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.     

Urinary arsenic levels influenced by abandoned mine tailings in the Southernmost Baja California Peninsula,Mexico

Gold has been mined at San Antonio-El Triunfo, (Baja California Sur, Mexico) since the 18th century. This area has approximately 5,700 inhabitants living in the San Juan de Los Planes and El Carrizal hydrographic basins, close to more than 100 abandoned mining sites containing tailings contaminated with potentially toxic elements such as arsenic. To evaluate the arsenic exposure of humans living in the surrounding areas, urinary arsenic species, such as inorganic arsenic (iAs) and the metabolites mono-methylated (MMA) and di-methylated arsenic acids (DMA), were evaluated in 275 residents (18–84 years of age). Arsenic species in urine were analyzed by hydride generation-cryotrapping-atomic absorption spectrometry, which excludes the non-toxic forms of arsenic such as those found in seafood. Urinary samples contained a total arsenic concentration (sum of arsenical species) which ranged from 1.3 to 398.7 ng mL^?1, indicating 33 % of the inhabitants exceeded the biological exposition index (BEI = 35 ng mL^?1), the permissible limit for occupational exposure. The mean relative urinary arsenic species were 9, 11 and 80 % for iAs, MMA and DMA, respectively, in the Los Planes basin, and 17, 10 and 73 %, respectively, in the El Carrizal basin. These data indicated that environmental intervention is required to address potential health issues in this area.     

Polychlorobenzenes and polychlorinated biphenyls in ash and soil from several industrial areas in North Vietnam: residue concentrations,profiles and risk assessment

Polychlorinated benzenes (PCBzs) including penta- and hexachlorobenzene can be unintentionally formed from thermal processes in different industrial activities, and very little information is available on the contamination and emission characteristics of these new persistent organic pollutants from industries in Vietnam. In this study, contamination of PCBzs (including penta- and hexachlorobenzene, named PeCBz and HCB, respectively) and PCBs (including CB-28, 52, 101, 153, 138, 180) in fly ash, bottom ash and soil from combustion processes of waste incineration, metallurgy (steel making and zinc production) and cement production from several provinces in the Northern Vietnam, including Hai Duong, Hanoi, Bac Ninh, Hai Phong and Thai Nguyen, was preliminary investigated. The PCBzs concentrations in fly ash, bottom ash and soil ranged from 2.7 to 100 ng g^?1, from 2.7 to 159 ng g^?1 and from 0.28 to 33.9 ng g^?1, respectively. Relatively high residues of PeCBz in fly ash and bottom ash from municipal waste incinerators in some provinces from the Northern Vietnam were encountered. Total PCBs concentrations ranged from 18.0 to 8260 ng g^?1, from 1.0 to 10600 ng g^?1 and from 14.5 to 130 ng g^?1 for the fly ash, bottom ash and soil, respectively. Daily intakes of PeCBz, HCB and PCBs through soil ingestion and dermal exposure estimated for children ranged 0.33–9.93 (mean 3.14), 0.39–21.1 (mean 4.9) and 6.09–1530 ng/kg bw/day (mean 346), respectively; and these intakes were about 4.7–5.4 times higher than those estimated for adult. The intakes of PeCBz and HCB were relatively low, while those for PCBs exceeded WHO TDI for some samples.     

Distribution,sources and potential risk of HCH and DDT in soils from a typical alluvial plain of the Yangtze River Delta region,China

