A picture of pharmaceutical pollution in landfill leachates: Occurrence, regional differences and influencing factors.

Municipal solid waste (MSW) landfill sites have been identified as a significant source of pharmaceuticals in the environment because unused or expired pharmaceuticals are discarded into MSW, which eventually percolate into leachates. However, the contamination of pharmaceuticals in landfill leachate in China is not comprehensively understood. Previous research into factors influencing pharmaceutical concentrations focused on a limited number and type of target pollutants or restricted study area. In the present study, 66 pharmaceuticals were analyzed (including 45 antibiotic and 21 non-antibiotic pharmaceuticals, also categorized as 59 prescription and 7 non-prescription pharmaceuticals) in leachate samples from landfill sites with various characteristics in different regions of China. The results indicated that non-antibiotic pollutants were present at significantly higher concentrations than antibiotic pollutants, with median concentrations of 1.74 µg/L and 527 ng/L, respectively. Non-antibiotic pollutants also presented a higher environmental risk than antibiotic pollutants, by 2 to 4 orders of magnitude, highlighting that non-antibiotic pharmaceuticals should not be overlooked during the assessment of landfill leachate. Pharmaceutical concentrations in landfill leachate samples exhibited regional differences; the population size served by the landfills was the dominant factor contributing to the observed differences. In addition, landfill characteristics such as the solid waste composition and MSW loading can also affect pharmaceutical concentrations in landfill leachate. Despite the implementation of the classification and disposal policy of MSW in Shanghai, China since July 2019, specifying that unused or expired pharmaceuticals should be discarded as hazardous waste, high levels of pharmaceutical contaminations were detected in leachate from the main components of classified MSW (i.e., residual and food waste). These findings emphasize the importance of pharmaceutical management in solid waste systems.

Microplastics in different municipal solid waste treatment and disposal systems: Do they pose environmental risks?

Microplastic (MP) pollution is a significant worldwide environmental and health challenge. Municipal solid waste (MSW) can be an important source of MPs in the environment if treated and disposed of inappropriately, causing potential ecological risks. MSW treatment and disposal methods have been gradually shifting from landfilling/dumping to more sustainable approaches, such as incineration or composting. However, previous studies on MP characteristics in different MSW treatment and disposal systems have mainly focused either on landfills/dumpsites or composts. The lack of knowledge of multiple MSW treatment and disposal systems makes it difficult to ensure effective MP pollution control during MSW treatment and disposal. Therefore, this study systematically summarizes the occurrence of MPs in different MSW treatment and disposal systems (landfill/dumpsite, compost, and incineration) on the Eurasian scale, and discusses the factors that influence MPs in individual MSW treatment and disposal systems. In addition, the paper assesses the occurrence of MPs in the surrounding environment of MSW treatment and disposal systems and their ecological risks using the species sensitivity distribution approach. The study also highlights recommendations for future research, to more comprehensively describe the occurrence and fate of MPs during MSW treatment and disposal processes, and to develop appropriate pollution control measures to minimize MP pollution.

Absorption and translocation of selected pharmaceuticals in Pistia stratiotes: Spatial distribution analysis using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.

