Up-scaling application of microbial carbonate precipitation: optimization of urease production using response surface methodology and injection modification

In order to reduce the cost of the microbial-induced carbonate precipitation, mixotrophic growth of Sporosarcina pasteurii was carried out at different yeast extract/sodium acetate concentrations and constant chemical oxygen demand for optimal production of urease enzyme. Optimization of cultivation conditions was also investigated using a 3-level central composite design approach based on the response surface methodology. A good agreement between predicted values of enzyme activity and experimental results was observed (R ² value of 0.973). All three chosen independent variables had statistically great effects on the efficiency of urease activity. The maximum activity of 2.98 mM urea min^?1 was achieved at yeast extract concentration of 5 g L^?1, NH₄ concentration of 9.69 g L^?1, and incubation time of 60 h as the optimal conditions. Thereafter, a novel injection procedure as sequencing batch mode injection has been proposed for bacteria and cementation fluid injection at obtained optimal urease activity. After fourth injection of bacteria and cementation fluid, uniform CaCO₃ distribution with unconfined compression strength of 795 kPa was obtained even for poorly graded sand. The presented experimental approach for optimizing urease activity and strength production in porous media can be used to design the treatment protocol for practical engineering applications.     

Spatial and Temporal Variability of the CO2 Fluxes in a Tropical, Highly Urbanized Estuary

The spatial and temporal variations of the flux of CO₂ were determined during 2007 in the Recife estuarine system (RES), a tropical estuary that receives anthropogenic loads from one of the most populated and industrialized areas of the Brazilian coast. The RES acts as a source of nutrients (N and P) for coastal waters. The calculated CO₂ fluxes indicate that the upstream inputs of CO₂ from the rivers are largely responsible for the net annual CO₂ emission to the atmosphere of +30 to +48 mmol m^?2 day^?1, depending on the CO₂ exchange calculation used, which mainly occurs during the late austral winter and early summer. The observed inverse relationship between the CO₂ flux and the net ecosystem production (NEP) indicates the high heterotrophy of the system (except for the months of November and December). The NEP varies between ?33 mmol m^?2 day^?1 in summer and ?246 mmol m^?2 day^?1 in winter. The pCO₂ values were permanently high during the study period (average ~4,700 μatm) showing a gradient between the inner (12,900 μatm) and lower (389 μatm) sections on a path of approximately 30 km. This reflects a state of permanent pollution in the basin due to the upstream loading of untreated domestic effluents (N/P?=?1,367:6 μmol kg^?1 and pH?=?6.9 in the inner section), resulting in the continuous mineralization of organic material by heterotrophic organisms and thereby increasing the dissolved CO₂ in estuarine waters.     

Ameliorating nitrite inhibition in a low-temperature nitritation–anammox MBBR using bacterial intermediate nitric oxide

The long-term sustainability of an anaerobic ammonium oxidation (anammox) process in a moving bed biofilm reactor (MBBR) treating highly concentrated (mean of 740 mg NH₄ ⁺-N L^?1) wastewater was demonstrated by 1600 days of efficient operation. A high maximum total nitrogen removal rate (TNRR) of 1.5 g N m^?2 d^?1 was achieved at the low temperature of 20 °C. For nitrogen removal recovery in cases of nitrite inhibition, anammox intermediate nitric oxide (NO) was tested in batch experiments as an N-removal accelerating agent. The effect of the addition of various NO dosages (8–72 mg NO-N L^?1) was studied under inhibitory nitrite concentrations (>100 mg NO₂ ^?-N L^?1) for anammox bacteria. Optimal maintained NO concentration was 58 mg NO-N L^?1 and brought about the highest biofilm-specific anammox activity (SAA). Compared to a blank test, the minimum concentration of added NO of 40 mg NO-N L^?1 showed a statistically significant (p < 0.05) accelerating effect on SAA. No inhibition of SAA by NO was observed, although at NO concentrations exceeding 72 mg NO-N L^?1, the acceleratory effect upon SAA was decreased by 8%. Changes in the bacterial consortia involved in nitrogen conversion were determined concurrently for the different nitrogen removal rates and operational conditions. Quantities of Planctomycetales clone P4 strains, which are the closest (99% similarity) relative to Candidatus Brocadia fulgida, increased from 1 × 10³ to 1 × 10⁶ anammox gene copies per g total suspended solids during reactor operation days 568–1600, which was determined by quantitative polymerase chain reaction. During the operation of the MBBR, the abundance of ammonium-oxidizing bacteria (AOB) increased proportionally (up to 30%). The abundance of nitrite-oxidizing bacteria (NOB) did not increase (remaining below 10%) during days 232–860. AOB became predominant over NOBs owing to the inhibition of free ammonia spiking on NOBs.     

