Ultracentrifugation as a direct method to concentrate viruses in environmental waters: virus-like particle enumeration as a new approach to determine the efficiency of recovery

Some health important enteric viruses are considered to be emerging waterborne pathogens and so the improvement of detection of these viruses in the aquatic environment is one of the most important steps in dealing with these pathogens. Since these viruses may be present in low numbers in water, it is necessary to concentrate water samples before viral detection. Although there are several methods to concentrate viruses in environmental waters, all present some drawbacks and consequently the method should be chosen that, despite its limitations, is adequate to achieve the aim of each study. As the effectiveness of the concentration methods is evaluated by determining the efficiency of viral recovery after concentration, it is important to use a simple and effective approach to evaluate their recovery efficiency. In this work ultracentrifugation, usually used as a secondary step for virus concentration, was evaluated as the main method to concentrate directly viruses in environmental water samples, using the microscopic enumeration of virus-like particles (VLP) as a new approach to estimate the efficiency of recovery. As the flocculation method is currently employed to concentrate viruses in environmental waters, it was also used in this study to assess the efficiency of the ultracentrifugation as the main viral concentration method in environmental waters. The results of this study indicate that ultracentrifugation is an adequate approach to concentrate viruses directly from environmental waters (recovery percentages between 66 and 72% in wastewaters and between 66 and 76% in recreational waters) and that the determination of VLP by epifluorescence microscopy is a simple, fast and cheap alternative approach to determine the recovery efficiency of the viral concentration methods.     

Radiological aspects of some Egyptian thermo-mineral springs

In Egypt, nineteen water springs with temperatures exceeding 35 degrees C, which can be considered thermal waters, were reported. The radiological aspects of thermal water in three northern regions of Egypt (Gulf of Suez, Cairo, and Bahariya Oasis) were investigated. The activity concentrations of natural radionuclides of 226Ra, 40K, total uranium and 210Pb (210Po) in water samples were determined using gamma spectrometry, laser fluorimetry and alpha spectrometry after chemical separation, respectively. The highest concentrations are detected in two locations, namely Sudr and Hammam Faroun springs, which are the hottest waters in Egypt (89 and 72 degrees C respectively). It seems that the presence of 226Ra is correlated to the water mineralization and the depth and the temperature of the reservoir's base. Also, these results seem evidence of uranium accumulation at depth in the mother bedrock and/or uranium immobilization due to uranium reduction to the immobile 4+-oxidation state in the reservoir base. The average activity concentrations of 40K are dependent on the water's origin, i.e. meteoric water mixed with sea water (Gulf of Suez springs) and meteoric water (Bahariya Oasis wells). There is no prescribed dose limit for short term and temporary exposure to thermal water. Workers at the thermal springs should be regularly monitored because of their continuous exposure to enhanced radiation levels over a long period of time. The hydrochemical characteristics, environmental isotopes aspects and water origin are briefly discussed based on published data.     

Chemical speciation of inorganic pollutants in river–estuary–sea water systems

Monitoring studies and thermodynamic modeling were used to reveal the changes of inorganic chemical species of some water pollutants (nutrients and trace metals such as Fe, Mn, Zn, Cu, Cd and Pb) inthe river-estuary-sea water system. The case studies were two rivers, Kamchiya and Ropotamo, representing part of the Bulgarian Black Sea water catchment area, and having different flow characteristics. There were no major differences in inorganic chemical species of the two river systems. NO3(-) and NO2(-) chemical species showed no changes along the river-estuary-sea water system. Concerning phosphates six different species were calculated and differences between the three parts of the systems were established. The HPO4(2-) and H2PO4(-) species were found to be dominant in river waters. The H2PO4(-) species quickly decreased at the expense of HPO4(2-) and Ca, Mg and Na phosphate complexes in estuary and seawater. Trace metals showed a great variety of chemical species. Fe(OH)2(+) species prevailed in river waters, and Fe(OH)3(0) species--in sea waters. Me2+ and MeCO3(0) (Me = Cu, Pb) and PbHCO3(+) were dominant in river waters, while Cu(CO3)2(2-) and PbCl(-) species appear also in sea waters. Cd2+ species prevailed in river and estuary waters, and CdCln(2-n) (n = 1-3) species, in seawater. Free Zn2+ species predominated in all systems but downstream their percentage decreased at the expense of Zn phosphates, carbonates,sulfates and chlorides complexes. Only free Mn2+ species were dominant along the systems.     

