ABSTRACT
Microplastics (MPs) pollution in freshwater poses a risk to various ecosystems and health security. In 2018, the Chinese government banned fishing since 2018 in the Three Gorges Reservoir (TGR), but the fate and risk of MPs in wild fish remain unclear. Therefore, a detailed investigation was conducted into the occurrence of MPs in 18 wild fish species in the TGR using a Micro Fourier Transform Infrared Spectrometer, and the trophic transfer and risks were assessed. MPs in fish were aged, with abundances ranging from 0.68 ± 0.98 to 4.00 ± 2.12 items/individual. Most particles were less than 1 mm in size (73.4 %), with fibers being the dominant shape (48.9 %) and transparent as the dominant color (35 %). Polyethylene (PE) was the most prevalent type. The bioconcentration factor (BCF), bioaccumulation factor (BAF), trophic magnification factor (TMF) and polymer hazard index (PHI) were low, suggesting no trophic transfer and a low risk of MPs. The BAF may provide a more reasonable description of the degree of enrichment of MPs, and 'items/individual' or 'g/individual' can be used to describe MPs concentrations in fish. This study proposes new insights and prospectives that can help researchers better understand MPs enrichment in fish across various trophic levels.
ABSTRACT
Triphenyltin (TPT) is widely used in crop pest control and ship antifouling coatings, which leads to its entry into aquatic environment and poses a threat to aquatic organisms. However, the effects of TPT on the early life stages of wild fish in natural water environments remains unclear. The aim of this study was to assess the toxic effects of TPT on the early life stages of fish under two different environments: field investigation and laboratory experiment. The occurrence of deformities in wild fish embryos and larvae in the Three Gorges Reservoir (TGR) and the developmental toxicity of TPT at different concentrations (0, 0.15, 1.5 and 15 µg Sn/L) to zebrafish embryos and larvae were observed. The results showed that TPT content was higher in wild larvae, reaching 27.21 ng Sn/g w, and the malformation of wild fish larvae mainly occurred in the eyes and spine under natural water environment. Controlled experiment exposure of zebrafish larvae to TPT also resulted in eye and spinal deformities. Gene expression analysis showed that compared with the control group, the expression levels of genes related to eye development (sox2, otx2, stra6 and rx1) and spine development (sox9a and bmp2b) were significantly up-regulated in the 15 µg Sn/L exposure group, which may be the main cause of eye and spine deformity in the early development stage of fish. In addition, the molecular docking results further elucidate that the strong hydrophobic and electrostatic interactions between TPT and protein residues are the main mechanism of TPT induced abnormal gene expression. Based on these results, it can be inferred that TPT is one of the teratogenic factors of abnormal eye and spine development in the early life stage of fish in the TGR. These findings have important implications for understanding the toxicity of TPT on fish.
Subject(s)
Embryo, Nonmammalian , Larva , Organotin Compounds , Water Pollutants, Chemical , Zebrafish , Animals , Organotin Compounds/toxicity , Water Pollutants, Chemical/toxicity , Larva/drug effects , Embryo, Nonmammalian/drug effects , Spine/drug effects , Spine/abnormalities , Eye/drug effects , Eye/embryologyABSTRACT
Organotin compounds (OTs) accumulate in fish easily, however, research on their influencing factors is still limited. This study collected 25 species of fish with different diets, habitats, and age from the Three Gorges Reservoir (TGR), the largest deep-water river channel-type reservoir in China, and analyzed the accumulation characteristics of OTs in these fish. The results showed that tributyltin (TBT) and triphenyltin (TPhT) were the dominant OTs in fish from the TGR. The correlation between OTs concentration and age, body length, and body weight varied with fish species. The concentrations of TBT and TPhT in carnivorous fish (mean, 25.78 and 11.69 ng Sn/g dw, respectively) were higher than those in other diet fish (P<0.01), but there was no significant difference in fish at different habitat water layers (P>0.05). In addition, the degradation rates of TBT and TPhT in different fish species were all below 50%. In summary, the accumulation of TBT and TPhT in fish is mainly influenced by diet, and both TBT and TPhT were difficult to degrade in fish. These results reveal the pollution characteristics of OTs in fish from the TGR, and can improve our understanding of the factors influencing TBT and TPhT accumulation in freshwater fish.
