Burdens of PBBs, PBDEs, and PCBs in tissues of the cancer patients in the e-waste disassembly sites in Zhejiang, China

This study was conducted to explore the burdens of PBBs, PBDEs, and PCBs among cancer patients living in the e-waste disassembly sites. The contents of 23 PBB congeners, 12 PBDE congeners, and 27 PCB congeners in kidney, liver, and lung samples were measured by GC-MS. The results showed that low-brominated PBBs and PBB153 were the predominant congeners. PBDE47 were the most predominant PBDE congeners. PBDE209 were detected in > 70% of the samples, with geometric means ranging from 64.2 to 113.9 ng g^− 1 lipid. Among the three subfamilies of PHAHs, PCB concentrations were the highest. The detected levels of PHAHs were in the same order of magnitude in the three tissues, which indicated that any of the three tissues could be the suitable indicator for assessing body burdens of PHAHs. PBB contents (181-192 ng g^− 1 lipid) were obviously higher than those reported in the general USA population (3-8 ng g^− 1 lipid). PBDE levels (174.1-182.3 ng g^− 1 lipid) were comparable to those reported in the USA population, but significantly higher than those of the European population. PCBs levels were comparable to those of the European population. The high cancer incidence in the disassembly sites may be related to higher burdens of PBBs, PBDEs, and PCBs in tissues.     

Mercury bioacumulation in four tissues of Podocnemis erythrocephala (Podocnemididae: Testudines) as a function of water parameters

A number of environmental factors influence the dynamics of Hg in aquatic ecosystems, yet few studies have examined these factors for turtles, especially from South America. Red-headed river turtle (Podocnemis erythrocephala) is easy to capture in the black waters of Rio Negro, making it the turtle species that is consumed most often by people of the region. In this study, environmental factors and turtle size were investigated to determine their influence on the Hg concentration in blood, muscle, liver and carapace of the red-headed river turtle. Factors investigated included turtle length, pH, dissolved organic carbon and availability of potential methylation sites (floodplain forests and hydromorphic soils). The study was conducted in the Rio Negro basin, where we collected water and turtle blood, muscle, liver and carapace samples from 12 tributaries for chemical analysis. Through radar imagery and existing soil maps with GIS, the percentage of alluvial floodplains and hydromorphic soils (potential methylation sites) was estimated for each drainage basin at sampling points. The mean Hg concentration in blood of P. erythrocephala was 1.64 ng g^− 1 (SD = 1.36), muscle 33 ng g^− 1 (SD = 11), liver 470 ng g^− 1 (SD = 313) and carapace 68 ng g^− 1 (SD = 32). Sex or length did not influence the Hg concentration in P. erythrocephala blood, muscle and liver, but Hg increased in carapace tissue when length size increased (ANCOVA p = 0.007). In the multiple regression analysis, none of the environmental factors studied had a significant relation with blood, muscle, liver and carapace. P. erythrocephala moves among habitats and in the open and interconnected aquatic systems of the Amazon basin, characterized by high levels of limnological variability, a good bioindicator of Hg concentration needs to be relatively sedentary to represent a specific habitat. However, the levels of Hg in liver were sufficient to pose a potential risk to humans that consume them, suggesting the usefulness of P. erythrocephala as a bioindicator.     

Simultaneous determination of microcystin contaminations in various vertebrates (fish, turtle, duck and water bird) from a large eutrophic Chinese lake, Lake Taihu, with toxic Microcystis blooms

This is the first to conduct simultaneous determination of microcystin (MC) contaminations in multi-groups of vertebrates (fish, turtle, duck and water bird) from Lake Taihu with Microcystis blooms. MCs (-RR, -YR, -LR) in Microcystis scum was 328 μg g^− 1 DW. MCs reached 235 μg g^− 1 DW in intestinal contents of phytoplanktivorous silver carp, but never exceeded 0.1 μg g^− 1 DW in intestinal contents of other animals. The highest MC content in liver of fish was in Carassius auratus (150 ng g^− 1 DW), followed by silver carp and Culter ilishaeformis, whereas the lowest was in common carp (3 ng g^− 1 DW). In livers of turtle, duck and water bird, MC content ranged from 18 to 30 ng g^− 1 DW. High MC level was found in the gonad, egg yolk and egg white of Nycticorax nycticorax and Anas platyrhynchos, suggesting the potential effect of MCs on water bird and duck embryos. High MC contents were identified for the first time in the spleens of N. nycticorax and A. platyrhynchos (6.850 and 9.462 ng g^− 1 DW, respectively), indicating a different organotropism of MCs in birds. Lakes with deaths of turtles or water birds in the literatures had a considerably higher MC content in both cyanobacteria and wildlife than Lake Taihu, indicating that toxicity of cyanobacteria may determine accumulation level of MCs and consequently fates of aquatic wildlife.     