Spatial distribution, sources and potential health risks of organochlorine pesticides (OCPs), including hexachlorocyclohexane (HCH) and dichlorodiphenyltrichloroethane (DDT), in surface soils (n = 544) collected from a typical alluvial plain of the Yangtze River Delta region, China, were elucidated. Concentrations of ΣHCH and ΣDDT in soils ranged from less than the limit of detection (<LOD) to 99.0 ng g^?1, dry weight (dw) (mean 3.23 ng g^?1 dw) and <LOD to 600 ng g^?1 dw (mean 88.8 ng g^?1 dw), respectively. Historical applications of HCH and DDT were the major sources of the residue in soils. HCH was mainly distributed in Anthrosols in the southern part of the watershed, while DDT was mainly distributed in Cambosols in the northern part. The 95 % cumulative probability incremental lifetime cancer risks (ILCRs) of different age groups such as children, youths, and adults all exceeded the acceptable risk level of 10^?6 recommended by USEPA for carcinogenic chemicals. The spatial distributions of ∑ILCRs were consistent with concentrations of OCPs in soils, while they were slight different for the different age groups. Adult females had the greatest risk of OCPs in soils, followed by children, while youths had the least risk. The ingestion of OCPs in soils was the more important route of exposure compared with dermal and inhalation exposures. The concentration of OCPs in soils, the particulate emission factor, the fraction of dermal exposure ratio, and the soil ingestion rate were the major contributing variables to total ILCRs according to sensitivity analyses.     

Spatial distributions,source apportionment and ecological risk of SVOCs in water and sediment from Xijiang River,Pearl River Delta

Xijiang River is an important drinking water source in Guangxi Province, China. Along the Xijiang River and surrounding tributary, the pollution profile of three important groups of semi-volatile organic compounds, including polycyclic aromatic hydrocarbons (PAHs), organochlorine pesticides (OCPs) and phthalate esters (PAEs), was analyzed. Relatively low levels of PAHs (64–3.7 × 10² ng L^?1) and OCPs (16–70 ng L^?1), but high levels of PAEs (7.9 × 10²–6.8 × 10³ ng L^?1) occurred in the water. Comparatively, low levels of OCPs (39–1.8 × 10² ng g^?1) and PAEs (21–81 ng g^?1), but high levels of PAHs (41–1.1 × 10³ ng g^?1) were found in sediment. Principal component analyses for source identification indicated petroleum-derived residues or coal and biomass combustion, and vehicular emission was the main sources for PAHs. The OCPs sources of each category were almost independent, whereas the new input of HCHs and p,p′-DDTs probably existed in some areas. PAEs were mainly originated from personal care products of urban sewage, plastic and other industrial sources. Ecological risk through the risk quotient analysis indicated a small or significant potential adverse effect on fish, daphnia and green algae. Nevertheless, the integrated risk of all pollutants should be taken into account in future study.     

Organochlorine pesticides (HCHs and DDTs) in soils along the north coastal areas of the Bohai Sea,China

A systematic survey of organochlorine pesticides (OCPs) including hexachlorocyclohexane isomers (α-HCH, β-HCH, γ-HCH, δ-HCH and ΣHCH) and dichlorodiphenyltrichloroethane metabolites (p,p′-DDT, p,p′-DDE, o,p′-DDT, p,p′-DDD and ∑DDT) in soils along the north coastal areas of the Bohai Sea, China, has been lacking. In this study, 31 representative surface soil samples were collected along the north coastal and riverine areas of the Bohai Sea to characterise the potential for adverse effects of ∑HCH, ∑DDT and their individual isomers and transformation products. Concentrations of ΣHCH and ΣDDT in soils ranged from less than the limit of detection (1 ng · g^?1 dw (mean: 3.5 ng · g^?1 dw) and2 ng · g^?1 dw (mean: 1.7 × 10¹ ng · g^?1 dw), respectively. Compared with studies of OCPs in soils from other locations, concentrations of HCHs and DDTs observed in this study were moderate. Concentrations of OCPs observed in soils were generally less than proposed reference values. HCH residues were a mixture of historical technical HCH and current lindane sources. The pattern of DDTs was consistent with historical releases of technical DDTs. Selected soil physicochemical properties did not explain the sorption and/or partitioning of HCHs or DDTs.     