Phytoremediation can eliminate pharmaceuticals from aquatic environments through absorption; however, understanding of absorption and transport processes in plants remains limited. In this study, a matrix-assisted laser desorption/ionization time-of-flight mass spectrometry imaging (MALDI-MSI) method was developed to explore the absorption and translocation mechanisms of seven common pharmaceuticals in Pistia stratiotes. Results showed that 2,3-dicyanohydroquinone, an infrequently used matrix, exhibited outstanding performance in MALDI-MSI analysis, producing the highest signal intensity for four of the seven pharmaceuticals. Region of Interest (ROI) analysis revealed that charge speciation of pharmaceuticals significantly influenced their ability to enter vascular bundle. Neutral and positively charged pharmaceuticals easily entered vascular bundle, while negatively charged pharmaceuticals faced difficulty. ROI results for neutral and negatively charged pharmaceuticals exhibited positive correlation with their transfer factor values, indicating that their translocation ability from root to shoot was related to their capacity to enter vascular bundle. However, no correlation was observed for positively charged pharmaceuticals, suggesting that these compounds, upon entering vascular bundle, encountered difficulties in upward translocation through the xylem. This study introduces an innovative approach and offers novel insights into the retention and migration of pharmaceuticals in plant tissues, aiming to enhance the understanding of pharmaceutical accumulation in plants. ENVIRONMENTAL IMPLICATION: Pharmaceuticals in aquatic environment can inflict detrimental effects on both human health and ecosystem. Phytoremediation can remove pharmaceuticals from aquatic environments through absorption. However, our understanding of absorption and transportation of pharmaceuticals in plants remains limited. This study developed a matrix-assisted laser desorption/ionization time-of-flight mass spectrometry imaging (MALDI-MSI) method for pharmaceuticals in plant roots, and to explore the absorption and translocation mechanisms of pharmaceuticals. The study offers direct evidence of differences in accumulation behavior of pharmaceuticals in plants, providing valuable insights for targeted and effective strategies in using plants for remediating the aquatic ecosystem from pharmaceuticals.

Occurrence, behaviors, and fate of per- and polyfluoroalkyl substances (PFASs) in typical municipal solid waste disposal sites.

Per- and polyfluoroalkyl substances (PFASs) have become a crucial environmental concern owing to their exceptional persistence, ability to bioaccumulate within ecosystems, and potential to adversely affect biota. Products and materials containing PFASs are usually discarded into municipal solid waste (MSW) at the end of their life cycle, and the fate of PFASs may differ when different disposal methods of MSWs are employed. To date, limited research has focus on the occurrence, behaviors, and fate of PFASs emitted from various MSW disposal sites. This knowledge gap may lead to an underestimation of the contribution of MSW disposal sites as a source of PFASs in the environment. In this review, we collated publications concerning PFASs from typical MSW disposal sites (i.e., landfills, incineration plants, and composting facilities) and explored the occurrence patterns and behaviors of PFASs across various media (e.g., landfill leachate/ambient air, incineration plant leachate/ash, and compost products) in these typical MSW disposal sites. In particular, this review highlighted ultrashort-chain perfluoroalkyl acids and "unknown"/emerging PFASs. Additionally, it meticulously elucidated the use of non-specific techniques and non-target analysis for screening and identifying these overlooked PFASs. Furthermore, the composition profiles, mass loads, and ecological risks of PFASs were compared across the three typical disposal methods. To the best of our knowledge, this is the first review regarding the occurrence, behaviors, and fate of PFASs in typical MSW disposal sites on a global scale, which can help shed light on the potential environmental impacts of PFASs harbored in MSWs and guide future waste management practices.

FOXO3a Induces Myocardial Fibrosis by Upregulating Mitophagy.