Accumulation of polychlorinated biphenyls and organochlorine pesticide in pet cats and dogs: Assessment of toxicological status

PCB and DDT concentrations were determined in the adipose tissue of cats and dogs from Southern Italy. In cats p,p′-DDE was the most abundant DDT component (95.0%), while in dogs these compounds were absent, except in two specimens. PCB concentrations were higher in cats (199.02 ng g^− 1 lipid weight) than in dogs (41.61 ng g^− 1 lipid weight). Also there were inter-specific differences in the contribution of the different congeners to PCBs, although PCB 138, PCB 153 and PCB 180 were the most representative congeners in both species. Animals from one location, Taranto City, had significantly elevated concentrations of dioxin-like PCBs compared to the other locations. Consequently the estimated mean 2,3,7,8-tetrachlorodibenzo-p-dioxin toxic equivalents (TEQs) of coplanar PCBs were higher in these animals (cats: 0.65 pg g^− 1 lipid weight; dogs 0.29 pg g^− 1 lipid weight) than in the other ones (cats: 0.12 pg g^− 1 lipid weight; dogs: 0.001 pg g^− 1 lipid weight).     

Pharmaceutical and personal care products in tile drainage following surface spreading and injection of dewatered municipal biosolids to an agricultural field

Land application of municipal biosolids can be a source of environmental contamination by pharmaceutical and personal care products (PPCPs). This study examined PPCP concentrations/temporally discrete mass loads in agricultural tile drainage systems where two applications of biosolids had previously taken place. The field plots received liquid municipal biosolids (LMB) in the fall of 2005 at an application rate of ∼ 93,500 L ha^− 1, and a second land application was conducted using dewatered municipal biosolids (DMB) applied at a rate of ∼ 8 Mt dw ha^− 1 in the summer of 2006. The DMB land application treatments consisted of direct injection (DI) of the DMB beneath the soil surface at a nominal depth of ∼ 0.11 m, and surface spreading (SS) plus subsequent tillage incorporation of DMB in the topsoil (∼ 0.10 m depth). The PPCPs examined included eight pharmaceuticals (acetaminophen, fluoxetine, ibuprofen, gemfibrozil, naproxen, carbamazepine, atenolol, sulfamethoxazole), the nicotine metabolite cotinine, and two antibacterial personal care products triclosan and triclocarban. Residues of naproxen, cotinine, atenolol and triclosan originating from the fall 2005 LMB application were detected in tile water nearly nine months after application (triclocarban was not measured in 2005). There were no significant differences (p > 0.05) in PPCP mass loads among the two DMB land application treatments (i.e., SS vs. DI); although, average PPCP mass loads late in the study season (> 100 days after application) were consistently higher for the DI treatment relative to the SS treatment. While the concentration of triclosan (∼ 14,000 ng g^− 1 dw) in DMB was about twice that of triclocarban (∼ 8000 ng g^− 1 dw), the average tile water concentrations for triclosan were much higher (43 ± 5 ng L^− 1) than they were for triclocarban (0.73 ± 0.14 ng L^− 1). Triclosan concentrations (maximum observed in 2006 ∼ 235 ng L^− 1) in tile water resulting from land applications may warrant attention from a toxicological perspective.     

Biostrome communities and mercury and selenium bioaccumulation in the Great Salt Lake (Utah, USA)