Subject(s)
Organotin Compounds , Trialkyltin Compounds , Water Pollutants, Chemical , Animals , Trialkyltin Compounds/metabolism , Fishes/metabolism , China , Environmental Monitoring , Water , Water Pollutants, Chemical/analysisABSTRACT
This study investigated the behavior of veterinary antibiotics (VAs) in a small farm ecosystem. Manure and environmental samples were collected around a large pig farm in northeast China. Thirty-four VAs in six categories were analyzed. Then, a multimedia fugacity model was used to estimate the fates of VAs in the environment. The results showed that VAs were prevalent in manure, soil, water, and sediment, but not in crops. Compared with fresh manure, VA levels were significantly lower in surface manure piles left in the open air for 3-6 months. The main VAs, tetracyclines and quinolones, decreased by 427.12 and 158.45 µg/kg, respectively. VAs from manure piles were transported to the surroundings and migrated vertically into deep soil. The concentrations of ∑VAs detected in agricultural soils were 0.03-4.60 µg/kg; > 94% of the mass inventory of the VAs was retained in soil organic matter (SOM), suggesting that SOM is the main reservoir for antibiotics in soil. Risk assessment and model analysis indicated that the negative impact of mixed antibiotics at low concentrations in farmland on crops may be mediated by indirect effects, rather than direct effects. Our findings highlight the environmental fates and risks of antibiotics from livestock farms.
Subject(s)
Anti-Bacterial Agents , Environmental Monitoring , Soil Pollutants , Veterinary Drugs , Animals , Anti-Bacterial Agents/analysis , China , Crops, Agricultural , Ecosystem , Environmental Monitoring/methods , Farms , Manure/analysis , Soil , Soil Pollutants/analysis , Swine , Veterinary Drugs/analysisABSTRACT
Triphenyltin (TPhT) and tributyltin (TBT) remain widely present in various aquatic environments despite restrictions on their use in many countries for many years. The biomagnification of these compounds in the aquatic food web remains controversial. This study reports the bioaccumulation of TPhT and TBT in aquatic animals in the Three Gorges Reservoir (TGR), a deep-water river channel-type reservoir and the largest reservoir in China. We measured TPhT, TBT and their metabolites in 2 invertebrates, 27 fish and the aquatic environment. The logarithmic bioaccumulation factors of TPhT and TBT were 4.37 and 3.77, respectively, indicating that TPhT and TBT were enriched in organisms of the TGR. Both TPhT and TBT concentrations were significantly and positively correlated with trophic level, with trophic magnification factors of 3.71 and 3.63, respectively, indicating that TPhT and TBT exhibited similar trophic enrichment in the freshwater food web of the TGR. The results of health risk assessment showed that although all hazard index (HI) values were <1, more attention should be paid to the health risk to children associated with consumption of aquatic products (HIâ¯=â¯0.67). This study provides powerful evidence of trophic enrichment of TPhT and TBT in a freshwater food web in a deep-water river channel-type reservoir and provides valuable data regarding organotins in aquatic animals in the TGR.
Subject(s)
Organotin Compounds , Water Pollutants, Chemical , Animals , China , Environmental Monitoring/methods , Food Chain , Rivers , Water , Water Pollutants, Chemical/analysisABSTRACT
Municipal solid waste incineration (MSWI) fly ash contains many harmful components that may limit its potential for recycling. An effective pretreatment is therefore required before any recycling can be implemented. In this study, the effects of four pretreatment methods (water washing, CO2-aided washing, CO32--aided washing, and CO2 and CO32--aided washing) on the extraction behavior of chloride, sulfate, and heavy metals were evaluated. Water washing was found to be effective for the extraction of all easily and moderately soluble Cl-bearing salts, achieving Cl extraction ratios of 88%, 90%, and 96% for ash from Chongqing (CQ), Qingdao (QD), and Tianjin (TJ), respectively. Injection of CO2 during washing facilitated decomposition of the hardly soluble Cl-bearing salts, increasing the Cl extraction efficiency by 6% for CQ ash and 9% for QD ash. However, for the TJ ash that contained few insoluble Cl-bearing minerals, CO2 injection decreased the Cl extraction rate. The addition of CO32- had a negative influence on Cl extraction for all ashes, but it slightly promoted sulfate extraction. Despite the high Cl removal rate, only 23-37% of the sulfate and 0.1-12% of heavy metals were removed. Overall, water-based pretreatment, especially CO2-aided washing, significantly altered the physical, chemical, and mineralogical characteristics of the fly ash, making it more suitable for recycling. Consequently, the blending ratio of the fly ash for cement clinker manufacture increased from 0.2 to 0.3% in the raw ash to 3.5-5.5% in the treated ash, enabling the extensive use of ash materials.
