Contamination and impacts of new antifouling biocide Irgarol-1051 on subtropical coral reef waters

Coral reefs are deteriorating worldwide due to various stresses, including pollution of hazardous chemicals such as antifouling chemicals. Occurrence and impacts of a new antifouling biocide Irgarol-1051 (2-methylthio-4-tert- butylamino -6-cyclopropylamino -s-triazine) have been studied in coral reef waters around Okinawa Islands, Japan. The average concentration of Irgarol detected at commercial and fisheries Ports was 24.70 ± 9.88 ng/L. In Naha Bay, the average concentration of Irgarol was 10.00±12.98 ng/L. The average level detected around the Ports has already approaches the environmental risk limit for the marine organisms. Irgarol was detected in waters at the frequency of 92.3 % (24/26) of the total samples collected during two sampling campaigns (September and December, 2007) at the Ports. In Naha Bay, Irgarol was detected by 40.5 % (17/42) of the total water samples collected monthly from Sep., 2007 to Feb., 2008, indicating that Irgarol is widely detected along the coastal shorelines of Okinawa Island. The eco- toxicological study revealed that the rate of photosynthesis in the coral Galaxea fascicularis was significantly reduced by 18 % and 121 % relative to control when the corals were exposed to 1000 and 10,000 ng/L of Irgarol, respectively. The calcification rate dropped by 98.3 % relative to control when the corals were exposed to 10,000 ng/L of Irgarol. The results of the present study report the wide occurrence of new antifouling biocide Irgarol around coastal areas of Okinawa Island. However, the contamination does not pose serious threat on the photosynthesis and calcification of corals under short term exposure (96 h).     

Determination of the radiation dose due to radon ingestion and inhalation

The distribution of radon in ground and surface water samples in Sankey Tank and Mallathahalli Lake areas was determined using Durridge RAD-7 analyzer with RAD H₂O accessory. The radiation dose received by an individual falling under different age groups (viz., 3 months; 1, 5, 10, 15 years and adult) depending upon their average annual water consumption rate was attempted. The mean radon activity in surface water of Sankey Tank and Mallathahalli Lake was 7.24 ± 1.48 and 11.43 ± 1.11 Bq/L, respectively. The average radon activities ranged from 11.6 ± 1.7 to 381.2 ± 2.0 Bq/L and 1.50 ± 0.83 to 18.9 ± 1.59 Bq/L, respectively, in 12 groundwater samples each around Sankey Tank and Mallathahalli Lake areas. Majority of the measured groundwater samples (viz., 100 % in Sankey Tank area and 75 % in Mallathahalli Lake area) showed mean radon values above the EPA’s maximum contaminant level of 11.1 Bq/L and only 66.67 % of samples in Sankey Tank area showed radon above the WHO and EU’s reference level of 100 Bq/L. The overall radiation dose due to radon emanating from water in the study area was increasing with increase in age and water consumption rates, but significantly lower than UNSCEAR and WHO recommended limit of 1 mSv/year except for few groundwater samples in Sankey Tank area (i.e., 0.92, 0.99 and 1.39 mSv/year). The radiation dose rate received by bronchial epithelium via inhalation was very high compared to that by stomach walls via ingestion.     

Antibiotics pollution in Gonghu Bay in the period of water diversion from Yangtze River to Taihu Lake

