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• EtHg artifact during propylation links to Hg2+ in the extract for derivatization. • CuSO 4 HNO 3 CH 2 Cl 2 extraction offers excellent EtHg recovery with minimal artifacts. • EtHg is prevalent in soils/sediments across 14 Chinese wetlands. • All Yellow River Delta samples contained MeHg, with EtHg detected in 48% of them. Ethylmercury (EtHg), similar to methylmercury (MeHg), is highly neurotoxic and bioaccumulative. Although recent studies suggested its occurrence in natural soils and sediments, the common propylation derivatization for EtHg analysis might generate EtHg artifacts, potentially leading to its overestimation in environmental samples. Furthermore, the extensive environmental prevalence of EtHg remains unverified, keeping its importance largely uncertain. This study investigated the formation of EtHg artifacts during propylation derivatization, evaluating artifacts formation and recoveries under different extraction methods with real samples, and confirmed the widespread occurrence of EtHg in Chinese wetlands. EtHg artifacts were obviously present during the propylation derivatization and strongly dependent on the levels of Hg2+ (0.1–10 ng) in the derivatization solution (R² = 0.99), accounting for 1.38–2.14% of Hg2+. CuSO 4 -HNO 3 CH 2 Cl 2 extraction (effectively removing Hg2+) combined with propylation derivatization offers excellent recovery (81–86%) and low artifacts (< LOD: 1.98 × 10−4 ng/g) for EtHg measurement in soils/sediments, with results aligning with those from online solid phase extraction-high performance liquid chromatography-inductively coupled plasma mass spectrometry (R2 = 0.99). Additionally, we observed the occurrence of EtHg in soil and sediment samples across 14 Chinese wetlands, with concentrations varying from 6.08 to 171 pg/g, similar to MeHg concentrations at some sites. EtHg positively correlates with MeHg, total Hg, and total organic carbon across all samples, indicating a possible biological formation. These findings help better understand and predict the prevalence of EtHg in wetlands and its key role in environmental Hg cycle. [Display omitted] [ABSTRACT FROM AUTHOR]

• Micropollutants of 216 were detected in effluents from 46 WWTPs across China. • The exposure and hazard potential of pollutants were defined based on multivariate analysis. • PI method was proposed to prioritize multi-class micropollutants in effluents of WWTPs. • Priority criteria involved concentration, detection rate, persistence, bioaccumulation and toxicity. • Pollutants with high PI scores mainly included POPs and their alternatives. Identifying priority pollutants in wastewater treatment plant (WWTP) effluents is crucial for optimizing monitoring efforts, improving regulations, and developing targeted mitigation strategies. Despite the presence of numerous trace organic pollutants in WWTP effluents, a comprehensive prioritization scheme is lacking, hindering effective control. This study screened 216 micropollutants, including pharmaceuticals, pesticides, and industrial chemicals, which had been detected in effluents from 46 WWTPs across China. A multi-criteria prioritization method was developed, considering exposure potential based on median concentrations and detection frequencies, as well as hazard potential determined by persistence, bioaccumulation, in vitro toxicity, and in vivo toxicity. Pollutants with low exposure or hazard potential were filtered out, and a priority index was calculated to rank the remaining 59 substances. The top 15 priority pollutants included regulated persistent organic pollutants like perfluorooctanoic acid and their alternatives such as perfluorobutane sulfonate, pesticide transformation products, and emerging contaminants such as bisphenol A, which are not currently regulated in WWTP effluents. This study provides a systematic approach to identify priority pollutants and generates a guiding framework for monitoring, regulation, and control of both well-recognized and overlooked contaminants in WWTP effluents. [Display omitted] [ABSTRACT FROM AUTHOR]

• PFBSA was detected in > 90% of sampled seawater from East China Sea and Antarctic Ocean. • Field-based log K oc of PFBSA was calculated in East China Sea and Antarctic Ocean. • Bioaccumulation potential of PFBSA was examined in collected marine fishes. • This study provides the first data on behaviors of PFBSA in the marine environment. Environmental occurrence of perfluorobutane sulfonamide (PFBSA) has only been recently discovered. The current knowledge regarding the occurrence and environmental behaviors of PFBSA in the marine environment is still relatively limited. In this study, PFBSA and other 37 poly- and perfluoroalkyl substances were analyzed in seawater (n = 43), sediment (n = 43), and marine fish (n = 176) samples collected from East China Sea and Antarctic Ocean. PFBSA was detected in > 90% of seawater from East China Sea and Antarctic Ocean, with the concentrations of 1.0 − 19 ng/L and < LOD−228 pg/L, respectively. The field-based mean log-transformed sediment-seawater partitioning coefficients of PFBSA were 1.6 ± 0.19 L/kg dw and 1.1 ± 0.19 L/kg dw in East China Sea and Antarctic Ocean, respectively, which are lower than that of perfluorooctanoate and perfluorooctane sulfonate. This indicates its long-range transport potential in global oceans with ocean currents. The mean log-transformed bioaccumulation factor values of PFBSA determined in the multiple species of whole-body marine fishes from East China Sea and Antarctic Ocean were 2.3 L/kg ww and 2.4 L/kg ww, respectively, which are comparable to that of perfluoroheptanoate (2.3 L/kg ww) in marine fishes from East China Sea. We did not observe an obvious biomagnification or biodilution of PFBSA along the marine food chain in East China Sea or Antarctic Ocean. This study provides the first data on the environmental behaviors of PFBSA in the marine environment. [Display omitted] [ABSTRACT FROM AUTHOR]

• Mixtures of pesticide residues were detected in all small water bodies. • Herbicides were found in levels significantly higher than fungicides and insecticides. • 38 % of the pesticides found in water are no longer approved as PPP in the EU. • The total pesticide concentration exceeded the threshold value in 8 out of 11 CSS. • Risk ratios for pesticide mixtures suggested potential risk for aquatic organisms. Freshwater ecosystems face a particularly high risk of biodiversity loss compared to marine and terrestrial systems. The use of pesticides in agricultural fields is recognized as a relevant stressor for freshwater environments, exerting a negative impact worldwide on the overall status and health of the freshwater communities. In the present work, part of the Horizon 2020 funded SPRINT project, the occurrence of 193 pesticide residues was investigated in 64 small water bodies of distinct typology (creeks, streams, channels, ditches, rivers, lakes, ponds and reservoirs), located in regions with high agricultural activity in 10 European countries and in Argentina. Mixtures of pesticide residues were detected in all water bodies (20, median; 8–40 min-max). Total pesticide levels found ranged between 6.89 and 5860 ng/L, highlighting herbicides as the dominant type of pesticides. Glyphosate was the compound with the highest median concentration followed by 2,4-D and MCPA, and in a lower degree by dimethomorph, fluopicolide, prothioconazole and metolachlor(-S). Argentina was the site with the highest total pesticide concentration in water bodies followed by The Netherlands, Portugal and France. One or more pesticides exceeded the threshold values established in the European Water Framework Directive for surface water in 9 out of 11 case study sites (CSS), and the total pesticide concentration surpassed the reference value of 500 ng/L in 8 CSS. Although only 5 % (bifenthrin, dieldrin, fipronil sulfone, permethrin, and terbutryn) of the individual pesticides denoted high risk (RQ > 1), the ratios estimated for pesticide mixtures suggested potential environmental risk in the aquatic compartment studied. [Display omitted] [ABSTRACT FROM AUTHOR]

