Environmental occurrence,origin, physical and geochemical properties,and carcinogenic potential of erionite near San Miguel de Allende,Mexico

Detailed geologic surveys and different microscopic and analytical techniques were conducted near Tierra Blanca de Abajo where lung cancer and malignant mesothelioma (MM) are the primary causes of death. Results show that erionite-K occurs as a diagenetic product in altered Oligocene–Miocene rhyolitic tuffs. The microscopic structure of erionite minerals shows concentrations of individual fibers in the range of 0.14–0.547 μm in diameter and 2.81–50 μm in length, with a few “bundles” about 0.2–2.5 μm wide by 10–50 μm long. Chemical properties of erionite show Si/Al in the range of 3.23–3.58 (at.%) and T _Si in the range of 0.76–0.78 (at.%). Potassium is the dominant cation (K > Ca > Mg > Fe). Associated minerals are heulandite, clinoptilolite, quartz, sanidine, anorthite, smectite and opal. This mineral assemblage formed in the lower part of an open catchment, where bicarbonate-rich (T > 30 °C, pH > 8) groundwater discharge conditions prevailed in the past. The physical and chemical characteristics of erionite near San Miguel de Allende are similar to those of erionite from the Cappadocian region of Turkey where erionite is associated with MM. The presence of erionite and the type of respiratory diseases that occur in the village strongly suggest the need for detailed health-based studies in the region. Pliocene–Holocene fine-grain deposits, used in the past for the construction of adobe-houses and exposed in recreational areas, also contain erionite associated with erosion and alluvial transport from the rhyolitic tuffs, potentially affecting more than 13 villages located downstream toward the Allende Dam.     

Hair burning and liming in tanneries is a source of pollution by arsenic,lead, zinc,manganese and iron

Heavy metals in the environment may be toxic for human and animals. Tanneries are a source of pollution by heavy metals. There is little information on heavy metals pollution in tanneries, especially on metals produced by the process of hair burning and liming. Liming is the first stage of chemical treatment where animal hair or wool is removed with sodium sulphide and calcium oxide. Here we studied cow, goat, buffalo and sheep hair, conventional liming agents and liming wastewaters from several sources. Samples were acid-digested and aliquots were analysed by atomic absorption spectroscopy following APHA standard method to measure concentrations of arsenic, lead, cadmium, zinc, manganese and iron. Results show that the range of metal contents in hair or wool and liming agents are 1.3–8.2 mg/kg for arsenic, 0.02–21.8 mg/kg for lead, 17.7–121.0 mg/kg for manganese, 7.3–141.1 mg/kg for zinc and 119.6–10613.8 mg/kg for iron. Liming wastewaters contain 1.9–5.6 µg/L arsenic, 0.03–6.05 µg/L lead, 38.6–139.0 µg/L manganese, 144.0–171.5 µg/L zinc and 399.5–1069.0 µg/L iron. Cadmium was below detection limits. This is the first investigation that reveals that hair burning liming operation is a potential source of heavy metals in the environment.     

Seasonal variation assessment of impact of industrial effluents on physicochemical parameters of surface water of River Challawa,Kano, Nigeria

The physicochemical characteristics of the River Challawa in the Kumbotso Local Government Area of Kano State were studied across four seasons (warm and dry, cold and dry, hot and dry, and warm and wet seasons) between October 2006 and August 2008. Physicochemical parameters like pH, electrical conductivity (EC), total dissolved solids (TDSs), total suspended solids (TSS), alkalinity, turbidity, hardness, dissolved oxygen (DO), biological oxygen demand (BOD), chemical oxygen demand (COD), ammonia, chloride, nitrate, sulfate, and phosphate were analyzed and compared with standard permissible limits. The mean range of parameters determined across the seasons revealed: 8.36–8.59 for pH; 209.57–335.27 µS cm^?1 for EC; 134.05–208.5 mg L^?1 for TDS; 182.4–273.45 mg L^?1 for TSS; 125.3–276.07 mg L^?1 for hardness; 16.11–40 mg L^?1 of CaCO₃ for alkalinity; 2.76–3.78 mg L^?1 for DO; 1.9–43.33 mg L^?1 for BOD; 231.67–310.06 mg L^?1 for COD; 221.67–441.67 mg L^?1 for turbidity; 17.98–35.89 mg L^?1 for chloride; 5.12–8.89 mg L^?1 for nitrate; 37–558.83 mg L^?1 for sulfate; and 0.47–0.81 mg L^?1 for phosphate. Data showed that all parameters determined were significantly different among the various sampled sites across seasons. With the exception of COD, EC, and phosphate, all other parameters determined were within the WHO and USPH standard limits.     