As a famous project in China, the water diversion from Yangtze River to Taihu Lake Project has impacts on the water quality of Taihu Lake, especially Gonghu Bay, which is the entrance of the diversion water and the drinking water source for Wuxi and Suzhou. To investigate contamination of the antibiotics in Gonghu Bay in the period of water diversion, 16 antibiotics in 14 water samples collected from Wangyu River and Gonghu Bay in China were analyzed by liquid chromatography–tandem mass spectrometry. The results indicated that the concentration of total antibiotics in Wangyu River and Gonghu Bay ranged from 1320 to 17,209 ng/L (mean: 3920?±?3841 ng/L). The average level of different antibiotics was tetracyclines (range 1082–15,310 ng/L, mean 3161?±?3479 ng/L)?>?quinolones (range 225–1325 ng/L, mean 463?±?276 ng/L)?>?sulfonamides (range n.d.–888 ng/L, mean 402?±?248 ng/L)?>?macrolides (range 12–17 ng/L, mean 14?±?2 ng/L), and levels of the detected antibiotics in Gonghu Bay were higher than that in Wangyu River, indicating that the antibiotics pollution in Gonghu Bay were much severer than Wangyu River. Ecological risk evaluation showed that in the Wangyu and Gonghu water, trimethoprim (TMP), sulfacetamide (SAAM), sulfamethoxypyridazine (SMP), and sulfamerazine (SMRZ) presented low ecological risk levels, chlortetracycline (CTC), tetracycline (TC), roxithromycin (ROM), and sulfamethoxazole (SMX) had medium level of risk, and oxytetracycline (OTC), norfloxacin (NOR), ofloxacin (OFL), ciprofloxacin (CIP), and enrofloxacin (ENR) had high level of ecological risk. The total hazard quotient of antibiotic mixtures for each sample site indicated high risk of antibiotics in Wangyu River and Gonghu Bay. In summary, the water diversion could mitigate antibiotic pollution in Gonghu Bay to a certain degree. However, the risk of antibiotics in the Wangyu River and Gonghu Bay is still high.     

In situ and laboratory treatment tests for lowering of excess manganese and iron in drinking water sourced from river–groundwater interaction

Manganese and iron are essential nutrients at low doses. However, long-term exposure in high doses may be harmful. Human activities and natural sources are responsible for manganese and iron contamination in water. This study aimed to investigate the source of high manganese and iron contents in shallow groundwater, where the groundwater is used for drinking purpose, and to decrease the excess manganese and iron from shallow groundwater. Based on the on-site analytical results taken from the wells in the study area, iron contents in water samples varied between 30 and 200 μg/L, which were under the allowable limits of Turkish Drinking Water Standards (TDWS) (Water intended for human consumption, http://rega.basbakanlik.gov.tr/eskiler/2005/02/20050217-3.htm, 2005). However, manganese levels varied from 30 to 248 μg/L, which some of them are higher than the allowable limits of TDWS (Water intended for human consumption, http://rega.basbakanlik.gov.tr/eskiler/2005/02/20050217-3.htm, 2005) (50 μg/L), and EPA (http://water.epa.gov/drink/contaminants/index.cfm, 2006) (50 μg/L). The source of excess manganese is originated mainly from geogenic source besides Porsuk River interaction in shallow aquifer in the specific section of the study area. To decrease high manganese content from the well water and reservoir water, laboratory and in situ treatment tests were applied. Among these tests, chlorination, associated with filtration (by fine sand, active carbon and zeolite) and the use of different filtration procedures by cation exchange resin were determined as the most effective methods, which was not previously applied on-site as a combinative approaches to reduce the excess manganese in water.     

Survey of polycyclic aromatic hydrocarbons and nitrated polycyclic aromatic hydrocarbons in Jiaxing city, China

Polycyclic aromatic hydrocarbon (PAH) and nitrated PAH (NPAH) products are toxic. Thus, determination of their concentrations is of great interest to researchers of soil and water pollution control. In this work, soil samples, surface water samples, and groundwater samples were collected, and the concentrations of 16 priority PAHs and 15 NPAHs were determined using an HPLC-ultraviolet detector. Results showed that the total PAH concentrations ranged within 489.69–1,670.11 ng/g (average = 905.89 ng/g) in soil samples, 4.00–23.4 μg/l (average = 9.84 μg/l) in surface water samples, and 2.14–22.3 μg/l (average = 8.37 μg/l) in groundwater samples. The NPAH concentrations were one to two orders of magnitude lower than the PAH concentrations and ranged within 22.72–128.70 ng/g (average = 63.88 ng/g) in soil samples. 2-Nitropyrene and 6-nitrochrysene were the most abundant compounds, accounting for about 14.3 and 26.5 %, respectively. Source analysis revealed that most PAHs originated from coal combustion around the study area, whereas NPAH studies suggested that the primary emission of gasoline engines and daytime OH reactions were the dominant sources of these compounds.     

