Distribution of bisphenol-A, triclosan and n-nonylphenol in human adipose tissue, liver and brain

In this study, an analytical method was optimized for the determination of bisphenol-A (BPA), triclosan (TCS) and 4-n-nonylphenol (4n-NP), environmental contaminants with potential endocrine disruptive activities, in human tissues. The method consisted of a liquid extraction step, derivatization with pentafluorobenzoylchloride followed by a clean-up on acidified silica and detection with gas chromatography coupled with mass spectrometry (GC-ECNI/MS). Recoveries ranged between 92% and 102% with a precision below 5%. Limits of quantification ranged between 0.3-0.4 ng g⁻¹, 0.045-0.06 ng g⁻¹ and 0.003-0.004 ng g⁻¹ for BPA, TCS and 4n-NP in different tissues, respectively. The method was applied for the determination of BPA, TCS and 4n-NP in paired adipose tissue, liver and brain samples from 11 individuals. BPA could be detected in almost all tissues, with the highest concentrations found in adipose tissue (mean 3.78 ng g⁻¹), followed by liver (1.48 ng g⁻¹) and brain (0.91 ng g⁻¹). TCS showed the highest concentrations in liver (3.14 ng g⁻¹), followed by adipose tissue (0.61 ng g⁻¹), while it could be detected in only one brain sample. Levels of 4n-NP were much lower, mostly undetected, and therefore 4n-NP is considered of minor importance for human exposure. Despite the measurable concentrations in adipose tissue, these compounds seem to have a low bioaccumulation potential. The reported concentrations of free BPA in the various tissues are slight disagreement with pharmacokinetic models in humans and rats and therefore the possibility of external contamination with BPA during sample collection/storage cannot be ruled out.     

Plant biodiversity and ethnobotany inside the projected impact area of the Upper Seti Hydropower Project,Western Nepal

A survey of plant biodiversity and ethnobotany was conducted along the Seti river banks in the Tanahun district of Western Nepal. This area, home of the Magar ethnic group, will be impacted by a major hydropower project, currently under feasibility study. The objective of the study was to document plant biodiversity and ethnobotany in order to suggest appropriate conservation and management strategies. Botanical sampling was conducted inside quadrats and along transects. A total of 221 plant species were recorded in the study area, distributed as herbs (80 species), trees (68), shrubs (28), climbers (19), pteridophytes (18), lianas (5), and epiphytes (3). Twelve of the inventoried species figure in one or more conservation categories identified by various national or international agencies. Group discussions and personal interviews allowed to find out that 43% of the species were ethnobotanically important for the local people and that most were used as medicine, food, or timber. We propose specific species for sustainable use programs based on certain criteria. The area is very important in terms of plant biodiversity and ethnobotany, and hence, immediate implementation of conservation measures is recommended to maintain the high social, ecological and economic values of the area.     

What can we learn from monitoring PCBs in the European eel? A Belgian experience

Between 2000 and 2007 pooled muscle tissue samples of the European eel (Anguilla anguilla) from 48 sites in Flanders (Belgium) were analysed for 30 polychlorinated biphenyl (PCB) congeners. There was a large variation between individual sites (range 11-7752 ng/g wet weight (ww) for the sum of the ICES 7 PCBs), eels from the River Meuse basin (mean 1545 ng/g ww) being considerably more polluted than those from the River Scheldt (615) and IJzer (61) basins. Overall, PCB 153, PCB 138 and PCB 180 were the most prominent congeners, however PCB patterns varied between the monitored locations. Analysis of the weight percentage of congeners demonstrates obvious differences in PCB composition between sites, indicating differential sources of pollution. Due to the variation in patterns, atmospheric fallout does not seem to be the main source of the PCB spread, but instead both local and upstream sources linked to industrial activities seem to be the main cause for PCB presence in Flanders. Considering the levels of the Sum 7 PCBs, eels are not compliant with the Belgian legal limits for consumption (75 ng/g ww) in 71% of the sites. Regular consumption of eels from polluted sites leads to a considerable excess of the WHO Acceptable Daily Intake value. Consumption of wild eels should by all means be prevented, as it presents risks for human health, especially for local anglers consuming their catch.     