BACKGROUND: Atrial fibrillation is one of the most common cardiac arrhythmias. Myocardial fibrosis is closely associated with atrial remodeling, which leads to heightened risk of atrial fibrillation. This study aimed to explore whether forkhead box protein O3 (FOXO3a) impacts myocardial fibrosis incidence by regulating mitophagy. METHODS: Cell viability was assessed by cell counting kit-8 (CCK-8) assays. The expression of vimentin and cytochrome C was detected by immunofluorescence assays. Quantitative real-time polymerase chain reaction (PCR) was used to analyze the relative mRNA level of FOXO3a. Expression of FOXO3a, phosphorylated FOXO3a, Collagen I, Collagen III, alpha-smooth muscle actin (α-SMA), matrix metalloprotease 9 (MMP9), light chain 3 (LC3), phosphatase and tensin homolog (PTEN)-induced kinase 1 (PINK1), Parkin, and sequestosome-1 (p62) proteins were determined by western blotting. 5-ethynyl-2'-deoxyuridine (EDU) incorporation was employed to measure cell proliferation. Changes in mitochondrial membrane potential were determined by 5,5',6,6'-tetrachloro-1,1',3,3'-tetraethyl-imidacarbocyanine iodide (JC-1) staining. A wound healing assay was used to examine cell migration, and the levels of reactive oxygen species were determined by flow cytometry. RESULTS: The expression of FOXO3a was upregulated in cardiac fibroblasts treated with angiotensin II (AngII), while the expression of phosphorylated FOXO3a was downregulated under these conditions. FOXO3a knockdown significantly inhibited the proliferation, migration and collagen secretion of cardiac fibroblasts treated with AngII. The ratio of LC3 II/I as well as expression of PINK1 and Parkin was increased, and the expression of p62 was decreased, in cardiac fibroblasts treated with AngII. Moreover, these effects were limited by FOXO3a knockdown. Finally, the mitophagy inducer everolimus (RAD001) attenuated the suppressive effect of FOXO3a knockdown on cardiac fibroblast activation. CONCLUSIONS: FOXO3a promotes the progress of myocardial fibrosis by triggering mitophagy in cardiac fibroblasts.

Perfluoroalkyl acid precursors in agricultural soil-plant systems: Occurrence, uptake, and biotransformation.

Perfluoroalkyl acid (PFAA) precursors have been used in various consumer and industrial products due to their hydrophobic and oleophobic properties. In recent years, PFAA precursors in agricultural soil-plant systems have received increasing attention as they are susceptible to biotransformation into metabolites with high biotoxicity risks to human health. In this review, we systematically assessed the occurrence of PFAA precursors in agricultural soils, taking into account their sources and biodegradation pathways. In addition, we summarized the findings of the relevant literature on the uptake and biotransformation of PFAA precursors by agricultural plants. The applications of biosolids/composts and pesticides are the main sources of PFAA precursors in agricultural soils. The physicochemical properties of PFAA precursors, soil organic carbon (SOC) contents, and plant species are the key factors influencing plant root uptakes of PFAA precursors from soils. This review revealed, through toxicity assessment, the potential of PFAA precursors to generate metabolites with higher toxicity than the parent precursors. The results of this paper provide a reference for future research on PFAA precursors and their metabolites in soil-plant systems.

Organic pollutants adsorbed on microplastics: Potential indicators for source appointment of microplastics.

Pollution by microplastics (MPs) has caused potential threats to the environment. Understanding the sources of MPs in the environment can help control their emissions and reduce environmental risks. Source apportionment of MPs has been conducted according to the characteristics of MPs themselves (such as types of polymers and morphological characteristics). However, the specificity and resolution of the appointments of sources need to be improved. Organic pollutants adsorbed on MPs can be used as a novel and reliable indicator to identify the source of MPs in the environment. In the present work, the analytical methods of MPs and organic pollutants adsorbed on MPs were critically reviewed, and the occurrence of organic pollutants and factors influencing their adsorption on MPs were discussed. Furthermore, the potential applications of organic pollutants adsorbed on MPs as indicators for determining the sources of MPs were highlighted. The study would help recognize the sources of MPs, which will support efforts aimed at reducing their emissions and further pollution of the ecosystem.

FeS as excellent co-activator driving nano calcium peroxide oxidation for contaminants degradation: Performance and mechanisms.