Size and resin fractionations of dissolved organic matter and trihalomethane precursors from four typical source waters in China

Dissolved organic matter (DOM) and its potential to form disinfection by-products (DBPs) during drinking water treatment raise challenges to water quality control. Understanding both chemical and physical characteristics of DOM in source waters is key to better water treatment. In this study, the DOM from four typical source waters in China was fractionated by XAD resin adsorption (RA) and ultrafiltration (UF) techniques. The trihalomethane formation potential (THMFP) of all fractions in the DOM were investigated to reveal the major THM precursors. The fraction distributions of DOM could be related to their geographical origins in a certain extent. The dominant chemical fraction as THM precursors in the DOM from south waters (East-Lake reservoir in Shenzhen and Peal rivers in Guangzhou) was hydrophobic acid (HoA). The size fraction with molecular weight (MW) <1 kDa in both south waters had the highest THMFP. The results of cluster analysis showed that the parameters of fractions including DOC percentage (DOC%), UV₂₅₄%, SUVA₂₅₄ (specific UV₂₅₄ absorbance) and THMFP were better for representing the differences of DOM from the studied waters than specific THMFP (STHMFP). The weak correlation between SUVA₂₅₄ and STHMFP for either size or XAD fractions suggests that whether SUVA₂₅₄ can be used as an indicator for the reactivity of THM formation is highly dependent on the nature of organic matter.     

Quality assessment of various bottled waters marketed in Saudi Arabia

This study focuses on the chemical analysis of the available brands of domestic bottled water in Riyadh City, Saudi Arabia. The distribution of the chemical constituents (major, minor, and trace elements) is determined and compared with the chemical content labeled on the bottles and with drinking water standards of Saudi Arabian, World Health Organization, and U.S. Environmental Protection Agency. The obtained results indicated that except for fluoride and bromate, the concentrations of dissolved salts, soluble cations and anions, nitrate, and trace elements of most bottled waters on sale were within the permissible limits set by standards used. On the other hand, the comparison between determined and reported label values recorded a substantial variation in some parameter values. Results indicated that more than 18 % of the sampled bottled waters exceeded the allowable limits for drinking water. Generated Piper diagrams revealed that the majority of investigated waters were sodium chloride–sulfate type; however, the hydrochemical modeling indicated that all water samples were undersaturated for anhydrite, gypsum, and halite.     

The Quality of Water Resources in Dalmatia

The purpose of this study was to monitor and record the specific characteristics and properties of most of the important water resources in Dalmatia located in Southern Croatia for a period of 5 years (1998–2002) according to established standards for drinking water. The paper presents a detailed account of their chemical content, the classification and the concentration of salts. The bacteriological pollution levels are indicated by the total coliform bacterial levels (MPN coli/100 mL). The water characteristics are expressed by coefficients, which represent the ratios between water ingredients. The Ca/Mg eq ratio, SO₄/Cl eq ratio and K₁, K₂ for bicarbonate hardness were calculated. The hygienic characteristics of the water samples were expressed by the total coliform bacteria estimation (MPN coli/100 mL), the permanganate consumption (KMnO₄) and biological oxygen demand (BOD₅). Karst waters in Dalmatia are moderately hard, the SO₄/Cl ratio is 0.38–1.6, non-corrosive (K₁ lower than 0.2) and not significantly mineralised (< 500 mg/L minerals). Sulphate waters are generally hard, the SO₄/Cl ratio is higher than 1.6, K₁ is 0.2–0.65. Marine waters are quite hard or hard, particularly at the river estuaries, the SO₄/Cl ratio is lower than 0.38, and K₁ is higher than 0.65. The groundwater and springs in Dalmatia are less polluted than surface waters. A majority of these have a geometric average value of MPN coli < 150/100 mL of water observed in 24 of 42 locations studied. The highest bacteriological pollution was found in nine locations where MPN coli > 1000/100 mL and moderate pollution was found in nine locations where MPN coli is between 150 and 1000/100 mL of water. The physical and chemical parameters determined for the most sources in Dalmatia are safe below the international permissible limits.     