Subject(s)
Metals, Heavy , Refuse Disposal , Carbon/chemistry , Carbon Dioxide , Chlorides , Coal Ash/chemistry , Incineration/methods , Metals, Heavy/analysis , Particulate Matter , Refuse Disposal/methods , Salts , Solid Waste/analysis , Sulfates , WaterABSTRACT
With the wide utilization of organophosphate esters (OPEs) in recent years, OPEs have been detected more frequently in the aquatic environment. However, the distribution of OPEs in drinking source water has rarely been investigated across a large region. In this study, the occurrence and distribution of 13 OPEs were investigated in 23 source water sites from Northeast to Southeast (spacing greater than 3320 km) with a direct injection ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method. Total OPEs ranged from 218.8 to 636.6 ng/L, with a mean of 380.8 ng/L. The average detected concentration of OPEs in southern cities was higher than that in northern cities. Chlorinated OPEs accounted for 64.74% of the total concentration. Triethyl phosphate (TEP), tri (2-chloroethyl) phosphate (TCEP), and tri (chloropropyl) phosphate (TCPP) were detected in all water samples. Rainfall is a significant factor that affects the OPE concentration (less rainfall, higher concentration). China's OPE concentrations have rapidly reached a median level when compared to those of other countries. Ecological risk assessment showed that most OPEs have no or low risk to organisms (fish, crustacea, algae), except tricresyl phosphate (TCP), which is medium risk. The risk of OPEs in less-rain regions needs to be of greater concern, especially TCP.
Subject(s)
Drinking Water , Flame Retardants , Animals , China , Chromatography, Liquid , Drinking Water/analysis , Environmental Monitoring/methods , Esters/analysis , Flame Retardants/analysis , Organophosphates/analysis , Phosphates/analysis , Risk Assessment , Tandem Mass SpectrometryABSTRACT
Organophosphate esters (OPEs) in the environment have been the focus of increasing attention due to their ubiquity and potential toxicity. However, there is little information on the occurrence and characteristics of OPEs in rural areas, especially those with cold year-round temperatures and frozen soil in winter. In this study, environmental samples were collected, in summer and winter, from villages and towns in Northeast China differing in the types and intensities of their anthropogenic activities. The samples were analyzed for 12 OPEs. The results showed the widespread presence of alkyl-OPEs, Cl-OPEs, and aryl-OPEs in the water, soil, snow, and ice of the study sites. In summer, tris(1-chloro-2-propyl) phosphate (TCPP) and tris(2-chloroethyl) phosphate (TCEP) were the primary compounds in water and soil, respectively. The ∑12OPE concentration in three villages varied from 46.26 to 257.37 ng/L in water, and from 6.62 to 19.46 ng/g in soils. The ∑12OPE concentrations in water were lower in winter than summer, but conversely, ∑12OPE concentrations in frozen soils in winter were higher than those in soils in summer. In winter, there was a shift in the predominant OPEs in water and frozen soils, with dominance of TCEP and complex compounds, respectively. Obvious seasonal characteristics of the potential sources and ecological risks of OPEs in these areas were also determined, with more complex sources of OPEs seen in summer than winter. In summer, only 2-ethylhexyl diphenyl phosphate (EHDPP) in water posed a potential risk, while in summer and, especially, in winter, EHDPP and tris(2-ethylhexyl) phosphate posed potential risks in soils. The high ∑12OPE concentration in snow (56.77 ng/L) implied that wet deposition can amplify OPEs in other environmental compartments. This is the first systematic report on OPEs in a cold rural area. Our findings highlight the need for seasonal monitoring of OPEs in similar areas.
