Identification of microcystins contamination in surface water samples from the Three Gorges Reservoir, China

Physicochemical and biological parameters related to water quality and microcystins (MCs) contamination in aquatic environment of the Three Gorges Reservoir were investigated in August 2004 and January 2005. A solid-phase extraction method and an HPLC equipped with photodiode array were used for MC-LR detection. A quantitative analysis showed the total MC-LR concentrations of water samples ranged from non-detectable to 0.57 μg L?1 among the seven sampling sites. The highest MC-LR concentration was found at sampling site G (Wushan), which was followed by F (Kaixian), E (Wanzhou), D (Fuling), C (Cuntan), and A (Daxigou). The correlation analysis showed the MC-LR concentration was positively correlated with chlorophyll-a concentration. This result suggests that MC concentration in water can be indirectly estimated by analyzing the chlorophyll-a concentration. Overall, the results of this study suggest that more importance should be placed on monitoring of MC contamination and water quality in the Three Gorges Reservoir to ensure drinking water safety and reduce the potential exposure of people to these health hazards.     

A nanosilver-based spectrophotometric method for determination of malachite green in surface water samples

A new spectrophotometric method is reported for the determination of nanomolar level of malachite green in surface water samples. The method is based on the catalytic effect of silver nanoparticles on the oxidation of malachite green by hexacyanoferrate (III) in acetate–acetic acid medium. The absorbance is measured at 610 nm with the fixed-time method. Under the optimum conditions, the linear range was 8.0?×?10^?9–2.0?×?10^?7?mol?L^?1 malachite green with a correlation coefficient of 0.996. The limit of detection (S/N?=?3) was 2.0?×?10^?9?mol?L^?1. Relative standard deviation for ten replicate determinations of 1.0?×?10^?8?mol?L^?1 malachite green was 1.86 %. The method is featured with good accuracy and reproducibility for malachite green determination in surface water samples without any pre-concentration and separation step.     

Monitoring of aminophenol isomers in surface water samples using a new HPLC method

A new HPLC method was developed for the simultaneous determination of aminophenol isomers by means of a mixed-mode stationary phase containing both SCX and C18 moieties. All factors influencing the separation were discussed and optimized. The chromatographic conditions for the separation of aminophenols are the stationary phase duet SCX/C18, the mobile phase of aqueous phosphate buffer (pH 4.85):methanol?=?85:15 (v/v) delivered with a flow rate of 1 mL/min and a detection at 285 nm. The method proposed was validated in terms of linearity, limits of detection and quantification, accuracy and precision. The HPLC method elaborated here was applied with good results on river water samples. In order to survey the quality of surface rivers entered in treatment plants which deliver water for Bucharest, two major rivers were included in a monitoring program which last more than 1 year.     

Storm water contamination and its effect on the quality of urban surface waters

We studied the effect of storm water drained by the sewerage system and discharged into a river and a small reservoir, on the example of five catchments located within the boundaries of the city of Poznań (Poland). These catchments differed both in terms of their surface area and land use (single- and multi-family housing, industrial areas). The aim of the analyses was to explain to what extent pollutants found in storm water runoff from the studied catchments affected the quality of surface waters and whether it threatened the aquatic organisms. Only some of the 14 studied variables and 22 chemical elements were important for the water quality of the river, i.e., pH, TSS, rain intensity, temperature, conductivity, dissolved oxygen, organic matter content, Al, Cu, Pb, Zn, Fe, Cd, Ni, Se, and Tl. The most serious threat to biota in the receiver came from the copper contamination of storm water runoff. Of all samples below the sewerage outflow, 74 % exceeded the mean acute value for Daphnia species. Some of them exceeded safe concentrations for other aquatic organisms. Only the outlet from the industrial area with the highest impervious surface had a substantial influence on the water quality of the river. A reservoir situated in the river course had an important influence on the elimination of storm water pollution, despite the very short residence time of its water.     

