Occurrence of sulfonamide residues along the Ebro River basin: removal in wastewater treatment plants and environmental impact assessment

Sulfonamides (SAs) have become one of the antibiotic families most frequently found in all kind of environmental waters. In the present work, the presence of 16 SAs and one of their acetylated metabolites in different water matrices of the Ebro River basin has been evaluated during two different sampling campaigns carried out in 2007 and 2008. Influent and effluent samples from seven wastewater treatment plants (WWTPs), together with a total of 28 river water samples were analyzed by on-line solid phase extraction-liquid chromathography-tandem mass spectrometry (on-line SPE-LC-MS/MS). Sulfamethoxazole and sulfapyridine were the SAs most frequently detected in WWTPs (96-100%), showing also the highest concentrations, ranging from 27.2 ng L(-1) to 596 ng L(-1) for sulfamethoxazole and from 3.7 ng L(-1) to 227 ng L(-1) for sulfapyridine. Sulfamethoxazole was also the SA most frequently detected in surface waters (85% of the samples) at concentrations between 11 ng L(-1) and 112 ng L(-1). In order to assess the effectiveness of the wastewater treatment in degrading SAs, removal efficiencies in the seven WWTPs were calculated for each individual SA (ranging from 4% to 100%) and correlated to the corresponding hydraulic retention times or residence times of the SAs in the plants. SAs half-lives were also estimated, ranging from to 2.5 hours (sulfadimethoxine) to 128 h (sulfamethazine). The contribution of the WWTPs to the presence of SAs depends on both the load of SAs discharging on the surface water from the WWTP effluent but also on the flow of the receiving waters in the discharge sites and the dilution exerted; WWTP4 exerts the highest pressure on the receiving water course. Finally, the potential environmental risk posed by SAs was evaluated calculating the hazard quotients (HQ) to different non-target organisms in effluent and river water. The degree of susceptibility resulted in algae>daphnia>fish. Sulfamethoxazole was the only SA posing a risk to algae in effluent water, with an HQ>7.     

Tritium in surface waters of the Yenisei River basin

This paper reports an investigation of the tritium content in the surface waters of the Yenisei River basin near the Mining and Chemical Combine (MCC). In 2001 the maximum tritium concentration in the Yenisei River did not exceed 4 +/- 1 Bq l(-1), which is consistent with the data of 1998-99. However, it has been found that there are surface waters containing enhanced tritium as compared with the background values for the Yenisei River. For instance, in the Ploskii Stream and the Shumikha River the maximum tritium concentrations amount to 168 and 81 Bq l(-1), respectively. The source of tritium in these surface waters is the last operating reactor at the MCC, which still uses the Yenisei water as coolant. In water and sediment samples of the Bolshaya Tel River (a tributary of the Yenisei River) the tritium content turned out to be at least 10 times higher than the background values for the Yenisei River. The measurements conducted at the RPA RADON (Moscow) revealed not only tritium but also the artificial radionuclide (14)C in the Bolshaya Tel samples. The data obtained suggest that the Bolshaya Tel River receives the major part of tritium from sediments rather than from the water catchment area. This allows the conclusion that there is water exchange between the surface waters and the radioactively contaminated underground horizons of the "Severny" testing site.     

Occurrence and distribution of organochlorine pesticides - lindane, p,p'-DDT, and heptachlor epoxide - in surface water of China

