Comparative distribution of the scalp hair trace metal contents in the benign tumour patients and normal donors

The scalp hair samples of benign tumour patients (n = 77) and normal donors (n = 86) were analysed for selected trace metal contents using atomic absorption spectrophotometry. In the scalp hair of benign tumour patients, highest average levels were found for Ca (1,401 microg/g), followed by Na (476.9 microg/g), Mg (441.6 microg/g), Zn (438.3 microg/g), K (119.2 microg/g) and Fe (96.38 microg/g) while in comparison, the maximum mean levels in the scalp hair of normal donors were shown by Ca (556.5 microg/g), followed by Zn (154.2 microg/g), Mg (153.4 microg/g), Na (97.45 microg/g) and Fe (81.68 microg/g). Almost all metal levels revealed higher dispersion and asymmetry in the scalp hair of benign tumour patients compared with the normal donors. The average concentrations of Ca, Cd, Co, K, Mg, Mn, Na, Ni, Pb, Sb, Sr and Zn were significantly higher in the hair of benign tumour patients compared with the normal donors. Significant gender-based differences were also observed in the scalp hair metal contents of benign tumour patients. Strong positive correlations were found between Cd-Cr (0.547) and Cd-Co (0.507) in the hair of benign tumour patients whereas Ca-Mg, Mg-Sr, Co-Cd, Cr-Cd, Li-Cr, Li-Co, Li-Cd, Na-Cd, Na-Co and Na-Li exhibited strong relationships (r > 0.50) in the hair of normal donors. Cluster analysis (CA) and principal component analysis (PCA) were used for the source identification and apportionment of scalp hair trace metals in the two donor groups. The scalp hair of benign tumour patients and normal donors revealed six and five main clusters of trace metals, respectively. PCA extracted seven principal components of trace metals in the scalp hair of benign tumour patients while six principal components were observed in the case of normal donors. The study evidenced significantly different patterns of metal distribution in the hair of benign tumour patients in comparison with normal donors.     

Hydrochemistry of Wet Atmospheric Precipitation Over an Urban Area in Northern Indo-Gangetic Plains

Rain water samples were collected to study the chemical composition of wet atmospheric precipitation (first event) over the Lucknow city in the northern Indo-gangetic alluvial plains. The samples were collected in the month of July, 2005 from different sites. The wet precipitation samples were analyzed for pH, EC, major ions (, Cl⁻, , , , F⁻, Na⁺, K⁺, Ca²⁺, Mg²⁺, ) and heavy metals (As, Cd, Al, Co, Cr, Cu, Fe, Mn, Mo, Ni, Hg, Pb, Se, Sn, Ti, V, Zn). The pH values of wet precipitation samples ranged between 6.5 and 8.7. The analysis of linear regression applied to the set of studied variables and computation of neutralization factors showed that neutralization occurred in precipitation samples and Ca²⁺ had the maximum neutralization capacity. It was found that Cl⁻, , Ca²⁺, Mg²⁺, Na⁺ and K⁺ in the precipitation samples originated mainly from crustal/anthropogenic sources in the region. On an average Fe, and Al accounted for >72% of the total concentration of trace metals in the wet precipitation samples followed by Zn (>10%). Enrichment factors calculated for heavy metals over reference background level in seawater and Earth’s crust showed relatively higher enrichment of Zn. The principal component analysis (PCA) identified the possible sources of ionic species and heavy metals in the wet precipitation samples.     

Persistent Organochlorine Pesticide Residues in Soil and Surface Water of Northern Indo-Gangetic Alluvial Plains

This study reports the concentration levels and distribution pattern of the organochlorine pesticide (OCPs) residues in the soil and surface water samples collected from the northern Indo-Gangetic alluvial plains. A total of 31 soil and 23 surface water samples were collected from the study region in Unnao district covering an area of 2150 km² and analyzed for aldrin, dieldrin, endrin, HCB, HCH isomers, DDT isomers/metabolites, endosulfan isomers (α and β), endosulfan sulfate, heptachlor and its metabolites, α-chlordane, γ-chlordane and methoxychlor. In both the soil and surface water samples β- and δ-isomers of HCH were detected most frequently, whereas, methoxychlor was the least detected pesticide. The results showed contamination of soil and surface water of the region with several persistent organic pesticides. The total OCPs level ranged from 0.36–104.50 ng g^–1 and 2.63–3.72 μg L^–1 in soil and surface water samples, respectively.     

