Computer simulated versus observed NO2 and SO2 emitted from elevated point source complex

ISC-AERMOD dispersion model was used to predict air dispersion plumes from an diesel power plant complex. Emissions of NO₂and SO₂from stacks (5 numbers) and a waste oil incinerator were studied to evaluate the pollutant dispersion patterns and the risk of nearby population. Emission source strengths from the individual point sources were also evaluated to determine the sources of significant attribution. Results demonstrated the dispersions of pollutants were influenced by the dominant easterly wind direction with the cumulative maximum ground level concentrations of 589.86 μg/m³ (1 h TWA NO₂) and 479.26 μg/m³ (1 h TWA SO₂). Model performance evaluation by comparing the predicted concentrations with observed values at ten locations for the individual air pollutants using rigorous statistical procedures were found to be in good agreement. Among all the emission sources within the facility complex, SESB-Power (diesel power plant) had been singled out as a significant source of emission that contributed >85% of the total pollutants emitted.     

Assessment of environmental impact of open burning of scrap tyres on ambient air quality

Open burning of scrap (bicycle, motorcycle, car and truck) tyres (OBST) was simulated in the laboratory to investigate their impact on the ambient air quality. The tyre samples were burnt in combustion chamber, and gaseous pollutants (CO, NO₂ and SO₂) emitted were quantified, while concentrations and elemental compositions of emitted total suspended particulates (TSP) were determined. Emission level of SO₂ from all the tyre samples exceeded USEPA allowable (156.74 µg/m³) limit. CO due to car and truck tyres exceeded USEPA allowable (10,285.71 µg/m³) limit, while NO₂ concentration was below the allowable limit (56.33 µg/m³) only in bicycle tyre. 25% of all the gaseous pollutants emitted are within the Air Quality Index range of 101–150. TSP concentrations from all the tyre samples were higher than the Federal Ministry of Environment standard (250 µg/m³) for ambient TSP. There is strong correlation (R) of 0.885, 0.949 and 0.802 among all the gaseous (CO/NO₂, CO/SO₂ and NO₂/SO₂) pollutants, respectively, while the highest (0.999) and lowest (0.079) positive correlations were observed between Mg and Mn as well as Cd and Zn, respectively. The results of this study show that OBST emits hazardous pollutants, which pose serious threat to human health and environment.     

Ammonia emission from CO<Subscript>2</Subscript> capture pilot plant using aminoethylethanolamine

Amine post-combustion carbon capture technology is based on washing the flue gas with a solvent that captures CO₂. Thus, a small fraction of this solvent can be released together with the cleaned flue gas. This release may cause environmental concerns, both directly and indirectly through subsequent solvent degradation into other substances in the atmosphere. The paper presents the ammonia emission from CO₂ capture pilot plant (1 tonne CO₂ per day) using 40 wt% aminoethylethanolamine solvent, along with the efficiency of the water wash unit. In addition, the temperature effect of lean amine entering the absorber on ammonia emission was studied. Furthermore, the concentrations of other compounds such as SO₂, SO₃, NO₂, CS₂ and formaldehyde were monitored. The literature review on the NH₃ emission from a pilot plant using aminoethylethanolamine solvent has not been published. The results show that the main source of ammonia emission is the absorber and that emission (in the range 27–50 ppm) corresponds to typical NH₃ release from CO₂ capture pilot plant using an amine solvent. The emission of amines and amine degradation products is a complex phenomenon which is difficult to predict in novel solvents, and for this reason the significance of new solvents testing in a pilot scale has been highlighted.     