Persistent organochlorine pesticides,polychlorinated biphenyls,polybrominated diphenyl ethers in fish from coastal waters off Savannah,GA, USA

Contamination profiles of organochlorine pesticides (OCPs), polychlorinated biphenyls (PCBs), and polybrominated diphenyl ethers (PBDEs) were determined in six fish species from three selected regions along coastal waters off Savannah, GA, USA. Concentrations of PCBs were predominant (12–493 ng g^?1 lw) followed by PBDEs (10–337 ng g^?1 lw), OCPs such as DDTs (2.7–153 ng g^?1 lw), chlordanes (3.8–34 ng g^?1 lw), cyclodienes (<0.1–35 ng g^?1 lw), mirex (<0.1–8.6 ng g^?1 lw), γ-hexachlorocyclohexane (<0.1–1.4 ng g^?1 lw), and hexachlorobenzene (<0.1–0.68 ng g^?1 lw). The results indicated no region-specific difference in the contaminants however inter-species as well as intra-species differences were evident. Comparison of DDTs, PCBs, and PBDEs profiles in fish with those from other countries revealed that fish from coastal waters off Savannah contained relatively less concentrations of PCBs and chlorinated pesticides, while PBDE concentrations were comparable or even higher than fish samples from other regions. Polychlorinated biphenyl congeners and chlorinated pesticide tempoal trend data exhibited no increase of contamination levels. The levels of PCBs and chlorinated pesticides in fish from Savannah coastal waters were below the Food and Drug Administrations (FDA) established limits for human consumption.     

Polychlorinated-dibenzo-p-dioxins, -dibenzofurans and -dioxin-like polychlorinated biphenyls in aquatic organisms from lake Kasumigaura,Japan

Polychlorinated-dibenzo-p-dioxins (PCDDs), -dibenzofurans (PCDFs) and -dioxin-like polychlorinated biphenyls (DLPCBs) were determined in aquatic wildlife of Kasumigaura Lake (KUL), Japan from 1978 to 2001. Two plankton species elucidated several fold greater concentrations (2400–7800) than small tiger fish (310–6500), shrimp (160–1100), and three large fish namely, black bass (120–240), carp (94–120) and mullet (54) on pg/g fat. PCDD homologues were predominant accumulants with >68–<95% contribution and remaining was shared by PCDFs. Accumulation, non-ortho DLPCBs in plankton (3500–9200), shrimp (1600–8600) and small fish (2000–8800) and large fish (1300–3900) on ng/g fat basis were several orders magnitude greater than PCDD/DFs. The mono-ortho DLPCBs in large fish species were 23?000–83?000?ng/g fat and which it is accounted 94.3–95.9% the total dioxin-like PCBs accumulation. Temporal trends of PCDDs, PCDFs, non-ortho PCBs and TEQ in shrimp and small tiger fish were varied. The mullet had minimum toxic equivalency “TEQ” (14?pg?TEQ/g) followed by plankton Neomysis intermedia (25?pg?TEQ/g), small tiger fish (mean: 33, ranges 14–66?pg?TEQ/g), plankton Cyclopus vicinus (34?pg?TEQ/g), carp (mean: 35, ranges 32–38?pg?TEQ/g), shrimp (mean: 38, ranges 11–68?pg?TEQ/g) and black bass (mean: 59, ranges 38–79?pg?TEQ/g) on fat basis. In all the samples, PCDD was predominant TEQ contributor followed by PCDFs and DLPCBs. The contribution of mono-ortho DLPCBs to the total TEQ was 0.52–0.92 in large fish.     

