Environmental human silver exposure

Environmental exposure to silver (Ag) was assessed in occupationally non-exposed adult human population by analyzing Ag in the hair (H?·?Ag) and whole blood (WB?·?Ag). H?·?Ag was analyzed in 311 (123 men, M; 188 women, W); while WB?·?Ag was determined in 235 of these individuals (90 M, 145 W). Women had more H?·?Ag than men (M 0.05 vs. W 0.076), whereas WB?·?Ag concentrations in men and women were not significantly different. A natural distribution of the median derivatives was utilized to generate the dataset to fit the logistic sigmoid curve to assess the current human body burden of environmental Ag population exposure for M and W separately. The H?·?Ag (µg?g^?1) below 0.0105 for M and 0.0145 for W, reflects low level of environmental Ag exposure. The adaptive physiological saturation phase followed where H?·?Ag rose rapidly, first for M and then for W in parallel with biological assay. Both parallel saturation curves converged and plateaued at 0.215 for M and 0.965 for W (µg?g^?1). The current level of human environmental Ag exposure is low, but cases of high Ag exposure occurred sporadically. In conjunction with the medical histories overt clinical neural toxicity may be expected for H?·?Ag at 4?µg?g^?1and higher. There were no significant correlation between the H?·?Ag and WB?·?Ag.     

Determination of persistent organic pollutants in sediment and fish of the western coast of Alexandria,Egypt

Persistent organic pollutants (POPs) were recorded in sediment and fish samples collected from the western coast of Alexandria. Total hydrocarbons (aliphatic+PAHs ) in sediment ranged from 683.8 to 34670.1 ng g ^?1 with an average of 9286.9 ng g ^?1. The sum of C16–C34 of aliphatic fractions was<4000?ng g;^?1, indicating the presence of a fresh petroleum source. For all sediments, the anthracene/phenanthrene ratio was>0.1, suggesting the dominance of a pyrolytic source. Total aliphatics in different fish species ranged from 253 to 11?132 ng g;^?1, while total PAHs ranged from 3862 to 35?746 ng g;^?1 wet weight. Benzo[a]pyrene was the most dominant PAH fraction ranged from 1902.7 to 32 905.5 with an average of 9464.5?ng g;^?1 wet weight in all fish species. Concentrations of polychlorinated biphenyls (PCBs) ranged from 0.79 to 64.9?ng g;^?1 with an average 12.14?ng g;^?1 wet weight. The concentrations of organochlorines in fish species (Euthynnus alleferatus, Scomberomorus commerson, Sphyraena Sphyraena, Diplodus vulgaris, and Alepes djedaba) decreased following the order: PCBs>DDTs>HCHs>total cyclodienes. Concentrations of DDTs in fish tissues ranged from 4.89 to 36.37 ng g^?1 with an average of 16.4?ng g;^?1 wet weight. The concentrations of total HCHs ranged from 0.3 to 65.7?ng g;^?1 with an average of 16.35?ng g;^?1. The present study indicates: (1) fresh petroleum input where Pr/Ph>1; (2) PAHs in sediment<4000 ng g ^?1; (3) BaP concentration exceeded the permissible levels in Alepes djedaba species; (4) DDTs in sediment were below the effective range low level; (5) PCBs>effective range low and相似文献   

Assessment of metals in soil extracts and their uptake and movement within Tamarix nilotica at Lake Nasser banks,Egypt