The Great Salt Lake has a salinity near 150 g/L and is habitat for over 200 species of migratory birds. The diet of many of these birds is dependent on the food web of carbonaceous biostromes (stromatolites) that cover 260 km² of the lake's littoral zone. We investigated the biostrome community to understand their production processes and to assess whether they are a potential vector for bioconcentration of high mercury and selenium levels in the lake. The periphyton community of the biostromes was > 99% colonial cyanobacteria. Periphyton chlorophyll levels averaged 900 mg m⁻² or nine times that of the lake's phytoplankton. Lake-wide estimates of chlorophyll suggest that their production is about 30% of that of the phytoplankton. Brine fly (Ephydra gracilis) larval densities on the biostromes increased from 7000 m⁻² in June to 20000 m⁻² in December. Pupation and adult emergence halted in October and larvae of various instars overwintered at temperatures < 5 °C. Mean total dissolved and dissolved methyl mercury concentrations in water were 5.0 and 1.2 ηg L⁻¹. Total mercury concentrations in the periphyton, fly larvae, pupae, and adults were, respectively, 152, 189, 379 and 659 ηg g⁻¹ dry weight, suggesting that bioconcentration is only moderate in the short food web and through fly developmental stages. However, common goldeneye ducks (Bucephala clangula) that feed primarily on brine fly larvae at the Great Salt Lake had concentrations near 8000 ηg Hg g⁻¹ dry weight in muscle tissue. Data from a previous study indicated that selenium concentrations in periphyton, brine fly larvae and goldeneye liver tissue were high (1700, 1200 and 24,000 ηg g⁻¹, respectively) and Hg:Se molar ratios were < 1.0 in all tissues, suggesting that the high mercury concentration in the ducks may be partially detoxified by combining with selenium. The study demonstrated that the high mercury levels in the Great Salt Lake are routed through the biostrome community resulting in invertebrate prey that may provide health risks for birds and humans that consume them.     

Uptake, depuration, and radiation dose estimation in zebrafish exposed to radionuclides via aqueous or dietary routes

Understanding uptake and depuration of radionuclides in organisms is necessary to relate exposure to radiation dose and ultimately to biological effects. We investigated uptake and depuration of a mixture of radionuclides to link bioaccumulation with radiation dose in zebrafish, Danio rerio. Adult zebrafish were exposed to radionuclides (⁵⁴Mn, ⁶⁰Co, ⁶⁵Zn, ⁷⁵Se, ¹⁰⁹Cd, ^110mAg, ¹³⁴Cs and ²⁴¹Am) at tracer levels (< 200 Bq g⁻¹) for 14 d, either via water or diet. Radioactivity concentrations were measured in whole body and excised gonads of exposed fish during uptake (14 d) and depuration phases (47 d and 42 d for aqueous and dietary exposures respectively), and dose rates were modelled from activity concentrations in whole body and exposure medium (water or diet). After 14-day aqueous exposure, radionuclides were detected in decreasing activity concentrations: ⁷⁵Se > ⁶⁵Zn > ¹⁰⁹Cd > ^110mAg > ⁵⁴Mn > ⁶⁰Co > ²⁴¹Am > ¹³⁴Cs (range: 175-8 Bq g¹). After dietary exposure the order of radionuclide activity concentration in tissues (Bq g⁻¹) was: ⁶⁵Zn > ⁶⁰Co > ⁷⁵Se > ¹⁰⁹Cd > ^110mAg > ²⁴¹Am > ⁵⁴Mn > ¹³⁴Cs (range: 91-1 Bq g⁻¹). Aqueous exposure resulted in higher whole body activity concentrations for all radionuclides except ⁶⁰Co. Route of exposure did not appear to influence activity concentrations in gonads, except for ⁵⁴Mn, ⁶⁵Zn, and ⁷⁵Se, which had higher activity concentrations in gonads following aqueous exposure. Highest gonad activity concentrations (Bq g⁻¹) were for ⁷⁵Se (211), ¹⁰⁹Cd (142), and ⁶⁵Zn (117), and highest dose rates (μGy h⁻¹) were from ²⁴¹Am (aqueous, 1050; diet 242). This study links radionuclide bioaccumulation data obtained in laboratory experiments with radiation dose determined by application of a dosimetry modelling tool, an approach that will enable better linkages to be made between exposure, dose, and effects of radionuclides in organisms.     

