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Patel, D.; Pamidimukkala, P.; Chakraborty, D. |
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Title |
Groundwater quality evaluation of Narmada district, Gujarat using principal component analysis |
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Journal Article |
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Year |
2024 |
Publication |
Groundwater for Sustainable Development |
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24 |
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101050 |
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Keywords |
Fluoride, Groundwater quality index, Principal component analysis, Uranium |
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Abstract |
In the present study, the ground water quality parameters were monitored during pre- and post-monsoon seasons across Narmada district, Gujarat, India. Monitoring was done in 89 drinking water samples collected by grid sampling method from the study area. Uranium and fluoride were analyzed along with associated parameters such as pH, dissolved oxygen, Cl−, NO3−, F−, SO42−, total alkalinity, total dissolved solids and hardness. In 4% samples the fluoride content was found to be above WHO permissible limits of 1.5 mg/L (2.36 mg/L in Undaimandava, 1.55 mg/L in Shira, 3.04 mg/L in Fatehpur and 1.83 mg/L in Dholivav) during pre-monsoon season (PRM) and 4.74 mg/L, 2.41 mg/L, 2.34 mg/L and 3.99 mg/L respectively in Bantawadi, Shira, Undai Mandava and Fatepur villages during post-monsoon (POM). The uranium level was within WHO limits in both POM and PRM seasons. The quality of the water was evaluated by Principal Component and Pearson Correlation statistical analysis techniques. The PRM and POM correlation study indicated a strong correlation of TDS with EC, Chloride, total alkalinity and bicarbonate and U while moderately strong correlation of TDS with fluoride were observed indicating that chloride, total alkalinity, bicarbonate, U and fluoride contributed to TDS and EC. Principal component analysis was applied for 14 variables, from which 3 factors were extracted during PRM and POM seasons. The extracted components, contributed 84.391% and 83.315%, to variation during PRM and POM seasons respectively. The study indicated that the analyzed water samples in Narmada district were safe for drinking purpose. However, Tilakwada tehsil groundwater was observed to be unsustainable for drinking, without further water treatment, but was appropriate for agricultural purposes. The study will help the residents of the district to understand the present water quality status and will also help in future management to protect the ground water of Narmada district. |
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2352-801x |
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THL @ christoph.kuells @ patel_groundwater_2024 |
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148 |
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Pastukhov, A.M.; Rychkov, V.N.; Smirnov, A.L.; Skripchenko, S.Y.; Poponin, N.A. |
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Title |
Purification of in situ leaching solution for uranium mining by removing solids from suspension |
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Journal Article |
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Year |
2014 |
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Minerals Engineering |
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55 |
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1-4 |
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Bag filter, Firm particles, In situ leaching mining, Injection wells, Intake capacity, Purification |
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This study investigated the process of in situ leaching (ISL) method of uranium mining, and the removal of solid particles from the leaching solution. Investigations were carried out for 4months. The content of firm suspensions in the productive solutions arriving from the well field was up to standard of 3–5mg/l. After keeping in a settler of productive solutions within one hour concentration of suspensions decreases to 2–2.5mg/l. To increase the life of the wells requires more fine purification of the ISL solutions. The best results can be obtained but using filtration. Bag filters were used in experiments carried out at the extraction site. All samples of polypropylene bag filter was produced by the Tamfelt Corporation. The best results were obtained for fabrics S-51M03-L2K4 (pore size 3μm). After three month of trials following indicators of wells work were fixed: on the trial cell decrease in intake capacity did not occur; on the other cells of well field injectability of holes for the same period of time decreased for 15–40%. The results illustrated the high efficiency of this method, which allows injection wells to reach a constant intake capacity, making it possible for technological cells to achieve a constant productivity and balance. Purification of solutions allows to reduce acidulation term of new technological cells from 3–4 to 1.5–2months. |
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0892-6875 |
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THL @ christoph.kuells @ pastukhov_purification_2014 |
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204 |
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Paradis, C.J.; Hoss, K.N.; Meurer, C.E.; Hatami, J.L.; Dangelmayr, M.A.; Tigar, A.D.; Johnson, R.H. |
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Elucidating mobilization mechanisms of uranium during recharge of river water to contaminated groundwater |
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Journal Article |
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2022 |
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Journal of Contaminant Hydrology |
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251 |
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104076 |
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Desorption, Dissolution, Groundwater, Surface water, Tracer, Uranium |