Abstract The release of persistent and mobile organic chemicals (PMOCs) into the aquatic environment puts the quality of water resources at risk. PMOCs are challenging to analyze in water samples, due to their high polarity. The aim of this study was to develop novel analytical methods for PMOCs and to investigate their occurrence in surface and groundwater samples. The target compounds were culled from a prioritized list of industrial chemicals that were modeled to be persistent, mobile, and emitted into the environment. Analytical screening methods based on mixed-mode liquid chromatography (LC), hydrophilic interaction LC, reversed phase LC, or supercritical fluid chromatography in combination with mass spectrometric detection were successfully developed for 57 target PMOCs and applied to 14 water samples from three European countries. A total of 43 PMOCs were detected in at least one sample, among them 23 PMOCs that have not been reported before to occur in environmental waters. The most prevalent of these novel PMOCs were methyl sulfate, 2-acrylamino-2-methylpropane sulfonate, benzyltrimethylammonium, benzyldimethylamine, trifluoromethanesulfonic acid, 6-methyl-1,3,5-triazine-diamine, and 1,3-di- o -tolylguanidine occurring in ≥50% of the samples at estimated concentrations in the low ng L−1 up to μg L−1 range. The approach of focused prioritization combined with sensitive target chemical analysis proved to be highly efficient in revealing a large suite of novel as well as scarcely investigated PMOCs in surface and groundwater. Graphical abstract Image 1 Highlights • Persistent and mobile organic chemicals (PMOCs) occur in drinking water resources. • Innovative methods for analysis of PMOCs in water samples are presented. • 57 PMOCs are selected and analyzed in 14 European water samples. • 43 PMOCs (75%) are detected, among them 23 for the first time. • PMOC concentrations range up to μg L−1 in surface and groundwater. [ABSTRACT FROM AUTHOR]

Abstract Microplastics have aroused increasing concern as they pose threats to aquatic species as well as human beings. They do not only contribute to accumulation of plastics in the environment, but due to absorption they can also contribute to spreading of micropollutants in the environment. Studies indicated that wastewater treatment plants (WWTPs) play an important role in releasing microplastics to the environment. Therefore, effective detection of the microplastics and understanding their occurrence and fate in WWTPs are of great importance towards microplastics control. In this review, the up-to-date status on the detection, occurrence and removal of microplastics in WWTPs are comprehensively reviewed. Specifically, the different techniques used for collecting microplastics from both wastewater and sewage sludge, and their pretreatment and characterization methods are reviewed and analyzed. The key aspects regarding microplastics occurrence in WWTPs, such as concentrations, total discharges, materials, shapes and sizes are summarized and compared. Microplastics removal in different treatment stages and their retention in sewage sludge are explored. The development of potential microplastics-targeted treatment technologies is also presented. Although previous researches in microplastics have undoubtedly improved our level of understanding, it is clear that much remains to be learned about microplastics in WWTPs, as many unanswered questions and thereby concerns still remain; some of these important future research areas are outlined. The key challenges appear to be to harmonize detection methods as well as microplastics mitigation from wastewater and sewage sludge. Graphical abstract Image 1 Highlights • The detection, occurrence and behavior of microplastics in WWTPs are reviewed. • The collection, pretreatment and characterization of microplastics are analyzed. • The concentrations, materials and properties of microplastics are summarized. • The microplastics removal in WWTPs and retention in sewage sludge are explored. [ABSTRACT FROM AUTHOR]

Abstract Hepatitis E virus (HEV) is an enteric virus divided into eight genotypes. Genotype 1 (G1) and G2 are specific to humans; G3, G4 and G7 are zoonotic genotypes infecting humans and animals. Transmission to humans through water has been demonstrated for G1 and G2, mainly in developing countries, but is only suspected for the zoonotic genotypes. Thus, the water-related HEV hazard may be due to human and animal faeces. The high HEV genetic variability allows considering the presence in wastewater of not only different genotypes, but also quasispecies adding even greater diversity. Moreover, recent studies have demonstrated that HEV particles may be either quasi-enveloped or non-enveloped, potentially implying differential viral behaviours in the environment. The presence of HEV has been demonstrated at the different stages of the water cycle all over the world, especially for HEV G3 in Europe and the USA. Concerning HEV survival in water, the virus does not have higher resistance to inactivating factors (heat, UV, chlorine, physical removal), compared to viral indicators (MS2 phage) or other highly resistant enteric viruses (Hepatitis A virus). But the studies did not take into account genetic (genogroups, quasispecies) or structural (quasi- or non-enveloped forms) HEV variability. Viral variability could indeed modify HEV persistence in water by influencing its interaction with the environment, its infectivity and its pathogenicity, and subsequently its transmission by water. The cell culture methods used to study HEV survival still have drawbacks (challenging virus cultivation, time consuming, lack of sensitivity). As explained in the present review, the issue of HEV transmission to humans through water is similar to that of other enteric viruses because of their similar or lower survival. HEV transmission to animals through water and how the virus variability affects its survival and transmission remain to be investigated. Graphical abstract Image 1 Highlights • Hepatitis E virus (HEV) is a highly variable virus, waterborne in some cases. • HEV seems sensitive to water treatments compared to other enteric viruses. • Cell culture methods should be improved especially for HEV detection in water. • Role of water for animal transmission of HEV should be investigated. • Presence of enveloped HEV particles in the environment may be explored. [ABSTRACT FROM AUTHOR]

Abstract Fecal indicator bacteria, such as Escherichia coli (E.coli) and Enterococcus , have been widely used to indicate the presence of pathogens. However, the suitability of fecal indicator bacteria to represent health risks is still being challenged, particularly in tropical aquatic environments. The objective of this study is to understand the occurrence and prevalence of indicators and pathogens in areas with contrasting land use, as well as to identify the major correlations between indicators, pathogens and environmental parameters. The spatial and temporal variation of indicators and pathogens was studied to examine the distribution patterns for areas with different land use, and the impact of seasonal changes on microbial populations. A total of 234 water samples were sampled for two years from reservoirs and their tributaries, and tested for fecal indicator bacteria, coliphages, human specific markers, pathogenic bacteria and viruses. The prevalence of indicators and pathogens in reservoirs were generally low, while relatively high concentrations were observed in tributaries to varying degrees. Of the enteric viruses, norovirus GII was among the most prevalent and had the highest concentration. Although strong correlations were found between indicators, only relatively weak correlations were found between indicators and pathogens. The results in this study showed that none of the bacteria/phage indicators were universal predictors for pathogens. Inclusion of the alternative indicators, Methanobrevibacter smithii , Bacteroides and human polyomaviruses (HPyVs) to monitoring programs could help to determine whether the fecal source was human. The microbial distribution patterns allow the classification of sampling sites to different clusters and thus, help to identify sites which have poor water quality. This approach will be useful for water quality management to pinpoint factors that influence water quality and help to prioritize sites for restoration of water quality. Graphical abstract Image 1 Highlights • Norovirus GII was the most prevalent enteric viruses. • Land use classification was correlated to the distribution of pathogens/indicators. • Alternative indicators helped to improve the prediction of enteric viruses. • Cluster analysis identified sites with poor water quality. [ABSTRACT FROM AUTHOR]