Subject(s)
Flame Retardants , China , Environmental Monitoring/methods , Esters , Flame Retardants/analysis , Organophosphates , Phosphates , Seasons , Soil , WaterABSTRACT
Persulfate (PS)-based advanced oxidation processes have been frequently employed for contaminant remediation, but the effectiveness of PS oxidation for the elimination of cyanide-bearing contaminants from soil, and the underlying mechanisms, have rarely been explored. This study investigated the degradation of two iron-cyanide (Fe-CN) complexes (ferricyanide and ferrocyanide) with thermally activated PS via two remediation strategies, namely one-step oxidation (direct PS oxidation) and two-step oxidation (alkaline extraction followed by PS oxidation). The two-step oxidation process was more effective for the elimination of cyanide pollutants from soil, reaching >94% remediation efficiency for both Fe-CN complexes studied. The presence of dissolved soil components, especially soil organic matter, increased consumption of PS during the remediation process. A combined analysis based on electron paramagnetic resonance (EPR), free radical scavenging, and degradation product identification revealed that SO4- and HO were the principal reactive radicals responsible for Fe-CN degradation. Based on the determination of radical species and identification of decomposition products, a transformation pathway for Fe-CN complexes during thermally activated PS oxidation is proposed. Overall, this study demonstrates the effectiveness of the thermally activated PS oxidation technique for cyanide elimination from polluted soil. Further study is required to verify the feasibility of this method for field applications.
Subject(s)
Soil Pollutants , Water Pollutants, Chemical , Cyanides , Environmental Pollution , Oxidation-Reduction , Soil , Soil Pollutants/analysis , SulfatesABSTRACT
Organophosphate esters (OPEs) are widely used flame retardants that are frequently released into the environment, causing potential harm to humans and ecosystems. Tibet is located on the Tibetan Plateau, known as the "roof of the world", but the occurrence of OPEs in Tibet remains unclear. This is the first report of the occurrence, potential sources and risks of 12 OPEs in water, soil, sediment and snow from Xainza, a typical town at high-elevation in Tibet (average elevation = 4700 m). Ten OPEs were observed, with ∑OPE concentrations of 46.45-1744.73 ng/L in surface water, 29.74-73.85 ng/g in soil, and 13.30-32.23 ng/g in sediment. Moreover, the mean ∑OPE concentration in snow was 413.90 ng/L. Tris (2-chloroethyl) phosphate (TCEP) and tris (2-chloroisopropyl) phosphate (TCPP) were the main OPEs in surface water and snow, while 2-ethylhexyl diphenyl phosphate (EHDPP) was dominant in soil and sediment. Local human activities and long-distance atmospheric transport may be the main sources of OPEs in Xainza. The assessment of ecological risk indicated that EHDPP in soil poses potential risk. The occurrence of OPEs in Xainza showed that more attention should be paid to persistent organic pollutants in high-elevation regions.
Subject(s)
Environmental Monitoring , Flame Retardants , China , Ecosystem , Esters , Flame Retardants/analysis , Humans , Organophosphates , TibetABSTRACT
Acicular mullite was modified by ferromanganese binary metal oxide (Mn-Fe) to improve the removal efficiency of endocrine disruptors by traditional water treatment practices, using the commercial ceramsite for comparison. The physicochemical properties of synthesized samples were characterized, and batch adsorption experiments were carried out to study the adsorption efficiency of bisphenol A (BPA) and 17α-ethinylestradiol (EE2) on synthesized samples, investigating how solution chemistry and regeneration may affect the adsorption efficiency. Results show that the manganese oxide loaded on the acicular mullite was manganite with an average particle size of 450 nm. After Mn-Fe impregnation, the specific surface area, cumulative pore volume, and mesoporous ratio of the acicular mullite were significantly increased. The virgin acicular mullite had no removal ability for BPA and EE2, and the removal efficiency of BPA and EE2 by Mn-Fe impregnated acicular mullite were significantly increased. Acicular mullite was more suitable as support material for modified filter material. The adsorption kinetics of BPA and EE2 on Mn-Fe-M were fitted with the intra-particle diffusion model, and found to be mainly affected by intra-particle diffusion. The isothermal adsorption data was best fitted to the Langmuir-Freundlich model, and the maximum adsorption capacities of BPA and EE2 were 5.043 mg·g-1 and 3.990 mg·g-1, respectively. Thermodynamic experiments showed that the adsorption of BPA and EE2 by Mn-Fe embedded in acicular mullite was an endothermic reaction, and the temperature increase is beneficial to the adsorption. The adsorption amount of BPA and EE2 on Mn-Fe embedded in acicular mullite decreased with increasing pH. The increase of ionic strength favored the adsorption removal of BPA and EE2. The co-existing anion of SO42- promoted the adsorption of both BPA and EE2, while CO32- and PO43- inhibited the adsorption of both BPA and EE2 on Mn-Fe embedded in acicular mullite. The adsorbent regeneration test showed that Mn-Fe embedded acicular mullite was an easily recyclable adsorbent. Mn-Fe embedded in high-porosity acicular mullite can effectively remove typical endocrine disruptors in water, and it can be potentially extensively used to alleviate the problem of low removal efficiency of endocrine disrupting chemicals in traditional water treatment practice.