Removal of Pharmaceutical and Personal Care Products (PPCPs) under nitrifying and denitrifying conditions

The contribution of volatilization, sorption and transformation to the removal of 16 Pharmaceutical and Personal Care Products (PPCPs) in two lab-scale conventional activated sludge reactors, working under nitrifying (aerobic) and denitrifying (anoxic) conditions for more than 1.5 years, have been assessed. Pseudo-first order biological degradation rate constants (k_biol) were calculated for the selected compounds in both reactors. Faster degradation kinetics were measured in the nitrifying reactor compared to the denitrifying system for the majority of PPCPs. Compounds could be classified according to their k_biol into very highly (k_biol > 5 L g_SS⁻¹ d⁻¹), highly (1 < k_biol < 5 L g_SS⁻¹ d⁻¹), moderately (0.5 < k_biol < 1 L g_SS⁻¹ d⁻¹) and hardly (k_biol < 0.5 L g_SS⁻¹ d⁻¹) biodegradable.Results indicated that fluoxetine (FLX), natural estrogens (E1 + E2) and musk fragrances (HHCB, AHTN and ADBI) were transformed to a large extent under aerobic (>75%) and anoxic (>65%) conditions, whereas naproxen (NPX), ethinylestradiol (EE2), roxithromycin (ROX) and erythromycin (ERY) were only significantly transformed in the aerobic reactor (>80%). The anti-depressant citalopram (CTL) was moderately biotransformed under both, aerobic and anoxic conditions (>60% and >40%, respectively). Some compounds, as carbamazepine (CBZ), diazepam (DZP), sulfamethoxazole (SMX) and trimethoprim (TMP), manifested high resistance to biological transformation.Solids Retention Time (SRT_aerobic >50 d and <50 d; SRT_anoxic >20 d and <20 d) had a slightly positive effect on the removal of FLX, NPX, CTL, EE2 and natural estrogens (increase in removal efficiencies <10%). Removal of diclofenac (DCF) in the aerobic reactor was positively affected by the development of nitrifying biomass and increased from 0% up to 74%. Similarly, efficient anoxic transformation of ibuprofen (75%) was observed after an adaptation period of 340 d. Temperature (16-26 °C) only had a slight effect on the removal of CTL which increased in 4%.     

DDT contamination from indoor residual spraying for malaria control

The insecticide DDT is still used in specific areas of South Africa for indoor residual spray (IRS) to control malaria vectors. Local residents could be exposed to residues of DDT through various pathways including indoor air, dust, soil, food and water. The aims of this study were to determine the levels of DDT contamination, as a result of IRS, in representative homesteads, and to evaluate the possible routes of human exposure. Two villages, exposed (DV) and reference (TV) were selected. Sampling was done two months after the IRS process was completed. Twelve homesteads were selected in DV and nine in TV. Human serum, indoor air, floor dust, outside soil, potable water, leafy vegetables, and chicken samples (muscle, fat and liver) were collected and analyzed for both the o,p′- and p,p′-isomers of DDT, DDD and DDE. DDT was detected in all the media analyzed indicating a combination of potential dietary and non-dietary pathways of uptake. DV had the most samples with detectable levels of DDT and its metabolites, and with the exception of chicken muscle samples, DV also had higher mean levels for all the components analyzed compared to TV. Seventy-nine percent of participants from DV had serum levels of DDT (mean ∑ DDT 7.3 µg g⁻¹ lipid). These residues constituted mainly of p,p′-DDD and p,p′-DDE. ∑ DDT levels were detected in all indoor air (mean ∑ DDT 3900.0 ng m^− 3) and floor dust (mean ∑ DDT 1200.0 µg m^− 2) samples. Levels were also detected in outside soil (mean ∑ DDT 25.0 µg kg^− 1) and potable water (mean ∑ DDT 2.0 µg L^− 1). Vegetable sample composition (mean ∑ DDT 43.0 µg kg^− 1) constituted mainly p,p′-DDT and p,p′-DDD. Chicken samples were highly contaminated with DDT (muscle mean ∑ DDT 700.0 µg kg^− 1, fat mean ∑ DDT 240,000.0 µg kg^− 1, liver mean ∑ DDT 1600.0 µg kg^− 1). The results of the current study raise concerns regarding the potential health effects in residents living in the immediate environment following DDT IRS.     