Associations of Decadal to Multidecadal Sea‐Surface Temperature Variability with Upper Colorado River Flow1

Abstract: The relations of decadal to multidecadal (D2M) variability in global sea‐surface temperatures (SSTs) with D2M variability in the flow of the Upper Colorado River Basin (UCRB) are examined for the years 1906‐2003. Results indicate that D2M variability of SSTs in the North Atlantic, North Pacific, tropical Pacific, and Indian Oceans is associated with D2M variability of the UCRB. A principal components analysis (with varimax rotation) of detrended and 11‐year smoothed global SSTs indicates that the two leading rotated principal components (RPCs) explain 56% of the variability in the transformed SST data. The first RPC (RPC1) strongly reflects variability associated with the Atlantic Multidecadal Oscillation and the second RPC (RPC2) represents variability of the Pacific Decadal Oscillation, the tropical Pacific Ocean, and Indian Ocean SSTs. Results indicate that SSTs in the North Atlantic Ocean (RPC1) explain as much of the D2M variability in global SSTs as does the combination of Indian and Pacific Ocean variability (RPC2). These results suggest that SSTs in all of the oceans have some relation with flow of the UCRB, but the North Atlantic may have the strongest and most consistent association on D2M time scales. Hydroclimatic persistence on these time scales introduces significant nonstationarity in mean annual streamflow, with critical implications for UCRB water resource management.     

3-to-1: unraveling structural transitions in ureases

Ureases are nickel-dependent enzymes which catalyze the hydrolysis of urea to ammonia and carbamate. Despite the apparent wealth of data on ureases, many crucial aspects regarding these enzymes are still unknown, or constitute matter for ongoing debates. One of these is most certainly their structural organization: ureases from plants and fungi have a single unit, while bacterial and archaean ones have three-chained structures. However, the primitive state of these proteins — single- or three-chained — is yet unknown, despite many efforts in the field. Through phylogenetic inference using three different datasets and two different algorithms, we were able to observe chain number transitions displayed in a 3-to-1 fashion. Our results imply that the ancestral state for ureases is the three-chained organization, with single-chained ureases deriving from them. The two-chained variants are not evolutionary intermediates. A fusion process, different from those already studied, may explain this structural transition.     

Inter-species differences for polychlorinated biphenyls and polybrominated diphenyl ethers in marine top predators from the Southern North Sea: Part 2. Biomagnification in harbour seals and harbour porpoises

Harbour porpoises (Phocoena phocoena) and harbour seals (Phoca vitulina) were found to differ in the ability to metabolize polychlorinated biphenyls (PCBs) and polybrominated diphenyl ethers (PBDEs). Biomagnification factors (BMFs), calculated between both predators and their prey (sole - Solea solea and whiting - Merlangius merlangus), had a large range of variation (between 0.5 and 91 for PCBs and between 0.6 and 53 for PBDEs). For the higher chlorinated PCBs and the highest brominated PBDEs, the BMF values in adult males were significantly higher than in the juvenile individuals of both species. BMF values of hexa- to octa-PCBs were the highest, suggesting reduced ability to degrade these congeners. Harbour porpoises had higher BMFs for lower chlorinated PCBs and for all PBDEs compared to harbour seals. Other factors, which may influence biomagnification, such as the octanol-water partition coefficients and the trophic level position measured through stable isotope (δ¹⁵N) analysis, were found to be of lesser importance to predict biomagnification in the studied food chain.     