This study aims to determine heavy-metal levels in soil from the banks of Lake Nasser, the ability of Tamarix nilotica to accumulate such metals from soil and hence its potential for phytoextraction. Soil and Tamarix samples were collected from the banks of four bights around Lake Nasser and analysed for Fe, Mn, Ca, Mg, Cr, Cu, Ni, Zn, Cd and Pb by atomic absorption spectrometry, whereas Na and K were measured by atomic emission spectrophotometry. Three different methods of extraction were used for the soil samples. Lead, copper and zinc were equally distributed between the exchangeable phase and Fe/Mn oxide-bound form, while other measured metals were mainly present in the Fe/Mn oxide fraction. With the exception of iron, all metals studied showed total concentrations within the geochemical background values. T. nilotica exhibited elevated concentrations of Na (36.2–48.5?mg?g^?1) and K (2.74–4.33?mg?g^?1) in stems, and relatively high concentrations of Pb, Cd and Co (0.39–1.03?µg?g^?1, 0.24–1.3?µg?g^?1 and 1.94–5.3?µg?g^?1, respectively) are found in plant leaves. Bioaccumulation factors of Na and K (9.3 and 12.63, respectively) were high in T. nilotica stems. While the bioaccumulation of Pb, Cd, Co and Ni (2870.1, 2035.4, 10.5 and 5313.2, respectively) was high in plant leaves, Fe, Mn, Ca and Mg were accumulated relatively equally in plant stems and leaves. T. nilotica was found to secrete high amounts of Na, Ca and K, in addition to small amounts of all accumulated metals except Cd and Cu. These secreted metals appeared as salt crystals (67.5% Na; 25.8% Ca; 5% Mg; 1.5% K and 0.16% trace and minor elements) on the plant surface. The concentrations of all the metals studied in T. nilotica were higher than in the salt crystals. Statistical analysis of the database suggests bioaccumulation of these metals from soil to T. nilotica. This reflects the importance of using T. nilotica as a model in the phytoremediation process as an established environmental clean-up technology.     

Leaching characteristics of bisphenol A from epoxy-resin pavement materials

We investigated the leaching characteristics of bisphenol A (BPA) from two kinds of epoxy-resin pavement materials, one containing epoxy resins (EPs) and the other containing epoxy-acrylate resins (EPAs). Both samples contained residual BPA monomer, at levels of 9.0?µg?g^?1 for the EP resin sample and 4.4?µg?g^?1 for the EPA resin sample. These amounts were larger than amounts previously measured for polycarbonate samples. The amount of BPA leached from the samples increased with temperature. The leaching of BPA from EP was more strongly affected by temperature than the leaching from EPA. The pH also affected the amount of leached BPA. The maximum leached amount was observed under alkaline conditions (pH 10.8) for both sample types. The amounts of BPA that might leach from pavement materials during 1?h of heavy rain were estimated to be 0.9?µg?m^?2 for EP and 3.5?µg?m^?2 for EPA. Our results indicate that EPs disposed of in waste landfills without any treatment may be a source of BPA in leachate at landfill sites.     

Concentrations of lead in cosmetics commonly used in South Africa

In this study, we present evidence of lead in lip liner, oil absorbent powder, mascara, concealer, lipsticks, lip gloss, and foundation. The samples were analyzed for lead by flame atomic absorption spectrometry. The levels of lead in concealer, mascara, lip liner, and oil absorbent powder were found to be 7.4?±?1.3?µg?g^?1, 15.8?±?0.2?µg?g^?1, 29.0?±?9.2?µg?g^?1, and 17.3?±?2.9?µg?g^?1, respectively. The levels of lead in lipsticks, lip gloss, and foundation ranged from not detected to 73.1?±?5.2?µg?g^?1, 4.7 to 11.7?±?2.8?µg?g^?1, and 7.8 to 32.9?±?1.4?µg?g^?1, respectively. Thus, in the majority of samples, the concentrations of lead are higher than the USFDA maximum permissible concentration of 0.10?µg?g^?1 in candy and cosmetics. In lipsticks alone, only 25% of 40 samples were found to meet the requirement. Therefore, continuous use of cosmetic products in which lead concentration exceeds the maximum permissible level may pose a health hazard for the female population of South Africa in the long run.     