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   

Perfluorinated compounds in water and sediment from coastal regions of the northern Bohai Sea,China

Concentrations of perfluorooctanesulfonate (PFOS), perfluorooctanoic acid (PFOA) and other perfluorinated compounds (PFCs) were measured in water and sediment from coastal Bohai Bay and surrounding rivers flowing into the bay. Of the 15 PFCs measured, PFOS and PFOA were detected with the greatest frequency. Concentrations in water ranged from<0.2 to 31 ng·L^?1 and<1.0 to 82 ng·L^?1 for PFOS and PFOA, respectively. Concentrations of PFOS and PFOA in sediments ranged from<0.1 to 2.0 ng·g^?1 dw and<0.1 to 0.5 ng·g^?1 dw, respectively. Concentrations of PFCs in Bohai Bay were less than those observed in other areas in Asia, but greater concentrations of ∑PFCs were observed in the Dalin River with concentrations increasing from upstream to downstream, and the greatest concentrations in sediment were observed in tidal flats. The ratio of ∑PFCs in sediment and water indicated that sediment could serve as a significant sink for PFUnA.     

Daily dietary fluoride intake in rural villages of the Ethiopian Rift Valley

Dental and skeletal fluorosis is widespread in the Ethiopian Rift Valley region. Drinking water has been considered the main reason for the development of fluorosis, but dietary intake may also be a contributor in areas with high concentration of fluoride in water, soil, and biota. The purpose of this study is to assess the total daily dietary fluoride intake by adults in a rural part of the Ethiopian Rift Valley. The food, beverage, and water samples were collected from selected households of three neighboring villages with similar dietary pattern, but with different fluoride content in their water sources. Village A uses water with 1.0 mg L^?1 fluoride, village B uses water with 3.0 mg L^?1 fluoride, and village C uses water with 11.5 mg L^?1 fluoride both for food preparation and for drinking. The level of fluoride was determined in all food ingredients, in the prepared food, beverages, and in the water used for food preparation and drinking. Recipe and food frequency questionnaires were used to gather household food preparation and consumption patterns. An alkali fusion method was used for digestion of food samples and for subsequent determination of fluoride with ion-selective electrode. The daily fluoride intake varied depending on its concentration in the water used for cooking and drinking. In households using water with 1 mg L^?1, 3 mg L^?1, and 11.5 mg L^?1 fluoride, the total personal intake was found to be 10.5, 16.6, and 35.3 mg d^?1, respectively. Contribution of the water to the daily fluoride intake was 33%, 58%, and 86%, respectively. Even in households using water containing fluoride at a concentration of 1 mg L^?1, the daily intake was higher than the recommended safe intake of 1.5–4.0 mg d^?1 for adults, which indicates that the fluoride intake through food may cause health risks. Minimizing the fluoride concentration in water to the lowest possible level will greatly reduce the daily intake. The form of fluorine (organic or inorganic) in the food items and the associated health risk factors need further investigation.     

Polycyclic aromatic hydrocarbons (PAHs) in multimedia environment of Heshan coal district,Guangxi: distribution,source diagnosis and health risk assessment

Mining activities are among the major culprits of the wide occurrences of soil and water pollution by PAHs in coal district, which have resulted in ecological fragilities and health risk for local residents. Sixteen PAHs in multimedia environment from the Heshan coal district of Guangxi, South China, were measured, aiming to investigate the contamination level, distribution and possible sources and to estimate the potential health risks of PAHs. The average concentrations of 16 PAHs in the coal, coal gangue, soil, surface water and groundwater were 5114.56, 4551.10, 1280.12 ng g^?1, 426.98 and 381.20 ng L^?1, respectively. Additionally, higher soil and water PAH concentrations were detected in the vicinities of coal or coal gangue dump. Composition analysis, isomeric ratio, Pearson correlation analysis and principal component analysis were performed to diagnose the potential sources of PAHs in different environmental matrices, suggesting the dominant inputs of PAHs from coal/coal combustion and coal gangue in the soil and water. Soil and water guidelines and the incremental lifetime risk (ICLR) were used to assess the health risk, showing that soil and water were heavily contaminated by PAHs, and mean ICLR_{coal/coal-gangue} and mean ICLR_soil were both significantly higher than the acceptable levels (1 × 10^?4), posing high potential carcinogenic risk to residents, especially coal workers. This study highlights the environmental pollution problems and public health concerns of coal mining, particularly the potential occupational health hazards of coal miners exposed in Heshan.     