基于Sentinel-3 OLCI影像的渤海FUI水色指数遥感提取及应用

水色是水体水文学特征的基本要素之一。水色测定主要是采用福莱尔比色表(Forel-Ule Scale)将自然水体按颜色从深蓝到红棕共分为21个级别,用以观测、记录海洋和内陆水体的颜色。基于2020—2021年大辽河口、黄河口西南及秦皇岛近岸海域的现场实测数据和同步Sentinel-3 OLCI影像,验证了FUI水色指数遥感提取结果的准确性,发现当现场测量时间与卫星过境时间接近时,FUI水色指数遥感提取结果与实测结果基本一致。利用2021年1—12月Sentinel-3 OLCI影像,提取了渤海月均FUI水色指数遥感产品,发现渤海FUI水色指数的主要变化区间为5~17,整体呈现辽东湾、渤海湾及莱州湾沿岸海域高,秦皇岛海域及其他离岸海域低的空间分布特征,且存在秋冬季高、春夏季低的时间变化规律。此外,FUI水色指数对诸多海洋生态环境问题具有显著的指示功能。尝试将其应用于海洋水色异常和海水水质类别观测,均取得了较好的应用效果。由此可见,FUI水色指数遥感提取将在今后的海洋生态环境监测与评价方面发挥重要作用。     

我国流域水生态完整性评价方法构建

流域水生态完整性评价是指通过对水生态系统中不同水生态指标(生物和非生物)的监测以及由数学方法综合形成的综合评价指数,来反映水生态系统完整性状况。近年来,世界各国水环境管理政策发生了变化,开始强调生态保护,重视水体的生态质量。中国现行的常规理化监测指标(如COD、氨氮、BOD5)很难满足水环境管理的需求,难以全面准确地反映水环境质量变化的趋势。因此,在借鉴欧美发达国家流域水生态完整性评价方法的基础上,结合中国目前监测现状以及流域水环境管理需求,构建了包括物理生境指标、理化指标、水生生物指标在内的流域水生态完整性监测与评价方法,以期为中国流域水质目标管理技术体系的业务化运行提供可资借鉴的技术支撑,实现从单一的化学指标监测转向综合的水生态系统监测,实现流域水生态完整性的监测与评价。     

Chemical markers of human waste contamination: analysis of urobilin and pharmaceuticals in source waters

Giving public water authorities another tool to monitor and measure levels of human waste contamination of waters simply and rapidly would enhance public protection. Most of the methods used today detect such contamination by quantifying microbes occurring in feces in high enough densities that they can be measured easily. However, most of these microbes, for example E. coli, do not serve as specific markers for any one host species and many can have origins other than feces. As an alternative, chemicals shed in feces and urine might be used to detect human waste contamination of environmental waters. One potential chemical marker of human waste is the compound urobilin. Urobilin is one of the final by-products of hemoglobin breakdown. Urobilin is excreted in both the urine and feces from many mammals, particularly humans. Source waters from 21 sites in New England, Nevada, and Michigan were extracted using hydrophilic-lipophilic balance (HLB) cartridges and then analyzed by high performance liquid chromatography-electrospray mass spectrometry (HPLC-ES-MS). As a marker of human waste, urobilin was detected in many of the source waters at concentrations ranging from not detectable to 300 ng L(-1). Besides urobilin, azithromycin, an antibiotic widely prescribed for human use only in the US, was also detected in many of these waters, with concentrations ranging from not detectable to 77 ng L(-1). This methodology, using both urobilin and azithromycin (or any other human-use pharmaceutical) could be used to give public water authorities a definitive method for tracing the sources of human waste contamination. The analysis and detection of urobilin in surface waters by HPLC-ES-MS has not been previously reported in the peer-reviewed literature.     