Organochlorines and mercury in livers of great cormorants (Phalacrocorax carbo sinensis) wintering in northeastern Mediterranean wetlands in relation to area, bird age, and gender

Wild birds are exposed to pollutants in their habitats. Top consumers of aquatic environments such as the fish-eating great cormorant (Phalacrocorax carbo sinensis) are especially affected due to the bioaccumulation of toxic substances in their tissues. This study analysed the livers of 80 great cormorants from Greece to estimate the concentration of organochlorines and mercury and to examine their possible toxic effects and origin. The results showed that mercury (geometric mean 8089 ng g⁻¹ dw), p,p′-DDE (2628 ng g⁻¹ dw), ∑ HCHs (47 ng g⁻¹ dw) and HCB (116 ng g⁻¹ dw) concentrations can be considered high compared with those found in great cormorant livers elsewhere except in highly polluted areas, whereas ∑ PCBs occurred in relatively low concentrations (1091 ng g⁻¹ dw). β-HCH was the dominant HCH isomer. Pollutant levels were generally unrelated to area, age and gender. However, p,p′-DDE and p,p′-DDD showed intersite differences, whilst the proportion of PCBs with 8 chlorine atoms were significantly higher in adult than 1st year great cormorants. Pollution did not reflect local patterns but rather these along the Baltic and Black Seas, whilst differences in p,p′-DDE concentration and ∑ DDTs/∑PCBs ratios between Evros, Axios or Amvrakikos, found on common migration route, suggested different bird origins. Most birds had toxic mercury concentrations; 83.7% above 4000 ng g⁻¹ dw and 16% above 17,000 ng g⁻¹ dw. Other pollutant levels were too low to have adverse effects.     

Analysis of composition, distribution and origin of hexachlorocyclohexane residues in agricultural soils from NW Spain

Concentrations of the isomers of the organochlorine pesticide hexachlorocyclohexane (HCH) were determined in 252 surface soil samples collected within a sampling network covering agricultural areas in Galicia (NW Spain). The concentration of total HCH (sum of α + β + γ + δ) ranged between 4 and 2305 ng g⁻¹ (dry weight), with the α-HCH and γ-HCH isomers predominating (< 1-1404 ng g⁻¹ and < 1-569 ng g⁻¹, respectively). The distribution of the pesticide residues was very heterogeneous, with the largest concentrations present in one of the studied areas (the province of A Coruña). The distribution of HCH was not found to be related to any soil property (organic matter, pH, clays, and metals). Multivariate statistical analysis of the data revealed that three populations of samples with a defined composition of HCH, can be related to the source of HCH: technical HCH (α/γ > 3), lindane (99% γ-HCH), or both. The existence of a third population consisting almost exclusively of α-HCH suggests that background contamination of anthropogenic origin dates from several decades ago. The detailed analysis of these populations enabled the possible temporal scale of the application of these pesticides to be deduced.     

Nitrous oxide production kinetics during nitrate reduction in river sediments

A significant amount of nitrogen entering river basins is denitrified in riparian zones. The aim of this study was to evaluate the influence of nitrate and carbon concentrations on the kinetic parameters of nitrate reduction as well as nitrous oxide emissions in river sediments in a tributary of the Marne (the Seine basin, France). In order to determine these rates, we used flow-through reactors (FTRs) and slurry incubations; flow-through reactors allow determination of rates on intact sediment slices under controlled conditions compared to sediment homogenization in the often used slurry technique. Maximum nitrate reduction rates (R_m) ranged between 3.0 and 7.1 μg N g⁻¹ h⁻¹, and affinity constant (K_m) ranged from 7.4 to 30.7 mg N-NO₃⁻ L⁻¹. These values were higher in slurry incubations with an R_m of 37.9 μg N g⁻¹ h⁻¹ and a K_m of 104 mg N-NO₃⁻ L⁻¹. Nitrous oxide production rates did not follow Michaelis-Menten kinetics, and we deduced a rate constant with an average of 0.7 and 5.4 ng N g⁻¹ h⁻¹ for FTR and slurry experiments respectively. The addition of carbon (as acetate) showed that carbon was not limiting nitrate reduction rates in these sediments. Similar rates were obtained for FTR and slurries with carbon addition, confirming the hypothesis that homogenization increases rates due to release of and increasing access to carbon in slurries. Nitrous oxide production rates in FTR with carbon additions were low and represented less than 0.01% of the nitrate reduction rates and were even negligible in slurries. Maximum nitrate reduction rates revealed seasonality with high potential rates in fall and winter and low rates in late spring and summer. Under optimal conditions (anoxia, non-limiting nitrate and carbon), nitrous oxide emission rates were low, but significant (0.01% of the nitrate reduction rates).     