Evaluation of effective nutritional parameters for <Emphasis Type="Italic">Scenedesmus</Emphasis> sp. microalgae culturing in a photobioreactor for biodiesel production

Recently, microalgae are considered as lipid sources for biodiesel production. A photobioreactor was designed and fabricated for Scenedesmus sp. microalgae cultivation. The effect of several nitrogen sources, light intensity, iron ions, silicon, magnesium sulfate and ethanol concentrations on Scenedesmus sp. microalgae growth were investigated. For incubation period of 8 days, sodium nitrate and ammonium carbonate were the best nitrogen sources with biomass concentrations of 2.373 and 2.254 g L^?1, respectively. Microalgae growth was reduced using nitrogen concentrations above 0.7 g L^?1. In the first 10 days of incubation, maximum cell dry weight (0.7 g L^?1) was obtained with light intensity of 10,000 lx, whiles after that, the results were desired (1 g L^?1) using interior lighting at 7500 lx. Magnesium sulfate had a positive effect on cell growth. The biomass concentration of 1.65 g L^?1 was obtained using 0.06 g L^?1 magnesium sulfate. Maximum obtained biomass with silicon (0.7 Mm), ethanol (1.8 mL L^?1) and ferric ammonium citrate (0.02 g L^?1) was 1.7 and 1.3 and 2.16 g L^?1, respectively. Logistic model was found to be a suitable model for cell growth forecast. Fatty acid analysis showed that composition of the most dominant synthesized fatty acids, palmitic and oleic acids, was 21.16 and 33.58%, respectively. Oil produced by Scenedesmus sp. microalgae composed of 49.08% saturated and 43.53% unsaturated fatty acids has a suitable composition for a desired biodiesel.     

High lipid content and productivity of microalgae cultivating under elevated carbon dioxide

This study examined the cell growth rate, lipid contents, lipid productivity, chlorophyll a concentration, and carbon dioxide tolerance of Chlorella vulgaris under various cultivation conditions. The pH, concentration of carbon dioxide in media, and light intensity variables were manipulated to obtain high lipid productivity. The optimum conditions were at pH 7.0, 2,930 lux, and 30 % carbon dioxide. Biomass concentration reached 1,288, 1,130, and 1,083 mg L^?1 at 15, 30, and 50 % CO₂ after 6 days, respectively, implying that this strain has appreciable tolerance to carbon dioxide. The highest concentration of chlorophyll a occurred at 2,930 lux and decreased with increasing light intensity gradually. The maximum specific growth rate was 3.25 day^?1 based on the dry weight and 4.63 day^?1 based on the cell number. The lipid content (45.68 %) and lipid productivity (86.03 mg day^?1 L^?1) obtained in this study are higher than reported values in literatures. Hence, C. vulgaris is a good candidate for subsequent research in biodiesel production under elevated carbon dioxide concentration by microalgae.     