Atmospheric oxidation of the pyritic waste rock in Maardu, Estonia. 1 field study and modelling

 A field survey and modelling of the oxidation and carbonate buffering reactions inside the alum-shale-containing waste rock dumps located in Maardu, Estonia, was accomplished. In the slope areas, the shale has been altered at high temperatures due to the spontaneous combustion and the pyritic acidity has been eliminated through migration of SO_x gases out from the dump. In the central parts of the waste rock plateaus, low temperature pyrite oxidation fronts develop towards the dump depth and towards the centres of individual shale lumps. The main secondary phases precipitating in the weathering profile are gypsum, ferric oxyhydroxide, K-jarosite and smectite. The respective field data made it possible to calibrate the two-stage oxygen diffusion model and the characteristic pyrite oxidation rate 0.06–0.08 mol of pyrite reacted per kg of available water (pyrox/H₂O value) was estimated to describe the first tens of years of dump performance. The model is capable to compare different shale disposal strategies that are illustrated with two case scenarios. The buffering of sulphuric acid by Mg-calcite appears to be an incongruent reaction with gypsum precipitating that leads to the build-up of the high Mg/Ca ratio in the leachate. Application of the Mg/Ca method estimates the pyrox/H₂O value in the range of 0.05–0.14 mol/kg. Received: 26 January 1999 · Accepted: 23. February 1999     

A quantitative approach to the influence of pyrite separation on Cu-processing tailings: a case study at Reps,Mirdita district,Albania

Sulfide-rich tailings are a well-known environmental threat due to their production of acid drainage (AD) and release of potential toxic elements (PTE) to the local environment. The presence of heterogeneous materials produces complex environmental signatures and complicates the quantitative prediction of contamination. The present work provides a method of quantifying such heterogeneities, starting from mineral processing data of the Reps, Mirdita (Albania) site. A quantitative flow sheet (QF) method was applied to a selected dump site of the Mirdita copper mining district where secondary pyrite separation had been used in the past. The site is subject to long-lasting (10³ years) AD processes with significant release of PTE into the local environment. The tailings at the Reps site are divided into two classes based on the sulfide S content, respectively, represented by high-sulfide-content (S > 10 wt%) materials (hS) and low-sulfide-content (S < 3 wt%) material (lS). The reconstruction of the QF allowed us to identify the hS tailings as the discharge of single-flotation processing lines. This material accounts for about 82% of the total potential H₂SO₄ production, even though it represents < 20% of the entire tailing discard. The QF is a useful tool for the evaluation of heterogeneity and consequently for the modeling of waste management within abandoned sites and in working plants. Given a good quantification, heterogeneity can in fact support the setting of pyrite separation lines or the separate management of pyrite-rich tailing dumps.     

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.     

Assessment of soil carbon pool,carbon sequestration and soil CO<Subscript>2</Subscript> flux in unreclaimed and reclaimed coal mine spoils

Surface coal mining inevitably deforests the land, reduces carbon (C) pool and generates different land covers. To re-establish the ecosystem C pool, post-mining lands are often afforested with fast-growing trees. A field study was conducted in the 5-year-old unreclaimed dump and reclaimed coal mine dump to assess the changes in soil CO₂ flux and compared with the reference forest site. Changes in soil organic carbon (SOC) and total nitrogen stocks were estimated in post-mining land. Soil CO₂ flux was measured using close dynamic chamber method, and the influence of environmental variables on soil CO₂ flux was determined. Woody biomass C and SOC stocks of the reference forest site were threefold higher than that of 5-year-old reclaimed site. The mean soil CO₂ flux was highest in 5-year-old reclaimed dump (2.37 μmol CO₂ m^?2 s^?1) and lowest in unreclaimed dump (0.21 μmol CO₂ m^?2 s^?1). Soil CO₂ flux was highly influenced by environmental variables, where soil temperature positively influenced the soil CO₂ flux, while soil moisture, relative humidity and surface CO₂ concentration negatively influenced the soil CO₂ flux. Change in soil CO₂ flux under different land cover depends on plant and soil characteristics and environmental variables. The study concluded that assessment of soil CO₂ flux in post-mining land is important to estimate the potential of afforestation to combat increased emission of soil CO₂ at regional and global scale.     