Chemical fractionation of metals in core sediments of Orogodo River,southern Nigeria

Sequential chemical extraction of metals (Cu, Ni, Mn, Fe, Pb, Cr, and Zn) from core sediments of the Orogodo River was carried out with a view of providing information on the phase distribution of these metals with respect to depths and seasons. The results indicate that copper was speciated into organic matter/sulfide, Fe–Mn oxides, and residual forms at 0–5?cm depth while at deeper sections copper was predominantly in the residual form. Nickel was speciated mainly into Fe–Mn oxides and residual forms. The average of lead in various particulate phases of the sediment are 0–100% for residual; 0–8% for carbonate; 0–16.2% for exchangeable; 0–10% for organic matter/sulfide form and 22–56% for Fe–Mn oxides bound metals. Manganese was speciated into exchangeable (10–36%) and Fe–Mn oxides bound (10–48%) at the surface layers of 0–20?cm depths and predominantly in the residual form in deeper sections implying partitioning into trioctahydral clay and/or well-defined crystalline oxides. Iron was predominantly in the Fe–Mn oxides and residual fractions, less than 8% in the organic fraction, and 24.4–37.3% in the exchangeable and carbonates fractions at the surface. The percentage contributions of iron in the exchangeable and carbonate fractions decreased to 3.2% at 55–60?cm depth. The amount of chromium in the exchangeable fraction ranged from 0% to 7% for exchangeable; 0–26.5% for organic matter/sulfide bound; 3.8–17.9% for Fe–Mn oxides; and 46.8–100% for residual fraction. The mobility factors of the metals indicated that these metals were relatively mobile at top sections as compared with deeper sections. The overall picture of metal mobility and availability indicates potential contamination risk by Fe, Zn, Mn, and Pb in the Orogodo River sediment system.     

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.     

Bioreduction of hexavalent chromium by Exiguobacterium indicum strain MW1 isolated from marine water of Paradip Port,Odisha, India

Hexavalent chromium-tolerant (1500?mg/L) bacterium MW1 was isolated from harbour water of Paradip Port and evaluated for Cr(VI) reduction potential. The isolate was identified as Exiguobacterium indicum by biochemical and 16S rRNA gene sequence methods. Salt tolerance of the bacterium was evaluated in a wide range of NaCl concentrations (0.5–13%, w/v). The Cr(VI) reduction of the strain was evaluated and optimised with varied Cr(VI) concentrations (100–1000?mg/L), pH (5.0–9.0), temperature (30–40°C) and shaking velocity (100–150?rpm) in two different minimal media (M9 and Acetate). Under optimised conditions, after 192?h of incubation nearly 92%, 50% and 46% reduction in the M9 minimal medium and 91%, 47% and 40% reduction in the acetate minimal medium were observed for 100, 500 and 1000?mg/L of Cr(VI), respectively. The exponential rate equation for Cr(VI) reduction yielded higher rate constant value, that is, 1.27?×?10^?2?h^?1 (M9) and 1.17?×?10^?2?h^?1 (Acetate) in case of 100?mg/L and became lower for 500 and 1000?mg/L Cr(VI) concentrations. Further, the association of bacterial cells with reduced product was ascertained by Fourier transform infrared spectrometer, UV–Vis–DRS and field-emission scanning electron microscope–energy-dispersive X-ray analyses. The above study suggests that the higher reducing ability of the marine bacterium E. indicum MW1 will be suitable for Cr(VI) reduction from saline effluents.     

Platinum pollution in road dusts,roadside soils,and tree barks in Seoul,Korea

This study presents the level of platinum in urban environment in and around Seoul, the capital city of Korea. Road dust, roadside soil, and tree bark samples were collected from the sites of various traffic volumes and from control sites in the suburbs. The above samples were analyzed for Pt by ICP-MS and other heavy metals by ICP-OES. Platinum levels in road dusts and roadside soils from Seoul were in the range of 3.8–444 ng/g (av. 115.0 ng/g) and 0.7–221 ng/g (av. 49.7 ng/g), respectively, whereas those in the suburbs were in the range of 2.3–5.2 ng/g (av. 3.9 ng/g) in road dusts and 0.4–5.1 ng/g (av. 2.4 ng/g) in roadside soils. The highest Pt levels in road dusts were found from major roads with high traffic volume. The remarkable difference in average Pt level between heavy traffic roads (av. 132.2 ng/g) and light traffic roads (av. 22.8 ng/g) reflects that an important source of Pt in roadside environment is automobile catalytic converter. High Pt level in road dust was found from the site of erratic stop–start driving condition, for example, 178 ng/g Pt in road dust around a vehicle crossing gate. Platinum level in tree barks ranged from 0.9 to 4.5 ng/g, which indicates the existence of Pt-containing particulate matter in the atmosphere. Road dusts with high Pt level were enriched in traffic-related heavy metals.