Estimation of uranium and radon concentration in some drinking water samples of Upper Siwaliks, India

Uranium and radon concentration was assessed in water samples taken from hand pumps, natural sources and wells collected from some areas of Upper Siwaliks, Northern India. Fission track registration technique was used to estimate the uranium content of water samples. The uranium concentration in water samples was found to vary from 1.08 +/- 0.03 to 19.68 +/- 0.12 microg l(-1). These values were compared with safe limit values recommended for drinking water. Most of the water samples were found to have uranium concentration below the safe limit of 15 microg l(-1) (WHO, World Health Organization, Guidelines for drinking-water quality (3rd ed.). Geneva, Switzerland: WHO, 2004). The radon estimation in these water samples was made using alpha-scintillometry to study its correlation with uranium. The radon concentration in these samples was found to vary from 0.87 +/- 0.29 to 32.10 +/- 1.79 Bq l(-1). The recorded values of radon concentration were within the recommended safe limit of 4 to 40 Bq l(-1) (UNSCEAR, United Nations Scientific Committee on the Effects of Atomic Radiations, Sources and effects of ionizing radiation. New York: United Nations, 1993). No direct correlation was found between uranium concentration and radon concentration in water samples belonging to Upper Siwaliks. The values of uranium and radon concentration in water were compared with that from the adjoining areas of Punjab state, India.     

The determination and distribution of Zn in surface water samples collected in the northeast Atlantic Ocean

Dissolved Zn concentrations were determined in surface water samples collected on-line along transects in the eastern North Atlantic in spring (March 1998). Two frontal zones could be identified in the research area by a change in salinity, temperature and nutrient concentrations. One zone was identified at 42 degrees N, separating the North Atlantic central water (NACW) and the Atlantic surface water (ASW) from each other, and another one crossing the continental slope at 12 degrees and 8 degrees E, respectively. Variability in Zn concentrations was observed near these zones, not only as a result of a change of water mass, but also due to external Zn sources. Surface Zn concentrations were 0.5-1 nM and 2 nM in the NACW and ASW, respectively, increasing to 4 nM over the continental shelf and finally 5-6 nM in the English Channel. Contributions of Zn derived from shelf sediments appear to be the major source for the enriched surface values in the continental zone.     

固相萃取-高效液相色谱法测定生活污水中壬基酚聚氧乙烯醚及其降解产物

比较了液-液萃取和固相萃取浓缩富集水体中壬基酚聚氧乙烯醚(NPnEO,n为聚合度)及其小分子代谢产物的效率,建立了复杂基体水样中壬基酚聚氧乙烯醚及其小分子代谢产物多成分同时测定的高分辨高灵敏的固相萃取(SPE)-正相高效液相色谱(NP-HPLC)-荧光检测(FL)方法。优化了影响SPE回收率的条件,洗脱溶剂和样品过柱的速度。SPE对NPnEO的回收率大于82%;使用1L水样,方法的检测限对壬基酚(NP)、NP1EO为0.01μgL,NP2EO、NP3EO为0.02μgL,NP4EO～NP12EO为0.05μgL。应用本方法测定了生活污水水样,检测到了NPnEO(n=1～12)及其小分子降解产物NP、NP1EO、NP2EO。     

分光光度法测定水中微量草酸盐

研究了在酸性介质中 ,锌与草酸的还原反应 ,生成的乙醛酸与盐酸苯肼反应生成乙醛酸苯腙 ,而苯肼转化为重氮盐后与乙醛酸苯腙反应生成粉红色偶氮化合物。据此建立了分光光度法测定微量草酸盐的分析方法。     

Use of preserved museum fish to evaluate historical and current mercury contamination in fish from two rivers in Oklahoma, USA