Potential correlation between perfluorinated acids and liver morphology in East Greenland polar bears (Ursus maritimus)

In this study, residual concentrations of chlorpyrifos (CPF) were determined in feed (40) and fodder (25) samples collected from various locations of Tarai region of Uttarakhand. For extracting residues, liquid–liquid partition followed by alumina column clean up was used and the detection and quantification of residues was undertaken with the help of high-performance liquid chromatography using C18 column and diode array detector at 220?nm. Of the total 40 feed samples analyzed, 7 (17.5%) samples were found positive for CPF with the mean residual concentration of 0.058?µg?g^?1; while out of 25 fodder samples, CPF residues were detected in a single (4%) sample with residual concentration of 0.39?µg?g^?1. However, none of the feed or fodder samples contained CPF residues above the prescribed limit.     

Organochlorines in urban soils from Central India: probabilistic health hazard and risk implications to human population

This study presents distribution of organochlorines (OCs) including HCH, DDT and PCBs in urban soils, and their environmental and human health risk. Forty-eight soil samples were extracted using ultrasonication, cleaned with modified silica gel chromatography and analyzed by GC-ECD. The observed concentrations of ∑HCH, ∑DDT and ∑PCBs in soils ranged between?<?0.01–2.54, 1.30–27.41 and?<?0.01–62.8 µg kg^?1, respectively, which were lower than the recommended soil quality guidelines. Human health risk was estimated following recommended guidelines. Lifetime average daily dose (LADD), non-cancer risk or hazard quotient (HQ) and incremental lifetime cancer risk (ILCR) for humans due to individual and total OCs were estimated and presented. Estimated LADD were lower than acceptable daily intake and reference dose. Human health risk estimates were lower than safe limit of non-cancer risk (HQ?<?1.0) and the acceptable distribution range of ILCR (10^?6–10^?4). Therefore, this study concluded that present levels of OCs (HCH, DDT and PCBs) in studied soils were low, and subsequently posed low health risk to human population in the study area.     

Screening of endogenous antioxidants in some medicinal plants

The evaluation of antioxidant enzymes and antioxidant metabolites was done in leaf tissues of Azadirachta indica, Butea monosperma, Cassia fistula, Mangifera indica, and Syzygium cumini growing in the Thar Desert, Rajasthan, India. The plants are naturally exposed to drought stress and high temperatures during summer. Enzymatic reactive oxygen species (ROS) scavenging mechanisms in plants include superoxide dismutase (SOD), ascorbate peroxidase (APX), glutathione reductase, catalase, and guaiacol peroxidase, and non-enzymatic antioxidants including the carotenoids, proline, and vitamin C were studied. The strategies to cope up with ROS under these extreme conditions are plant-specific. The highest activity of APX was found in M. indica (13.6?±?2.4?units?g^?1 fresh wt.). A. indica exhibited maximum guaiacol peroxidase activity (0.024?±?0.006?units?min?g^?1 fresh wt.), while S. cumini showed maximum SOD (12.5?±?2.3?units?g^?1 fresh wt.) and catalase activities (6.9?±?2.2?units?g^?1 fresh wt.). M. indica and S. cumini have been found to be more potent antioxidant systems among the studied plants.     

A novel extraction method for analysing available sulfamethoxazole in soil

A novel extraction method was established to determine the water-extractable (available) content of sulfamethoxazole (SMX) in soil. The SMX imprinted polymers (MIPs) were synthesised and the performance was evaluated by Fourier transform infrared spectroscopy, scanning electron microscopy and binding experiments. Results showed that the MIPs exhibited good selectivity for SMX, so the MIPs were applied as a sorbent. SMX in soil was extracted by water, sorbed from the extract to MIPs and analysed with a high performance liquid chromatography (HPLC) after its desorption from MIPs. Meanwhile, the classic organic solvent extraction was employed to measure the total SMX content in soil. Results showed that when SMX level in spiked soils varying from 1.0–500?μg?kg^?1, the observed recoveries of available SMX contents ranged from 63.27?±?3.11% to 82.11?±?2.77% (n?=?3), while the total SMX varied between 89.59?±?1.65% and 97.64?±?3.92% (n?=?3). The detection limit of the developed method for SMX in soils was 0.05?μg?kg^?1. Available SMX contents in five field soil samples ranged from 0.13 to 4.14?μg?kg^?1, which were only 0.35–25.40% of the respective total SMX contents. Results from this study manifest the importance of the extents of SMX immobilisation with different soils for assessing SMX's ecological and human health risks.     

