth, and organic acid exudation under Cr stress

Environmental Science and Pollution Research - Chromium (Cr), being a persistent toxic heavy metal, triggered the retardation of plant’s metabolic processes by initiating changes in...     

Source apportionment of PAHs and n-alkanes in respirable particles in Tehran,Iran by wind sector and vertical profile

The vertical concentration profiles and source contributions of polycyclic aromatic hydrocarbons (PAHs) and n-alkanes in respirable particle samples (PM₄) collected at 10, 100, 200 and 300-m altitude from the Milad Tower of Tehran, Iran during fall and winter were investigated. The average concentrations of total PAHs and total n-alkanes were 16.7 and 591 ng/m³, respectively. The positive matrix factorization (PMF) model was applied to the chemical composition and wind data to apportion the contributing sources. The five PAH source factors identified were: ‘diesel’ (56.3 % of total PAHs on average), ‘gasoline’ (15.5 %), ‘wood combustion, and incineration’ (13 %), ‘industry’ (9.2 %), and ‘road soil particle’ (6.0 %). The four n-alkane source factors identified were: ‘petrogenic’ (65 % of total n-alkanes on average), ‘mixture of petrogenic and biomass burning’ (15 %), ‘mixture of biogenic and fossil fuel’ (11.5 %), and ‘biogenic’ (8.5 %). Source contributions by wind sector were also estimated based on the wind sector factor loadings from PMF analysis. Directional dependence of sources was investigated using the conditional probability function (CPF) and directional relative strength (DRS) methods. The calm wind period was found to contribute to 4.4 % of total PAHs and 5.0 % of total n-alkanes on average. Highest average concentrations of PAHs and n-alkanes were found in the 10 and 100 m samples, reflecting the importance of contributions from local sources. Higher average concentrations in the 300 m samples compared to those in the 200 m samples may indicate contributions from long-range transport. The vertical profiles of source factors indicate the gasoline and road soil particle-associated PAHs, and the mixture from biogenic and fossil fuel source-associated n-alkanes were mostly from local emissions. The smaller average contribution of diesel-associated PAHs in the lower altitude samples also indicates that the restriction of diesel-fueled vehicle use in the central area of Tehran has been effective in reducing the PAHs concentration.     

Nutrient concentrations within and below root zones from applied chicken manure in selected Hawaiian soils

The objective of this study was to evaluate the effects of chicken manure (CM) application rates on nutrient concentrations within and below the root zone of sweet corn (Zea mays L. subsp. mays) under Hawaiian conditions. The research was conducted in leeward (Poamoho) and windward (Waimanalo) areas of Oahu, Hawaii, where contrasts exist in both climatic and soil conditions. Suction cup were used to collect soil solutions from 30 and 60 cm depths. Soil solutions were collected six times during the growing season at each location and analyzed for different nutrients (N, P, K, Ca, Mg, Na, Fe, Mn, Zn, and Cu), nitrate-nitrogen (NO₃–N), ammonium-nitrogen (NH₄–N), electrical conductivity (EC), and pH. Analysis showed that CM rates significantly affected the concentration of macro-nutrients below the root zone at Poamoho and within the root zone at Waimanalo. In general, nutrient concentration increased with the increasing rates of CM application. There was a significant effect of CM on micro-nutrients except below the root zone at Poamoho. CM significantly affected NO₃–N concentration within the root zone for 15, 60 days after planting (DAP) at Poamoho, and 16, 28 DAP at Waimanalo. The effect was also significant on total nitrogen (N) concentration in the root zone across the two growing seasons at Waimanalo. There was a highly significant correlation between total N and NO₃–N, and EC within and below the root zone.     

Toxic effects of deltamethrin and λ-cyhalothrin on Xenopus laevis tadpoles

This study evaluates the toxic effects of deltamethrin and λ-cyhalothrin on Xenopus laevis tadpoles after 168 h of exposure. The LC₅₀ of deltamethrin and λ-cyhalothrin at 168 h was calculated as the μg of active ingredient per liter (μg AI/L). According to these values, the LC₅₀ was 6.26 and 3.94 μg AI/L for deltamethrin and λ-cyhalothrin, respectively. Several enzymes were studied for early signs of intoxication following exposure to the pesticides for 24 h. Glutathione-S-transferase,carboxylesterase, and lactate dehydrogenase were inhibited by λ-cyhalothrin, and both pesticides inhibited acid phosphatase and aspartate aminotransferase. In contrast, acetylcholinesterase was activated by deltamethrin. The results suggest that X. laevis is sensitive to the pyrethroids that were tested, and the enzyme responses suggest that they are potential biomarkers for evaluating the toxic effect of pyrethroids on amphibians in environmental conditions.     