Persistent organochlorine pesticides pollutants (OCPs) have been reported to occur at relatively high concentrations in some Chinese waters. In order to map the distribution of organochlorine pesticides in the surface water throughout China, samples were collected from over 600 sites in seven major river basins and three main internal rivers drainage areas during 2003 and 2004. The surface water samples were analyzed for the representative organochlorine pesticides contaminants including lindane (gamma-HCH), p,p'-DDT and heptachlor epoxide. In general, the most frequently detected compound was lindane, being detected in 83.9% of samples (mean=31.3 ng/l; range <0.17-860 ng/l), and the highest concentration was present in the Yellow River basin. p,p'-DDT was detected in 63.1% of the samples collected (mean=14.6 ng/l; range <0.14-368 ng/l) with the highest concentration present in the Huaihe River basin. Heptachlor epoxide was detected in only 9.3% of water samples (range <0.11-10 ng/l). Measured concentrations for the three compounds were low and rarely exceed the environment quality standard for surface water of China. Lindane was more frequently detected at much higher concentrations in the rivers of northern China compared with those of southern China. The sites with higher concentration of lindane and p,p'-DDT mainly occurred in the Yellow River and Huaihe River basins, so the results of this investigation indicate that the organochlorine pesticide contamination of Yellow River and Huaihe River basins should be of particular concern relative to the other basins. When compared with other regions of the world, it appears that the Chinese surface water is moderately polluted by lindane and p,p'-DDT.     

Triclosan in wastewaters and biosolids from Australian wastewater treatment plants

Triclosan (TCS) is an antimicrobial agent widely used in many personal care products. This study investigated the occurrence of TCS in effluents, biosolids and surface waters, and its fate in wastewater treatment plants (WWTPs). The aqueous concentrations of TCS in nineteen effluents from Australian WWTPs ranged from 23 ng/L to 434 ng/L with a median concentration of 108 ng/L, while its concentrations in nineteen biosolids ranged from 0.09 mg/kg to 16.79 mg/kg on dry weight basis with a median concentration of 2.32 mg/kg. The removal rates for TCS in five selected WWTPs were found to range between 72% and 93%. Biological degradation was believed to be the predominant removal mechanism for TCS in the WWTPs. However, adsorption onto sludge also played a significant role in the removal of TCS in the WWTPs. TCS at concentrations up to 75 ng/L was detected in surface waters (outfall, upstream, and downstream) from five rivers receiving effluent discharge from WWTPs. Preliminary risk assessment based on the worst-case scenario showed that the TCS concentrations in surface waters might lead to risks to aquatic organisms such as algae. Based on the TCS levels in the biosolids, application of biosolids on agricultural land may also cause adverse effects in the soil environment.     

Urinary levels of bisphenol A,triclosan and 4-nonylphenol in a general Belgian population

Bisphenol A, triclosan and 4-nonylphenol are among the endocrine disruptors which are widely used in daily products. In this study, we reported total urinary levels of bisphenol A, triclosan and 4-nonylphenol, in order to evaluate the baseline contamination of a general population in Belgium. Bisphenol A and triclosan were detected in respectively 97.7% and 74.6% of the samples examined demonstrating that the general Belgian population is extensively exposed to both chemicals. On the other hand, 4-nonylphenol was not detected in any urine samples analyzed, suggesting either low exposure, inadequate biomarker, or that urine is an inappropriate biological matrix for assessing exposure to nonylphenol commercial mixtures. Geometric mean concentration was determined for bisphenol A at 2.55 μg/l and for triclosan at 2.70 μg/l. No significant difference was observed between levels and gender for both bisphenol A and triclosan. When classified by age, the 20–39 year group showed the highest triclosan levels, while all age groups seemed to be similarly exposed to bisphenol A. Both bisphenol A and triclosan urinary levels were not correlated with creatinine excretion in our healthy population, questioning the relevance of the creatinine adjustment in reporting these chemical levels. Bisphenol A levels in urine of people living in the same home and collected on the same time were fairly correlated, confirming the assumption that dietary intake would be the primary route of exposure. Triclosan urinary levels were not correlated with bisphenol A levels.     