Organochlorine residues in maternal milk from inhabitants of the Thohoyandou area,South Africa

The presence of organochlorine compounds (OC) such as DDT and their metabolites in the environment have created a significant environmental concern over the years due to adverse effects. Consequently, DDT has been banned in many countries. However, it is still used in some countries including South Africa, particularly for vector-borne disease eradication programmes. Since the presence of DDT and its metabolites may provide an indication of the general exposure and use of these compounds, there was a need for such a study. Human breast milk samples (n = 30) were collected from mothers within the age range of 19–40 years from the Thohoyandou area, South Africa. The liquid–liquid extraction method was used to extract DDT and its metabolites from the samples. The crude extracts were subjected to column chromatography for measurements of OC levels. The concentration ranges of the contaminants were as follows: not detected (ND) to1770 ng g^?1 (2,4′-DDE); ND to 3977 ng g^?1 (4,4′-DDE); ND to 3250 ng g^?1 (2,4′-DDD); ND to 2580 ng g^?1 (4,4′-DDD) and ND to 2847 ng g^?1 (4,4′-DDT). The mean ΣDDE, ΣDDD and ΣDDT obtained from the villages were 1180 ng g^?1, 830 ng g^?1 and 690 ng g^?1, respectively. The total DDT ranged from 820–7473 ng g^?1. The estimated daily intake varied from 260 to 4696 ng g^?1, ND-10551 ng g^?1 and ND-4237 ng g^?1 for DDE, DDD and DDT, respectively. These values are significantly higher than the FAO/WHO acceptable daily intake (ADI) of 20 ng g^?1. The ΣDDT was found to decrease with increasing age of the mothers. The observed high levels of DDE compared to DDT indicated chronic exposure of the mothers to DDT, which is metabolized to DDE and retained in the body.     

Development of a complex-based flow injection spectrophotometric method for determination of the herbicide pinoxaden in environmental samples

A flow injection (FI) spectrophotometric method for the determination of the herbicide pinoxaden (PXD) has been proposed. PXD was converted in alkaline media with hydroxylamine hydrochloride to the hydroxamate salt. The salt was reacted with iron(III) chloride, and the absorbance of the red colored tris iron hydroxamate complex was measured at 500?nm using a FI system. The method was found to be linear between 0.5 and 40?mg?L^?1 with a molar absorptivity of 1.53?×?10^4?L?mol^?1?cm^?1. The limit of detection and limit of quantification were found to be 0.1?±?0.01?mg?L^?1 and 0.6?±?0.05?mg?L^?1, respectively. Any interference of fenoxaprop-p-ethyl (FE) was avoided by the separation of PXD by liquid chromatography with a mixture of dichloromethane and n-hexane (1?:?1) as eluent. The method was applied to the determination of PXD in soil, water, and wheat grains with percent recoveries of 98?±?2, 100?±?2, and 98?±?5, respectively. Sample throughput of 60 samples per hour was achieved under optimized conditions.     