     

Platinum pollution in road dusts,roadside soils,and tree barks in Seoul,Korea

This study presents the level of platinum in urban environment in and around Seoul, the capital city of Korea. Road dust, roadside soil, and tree bark samples were collected from the sites of various traffic volumes and from control sites in the suburbs. The above samples were analyzed for Pt by ICP-MS and other heavy metals by ICP-OES. Platinum levels in road dusts and roadside soils from Seoul were in the range of 3.8–444 ng/g (av. 115.0 ng/g) and 0.7–221 ng/g (av. 49.7 ng/g), respectively, whereas those in the suburbs were in the range of 2.3–5.2 ng/g (av. 3.9 ng/g) in road dusts and 0.4–5.1 ng/g (av. 2.4 ng/g) in roadside soils. The highest Pt levels in road dusts were found from major roads with high traffic volume. The remarkable difference in average Pt level between heavy traffic roads (av. 132.2 ng/g) and light traffic roads (av. 22.8 ng/g) reflects that an important source of Pt in roadside environment is automobile catalytic converter. High Pt level in road dust was found from the site of erratic stop–start driving condition, for example, 178 ng/g Pt in road dust around a vehicle crossing gate. Platinum level in tree barks ranged from 0.9 to 4.5 ng/g, which indicates the existence of Pt-containing particulate matter in the atmosphere. Road dusts with high Pt level were enriched in traffic-related heavy metals.     

Evidence of new particle formation during post monsoon season over a high-altitude site of the Western Ghats,India

The formation of ultrafine particles, their growth, and associated characteristic features has been studied during new particle formation events over a high-altitude station of the Western Ghats during the 2014 post-monsoon season. Most of the events were observed during noon time where particle bursts in the nucleation-mode size range from 5 to 25 nm followed by sustained growth in size. This phenomenon persists for ～4–8 h with a growth rate of 1–2 nm h^–1. Peak concentrations of nucleation-mode particles during the event generally vary from 2300 to 5000 cm^–3. The mean growth rate is 1.4 ± 0.42 nm h^–1, particle formation rate is 1.14 ± 0.22 cm^–3 s^–1, coagulation sink is 0.35 ± 0.22 cm^–3 s^–1, and condensational sink is 15.4 ± 2.6?×?10^–3 s^–1. All these values are comparable with earlier results from Indian region. Comparison of size-segregated particle number concentration during days of new particle formation events and those without new particle formation were carried out showing a distinct variation in nucleation and Aitken mode with least variability associated with the accumulation mode.     

Seasonal variation of heavy metals in sediment of Lake Ulansuhai,China

Sediment samples were collected from 10 sites in Lake Ulansuhai during summer and winter 2009 to reveal seasonal variations in sediment heavy metal levels. The geoaccumulation index (GI) was calculated to assess the severity of metal pollution. The GI values suggest that, in winter, the lake sediments were polluted slightly with Cu (GI=0.66–1.34), Zn (GI=0.59–1.35), Cr (GI=0.49–0.82) and Pb (GI=0.60–0.96), and moderately with Cd (GI=1.03–4.23). The degree of pollution was higher in winter than in summer. By contrast, the degree of pollution was higher in summer than in winter for Hg and As. Correlation analysis can be used to identify factors influencing seasonal variations in heavy metals. The concetrations of Cu, Zn, Pb, Cr and Cd were negatively correlated with water temperature and hydrodynamic conditions, but positively correlated with organic matter concentration in the sediments and with a sediment particle size of<63 μm (p<0.01). Meanwhile, Hg and As concentrations were affected by redox state and salinity. Among the metals tested, Hg and Cd posed a more serious pollution risk.     

Acetaldehyde contamination of water,alcoholic, and non-alcoholic beverages stored in glass or plastic bottles