鄱阳湖蝶形湖泊水体氮磷等的变化及污染初步评价

分别于2014年夏季7月和冬季12月对鄱阳湖蝶形水域的9个湖泊进行了采样,并对湖泊水质基础性指标TN、TP、NH_3-N、NO_3~--N、NO_2~--N、溶解性磷酸盐、TOC、COD_(Mn)和叶绿素a进行了测定与分析。据此同时运用单因素评价法、均值型指数综合评价法和营养状态指数法对鄱阳湖蝶形水域的地表水水环境的污染现状和污染程度进行了评价,以更全面和准确地反映鄱阳湖蝶形水域的水质状况。结果显示:(1)鄱阳湖蝶形水域水质总体符合GB3838-2002III类水标准;(2)7月水质总体优于12月水质。12月总氮含量和总磷含量基本都高于7月,叶绿素a含量除中湖池12月值略低于7月外,其它点位12月值均高于7月。7月总氮值为0.6~1.3 mg/L,总磷值为0.02~0.15 mg/L,叶绿素a为2.2~6.7 mg/L;12月总氮值为0.6~2.0 mg/L,总磷值为0.04~0.19 mg/L,叶绿素a为3.8~34.7 mg/L;(3)7月和12月水质营养状态介于中营养和轻度富营养,水体主要污染物质为总氮和总磷。7月蚌湖营养状态为轻度富营养,其它点位为中营养,12月除常湖、梅溪湖和大汊湖营养状态为中营养,其它点位均为轻度富营养;(4)位于南部的象湖、常湖、白沙湖和大汊湖水质整体较其它蝶形湖泊差,主要是受到工业废水、生活污水和农业面源污染的赣江和饶河的污染输入影响所致。基于以上调查测试结果提出保护和改善鄱阳湖水环境的可行性措施,以促进鄱阳湖蝶形水域水资源的开发利用,实现经济与环境及资源的协调可持续发展。     

龙岩市省控断面水体中多环芳烃的污染特征、风险评价

对九龙江流域龙岩市省控断面2011年秋季、2012年冬季以及2012年春季河水中多环芳烃(PAHs)进行了分析。结果表明：该控断面河水中PAHs总量浓度变化为99~1788 ng/L，其组成特征是以3环(567%)、5环(246%)和4环(151%)为主，表明3环、4环及5环PAHs是九龙江流域龙岩市省控断面水中PAHs的最主要成分。地表水健康风险评价结果显示，红坊赤坑、雁石桥、捷步桥、顶坊4个采样点苯并\[a\]芘(BaP)毒性当量值(EBaP)均超出我国环境保护部(CEPA)制定的EBaP=2.8 ng/L的国家标准     

Measurement of flame retardants and triclosan in municipal sewage sludge and biosolids

As polybrominated diphenyl ethers (PBDEs) face increasing restrictions worldwide, several alternate flame retardants are expected to see increased use as replacement compounds in consumer products. Chemical analysis of biosolids collected from wastewater treatment plants (WWTPs) can help determine whether these flame retardants are migrating from the indoor environment to the outdoor environment, where little is known about their ultimate fate and effects. The objective of this study was to measure concentrations of a suite of flame retardants, and the antimicrobial compound triclosan, in opportunistic samples of municipal biosolids and the domestic sludge Standard Reference Material (SRM) 2781. Grab samples of biosolids were collected from two WWTPs in North Carolina and two in California. Biosolids samples were also obtained during three subsequent collection events at one of the North Carolina WWTPs to evaluate fluctuations in contaminant levels within a given facility over a period of three years. The biosolids and SRM 2781 were analyzed for PBDEs, hexabromobenzene (HBB), 1,2-bis(2,4,6-tribromophenoxy)ethane (BTBPE), 2-ethylhexyl 2,3,4,5-tetrabromobenzoate (TBB), di(2-ethylhexyl)-2,3,4,5-tetrabromophthalate (TBPH), the chlorinated flame retardant Dechlorane Plus (syn- and anti-isomers), and the antimicrobial agent 5-chloro-2-(2,4-dichlorophenoxy)phenol (triclosan). PBDEs were detected in every sample analyzed, and ΣPBDE concentrations ranged from 1750 to 6358 ng/g dry weight. Additionally, the PBDE replacement chemicals TBB and TBPH were detected at concentrations ranging from 120 to 3749 ng/g dry weight and from 206 to 1631 ng/g dry weight, respectively. Triclosan concentrations ranged from 490 to 13,866 ng/g dry weight. The detection of these contaminants of emerging concern in biosolids suggests that these chemicals have the potential to migrate out of consumer products and enter the outdoor environment.     