Polychlorinated biphenyl (PCB) residues in European roe deer (Capreolus capreolus) and red deer (Cervus elaphus) from north-western Poland

The purpose of this study was to evaluate polychlorinated biphenyls (PCBs) contamination levels in roe and red deer from north-western Poland and to assess environmental pollution in this area. A quantitative analysis was conducted using a capillary gas chromatography/mass spectrometry method. The mean concentrations of ΣPCBs (sum of PCBs: 28, 52, 101, 138, 153, 180) in liver samples were 30.24±12.35 ng·g^?1 of lipid weight (l.w.) in roe deer and 60.13±14.23 ng·g^?1 l.w. in red deer, compared with 24.21±10.02 and 45.22±9.77 ng·g^?1 in the lungs of roe and red deer, respectively. PCBs 138, 153 and 180 were the dominant congeners in the liver samples of the analysed animals, whereas PCB 138 and 153 in the lungs. TEQs levels calculated for only dioxin-like PCBs were low: 0.32 and 0.29 pg WHO-PCB-TEQ·g^?1 fat in liver of red deer and roe deer, respectively. The mean PCB concentrations obtained in our study for organs of roe deer and red deer were several times lower than those reported elsewhere. These findings show that the investigated roe and red deer originated from an area with low levels of PCB contamination.     

(Persistent) Organic pollutants in Germany: results from a pilot study within the 2015 moss survey

Background

Since 1990, every 5 years, moss sampling is conducted within the European moss monitoring programme to assess the atmospheric deposition of airborne pollutants. Besides many other countries, Germany takes regularly part at these evaluations. Within the European moss monitoring 2015, more than 400 moss samples across Germany were taken according to a harmonized methodology for the assessment heavy metal and nitrogen input. In a pilot programme, eight of these sites were chosen for additional investigations on a broad range of organic contaminants to evaluate their accumulation in moss and thereby their presence in atmospheric deposition in Germany. Target compound classes comprised polycyclic aromatic hydrocarbons (PAH), polychlorinated dibenzodioxins and –furans (PCDD/F), dioxin-like and non-dioxin-like polychlorinated biphenyls (dl-PCB, ndl-PCB), polyfluorinated alkyl substances, classical flame retardants as well as emerging chlorinated and brominated flame retardants. In total, 120 target compounds were analysed. For some analytes, comparisons of accumulation in moss and tree leave samples were possible.

Results

Except for certain flame retardants, PFAS, and ndl-PCB, substances of all other compound classes could be quantified in moss samples of all sites. Concentrations were highest for PAH (40–268 ng g^?1) followed by emerging flame retardants (0.5–7.7 ng g^?1), polybrominated diphenyl ethers (PBDE; 0.3–3.7 ng g^?1), hexabromocyclododecane (HBCD; 0.3–1.2 ng g^?1), dl-PCB (0.04–0.4 ng g^?1) and PCDD/F (0.008–0.06 ng g^?1).

Conclusions

Results show the widespread atmospheric distribution and deposition of organic contaminants across Germany as well as the suitability of moss as bioaccumulation monitor for most of these compound classes. Compared to nearby tree leaf samples, accumulation potential of moss appeared to be higher for pollutants of high octanol–air partition coefficient (K_OA) and octanol–water partition coefficient (K_OW).

     

Liver and renal histopathology of North Atlantic long-finned pilot whales (Globicephala melas) contaminated with heavy metals and organochlorine compounds