Filtration of fullerene and copper oxide nanoparticles using surface-modified microfilters

This study evaluated the filtration of engineered nanoparticles of fullerene and copper oxide (CuO) from water by using surface-modified microsized filters. The surfaces of microsized filters of cellulose acetate and glass fibers were coated with cationic and anionic surfactants to give them positively and negatively charged surfaces, respectively. Uncoated microfilters removed 30 % of a fullerene suspension, while no nanosized CuO suspension was removed. Cationic surfactant-coated filters enhanced the removal efficiency up to 70 % for the fullerene suspension, while the anionic surfactant-coated filters could not remove fullerene at all. The positively charged filters with cationic surfactant coating could easily adsorb negatively charged fullerenes on their surfaces. However, none of the surfactant-coated filters removed the CuO nanoparticles because the nanoparticles were not affected by the electrical charge of the filtration medium. The Hamaker constants of nanoparticles interacting with the filter materials in water were calculated to study these interactions. The Hamaker constant of fullerene interacting with cellulose acetate in water, 4.68E???21 J, was higher than that of interacting with quartz in water, 2.59E???21 J. However, the Hamaker constants of CuO interacting with quartz and cellulose acetate in water were both negative values, implying repulsive van der Waals interactions. The curves of potential energy of interaction between nanoparticles and the various filter media implied that the nanoparticles were very stable in water, and so, natural deposition of nanoparticles on the filters would not occur. Therefore, electrical bonding and hydrophobic interactions were the forces dominating fullerene removal by positively charged filters.     

The release of engineered nanomaterials to the environment

There is scientific agreement that engineered nanomaterial (ENM) production, use and disposal lead to environmental release of ENM. However, very little is known on emissions of ENM to the environment. Currently, techniques are lacking to quantitatively monitor ENM emissions to and concentrations in the environment, and hence data on emissions and environmental concentrations are scarce. One of the few available studies reports the detection of nano-TiO(2) in water leaching from exterior facades. Some experimental evidence is available on the release of nanosized materials from commercial textiles during washing. A handful of modeling studies have investigated ENM release to the environment. These studies modeled either the release of ENMs to the environment from ENM containing products during the consumer usage, or the release throughout the whole life cycle of ENM and ENM-containing products. Sewage sludge, wastewater, and waste incineration of products containing ENM were shown to be the major flows through which ENMs end up in the environment. However, reliable data are particularly lacking on release during ENM production and on the application amounts and empirical information on release coefficients for all life cycle stages and environmental compartments. Quantitative data linking occupational exposure measurements and ENM emission flows into the environment are almost completely missing. Besides knowing the amounts of ENM released into the environment, it is equally important to investigate in what form ENMs are released. First results show that much of the ENM released from products is present in matrix-bound form, but that also some fraction is released as single, dispersed nanoparticles.     

滇池水环境质量综合评价指标优选

在研究2000—2014年滇池流域水污染排放的时空变化、水环境质量时空变化和生态环境时空演替基础上,结合滇池目前水环境质量监测工作要求,采用模型计算、指标特性分析、专家调查等方法,筛选出36个评价指标,分别表征滇池水环境质量的物理、化学、生物、营养、重金属、有机污染等特性,将滇池湖体4个监测点位优选出的评价指标监测数据输入水生态健康评价系统。结果表明,优选指标和评价体系能全面、准确、宏观地反映滇池水环境质量状况。将滇池评价指标由现有的94个压缩至36个,极大节省人力、物力,且更符合滇池水环境特点。     

An assessment of the quality of various bottled mineral water marketed in Turkey

Fifteen bottled mineral waters purchased at random all over Turkey were analyzed for their chemical composition by OPTIMA-2000 ICP-AES Perkin Elmer techniques. Results show a wide spread in the chemical specification of these mineral waters, with differences in chemical composition observed in the regions being due to the geological environment and the majority of bottled mineral waters exceeding the pH limit of Turkish drinking water standards. When the concentrations of elements are evaluated, it can readily be seen that generally there are three types of mineral water in Turkey. The concentrations of Al, B, Ba, Cd, Cu, Cr, Fe, Mn Pb and Zn in mineral water were compared with the limits established by the Turkish Standard for Natural Mineral Waters (Turkish Official Gazette 2004); water standards prepared by World Health Organization (2006) and the United States of America Environmental Protection Agency (US EPA) drinking water standards (1993). Such a comparison shows that, except for Ba and Mn, the concentrations of the other heavy metals are lower than the limit of the US.EPA in Turkey. Some parameters examined were found to comprise strong correlations pair-wise.     