We examined the effects of a commonly used preservation technique on mercury concentration in fish tissue. After fixing fish muscle tissue in formalin followed by preservation in isopropanol, we found that mercury concentration in fish muscle tissue increased by 18%, reaching an asymptote after 40 days. We used formalin–isopropanol-preserved longear sunfish (Lepomis megalotis) from the Sam Noble Oklahoma Museum of Natural History to examine historical changes and predict current mercury concentrations in fish from two rivers in southeastern Oklahoma. Glover River was free-flowing, while Mountain Fork River was impounded in 1970 and a coldwater trout fishery was established upstream from the collection site in 1989. Mercury concentrations in longear sunfish from Glover River showed no historical changes from 1963 to 2001. Mercury concentrations in longear sunfish from Mountain Fork River showed no change from 1925 to 1993 but declined significantly from 1993 to 2003. We also compared mercury concentrations of the most recently collected longear sunfish in the museum to mercury concentrations of unpreserved fish collected from the rivers in 2006. Concentrations of mercury in museum fish were not significantly different from mercury concentrations in unpreserved fish we collected from the rivers. Our study indicates that preserved museum fish specimens can be used to evaluate historical changes and predict current levels of mercury contamination in fish.     

The 210Po and 210Pb levels in surface sediment samples in the Izmir Bay (Aegean Sea-Turkey)

Bottom sediments reflect in general the relative contamination of a sea area. Therefore, a great deal of monitoring work has been dedicated to the analysis of bottom sediments. Izmir Bay is a very important pollution centre in Turkish Aegean coast region due to a densely populated community, industrial complex and maritime transportation, and there are many streams flowing into the bay that pass through a number of industrial and agricultural areas. It had received the majority of domestic and industrial wastewaters until the wastewater treatment plant was constructed. It is well known that sediments play an important role as reservoirs of a fraction of the pollution in aquatic systems. Therefore, sediment samples were collected monthly from three stations which are located in the inner part of the bay during the period January to December 2003. Temporal variations and seasonal changes on their ²¹⁰Po and ²¹⁰Pb contents were examined, and the activity concentrations of ²¹⁰Po and ²¹⁰Pb were found to vary from 43±6 to 132±12 and 27±5 to 91±9 Bq kg^???1 dry wt, respectively. The highest values of those natural radionuclides were measured at Kar??yaka Station because of the current systems of the bay. Seasonally, the ²¹⁰Pb levels were found to increase during the winter time for all the stations.     

河南省地表水环境监测断面优化的原则及其运用

提出和运用了地表水环境监测断面优化的原则,包括网络功能专一化、分类有序优化、监测断面高效、监测断面与监测频率同时优化、监测断面分级管理等。     

Spatial and temporal properties of environmental exposure assessments related to ground water contamination

This paper describes a new methodology for modeling contaminant transport in ground water for (1) better quantifying the magnitude of exposure in a contaminated aquifer, (2) characterizing the spatial and temporal variation of exposure in a heterogeneous aquifer, and (3) providing more tools for characterizing population exposure. This methodology is also applied to a semi-hypothetical case study.     

Assessments of some metals contamination in lipsticks and their associated health risks to lipstick consumers in Iran

In this study, the concentrations of lead, cadmium, and chromium in lipstick samples were evaluated. The samples were from different brands and produced in different countries. The average lead, cadmium, and chromium concentrations in all lipstick samples were 1.851, 0.017, and 4.300 mg kg^?1 ww, respectively. There was a significant difference in the concentrations of lead, cadmium, and chromium among the brands (p?<?0.05). The concentrations of the measured elements in the brands did not exceed the values of the international standards provided for lipstick. The values of hazard quotient (HQ), health risk index (HI), relative intake index (RII), and estimated daily intake (EDI) indices were calculated. The results of the HQ and HI indices showed that in more than 50% of the lipstick brands, there is a potential threat to consumer health due to the presence of these elements in lipstick. Therefore, it can be concluded that, due to the simultaneous use of lipstick with other types of cosmetics and hence the potential exposure of consumers to toxic elements through all cosmetics, continuous monitoring of the concentrations of these elements in these types of products is necessary to avoid potential health risks.     