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The recharge of stream water below the baseflow water table can mobilize groundwater contaminants, particularly redox-sensitive and sorptive metals such as uranium. However, in-situ tracer experiments that simulate the recharge of stream water to uranium-contaminated groundwater are lacking, thus limiting the understanding of the potential mechanisms that control the mobility of uranium at the field scale. In this study, a field tracer test was conducted by injecting 100 gal (379 l) of oxic river water into a nearby suboxic and uranium-contaminated aquifer. The traced river water was monitored for 18 days in the single injection well and in the twelve surrounding observation wells. Mobilization of uranium from the solid to the aqueous phase was not observed during the tracer test despite its pre-test presence being confirmed on the aquifer sediments from lab-based acid leaching. However, strong evidence of oxidative immobilization of iron and manganese was observed during the tracer test and suggested that immobile uranium was likely in its oxidized state as U(VI) on the aquifer sediments; these observations ruled out oxidation of U(IV) to U(VI) as a potential mobilization mechanism. Therefore, desorption of U(VI) appeared to be the predominant potential mobilization mechanism, yet it was clearly not solely dependent on concentration as evident when considering that uranium-poor river water (\textless0.015 mg/L) was recharged to uranium-rich groundwater (≈1 mg/L). It was possible that uranium desorption was limited by the relatively higher pH and lower alkalinity of the river water as compared to the groundwater; both factors favor immobilization. However, it was likely that the immobile uranium was associated with a mineral phase, as opposed to a sorbed phase, thus desorption may not have been possible. The results of this field tracer study successfully ruled out two common mobilization mechanisms of uranium: (1) oxidative dissolution and (2) concentration-dependent desorption and ruled in the importance of advection, dispersion, and the mineral phase of uranium. |
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0169-7722 |
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THL @ christoph.kuells @ paradis_elucidating_2022 |
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135 |
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Orloff, K.G.; Mistry, K.; Charp, P.; Metcalf, S.; Marino, R.; Shelly, T.; Melaro, E.; Donohoe, A.M.; Jones, R.L. |
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Human exposure to uranium in groundwater |
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Journal Article |
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2004 |
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Environmental Research |
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94 |
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3 |
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319-326 |
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Groundwater, Human exposure, Uranium, Urine |
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High concentrations of uranium (mean=620μg/L) were detected in water samples collected from private wells in a residential community. Based on isotopic analyses, the source of the uranium contamination appeared to be from naturally occurring geological deposits. In homes where well water concentrations of uranium exceeded the drinking water standard, the residents were advised to use an alternate water source for potable purposes. Several months after the residents had stopped drinking the water, urine samples were collected and tested for uranium. Elevated concentrations of uranium (mean=0.40μg/g creatinine) were detected in urine samples, and 85 percent of the urine uranium concentrations exceeded the 95th percentile concentration of a national reference population. Urine uranium concentrations were positively correlated with water uranium concentrations, but not with the participants’ ages or how long they had been drinking the water. Six months later, a second urine sample was collected and tested for uranium. Urine uranium concentrations decreased in most (63 percent) of the people. In those people with the highest initial urine uranium concentrations, the urine levels decreased an average of 78 percent. However, urine uranium concentrations remained elevated (mean=0.27μg/g), and 87 percent of the urine uranium concentrations exceeded the 95th percentile concentration of the reference population. The results of this investigation demonstrated that after long-term ingestion of uranium in drinking water, elevated concentrations of uranium in urine could be detected up to 10 months after exposure had stopped. |
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0013-9351 |
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THL @ christoph.kuells @ orloff_human_2004 |
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136 |
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Ollivier, C.C.; Carrière, S.D.; Heath, T.; Olioso, A.; Rabefitia, Z.; Rakoto, H.; Oudin, L.; Satgé, F. |
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Ensemble precipitation estimates based on an assessment of 21 gridded precipitation datasets to improve precipitation estimations across Madagascar |
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Journal Article |
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2023 |
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Journal of Hydrology: Regional Studies |
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47 |
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101400 |
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Precipitation products, Remote sensing, Ensemble approach, Hydrology, Madagascar |
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Study region this study focuses on Madagascar. This island is characterized by a great diversity of climate, due to trade winds and the varying topography. This country is also undergoing extreme rainfall events such as droughts and cyclones. Study focus the rain gauge network of Madagascar is limited (about 30 stations). Consequently, we consider relevant satellite-based precipitation datasets to fill gaps in ground-based datasets. We assessed the reliability of 21 satellite-based and reanalysis precipitation products (P-datasets) through a direct comparison with 24 rain gauge station measurements at the monthly time step, using four statistical indicators: Kling-Gupta Efficiency (KGE), Correlation Coefficient (CC), Root Mean Square Error (RMSE), and Bias. Based on this first analysis, we produced a merged dataset based on a weighted average of the 21 products. New hydrological insights for the region based on the KGE and the CC scores, WFDEI (WATCH Forcing Data methodology applied to ERA-Interim), CMORPH-BLD (Climate Prediction Center MORPHing satellite-gauge merged) and MSWEP (Multi-Source Weighted Ensemble Precipitation) are the most accurate for estimating rainfall at the national scale. Additionally, the results reveal a high discrepancy between bio-climatic regions. The merged dataset reveals higher performance than the other products in all situations. These results demonstrate the usefulness of a merging approach in an area with a deficit of rainfall data and a climatic and topographic diversity. |
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2214-5818 |
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THL @ christoph.kuells @ Ollivier2023101400 |
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288 |
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