In this study, ferrous sulfide (FeS) was introduced to nano calcium peroxide (nCP)/Fe(III) system to facilitate the generation of Fe(II), more than 90% of naphthalene (NAP) could be removed at a wide pH range of 3-9. As a heterogeneous reductant, FeS could mitigate competitive reactions with reactive oxygen species (ROS), which favored the NAP degradation. As evidenced by scavenging experiments, HO• was the major ROS contributing to NAP degradation. The role of sulfur species (S2-, SO32-, and S2O32-) in nCP/Fe(III) system was investigated with S2O32- showing the preferable reactivity in Fe(III) reduction. In addition, the surface-bound HO• and surface Fe(II) were detected and the role of them on NAP degradation was revealed and concluded that both dissolved and surface Fe(II) contributed to NAP degradation, whereas surface-bound HO• was not superior to solution HO• in degrading NAP. Furthermore, nCP/Fe(III)/FeS system showed high feasibility to different solution matrixes and various types of water as well as the broad-spectrum reactivity to other toxic organic pollutants, exhibiting promise for practical application to remediate complex contaminants.

Effect of aggregation behavior on microplastic removal by magnetic Fe3O4 nanoparticles.

Magnetic nanotechnologies have been shown to be an efficient approach to the reduction of microplastic (MP) pollution in aquatic environments. However, uncertainties remain regarding the relationship between particle stability and MP removal under varying water conditions, hindering the practical application of magnetic nanotechnologies for MP removal. Herein, the influence of particle aggregation behavior on nano-scale MP removal by Fe3O4 nanoparticles (FNPs) was investigated, by monitoring dynamic light scattering parameters and analyzing the microstructures of particle aggregates. Results showed that 83.1 %-92.9 % of MPs could be removed by FNPs within 1 h, and MP removal exhibited a high degree of Pearson correlation (R = 0.95; P = 0.04) with particle aggregation behavior mediated by the FNPs dosage. Furthermore, pH-dependent electrostatic interactions significantly influenced particle aggregation behavior and the removal of MPs. Under pH <6.7 conditions, electrostatic attraction between electropositive FNPs and electronegative MPs led to charge neutralization-induced aggregation and efficient removal MP performance. Under increasingly saline conditions, compression of the electrical double layer enhanced the self-aggregation behavior of MPs, weakening the electrostatic repulsion between FNPs and MPs under alkaline conditions. Therefore, salinity improved the MP removal efficiency, especially under alkaline conditions, with MP removal increasing from 4.47 % to 55.1 % when the mass fraction of NaCl was increased from 0 % to 1 %. These findings further our understanding of the effect of aggregation behavior on MP removal by FNPs and highlight the potential for magnetic nanotechnology application in the removal of nano-scale MPs from aquatic environments, while also providing valuable insights for the design of FNP-based materials.

Comparative studies of organic contaminant removal in different calcium sulfite-enhanced oxidant/Fe(II) systems: Kinetics, mechanisms, and differentiated degradation pathways.

The application of S(IV) for the regeneration of Fe(II) has been widely investigated. As the common S(IV) sources, sodium sulfite (Na2SO3) and sodium bisulfite (NaHSO3) are soluble in the solution, resulting in excessive SO32- concentration and redundant radical scavenging problems. In this research, calcium sulfite (CaSO3) was applied as the substitution for the enhancement of different oxidant/Fe(II) systems. The advantages of CaSO3 could be summarized as follows: (1) it could sustainedly supplement SO32- for Fe(II) regeneration, preventing radical scavenging and unnecessary reagent waste; (2) the cost and toxicity of CaSO3 were extremely lower than that of other S(IV) sources; (3) the concentration of reactive species increased in the presence of CaSO3; and (4) after the reaction, SO42- would form CaSO4 precipitate, which would not increase the burden of SO42- in the solution. In the participation of CaSO3, the removal of trichloroethylene (TCE) and other organic contaminants were significantly promoted and different enhanced systems had high tolerance on complex solution conditions. The major reactive species in different systems were determined through qualitative and quantitative analyses. Eventually, the dechlorination and mineralization of TCE were measured and the differentiated degradation pathways in different CaSO3-enhanced oxidants/Fe(II) systems were elucidated.

The efficiency of full-scale subsurface constructed wetlands with high hydraulic loading rates in removing pharmaceutical and personal care products from secondary effluent.