Monitoring bacterial contamination of piped water supply in rural coastal Bangladesh

Safe drinking water is scarce in southwest coastal Bangladesh because of unavailability of fresh water. Given the high salinity of both groundwater and surface water in this area, harvested rainwater and rain-fed pond water became the main sources of drinking water. Both the government and non-government organizations have recently introduced pipe water supply in the rural coastal areas to ensure safe drinking water. We assessed the bacteriological quality of water at different points along the piped water distribution system (i.e., the source, treatment plant, household taps, street hydrants, and household storage containers) of Mongla municipality under Mongla Upazila in Bagerhat district. Water samples were collected at 2-month interval from May 2014 to March 2015. Median E. coli and total coliform counts at source, treatment plant, household taps, street hydrants, and household storage containers were respectively 225, 4, 7, 7, and 15 cfu/100 ml and 42,000, 545, 5000, 6150, and 18,800 cfu/100 ml. Concentrations of both of the indicator bacteria reduced after treatment, although it did not satisfy the WHO drinking water standards. However, re-contamination in distribution systems and household storage containers indicate improper maintenance of distribution system and lack of personal hygiene.     

Estimation of Polish cigarettes contamination with cadmium and lead, and exposure to these metals via smoking

To estimate exposure to cadmium (Cd) and lead (Pb) through cigarette smoking, the concentrations of both metals in the blood or/and urine of smokers (20 cigarettes or more per day for 10 years or longer) and their non-smoking counterparts inhabiting an environmentally unpolluted area (Bialystok, Poland) were evaluated, as well as Cd and Pb contents in the cigarette brands (produced in Poland) smoked by the participants, including intact cigarettes, pre-smoking (tobacco, paper and filter) and post-smoking (butt, ash and smoke) cigarette components. Blood and urinary Cd concentrations in the smokers have been already reported by us to be 2–4 times higher than in the non-smokers (Galażyn-Sidorczuk et al. Polish Journal of Environmental Studies, 13 (Suppl.1):91–95, 2004). All the other measurements are the subject of the present paper. Pb concentration in the blood of the cigarette smokers (52.12 ± 15.51 μg l⁻¹) was higher by 29% than in the non-smokers (40.42 ± 11.19 μg l⁻¹). The mean Cd and Pb contents in the cigarettes were 0.6801 ± 0.1765 and 0.6853 ± 0.0746 μg per cigarette, respectively. Under cigarette burning, performed using a machine for self-acting burning, on average 33% of Cd and 11% of Pb present in the whole cigarette was released into the smoke. For Cd, unlike Pb, there was a high positive correlation between the metal content in cigarettes and tobacco and its release into the smoke. Moreover, the subjects smoking cigarettes containing the highest Cd amount had higher blood Cd concentration than smokers of other cigarette brands. The results give clear evidence that in the case of inhabitants of areas unpolluted with Cd and Pb habitual cigarette smoking, due to tobacco contamination, creates a serious source of chronic exposure to these metals, especially to Cd.     

An investigation of arsenic contamination in Peninsular Malaysia based on Centella asiatica and soil samples

The first objective of this study was to provide data of arsenic (As) levels in Peninsular Malaysia based on soil samples and accumulation of As in Centella asiatica collected from 12 sampling sites in Peninsular Malaysia. The second objective was to assess the accumulation of As in transplanted C. asiatica between control and semi-polluted or polluted sites. Four sites were selected which were UPM (clean site), Balakong (semi-polluted site), Seri Kembangan (semi-polluted site) and Juru (polluted site). The As concentrations of plant and soil samples were determined by Instrumental Neutron Activation Analysis. The As levels ranged from 9.38 to 57.05 μg/g dw in soils, 0.21 to 4.33 μg/g dw in leaves, 0.18 to 1.83 μg/g dw in stems and 1.32–20.76 μg/g dw in roots. All sampling sites had As levels exceeding the CCME guideline (12 μg/g dw) except for Kelantan, P. Pauh, and Senawang with P. Klang having the highest As in soil (57.05 μg/g dw). In C. asiatica, As accumulation was highest in roots followed by leaves and stems. When the As level in soils were higher, the uptake of As in plants would also be increased. After the transplantation of plants to semi-polluted and polluted sites for 3 weeks, all concentration factors were greater than 50 % of the initial As level. The elimination factor was around 39 % when the plants were transplanted back to the clean sites for 3 weeks. The findings of the present study indicated that the leaves, stems and roots of C. asiatica are ideal biomonitors of As contamination. The present data results the most comprehensive data obtained on As levels in Malaysia.     