The dominant acetate degradation pathway/methanogenic composition in full-scale anaerobic digesters operating under different ammonia levels

Ammonia is a major environmental factor influencing biomethanation in full-scale anaerobic digesters. In this study, the effect of different ammonia levels on methanogenic pathways and methanogenic community composition of full-scale biogas plants was investigated. Eight full-scale digesters operating under different ammonia levels were sampled, and the residual biogas production was followed in fed-batch reactors. Acetate, labelled in the methyl group, was used to determine the methanogenic pathway by following the ¹⁴CH₄ and ¹⁴CO₂ production. Fluorescence in situ hybridisation was used to determine the methanogenic communities’ composition. Results obtained clearly demonstrated that syntrophic acetate oxidation coupled with hydrogenotrophic methanogenesis was the dominant pathway in all digesters with high ammonia levels (2.8–4.57 g NH₄ ⁺-N L^?1), while acetoclastic methanogenic pathway dominated at low ammonia (<1.21 g NH₄ ⁺-N L^?1). Thermophilic Methanomicrobiales spp. and mesophilic Methanobacteriales spp. were the most abundant methanogens at free ammonia concentrations above 0.44 g NH₃-N L^?1 and total ammonia concentrations above 2.8 g NH₄ ⁺-N L^?1, respectively. Meanwhile, in anaerobic digesters with low ammonia (<1.21 g NH₄ ⁺-N L^?1) and free ammonia (<0.07 g NH₃-N L^?1) levels, mesophilic and thermophilic Methanosaetaceae spp. were the most abundant methanogens.     

Groundwater Discharge as a Source of Dissolved Carbon and Greenhouse Gases in a Subtropical Estuary

Groundwater may be highly enriched in dissolved carbon species, but its role as a source of carbon to coastal waters is still poorly constrained. Exports of deep and shallow groundwater-derived dissolved carbon species from a small subtropical estuary (Korogoro Creek, Australia, latitude ?31.0478°, longitude 153.0649°) were quantified using a radium isotope mass balance model (²³³Ra and ²²⁴Ra, natural groundwater tracers) under two hydrological conditions. In addition, air-water exchange of carbon dioxide and methane in the estuary was estimated. The highest carbon inputs to the estuary were from deep fresh groundwater in the wet season. Most of the dissolved carbon delivered by groundwater and exported from the estuary to the coastal ocean was in the form of dissolved inorganic carbon (DIC; 687 mmol m^?2 estuary day^?1; 20 mmol m^?2 catchment day^?1, respectively), with a large export of alkalinity (23 mmol m^?2 catchment day^?1). Average water to air flux of CO₂ (869 mmol m^?2 day^?1) and CH₄ (26 mmol m^?2 day^?1) were 5- and 43-fold higher, respectively, than the average global evasion in estuaries due to the large input of CO₂- and CH₄-enriched groundwater. The groundwater discharge contribution to carbon exports from the estuary for DIC, dissolved organic carbon (DOC), alkalinity, CO₂, and CH₄ was 22, 41, 3, 75, and 100 %, respectively. The results show that CO₂ and CH₄ evasion rates from small subtropical estuaries surrounded by wetlands can be extremely high and that groundwater discharge had a major role in carbon export and evasion from the estuary and therefore should be accounted for in coastal carbon budgets.     

Methane cycle in the Barents Sea

Biogeochemical cycle of methane in the Barents Sea was studied using isotope geochemistry to determine the rates of microbial methane oxidation. It was established that microbiological processes (glucose consumption, ¹⁴CO₂ assimilation, sulfate reduction, and slow methane oxidation) in oxidized surface and weakly reduced sediments are marked by only insignificant change in SO ₄ ^2? concentration and absence of notable growth of total alkalinity and N/NH₄ downward the sediment core. Microbial methane productivity was 0.111 × 10⁶ mol day^?1. Taking into account the volume of water column, microbial methane consumption therein can be as much as 1.8 × 10⁶ mol day^?1.     

Energy generation from domestic wastewater using sandwich dual-chamber microbial fuel cell with mesh current collector cathode

A sandwich domestic wastewater-fed dual-chamber microbial fuel cell (MFC) was designed for energy generation and wastewater treatment. The generated power density by the MFC was observed to increase with increasing chemical oxygen demand (COD) of the domestic wastewater. The maximum power density was 251 mW m^?2 when the COD was 3400 mg L^?1 at a current density of 0.054 mA cm^?2 and external resistance of 200 Ω. These values dropped to 60 mW m^?2 (76 % lower) and 0.003 mA cm^?2 using wastewater 91 % diluted to 300 mg L^?1 COD. Maximum removals were: COD, 89 %; nitrite, 60 %; nitrate, 77 %; total nitrogen, 36 %; and phosphate, 26 %. Coulombic efficiency ranged from 5 to 7 %. The use of full-strength domestic wastewater reduces cost, and with improved reactor design, the ultimate goal of large-scale operation could be achieved.     