Constructed wetlands (CWs) are usually operated at low hydraulic load rates (HLRs) of < 0.5 m3/m2/d, and can efficiently remove pharmaceuticals and personal care products (PPCPs) from wastewaters. They however often occupy a large area of land, especially when treating the secondary effluent from wastewater treatment plants (WWTPs) in megacities. High-load CWs (HCWs) with an HLR ≥ 1 m3/m2/d, requiring smaller land areas, are a good option for urban areas. However, their performance for PPCP removal is not clear. In this study, we evaluated the performance of three full-scale HCWs (HLR: 1.0-1.3 m3/m2/d) to remove 60 PPCPs, and found they had a stable removal performance and a higher areal removal capacity than the previously reported CWs operated at low HLRs. We verified the advantages of HCWs by testing the efficiency of two identical CWs at a low HLR (0.15 m3/m2/d) and a high HLR (1.3 m3/m2/d) fed with the same secondary effluent. The areal removal capacity during the high-HLR operation was 6-9 times higher than that during the low-HLR operation. A high dissolved oxygen content, and low COD and NH4-N concentrations in the secondary effluent were critical for the robust PPCP removal by tertiary treatment HCWs.

Estimating the Mass of Pharmaceuticals Harbored in Municipal Solid Waste Landfills by Analyzing Refuse Samples at Various Ages and Depths.

Pharmaceuticals have been detected at high concentrations in municipal solid waste (MSW) landfill leachates, which are recognized as an underestimated source of pharmaceutical residues in the environment. However, limited efforts have been made to characterize pharmaceuticals in MSW landfill refuse, which is also of significant concern given the potential long-term environmental impact. Herein, we excavated landfill refuse from six cells with landfill ages of 7-27 years in the largest MSW landfill in Shanghai (in each cell, landfill refuse was collected from different depths of 2-8 m) and analyzed samples for the presence of 55 pharmaceuticals, including antibiotics and non-antibiotics. The results reveal the presence of 42 pharmaceuticals in landfill refuse, with median concentrations ranging from 0.30 to 116 µg/kg. Antibiotic and non-antibiotic pharmaceuticals exhibited diverse concentration trends with age, related to changes in policy intervention and consumption over time. Different concentration variations of individual pharmaceuticals were observed in refuse samples excavated at different depths and positively correlated to their sorption ability. The mass of pharmaceuticals in the investigated landfill was estimated from the obtained concentrations to be 80-220 tons with 95% probability, based on Monte Carlo analysis. To the best of our knowledge, this study provides the first estimate of pharmaceutical mass in an MSW landfill. The results will be helpful for understanding the potential long-term environmental impact of pharmaceuticals in landfills.

Mechanism and characterization of microplastic aging process: A review.

With the increasing production of petroleum-based plastics, the problem of environmental pollution caused by plastics has aroused widespread concern. Microplastics, which are formed by the fragmentation of macro plastics, are bio-accumulate easily due to their small size and slow degradation under natural conditions. The aging of plastics is an inevitable process for their degradation and enhancement of adsorption performance toward pollutants due to a series of changes in their physiochemical properties, which significantly increase the toxicity and harm of plastics. Therefore, studies should focus on the aging process of microplastics through reasonable characterization methods to promote the aging process and prevent white pollution. This review summarizes the latest progress in natural aging process and characterization methods to determine the natural aging mechanism of microplastics. In addition, recent advances in the artificial aging of microplastic pollutants are reviewed. The degradation status and by-products of biodegradable plastics in the natural environment and whether they can truly solve the plastic pollution problem have been discussed. Findings from the literature pointed out that the aging process of microplastics lacks professional and exclusive characterization methods, which include qualitative and quantitative analyses. To lessen the toxicity of microplastics in the environment, future research directions have been suggested based on existing problems in the current research. This review could provide a systematic reference for in-depth exploration of the aging mechanism and behavior of microplastics in natural and artificial systems.