Risk assessment of children's blood lead level in some rural habitations of western Uttar Pradesh,India

The objective of this study was to determine the blood lead level (BLL) of children aged under 5 living in western Uttar Pradesh, India. A total of 100 blood samples, 100 drinking water samples, and 21 vegetable samples were assessed for lead (Pb) contamination. BLL was observed in the range of 3–11.58?µg?dL^?1 with a maximal level of 11.58?±?0.05?µg?dL^?1 in Kazipur village. Lead in water samples was detected in the range of 0.006–0.095?ppm and identified at upto 9.5-fold higher than the stated permissible limit. A significant positive correlation (+0.679) was obtained between BLL and water Pb levels. All vegetable samples were also contaminated with Pb upto 12-fold higher than the permissible limit of 2.5?µg?g^?1 of Prevention of Food Adulteration Act (PFA) 1954. Untreated industrial effluents were identified as the responsible factors for Pb occurrence in the study area. The presence of lead may be associated with the increased antisocial activities of children living in western Uttar Pradesh. Children with elevated BLL had poorer nutritional status than those with background Pb levels. There is an urgent need for a national campaign to monitor the BLL of children in India.     

Fish as an indicator of aquatic environment: Multielemental neutron activation analysis of nutrient and pollutant elements in fish from Indian coastal areas

Fish is the main food in coastal areas and its analysis for toxic metals has been used as an indicator of the pollution status of the aquatic environment. Several different fish species from the three Indian coasts, Visakhapatnam in the east, Mumbai in the west and Mangalore in the south west and also inland freshwater fish from Nagpur in the central region for comparison were analyzed for up to 20 elements (As, Au, Ba, Br, Cl, Co, Cr, Cu, Fe, Hg, K, Mn, Na, P, Rb, Sb, Sc, Se, Sr, Zn) by instrumental neutron activation analysis (INAA). Dried fish samples in powdered form were irradiated with thermal neutrons in a nuclear reactor followed by high resolution gamma ray spectrometry at different intervals. Several Reference Materials (RMs) of biological origin were analyzed for quality assurance and data validation. Elemental contents in different fish species vary in a wide range depending on the species, its size, location, and aquatic environment. Fish from Mangalore showed highest mean contents of Cr (14.8?±?29.9?µg?g^?1), Cu (1005?±?643?µg?g^?1) and Sb (849?±?888?ng?g^?1) whereas those from Mumbai exhibited highest Hg (2066?±?2146?ng?g^?1) and P (20.3?±?4.63?µg?g^?1) but lowest Cu (6.30?±?3.10?µg?g^?1) contents. Fish from all the regions showed significant amounts of nutrient elements such as Na, K, P, Mn, Fe, Se and Zn as well as some pollutant elements (Br, Cr, Sb, Hg). No regularity in variation of elemental contents with the size was observed. Prawn (Panaeus latisulcatus), a popular fish species from four different regions showed wide variation in elemental contents of Cr, Mn, Fe, Zn, Se, P including toxic pollutants, Sb and Hg. An attempt has been made to calculate daily dietary intake (DDI) for some nutrient elements from Indian fish. Elemental data for Cr, Cu, Fe, Hg, Se, and Zn have been compared with those from other fish exporting countries.     

Occurrence and profiles of polybrominated diphenyl ethers (PBDEs) in riverine sediments of Shanghai: a combinative study with human serum from the locals

Herein, we studied the occurrence and profiles of thirteen PBDE congeners in 30 river sediment samples from Shanghai, China. The concentrations of Σ₁₃PBDEs ranged from 110 to 13,071 pg g ^?1 dw, with an average value of 2,841 pg g ^?1 dw. BDE-209 was the predominant congener accounting for more than 65 % of total PBDEs, demonstrating that the major source of PBDEs in sediment samples was associated with the prevalent use of technical deca-BDE products. Moreover, low brominated BDEs in sediments also came from the degradation of higher brominated BDEs. In addition, taking into consideration of dietary exposure, PBDEs in serum samples collected from the locals were also detected with range of 419–26,744 pg g^?1 (average 5,561 pg g ^?1), which suggested a relatively low burden of PBDEs contamination to human body compared with the condition in other place. And in serum, low brominated compounds constituted the majority of total PBDE congeners.     