Tunisian landfill leachate treatment using <Emphasis Type="Italic">Chlorella</Emphasis> sp.: effective factors and microalgae strain performance

The potential of the autoclaved Tunisian landfill leachate treatment using microalgae (Chlorella sp.) cultivation was investigated in this study. Landfill leachate was collected from Borj Chakir landfill, Tunisia. A full factorial experimental design 2² was proposed to study the effects of the incubation time and leachate ratio factors on the organic matter removal expressed in chemical oxygen demand (COD) and ammoniacal nitrogen (NH₄─N) and on the biological response of Chlorella sp. expressed by the cell density and chlorophyll content. All experiments were batch runs at ambient temperature (25 ± 2 °C). The Chlorella sp. biomass and chlorophyll a concentrations of 1.2 and 5.32 mg L^?1, respectively, were obtained with 10% leachate spike ratio. The obtained results showed that up to 90% of the ammoniacal nitrogen in landfill leachate was removed in 10% leachate ratio spiked medium with a residual concentration of 40 mg L^?1. The maximum COD removal rate reached 60% within 13 days of incubation time indicating that microalgae consortium was quite effective for treating landfill leachate organic contaminants. Furthermore, with the 10% leachate ratio spiked medium, the maximum lipid productivity was 4.74 mg L^?1 d^?1. The present study provides valuable information for potential adaptation of microalgae culture and its contribution for the treatment of Tunisian landfill leachate.     

The Dynamics of Benthic Respiration at a Mid-Shelf Station Off Oregon

Mid-shelf sediments off the Oregon coast are characterized as fine sands that trap and remineralize phytodetritus leading to the consumption of significant quantities of dissolved oxygen. Sediment oxygen consumption (SOC) can be delayed from seasonal organic matter inputs because of a transient buildup of reduced constituents during periods of quiescent physical processes. Between 2009 and 2013, benthic oxygen exchange rates were measured using the noninvasive eddy covariance (EC) method five separate times at a single 80-m station. Ancillary measurements included in situ microprofiles of oxygen at the sediment–water interface, and concentration profiles of pore water nutrients and trace metals, and solid-phase organic C and sulfide minerals from cores. Sediment cores were also incubated to derive anaerobic respiration rates. The EC measurements were made during spring, summer, and fall conditions, and they produced average benthic oxygen flux estimates that varied between ?2 and ?15 mmol m^?2 d^?1. The EC oxygen fluxes were most highly correlated with bottom-sensed, significant wave heights (H _s). The relationship with H _s was used with an annual record of deepwater swell heights to predict an integrated oxygen consumption rate for the mid-shelf of 1.5 mol m^?2 for the upwelling season (May–September) and 6.8 mol m^?2 y^?1. The annual prediction requires that SOC rates are enhanced in the winter because of sand filtering and pore water advection under large waves, and it counters budgets that assume a dominance of organic matter export from the shelf. Refined budgets will require winter flux measurements and observations from cross-shelf transects over multiple years.     

Identification of sulfate sources in groundwater using isotope analysis and modeling of flood irrigation with waters of different quality in the Jinghuiqu district of China

The main objective of this study was to identify the main sources and processes that control SO₄ ^2? groundwater concentrations in the Jinghuiqu irrigation district of China using isotope analysis. Lysimeter irrigation experiments and numerical modeling were used to assess the impact of long-term irrigation practices on sulfate transport, when different sources of irrigation water were used. SO₄ ^2? concentrations in the groundwater of the entire irrigation area increased significantly from the years 1990 (a mean value was 4.8 mmol L^?1) to 2009 (a mean value was 9.84 mmol L^?1). The δ³⁴S-SO₄ ^2? values (ranging from +5.27 to +10.69 ‰) indicated that sulfates in groundwater were initially predominantly derived from dissolution of minerals. However, no soluble sulfate minerals (gypsum and/or mirabilite) were detected after 1990. To better understand this seeming anomaly, water content and SO₄ ^2? data were collected before and after the field irrigation experiment and analyzed using the HYDRUS-1D and HP1 software packages. The experimental data were also used to assess sulfate leaching when different sources of irrigation water were used under current irrigation practices. The dissolved sulfate concentrations in the soil profile increased significantly when groundwater was used for infiltration compared to the use of surface water. Irrigation water sources had a great impact on the increase of sulfate concentrations in the shallow groundwater, especially when groundwater with elevated concentrations was used for irrigation.     