Impacts of garbage classification and disposal on the occurrence of pharmaceutical and personal care products in municipal solid waste leachates: A case study in Shanghai.

Leachate generated during the treatment and disposal of municipal solid wastes (MSWs) can be an important source of pharmaceutical and personal care products (PPCPs) in the environment. With the implementation of garbage classification policy in China, the disposal methods of MSWs have changed, while its impacts on the occurrence of PPCPs in the generated leachate remain unknown. In this study, we investigated 49 target PPCPs in the leachates of classified MSWs, i.e. residual waste leachate (RWL) and food waste leachate (FWL), and revealed the influence of garbage classification implementation on the occurrence of PPCPs in leachates to be treated. The results showed the concentration and mass load of target PPCPs in the RWL samples (median values: 34.9 ng/L and 52.3 mg/d, respectively) were significantly higher than those in the FWL samples (median values: 19.3 ng/L and 14.5 mg/d, respectively). Macrolide (ML) antibiotics were the predominant PPCPs in the RWL samples, while in the FWL samples, quinolone (QL) antibiotics exhibited the highest concentration and mass load. The implementation of garbage classification policy led to the reduction of PPCP mass load (from 739 g/d to 262 g/d) in leachates to be treated. The findings are helpful for better designing or managing MSW treatment and disposal processes to minimize the emission of PPCPs from MSW leachates.

Multiclass target analysis of contaminants of emerging concern including transformation products, soil bioavailability assessment and retrospective screening as tools to evaluate risks associated with reclaimed water reuse.

The occurrence of 200 multiclass contaminants of emerging concern (CECs) encompassing 168 medicinal products and transformation products (TPs), 5 artificial sweeteners, 12 industrial chemicals, and 15 other compounds was investigated in influent and effluent wastewater samples collected during 7 consecutive days from 5 wastewater treatment plants (WWTPs) located in Cyprus. The methodology included a generic solid-phase extraction protocol using mixed-bed cartridges followed by Ultra-High Performance Liquid Chromatography coupled with Quadrupole-Time of Flight Mass Spectrometry (UHPLC-QTOF-MS) analysis. A total of 63 CECs were detected at least in one sample, with 52 and 55 out of the 200 compounds detected in influents and effluents, respectively. Ten (10) out of the 24 families of parent compounds and associated TPs were found in the wastewater samples (influent or effluent). 1-H-benzotriazole, carbamazepine, citalopram, lamotrigine, sucralose, tramadol, and venlafaxine (>80 % frequency of appearance in effluents) were assessed with respect to their bioavailability in soil as part of different scenarios of irrigation with reclaimed water following a qualitative approach. A high score of 12 (high probability) was predicted for 2 scenarios, a low score of 3 (rare occasions) for 2 scenarios, while the rest 28 scenarios had scores 5-8 (unlikely or limited possibility) and 9-11 (possibly). Retrospective screening was performed with the use of a target database of 2466 compounds and led to the detection of 158 additional compounds (medicinal products (65), medicinal products TPs (15), illicit drugs (7), illicit drugs TPs (3), industrial chemicals (11), plant protection products (25), plant protection products TPs (10), and various other compounds (22). This work aspires to showcase how the presence of CECs in wastewater could be investigated and assessed at WWTP level, including an expert-based methodology for assessing the soil bioavailability of CECs, with the aim to develop sustainable practices and enhance reclaimed water reuse.

[Succession and PICRUSt2-based Predicted Functional Analysis of Microbial Communities During the Sludge Bulking Occurrence and Restoration in One-stage Combined Partial Nitritation and ANAMMOX Process].