ABSTRACT
Ultraviolet (UV) irradiation is an abiotic pathway for the transformation of complex phosphorus (P) components into inorganic P in ecosystems. To explore the effect of UV irradiation on organic P (OP) bioavailability in the water level fluctuation zone (WLFZ) soil, we collected representative soil samples from WLFZ of the Pengxi River, a tributary of the TGR, China. We determined the contents of different forms of OP in the WLFZ soil through sequential extraction. The bioavailability of different forms of OP and the effect of UV light were characterised using a combination of enzymatic hydrolysis and UV irradiation. The OP contents of the different extracts (Po) were ranked as NaOH-Po > NaHCO3-Po > H2O-Po, whereas those of enzymatically hydrolysable organic P (EHP) were ranked as NaOH-EHP > NaHCO3-EHP > H2O-EHP. UV irradiation was found to improve OP bioavailability, as demonstrated by increased levels of UV-sensitive P (UV-P) and EHP in the extracts after irradiation. The total contents of bioavailable Po in extracts were 5.6-35.3% higher after UV irradiation than before irradiation. Thus, the effect of UV irradiation on the OP bioavailability and release activity cannot be neglected in TGR WLFZ soil.
Subject(s)
Phosphorus/analysis , Soil , Biological Availability , China , Ecosystem , Ultraviolet Rays , WaterABSTRACT
Wastewater reclamation and reuse is considered an attractive and practical method for coping with water scarcity. However, the presence of micropollutants in reclaimed water, including endocrine disrupting chemicals (EDCs), is a major public health concern. This study attempted to identify unknown EDCs with liver X receptor (LXRα) agonist/antagonist activities in reclaimed wastewater, using nuclear receptors binding extraction coupled with high-resolution mass spectrometry (NRBE-HRMS). In total, 105 compounds in the reclaimed wastewater exhibited LXRα-binding activity. Among them, two previously unknown LXRα-antagonist compounds, catechol and 4-acetamidoantipyrine, were identified, based on authentic standards. The two LXRα-antagonist compounds exhibited weak LXRα-antagonist activities in a yeast two-hybrid assay. Catechol and 4-acetamidoantipyrine inhibited the ß-galactosidase activity induced by 60 nM of TO901317 in an LXRα yeast assay, with IC20 values of 79,938.9 nM and 6286.4 nM, respectively. To the best of our knowledge, this is the first study to identify EDCs in reclaimed wastewater with LXRα-agonist/antagonist activity using the NRBE-HRMS method.
Subject(s)
Liver X Receptors/metabolism , Endocrine Disruptors , Wastewater , Water Pollutants, ChemicalABSTRACT
In this study, the original Bohart-Adams model was employed to analyze the experimental data of 17α-ethinylestradiol (EE2) separation in lab-scale anthracite columns with low initial concentration. Besides, the assumptions for the simplified Bohart-Adams model were calculated and discussed. The results revealed that the breakthrough curves of EE2 separation in anthracite columns under different conditions were asymmetrical N-shaped and could be divided into three parts. The third part of the breakthrough curves was successfully fitted by the original Bohart-Adams model with high R2 values (higher than 0.918) and low ARS values (less than 0.141). As expected, the assumptions for the simplified Bohart-Adams model were not tenable during the whole experiment process. As a result, the EE2 separation capacities (N0° and N0s) obtained from the original and simplified Bohart-Adams model were quite different, and most N0° values were greater than N0s values. The N0° value used to evaluate the pollutant separation capacity in lab-scale column would be more accurate. In addition, physical interception and chemical adsorption simultaneously worked in the EE2 separation in anthracite columns. Physical interception and bed depth in anthracite columns at low flow rate were related in quadratic function (R2â¯>â¯0.988).