Light Rare Earth Elements enrichment in an acidic mine lake (Lusatia,Germany)

The distribution of Rare Earth Elements (REE) was investigated in the acidic waters (lake and groundwater) of a lignite mining district (Germany). The Fe- and SO₄-rich lake water (pH 2.7) displays high REE contents (e.g. La∼70 μg/l, Ce∼160 μg/l) and an enrichment of light REE (LREE) in the NASC normalised pattern. Considering the hydrodynamic model and geochemical data, the lake water composition may be calculated as a mixture of inflowing Quaternary and mining dump groundwaters. The groundwater of the dump aquifer is LREE enriched. Nevertheless, the leachates of dump sediments generally have low REE contents and display flat NASC normalised patterns. However, geochemical differences and REE pattern in undisturbed lignite (LREE enriched pattern and low water soluble REE contents) and the weathered lignite of the dumps (flat REE pattern and high water soluble REE contents) suggest that lignite is probably the main REE source rock for the lake water.     

Employing a novel nanocatalyst (Mn/Iranian hematite) for oxidation of SO<Subscript>2</Subscript> pollutant in aqueous environment

In this project, the oxidation of SO₂ pollutant by Mn/Iranian hematite (Mn/IH) as a novel nanocatalyst in aqueous solution was investigated and followed by conductometry in a semi-batch reactor. The removal of SO₂ gas is very important for decreasing the environmental pollution. The Mn/IH was prepared by coprecipitation method, and a novel way was used for converting SO₂ to sulfuric acid as an energy source. The characterization of catalyst was determined by X-ray diffraction, energy-dispersive X-ray spectroscopy, field emission scanning electron microscopy and X-ray fluorescence techniques. A Box–Behnken design was used to reduce the number of test runs and optimize the influencing factors such as the amount of nanocatalyst, temperature and the reaction time in oxidation of SO₂. The graphical counter plots and response surface were used to determine the optimum conditions. Analysis of variance showed a high determination coefficient value (\(R^{2} = 0.9999\), \(R_{\text{adj}}^{2} = 0.9996\) and \(R_{\text{pred}}^{2} = 0.9980\) for oxidation of SO₂) and satisfactory prediction second-order regression model. Based on the optimum results, the maximum efficiency for oxidation of SO₂ was 90.67%, and it was achieved at initial temperature of 286.03 K, concentration of Mn/IH at 951.11 mg/l and 35.75 min of reaction. The results showed that the temperature had the most significant effect on SO₂ oxidation compared with the other two variables.     

Estimation of atmospheric iodine emission from coal combustion

Coal combustion is the primary anthropogenic source of atmospheric iodine, which has important environmental and health effects. The iodine distribution in Chinese coals and the atmospheric iodine emission factors of coal-fired boilers are studied to estimate the iodine atmospheric flux from coal combustion in China from 1995 to 2009. The national average iodine content weighted by coal yield fluctuated from 2.61 mg kg^-1 in 1995 to 2.09 mg kg^-1 in 2009, recording an annual decline of 1.42 %. By establishing a monitoring program, iodine distribution in coal by-products after the coal is consumed in combustors is measured, and atmospheric iodine emission factors by sectors are calculated. Based on the coal consumption by sectors, the annual atmospheric iodine emission from coal combustion in China increased at an annual rate of 4.3 % from 3031.1 tons in 1995 to 4872.6 tons in 2009. Anthropogenic atmospheric iodine emission is significantly underestimated, and its environmental and health effects must be given more attention.     

Improving microbial oil production with standard and native oleaginous yeasts by using Taguchi design

Production of microbial oil has attracted a great attention in recent years. The potential of lipid production by the yeast strains is the reason for using microorganisms for biodiesel production. Microbial lipid has high similarity to the oil obtained from plants and animals in type and composition. Production of oil from yeasts must be economical, so optimization of the cultivation condition to reach higher production must be done. Native oleaginous yeast, Cryptococcus albidus, was isolated from soil by the nitrogen-limited medium and screened by Nile red staining. Yarrowia lipolytica DSM 8218 was used for lipid production as a standard strain. C. albidus was an excellent oleaginous yeast, and the lipid quantity, dry biomass and lipid productivity of this strain were 11.81 g/l, 19.65 g/l and 60.1 %, respectively, in shaking flask cultivation at 150 rpm and 25 °C in nitrogen-limited medium containing per liter 75 g glucose, 1 g (NH₄)₂SO₄, 1 g yeast extract, 3 g KH₂PO₄, 1.5 g MgSO₄.7H₂O, 0.15 g CaCl₂, 0.06 g MnSO₄.H₂O, 0.02 g ZnSO₄.7H₂O and 0.15 g FeCl₃.6H₂O with pH adjusted to 6.5. Fourier transform infrared spectroscopy was used for analyzing and confirming the production of microbial oil in this study.     