This study was based on the pilot one-stage combined partial nitritation and ANAMMOX process (CPNA), using data mining and analysis of 16S rRNA high-throughput sequencing data of activated sludge in the process of sludge bulking and recovery, combined with PISCRUSt2. The function prediction analysis aimed to reveal the microbial community changes and the characteristics of nitrogen metabolism and carbon metabolism at different stages of sludge bulking and recovery of the one-stage CPNA process. The results of the study showed that the microbial α-diversity in the sludge bulking and recovery process first increased and then declined. The relative abundance of Nitrosomonas, Candidatus_Brocadia, and Thaurea decreased in the sludge-bulking stage from 12.36%, 11.86%, and 0.272% to 5.97%, 8.30%, and 0.061%, whereas the relative abundance of Candidatus Kuenenia remained stable. The relative abundance of Levilinea, Longilinea, and Turicibacter increased from 0.031%, 0.018%, and 0.009% to 0.055%, 0.025%, and 0.033%. The PICRUSt2 function prediction analysis results showed that there were a total of 47 functional enzyme genes involved in nitrogen metabolism, of which nitrification, denitrification, dissimilative nitrate reduction (DNRA), assimilation nitrate reduction (ANRA), and nitrogen fixation were relatively abundant. The degrees of each had changed. During the sludge-bulking stage, the relative abundance of the ammonia monooxygenase gene (pmoABC-amoABC) and the hydroxylamine dehydrogenase gene hao decreased, whereas the relative abundance of the nitrate-reducing gene increased at the initial stage and then showed a downward trend. Carbon metabolism analysis showed that sodium acetate had a promoting effect on the heterotrophic growth of the CPNA process, but the energy metabolism and glucose production of sodium acetate were not active.

Non-antibiotics matter: Evidence from a one-year investigation of livestock wastewater from six farms in East China.

Livestock wastewater is an important source of pharmaceuticals in aquatic environments; however, most related studies only focused on antibiotics. This study investigated 18 pharmaceutical active compounds (PhACs), including 12 antibiotics and 6 non-antibiotics, in livestock wastewater during a one-year survey of six livestock farms in East China. The results showed that four non-antibiotic PhACs-caffeine, N,N-diethyl-m-toluamide, gemfibrozil, and diclofenac-exhibited high detection frequencies (80% to 97%), high concentrations (median 0.43 to 3.79 µg/L), poor removal efficiencies (3% to 53%), and high environmental risks. A ranking system was developed to prioritize PhACs based on their occurrence, removal, and environmental risks in livestock wastewater; diclofenac, N,N-diethyl-m-toluamide, sulfamethazine, sulfadiazine, and gemfibrozil, were identified as the top five priority PhACs that should be considered first. Finally, a preliminary source apportionment protocol using four priority PhACs was proposed to trace the emission originating from treated and untreated livestock wastewater and to indicate the major contributor (cattle or swine farms) in the region. To the best of our knowledge, this is the first long-term investigation on the pollution characteristics of non-antibiotics in livestock wastewater in China, and our findings highlight the importance of considering non-antibiotics and the prioritized PhACs for the pollution control of PhACs in livestock wastewater.

Discharge of pharmaceuticals from a municipal solid waste transfer station: Overlooked influence on the contamination of pharmaceuticals in surface waters.

During the temporal storage of municipal solid wastes (MSWs), pharmaceutically contained in MSWs may percolate into leachates and migrate into receiving waters via surface runoff. However, knowledge of their intra-event variations during the rainfall is quite limited. To fill in this gap, we collected runoff samples in a typical MSW transfer station over the full length of a rainfall event to comprehensively characterize the pharmaceutical contamination profiles. The results showed that 18 pharmaceuticals were detected in the runoff samples with high frequencies and concentrations ranging from below MQL to 18.6 µg/L. During the rainfall event, pharmaceuticals exhibited discrepant leachabilities as a result of different sorption capacities; two concentration peaks of each pharmaceutical were observed, suggesting the leaching effect by rainwater and the potential influence of human-related rinse. A further sampling campaign for one-week-long runoff samples generated by diurnal rinse water was conducted, and the results indicated comparable mass loads of pharmaceuticals in surface runoff receiving rinse water (0.37-8250 µg) to those in rainfall runoff (0.58-1754 µg), suggesting the similar discharge of pharmaceuticals from MSW transfer stations despite the weather. The estimated per capita discharge load of caffeine, one of the typical Pharmaceuticals, from MSW transfer stations was 4383 ng capita-1 d-1, higher than that in other emission sources, e.g. municipal wastewater effluent, indicating an overlooked influence of MSW transfer stations on its contamination in the surface waters in Shanghai.