Long-finned pilot whales (Globicephala melas) from the Faroe Islands are known to be heavily polluted with contaminants, such as mercury (Hg) and organochlorine compounds (OC). This is postulated to exert adverse health effects on whales as well as the human population who rely on its meat and blubber as food sources. It was therefore decided to conduct a screening pilot study to determine contaminant concentrations and histopathology of liver and renal tissues in a total of 14 specimens from this subpopulation. In blubber, the mean ∑OC concentration was 31,887 ng g^?1 lw (range: 18,170–47,425 ng g^?1 lw) of which ∑PCB concentration was 23,416 ng g^?1 lw (range: 13,947–34,543 ng g^?1 lw; n = 3). In liver, mean Hg concentration was 138 µg^?1 ww (range: 54–351 µg g^?1 ww; n = 7) and mean cadmium (Cd) concentration 15 µg g^?1 ww (range: 7–31 µg g^?1 ww; n = 7). In the kidney, the mean Cd concentration was 36 µg g^?1 ww (range: 23–47 µg g^?1 ww; n = 7). Of the liver Hg concentrations, two were at the suggested toxic threshold levels of 60 µg g^?1 ww and five were 2–6-fold above. Liver selenium (Se) : Hg was on average 1.11 (range: 0.97–1.41; n = 7) indicating that Se was in excess, which decreased the risk of acute Hg poisoning. Histopathological examinations showed high prevalence (>35%) of renal glomerular arteriosclerosis, glomerular capillary dilatation, dilatation and hyalinization of Bowman's space/capsule and tubular hyaline casts. In liver tissue, high prevalence was found for portal cell infiltrates, lipid granulomas, hepatocytic lipid accumulation, bile duct proliferation, lipid-filled Ito cells, and focal necrosis. In a single juvenile male, 4 of 8 renal and 3 of 7 liver lesions were present. Cadmium concentrations increased significantly in the presence of glomerular arteriosclerosis and a similar trend was found for tubular hyaline casts. Based on these findings, as well as the nature of the lesions, data indicate that the histopathological changes were a result of age and that contaminants are likely to be the co-factors in the development in at least three renal and four liver lesions.     

PAHs in organic film on glass window surfaces from central Shanghai,China: distribution,sources and risk assessment

Polycyclic aromatic hydrocarbons (PAHs) concentrations were analysed in the organic film on the glass surfaces of different functional areas in central Shanghai. Concentration levels of total PAHs in the organic film ranged from 1,348.5 to 4,007.9 ng m^?2. The concentration of PAHs was lowest in parks and green spaces (1,348.5 ng m^?2) and highest in traffic zones (4,007.9 ng m^?2). A concentration gradient of total PAHs was observed as follows: traffic zones > commercial areas > cultural and educational areas > parks and green spaces. The distribution of PAHs was characterised by 3–4 ring PAHs in the study areas. The most abundant PAHs were phenanthrene (20.5 %), fluorene (16.7 %), pyrene (12.4 %) and chrysene (Chry) (11.2 %). The mass of the bulk film was composed of organic and inorganic compounds and ranged from 246 to 1,288 mg m^?2. The bulk film thickness varied from 144 to 757 nm in the different functional areas. The ratios of An/178 and Fl/202 and principal component analysis suggested that PAHs came mainly from the mixed sources of fossil fuel, coal and incomplete combustion of biomass. Benzo[a]anthracene (BaA)/Chry is not suitable for use as a tracer for the transmission process of PAHs because of the rapid depletion of BaA in the organic film by photooxidation during daylight hours. The concentration of benzo[a]pyrene equivalent (BaPeq) varied from 21 to 701 ng g^?1, and the major carcinogenic contributors of the 16 PAHs were BaP, DahA, B[b/k]F and InP, accounting for 83 % of BaPeq.     

Levels and distribution of trace metals in surface sediments from Kongsfjorden, Svalbard, Norwegian Arctic

Trace metal contents (Cd, Co, Cr, Cu, Hg, Mn, Ni, Pb and Zn) have been measured in 27 surface sediment samples collected from Kongsfjorden, Svalbard, Norwegian Arctic. The analyses yielded concentration values (in mg kg^?1) of 0.13–0.63 for Cd, 11.89–21.90 for Co, 48.65–81.84 for Cr, 21.26–36.60 for Cu, 299.59–683.48 for Mn, 22.43–35.39 for Ni, 10.68–36.59 for Pb, 50.28–199.07 for Zn and 8.09–65.34 for Hg (in ng g^?1), respectively. Relative cumulative frequency method has been used to define the baseline values of these metals, which (in mg kg^?1) were 0.14 for Cd, 13.56 for Co, 57.86 for Cr, 25.14 for Cu, 364.08 for Mn, 26.22 for Ni, 17.46 for Pb, 70.49 for Zn and 9.76 for Hg (in ng g^?1), respectively. The enrichment factor analysis indicated that Hg showed some extent of anthropogenic pollution, while Pb, Zn and Cd showed limited anthropogenic contamination in the study areas.     