Mass-size distribution of PM10 and its characterization of ionic species in fine (PM2.5) and coarse (PM10−2.5) mode, New Delhi, India

Size distribution of PM₁₀ mass aerosols and its ionic characteristics were studied for 2 years from January 2006 to December 2007 at central Delhi by employing an 8-stage Andersen Cascade Impactor sampler. The mass of fine (PM_2.5) and coarse (PM_10?2.5) mode particles were integrated from particle mass determined in different stages. Average concentrations of mass PM₁₀ and PM_2.5 were observed to be 306 ± 182 and 136 ± 84 μg m^?3, respectively, which are far in excess of annual averages stipulated by the Indian National Ambient Air Quality Standards (PM₁₀: 60 μg m^?3 and PM_2.5: 40 μg m^?3). The highest concentrations of PM_10?2.5 (coarse) and PM_2.5 (fine) were observed 505 ± 44 and 368 ± 61 μg m^?3, respectively, during summer (June 2006) period, whereas the lower concentrations of PM_10?2.5 (35 ± 9 μg m^?3) and PM_2.5 (29 ± 13 μg m^?3) were observed during monsoon (September 2007). In summer, because of frequent dust storms, coarse particles are more dominant than fine particles during study period. However, during winter, the PM_2.5 contribution became more pronounced as compared to summer probably due to enhanced emissions from anthropogenic activities, burning of biofuels/biomass and other human activities. A high ratio (0.58) of PM_2.5/PM₁₀ was observed during winter and low (0.24) during monsoon. A strong correlation between PM₁₀ and PM_2.5 (r ² = 0.93) was observed, indicating that variation in PM₁₀ mass is governed by the variation in PM_2.5. Major cations (NH₄ ⁺, Na⁺, K⁺, Ca²⁺ and Mg²⁺) and anions (F^?, Cl^?, SO₄ ^2? and NO₃ ^?) were analyzed along with pH. Average concentrations of SO₄ ^2? and NO₃ ^? were observed to be 12.93 ± 0.98 and 10.33 ± 1.10 μg m^?3, respectively. Significant correlation between SO₄ ^2? and NO₃ ^? in PM_1.0 was observed indicating the major sources of secondary aerosol which may be from thermal power plants located in the southeast and incomplete combustion by vehicular exhaust. A good correlation among secondary species (NH⁺, NO₃ ^? and SO₄ ^2?) suggests that most of NH₄ ⁺ is in the form of ammonium sulfate and ammonium nitrate in the atmosphere. During winter, the concentration of Ca²⁺ was also higher; it may be due to entrainment of roadside dust particles, traffic activities and low temperature. The molar ratio (1.39) between Cl^? and Na⁺ was observed to be close to that of seawater (1.16). The presence of higher Cl^? during winter is due to western disturbances and probably local emission of Cl^? due to fabric bleaching activity in a number of export garment factories in the proximity of the sampling site.     

The thermal stability of sideronatrite and its decomposition products in the system Na2O–Fe2O3–SO2–H2O