Abstract This study aimed to examine the drivers in shaping the occurrence and distribution of total viruses and picoplankton in tropical freshwater ecosystems. Flow cytometry was used to quantify the concentrations of total viruses, picoheterotrophs, picophytoplankton, and picocyanobacteria. Three land use patterns (urban-, agriculture- and parkland-dominated) were evaluated using ArcGIS. Significant correlations were observed between water-borne microbial targets and water quality parameters (0.175 ≤ |r| ≤ 0.441), nutrients (0.250 ≤ r ≤ 0.570) and land use factors (0.200 ≤ |r| ≤ 0.460). In particular, the concentrations of total viruses and picoheterotrophic cells were higher in catchments whereas the abundances of picophytoplankton and picocyanobacteria were higher in reservoirs. Total viruses and picoplankton had higher concentrations in urban- and agriculture-dominated areas, probably due to anthropogenic inputs and agricultural inputs, respectively. Although surface water is a complex matrix influenced by niche-based (i.e., physicochemical properties, nutrients, land use impact etc.) and neutral-based factors (i.e., ecological drift, dispersal and species), land use patterns could help to elucidate the occurrence and distribution of the total microbial community at the macroscopic level. Meanwhile, inter-correlations among viruses, picoplankton and picoheterotrophs (0.715 ≤ r ≤ 0.990) also substantiates their mutual interactions in influencing the microbial community. Furthermore, the relationships between total microbial cells and bacterial and viral indicators were also investigated. Concentrations of total viruses, picoplankton and picoheterotrophs were positively correlated with bacterial indicators (0.427 ≤ r ≤ 0.590) and viral indicators (0.201 ≤ r ≤ 0.563). These results indicated that faecal and viral contamination could contribute to the numbers of total viruses and bacteria. Graphical abstract Image 1 Highlights • Viruses, bacteria and picophytoplankton in aquatic ecosystems were quantified by flow cytometry. • Microorganisms were correlated with water quality, nutrients and land use factors (0.18 < r < 0.57). • Total abundance of microorganisms correlated with bacterial and viral indicators (0.20 < r < 0.59). • The abundance of viruses, bacteria and picophytoplankton were impacted by land use patterns. [ABSTRACT FROM AUTHOR]

Abstract In this study, the spatial and temporal-distribution of 41-multiclass organic compounds were assessed in three estuaries of the Basque Country, from winter 2016 to winter 2017 by grab (active) sampling methods and an extra campaign combining both, grab and passive sampling methods. Wastewater treatment plant (WWTP) effluents were also evaluated to assess their impact on the estuaries. Moreover, the physicochemical features (phosphate and nitrate concentrations, pH, etc.) of each site were measured and included in the statistical analysis. Anti-inflammatory drugs (diclofenac and acetaminophen), hypertensive drugs (irbesartan and valsartan), a stimulant (caffeine), an artificial sweetener (acesulfame) and a corrosion inhibitor (2-hydroxybenzothiazole) were the most ubiquitous compounds. Due to the stratification of the waters in the estuary of Bilbao two independent sources were identified: WWTP and harbour activities. In the case of Gernika and Plentzia, both are estuaries with a high tidal dilution, and the main sources were localized in the effluents of the WWTPs. In addition to this, the use of POCIS provides an efficient way to monitor emerging pollutants over a relatively long sampling period. Finally, risk quotient (RQ) values of each contaminant were estimated from the maximum values determined at each estuary and WWTP effluent for acute and chronic effects. In the case of acute toxicity the highest RQ values (»1) were obtained for the angiotensin II receptor blockers (telmisartan, eprosartan, etc.), diuron and diclofenac. In the case of the chronic toxicity the highest RQ values (»1) were estimated for caffeine, diclofenac, bezafibrate and sulfadiazine. Graphical abstract Image 1 Highlights • Temporal distribution of 41 analytes was assessed in three estuaries and wastewater. • Different surface and bottom water distribution was observed in Bilbao estuary. • The use of pollution markers was studied to identify non-monitored effluent sources. • The suitability of POCIS samplers as an efficient monitor tool should be highlighted. • Sartan compounds ranked as highly concern compounds on the basis of risk assessment. [ABSTRACT FROM AUTHOR]

• EHPi method was proposed to integrate characteristics of pollutants in wastewater. • 34 typical pollutants in effluents were ranked by EHPi scores at a national level. • Pollutants that have synergistic effects with other pollutants were also identified. • Pollutants with high EHPi scores showed spatial differences. The identification of the priority control sequence of pollutants in effluents of wastewater treatment plants (WWTPs) has important implications for the management of water quality. This study chose 34 typical pollutants based on their representativeness and detection rates in municipal wastewater. The occurrence frequency and concentration of these pollutants in 168 Chinese WWTP effluents were measured at the national level. The data on in vitro toxicity (67 assays) and in vivo toxicity (216 species) for target pollutants were obtained from the public toxicity database and our experimental data. An environmental health prioritization index (EHPi) method was proposed to integrate the occurrence frequency, concentration, removal rate, and in vitro and in vivo toxicity to determine the priority control sequence of target pollutants. Ethynyl estradiol, 17β-estradiol, estrone, diclofenac, and atrazine were the top 5 pollutants identified by the EHPi score. Several pollutants with high EHPi scores showed spatial differences. Besides the EHPi method which was from the single pollutant perspective, the combined toxicity of pollutants (300 pairs of binary combinations) was also measured based on in vitro toxicity assays to evaluate the key pollutants from the pollutant-pollutant interacting perspective. The pollutants (such as ofloxacin and acetaminophen) that could have significant synergetic effects with many other pollutants are worthy of prior attention. This study shed new light on the identification of the priority control sequence of pollutants in WWTP effluents. The results provide meaningful data for the effective management and control of wastewater water quality. [ABSTRACT FROM AUTHOR]