High soil and groundwater arsenic levels induce high body arsenic loads,health risk and potential anemia for inhabitants of northeastern Iran

Arsenic bioavailability in rock, soil and water resources is notoriously hazardous. Geogenic arsenic enters the body and adversely affects many biochemical processes in animals and humans, posing risk to public health. Chelpu is located in NE Iran, where realgar, orpiment and pyrite mineralization is the source of arsenic in the macroenvironment. Using cluster random sampling strategy eight rocks, 23 soils, 12 drinking water resources, 36 human urine and hair samples and 15 adult sheep urine and wool samples in several large-scale herds in the area were randomly taken for quantification of arsenic in rock/soil/water, wool/hair/urine. Arsenic levels in rock/soil/water and wool/hair/urine were measured using inductively coupled plasma spectroscopy and atomic absorption spectrophotometry, respectively. While arsenic levels in rocks, soils and water resources hazardously ranged 9.40–25,873.3 mg kg^?1, 7.10–1448.80 mg kg^?1 and 12–606 μg L^?1, respectively, arsenic concentrations in humans’ hair and urine and sheep’s wool and urine varied from 0.37–1.37 μg g^?1 and 9–271.4 μg L^?1 and 0.3–3.11 μg g^?1 and 29.1–1015 μg L^?1, respectively. Local sheep and human were widely sick and slightly anemic. Hematological examination of the inhabitants revealed that geogenic arsenic could harm blood cells, potentially resulting in many other hematoimmunological disorders including cancer. The findings warn widespread exposure of animals and human in this agroecologically and geopolitically important region (i.e., its proximity with Afghanistan, Pakistan and Turkmenistan) and give a clue on how arsenic could induce infectious and non-infectious diseases in highly exposed human/animals.     

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.     

The evolution of pollution profile and health risk assessment for three groups SVOCs pollutants along with Beijiang River,China

Three important groups of semi-volatile organic compounds (SVOCs), polycyclic aromatic hydrocarbons (PAHs), organic chlorinated pesticides (OCPs) and phthalate esters (PAEs), were produced by various human activities and entered the water body. In this study, the pollution profiles of three species including 16 PAHs, 20 OCPs and 15 PAEs in water along the Beijiang River, China were investigated. The concentrations of Σ₁₆PAHs in the dissolved and particulate phases were obtained as 69–1.5 × 10² ng L^?1 and 2.3 × 10³–8.6 × 10⁴ ng g^?1, respectively. The levels of Σ₂₀OCPs were 23–66 ng L^?1 (dissolved phase) and 19–1.7 × 10³ ng g^?1 (particulate phase). Nevertheless, higher levels of PAEs were found both in the dissolved and particulate phases due to abuse use of plastic products. Furthermore, non-cancer and cancer risks caused by these SVOCs through the ingestion absorption and dermal absorption were also assessed. There was no non-cancer risk existed through two kinds of exposure of them at current levels, whereas certain cancer risk existed through dermal absorption of PAHs in the particulate phase in some sampling sites. The results will show scientific insights into the evaluation of the status of combined pollution in river basins, and the determination of strategies for incident control and pollutant remediation.     