Quantitatively identifying the emission sources of pharmaceutically active compounds (PhACs) in the surface water: Method development, verification and application in Huangpu River, China.

Recognizing the main sources of pharmaceutically active compounds (PhACs) found in surface waters has been a challenge to the effective control of PhAC contamination from the sources. In the present study, a novel method based on Characteristic Matrix (ChaMa) model of indicator PhACs to quantitatively identify the contribution of multiple emission sources was developed, verified, and applied in Huangpu River, Shanghai. Carbamazepine (CBZ), caffeine (CF) and sulfadiazine (SDZ) were proposed as indicators. Their occurrence patterns in the corresponding emission sources and the factor analysis of their composition in the surface water samples were employed to construct the ChaMa model and develop the source apportionment method. Samples from typical emission sources were collected and analyzed as hypothetical surface water samples, to verify the method proposed. The results showed that the calculated contribution proportions of emission sources to the corresponding source samples were 45%-85%, proving the feasibility of the method. Finally, the method was applied to different sections in Huangpu River, and the results showed that livestock wastewater was the dominant emission source, accounting for 55%-73% in the upper reach of Huangpu River. Untreated municipal wastewater was dominant in the middle and lower reaches of Huangpu River, accounting for 76%-94%. This novel source apportionment method allows the quantitative identification of the contribution of multiple PhAC emission sources. It can be replicated in other regions where the occurrence of localized indicators was available, and will be helpful to control the contamination of PhACs in the water environment from the major sources.

[Nitrite Regulation During Start-up of Combined Partial Nitritation and ANAMMOX Process].

Two types of full-scale reactors(SBR, 116.6 m3, activated sludge process; SBBR, 64.8 m3, activated sludge and biofilm process) were inoculated with activated sludge from a swine wastewater treatment plant. The effect of NO2--N concentration on ANAMMOX was investigated in the reactors during the start-up of the combined partial nitritation and ANAMMOX(CPNA) process by controlling the dissolved oxygen(DO), aeration mode, and NaNO2 dosing. The results showed that the SBBR was more suitable for rapid start-up of partial nitritation under the same operation conditions. Despite NO2--N inhibition(100-129 mg·L-1, 7 days), the ANAMMOX process was successfully started by the SBR on day 39, and the total nitrogen removal rate and efficiency(TNRR and TNRE) were 0.069 kg·(m3·d) -1 and 23.3%, respectively. However, 17 days of NO2--N inhibition(129-286 mg·L-1) had an unrecoverable effect on ANAMMOX activity in the SBBR. By adding NaNO2, the SBR successfully started the CPNA process on day 77. The TNRR, TNRE, and activity of ANAMMOX from day 51 to 77 increased rapidly from 0.070 to 0.336 kg·(m3·d) -1, 16.0% to 52.2%, and 0.012 to 0.307 kg·(kg·d) -1, respectively. The gene copy concentration of AOB and ANAMMOX bacteria in the SBR increased from the original 8.06×106 and 4.42×104 copies·mL-1 to 1.02×109 and 1.77×107 copies·mL-1, respectively, which indicated that the rapid enrichment of AOB and ANAMMOX bacteria in the SBR was achieved mainly by controlling DO, aeration mode, and NaNO2 dosing. Reasonable nitrite regulation is the key for the start of the CPNA process.