Acetaldehyde is a naturally found chemical in food substances characterized by a fruity aroma at low levels. However, high levels of acetaldehyde can add to or change the taste of foods and beverages. More importantly, acetaldehyde has recently been found to be possibly carcinogenic to humans (Group 2B). In this investigation, the amounts of acetaldehyde in several alcoholic and non-alcoholic beverages consumed in Greece, including red or white wine, retsina, tsipouro, grappa, fruit-based liqueurs, beers with different alcohol content as well as mineral water, soft drinks, and fruit juices were measured. The analytical method used is based on derivatization of acetaldehyde with 2,4-dinitrophenylhydrazine and its subsequent measurement using high performance liquid chromatography. High concentrations (median, min–max) were detected in grappa (29.4, 29.2–52.7 mg L^?1) and tsipouro (17.1, 0.8–55.6 mg L^?1), followed by beer (6.8, 6.7–6.9 mg L^?1) and red wine (3.7, 1.6–29.4 mg L^?1); the lowest levels were detected in soft drinks (0.067, 0.033–0.075 mg L^?1) and mineral water (0.04, 0.002--0.096 mg L^?1). Levels of acetaldehyde in retsina were very high (68.1, 63.9--68.3 mg L^?1) when after opening, the wine remained in plastic bottles for a long time, much higher than in samples taken from just opened bottles (7.2, 7.1–7.4 mg L^?1). The amount of acetaldehyde shows some positive correlation to the alcoholic content. These results suggest that regulatory measures and consumer guidance may be necessary for acetaldehyde in beverages.     

Distributions of total metals in the surface sediments of the Bandirma and Erdek Gulfs,Marmara Sea,Turkey

The aim of this study is to determine the contents of aluminum, iron, manganese, nickel, copper, zinc, chromium, cadmium, lead, and mercury in sediments at 1–30?m depths of the Band?rma and Erdek Gulfs in the Southern Inner Shelf of the Marmara Sea. Sediment samples were collected from different depths (1?m, 5?m, 10?m, 20?m, 30?m) at each region in February 2008. Primary hydrographic conditions, such as temperature (6.6–14.5°C), salinity (22.6–26.875 psu), percentage of dissolved oxygen saturation (35–83 %), and pH (8.0–8.4) were recorded for each sampling point. Moreover the total organic carbon (0.5–2.9%) and the total calcium carbonate contents (0.8–60%) of sediment samples were determined. In surface sediments of both gulfs, Pb (21–62?mg?kg^?1) and Cd (0.52–0.86?mg?kg^?1) contents were determined to be higher than the shale average (Pb 20?mg?kg^?1, Cd 0.2?mg?kg^?1) while the other metal contents were measured to be lower in general. On the other hand, generally Hg (0.06–1.1?mg?kg^?1) contents were higher than the shale average (0.3?mg?kg^?1)at all of the examined stations in the Band?rma Gulf and lower than the shale average in the Erdek Gulf.     

Identification of urinary metabolites in rats administered the fluorine-containing pyrethroids metofluthrin,profluthrin, and transfluthrin

The major metabolites in urine of rats administered the fluorine-containing pyrethroids transfluthrin, profluthrin, and metofluthrin, which are used widely recently as mosquito repellents or mothproof repellents, were identified to establish biological indexes for evaluating the absorption amounts of these pyrethroids in the general population. A single dose of 300?mg?kg^?1 body weight of each pyrethroid was separately administered intraperitoneally to male Sprague-Dawley rats and urine samples were collected until 24 hours after the administration. The metabolites identified by gas chromatography-mass spectrometry were as follows: 2,3,5,6-tetrafluorobenzyl alcohol, 2,3,5,6-tetrafluorobenzoic acid, and 3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylic acid (DCCA) for transfluthrin; 4-methyl-2,3,5,6-tetrafluorobenzyl alcohol, 4-methyl-2,3,5,6-tetrafluorobenzoic acid, 4-hydroxymethyl-2,3,5,6-tetrafluorobenzyl alcohol (HOCH₂–FB–Al), and 2,2-dimethyl-3-(1-propenyl)-cyclopropanecarboxylic acid (MCA) for profluthrin; 4-methoxymethyl-2,3,5,6-tetrafluorobenzyl alcohol, HOCH₂–FB–Al and MCA for metofluthrin. In addition, several compounds estimated to be metabolites were detected as follows: hydroxylated DCCA and its lactone for transfluthrin; 4-hydroxymethyl-2,3,5,6-tetrafluorobenzoic acid (HOCH₂–FB–Ac), hydroxylated MCA and its lactone for profluthrin; 4-methoxymethyl-2,3,5,6-tetrafluorobenzoic acid, HOCH₂–FB–Ac, hydroxylated MCA, and its lactone for metofluthrin. The pyrethroids administered underwent metabolic reactions such as ester hydrolysis and oxidation, and most of the metabolites were excreted as their conjugates into urine. These findings should be useful as basic data for evaluating the health effects of exposure to pyrethroids for the general population.     