The continuous increase in synthetic plastic production and poor management in plastic waste have led to a tremendous increase in the dumping into our aqueous environment. Consequently, microplastics commonly defined as sizes less than 5 mm are produced and stay in both seawater and freshwater environment. The presence of microplastics as a new type of emerging contaminant has become a great issue of concerns from public and government authorities. The sources of microplastics to freshwater systems are many with the largest portion from wastewater treatment plants. The abundance of microplastics varies with the location, from above 1 million pieces per cubic meter to less than 1 piece in 100 cubic meters. Microplastics can cause several harmful physical effects on humans and living organisms through such mechanisms as entanglement and ingestion. The microplastics can act as carriers of various toxins such as additives from industrial production processes and persistent contaminants by the sorption in waters. Those toxins may cause great health problems to humans. A few studies on the fishes demonstrated that the microplastics and the associated toxins are bio-accumulated and cause such problems as intestinal damage and change in metabolic profiles. In studies of microplastics, fresh water is first sampled by the nets with typical mesh size of 330 μm for collection of microplastics. After the volume reducing process, the samples will then go through the purification process including density separation by such inorganic salts as sodium chloride and digestion process by oxidizing agents or enzymes. The sequence of these two processes (namely purification and digestion) is dependent on the sample type. The purified samples can be studied by several analytical methods. The commonly used methods for the qualification studies are FTIR spectroscopy, Raman spectroscopy, pyrolysis-GC/MS, and liquid chromatography. A tagging method can be used in the quantification study. Our literature study finds that there is still no universal accepted quantification and qualification tools of microplastics in fresh waters. More work is anticipated so as to obtain accurate information on microplastics in freshwater, which can then be used for the better assessment of the environmental risk. [ABSTRACT FROM AUTHOR]

Emerging contaminants, such as antibiotics, pharmaceuticals, personal care products, hormones, and artificial sweeteners, are recognized as new classes of water contaminants due to their proven or potential adverse effects on aquatic ecosystems and human health. This review provides comprehensive data on the occurrence of 60 emerging contaminants (ECs) in influent, treated effluent, sludge, and biosolids in wastewater treatment plants (WWTPs). In particular, data on the occurrence of ECs in the influents and effluents of WWTPs are systematically summarized and categorized according to geographical regions (Asia, Europe, and North America). The occurrence patterns of ECs in raw influent and treated effluents of WWTPs between geographical regions were compared and evaluated. Concentrations of most ECs in raw influent in Asian region tend to be higher than those in European and North American countries. Many antibiotics were detected in the influents and effluents of WWTPs at concentrations close to or exceeding the predicted no-effect concentrations (PNECs) for resistance selection. The efficacy of EC removal by sorption and biodegradation during wastewater treatment processes are discussed in light of kinetics and parameters, such as sorption coefficients (K d ) and biodegradation constants (k biol ), and physicochemical properties (i.e. log K ow and pK a ). Commonly used sampling and monitoring strategies are critically reviewed. Analytical research needs are identified, and novel investigative approaches for future monitoring studies are proposed. [ABSTRACT FROM AUTHOR]

Recently, 13 new polar phenolic chlorinated and brominated disinfection byproducts (Cl- and Br-DBPs) were identified and quantified in simulated chlorinated drinking water by adopting product ion scan, precursor ion scan, and multiple reaction monitoring (MRM) analyses using ultra performance liquid chromatography/electrospray ionization-triple quadrupole mass spectrometry (UPLC/ESI-tqMS). The 13 new DBPs have been drawing increasing concern not only because they possess significantly higher growth inhibition, developmental toxicity, and chronic cytotoxicity than commonly known aliphatic DBPs, but also because they act as intermediate DBPs that can decompose to form the U.S. EPA regulated DBPs. In this study, through MS parameter optimization of the UPLC/ESI-tqMS MRM analysis, the instrument detection and quantitation limits of the 13 new DBPs were substantially lowered to 0.42–6.44 and 1.35–16.51 μg/L, respectively. The total levels of the 13 new DBPs formed in chlorination were much higher than those formed in chloramination within a contact time of 3 d. In chlorination, the 13 new DBPs formed quickly and decomposed rapidly, and their total concentration kept on decreasing with contact time. In chloramination, the levels of the dominant species (i.e., trihalo-phenols) firstly increased and then decreased with contact time, whereas the levels of the other new DBPs were relatively low and kept on increasing with contact time. An increasing of pH from 6.0 to 9.0 decreased the formation of the 13 new DBPs by 57.8% and 62.3% in chlorination and chloramination, respectively. Gallic acid was found to be present in various simulated and real source water samples and was demonstrated to be a precursor of the 13 new DBPs with elucidated formation pathways. Furthermore, 12 of the 13 new DBPs were detected in 16 tap water samples obtained from major cities in East China, at total levels from 9.5 to 329.8 ng/L. The concentrations of the new DBPs were higher in samples with source waters containing higher bromide levels. Ozone-activated carbon treatment prior to disinfection might reduce the formation of the new DBPs since it was effective in precursor reduction. [ABSTRACT FROM AUTHOR]

Human polyomaviruses (HPyVs) cause persistent infections in organs such as kidney, brain, skin, liver, respiratory tract, etc., and some types of HPyV are constantly excreted in the urine and/or feces of infected and healthy individuals. The use of an enteric virus as an indicator for human sewage/waste contamination in aquatic environments has been proposed; HPyVs are a good candidate since they are routinely found in environmental water samples from different geographical areas with relatively high abundance. HPyVs are highly human specific, having been detected in human waste from all age ranges and undetected in animal waste samples. In addition, HPyVs show a certain degree of resistance to high temperature, chlorine, UV, and low pH, with molecular signals (i.e., DNA) persisting in water for several months. Recently, various concentration methods (electronegative/positive filtration, ultrafiltration, skim-milk flocculation) and detection methods (immunofluorescence assay, cell culture, polymerase chain reaction (PCR), integrated cell culture PCR (ICC-PCR), and quantitative PCR) have been developed and demonstrated for HPyV, which has enabled the identification and quantification of HPyV in various environmental samples, such as sewage, surface water, seawater, drinking water, and shellfish. In this paper, we summarize these recent advancements in detection methods and the accumulation of environmental surveillance and laboratory-scale experiment data, and discuss the potential advantages as well as limitations of HPyV as a human-specific viral marker in aquatic environments. [ABSTRACT FROM AUTHOR]

Very little information on the occurrence and fate of multiple classes of antimicrobials in the aquatic environment is reported for the Southeast Asian region. This study provides the first and comprehensive data on the occurrence of ten different classes of antimicrobials in wastewater samples for Singapore. Among the investigated antimicrobials, 19 out of 21 target compounds were detected in 100% of the collected raw influent samples. Concentrations of the detected antimicrobials in raw influent varied from 23.8 to 43,740 ng/L. Removal of antimicrobials by conventional activated sludge (CAS) and membrane bioreactor (MBR) systems at a local wastewater treatment plant was evaluated. MBR exhibited better performance over CAS for most target antimicrobials. Beta-lactam, glycopeptide, and fluoroquinolone classes were largely eliminated by biological wastewater treatment processes, whereas trimethoprim and lincosamides appeared to be persistent. Effects of physicochemical properties and chemical structures of target antimicrobials on their removal efficiencies/mechanisms during wastewater treatment process were also discussed. [ABSTRACT FROM AUTHOR]