ABSTRACT
The Three Gorges Reservoir Region (TGRR) is one of the most sensitive areas of ecological environment in China. As vital backwater areas, the secondary anabranches of the TGRR were prone to eutrophication in Spring which would affect the distribution and transfer of organotins (OTs) among aquatic media. This study quantified the concentrations of butyltins (BTs) and phenyltins (PhTs) in water columns and aquatic media of two anabranches of the TGRR, the Daning River (DR) and the Xiaojiang River (XR) during the state of eutrophication. Our results showed that the average concentrations of BTs and PhTs in surface water are 43.91, 81.25â¯ng Sn L-1 in the DR, and 63.49, 69.21â¯ng Sn L-1 in the XR, respectively, and there were no obvious differences in the concentrations of BTs and PhTs across the water columns in the DR and XR. PhTs, especially monophenyltin (MPhT), are predominated in the dissolved phase, whereas BTs, especially dibutyltin (DBT), are predominated in both suspended particulate matter (SPM) and the sediment. Shipping and agricultural activity were likely the sources of OTs in both the DR and XR. High concentrations of tributyltin (TBT) and triphenyltin (TPhT) are still present in the aquatic media of the TGRR, and pose a significant risk to aquatic organisms due to the potential for bioaccumulation. Therefore, it is necessary to further monitor and assess OTs especially PhTs in surface water, and to continue to restrict the use of OTs to protect the aquatic environment of the TGRR.
Subject(s)
Environmental Monitoring/methods , Fresh Water/chemistry , Organotin Compounds/analysis , Water Pollutants, Chemical/analysis , Aquatic Organisms , China , Trialkyltin Compounds/analysisABSTRACT
The occurrence and health risks of organotins (OTs) in the waterworks and source water in the Three Gorges Reservoir Region (TGRR), China were assessed in this study. Water samples were collected at four waterworks (A, B, C, and D) in March and July 2012 to analyze butyltins (BTs) and phenyltins (PTs) using a gas chromatography-mass spectrometry (GC-MS) system. Our results showed that both the waterworks and their nearby water sources were polluted by OTs, with PTs being the most dominant species. Monobutyltin (MBT), monophenyltin (MPT), diphenyltin (DPT), and triphenyltin (TPT) were detected in most of the analyzed water samples. The highest concentrations of OTs in influents, effluents, and source water in March were 52.81, 17.93, and 55.32 ng Sn L-1, respectively. Furthermore, significant seasonal changes in OTs pollution were observed in all samples, showing pollution worse in spring compared with summer. The removal of OTs by the conventional treatment processes was not stable among the waterworks. The removal efficiency of OTs in July reached 100% at plant B, while that at plant C was only 38.8%. The source water and influents shared similar composition profiles, concentrations, and seasonal change of OTs, which indicated that OTs in the waterworks were derived from the source water. A health risk assessment indicated that the presence of OTs in the waterworks would not pose a significant health risk to the population, yet their presence should not be ignored.
Subject(s)
Organotin Compounds/toxicity , Rivers , Water Pollutants, Chemical/toxicity , China , Environmental Monitoring/methods , Gas Chromatography-Mass Spectrometry/methods , Organotin Compounds/analysis , Risk Assessment , Water Pollutants, Chemical/analysis , Water SupplyABSTRACT
Organotins (OTs) pollution in the aquatic environment of the Three Gorges Reservoir (TGR) was assessed during the reservoir's operating cycle. Butyltins (BTs) and phenyltins (PhTs) in the water phase and suspended particulate matter (SPM) at different water levels were analysed. It was found that the distribution of OTs in the surface and bottom water phases were similar, with the dominant OTs being BTs at the low water level and PhTs at the high water level. The detection rates and concentrations of OTs in the water phase at the high water level were both higher than those at the low water level, with most OTs being monobutyltin (MBT) at the low water level and monophenyltin (MPhT) at the high water level. The concentrations of OTs in SPM at the low water level were higher than those at the high water level, and BTs, especially dibutyltin (DBT) and tributyltin (TBT), were the predominant OTs whether surface or bottom layer at each water level. The BTs and SPM concentrations had a significant positive relationship in all samples, indicating that the SPM concentration would determine the distribution of BTs in the aquatic environment of the TGR region (TGRR). The difference in the distribution of OTs at the different water levels indicated that the hydrological and hydraulic behaviour of the TGR influences OTs transport in the aquatic environment of the TGRR.
