Investigating a surface water quality monitoring approach for QwaQwa, South Africa, by combining biological in vitro tests and chemical analyses

IntroductionWater quality assessment is a fundamental requirement for comprehensive water management. Access to water is not exclusively a quantitative issue, as human activities often lead to negative impacts on water quality due to pollution. This results in a need for the systematic monitoring of water bodies to surveil ongoing pollution dynamics and, if needed, facilitate the implementation of suitable solutions for water quality management.MethodsTo that effect, in March 2022 and July 2023, we conducted two sampling campaigns in four headwater streams in QwaQwa, South Africa, to assess the water quality under high (summer) and low (winter) flow conditions. The overarching aim was to support local decision-makers with relevant information on water quality in a semirural and less studied area. Beside the hydrological characterization of the catchment, which drains the mountainous areas around Phuthaditjhaba (the main town of the region), physicochemical and biological monitoring were conducted, including in vitro tests detecting endocrine disruption, dioxin-like impacts, and genotoxic potentials in the water.ResultsThe elemental analysis showed that at several sampling sites, Al, Cu, Mn, Fe, and Zn were above the Target-Water-Quality-Range (TWQR) for aquatic ecosystems and Fe, Al, and Mn were additionally above the TWQR for domestic use. Interestingly, the organic micropollutants (OMPs) revealed a region with a high incidence of HIV infections, given the occurrence of the drugs efavirenz, its transformation product 8-OH-efavirenz and nevirapine, among other micropollutants. Possibly, the signals from the in vitro tests for endocrine disruption are also induced by the detected micropollutants. Our results ultimately show that even though anthropogenic impacts increase from upstream to downstream, none of the sampling sites are without concern. This indicates the urgent need for measures to increase the water quality of these headwater streams in this region

Granular Natural Zeolites: Cost-Effective Adsorbents for the Removal of Ammonium from Drinking Water

Increasing food demand has resulted in an ever increasing demand for nitrogen fertilizers. Ammonium is the main constituent of these fertilizers and is a threat to aquatic environments around the world. With a focus on the treatment of drinking water, the scope of this study was to investigate the influence of key parameters on the suitability of granular natural zeolites as adsorbents for ammonium. Sorption experiments were performed in artificial matrices by varying the grain size, contact time, ammonium concentration, pH, content of competing ions, and regeneration solutions used. Additionally, natural matrices and the point of zero charge (pzc) were investigated. With an initial ammonium concentration of 10 mgN/L, the grain size was shown to have no significant effect on the sorption efficiency (97–98%). The experimental data obtained was best described by the Langmuir adsorption model (R2 = 0.99). Minor effects on sorption were observed at different pH values and in the presence of competing anions. In addition, the pHPZC was determined to be between pH 6.24 and pH 6.47. Potassium ions were shown to be better than sodium ions for the regeneration of previously loaded zeolites, potassium is also the main competitor to ammonium sorption. The use of tap, bank filtrate, river, and groundwater matrices decreased the ammonium sorption capacity of granular natural zeolites by up to 8%. Based on our results, granular natural zeolites are promising cost-effective adsorbents for drinking water treatment, especially in threshold and developing countries

Granular Natural Zeolites: Cost-Effective Adsorbents for the Removal of Ammonium from Drinking Water

Increasing food demand has resulted in an ever increasing demand for nitrogen fertilizers. Ammonium is the main constituent of these fertilizers and is a threat to aquatic environments around the world. With a focus on the treatment of drinking water, the scope of this study was to investigate the influence of key parameters on the suitability of granular natural zeolites as adsorbents for ammonium. Sorption experiments were performed in artificial matrices by varying the grain size, contact time, ammonium concentration, pH, content of competing ions, and regeneration solutions used. Additionally, natural matrices and the point of zero charge (pzc) were investigated. With an initial ammonium concentration of 10 mgN/L, the grain size was shown to have no significant effect on the sorption efficiency (97–98%). The experimental data obtained was best described by the Langmuir adsorption model (R2 = 0.99). Minor effects on sorption were observed at different pH values and in the presence of competing anions. In addition, the pHPZC was determined to be between pH 6.24 and pH 6.47. Potassium ions were shown to be better than sodium ions for the regeneration of previously loaded zeolites, potassium is also the main competitor to ammonium sorption. The use of tap, bank filtrate, river, and groundwater matrices decreased the ammonium sorption capacity of granular natural zeolites by up to 8%. Based on our results, granular natural zeolites are promising cost-effective adsorbents for drinking water treatment, especially in threshold and developing countries