Many pollutants such as pharmaceuticals and their transformation products (TPs) are not efficiently removed from wastewater treatment plants and enter into surface waters. The aim of this study was to investigate the occurrence and behavior of metformin, one of the most prescribed drugs worldwide, and its biological transformation product guanylurea, in eight wastewater treatment plants (WWTPs) of Greece. All WWTPs were equipped with conventional activated sludge treatment and the samples were taken from the influents and the effluents, over the four seasons of one year. The analytical method developed based on SPE followed by LC-UV/Vis-ESI/MS analysis, while positive findings were confirmed also by means of LTQ Orbitrap mass spectrometer. High polarity of both compounds led to the extraction with Oasis HLB and the use of the anionic surfactant SDS. The results showed that metformin dominated in the influents (bql-1167 ng/L), while guanylurea in the effluents (bql-627 ng/L) of the wastewater treatment plants, with Metformin/Guanylurea ratio ranging between 0.88 and 81.3 in the influents and between 0.005 and 0.78 in the effluents. Lack of a clear seasonal tendency in the occurrence and removal or formation was observed. Finally, an ecotoxicological risk assessment of metformin in effluent wastewaters took place by calculating the ratio between the environmental concentrations (MEC) and the predicted no effect concentrations (PNEC). Despite the fact that metformin presented low risk in all cases, an environmental concern is suspected for guanylurea since it is continuously released into the aquatic environment. [ABSTRACT FROM AUTHOR]

• Psychopharmaceuticals have limited occurrence (49%) and ecotoxicity (15%) data. • Only for 87 (12%) compounds could risk be assessed, with 23 (3.3%) demonstrating risk. • Risk correlated with the amount and diversity of data available per compound. • This indicates there may be hidden risks for understudied compounds. • Risks could not be calculated for some commonly prescribed psychopharmaceuticals. This study aimed to provide insights into the risk posed by psychopharmaceuticals and illicit drugs in European surface waters, and to identify current knowledge gaps hampering this risk assessment. First, the availability and quality of data on the concentrations of psychopharmaceuticals and illicit drugs in surface waters (occurrence) and on the toxicity to aquatic organisms (hazard) were reviewed. If both occurrence and ecotoxicity data were available, risk quotients (risk) were calculated. Where abundant ecotoxicity data were available, a species sensitivity distribution (SSD) was constructed, from which the hazardous concentration for 5% of the species (HC 5) was derived, allowing to derive integrated multi-species risks. A total of 702 compounds were categorised as psychopharmaceuticals and illicit drugs based on a combination of all 502 anatomical therapeutic class (ATC) 'N' pharmaceuticals and a list of illicit drugs according to the Dutch Opium Act. Of these, 343 (49%) returned occurrence data, while only 105 (15%) returned ecotoxicity data. Moreover, many ecotoxicity tests used irrelevant endpoints for neurologically active compounds, such as mortality, which may underestimate the hazard of psychopharmaceuticals. Due to data limitations, risks could only be assessed for 87 (12%) compounds, with 23 (3.3%) compounds indicating a potential risk, and several highly prescribed drugs returned neither occurrence nor ecotoxicity data. Primary bottlenecks in risk calculation included the lack of ecotoxicity data, a lack of diversity of test species and ecotoxicological end points, and large disparities between well studied and understudied compounds for both occurrence and toxicity data. This study identified which compounds merit concern, as well as the many compounds that lack the data for any calculation of risk, driving research priorities. Despite the large knowledge gaps, we concluded that the presence of a substantial part (26%) of data-rich psychopharmaceuticals in surface waters present an ecological risk for aquatic non-target organisms. [Display omitted] [ABSTRACT FROM AUTHOR]

• Legionella was below detection in chlorinated reservoirs and distribution piping • Legionella was detected in nontreated groundwater (61 of 61 wells) • Flushing wells at startup to turbidity <3 NTU reduced Legionella • Chlorine inactivation of Legionella followed the Chick-Watson model (R2=0.87) • ATP, turbidity, PO 4 3− and pump depth correlated with Legionella concentration Legionella occurrence monitoring is not required by United States Environmental Protection Agency (USEPA) drinking water regulations, and few occurrence studies exist for Legionella in source water or distribution systems. Legionella occurrence was monitored in Las Vegas Valley (Las Vegas, Nevada, USA) drinking water sources, including non-treated surface water, seasonal groundwater (61 wells, before and after chlorination), finished water (after treatment at water treatment facilities), and chlorinated distribution system water (at 9 reservoirs and 75 sample locations throughout the network). Legionella pneumophila was detected at least once at each of the wells sampled before chlorination, with an overall positivity rate of 38% (343/908). During well start-up (time<2 hours; turbidity>3 NTU), L. pneumophila concentrations averaged 2,792±353 MPN/100 mL, with a median of 105 MPN/100 mL, and range of <1 to 90,490 MPN/100 mL across 61 seasonally operated (typically April-October) groundwater wells. After initial flushing (turbidity<3 NTU), the average concentration decreased by more than two orders of magnitude to 24±3 MPN/100 mL but ranged from <1 to >2,273 MPN/100 mL. This trend indicates that stagnation (up to 391 days) contributed to greater initial concentrations, and flushing alone was incapable of complete L. pneumophila elimination. L. pneumophila concentration was significantly, positively correlated with total aqueous adenosine triphosphate (ATP) (p<0.00001, r=0.41-0.71), turbidity (p<0.00001, r=0.27-0.51), orthophosphate (p=0.35-0.076, r=0.51-0.59), and pump depth (p=0.032, r=0.40). During a full-scale assessment of chlorination (Ct= 0.7 to 10.5 mg-min/L; T=26.6-28.1°C), substantial reduction of Legionella spp. (up to 2.5 logs) was observed ; although, detectable concentrations were still measured. Extrapolating from a Chick-Watson model (log inactivation=0.28*(Ct); R2=0.87) constructed from the full-scale chlorination results, 3- and 4-log inactivation in Las Vegas Valley groundwater would require 10.8 and 14.3 mg-min/L, respectively; at least 3-log inactivation was required to bring Legionella spp. to below detection at the studied well. Chlorine exposure (Ct =0.1 to 10.9 mg-min/L) at most wells discharging directly to the distribution system was insufficient to fully inactivate Legionella spp. After discussing these findings with the state regulatory agency, direct-to-distribution wells (38 of 61 wells) remained out of operation; the distribution system, wells, and reservoirs were monitored for Legionella and chlorine residual, and additional treatment scenarios were identified for further evaluation. Legionella was either not detected or was well controlled in surface water, finished effluent from the drinking water treatment plant, chlorinated reservoirs, and the chlorinated distribution system. This study emphasizes the importance of utility-driven, non-regulatory research in order to protect public health and also identifies the need for greater occurrence monitoring and guidance for Legionella in groundwater supplies. [Display omitted] [ABSTRACT FROM AUTHOR]