The thermal stability of sideronatrite, ideally Na₂Fe³⁺(SO₄)₂(OH)·3(H₂O), and its decomposition products were investigated by combining thermogravimetric and differential thermal analysis, in situ high-temperature X-ray powder diffraction (HT-XRPD) and Fourier transform infrared spectroscopy (HT-FTIR). The data show that for increasing temperature there are four main dehydration/transformation steps in sideronatrite: (a) between 30 and 40 °C sideronatrite transforms into metasideronatrite after the loss of two water molecules; both XRD and FTIR suggest that this transformation occurs via minor adjustments in the building block. (b) between 120 and 300 °C metasideronatrite transforms into metasideronatrite II, a still poorly characterized phase with possible orthorhombic symmetry, consequently to the loss of an additional water molecule; X-ray diffraction data suggest that metasideronatrite disappears from the assemblage above 175 °C. (c) between 315 and 415 °C metasideronatrite II transforms into the anhydrous Na₃Fe(SO₄)₃ compound. This step occurs via the loss of hydroxyl groups that involves the breakdown of the [Fe³⁺(SO₄)₂(OH)] _∞ ^2? chains and the formation of an intermediate transient amorphous phase precursor of Na₃Fe(SO₄)₃. (d) for T > 500 °C, the Na₃Fe(SO₄)₃ compound is replaced by the Na-sulfate thenardite, Na₂SO₄, plus Fe-oxides, according to the Na₃Fe³⁺(SO₄)₃ → 3/2 Na₂(SO₄) + 1/2 Fe₂O₃ + SO_x reaction products. The Na–Fe sulfate disappears around 540 °C. For higher temperatures, the Na-sulfates decomposes and only hematite survives in the final product. The understanding of the thermal behavior of minerals such as sideronatrite and related sulfates is important both from an environmental point of view, due to the presence of these phases in evaporitic deposits, soils and sediments including extraterrestrial occurrences, and from the technological point of view, due to the use of these materials in many industrial applications.     

Flux of nutrients and heavy metals from the Melai River sub-catchment into Lake Chini, Pekan, Pahang, Malaysia

This study was carried out to determine the flux of nutrients and heavy metals from the Melai sub-catchment into Lake Chini through the process of erosion. Melai River is one of the seven feeder rivers that contributed to the present water level of Lake Chini. Three properties of soils, such as particle size, organic matter content, and soil hydraulic conductivity and three chemical soil properties, such as available nutrients, dissolved nutrients, and heavy metals, were analyzed and interpreted. Potential soil loss was estimated using the revised universal soil loss equation model. The results show that the soil textures in the study area consist of clay, silty clay, clay loam, and sandy silt loam. The organic matter content ranges from 3.40 to 9.92 %, while the hydraulic conductivity ranges from 5.2 to 25.3 cm/h. Mean values of available P, K, and Mg amount was 8.5 ± 3.7 μg/g, 24.5 ± 3.4 μg/g, and 20.7 ± 18.6 μg/g, respectively. The highest concentration of soluble nutrients was SO ₄ ^?2 (815.8 ± 624.1 μg/g), followed by NO₃ ^?-N (295.5 ± 372.7 μg/g), NH₄ ⁺-N (24.5 ± 22.1 μg/g) and PO₄ ^3? (2.0 ± 0.8 μg/g). The rainfall erosivity value was 1658.7 MJ mm/ha/h/year. The soil erodibility and slope factor ranges from 0.06 to 0.26 ton h/MJ/mm and 7.63 to 18.33, respectively. The rate of soil loss from the Melai sub-catchment in the present condition is very low (0.0028 ton/ha/year) to low (18.93 ton/ha/year), and low level flow of nutrients and heavy metals, indicating that the Melai River was not the contaminant source of sediments, nutrients, and heavy metals to the lake.     

Tree-ring growth recovers,but δ13C and δ15N do not change,after the removal of point-source air pollution: a case study for poplar (Populus cathayana) in northwestern China

Pollution from urban centers and fossil fuel combustion can decrease forest growth and interfere with physiological processes. To evaluate whether tree growth and the carbon isotope ratio (δ¹³C) and nitrogen isotope ratio (δ¹⁵N) in tree rings can serve as proxies for air pollution, this study compared these indices for poplar (Populus cathayana) growing at urban and suburban locations in Lanzhou, in northwestern China. Basal area increment values were much lower at the urban site than in the suburbs from 1985 to 2009, were negatively correlated with NO₂ (r = ?0.56, p < 0.01) and SO₂ (r = ?0.52, p < 0.05) emissions from 1990 to 2009, and increased abruptly after the Lanzhou urban steel factory closed. Urban tree-ring δ¹³C values were not significantly correlated with NO₂ and SO₂ concentrations, and did not differ significantly between the two sites, indicating that other environmental effects (such as precipitation) masked the pollution effects. Tree-ring δ¹⁵N values in the urban samples were much higher than the suburban values. Such differences may be attributable to uptake of ¹⁵N-enriched compounds caused by a higher urban N deposition rate. Tree growth is a promising tool for detecting ecophysiological responses of trees to both diffuse and point-source air pollution, but δ¹³C and δ¹⁵N in poplar were not sensitive to point-source air pollution in a heavily polluted environment.     