Natural Zeolites for the Sorption of Ammonium: Breakthrough Curve Evaluation and Modeling

The excessive use of ammonium fertilizer and its associated leakage threatens aquatic environments around the world. With a focus on the treatment of drinking water, the scope of this study was to evaluate and model the breakthrough curves for NH4+ in zeolite-filled, fixed-bed columns. Breakthrough experiments were performed in single- and multi-sorbate systems with the initial K+ and NH4+ concentrations set to 0.7 mmol/L. Breakthrough curves were successfully modeled by applying the linear driving force (LDF) and Thomas models. Batch experiments revealed that a good description of NH4+ sorption was provided by the Freundlich sorption model (R2 = 0.99), while unfavorable sorption was determined for K+ (nF = 2.19). Intraparticle diffusion was identified as the rate limiting step for NH4+ and K+ during breakthrough. Compared to ultrapure water, the use of tap, river, and groundwater matrices decreased the treated bed volumes by between 25% and 69%—as measured at a NH4+ breakthrough level of 50%. The concentrations of K+ and of dissolved organic carbon (DOC) were identified as the main parameters that determine NH4+ sorption in zeolite-filled, fixed-bed columns. Based on our results, the LDF and Thomas models are promising tools to predict the breakthrough curves of NH4+ in zeolite-filled, fixed-bed columns

A Water Quality Appraisal of Some Existing and Potential Riverbank Filtration Sites in India

There is a nationwide need among policy and decision makers and drinking water supply engineers in India to obtain an initial assessment of water quality parameters for the selection and subsequent development of new riverbank filtration (RBF) sites. Consequently, a snapshot screening of organic and inorganic water quality parameters, including major ions, inorganic trace elements, dissolved organic carbon (DOC), and 49 mainly polar organic micropollutants (OMPs) was conducted at 21 different locations across India during the monsoon in June–July 2013 and the dry non-monsoon period in May–June 2014. At most existing RBF sites in Uttarakhand, Jammu, Jharkhand, Andhra Pradesh, and Bihar, surface and RBF water quality was generally good with respect to most inorganic parameters and organic parameters when compared to Indian and World Health Organization drinking water standards. Although the surface water quality of the Yamuna River in and downstream of Delhi was poor, removals of DOC and OMPs of 50% and 13%–99%, respectively, were observed by RBF, thereby rendering it a vital pre-treatment step for drinking water production. The data provided a forecast of the water quality for subsequent investigations, expected environmental and human health risks, and the planning of new RBF systems in India

Portable Analyzer for On-Site Determination of Dissolved Organic Carbon — Development and Field Testing

Dissolved organic carbon (DOC) is a sum parameter that is frequently used in water analytics. Highly resolved and accurate DOC data are necessary, for instance, for water quality monitoring and for the evaluation of the efficiency of treatment processes. The conventional DOC determination methods consist of on-site sampling and subsequent analysis in a stationary device in a laboratory. However, especially in regions where no or only poorly equipped laboratories are available, this method bears the risk of getting erroneous results. For this reason, the objective of the present study was to set up a reliable and portable DOC analyzer for on-site analysis. The presented DOC system is equipped with an electrolysis-based decomposition cell with boron-doped diamond electrodes (BDD) that oxidizes the organic compounds to carbon dioxide. Within this study, the influence of different electrode materials and the composition of the applied electrolytes on the DOC decomposition in an undivided electrolytic cell were systematically investigated. Furthermore, some technical aspects of the portable prototype are discussed. After a detailed validation, the prototype was used in an ongoing monitoring program in Northern India. The limit of detection is 0.1 mg L−1 C with a relative standard deviation of 2.3% in a linear range up to 1000 mg L C−1. The key features of the portable DOC analyzer are: No need for ultra-pure gases, catalysts or burning technology, an analyzing time per sample below 5 min, and a reliable on-site DOC determination