• HHBNs were identified as a new group of halogenated aromatic DBPs in drinking water. • Seven HHBN species showed 100% detection frequency in drinking water at ng/L levels. • HHBNs exhibited significantly higher cytotoxicity in CHO cells than regulated DBPs. • HHBNs underwent transformation during chlorination with half-lives of 9–63 h. • HHBNs were evaluated to show comparable risk to halonitrophenols in drinking water. Halogenated aromatic disinfection byproducts (DBPs) exhibited similar total organic halogen levels in chlorinated drinking water samples as compared with aliphatic ones, and they predominantly accounted for the overall toxicity of the samples. Among the reported halogenated aromatic DBPs, halonitrophenols (HNPs) have received particular attention in recent years due to the relatively high risk in drinking water. In this study, a new group of halogenated aromatic DBPs were detected and then proposed to be halohydroxybenzonitriles (HHBNs) by employing the ultra-performance liquid chromatography/tandem mass spectrometers. Thereafter, the specific HHBN species in drinking water were theoretically speculated and then thoroughly identified with standard compounds. Their occurrence in drinking water was investigated, their cytotoxicity was evaluated, and their stability in the presence of chlorine was assessed. Seven newly identified HHBNs, including 3,5-dichloro-4-hydroxybenzonitrile, 3,5-dichloro-2-hydroxybenzonitrile, 5-bromo-3-chloro-4-hydroxybenzonitrile, 5-bromo-3-chloro-2-hydroxybenzonitrile, 3,5-dibromo-4-hydroxybenzonitrile, 3,5-dibromo-2-hydroxybenzonitrile, and 3,5-diiodo-4-hydroxybenzonitrile, showed 100% detection frequency in the collected drinking water samples with concentrations up to 36 ng/L. HHBNs exhibited significantly higher cytotoxicity in Chinese hamster ovary cells than regulated DBPs (e.g., trihalomethanes and haloacetic acids), which might be contributed by their cellular uptake efficiency and nucleophilicity. The seven HHBNs were proved to undergo transformation during chlorination following pseudo-first-order decay with half-lives in the range of 9–63 h. More importantly, in comparison to HNPs, which showed relatively high toxicity and strong stability among the halogenated aromatic DBPs, HHBNs presented comparable concentration-cytotoxicity contribution (50%) and slightly weaker stability (43%), suggesting that HHBNs should be a new group of DBPs of concern in drinking water. [Display omitted] [ABSTRACT FROM AUTHOR]

Ketamine has been increasingly used both recreationally and medicinally around the world. Although the metabolic pathways to form its metabolite norketamine have been carefully investigated in humans and animals, knowledge of their environmental occurrence and fate is limited. In this study, we investigated the occurrence of ketamine and norketamine in 20 natural bodies of water, effluents from 13 hospitals, two wastewater treatment plants and one water supply plant. Ketamine was found at concentrations as high as 10 μg/L. Ketamine and norketamine were consistently found in similar concentrations (ketamine/norketamine ratio: 0.3–4.6) in the collected water samples, and this ratio similar to that found in urine samples. Dark incubation experiments have shown that ketamine is not susceptible to microbial degradation or hydrolysis. Phototransformation was demonstrated to significantly reduce the concentration of ketamine and norketamine in river waters (t 1/2 = 12.6 ± 0.4 and 10.1 ± 0.4 h, respectively) and resulted in byproducts that are similar to human metabolites. Both direct and indirect photolysis led to the N-demethylation of ketamine to form norketamine and other byproducts, including hydroxy-norketamine (HNK), dehydronorketamine (DNK), hydroxy-ketamine (HK) and isomer forms of ketamine and norketamine. Irradiated solutions exhibited higher toxicity (via the Microtox® test). Although a final risk assessment could not be made due to a lack of studies on the chronic effects on aquatic organisms, the high and persistent environmental occurrences of ketamine and norketamine as well as the increasingly acute toxicity of the photo byproducts demonstrate the importance of including metabolites in evaluation of the overall risk of ketamine. [ABSTRACT FROM AUTHOR]

Abstract: The near ubiquitous presence of poly- and perfluoroalkyl substances (PFASs) in humans has raised concerns about potential human health effects from these chemicals, some of which are both extremely persistent and bioaccumulative. Because some of these chemicals are highly water soluble, one major pathway for human exposure is the consumption of contaminated drinking water. This study measured concentrations of PFASs in 18 raw drinking water sources and 2 treated wastewater effluents and evaluated 15 full-scale treatment systems for the attenuation of PFASs in water treatment utilities throughout the U.S. A liquid-chromatography tandem mass-spectrometry method was used to enable measurement of a suite of 23 PFASs, including perfluorocarboxylic acids (PFCAs) and perfluorosulfonic acids (PFSAs). Despite the differences in reporting levels, the PFASs that were detected in >70% of the source water samples (n = 39) included PFSAs, perfluorobutane sulfonic acid (74%), perfluorohexane sulfonic acid (79%), and perfluorooctane sulfonic acid (84%), and PFCAs, perfluoropentanoic acid (74%), perfluorohexanoic acid (79%), perfluoroheptanoic acid (74%), and perfluorooctanoic acid (74%). More importantly, water treatment techniques such as ferric or alum coagulation, granular/micro-/ultra- filtration, aeration, oxidation (i.e., permanganate, ultraviolet/hydrogen peroxide), and disinfection (i.e., ozonation, chlorine dioxide, chlorination, and chloramination) were mostly ineffective in removing PFASs. However, anion exchange and granular activated carbon treatment preferably removed longer-chain PFASs and the PFSAs compared to the PFCAs, and reverse osmosis demonstrated significant removal for all the PFASs, including the smallest PFAS, perfluorobutanoic acid. [Copyright &y& Elsevier]

Fungi are known to occur ubiquitously in the environment. In the past years, the occurrence of filamentous fungi in the aquatic environment has been a subject of growing interest. This study describes the occurrence of various fungal genera in different drinking water sources being Penicillium and Trichoderma the most representative ones (30% and 17%, respectively). Also, 24 fungal species that have not been previously described in the aquatic environment are reported in this study, being once again the major species from the Penicillium genera. This study therefore contributes to the knowledge on the richness of fungi diversity in water. 68% of the described species were found to be able to grow at 30 °C but only Aspergillus fumigatus, Aspergillus viridinutans and Cunninghamella bertholletiae were able to grow at the higher temperature tested (42 °C). 66% of the species that were able to grow at 30 °C have spore sizes below 5 μm which enables them to cause breathing infections. These were therefore identified as potential pathogenic species. [ABSTRACT FROM AUTHOR]