Accumulation and release of 241Am by a macrophyte of the Yenisei River (Elodea canadensis)

The source of radioactive contamination of the Yenisei River floodplain, including contamination with transuranic elements, is the Mining-and-Chemical Combine of the Russian Ministry of Atomic Energy, which has for many years been producing weapons-grade plutonium. Transuranic elements have been detected not only in the soil and sediment of the river but also in the biomass of aquatic plants. This work is an investigation of accumulation and release of 241Am by a submerged macrophyte of the Yenisei River (Elodea canadensis) in laboratory experiments. In 2000-2003, laboratory experiments were carried out with biomass of E. canadensis Mich. and filtered river water. The samples were collected from the Yenisei River upstream of the discharge of the Combine's radioactive effluent. The experiments showed that 241Am is accumulated by Elodea biomass: the activity concentration of 241Am can reach 3280+/-240 Bq/g, with the concentration factor for 241Am 16 600+/-2200l/kg. Results of chemical fractionation have proved that in the course of 241Am accumulation by Elodea biomass, 241Am tightly bound to biomass increases from 11% to 27% of the total 241Am in the biomass. Release of 241Am from the decaying Elodea biomass has been evaluated experimentally. By the end of the experiment (lasting up to 127 days), the Elodea plants had lost up to 65% of their initial 241Am activity and the rate of 241Am release into the water environment reached 23 Bq/day.     

Rare earth elements in the Rhine River, Germany: first case of anthropogenic lanthanum as a dissolved microcontaminant in the hydrosphere

The distribution of dissolved rare earth elements (REE) in the Rhine River, Germany, shows the anthropogenic gadolinium (Gd) microcontamination that is commonly observed in rivers in densely populated countries with a highly evolved health care system. However, the Rhine River also carries anomalously high concentrations of lanthanum (La), which produce very large positive La anomalies in normalized REE distribution patterns. These positive La anomalies first occur north of the City of Worms and then decrease in size downstream, but are still significant approximately 400 km downstream, close to the German-Dutch border. The strong La enrichment is of anthropogenic origin and can be traced back to effluent from a production plant for fluid catalytic cracking catalysts at Rhine river-km 447.4. This effluent is characterized by extremely high dissolved total REE and La concentrations of up to 52 mg/kg and 49 mg/kg, respectively. Such La concentrations are well-above those at which ecotoxicological effects have been observed. The Rhine River is the first case observed to date, where a river's dissolved REE inventory is affected and even dominated by anthropogenic La. Our results suggest that almost 1.5t of anthropogenic dissolved La is exported via the Rhine River into the North Sea per year. This reveals that the growing industrial use of REE (and other formerly "exotic" elements) results in their increasing release into the environment, and highlights the urgent need to determine their geogenic background concentrations in terrestrial surface waters.     

九龙江流域河水溶解态碳的时空变化

为了研究九龙江流域河流中溶解碳变化规律，分别于2017年7月与2018年1月对九龙江河水溶解无机碳（DIC）与溶解有机碳（DOC）进行了分析。丰水季河水DIC浓度为7.50~49.04 mg/L，平均值为22.12 mg/L，枯水季DIC浓度为8.84~84.91 mg/L，平均浓度41.17 mg/L，丰水季河水中的DOC浓度为0.54~2.89 mg/L，平均值为1.04 mg/L，枯水季河水中DOC浓度变化在1.34~3.56 mg/L之间，平均值为2.34 mg/L，据此计算了九龙江河水DOC、DIC的入海通量。研究结果表明九龙江河水中溶解碳具有显著的时空变化特征，通过与中国其他河流溶解碳数据对比，解释了碳酸盐岩的风化、气候变化、河流中浮游植物以及人类活动对九龙江河流溶解碳浓度的影响。     