Biomonitoring of Cd, Cr, Hg and Pb in the Baluarte River basin associated to a mining area (NW Mexico)

With the purpose of knowing seasonal variations of Cd, Cr, Hg and Pb in a river basin with past and present mining activities, elemental concentrations were measured in six fish species and four crustacean species in Baluarte River, from some of the mining sites to the mouth of the river in the Pacific Ocean between May 2005 and March 2006. In fish, highest levels of Cd (0.06 μg g^− 1 dry weight) and Cr (0.01 μg g^− 1) were detected during the dry season in Gobiesox fluviatilis and Agonostomus monticola, respectively; the highest levels of Hg (0.56 μg g^− 1) were detected during the dry season in Guavina guavina and Mugil curema. In relation to Pb, the highest level (1.65 μg g^− 1) was detected in A. monticola during the dry season. In crustaceans, highest levels of Cd (0.05 μg g^− 1) occurred in Macrobrachium occidentale during both seasons; highest concentration of Cr (0.09 μg g^− 1) was also detected in M. occidentale during the dry season. With respect to Hg, highest level (0.20 μg g^− 1) was detected during the rainy season in Macrobrachium americanum; for Pb, the highest concentration (2.4 μg g^− 1) corresponded to Macrobrachium digueti collected in the dry season. Considering average concentrations of trace metals in surficial sediments from all sites, Cd (p < 0.025), Cr (p < 0.10) and Hg (p < 0.15) were significantly higher during the rainy season. Biota sediment accumulation factors above unity were detected mostly in the case of Hg in fish during both seasons. On the basis of the metal levels in fish and crustacean and the provisional tolerable weekly intake of studied elements, people can eat up to 13.99, 0.79 and 2.34 kg of fish in relation to Cd, Hg and Pb, respectively; regarding crustaceans, maximum amounts were 11.33, 2.49 and 2.68 kg of prawns relative to levels of Cd, Hg and Pb, respectively.     

The MERSADE (European Union) project: Testing procedures and environmental impact for the safe storage of liquid mercury in the Almadén district, Spain

The MERSADE Project (LIFE — European Union) tested the Las Cuevas decommissioned mining complex (Almadén mercury district, Spain) as a potential site for the installation of a future European prototype safe deposit of surplus mercury from industrial activities. We here present the results of a baseline study on the distribution of mercury in soils and air in the Las Cuevas complex and surrounding areas, and show the results of a plume contamination model using the ISC-AERMOD software. Despite restoration works carried out in 2004, the Las Cuevas complex can still be regarded as hotspot of mercury contamination, with large anomalies above 800 μg g^− 1 Hg (soils) and 300 ng Hg m^− 3 (air). In the case of soils, high, and persistent concentrations above 26 μg g^− 1 Hg extend well beyond the complex perimeter for more than 2 km. These concentrations are about three orders of magnitude above world baselines. The same applies to mercury in air, with high concentrations above 300 ng Hg m^− 3 inside the perimeter, which nonetheless fade away in a few hundred meters. Air contamination modelling (Hg gas) predicts formation of a NW-SE oriented narrow plume extending for a few hundred meters from the complex perimeter. The geographic isolation of Las Cuevas and its mining past make the complex an ideal site for mercury stocking. The only potential environmental hazards are the raising of livestock only a few hundred meters away from the complex and flash floods.     

The effects of changes in cadmium and lead air pollution on cancer incidence in children

This article presents the results of research on the effects of air pollution on cancer incidence in children in the region of Silesia (Poland), which has undergone one of the most profound anthropogenic transformations in Europe. The main objective of the research was to specify the impact of changes in cadmium and lead pollution in the years 1990-2005 on the incidence of cancers reported in children. Lead concentration ranged from 0 to 1490 · 10^-9 G m⁻²/year, and cadmium concentration ranged from 0 to 33.7 · 10^-9 G  m⁻²/year. There was no strong significant correlation (max 0.3) between air pollution and incidence rate (IR) in the general population of children in any particular year. Alongside the cartographic presentation of dependences, correlation coefficients between the variables in question were calculated. This made it possible to determine the relationship between the pollution levels and incidence rates in the area. There was a significant reduction in the level of pollution during the investigated period. The study of the relationship between the number of cancers reported and the condition of the natural environment revealed increased sensitivity to toxins in boys (correlation coefficient 0.3). In addition, the spatial distribution of the number of cases reported in boys suggests a correlation with the spatial distribution of the coefficients for the entire group of children included in the study. The yearly average IR of childhood cancer in specific districts ranged from 0 to 61.48/100,000 children under 18 years of age during the 1995-2004 period.     