Abstract: Recent studies have demonstrated the presence of trace-level pharmaceutically active compounds (PhACs) and endocrine disrupting compounds (EDCs) in a number of finished drinking waters (DWs). Since there is sparse knowledge currently available on the potential effects on human health associated with the chronic exposure to trace levels of these Emerging Contaminants (ECs) through routes such as DW, it is suggested that the most appropriate criterion is a treatment criterion in order to prioritize ECs to be monitored during DW preparation. Hence, only the few ECs showing the lowest removals towards a given DW Treatment (DWT) process would serve as indicators of the overall efficiency of this process and would be relevant for DW quality monitoring. In addition, models should be developed for estimating the removal of ECs in DWT processes, thereby overcoming the practical difficulties of experimentally assessing each compound. Therefore, the present review has two objectives: (1) to provide an overview of the recent scientific surveys on the occurrence of PhACs and EDCs in finished DWs; and (2) to propose the potential of Quantitative-Structure-Activity-Relationship-(QSAR)-like models to rank ECs found in environmental waters, including parent compounds, metabolites and transformation products, in order to select the most relevant compounds to be considered as indicators for monitoring purposes in DWT systems. [Copyright &y& Elsevier]

Abstract: Metformin, an antidiabetic drug with one of the highest consumption rates of all pharmaceuticals worldwide, is biologically degraded to guanylurea in wastewater treatment plants. Due to high metformin influent concentrations of up to 100 μg/L and its high but incomplete degradation both compounds are released in considerable amounts of up to several tens of μg/L into recipient rivers. This is the first systematic study on their environmental fate and the effectiveness of treatment techniques applied in waterworks to remove metformin and guanylurea from surface water influenced raw waters. The concentrations in surface waters depend strongly on the respective wastewater burden of rivers and creeks and are typically in the range of about 1 μg/L for metformin and several μg/L for guanylurea but can reach elevated average concentrations of more than 3 and 20 μg/L, respectively. Treatment techniques applied in waterworks were investigated by an extended monitoring program in three facilities and accompanied by laboratory-scale batch tests. Flocculation and activated carbon filtration proved to be ineffective for removal of metformin and guanylurea. During ozonation and chlorination experiments with waterworks-relevant ozone and chlorine doses they were partly transformed to yet unknown compounds. The effectiveness of the treatment steps under investigation can be ordered chlorination > ozonation > activated carbon filtration > flocculation. However, most effective for removal of both compounds at the three full-scale waterworks studied proved to be an underground passage (riverbank filtration or artificial groundwater recharge). A biological degradation is most likely as sorption can be neglected. This is based on laboratory batch tests conducted with three different soil materials according to OECD guideline 106. Since such treatment steps were implemented in all three drinking water treatment plants, even traces of metformin and its metabolite guanylurea could not be detected at the end of the treatment trains. Both can only be expected in finished drinking water if surface influenced raw water is used by direct abstraction without underground passage. [Copyright &y& Elsevier]

Abstract: The site-specific daily fluctuations and scale-dependent variability of influent water quality, particularly concentrations of trace organic chemicals (TOrCs), have not yet been well described. In this study, raw wastewater from three distinct sewershed scales was sampled including a centralized wastewater treatment facility in Boulder, Colorado (population ∼125,000) and two decentralized wastewater catchments in Golden, Colorado (clustered system population 400, and septic system population 32). Each site was sampled hourly for 26 h and samples were subsequently analyzed in triplicate for 32 TOrCs using liquid chromatography with tandem mass spectrometry and stable isotope dilution. Detection frequency (DF) of the various TOrCs was positively correlated with sewershed size with the greatest DF of the targeted TOrCs at the Boulder site and with decreasing DF with decreasing sewershed size. Site-specific fluctuations were both scale and compound-specific. The 11 TOrCs detected greater than 75% of the time across all three sites were used to further investigate and quantify variability and to develop a statistical model to investigate the flow-dependence and time-dependence of TOrC variability. Sewershed scale was inversely correlated to variability with coefficients of variation ranging from 0.24 to 0.96, 0.39 to 2.22, and 0.32 to 3.93 for the Boulder, cluster, and septic sites, respectively. A significant linear relationship was observed between concentration and flow and concentration and the concentration at prior time points for most TOrCs at the Boulder site. This suggests less variable influent concentrations result from dispersion and mixing in the conveyance system and a larger number of discrete inputs. A notable exception was the chlorinated flame retardant TCPP, which is likely associated with a high concentration, low-flow industrial input. A significant linear relationship between flow and concentration and sequential time points was not common at the decentralized sites. Scientists and engineers developing decentralized treatment systems must consider a larger range of influent qualities, particularly with respect to TOrCs. [Copyright &y& Elsevier]

Abstract: Lead samples were collected at the tap from homes with lead service lines (LSLs) in a full-scale utility using both random daytime (RDT) and particulate stimulation sampling (PSS) protocols. Analysis of the results revealed two sources and occurrences of particulate lead. A first source is due to corrosion of lead-bearing elements in the premise plumbing (PP) and occurs mostly at low to moderate concentrations <3μg/L, with some sporadic higher concentrations (4–12μg/L). These spikes were consistently observed and considerably increased using PSS, showing that current sampling protocols may miss a significant portion of particulate lead. The second source results from the adsorption of dissolved lead onto iron deposits in LSL/PP, and is continuously present at low to moderate concentrations. Statistical analyses were validated by physical analyses of: (i) lead scales from LSLs; and (ii) lead particles from tap aerators. [Copyright &y& Elsevier]

Abstract: Synthetic musk compounds (SMCs) occur widely in water environments. The aims of this paper were to investigate the occurrence and fate of SMCs in sewage treatment plants (STPs) and surface waters. Total SMC concentrations ranged from 3.69 to 7.33μg/L (influent) and from 0.96 to 2.69μg/L (effluent) in 10 STPs. The SMC concentrations varied with the input source and treatment volume of each STP. Biological treatment processes had a greater SMCs removal effect than chemical treatment, filtration and disinfection processes. The SMC concentrations in surface waters ranged from 0.15 to 16.72μg/L and exhibited similar SMCs occurrence patterns generally. The fate of SMCs in water environments depends on their physical–chemical properties and their concentrations can be predicted from other SMC concentrations due to their similar fates. [Copyright &y& Elsevier]