Mechanism and numerical simulation of multicomponent solute transport in sodic soils reclaimed by calcium sulfate

The mechanism for reclaiming sodic soils using calcium sulfate (CaSO₄) could provide a theoretical basis for the field application of CaSO₄ substitutes, including the by-products of flue gas desulfurization (BFGD), fly ash, and phosphorus gypsum. In this study, Ca²⁺ application experiment was conducted to analyze the dynamic changes of the cations in the reclamation of sodic soils with CaSO₄. A multicomponent solute transport model (UNSATCHEM) that considers ion adsorption exchange and dynamic changes in the soil’s hydraulic conductivity was subsequently used to simulate and predict the movement of ions. The Ca²⁺ application experiment consisted of four treatments with four CaSO₄ concentrations (0.5, 1, 1.5, and 2 g L^?1). When the Ca²⁺ concentrations in the supplied water were 14.71, 22.06, and 29.41 mmol L^?1, Ca²⁺ achieved penetration, and this process was faster when the Ca²⁺ concentration in the supplied water was higher. Ca²⁺ did not achieve penetration when the Ca²⁺ concentration was 7.35 mmol L^?1. UNSATCHEM was able to simulate the transportation mechanism of Ca²⁺ and Na⁺ in the soil solution in the Ca²⁺ application experiment, the adsorption and exchange between the Na⁺ in the soil colloid and Ca²⁺ in the soil solution, and the precipitation and dissolution of CaSO₄ with a high degree of accuracy. Sodic soil reclamation with CaSO₄ was not a short-term process. Compared with applying CaSO₄ only once, applying CaSO₄ in batches decreased the accumulation of soil salts and promoted its dissolution.     

Groundwater,Acid and Carbon Dioxide Dynamics Along a Coastal Wetland,Lake and Estuary Continuum

Coastal wetlands are hotspots for biodiversity and biological productivity, yet the hydrology and carbon cycling within these systems remains poorly understood due to their complex nature. By using a novel spatiotemporal approach, this study quantified groundwater discharge and the related inputs of acidity and CO₂ along a continuum of a modified coastal acid sulphate soil (CASS) wetland, a coastal lake and an estuary under highly contrasting hydrological conditions. To increase the resolution of spatiotemporal data and advance upon previous methodologies, we relied on automated observations from four simultaneous time-series stations to develop multiple radon mass balance models to estimate groundwater discharge and related groundwater inputs of acidity and dissolved inorganic carbon (DIC), along with surface water to atmosphere CO₂ fluxes. Spatial surveys indicated distinct acid hotspots with minimum surface water pH of 2.91 (dry conditions) and 2.67 (flood conditions) near a non-remediated (drained) CASS area. Under flood conditions, groundwater discharge accounted for ～14.5 % of surface water entering the lake. During the same period, acid discharge from the acid sulphate soil section of the continuum produced ～4.8 kg H₂SO₄?ha^?1 day^?1, a rate much higher than previous studies in similar systems. During baseflow conditions, the low pH water was rapidly buffered within the estuarine lake, with the pH increasing from 4.22 to 6.07 over a distance of ～250 m. The CO₂ evasion rates within the CASS were extremely high, averaging 2163?±?125 mmol m^?2 day^?1 in the dry period and 4061?±?259 mmol m^?2 day^?1 under flood conditions. Groundwater input of DIC could only account for 0.4 % of this evasion in the dry conditions and ～5 % during the flood conditions. We demonstrated that by utilising a spatiotemporal (multiple time-series stations) approach, the study was able to isolate distinct zones of differing hydrology and biogeochemistry, whilst providing more reasonable groundwater acid input estimates and air–water CO₂ flux estimates than some traditional sampling designs. This study highlights the notion that modified CASS wetlands can release large amounts of CO₂ to the atmosphere because of high groundwater acid inputs and extremely low surface water pH.     