Post-irrigation impact of domestic sewage effluent on composition of soils,crops and ground water--a case study

Long-term irrigation with sewage water adds large amounts of carbon, major and micro- nutrients to the soil. We compared the spatial distribution of N, P, K and other micronutrients and toxic elements in the top 0.6 m of an alluvial soil along with their associated effects on the composition of crops and ground waters after about three decades of irrigation with domestic sewage effluent as a function of distance from the disposal point. Use of sewage for irrigation in various proportions improved the organic matter to 1.24-1.78% and fertility status of soils especially down to a distance of 1 km along the disposal channel. Build up in total N was up to 2908 kg ha(-1), available P (58 kg ha(-1)), total P (2115 kg ha(-1)), available K (305 kg ha(-1)) and total K (4712 kg ha(-1)) in surface 0.15 m soil. Vertical distribution of these parameters also varied, with most accumulations occurring in surface 0.3 m. Traces of NO3-N (up to 2.8 mg l(-1)), Pb (up to 0.35 mg l(-1)) and Mn (up to 0.23 mg l(-1)) could also be observed in well waters near the disposal point thus indicating initiation of ground water contamination. However, the contents of heavy metals in crops sampled from the area were below the permissible critical levels. Though the study confirms that the domestic sewage can effectively increase water resource for irrigation but there is a need for continuous monitoring of the concentrations of potentially toxic elements in soil, plants and ground water.     

BOD-DO modeling and water quality analysis of a waste water outfall off Kochi, west coast of India

Water quality scenarios around an offshore outfall off Kochi were simulated using MIKE21 water quality model, assuming a high Biochemical Oxygen Demand (BOD=50 mg l(-1)) effluent discharge. The discharge is introduced into the model through an outfall located at a distance of 6.8 km from the shore at a depth of 10 m. Three scenarios were simulated with different discharge rates such as 2, 5 and 10 m3 s(-1), with BOD load of 8640, 21,600 and 43,200 kg day(-1) respectively. Model simulations were carried out to estimate the assimilation capacity of the waters off Kochi for the three discharge rates. The results show that for 10 m3 s(-1) effluent discharge, the initial BOD of 50 mg l(-1) reduced to 3.33 mg l(-1) at the outfall after 48 h. High BOD values were confined to an elliptical area of approximately 8 km2 around the outfall. Based on this, the assimilative capacity of the waters off Kochi in terms of BOD can be estimated as 38,000 kg day(-1). It is suggested that offshore waters could be used as a feasible alternative to the Kochi backwaters for the disposal of treated effluent.     

Evaluation of the water genotoxicity from Santos Estuary (Brazil) in relation to the sediment contamination and effluent discharges

The genotoxic activity of water samples collected in 9 different sites within the area of the Santos estuary was preliminary evaluated, and related to previous data on the genotoxicity of sediments and the contents of PAHs in both water and sediment samples. The liquid discharge of a steel mill (coke plant), known to be mutagenic, was chemically analyzed to determine its PAH content. For the water evaluation we employed the Salmonella/microsome assay with the strains TA98 and TA100 with and without S9 mix in the plate incorporation method. The water was filtered with an AP20 membrane before being extracted with XAD4 at natural and acidic pH. The industrial effluent was filtered in 0.45 microm membranes before being extracted with the liquid/liquid method. Both membranes containing the particulate material were extracted using ultrasonication. PAHs were found associated with the suspended particles present in the industrial effluent in accordance with mutagenicity data previously reported. In relation to the estuarine waters, sites 1 and 5 presented low levels of mutagenic activity only in the filtered water (liquid fraction) extracts. At site 3, both the filtered water and particulate solids presented also low mutagenicity. Results show that the mutagenic activity observed in water could not be directly related to the genotoxic activity and PAHs contents of the bottom sediments.     