Adsorption of malachite green on groundnut shell waste based powdered activated carbon

In the present technologically fast changing situation related to waste management practices, it is desirable that disposal of plant waste should be done in a scientific manner by keeping in view economic and pollution considerations. This is only possible when the plant waste has the potential to be used as raw material for some useful product. In the present study, groundnut shell, an agricultural waste, was used for the preparation of an adsorbent by chemical activation using ZnCl2 under optimized conditions and its comparative characterisation was conducted with commercially available powdered activated carbon (CPAC) for its physical, chemical and adsorption properties. The groundnut shell based powdered activated carbon (GSPAC) has a higher surface area, iodine and methylene blue number compared to CPAC. Both of the carbons were used for the removal of malachite green dye from aqueous solution and the effect of various operating variables, viz. adsorbent dose (0.1-1 g l(-1)), contact time (5-120 min) and adsorbate concentrations (100-200 mg l(-1)) on the removal of dye, has been studied. The experimental results indicate that at a dose of 0.5 g l(-1) and initial concentration of 100 mg l(-1), GSPAC showed 94.5% removal of the dye in 30 min equilibrium time, while CPAC removed 96% of the dye in 15 min. The experimental isotherm data were analyzed using the linearized forms of Freundlich, Langmuir and BET equations to determine maximum adsorptive capacities. The equilibrium data fit well to the Freundlich isotherm, although the BET isotherm also showed higher correlation for both of the carbons. The results of comparative adsorption capacity of both carbons indicate that groundnut shell can be used as a low-cost alternative to commercial powdered activated carbon in aqueous solution for dye removal.     

Heavy metal accumulation in edible fish species from Rawal Lake Reservoir, Pakistan

The aim of the present study was to describe the accumulation of trace metals in the liver, kidney, gills, muscles, and skin of four edible fish species (Tor putitora, Cirrhinus mrigala, Labeo calbasu, and Channa punctatus) of Rawal Lake Reservoir, Pakistan. The fish samples were collected in the pre-monsoon (May 2008) and post-monsoon (October 2007) seasons and were analyzed for heavy metals by using an atomic absorption spectrometer. Kidney and liver showed relatively high concentrations of heavy metals. The accumulation of metals in the different organs of the fish (skin, muscles, and gills) in post-monsoon was higher than in pre-monsoon. In pre-monsoon, the metals followed the trend Zn > Pb > Fe > Cr > Ni > Mn > Co > Cu > Cd > Li, while in the post-monsoon season, the trend was Fe > Pb > Cr > Ni > Zn > Cu > Co > Mn > Cd > Li. The concentrations of Ni, Cr, and Pb in the muscle of all fish species were higher than the WHO guideline values of heavy metals in fishes for human consumption except in T. putitora. Cu level was nearly equal to the WHO maximum levels in C. mrigala and L. calbasu, while it was lower in T. putitora and C. punctatus. It is strongly advocated that risk assessment studies should be conducted and there is an urgent need for water quality restoration and management of Rawal Lake Reservoir.     