Effect of rising atmospheric CO2 on sediment and water 15N interactions in experimental riparian wetland

The experiment was conducted to ascertain net production and consumption rates of ¹⁵NH₄ ⁺ and ¹⁵NO₃ ^? for water and sediment in a wetland. This was done using ¹⁵N isotope pool dilution methodology under ambient and elevated atmospheric CO₂ concentrations in experimental riparian wetlands to obtain the gross N transformation rates. The ¹⁵N budget for sediment was also estimated. The results suggested that the differences in high proportion of ¹⁵N concentration in the overlying water body under elevated CO₂ could be attributed to the low production and high consumption rates of ¹⁵NH₄ ⁺ in sediment. The elevated CO₂ effect on production and consumption of NH₄ ⁺ decreased by 144 % (P = 0.014) and increased by 153 % (P = 0.009), respectively. Thereby, ¹⁵NH₄ ⁺ production rates are negatively related with ¹⁵NO₃ ^? consumption rates and this accounted for the decreases in net ¹⁵NO₃ ^? consumption under CO₂ enrichment in the wetland sediment by 11 % (P = 0.528). Therefore, ¹⁵NO₃ ^? production and consumption rates may strongly depend on NH₄ ⁺ production. Inorganic ¹⁵N and total ¹⁵N exported from sediment to overlying water body by the effect of CO₂ were 41 % (P = 0.071) and 18 % (P = 0.000), respectively. Therefore, low net ¹⁵NH₄ ⁺ production and high ¹⁵NH₄ ⁺ consumption rates under elevated CO₂ may partly explain the significant reduction of N from the sediment.     

Effects of organic acids on dissolution of Fe and Mn from weathering coal gangue

Understanding the effects of organic acids (OA) on the transformation of Fe and Mn to surface water from the weathering coal gangue is of great benefit to risk assessment and remediation strategies for contaminated water and soil. Based on the investigation on surface water in the central coal districts of the Guizhou Province, 18 water samples were collected for heavy metal analysis. The results indicated that the pH value of surface water is low (3.11–4.92), and Fe concentration (1.31–5.55 mg L^?1) and Mn concentration (1.90–5.71 mg L^?1) were, on average, 10.86 and 34.33 times the limit of Surface Water Quality Standards, respectively. In order to evaluate the effects of the OA on the dissolution of Fe and Mn from the weathering coal gangue, column elution and batch leaching experiments were conducted. The results show that the low molecular weight of organic acids (LMWOAs, i.e., oxalic, tartaric, malic and citric acids) and fulvic acids significantly accelerated the dissolution of Fe and Mn; in addition, when the concentration of OA reached 25 mmol L^?1, the concentrations of Fe, and Mn were 1.14–67.08 and 1.11–2.32 times as high as those in 0.5 mmol L^?1 OA, respectively. Furthermore, the migration of Fe and Mn was significantly influenced by the pH and Eh, especially for Fe; the ion Mn was dissolved from the gangue more easily than the ion Fe in the column leaching, which was contrary to the results of batch leaching.     