Assessment of the retardation of selected herbicides onto Danube sediment based on small column tests

Purpose: This study utilizes column tests to investigate the retardation of certain herbicides with different hydrophobicities (atrazine, alachlor and trifluralin) during transport through surface Danube sediment. The influence of water matrix on the retardation factor Rd and Freundlich constant Kf is investigated. The results are compared with batch tests to establish whether different methodologies result in similar or different conclusions. Materials and methods: A stainless steel column was filled with natural Danube sediment. Three water matrices were investigated: synthetic, Danube surface, and deep groundwater rich in natural organic matter (NOM). The goal was to examine whether different water matrices would result in changes in the Rd and corresponding Kf values. After a tracer experiment, single herbicide solutions were tested in the three water matrices. Herbicides were analyzed by gas chromatography coupled with electron capture detector (GC/ECD). Retardation factors obtained in the column experiments were calculated using Transmod software (version 2.2). The Kf values calculated were compared with the values obtained in previous batch experiments. Results and discussion: A breakthrough curve (BTC) for trifluralin could not be obtained during the experiment. Atrazine Rd values were almost the same in the natural matrices (54 and 55 for the ground and surface waters, respectively), and lower in the synthetic water (40). Alachlor Rd values in the three water matrices were very similar (30–35). The corresponding Kf values for alachlor (8.47–17.4) were lower than those of atrazine (13.5–27.9). These results differ from those obtained by earlier batch tests, which showed similar Kf values for both atrazine (4.4–9.2) and alachlor (4.43–10.35) in all three matrices. In contrast to the results observed during the batch tests, the column tests exhibited higher Kf values in the natural water matrices than the synthetic water, possibly due to the influence of dissolved organic carbon on herbicide sorption. Conclusions: Of the three herbicides investigated, the smallest retardation was observed for alachlor. This was unexpected given the relative hydrophobicities of alachlor and atrazine. The potential risk of transport through the sediment may therefore be greater for alachlor than the other two herbicides. This was indicated neither by the batch tests nor from the Koc–Kow estimations. Both herbicides exhibited similar Kd and Kf values in the batch tests, and lower values in the natural water matrices. In comparison, the column tests showed higher Kf values, with higher values in the natural matrices than in the synthetic water matrix

Identification and Expression Analyses of Putative Sesquiterpene Synthase Genes in Phormidium sp. and Prevalence of geoA-Like Genes in a Drinking Water Reservoir▿

The occurrence of taste and odor problems in drinking water supplies is a widespread phenomenon. From a Saxonian water reservoir we isolated a cyanobacterial species which was classified as Phormidium sp. Under laboratory conditions it produced an earthy-musty smell due to the synthesis of geosmin. The only genes shown to be involved in geosmin biosynthesis are cyc2 and geoA of Streptomyces. Based on the alignment of Cyc2 with a putative sesquiterpene synthase of Nostoc punctiforme, a degenerate primer pair was designed. By PCR, we could amplify two similar genes in Phormidium sp., which we named geoA1 and geoA2. Their expression was studied by reverse transcription-PCR. This revealed that both genes are expressed at 20°C and a light-dark cycle of 12 h. Expression was not detectable at the end of a 24-h dark period. To analyze the prevalence of geoA1 and geoA2 in samples from the phytobenthos, we generated PCR fragments with the same degenerate primer pair. Fifty-five different sequences that might represent geoA variants were obtained. The GC content ranged from 42% to 67%, suggesting that taxonomically very different bacteria might contain such genes

Behavior of Organic Micropollutants During River Bank Filtration in Budapest, Hungary

This paper summarizes results from a half-year sampling campaign in Budapest, when Danube River water and bank filtrate were analyzed for 36 emerging micropollutants. Twelve micropollutants were detected regularly in both river water and bank filtrate. Bisphenol A, carbamazepine, and sulfamethoxazole showed low removal (<20%) during bank filtration on Szentendre Island and Csepel island, whereas 1H-benzotriazole, tolyltriazole, diclofenac, cefepime, iomeprol, metazachlor, and acesulfame showed medium to high removal rates of up to 78%. The concentration range in bank filtrate was much lower compared to river water, proving the equilibration effect of bank filtration for water quality