Compositions and sources of extractable organic matter in Mesopotamian marshland surface sediments of Iraq: II. Polar compounds

The concentrations of polar organic compounds including n-alkanoic acids, n-alkanols, steroids and triterpenoids were determined in extracts of shallow sediments from the Mesopotamian marshlands of Iraq. The sediments were collected by a stainless steel sediment corer, extracted with a dichloromethane and methanol mixture (3:1 v:v) by ultrasonic agitation and then analyzed by gas chromatography–mass spectrometric (GC–MS). The analysis results showed that the n-alkanoic acids ranged from C₈ to C₂₀ with concentrations of 7.8 ± 1.2 μg/g sample, whereas the concentrations of n-alkanols, which ranged from C₁₂ to C₃₉ were from 28.6 ± 4.3 to 121.7 ± 18.3 μg/g sample. The steroids and triterpenoids included stenols, stanols, stenones, stanones, tetrahymanol, tetrahymanone and extended ββ-hopanes. The total concentrations of steroids and triterpenoids ranged from 26.8 ± 4.1 to 174.6 ± 26.2 μg/g and from 0.74 ± 0.11 to 11.2 ± 1.7 μg/g sample, respectively. The major sources of these lipids were from natural vegetation, microbial (plankton) residues and bacteria in the sediments, with some contribution from anthropogenic sources (livestock, sewage and petroleum). Further studies of these wetlands are needed to characterize the input rate, transformation and diagenesis of the organic matter and to assess its various sources.     

Polycyclic aromatic hydrocarbons in Niger Delta soil: contamination sources and profiles

The distribution and sources of PAHs in soil as well as PAHs profiles have been investigated in areas with anthropogenic pollution in the Niger Delta (Nigeria) such as Warri and Ughelli. PAHs were identified in 21 soil samples (0–10cm upper layer) collected in May, 2003. The typical total PAHs level in Niger Delta soil ranged from 182 ± 112 - to - 433 ±256 íg/kg dw. PAH concentrations in soil samples from Warri Refinery, Tanker Loading point and Ugboko via Rapele oil field were quite high ( the mean ÓPAH concentrations were 433, 402 and 384 íg/kg dry weight respectively). The dominant PAHs in soil samples were pyrene, naphthalene and benzo[k]fluoranthene. The soil total PAHs (PAH_tot.) concentration, normalized to organic carbon content (OC), ranged from 11.4 to 47.2 mg PAH_tot. /kg OC; and showed that organic matter of the soil samples from Quality Control Centre, Ugelli West is highly contaminated with PAHs and had a value of 47.2 ± 31.2 mg PAH_tot./kg OC. Two and three ring aromatic hydrocarbons predominated in soil samples from Ughelli West, Tanker Loading point and Delta Steel Company, which is indicative of petrogenic origin.     

Determination of cadmium and lead in human milk

The objectives of this study were to determine cadmium and lead concentrations in the breast milk of healthy lactating women who were living in Zarrinshahr, an industrial area of Iran and to investigate the effect of mother’s age, parity and smoking habits in families living in the vicinity of areas contaminated with heavy metals. Cadmium and lead concentrations were determined by graphite furnace atomic absorption spectrometry in 44 milk samples from healthy lactating women collected on first to sixth postpartum week. Accuracy of the analysis was checked by various methods including the use of reference material. The mean ± standard deviation of cadmium and lead concentrations in human milk were 2.44 ± 1.47 μg/L (range 0.62–6.32 μg/L) and 10.39 ± 4.72 μg/L (range 3.18–24.67 μg/L), respectively. There was a positive correlation between the concentrations of lead in milk samples and mother’s age and parity (P < 0.05). Also the concentration of cadmium in breast milk significantly increased (P < 0.05) in mothers who were actively and/or passively exposed to smoking. The results of this study showed that lead and cadmium concentrations in milk samples from lactating women in Zarrinshahr were high. This can be a major public health hazard for the inhabitants living in this industrial region of Iran.     