Variability in Concentrations and Fluxes of Methane in the Indian Estuaries

In order to examine the fluxes of methane (CH₄) from the Indian estuaries, measurements were carried out by collecting samples from 26 estuaries along the Indian coast during high discharge (wet) and low water discharge (dry) periods. The CH₄ concentrations in the estuaries located along the west coast of India were significantly higher (113?±?40 nM) compared to the east coast of India (27?±?6 nM) during wet and dry periods (88?±?15 and 63?±?12 nM, respectively). Supersaturation of CH₄ was observed in the Indian estuaries during both periods ((0.18 to 22.3?×?10³ %). The concentrations of CH₄ showed inverse relation with salinity indicating that freshwater is a significant source. Spatial variations in CH₄ saturation were associated with the organic matter load suggesting that its decomposition may be another source in the Indian estuaries. Fluxes of CH₄ ranged from 0.01 to 298 μmol m^?2 day^?1 (mean 13.4?±?5 μmol m^?2 day^?1) which is ~30 times lower compared to European estuaries (414 μmol m^?2 day^?1). The annual emission from Indian estuaries, including Pulicat and Adyar, amounted to 0.39?×?10¹⁰ g CH₄?year^?1 with the surface area of 0.027?×?10⁶ km² which is significantly lower than that in European estuaries (2.7?±?6.8?×?10¹⁰ g CH₄?year^?1 with the surface area of 0.03?×?10⁶ km²). This study suggests that Indian estuaries are a weak source for atmospheric CH₄ than European estuaries and such low fluxes were attributed to low residence time of water and low decomposition of organic matter within the estuary. The CH₄ fluxes from the Indian estuaries are higher than those from Indian mangroves (0.01?×?10¹⁰ g CH₄?year^?1) but lower than those from Indian inland waters (210?×?10¹⁰ g CH₄?year^?1).     

Assessment of hydrogeochemistry and contamination of Varamin deep aquifer,Tehran Province,Iran

The present study investigates the hydrogeochemistry and contamination of Varamin deep aquifer located in the southeast of Tehran province, Iran. The study also evaluates groundwater suitability for irrigation uses. The hydrogeochemical study was conducted by collecting and analyzing 154 groundwater samples seasonally during 2014. Based on evolutionary sequence of Chebotarev, the aquifer is in the stage of SO₄ + HCO₃ in the north half of the plain and it has evolved into SO₄ + Cl in the south half. The unusual increase in TDS and Cl^? toward the western boundaries of the aquifer indicates some anomalies. These anomalies have originated from discharge of untreated wastewater of Tehran city in these areas. The studied aquifer contains four dominant groundwater types including Na–Ca–SO₄ (55%), Na–Ca–HCO₃ (22%), Na–Cl (13%) and Ca–Cl (10%). The spatial distributions of Na–Cl and Ca–Cl water types coincide with observed anomalies. Ionic relationships of SO₄ ^2? versus Cl^? and Na⁺ versus Cl^? confirm that water–rock interaction and anthropogenic contribution are main sources of these ions in the groundwater. The main processes governing the chemistry of the groundwater are the dissolution of calcite, dolomite and gypsum along the flow path, and direct ion exchange. Reverse ion exchange controls the groundwater chemistry in the areas contaminated with untreated wastewater. Based on Na% and SAR, 10.3 and 27% of water samples are unsuitable for irrigation purposes, respectively. Regarding residual sodium carbonate, there is no treat for crop yields. Only 6% of water samples represent magnesium adsorption ratios more than 50% which are harmful and unsuitable for irrigation.     