我国内陆流域各类水体中天然放射性核素浓度

1985年～1989年由新疆、甘肃、青海、西藏、内蒙古、陕西、宁夏等省、自治区环境监测站(研究所)对内陆流域各类水体中U、Th、~(226)Ra、~(40)K浓度进行调查,由调查的29条内陆河、23个湖泊、15座水库、55处井泉和34个自来水的统计结果表明,流域内各水体中U和~(40)K浓度的平均值与同期调查的黄河水系同类水体的浓度相近,明显高于长江水系,与全国同类水体相比亦属偏高。Th和~(226)Ra的平均浓度与全国同类水体的浓度相近,甘、新内陆区浓度较低。调查发现,一些咸水湖、井水和自来水中U、~(226)Ra,或~(40)K浓度异常偏高。     

Influence of multi-industrial activities on trace metal contamination: an approach towards surface water body in the vicinity of Dhaka Export Processing Zone (DEPZ)

Industrial wastewater discharged into aquatic ecosystems either directly or because of inadequate treatment of process water can increase the concentrations of pollutants such as toxic metals and others, and subsequently deteriorate water quality, environmental ecology and human health in the Dhaka Export Processing Zone (DEPZ), the largest industrial belt of 6-EPZ in Bangladesh. Therefore, in order to monitor the contamination levels, this study collected water samples from composite effluent points inside DEPZ and the surrounding surface water body connected to effluent disposal sites and determined the environmental hazards by chemical analysis and statistical approach. The water samples were analysed by inductively coupled plasma mass spectrometry to determine 12 trace metals such as As, Ag, Cr, Co, Cu, Li, Ni, Pb, Se, Sr, V and Zn in order to assess the influence of multi-industrial activities on metal concentrations. The composite effluents and surface waters from lagoons were characterized by a strong colour and high concentrations of biochemical oxygen demand, chemical oxygen demand, electrical conductivity, pH, total alkalinity, total hardness, total organic carbon, Turb., Cl(-), total suspended solids and total dissolved solids, which were above the limit of Bangladesh industrial effluent standards, but dissolved oxygen concentration was lower than the standard value. The measurement of skewness and kurtosis values showed asymmetric and abnormal distribution of the elements in the respective phases. The mean trend of variation was found in a decreasing order: Zn > Cu > Sr > Pb > Ni > Cr > Li > Co > V > Se > As > Ag in composite industrial effluents and Zn > Cu > Sr > Pb > Ni > Cr > Li > V > As > Ag > Co > Se in surface waters near the DEPZ. The strong correlations between effluent and surface water metal contents indicate that industrial wastewaters discharged from DEPZ have a strong influence on the contamination of the surrounding water bodies by toxic metals. The average contamination factors were reported to be 0.70-96.57 and 2.85-1,462 for industrial effluents and surface waters, respectively. The results reveal that the surface water in the area is highly contaminated with very high concentrations of some heavy/toxic metals like Zn, Pb, Cu, Ni and Cr; their average contamination factors are 1,460, 860, 136, 74.71 and 4.9, respectively. The concentrations of the metals in effluent and surface water were much higher than the permissible limits for drinking water and the world average concentrations in surface water. Therefore, the discharged effluent and surface water may create health hazards especially for people working and living inside and in the surrounding area of DEPZ.     

Occurrence of dissolved PAHs in the Jinsha River (Panzhihua)--upper reaches of the Yangtze River,Southwest China

16 priority polycyclic aromatic hydrocarbons (PAHs) were determined in water samples from the Jinsha River (Panzhihua part), Southwest China. Total dissolved PAH concentrations varied from 21.89 microg l(-1) to 382.8 microg l(-1). It was found that the concentration of PAHs decreased along the flow direction due to the higher density distribution of coal chemical industry in the upstream of our study rivers. The pollution levels in our study area are significantly higher than previously reported values in other waters both in China and other countries. The predominance of benzo[k]fluoranthene and indeno[1,2,3-cd]pyrene was clearly observed in all water samples. On average these two compounds accounted for 98.3% of the total dissolved PAH concentration in water. The results showed the positive correlations among total dissolved PAHs, benzo[k]fluoranthene and indeno[1,2,3-cd]pyrene, which suggested that these two predominant PAHs have similar source and environmental behaviors in our study area. When compared with the survey results of organic micropollutants two decades ago, it was found that hydrocarbon pollution both predominated and even increased with the development of coal chemical industry in this area during the past 20 years. The results therefore provide important information on the current contamination status of a key industrial city in China, and points to the need for urgent action to investigate the relationship between the PAH composition and concentration in water from the Jinsha River and the wastewater discharge from coal chemical industry, and to identify the source, transport pathway and fate of PAHs in the area. It should then be necessary to adopt appropriate and instant measures to control the pollution around this area.     