Calcite and aragonite saturation States of Kamaran strait surface seawater, Yemen: summer time

Surface seawater samples from Kamaran Strait of Yemen were collected for physical and chemical parameter determinations. This work reports the results of air and surface seawater temperature, salinity, pH, and total alkalinity measurements. The air temperature ranged from 29.9°C to 36.5°C with an average value of 31.5?±?1.5°C, whereas the seawater surface temperature ranged from 34.0°C to 36.0°C with a mean value of 34.5?±?0.5°C. The salinity was observed to be high, ranging from 38.03 to 38.81 with an average value of 38.45?±?0.22. The pH ranged from 7.74 to 8.27 with a mean value of 8.11?±?0.10. The total alkalinity was found to range from 2.3860 to 2.5000 meq L^?1 with an average value of 2.4288?±?0.0351 meq L^?1. The result of the study showed that there was a negative correlation between the pH and surface seawater temperature and salinity. The surface seawater of the Kamaran Strait was found to be several fold supersaturated with respect to calcium carbonate. The measured percent degree of saturation ranged from 454% to 668% with respect to calcite and from 246% to 361% with respect to aragonite. The lowest value of supersaturation with respect to both calcite and aragonite were found in front of as-Salif port, where human and developmental activities are intensively increased. The visual inspection of coral reefs distribution and their intensity were obviously observed in areas of high value of supersaturation with respect to both minerals, high transparency of seawater column, and low human activities. Further studies are needed to investigate the occurrence, distribution, and mineralogy of corals and the effects of physical and chemical parameters upon their growth in the region.     

Health risk assessment of trace elements in drinking water from Najran City,southwestern Saudi Arabia

The concentrations of 16 trace elements (Ag, Al, As, B, Ba, Cd, Cr, Cu, Hg, Mn, Ni, Pb, Se, Ti, U, and Zn) in drinking water from Najran City, Saudi Arabia, were determined by inductively coupled plasma-mass spectrometry (ICP-MS) and compared with local, regional, and international guidelines. Water samples from 22 water treatment plants and 13 commercial bottled water brands were analyzed. Except for B and U, the trace element concentrations were below the permitted limits defined in SASO, GSO, and WHO drinking water quality guidelines. The B concentrations in three brands of bottled water were 533.19, 602.29, and 1471.96 μg/L, which were all higher than the GSO and SASO limit (500 μg/L). The U concentrations were higher than the SASO limits for drinking water in two samples; one in treatment plant (2.39 μg/L) and another in foreign bottled water (2.17 μg/L). The median As, Ba, Cu, Ni, U, and Zn concentrations were statistically significantly higher in the treatment plant water samples than those in the bottled water samples, and conversely, the B concentrations were higher in the bottled water samples. The Cd, Hg, and Ti concentrations were below the detection limits of ICP-MS in all of the water samples. Apart from few exceptions, trace element concentrations in drinking water of Najran City were all within limits permitted in the national, regional, and international drinking water quality guideline values.     

Biomonitoring of trace element accumulation in plants growing at Murat Mountain

The purpose of this study is to determine the present levels of atmospheric trace element pollution in the Murat Mountain of Aegean Region in the western part of Turkey. Therefore, 29 different plants were selected as potential biomonitors of trace elements including nickel, zinc, iron, lead, cadmium and manganese (??g/g, dry weight). The samples were collected from two different heights of Murat Mountain. Atomic absorption spectrometry was used to determine the concentrations of trace elements. The mean concentrations determined at 1,000?m altitude ranged from 0.139 to 4.518, 0.223 to 0.986, 0.359 to 6.930, 0.443 to 0.727 and 0.077 to 3.222???g/g, dry weight, for nickel, zinc, iron, lead and manganese, respectively. At 1,600?m altitude, the values ranged from 0.191 to 6.248, 0.302 to 1.008, 2.387 to 8.896, 0.345 to 0.570 and 0.195 to 3.502???g/g, dry weight, for nickel, zinc, iron, lead and manganese, respectively. No cadmium was found at both altitudes. For determination of existence of any differences between the averages of the herbaceous and woody plants, comparisons were made by the independent sample t test. In the statistical analysis, comparison of trace element pollution values of herbaceous and woody plants for nickel, lead and manganese was significant (P?<?0.05), while it was not for iron and zinc.     