Concentrations of brominated flame retardants in dust from United Kingdom cars, homes, and offices: causes of variability and implications for human exposure

Average concentrations of polybrominated diphenyl ethers (PBDEs) in dust in 30 homes, 18 offices, and 20 cars were 260,000, 31,000, and 340,000 ng SigmaPBDEs g(-1) respectively. Concentrations of BDEs 47, 99, 100, and 154 in cars exceeded significantly (p<0.05) those in homes and offices. Average concentrations of 1,2-bis(2,4,6-tribromophenoxy)ethane (TBE) and decabromodiphenyl ethane (DBDPE) in homes, offices, and cars respectively were lower at 120, 7.2, and 7.7 ng g(-1) (TBE) and 270, 170, and 400 ng g(-1) (DBDPE). BDE-209 concentrations in three samples are the highest to date at 2,600,000 (car), 2,200,000 (home), and 1,400,000 ng g(-1) (home). UK toddlers daily consuming 200 mg dust contaminated at the 95th percentile concentration, ingest 180 ng (Sigma)tri-hexa-BDEs and 310 microg BDE-209 day(-1). For TBE, exposure was lower than for PBDEs and hexabromocyclododecanes (HBCDs), while that for DBDPE was similar in magnitude to (Sigma)tri-hexa-BDEs, but less than for BDE-209 and HBCDs. BDE-209 concentrations recorded in ten samples taken at monthly intervals in one room varied 400-fold, implying caution when using single measurements of dust contamination for exposure assessment. Significant negative correlation was observed in one room between concentrations of BDE-47, 99, and 153 and dust loading (g dust m(-2) floor), suggesting "dilution" occurs at higher dust loadings.     

Five Hundred Years of Hydrological Drought in the Upper Colorado River Basin1

Abstract: This article evaluates drought scenarios of the Upper Colorado River basin (UCRB) considering multiple drought variables for the past 500 years and positions the current drought in terms of the magnitude and frequency. Drought characteristics were developed considering water‐year data of UCRB’s streamflow, and basin‐wide averages of the Palmer Hydrological Drought Index (PHDI) and the Palmer Z Index. Streamflow and drought indices were reconstructed for the last 500 years using a principal component regression model based on tree‐ring data. The reconstructed streamflow showed higher variability as compared with reconstructed PHDI and reconstructed Palmer Z Index. The magnitude and severity of all droughts were obtained for the last 500 years for historical and reconstructed drought variables and ranked accordingly. The frequency of the current drought was obtained by considering two different drought frequency statistical approaches and three different methods of determining the beginning and end of the drought period (annual, 5‐year moving, and ten year moving average). It was concluded that the current drought is the worst in the observed record period (1923‐2004), but 6th to 14th largest in terms of magnitude and 1st to 12th considering severity in the past 500 years. Similarly, the current drought has a return period ranging from 37 to 103 years based on how the drought period was determined. It was concluded that if the 10‐year moving average is used for defining the drought period, the current drought appears less severe in terms of magnitude and severity in the last 500 years compared with the results using 1‐ and 5‐year averages.     

A one year investigation of the occurrence of illicit drugs in wastewater from Brussels, Belgium

Daily 24 hour composite influent wastewater samples were collected from the wastewater treatment plant of Brussels-North (Belgium) for eight months to study variations in the concentrations and mass loads of nine illicit drugs and metabolites: cocaine (COC) and its metabolites benzoylecgonine (BE) and ecgonine methyl ester (EME), amphetamine (AMP), methylenedioxymethamphetamine (MDMA), methamphetamine (METH), methadone (MTD) and its metabolite 2-ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine (EDDP) and the specific metabolite of heroin, 6-monoacetylmorphine (6-MAM). Samples were analyzed using a validated analytical method based on solid-phase extraction and hydrophilic interaction liquid chromatography coupled to tandem mass spectrometry. The selected compounds could be detected and quantified in all samples. The measured concentrations were in agreement with earlier published concentrations, when available. All illicit drugs showed significant differences in mass loads between months. Daily variations were observed for MDMA, AMP and COC and metabolites, with higher mass loads observed during the weekend. This is probably related to their recreational consumption pattern and was further confirmed when holiday periods (New Year's Eve, Belgian national holiday) were in detail investigated. For METH, 6-MAM, MTD and EDDP, stable and consistent amounts were observed during the week. In all samples, the ratio of the concentration of the parent compound to its metabolite(s) was calculated to evaluate whether measured concentrations reflect human excretion of the illicit drugs. For MTD, the ratio of parent compound/metabolite was in agreement with the excretion pattern, while for COC some deviations were observed, resulting from excretion pattern uncertainties, and stability and discharge issues.