Hydrochemical characteristics and quality assessment of regolith aquifers in Enugu metropolis, southeastern Nigeria

Twenty groundwater samples were collected from Enugu metropolis over two seasonal periods in order to characterize the groundwater and to determine its quality for domestic and irrigation purposes. The results show that groundwater of the area is strongly acidic to slightly alkaline in nature and varied from “soft water” to “moderately hard” water type. The major ionic trend is in the order Cl^? > Na⁺ > HCO₃ ^? > K⁺ > Mg²⁺ > Ca²⁺ > SO₄ ^2?and Mg²⁺ > Cl^? > Na⁺ > K⁺ > Ca²⁺ > HCO ₃ ^?  > SO₄ ^2? in abundance for dry and rainy seasons, respectively. The results also reveal that there is an increase in trend of the ionic concentrations during the dry season, which arises from weathering of the host rocks and anthropogenic activities. Two hydrochemical facies were identified, namely, Na⁺ –K⁺ –Cl^? –SO₄ ^2?and Ca²⁺ –Mg²⁺ –Cl^? –SO₄ ^2? _, with Na⁺ –K⁺ –Cl^? –SO₄ ^2? as the dominant facies for the two seasons. Groundwater quality ranges from “very poor water” to “good water” and “water unsuitable for drinking purposes” to “good water” for the dry season and rainy season investigations, respectively. The groundwater is suitable for irrigation purposes for the two seasons.     

Deep pre-eruptive storage of silicic magmas feeding Plinian and dome-forming eruptions of central and northern Dominica (Lesser Antilles) inferred from volatile contents of melt inclusions

Volatiles contribute to magma ascent through the sub-volcanic plumbing system. Here, we investigate melt inclusion compositions in terms of major and trace elements, as well as volatiles (H₂O, CO₂, SO₂, F, Cl, Br, S) for Quaternary Plinian and dome-forming dacite and andesite eruptions in the central and the northern part of Dominica (Lesser Antilles arc). Melt inclusions, hosted in orthopyroxene, clinopyroxene and plagioclase are consistently rhyolitic. Post-entrapment crystallisation effects are limited, and negligible in orthopyroxene-hosted inclusions. Melt inclusions are among the most water-rich yet recorded (≤?8 wt% H₂O). CO₂ contents are generally low (<?650 ppm), although in general the highest pressure melt inclusion contain the highest CO₂. Some low-pressure (<?3 kbars) inclusions have elevated CO₂ (up to 1100–1150 ppm), suggestive of fluxing of shallow magmas with CO₂-rich fluids. CO₂-trace element systematics indicate that melts were volatile-saturated at the time of entrapment and can be used for volatile-saturation barometry. The calculated pressure range (0.8–7.5 kbars) indicates that magmas originate from a vertically-extensive (3–27 km depth) storage zone within the crust that may extend to the sub-Dominica Moho (28 km). The vertically-extensive crustal system is consistent with mush models for sub-volcanic arc crust wherein mantle-derived mafic magmas undergo differentiation over a range of crustal depths. The other volatile range of composition for melt inclusions from the central part is F (75–557 ppm), Cl (1525–3137 ppm), Br (6.1–15.4 ppm) and SO₂ (<?140 ppm), and for the northern part it’s F (92–798 ppm), Cl (1506–4428 ppm), Br (not determined) and SO₂ (<?569; one value at 1015 ppm). All MIs, regardless of provenance, describe the same Cl/F correlation (8.3?±?2.7), indicating that the magma source at depth is similar. The high H₂O content of Dominica magmas has implications for hazard assessment.     

Pyrometamorphism of 19th‐century kiln artifacts from Caledonia Springs,Ontario, Canada

Marked, 19th‐century kiln bricks and rocks from Caledonia Springs (CS) have black glass coatings that can easily be mistaken for glass produced at the elusive CS glassworks (c. 1844–1846). The glass‐on‐brick material, however, is more aluminous (nearly 20% Al₂O₃) than virtually any analyzed historical glass, and the glass‐on‐rock is compositionally similar to the rock itself, which shows clear signs of having undergone extensive melting. Mineral thermometry (Cpx‐Ol, Pl‐melt) indicates that parts of the kiln‐achieved temperatures of approximately 1200–1300°C. The CS samples show that caution must be exercised when identifying seemingly obvious waste glass near defunct glassworks sites. © 2005 Wiley Periodicals, Inc.