Assessment of Zn, Cu, Pb and Ni contamination in wetland soils and plants in the Lake Victoria basin

The impact of waste disposal on trace metal contamination was investigated in eleven wetlands in the Lake Victoria Basin. Samples of soil, water and plants were analysed for total Zn, Cu, Pb and Ni concentrations using flame atomic absorption spectrophotometry. The trace metal concentrations in soil were the highest in Katanga wetland with the highest mean concentrations of 387.5±86.5 mg/kg Zn, 171.5±36.2 mg/kg Pb, 51.20±6.69 mg/kg Cu and 21.33±2.23 mg/kg Ni compared to the lowest levels observed at Butabika (30.7±3.2 mg/kg Zn, 15.3±1.7 mg/kg Pb, 12.77±1.35 mg/kg Cu and 6.97±1.49 mg/kg Ni). Katanga receives waste from multiple industrial sources including a major referral city hospital while Butabika is a former solid waste dumpsite. Wetland soil near a copper smelter had a Cu concentration of 5936.3±56.2 mg/kg. Trace metal concentrations in industrial effluents were above international limits for irrigation water with the highest concentrations of 357,000 μg/L Cu and 1480 μg/L Zn at a Cu smelter and 5600 μg/L Pb at a battery assembling facility compared to the lowest of 50 μg/L Cu and 50 μg/L Zn in water discharged from Wakaliga dumpsite. Uptake of trace metals from soil differed from plant to plant and site to site. Higher levels of trace metals accumulated in the root rather than in the rhizome and the least amount was in the leaf. The study identifies industry as a potential source of trace metal contamination of water and the environment pent-up need for policy intervention in industrial waste management.     

Occurrence of nonylphenol an endocrine disrupter in Karun River,Khuzestan Province,Iran

The important Iranian Karun River has never been investigated for the presence of potentially endocrine-disrupting chemicals, nonylphenol (NP). In this study, concentrations of NP were measured in water from Karun River and five wastewater discharge points into this river, collected during April to July 2010. The analytes were extracted by solid-phase extraction, and quantitative analyses were performed by HPLC–FLD. NP was detected in water and wastewater samples with 0.17–1.83 and 15.27–21.79 μg/L, respectively. The results showed that the NP content of aqueous phase of all wastewater samples higher than particulate phase, which were detected in the aqueous and particulate phases with mean concentrations of 12.8 ± 2.4 and 5.2 ± 1.2 μg/L, respectively. These data suggest that the NP levels in Karun river water are likely attributable to untreated municipal wastewaters discharged directly into the river. To our knowledge; this is the first study to evaluate NP concentrations in water and wastewater in Iran.     

Predictive environmental impact assessment of total petroleum hydrocarbons in petrochemical wastewater effluent and surface sediment

The contamination level of total petroleum hydrocarbons (TPH) in wastewater and surface sediment samples from the Petrochemical Special Economic Zone (PETZONE) and adjacent coastal area in Musa Bay (in Northwest of Persian Gulf) was examined. Concentrations of TPH in the Musa Bay sediments ranged from 16.48 to 97.15 µg/g dry weight (dw) with average value of 48.98 ± 30.36 µg/g dw. The highest concentrations were estimated in stations close to the coastline, locations affected by intensive petrochemical discharges and shipping activities. The average TPH concentration in the PETZONE wastewater effluent samples was 5.22 mg/L, with a range of 0.06–35.33 mg/L. Regarding environmental impact assessment, the concentration of TPH was lower than the wastewater effluent discharge standard at most of the monitoring stations inside PETZONE companies, with the exception of stations 15, 16 (Imam Khomeini petrochemical company 1, 2) and 17 (Razi petrochemical company). These stations were considered as moderate environmental aspects, suggesting that concentration of TPH in the wastewater effluents of these petrochemical companies could be considered as contaminants of concern in the PETZONE area.     

Determination of trihalomethanes and the ionic composition of groundwater at Amman City, Jordan

A water-chemistry evaluation was made of the available springs and wells in Amman and vicinity. Trihalomethanes (THM) were found in all analysed samples with concentrations ranging from 0.2–31.88 μg/L. The probable sources of trihalomethanes in the aquifers originate from three sources: (1) chlorinated Deir Alla surface water, (2) reaction of excess chlorine in the leaky, corroded water-distribution network with organic matter in the vadose zone, and (3) sewage seepage from cesspools in the area. Total organic carbon (TOC) ranged from 0.2–1.4 mg/L. Its probable source is either from the vadose zone or the treated surface water at Deir Alla. It was found that TOC was of vital importance in the formation of THM in the presence of chlorine from the water-distribution system. Major ionic composition of the analysed samples reflected the limestone lithology of the aquifer in the investigated area. Heavy-metal content was relatively low due to the high pH of the groundwater samples. Electronic Publication     