The level and distribution of selected organochlorine pesticides in sediments from River Chenab,Pakistan

Organochlorine pesticides (OCPs), viz. β-hexachlorocyclohexane (β-HCH), γ-HCH, aldrin, dieldrin, endrin, heptachlor, endosulfan-I, endosulfan-II, heptachlor endoepoxide, heptachlor exoepoxide, mirex, dicofol, o,p′-dichlorodiphenyltrichloroethane (o,p′-DDT), p,p′-dichlorodiphenyltrichloroethane (p,p′-DDT), dichlorodiphenyldichloroethane (DDD), and dichlorodiphenyltrichloroethylene (DDE) and 12 other physicochemical parameters were measured in surface sediments from River Chenab during two sampling seasons (summer and winter, 2007) to evaluate spatial and temporal trends of sediment pollution. Hierarchical agglomerative cluster analysis identified three groups of sites based on spatial similarities in physicochemical parameters and OCP residual concentrations. Spatial discriminant function analysis (DFA) segregated 14 parameters, viz. dicofol, endosulfan-I, heptachlor endoepoxide, dieldrin, DDD, DDE, endosulfan-II, o,p′-DDT, p,p′-DDT, pH, electrical conductivity (EC), Cl⁻¹, total P (%), and silt, which explained 96% of total variance between spatial groups. γ-HCH was the most frequently detected (63%) pesticide, followed by DDD (56%). The ratio of DDTs to their metabolites indicated current input and anaerobic biodegradation. Temporal DFA highlighted aldrin, heptachlor endoepoxide, Cl⁻¹, total P, and EC as important variables which caused variations between summer and winter. DDTs were relatively more prevalent as compared to other OCPs in the sediments samples during both seasons. DDT metabolites were detected at greater frequencies and concentrations in winter, whereas DDT isomers were more prevalent in summer sediment samples. Factor analysis identified agricultural and industrial activities as major sources of sediment OCP contamination. Concentrations of γ-HCH, heptachlor endoepoxide, dieldrin, and DDTs (isomers and metabolites) in all sediment samples were well above interim sediment quality guidelines (ISQGs) and probable effect limits (PEL) given by Canadian Sediment Quality Guidelines (CSQGs).     

Organochlorine residual concentrations in cattle egret from the Punjab Province, Pakistan

In this study, residual concentration of organochlorine pesticides (OCPs) in the sediments, prey, and eggs of Bubulcus ibis were measured from three breeding heronries from the Punjab province of Pakistan. Pattern of contamination in eggs followed the order: DDTs > HCHs > heptachlor > aldrin. Overall, pesticide residual concentrations were greater in eggs of cattle egrets collected from heronry on the River Ravi. Among HCHs, ??-HCH was more prevalent in eggs, whereas DDTs followed the order: DDD > DDE > p,p ^??-DDT > o,p ^??-DDT. Eggshell thinning was detected which showed negative relationship with residual concentration of DDE. In prey samples, residual concentration of POPs followed the order: DDTs > HCHs > dicofol > heptachlor; however, contamination pattern in sediments followed a slightly different order: DDTs > heptachlor > dicofol > HCHs > dieldrin > aldrin. Concentration of ??-HCH was more prevalent in sediments and comparatively greater concentrations of POPs were measured in sediments collected from the River Ravi. Dicofol was found for the very first time in the biological samples from Pakistan, and its concentration was measured as relatively high in eggs from heronry from the River Chenab. Residual concentrations measured in eggs were below the levels that could affect egret populations. Biomagnification of the total OCPs through the food chain was evident in three breeding heronries. The concentration of DDE measured in eggs of the cattle egret suggests the need for monitoring this contaminant in other bird species at different trophic levels.     

Nexus between willingness to pay for renewable energy sources: evidence from Turkey

Environmental Science and Pollution Research - The willingness to pay (WTP) plays a central role in directing appropriate policy regarding ambitious renewable energy targets. Based on this...     

Further Results on Permit Markets with Market Power and Cheating

This paper examines a market for pollution permits in which one firm has market power and one or more firms is noncompliant. I show that the firm with market power may choose to hold more permits than it needs, effectively retiring permits from the market. I also show that some noncompliance may be socially desirable because it can mitigate the distortion caused by market power. Similarly, some degree of market power may be socially desirable because it can, in turn, mitigate the distortion caused by noncompliance.