Utilization of statistics based classification approach to investigate water supply profile of Turkey

In the paper water supply profile of Turkey was examined. In this scope, the questionnaire survey conducted by Turkish Statistical Institute in 2004 to investigate annual amount of water abstracted to drinking water networks by type of resources in 81 provinces was evaluated. In the questionnaire, sources were grouped under five categories as spring, (artificial) lake, river, reservoir and well. Due to the complex and multivariate characteristics of the data sets, to replace a large collection of variables with a smaller number of factors the statistical method "factor analysis" was performed. Results revealed that, water supply systems in the country were mainly governed by groundwater sources (well and/or spring). However, in the northeastern part of the country, rivers were allocated for drinking water supply. On the other hand, reservoir dependent cities were densely located in Marmara, Central Anatolia and Southeast Anatolia Regions. This study showed that statistics based classification methods assist decision makers to extract information from multidimensional complex data sets representing environmental conditions.     

An assessment of heavy metal contamination in surface sediment using statistical analysis

The distribution and accumulation of heavy metals in the sediments, especially those nearest of wastewater discharges of south of Spain, were investigated. Sediment samples from 14 locations were collected and characterised for metal content (e.g. Ni, Cu, Zn, Cr, Pb, Mn, Cd and Hg), organic carbon, total nitrogen, total phosphorous, n-hexane-extractable material, carbonates and grain size. Concentration data were processed using correlation analysis and factor analysis. The correlation analysis of concentrations data showed important positive correlations among organic carbon, total phosphorus, Cu, Zn, Cd and Hg, otherwise weak correlations among Mn, Cr, Ni and CO₃ ^2???, indicating that these metals have complicated geochemical behaviours. The use of statistical factor analysis also confirmed these results. Sediments pollution assessment was carried out using geoaccumulation and metal pollution indexes (MPI₈). The results revealed that sediments of Cádiz bay and Sancti Petri channel were uncontaminated with the studied metals.     

Analysis of selected biomonitors to evaluate the suitability for their complementary use in monitoring trace element atmospheric deposition

The biomonitoring properties of oak tree bark compared with the epiphytic moss Hypnum cupressiforme and the influence of the tree bark, as its growth substrate, on the content of heavy metals in moss were investigated. Samples of the epiphytic moss H. cupressiforme and oak tree bark (Quercus spp.) were collected in Eastern Romania at a total of 44 sampling sites. Parallel moss and bark samples were collected from the same sides of the trunk circumference. V, Cr, Ni, Cu, Zn, As, Mo, Cd, In, Tl, Sn, Pb, and Bi were determined by ICP-MS. Principal component analysis was used to identify possible sources of metals in bark and moss. Six factors explaining 87 % of the total variance in the data set were chosen. The main factors represent long-range atmospheric transport of elements (Zn, Cd, (Pb), Bi, (Mo), (Tl)), local emissions from industrial sources (As, Cr, Ni, V), road traffic (Pb, Zn) and agricultural activities (Cu, (Zn)). The element concentrations in moss and bark samples are of the same order of magnitude. For almost all the elements, higher concentrations were obtained in moss. Significant correlations between concentrations in moss and bark samples were obtained for 7 of the 13 elements: V, Ni, Cu, Zn, Cd, In, and Bi, all typical anthropogenic pollutants. The use of tree bark for monitoring purposes might be an alternative in areas where there is a scarcity of mosses.