Arsenic contamination of natural waters in San Juan and La Pampa, Argentina

Arsenic (As) speciation in surface and groundwater from two provinces in Argentina (San Juan and La Pampa) was investigated using solid phase extraction (SPE) cartridge methodology with comparison to total arsenic concentrations. A third province, Río Negro, was used as a control to the study. Strong cation exchange (SCX) and strong anion exchange (SAX) cartridges were utilised in series for the separation and preservation of arsenite (As^III), arsenate (As^V), monomethylarsonic acid (MA^V) and dimethylarsinic acid (DMA^V). Samples were collected from a range of water outlets (rivers/streams, wells, untreated domestic taps, well water treatment works) to assess the relationship between total arsenic and arsenic species, water type and water parameters (pH, conductivity and total dissolved solids, TDS). Analysis of the waters for arsenic (total and species) was performed by inductively coupled plasma mass spectrometry (ICP-MS) in collision cell mode. Total arsenic concentrations in the surface and groundwater from Encon and the San José de Jáchal region of San Juan (north-west Argentina within the Cuyo region) ranged from 9 to 357 μg l^?1 As. Groundwater from Eduardo Castex (EC) and Ingeniero Luiggi (LU) in La Pampa (central Argentina within the Chaco-Pampean Plain) ranged from 3 to 1326 μg l^?1 As. The pH range for the provinces of San Juan (7.2–9.7) and La Pampa (7.0–9.9) are in agreement with other published literature. The highest total arsenic concentrations were found in La Pampa well waters (both rural farms and pre-treated urban sources), particularly where there was high pH (typically > 8.2), conductivity (>2,600 μS cm^?1) and TDS (>1,400 mg l^?1). Reverse osmosis (RO) treatment of well waters in La Pampa for domestic drinking water in EC and LU significantly reduced total arsenic concentrations from a range of 216–224 μg l^?1 As to 0.3–0.8 μg l^?1 As. Arsenic species for both provinces were predominantly As^III and As^V. As^III and As^V concentrations in San Juan ranged from 4–138 μg l^?1 to <0.02–22 μg l^?1 for surface waters (in the San José de Jáchal region) and 23–346 μg l^?1 and 0.04–76 μg l^?1 for groundwater, respectively. This translates to a relative As^III abundance of 69–100% of the total arsenic in surface waters and 32–100% in groundwater. This is unexpected because it is typically thought that in oxidising conditions (surface waters), the dominant arsenic species is As^V. However, data from the SPE methodology suggests that As^III is the prevalent species in San Juan, indicating a greater influence from reductive processes. La Pampa groundwater had As^III and As^V concentrations of 5–1,332 μg l^?1 and 0.09–592 μg l^?1 for EC and 32–242 μg l^?1 and 30–277 μg l^?1 As for LU, respectively. Detectable levels of MA^V were reported in both provinces up to a concentration of 79 μg l^?1 (equating to up to 33% of the total arsenic). Previously published literature has focused primarily on the inorganic arsenic species, however this study highlights the potentially significant concentrations of organoarsenicals present in natural waters. The potential for separating and preserving individual arsenic species in the field to avoid transformation during transport to the laboratory, enabling an accurate assessment of in situ arsenic speciation in water supplies is discussed.     

Concentrations and classification of HCHs and DDTs in soil from the lower reaches of the Jiulong River, China

Soil is an important source to other environmental media and organisms for organochlorine pesticides (OCPs) bioaccumulation. Twenty-four representative surface soil samples were collected from the lower reaches of the Jiulong River, China, in 2009. The concentrations of hexachlorocyclohexane isomers (HCHs) ranged from 0.38 to 39.52 ng·g^?1, with a mean value of 9.51 ng·g^?1. The concentrations of dichlorodiphenyltrichloroethanes (DDTs) and their metabolites were within the ranges of 0.94–700.99 ng·g^?1, with a mean value of 71.17 ng·g^?1. The concentrations of HCHs and DDTs in the soil were lower than the first grade level (50 ng·g^?1) of the Chinese Environmental Quality Standard (GB15618-1995). Hierarchical Cluster Analysis (HCA) and Pearson’s bivariate Correlations Analysis (PCA) were used to analyse the distribution and contamination levels of OCPs in this region. The results showed that DDTs were the major contaminants and there were no significant correlations between various OCPs concentrations and the total organic carbon (TOC) contents. A significant positive correlation was observed between HCHs and DDTs (p<0.01), which indicates that HCHs and DDTs may have similar sources and fate in the study area.