Subject(s)
Environmental Monitoring , Organotin Compounds/analysis , Rivers/chemistry , Water Pollutants, Chemical/analysis , China , Particulate Matter/analysis , Water Movements , Water Pollution, Chemical/statistics & numerical dataABSTRACT
The water quality security of the Three Gorges Reservoir during different operating periods has been a subject of recent concern. This study is the first to report the spatiotemporal variability of organotins (OTs) in surface water under dynamic water level conditions in the Three Gorges Reservoir Region (TGRR). TGRR surface water was collected during three monitoring campaigns to analyze butyltins (BTs) and phenyltins (PTs) using a gas chromatography-mass spectrometry system. Our results showed that TGRR surface water was polluted by BTs and PTs, with mono-OTs being the dominant species. A wide range of BTs and PTs concentrations was observed across the study area, but tributyltin (TBT) displayed extensive spatial distribution, and the highest concentrations consistently occurred in the downstream region of the TGRR study area, with a maximum of 393.35 ng Sn/L in Zigui (S27). The total OTs contamination level decreased over time. The diphenyltin concentration exhibited significant seasonal variation, while other OTs showed seasonal changes only during two monitoring campaigns, with the exception of dibutyltin. An ecological risk assessment indicated that both TBT and triphenyltin posed risks to aquatic organisms in TGRR surface water. We urgently recommend continuous monitoring and further measures to prevent and control OTs pollution in the TGRR.
Subject(s)
Environmental Monitoring , Organotin Compounds/analysis , Organotin Compounds/toxicity , Rivers/chemistry , Spatio-Temporal Analysis , Water Pollutants, Chemical/analysis , Water Pollutants, Chemical/toxicity , Aquatic Organisms/drug effects , China , Gas Chromatography-Mass Spectrometry , Organotin Compounds/chemistry , Risk Assessment , Water Pollutants, Chemical/chemistryABSTRACT
Triphenyltin (TPhT) is a kind of organotin compounds which have been used ubiquitously as herbicide, pesticide, and fungicide in agriculture. The present study provides the possibility to detect and monitor TPhT with normal Raman spectroscopy and surface enhanced Raman scattering (SERS) spectroscopy. Firstly, the complete vibrational Raman spectra characterization of TPhT along with the IR spectroscopy were reported for the first time. Then a wide range of pH values were carried out to choose the optimal pH value in TPhT detection by using Raman spectroscopy. Afterwards, Raman spectra of various TPhT solutions were collected and analyzed. The results indicate that the optimal pH value for TPhT detection by Raman spectroscopy is 5.5, and with silver nanoparticles (Ag NPs) as SERS substrate is an effective technique for trace TPhT detection with an enhancement by 5 orders of magnitude and the detection limit can be as low as 0.6 ng/L within less than 30 s. Finally, in this study, the residual of TPhT on apple peel was investigated by casting different concentrations of TPhT on apple peel under the current optimized condition. The result demonstrates that TPhT could be detected based on its SESR spectra at 6.25 ng/cm(2) in standard solutions.
Subject(s)
Environmental Monitoring/methods , Organotin Compounds/analysis , Spectrum Analysis, Raman , Limit of Detection , Metal Nanoparticles/chemistry , Silver/chemistry , SolutionsABSTRACT
As important constituents of activated sludge flocs, extracellular polymeric substances (EPS) play significant roles in pollutants adsorption, the formation and maintenance of microbial aggregates, and the protection of microbes from external environmental stresses. In this work, EPS in activated sludge from a municipal wastewater treatment plant (M-WWTP) with anaerobic/anoxic/oxic (A(2)/O) process and a hyperhaline wastewater treatment plant (H-WWTP) with anaerobic/oxic (A/O) process were extracted by ultrasound method. The proteins and polysaccharides contents in EPS were determined by using a modified Lowry method and anthrone colorimetry respectively to analyze the detail differences in two types of WWTPs. Fourier transform-infrared spectroscopy and three-dimensional excitation-emission matrix fluorescence spectroscopy demonstrated proteins and polysaccharides were the dominant components of the two types of EPS, and the aromatic protein-like substances accounted for a larger proportion in EPS proteins. The results of the aggregation test indicated that EPS were good for the sludge aggregation, and the EPS in oxic sludge were more beneficial to sludge aggregation than that in anoxic sludge. Anoxic sludge EPS in H-WWTP showed a negligible effect on sludge aggregation. Comparative study on EPS of different tanks in the M-WWTP and H-WWTP was valuable for understanding the characteristics of EPS isolated from two typical wastewater treatment processes.