Long-term (1243 days), low-temperature (4-15 °C), anaerobic biotreatment of acidified wastewaters: Bioprocess performance and physiological characteristics

The feasibility of long-term (>3 years), low-temperature (4-15 °C) and anaerobic bioreactor operation, for the treatment of acidified wastewater, was investigated. A hybrid, expanded granular sludge bed-anaerobic filter bioreactor was seeded with a mesophilic inoculum and employed for the mineralization of moderate-strength (3.75-10 kg chemical oxygen demand (COD) m⁻³) volatile fatty acid-based wastewaters at 4-15 °C. Bioprocess performance was assessed in terms of COD removal efficiency (CODRE), methane biogas concentration, and yield, and biomass retention. Batch specific methanogenic activity assays were performed to physiologically characterise reactor biomass.Despite transient disimprovements, CODRE and methane biogas concentrations exceeded 80% and 65%, respectively, at an applied organic loading rate (OLR) of 10 kg COD m⁻³ d⁻¹ between 9.5 and 15 °C (sludge loading rate (SLR), 0.6 kg COD kg[VSS]⁻¹ d⁻¹). Over 50% of the granular sludge bed was lost to disintegration during operation at 9.5 °C, warranting a reduction in the applied OLR to 3.75-5 kg COD m⁻³ d⁻¹ (SLR, c. 0.4-0.5 kg COD kg[VSS]⁻¹ d⁻¹). From that point forward, remarkably stable and efficient performance was observed during operation at 4-10 °C, with respect to CODRE (≥82%), methane biogas concentration (>70%) and methane yields (>4 l_Methane d⁻¹), suggesting the adaptation of our mesophilic inoculum to psychrophilic operating conditions.Physiological activity assays indicated the development of psychroactive syntrophic and methanogenic populations, including the emergence of putatively psychrophilic propionate-oxidising and hydrogenotrophic methanogenic activity. The data suggest that mesophilic inocula can physiologically adapt to sub-optimal operational temperatures: treatment efficiencies and sludge loading rates at 4 °C (day, 1243) were comparable to those achieved at 15 °C (day 0). Furthermore, long-term, low-temperature bioreactor operation may act as a selective enrichment for psychrophilic methanogenic activity from mesophilic inocula. The observed efficient and stable bioprocess performance highlights the potential for long-term, low-temperature bioreactor operation.     

Determination of 210Po in various foodstuffs and its annual effective dose to inhabitants of Qena City, Egypt

The concentration of ²¹⁰Po was determined in different foodstuffs of plant origin purchased from markets in Qena City, Upper Egypt. Measurement of ²¹⁰Po has been carried out using alpha spectrometry technique in different food categories such as vegetables, fruits, cereals beverages and herbs. The general range of ²¹⁰Po activity levels ranged widely from < 0.010-18.6 ± 0.910 mBq g^− 1, with minimum being in cereal samples and maximum being in beverage samples. Tea samples recorded highest activity concentrations of ²¹⁰Po with lowest value of 10 ± 0.54 mBq g⁻¹ for Crown tea and highest value of 18.6 ± 0.910 mBq g⁻¹ for El maabad tea. The daily intake of ²¹⁰Po from food consumption reveals that vegetables are the biggest contributors, while beverages are the lowest. The effective ingestion dose has been estimated for Qena City residents and it was found in the range 0.008-38.3 μSv y⁻¹.     

Temporal and spatial distributions of total gaseous mercury concentrations in ambient air in a mountainous area in southwestern China: Implications for industrial and domestic mercury emissions in remote areas in China

Spatial and temporal distributions of total gaseous mercury (TGM) concentrations in ambient air were investigated in the Mt. Gongga area (Sichuan province, PR China) from April 2006 to June 2007. The annual geometric mean TGM concentration at the Moxi baseline station was 3.90 ± 1.20 ng m^− 3. Geometric mean TGM concentrations at 14 representative sampling sites during the warm season ranged from 1.60 to 20.1 ng m^− 3 and varied spatially, with levels decreasing between urbanized areas and more remote regions: urban area (U1-U3: 7.76 ± 4.57 to 20.1 ± 15.1 ng m^− 3), town (T1: 4.61 ± 1.15 ng m^− 3) and village (V1-V4: 3.26 ± 0.63 to 8.45 ± 3.06 ng m^− 3), and remote area (R1-R6: 1.60 ± 0.43 to 3.41 ± 1.26 ng m^− 3). Our study suggested that industrial activities, especially non-ferrous smelting activities, were an important source of atmospheric Hg and played a vital role in the regional distribution of TGM. In addition, domestic coal and biomass combustion to heat residential homes were important sources of TGM in densely populated areas during the winter months.     