Rapid changes in growth,condition, size and age of small pelagic fish in the Mediterranean

Since 2007, the ecosystem of the Gulf of Lions has shifted to a different regime, characterised by a low anchovy (Engraulis encrasicolus) and sardine (Sardina pilchardus) biomass and a remarkably high sprat (Sprattus sprattus) biomass. Surprisingly, the abundance and recruitment of anchovy and sardine remained high. To understand which processes (bottom-up or top-down control, etc.) could have caused this shift, we studied the changes in body condition, growth and size and age of anchovy, sardine and sprat over 1984–1985 and 1992–2012, using data from scientific surveys. The annual age structure of anchovy and sardine was estimated using Bayesian mixture models based on size frequency data with priors on the age–length relationship derived from independent otolith readings. The results indicated periods during which anchovy and sardine were in an average (1992–2004), good (2005–2007) or poor (2008–2012) overall state of condition. For sardine, the shift towards smaller fish observed during these past 4 years was explained by a combination of slower growth and the disappearance of older individuals (ages 2+). Despite the increase in biomass of sprat since 2008, indications were found that sprat was also smaller than in the past. As growth and condition decreased and overexploitation has not been documented or suspected for those three species in this area, we propose that the current decline in sardine and anchovy biomass could be due to qualitative and/or quantitative modifications in the planktonic production (i.e. a bottom-up control) or mass mortalities of adults due to an epidemic disease.     

Residues,half-life times,dissipation, and safety evaluation of the acaricide fenpyroximate applied on grapes

A validated high-performance liquid chromatography–diode array detector method for simultaneous determination of the acaricide fenpyroximate on grape was developed. Estimated limit of detection and limit of quantification for fenpyroximate were 0.01 and 0.05 mg kg^?1, respectively. The intra- and inter-day precisions performed with relative standard deviation were better than 9.3% and 8%, respectively, while recoveries were in the range of 88.5%–100.4%. Residue levels of fenpyroximate in grape samples collected 10 days after field application were below the established maximum residue level values. The dissipation rates of fenpyroximate were described using first-order kinetics and its half-life, were approximately 3.5 days in grape. This study provides basic information for developing regulations to safeguard the use of fenpyroximate in grapes and prevent any potential health concerns for consumers.     

Preparation,characterization, and kinetics of nanoscale iron in nitrate nitrogen removal from polluted water

The aim of this study was to examine the production of nanoscale ions via the liquid phase reduction method and the effectiveness of the removal of nitrate nitrogen (NO₃^?–N) as well as measure the products and kinetics of the reactions. The nanoparticles obtained were approximately 50 nm in diameter and the main component was iron (Fe). This custom-made nanoscale Fe was highly positively charged, and reacted rapidly with NO₃^?–N in oxygen-free and neutral conditions at room temperature. A 90% removal rate was achieved when the reaction occurred for 30 min in simulation sample water with vigorous shaking at 250 r/min at NO₃^?–N concentrations of 30, 50, 80 or120 mg N/L. The nanometer Fe dosage was maintained throughout the experiment at 4 g/L. A first-order kinetics equation was applied to the obtained experimental data which followed a pseudo first-order reaction. Data demonstrated that the removal of nitrate nitrogen from polluted groundwater using a nanoscale Fe iron was effective and rapid.     

Elemental composition of particulate matters around Urmia Lake,Iran

Atmospheric particulate matters and their elements were concurrently measured at two sites located in the north and southeast parts of Urmia Lake from January to September 2013. At both sampling sites, average concentrations of total suspended particulate, particles with the aerodynamic diameter of smaller than 10 µm, smaller than 2.5 µm, and smaller than 1 µm were 260 ± 106, 180 ± 73, 30 ± 8, and 25 ± 7 µg m^?3, respectively. The analyzed water soluble ions accounted for approximately 11%–13% mass concentrations of total suspended particulate and 8%–9% of particles smaller than 10 µm, and the sum of the concentrations of the analyzed elements associated with both ranged from 9 to 41 µg m^?3 (6.5%–9.6% in mass) and 7 to 26 µg m^?3 (5.5%–11.3% in mass), respectively. Thus, particulate matter was composed of a complex mixture of minerals such as halite, quartz, gypsum, hexahydrite, and Bassanite.