Comparative evaluation of trace elements in the scalp hair of arthritis patients and healthy donors

This study was aimed to evaluate the comparative distribution, correlation and apportionment of selected elements (Ca, Cd, Co, Cr, Cu, Fe, Mg, Mn, Pb and Zn) in the scalp hair of arthritis patients and healthy subjects. The hair samples collected from the patients (rheumatoid and osteoarthritis) and healthy donors were digested in nitric acid and perchloric acid mixture, followed by the quantification of trace elements using atomic absorption spectrometry. In the case of healthy donors, highest mean concentration was shown by Ca (3240?µg?g^?1), followed by Mg (340?µg?g^?1), Zn (192?µg?g^?1), Fe (184?µg?g^?1) and Pb (27?µg?g^?1), whereas, the estimated average metal levels in rheumatoid arthritis and osteoarthritis patients were 3160, 290, 197, 61 and 23?µg?g^?1, and 3090, 300, 182, 50 and 21?µg?g^?1, respectively. Most of the elements revealed diverse and random distribution in the scalp hair of the donor groups. The correlation study pointed out significant disparities in the mutual relationships among the trace elements in the patients and controls. Principal component analysis and cluster analysis of the element data manifested diverse apportionment of the selected elements in the scalp hair of the patients compared with the healthy counterparts.     

Assessment of PAHs in water and fish tissues from Great Bitter and El Temsah lakes,Suez Canal,as chemical markers of pollution sources

Sea water and fish tissue samples were collected from nine sampling stations from the Great Bitter and El Temsah lakes in the Suez Canal and analysed for polycyclic aromatic hydrocarbon (PAH). The compositions of PAH determined in the dissolved fraction of sea water were measured in order to use them as chemical markers for identifying different sources of PAH pollution in this region. PAHs determined in fish tissues were measured for comparison with human health standards as consumption. The total mean PAHs concentrations in the sea water samples ranged from 0.28 to 39.57 μg l^?1 with an overall mean of 10.78 and 12.38 μg l^?1 for El Temsah and Bitter Lakes water, respectively. Total PAHs fractions recorded in muscle tissues of all different Osteicthyes fishes collected from Great Bitter lakes ranged from 5.8 to 218.5 μg g^?1 with an overall mean of 57.98 μg g^?1 during all seasons. However, they ranged from 68 to 623 μg g^?1 with an overall mean of 87.69 μg g^?1 recorded in El Temsah lake during four seasons (2003–2004). Benzo(a)pyrene was the most dominant PAHs found in the sea water samples from both lakes with an average concentration of 3.8 μ g l^?1. Dibenzo(a,h)anthracene (DBA) was the most dominant PAHs recorded in fish samples. A maximum of 533 μg g^?1 of DBA was recorded in Dahbana sp. collected from Bitter lakes during January 2004. However, a maximum of 68.7 μ g g^?1 was recorded in Liza carinata species collected from El Temsah lake during July, 2004. The simultaneous occurrence of isomer ratios PHE/ANT<10 for all stations indicated that the major PAH input to water was from combustion of fossil fuel (pyrolytic source). The average ratios were 1.21 and 12.9 during winter (January 2004) and 4.3 and 8.63 during spring (April 2004) for all water samples of Great Bitter lakes and El Temsah lake, respectively. In addition, the present data demonstrate that PAHs from fossil fuel sources (MW<178) were the least significant source of PAHs in this region.     

Organochlorines in the surface sediments of the Bahiret el Bibane lagoon (Tunisia,Southwestern Mediterranean Sea)

Organochlorines (including organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs)) were analysed in 10 surface sediment samples collected from the Bahiret el Bibane lagoon, which is one of the most productive lagoons and one of the most important active commercial fish traps in the southern Tunisia. The aim was to obtain information concerning the recent deposition of these compounds in this area, together with the levels, the distribution and any potential biological risk. Total concentrations of OCPs and PCBs in the sediments ranged from below the limit of detection (?1 and from 29.5 to 88.2?ng?g^?1?dw, respectively. The spatial distribution of PCBs suggested that the sources of these contaminants are probably located outside the lagoon and are transported by water currents and atmospheric deposition. Compared with some other regions of the world, the Bahiret el Bibane lagoon exhibited low to moderate levels of PCBs and OCPs. According to established sediment quality guidelines, PCBs and Lindane at most of the study sites would be more concerned for the ecotoxicological risk in the Bahiret el Bibane lagoon. The results of this study could provide a useful aid for the sustainable marine management of the region.     