Use of Pyracantha coccinea Roem. as a possible biomonitor for the selected heavy metals

In this study, copper, iron, manganese and nickel levels of branches and leaves of Pyracantha coccinea Roem. (firethorn) were measured for determining the heavy metal pollution in Mugla Province. Plant samples were collected from 34 different localities in four different areas of Mugla Province, during 2006 vegetation period. Unwashed and washed leaf samples and unwashed branch samples were subjected to analysis and copper, iron, manganese and nickel concentrations of samples were measured by inductively coupled plasma optical emission spectrometry. The obtained data were analyzed with “statistical package for the social sciences” statistics program. As a result of measurements, the highest average and lowest values and their collected stations were as follows; the highest average (5.89 ± 0.04 μg/g dw) and the lowest (5.20 ± 0.03 μtg/g dw) values of copper were measured near highways. The average highest iron value (9.53 ±1.68 μtg/g dw) was in industrial area while the lowest was near highways (1.73 ± 0.54 μtg/g dw). The highest value of magnesium accumulation (1.00 ± 0.16 μtg/gdw) was measured near highways. The lowest value was determined in urban area (0.40 ± 0.14 μtg/g dw). The average highest level of nickel was in industrial area while the lowest was determined in urban area. The values were 14.34 ± 1.59 μtg/g and 4.05 ± 0.51 μtg/g dw. As a result, it was proven that P. coccinea could be used as a biomonitor species for some of these heavy metals especially for copper and nickel.     

Aerosol-trace gases interactions and their role in air quality control of Delhi city (India)

Atmospheric dust is considered to be the major cause of poor air quality due to its contribution to high particulate levels, but their interaction with the acidic gases helps in controlling the level of SO₂ and NO₂ through ambient neutralization reactions. In the present study, the interaction of acidic gases such as SO₂ and NO₂ with alkaline dust was investigated during October, 2013–July, 2014 at a site named as Babarpur located at the Trans-Yamuna region of Delhi. The concentration of SO₂ ranged from 10 to 170 μg/m³ with an average of 36 μg/m³ while that of NO₂ ranged from 15 to 54 μg/m³ with an average of 26?±?8 μg/m³. The results were observed to be well within the National Ambient Air Quality Standard (NAAQS) limits prescribed by the Central Pollution Control Board (CPCB). The average concentrations of SO₂ during day and night time were recorded as 31?±?18 and 43?±?53 μg/m³ respectively while the mean concentrations of NO₂ during day and night time were recorded as 26?±?7 and 27?±?12 μg/m³ respectively. A positive correlation between SO₄^2? and NO₃^? was also observed indicating their secondary aerosol formation. In aerosol phase, average concentrations of SO₄^2? during day and night time were 3.9?±?0.3 and 6.5?±?2.3 μg/m³ respectively while that of NO₃^? were 9.5?±?1.5 and 7.3?±?0.5 μg/m³ respectively. Molar ratios of Ca²⁺/SO₄^2?, NH₄⁺/SO₄^2?, and NH₄⁺/NO₃^? were observed as 8, 5, and 1.7 during daytime and 1.5, 0.4, and 0.8 during nighttime respectively. Such molar ratios confirmed high concentrations of sulphate (SO₄)^2? and low concentrations of nitrate (NO₃^?) during night time, thereby indicating different pathway of aerosol formation during day and night time. Surface morphology and elemental composition of aerosol samples showed various oval, globular, and platy shapes where the diameter varied from few nm to ~5 μm depending on their precursors. There were certain shapes like grossularite, irregular aggregate, grape-like, triangular, and flattened which indicate the crustal origin of aerosols and their possible role in SO₂ and NO₂ adsorption.     