Assessment of environmental variations caused by a very large floating structure in a semi-closed bay

To assess the environmental impacts of large floating structures, various physical, chemical, and biological parameters were measured. The current and water quality were monitored around a prototype floating structure called the Phase-II Mega-Float model (MF-II model), which was moored off Yokosuka in Tokyo Bay during the period 1999–2000. The effects of the MF-II model on the condition of the physical environment, e.g., the direction and flow rate of water currents and the stratification structure, were negligible. Analysis of water quality showed that the concentrations of chlorophyll a and nutrients only varied just below the MF-II model. However, such variations were localized to within 5 m below the MF-II model since the waters were exchanged because of the tidal current. The minor changes in water quality are attributable to the impedance of photosynthesis due to the sea-covering effect and the activities of sessile organisms fouling the bottom surface of the MF-II model.     

中国1998年度环境质量状况

对我国１９９８年度的环境空气质量,酸雨,主要流域水质,近岸域海水水质,地下水水位与水质,城市声环境、射环境质量,典型区域生态环境的状况进行了综述了与分析,指出了我国的环境污染问题主要是城市空气污染,地面水体污染和城市噪声污染。     

Contamination from historic metal mines and the need for non-invasive remediation techniques: a case study from Southwest England

The UK is legally required by the EU Water Framework Directive (WFD) to improve the environmental quality of inland and coastal waters in the coming years. Historic metal mine sites are recognised as an important source of some of the elements on the WFD priority chemicals list. Despite their contamination potential, such sites are valued for their heritage and for other cultural and scientific reasons. Remediating historic mining areas to control the contamination of stream waters, whilst also preserving the integrity of the mine site, is a challenge but might be achieved by novel forms of remediation. In this study, we have carried out environmental monitoring at a historic, and culturally-sensitive, lead-silver mine site in southwest England and have undertaken a pilot experiment to investigate the potential for a novel, non-invasive remediation method at the site. Concentrations of Pb and Zn in mine spoil were clearly elevated with geometric mean concentrations of 6,888 and 710 microg g(-1), respectively. Mean concentrations of Pb in stream waters were between 21 and 54 microg l(-1), in exceedance of the WFD environmental quality standard (EQS) of 7.2 microg l(-1) (annual average). Mean Zn concentrations in water were between 30 and 97 microg l(-1), compared to the UK EQS of 66.5 microg l(-1) (average). Stream sediments within, and downstream from, the mining site were similarly elevated, indicating transport of mine waste particles into and within the stream. We undertook a simple trial to investigate the potential of hydroxyapatite, in the form of bonemeal, to passively remove the Pb and Zn, from the stream waters. After percolating through bonemeal in a leaching column, 96-99% of the dissolved Pb and Zn in stream water samples was removed.     

Laser-induced breakdown spectroscopy application in environmental monitoring of water quality: a review

Water quality monitoring is a critical part of environmental management and protection, and to be able to qualitatively and quantitatively determine contamination and impurity levels in water is especially important. Compared to the currently available water quality monitoring methods and techniques, laser-induced breakdown spectroscopy (LIBS) has several advantages, including no need for sample pre-preparation, fast and easy operation, and chemical free during the process. Therefore, it is of great importance to understand the fundamentals of aqueous LIBS analysis and effectively apply this technique to environmental monitoring. This article reviews the research conducted on LIBS analysis for liquid samples, and the article content includes LIBS theory, history and applications, quantitative analysis of metallic species in liquids, LIBS signal enhancement methods and data processing, characteristics of plasma generated by laser in water, and the factors affecting accuracy of analysis results. Although there have been many research works focusing on aqueous LIBS analysis, detection limit and stability of this technique still need to be improved to satisfy the requirements of environmental monitoring standard. In addition, determination of nonmetallic species in liquid by LIBS is equally important and needs immediate attention from the community. This comprehensive review will assist the readers to better understand the aqueous LIBS technique and help to identify current research needs for environmental monitoring of water quality.