Ingestion of lead from ammunition and lead concentrations in white-tailed sea eagles (Haliaeetus albicilla) in Sweden

In this study we show for the first time that lead poisoning from ammunition is a significant mortality factor for white-tailed sea eagle (WSE) (Haliaeetus albicilla) in Sweden. We analyzed 118 WSEs collected between 1981 and 2004 from which both liver and kidney samples could be taken. A total of 22% of all eagles examined had elevated (> 6 µg/g d.w.) lead concentrations, indicating exposure to leaded ammunition, and 14% of the individuals had either liver or kidney lead concentrations diagnostic of lethal lead poisoning (> 20 µg/g d.w.). Lead concentrations in liver and kidney were significantly correlated. In individuals with lead levels < 6 µg/g, concentrations were significantly higher in kidney than in liver; in individuals with lead levels > 20 µg/g, concentrations were significantly higher in liver. The lead isotope ratios indicate that the source of lead in individuals with lethal concentrations is different from that of individuals exhibiting background concentrations of lead (< 6 µg/g d.w.) There were no significant sex or age differences in lead concentrations. A study from the Baltic reported in principle no biomagnification of lead, but background lead concentrations in WSE liver in this study were still four to > 10 times higher than concentrations reported for Baltic fish from the same time period. In contrast to other biota there was no decrease in lead concentrations in WSE over the study period. The proportion of lead poisoned WSE remained unchanged over the study period, including two years after a partial ban of lead shot was enforced in 2002 for shallow wetlands. The use of lead in ammunition poses a threat to all raptors potentially feeding on shot game or offal. The removal of offal from shot game and alternatives to leaded ammunition needs to be implemented in order to prevent mortality from lead in raptors and scavengers.     

Investigating the potential role of ammonia in ion chemistry of fine particulate matter formation for an urban environment

To investigate the potential role of ammonia in ion chemistry of PM_2.5 aerosol, measurements of PM_2.5 (particulate matter having aerodynamic diameter < 2.5 µm) along with its ionic speciation and gaseous pollutants (sulfur dioxide (SO₂), nitrogen oxides (NO_x), ammonia (NH₃) and nitric acid (HNO₃)) were undertaken in two seasons (summer and winter) of 2007-2008 at four sampling sites in Kanpur, an urban-industrial city in the Ganga basin, India. Mean concentrations of water-soluble ions were observed in the following order (i) summer: SO₄²⁻ (26.3 µg m^− 3) > NO₃⁻ (16.8) > NH₄⁺ (15.1) > Ca²⁺ (4.1) > Na⁺ (2.4) > K⁺ (2.1 µg m^− 3) and (ii) winter: SO₄²⁻ (28.9 µg m^− 3) > NO₃⁻ (23.0) > NH₄⁺ (16.4) > Ca²⁺(3.4) > K⁺(3.3) > Na⁺ (3.2 µg m^− 3). The mean molar ratio of NH₄⁺ to SO₄²⁻ was 2.8 ± 0.6 (mostly >2), indicated abundance of NH₃ to neutralize H₂SO₄. The excess of NH₄⁺ was inferred to be associated with NO₃⁻ and Cl⁻. Higher sulfur conversion ratio (F_s: 58%) than nitrogen conversion ratio (F_n: 39%) indicated that SO₄²⁻ was the preferred secondary species to NO₃⁻. The charge balance for the ion chemistry of PM_2.5 revealed that compounds formed from ammonia as precursor are (NH₄)₂SO₄, NH₄NO₃ and NH₄Cl. This study conclusively established that while there are higher contributions of NH₄⁺, SO₄²⁻ to PM_2.5 in summer but for nitrates (in particulate phase), it is the winter season, which is critical because of low temperatures that drives the reaction between ammonia and HNO₃ in forward direction for enhanced nitrate formation. In summary, inorganic secondary aerosol formation accounted for 30% mass of PM_2.5 and any particulate control strategy should include optimal control of primary precursor gases including ammonia.