Heavy metal fractionation in roof run off in Ile-Ife, Nigeria

Runoff was collected from three different roofing materials that are commonly used for roofing in Ile-Ife, Nigeria, between the months of June to August, 2004. The samples were collected in four geographical locations in the town. The run offs were analysed for pH, Temp, TDS, CI?, S0₄ ^2?, PO₄ ^3? N0₃ ^2?, EC and some heavy metals both as regards total, dissolved and particulate fractions. Analysis of the heavy metals was done using flame Atomic Absorption Spectrophotometer. The quantity of these parameters varies with the different roofing materials. In terms of dissolved metals, Fe is the most predominant metal with mean values 0.59 ± 0.29, 0.82 ± 0.14, and 1.04 ± 0.27 mg/L for asbestos, ceramic tiles and metal sheets respectively. The tendency of the roofing materials to release dissolved metals is arranged as follows: Zn, Cr and Fe (metal sheet > Ceramic > asbestos); Cd and Pb (asbestos > ceramic > metal sheet). In terms of particulate metals, the concentration of Cd and Pb are higher in the asbestos than other roofing stuffs. The sequence of their predominance in asbestos is as follows: Pb (0.83±0.55 mg/L) > Cd (0.29 ± 0.07 mg/L). In all the roofs, both particulate and dissolved metals except Zn exceeded WHO permissible limits for drinking water. The high levels of the metals obtained in this study may likely result in consumer complaints since some of the metals are not only carcinogenic but are also liable of impacting bad taste in water.     

The influence of hydrology and climate on the isotope geochemistry of playa carbonates: a study from Pilot Valley, NV, USA

Carbonates often accompany lake and lake‐margin deposits in both modern and ancient geological settings. If these carbonates are formed in standing water, their stable isotope values reflect the aquatic chemistry at the time of precipitation and may provide a proxy for determining regional hydrologic conditions. Carbonate rhizoliths and water samples were collected from a playa lake in eastern Nevada. Pilot Valley (～43°N) is a closed‐basin, remnant playa from the Quaternary desiccation of palaeo‐Lake Bonneville. Water is added to the playa margin by free convection of dense brines to the east and forced convection of freshwater off the alluvial fan to the west. Both freshwater and saline springs dot the playa margin at the base of an alluvial fan. Water samples collected from seven springs show a range from ?16 to ?0·2‰ (Vienna Standard Mean Ocean Water), and are consistent with published values. The δ¹⁸O_calcite values from rhizolith samples range from ?18·3 to ?6·7‰ (Vienna Pee Dee Belemnite), and the average is ?12‰ V‐PDB (1 ? σ SD 2‰). With the exception of samples from Little Salt Spring, the range in the δ¹⁸O_calcite values collected from the rhizoliths confirms that they form in equilibrium with ambient water conditions on the playa. The initial geochemical conditions for the spring waters are dictated by local hydrology: freshwater springs emerge in the northern part of the basin to the east of a broad alluvial fan, and more saline springs emerge to the south where the influence of the alluvial fan diminishes. Rhizoliths are only found near the southern saline springs and their δ¹³C_calcite values, along with their morphology, indicate that they only form around saltgrass (Distichlis sp.). As the residence time of water on the playa increases, evaporation, temperature change and biological processes alter the aquatic chemistry and initiate calcite precipitation around the plant stems. The range in δ¹⁸O_calcite values from each location reflects environmental controls (e.g. evaporation and temperature change). These rhizoliths faithfully record ambient aquatic conditions during formation (e.g. geochemistry and water depth), but only record a partial annual signal that is constrained by saltgrass growth and the presence of standing water on the playa margin.     

Organic compounds in produced waters from coalbed natural gas wells in the Powder River Basin,Wyoming, USA

The organic composition of produced water samples from coalbed natural gas (CBNG) wells in the Powder River Basin, WY, sampled in 2001 and 2002 are reported as part of a larger study of the potential health and environmental effects of organic compounds derived from coal. The quality of CBNG produced waters is a potential environmental concern and disposal problem for CBNG producers, and no previous studies of organic compounds in CBNG produced water have been published. Organic compounds identified in the produced water samples included: phenols, biphenyls, N-, O-, and S-containing heterocyclic compounds, polycyclic aromatic hydrocarbons (PAHs), aromatic amines, various non-aromatic compounds, and phthalates. Many of the identified organic compounds (phenols, heterocyclic compounds, PAHs) are probably coal-derived. PAHs represented the group of organic compounds most commonly observed. Concentrations of total PAHs ranged up to 23 μg/L. Concentrations of individual compounds ranged from about 18 to <0.01 μg/L. Temporal variability of organic compound concentrations was documented, as two wells with relatively high organic compound contents in produced water in 2001 had much lower concentrations in 2002.