Abstract: In order to determine the occurrence of fungi in different drinking water sources and capture variability in terms of matrix composition and seasonal effects, surface water, spring water, and groundwater samples were collected in numerous sampling events. The occurrence and significance of fungi detected in the different water sources are reported and discussed in terms of colony-forming units per millilitre and by the identification of the most frequently detected isolates, at the species level, based on morphology and other phenotypic characters. All the samples were also analyzed in terms of total coliforms and Escherichia coli that are widely monitored bacteria considered as microbiology indicators of water quality. All the groundwater samples showed significantly lower levels of total coliforms, E. coli, and fungi compared to the surface and spring water samples. No significant correlations were found between the levels of fungi detected in all the matrices and the physico-chemical parameters and bacteria regularly monitored by drinking water utilities. Fifty-two fungi isolates were identified in this study, most of which have never been described to occur in water sources. The results obtained show that fungi occur widely in drinking water sources and that further studies should be conducted to address their biodegradation potential as well as if the drinking water treatment processes currently used are effective in removing these organisms and the potential secondary metabolites produced. [Copyright &y& Elsevier]

The presence of earthy-musty odors in drinking water is a major concern for water suppliers and consumers worldwide. While geosmin and 2-methylisoborneol are the most studied earthy-musty odor-causing compounds, pyrazine and its alkyl and methoxy compounds possess similar odors and are widely distributed in nature, foods, and beverages. In this study, odor characteristics of pyrazines and their presence in natural and treated waters were determined. Pyrazine, 2,6-dimethyl-pyrazine (DMP), 2,3,5-trimethyl-pyrazine (TrMP), 2-ethyl-5(6)-methyl-pyrazine (EMP), 2,3,5,6-tetramethyl-pyrazine (TeMP), 2-isobutyl-3-methoxy-pyrazine (IBMP) and 2-isopropyl-3-methoxy-pyrazine (IPMP) were measured in source and finished drinking water across China. 2-Methoxy-3,5-dimethyl-pyrazine (MDMP), IBMP, and IPMP were investigated in rivers in Virginia, USA. The results showed that "musty" and "sweet" were the most common descriptors for pyrazine, DMP, MDMP, TrMP, and TeMP. While IBMP and IPMP were never detected in 140 source or drinking water samples from across China, pyrazine, DMP, MDMP, TrMP, and TeMP occurred throughout with concentrations of n.d.−62.2 ng/L-aq in source water and n.d.−39.6 ng/L-aq in finished water. IBMP, IPMP, and MDMP were present in two Virginia rivers; MDMP occurred in 18% of the samples with concentrations of n.d.−4.4 ng/L, many of which were above the aqueous odor threshold of 0.043 ng/L MDMP. The removal efficiencies through conventional water treatment were poor, ranging from negative removals to ∼10%. Advanced oxidation water treatment could only remove EMP and TrMP. The widespread presence of earthy-musty-sweet pyrazines in source and drinking waters on two continents, their poor removal during water treatment, and ng/L odor threshold concentrations confirm their potential to be T&O issues for consumers. Image 1 • Pyrazines co-occur widely and are often found in source and drinking waters. • "Musty" and "sweet" were the dominant descriptors applied to all five pyrazines. • Pyrazines can have low ng/L OTCs and are overlooked as T&O contributors. • Conventional and advanced oxidation treatment showed limited removal of pyrazines. • Using Henry's Law and OTCs in water to predict OTCs in air could be a powerful tool. [ABSTRACT FROM AUTHOR]

Coronaviruses (CoV) are a large family of viruses causing a spectrum of disease ranging from the common cold to more severe diseases as Middle East Respiratory Syndrome (MERS-CoV) and Severe Acute Respiratory Syndrome (SARS-CoV). The recent outbreak of coronavirus disease 2019 (COVID-19) has become a public health emergency worldwide. SARS-CoV-2, the virus responsible for COVID-19, is spread by human-to-human transmission via droplets or direct contact. However, since SARS-CoV-2 (as well as other coronaviruses) has been found in the fecal samples and anal swabs of some patients, the possibility of fecal-oral (including waterborne) transmission need to be investigated and clarified. This scoping review was conducted to summarize research data on CoV in water environments. A literature survey was conducted using the electronic databases PubMed, EMBASE, and Web Science Core Collection. This comprehensive research yielded more than 3000 records, but only 12 met the criteria and were included and discussed in this review. In detail, the review captured relevant studies investigating three main areas: 1) CoV persistence/survival in waters; 2) CoV occurrence in water environments; 3) methods for recovery of CoV from waters. The data available suggest that: i) CoV seems to have a low stability in the environment and is very sensitive to oxidants, like chlorine; ii) CoV appears to be inactivated significantly faster in water than non-enveloped human enteric viruses with known waterborne transmission; iii) temperature is an important factor influencing viral survival (the titer of infectious virus declines more rapidly at 23°C–25 °C than at 4 °C); iv) there is no current evidence that human coronaviruses are present in surface or ground waters or are transmitted through contaminated drinking-water; v) further research is needed to adapt to enveloped viruses the methods commonly used for sampling and concentration of enteric, non enveloped viruses from water environments. The evidence-based knowledge reported in this paper is useful to support risk analysis processes within the drinking and wastewater chain (i.e., water and sanitation safety planning) to protect human health from exposure to coronavirus through water. • SARS Coronavirus has been detected in wastewater but not as infectious particles. • Temperature is an important environmental factor affecting CoV survival in water. • CoV show limited environmental stability and sensitivity to oxidants as chlorine. • There is no evidence of CoV transmission through contaminated water. • Methods for CoV concentration from waters should be optimized. [ABSTRACT FROM AUTHOR]

The seasonal and diurnal patterns of N -nitrosomorpholine (NMOR) and its formation potential (NMOR FP) were examined with water samples taken from five outlets of four sewage treatment plants (STPs), seven main stream sites, and five tributary sites in the Yodo River basin. STPs were shown to be the main sources of downstream NMOR load. The highest NMOR levels were found in the discharge from one STP (26.4–171 ng/L). Continuous sequential samplings over a period of 24 h at this STP revealed that NMOR flux at the influent point fluctuated in both summer (0.4–3.2 g/h) and winter (0.3–5.4 g/h), while it was steady in the effluent. In addition, levels of NMOR remained stable during the biological treatment and disinfection processes. The present research demonstrated that NMOR could be formed from morpholine (MOR) in raw sewage treated by this STP, with a possible mechanism being formaldehyde-catalyzed nitrosation of MOR by nitrites, prior to raw sewage entering the STP. This implies that the NMOR detected here might not be a disinfection byproduct per se under low-chlorine disinfection (around 1.0 mg/L), but is primarily a contaminant that is difficult to remove during sewage treatment. NMOR attenuated significantly in the rivers in the daytime with production of MOR, but persisted during nights, which demonstrated the importance of monitoring NMOR levels in the water environment during periods of low UV intensity, especially nights. Image 1 • Seasonal and diurnal patterns of NMOR and NMOR FP were investigated. • NMOR can form via formaldehyde-catalyzed nitrosation of MOR by nitrites before STPs. • NMOR was stable during biological treatment and disinfection processes. • NMOR in rivers attenuated significantly during the day but persisted at night. [ABSTRACT FROM AUTHOR]