Equilibrium, kinetic, and thermodynamic biosorption of Pb(II), Cr(III), and Cd(II) ions by dead anaerobic biomass from synthetic wastewater

Purpose

Heavy metals are toxic pollutants released into the environment as a result of different industrial activities. Biosorption of heavy metals from aqueous solutions is a new technology for the treatment of industrial wastewater. The aim of the present research is to highlight the basic biosorption theory to heavy metal removal.

Materials and methods

Heterogeneous cultures mostly dried anaerobic bacteria, yeast (fungi), and protozoa were used as low-cost material to remove metallic cations Pb(II), Cr(III), and Cd(II) from synthetic wastewater. Competitive biosorption of these metals was studied.

Results

The main biosorption mechanisms were complexation and physical adsorption onto natural active functional groups. It is observed that biosorption of these metals was a surface process. The main functional groups involved in these processes were hydroxyl (–OH) and carboxylic groups (C=O) with 37, 52, and 31 and 21, 14, and 34 % removal of Pb(II), Cr(III), and Cd(II), respectively. Langmuir was the best model for a single system. While extended Langmuir was the best model for binary and ternary metal systems. The maximum uptake capacities were 54.92, 34.78, and 29.99 mg/g and pore diffusion coefficients were 7.23, 3.15, and 2.76?×?10^?11 m²/s for Pb(II), Cr(III), and Cd(II), respectively. Optimum pH was found to be 4. Pseudo-second-order was the best model to predict the kinetic process. Biosorption process was exothermic and physical in nature.

Conclusions

Pb(II) offers the strongest component that is able to displace Cr(III) and Cd(II) from their sites, while Cd(II) ions are the weakest adsorbed component.     

Biochemical response to exposure to six textile dyes in early developmental stages of Xenopus laevis

The present study was undertaken to determine the toxic effect of a lethal concentration of six different commercially used textile dyes on the 46th stage of Xenopus laevis tadpoles. The tadpoles were exposed to Astrazon Red FBL, Astrazon Blue FGRL, Remazol Red RR, Remazol Turquoise Blue G-A, Cibacron Red FN-3G, and Cibacron Blue FN-R for 168 h in static test conditions, and thus, 168-h median lethal concentrations (LC₅₀s) of each dye were determined to be 0.35, 0.13, 112, 7, 359, and 15.8 mg/L, respectively. Also, to evaluate the sublethal effects of each dye, tadpoles were exposed to different concentrations of dyes (with respect to 168-h LC₅₀s) for 24 h. The alteration of selected enzyme activities was tested. For this aim, glutathione S-transferase (GST), carboxylesterase, and lactate dehydrogenase (LDH) were assayed. After dye exposure, the GST induction or inhibition and LDH induction indicated some possible mechanisms of oxidative stress and deterioration in aerobic respiration processes induced by the tested dyes. Findings of the study suggest that selected biomarker enzymes are useful in understanding the toxic mechanisms of these dyes in X. laevis tadpoles as early warning indicators. Therefore, these selected biomarkers may evaluate the effect of environmental factors, such as textile dye effluents and other industrial pollutants, on amphibians in biomonitoring studies.     

A new catalytic oxidation method for sensitive quantification of bromate in flours and bottled water using AgNPs

In this paper, a simple and sensitive spectrophotometric method for the determination of nanomolar level of bromate, based on the catalytic effect of silver nanoparticles on the oxidation of acid red 14 by potassium bromate, is described. The reaction rate was monitored spectrophotometrically by measuring the decrease in absorbance of acid red 14 at 516 nm. The detection limit of the method was 8 ng/mL, and the linear range was between 15 and 130 ng/mL. The effects of acidity, concentration of reactants and reaction time, and external ions were also discussed. The optimum reaction conditions were fixed, and some kinetic parameters determined. The relative standard deviation for the determination of bromate at the concentration of 50 ng/mL was calculated to be 0.996 % (n?=?10). The method has been successfully applied to the determination of bromate in flours and bottled waters.