Removal of acetaminophen from hospital wastewater using electro-Fenton process

The current work deals with efficient removal of acetaminophen (AC) from hospital wastewater using electro-Fenton (EF) process. The degradation yield of 99.5% was obtained under optimal experimental conditions, namely 5.75 mg L^?1 initial AC concentration, 2.75 pH solution, 3-cm inter-electrode distance, 100 mg L^?1 KCl electrolyte, 122.5 µL L^?1 H₂O₂, 8 mA cm^?2 current density at equilibrium time of 8 min. Analysis of variance (ANOVA) suggested that the effect of mentioned operating parameters was statistically significant on the AC removal. The low probability amount of P value (P < 0.0001), the Fisher’s F-value of 65.91, and correlation coefficient of the model (R² = 0.9545) revealed a satisfactory correlation between the experimental and the predicted values of AC removal. The predicted removal efficiency of 99.4% was in satisfactory agreement with the obtained experimental removal efficiency of 98.7%. The AC degradation during the EF followed a first-order kinetic model with rate constants (K_app) of 0.6718 min^?1. Using the ordinary radical scavengers revealed that main mechanism of AC degradation controlled by the hydroxyl free radicals produced throughout the EF process. The excess amount of iron (II) scavenged the active radicals and diminished the concentration of ^·OH available to react with AC. The optimum molar ratio of H₂O₂ to Fe²⁺ was found to be 2.5. The developed EF process as a promising technique applied for treatment of real samples.     

Spatial variability of groundwater quality and its suitability for drinking and irrigation in the Amik Plain (South Turkey)

In this study, it is determined physicochemical properties of the groundwater and the spatial variability of physicochemical properties of the groundwater in the Amik plain and as well as assess its suitability for drinking and irrigation. A total 92 groundwater samples were collected from drilled well in June 2012. In addition, the 42 of 92 drilled wells were also sampled in September 2012 to evaluate the changes of groundwater properties. According to t test values, the mean Ca²⁺, SO₄ ^2?, Mg²⁺ and TH values in the June period were significantly lower than those of the September period. On the other hand, the mean (CO ₃ ^2?  + HCO₃ ^?) and RSC and MR values in the June period were significantly higher than those of the September period. The order of relative abundance of major cations in the groundwater (in mg L^?1) is in order Na⁺ > Mg²⁺ > Ca²⁺ > K⁺. The order of the anions abundance (mg L^?1) is SO₄ ^2? > Cl^? > HCO₃ ^? > CO₃ ^2? in this research. Log and square-root transformation were carried out for the most of the water properties before the calculation of semivariance. The nugget ratio showed all the variables were strongly spatial dependent except for K⁺ and Mg²⁺ and (CO₃ ^2? + HCO₃ ^?) which showed moderate spatial dependence (ratio ranging from 28 to 49.9 %). Spatial distribution analysis of groundwater quality indicated that The EC, TDS values and Na and Cl^? contents which is important water quality parameters increase from northern towards southern. The total hardness values increase also from northwestern towards southwestern.     

Hydrogeochemistry of coal mine water of North Karanpura coalfields,India: implication for solute acquisition processes,dissolved fluxes and water quality assessment

Mine water samples collected from different mines of the North Karanpura coalfields were analysed for pH, electrical conductivity, total dissolved solids (TDS), total hardness (TH), major anions, cations and trace metals to evaluate mine water geochemistry and assess solute acquisition processes, dissolved fluxes and its suitability for domestic, industrial and irrigation uses. Mine water samples are mildly acidic to alkaline in nature. The TDS ranged from 185 to 1343 mg L^?1 with an average of 601 mg L^?1. Ca²⁺ and Mg²⁺ are the dominant cations, while SO₄ ^2? and HCO₃ ^? are the dominant anions. A high concentration of SO₄ ^2? and a low HCO₃ ^?/(HCO₃ ^? + SO₄ ^2?) ratio (<0.50) in the majority of the water samples suggest that either sulphide oxidation or reactions involving both carbonic acid weathering and sulphide oxidation control solute acquisition processes. The mine water is undersaturated with respect to gypsum, halite, anhydrite, fluorite, aluminium hydroxide, alunite, amorphous silica and oversaturated with respect to goethite, ferrihydrite, quartz. About 40% of the mine water samples are oversaturated with respect to calcite, dolomite and jarosite. The water quality assessment shows that the coal mine water is not suitable for direct use for drinking and domestic purposes and needs treatment before such utilization. TDS, TH, F^?, SO₄ ^2?, Fe, Mn, Ni and Al are identified as the major objectionable parameters in these waters for drinking. The coal mine water is of good to suitable category for irrigation use. The mines of North Karanpura coalfield annually discharge 22.35 × 10⁶ m³ of water and 18.50 × 10³ tonnes of solute loads into nearby waterways.