Contaminant mobility in diked containment areas

Nine dredged material land containment areas, located at upland, lowland, and island sites, were monitored during hydraulic dredging operations in fresh and brackish-water riverine, lake, and estuarine environments. Influent/effluent sampling at the diked disposal areas showed that, with proper retention of suspended solids, most chemical constituents could be removed to near background water levels. Most heavy metals, oil and grease, chlorinated pesticides, and PCBs were almost totally associated with solids in both the influent and effluent samples. The parameters that appear to have the greatest potential impact as a result of land disposal of dredged material are ammonia, soluble manganese, total mercury, and dissolved oxygen; soluble iron, zinc, and copper may occasionally exceed criteria or background levels.v However, none of these should present serious problems after dillution of the effluent discharge in the receiving waters. Actively growing vegetation in disposal areas appeared to be efficient in removing ammonium nitrogen to low levels and also for filtering out suspended solids. Dissolved oxygen in effluents ranged from 0.6 to 12.5 ppm. Geochemical phase partitioning of influent and effluent solids indicated that carbonate solids of several heavy metals tended to form during dredged slurry containment, promoted by high alkalinity and increased pH in site waters. Metal adsorption onto effluent suspended particles (exchangeable phase) increased slightly, along with a significant increase in cation exchange capacity.     

Modelling changes in nitrogen emissions into the Oder River System 1875–1944

Studies of nutrient emissions into surface waters are usually only performed for years in recent decades. However, estimating nutrient emissions for the more distant past enables us to identify the main factors responsible for the increasing nutrient contamination since the end of the nineteenth century. We focussed on the Oder River System for 1875–1944, divided into 10-year periods. Nutrient emissions into surface waters were calculated with the model MONERIS (MOdelling Nutrient Emissions in RIver Systems). For seven different pathways and eight sources, the total nitrogen (TN) emissions were quantified. The TN-emissions into the surface waters for 1880 amounted to 25,300 t?year^?1, and by 1940, this value had almost doubled to 46,600?t?year^?1. In 1880, 57% of TN-emissions into the surface waters derived from urban systems, due to the high amount of untreated waste water. In 1940, only 34% of TN-emissions into surface waters derived from urban systems, despite a population growth of about 27% since 1880; point sources via newly constructed waste water treatment plants (WWTPs) increased from 4% (1880) to 26% (1940). During the study period, the main changes in diffuse TN-emissions from agriculture were caused by inorganic fertilizer application and nitrogen deposition, while TN-emissions via urban sources were shifted to point sources due to population growth and the construction of new WWTPs. Furthermore, estimated TN-concentrations could make a contribution to construct benchmarks for nutrient concentrations according to the physiochemical properties to implement the European Water Framework Directive (WFD 2000).     

Distributions of heavy metals in the surface sediments of the Gulf of Saros, NE Aegean Sea

The Gulf of Saros in the northeastern Aegean Sea (Turkey) is a relatively unpolluted marine environment. There is almost no industry and only small settlements in the surrounding region. The main sources of fresh water and sediment to the Gulf are the Meric River in the northwest and the Kavak Creek in the east. It has an asymmetric bathymetry with a 10-km-wide shelf to the north and up to 15-km-wide, 700-m-deep trough in the south. Water circulation in the Gulf is characterized by longshore currents and anticyclonic eddies. The Black Sea waters, leaving the Sea of Marmara through the Canakkale Strait, are known to enter the southern Gulf during the summer. The surface sediments on the northern shelf consist mainly of sand, whereas those on the slope and the deep trough are mainly silt and clay. The ranges of Fe, Mn, Cu, Zn, Pb, Ni, and Hg contents of the surface sediments from the Gulf of Saros are 0.25 4.60%, 114 1740 ppm, 6-44 ppm, 23-154 ppm, 2-80 ppm, 14-145 ppm, and 10-130 ppb, respectively. These values are low compared to those from the other neighboring marine environments, indicating the pristine nature of the Gulf in terms of metal pollution. However, most metal and organic carbon (Corg) distributions in the Gulf sediments show the effect of anthropogenic and natural inputs to the northwestern and eastern shelf areas from the Meric River and the Kavak Creek and to the deep trough from the Black Sea waters.     