A screening of liver,kidney, and thyroid gland morphology in organochlorine-contaminated glaucous gulls (Larus hyperboreus) from Svalbard

Concentrations of organochlorine (OC) contaminants and histomorphology of liver, kidney, and thyroid tissues were studied in nine adult and one subadult glaucous gulls (Larus hyperboreus) collected at Svalbard on 2 August 2011. Concentrations of liver polychlorinated biphenyls (PCB; range: 150–2820?ng?g^?1 ww), dichlorodiphenyltrichloroethane (DDT; range: 58–724?ng?g^?1 ww), and chlordanes (CHL; range: 11–126?ng?g^?1 ww) dominated the OC profile followed by hexachlorobenzene (HCB; range: 11–42?ng?g^?1 ww), mirex (range: 2–52?ng?g^?1 ww), and β-hexachlorocyclohexane (β-HCH; range: 1–7?ng?g^?1 ww). Histological examination of the liver showed mononuclear cell infiltrations and granulomas in 10 and 6 gulls, respectively, while intense intrahepatic lipid accumulation (steatosis) was found in two and focal necrosis in one gull. In kidney, glomerular sclerosis and adhesions was found in five and one gull, respectively. Thickening of the glomerular basement membranes and tubular necrosis was found in four and seven gulls, respectively, while mononuclear cell infiltrations were found in two individuals. In the thyroid gland, a high density of small follicles accompanied by follicular epithelial cell proliferation was observed in five glaucous gulls. Gulls with hepatic steatosis had significantly higher ΣDDT levels than the gulls without hepatic steatosis and a similar trend was found for ΣPCB. When normalizing OC concentrations for lipid content in liver, gulls with lipid granulomas had significantly lower β-HCH and significantly higher mirex levels, respectively, than gulls without lipid granulomas. Also; gulls with thickening of the glomerular basement membranes had non-significantly higher ΣPCB levels than gulls without. The histological findings were similar to those of controlled laboratory studies and OC-contaminated wildlife (e.g., polar bears; Ursus maritimus) and the data of this study therefore suggest that OC exposure may be a co-factor in the development of organ alterations in glaucous gulls. However, other environmental factors such as age, element exposure, and infectious micropathogens cannot be ruled out as co-factors, and it is uncertain if the tissue changes found exert adverse health effects on the population of Svalbard glaucous gulls.     

Quantitative analysis and sorption of cadmium in environmental samples with a functionalized synthetic polymer

Quantitative analysis of cadmium in environmental samples was achieved with a polymeric sorbent synthesized by copolymerization of N,N-dimethylacrylamide and allyl glycidyl ether/iminodiacetic acid as chelating monomers with N,N′-methylenebisacrylamide as cross-linker. The polymer was characterized by Fourier transform infrared spectroscopy, thermogravimetric analysis, elemental analysis, and scanning electron microscopy. The sorption capacity of the functionalized sorbent was 70 mg g^?1. The equilibrium sorption data of Cd(II) on polymeric sorbent were analyzed using Langmuir, Freundlich, Temkin, and Redlich–Peterson models. Based on equilibrium adsorption data, the constants at pH 4.2 and 20 °C were determined for the first three as 0.33 (L mg^?1), 17.5 (mg g^?1) (L mg^?1)^1/n, and 12.9 (J mol^?1). Recovery of 94% of the metal ion was obtained with 0.5 mol L^?1 nitric acid as an eluting agent.