西苕溪干流水体、悬浮物和表层沉积物中营养盐分布特征与水质评价

了解不同介质的营养盐分布可以全面掌握河流的环境现状。为了调查西苕溪干流的营养盐分布特征和水质现状,沿着干流采集了11个点位的水体、悬浮物和表层沉积物样品,并对水体、悬浮物和表层沉积物中的营养盐特征进行了分析,拟为苕溪流域的水污染防治提供基础数据。研究表明:整个西苕溪干流,水体和沉积物中总氮(TN)和总磷(TP)浓度均存在丰水期明显高于枯水期的季节变化特征,水体中总氮的浓度均超出地表水环境质量Ⅴ类的标准,显示氮污染是西苕溪流域的特点。相关性分析结果表明,悬浮物中的TN和有机质(OM)呈极显著性正相关(r=0.974,p0.01);水体中的TN和悬浮物的各营养盐指标之间的相关性均达到了极显著水平,但沉积物营养盐指标与水体的TN和TP相关性不明显,显示沉积物并不能很好反映流域水质的现状。     

鄱阳湖表层水中全氟辛酸和全氟辛烷磺酸污染现状调查

为阐明鄱阳湖表层水中全氟辛酸（PFOA）和全氟辛烷磺酸（PFOS）的污染现状，于2011年4月7～9日采集鄱阳湖的表层水样30份和长江水样2份，采用超高效液相色谱－三重四极杆串联质谱/质谱法检测样品中PFOS和PFOA含量，探索鄱阳湖表层水中PFOS和PFOA的污染水平及空间分布特征。结果表明： PFOS和PFOA的浓度范围分别为未检出~071 ng/L和030 ~189 ng/L，均值分别为035 ng/L和110 ng/L。而位于长江的0号点水中PFOA和PFOS含量分别为1511 ng/L和081 ng/L。鄱阳湖表层水中的PFOS和PFOA在整体上都呈现南部高于北部的趋势，这可能是由鄱阳湖的水动力条件和其周边PFCs污染源分布不同所致。以上研究结果显示，鄱阳湖表层水中PFOS和PFOA处于较低的污染水平     

Drugs of abuse in surface and tap waters of the Tagus River basin: Heterogeneous photo-Fenton process is effective in their degradation

This work investigates for the first time the occurrence of drugs of abuse and metabolites in surface waters from the Tagus River on its way through the province of Toledo (downstream Madrid metropolitan area) and in drinking waters in two nearby cities. Some of the studied drugs are used for therapeutic purposes but they can also be consumed as illicit drugs. The results of this preliminary study have revealed the presence of 12 out of 22 drugs of abuse analyzed in fluvial water at concentrations ranging from 1.14 to 40.9 ng/L. The largest concentrations corresponded to the anxiolytics diazepam and lorazepam, the cocaine metabolite benzoilecgonine, the amphetamine-like compound ephedrine, and the methadone metabolite EDDP. All these substances, except for lorazepam, were detected in all the sampling points. Traces of methadone and ephedrine were detected in some samples of tap water. Despite the low concentrations of these pollutants, effects on wildlife or human health cannot be disregarded, especially on vulnerable population. Thus, the treatment of these substances using a heterogeneous photo-Fenton process has been evaluated, rendering a remarkable effectiveness for their degradation.