Atmospheric vapour phase and particulate phase mercury in a coastal desert climate

Vapour (T-Hg(v)) and particulate (T-Hg(p)) mercury were measured in the lower atmosphere at a ground station in Kuwait Bay. The concentration of T-Hg(v) varied from 0-86 ng m(-3) with a mean of 3.8 +/- 5.5 ng m(-3)(n= 13 326). About 40% of the measured T-Hg(v) values over Kuwait Bay are higher than the global range (1-3 ng m(-3)). Car exhausts contributed to the increase of T-Hg(v) during the rush hours. However the contribution of T-Hg(v) from air crossing Kuwait Bay exceeds that T-Hg(v) produced by traffic probably because of the effects of the substantial load of industrially-derived mercury in the sediments of this shallow region. Thermal inversions have a major impact on the levels during the evening hours. The concentration of T-Hg(p) varied from 0.00-0.22 ng m(-3) with a mean of 0.03 +/- 0.03 ng m(-3)(n= 175). The T-Hg(p)/T-Hg(v)% ratio varied from 0-11.1 (n= 171) with a mean of 1.0 +/- 1.5%. Meteorological parameters influence the T-Hg(v) and T-Hg(p) concentrations with dust storms having a major impact on T-Hg(p) concentrations.     

Spatial distribution and quantification of endocrine-disrupting chemicals in Sado River estuary, Portugal

The important Portuguese Sado River estuary has never been investigated for the presence of potentially endocrine-disrupting chemicals (EDCs), such as natural estrogens (estradiol, estrone), pharmaceutical estrogens (17α-ethynylestradiol), phytoestrogens (daidzein, genistein and biochanin A), or industrial chemicals (4-octylphenol, 4-nonylphenol, and bisphenol A). Thus, the main objective of this study was to evaluate their presence at 13 sampling points distributed between both the industrial and the natural reserve areas of the estuary, zones 1 and 2, respectively. For that, water samples collected in summer and winter were processed by solid phase extraction and analyzed by high-performance liquid chromatography with photodiode array detection and gas chromatography–mass spectroscopy. Results showed that estrone, ethynylestradiol, all the aforementioned phytoestrogens as well as bisphenol A and 4-octylphenol were found in zone 1. In zone 2, neither estrogens nor 4-OP were found. However, in the same zone, daidzein (500 ng/L) and genistein (320 ng/L) attained their highest levels in summer, whereas biochanin A peaked in winter (170 ng/L). Furthermore, bisphenol A was also found in some areas of zone 2, but showed similar concentrations in both surveys (about 220 ng/L). This study demonstrated that the Sado River estuary had low EDCs levels, suggesting that the Sado’s high hydrodynamic activity may be involved in the dilution of local pollution. It was suggested that at the current levels of concentrations, all assayed EDCs are unlikely to individually cause endocrine disruption in local animals. However, under a continuous exposure scenario, an additive and/or synergistic action of the estrogenic chemicals load can not be excluded, and so, continuous monitoring is advisable.     

Water quality of a tributary of the Pearl River, the Beijiang, Southern China: implications from multivariate statistical analyses

Water quality information of Beijiang River, a tributary of Pearl River in Guangdong, China, was analyzed to provide an overview of the hydrochemical functioning of a major agricultural/rural area and an industrial/urban area. Eighteen water quality parameters were surveyed at 13 sites from 2005 to 2006 on a monthly basis. A bivariate correlation analysis was carried out to evaluate the regional correlations of the water quality parameters, while the principal component analysis (PCA) technique was used to extract the most influential variables for regional variations of river water quality. Six principal components were extracted in PCA which explained more than 78% and 84% of the total variance for agricultural/rural and industrial/urban areas, respectively. Physicochemical factor, organic pollution, sewage pollution, geogenic factor, agricultural nonpoint source pollution, and accumulated pesticide usage were identified as potential pollution sources for agricultural/rural area, whereas industrial wastewaters pollution, mineral pollution, geogenic factor, urban sewage pollution, chemical industrial pollution, and water traffic pollution were the latent pollution sources for industrial/urban area. A multivariate linear regression of absolute principal component scores (MLR-APCS) technique was used to estimate contributions of all identified pollution sources to each water quality parameter. High coefficients of determination of the regression equations suggested that the MLR-APCS model was applicable for estimation of sources of most water quality parameters in the Beijiang River Basin.     

Characteristics of and Human Influences on Nitrogen Contamination in Yellow River System, China

Nitrogen (N) contamination in the Yellow River mainstream and its tributaries was studied using data from 1960 to 2000 from 312 monitoring sites in the Yellow River system. Data showed that N concentrations in the Yellow River have increased since 1960, especially after 1990. N concentrations in the Yellow River mainstream increased from the upper reaches (less than 1.0 mg L(-1) for TN and less than 0.10 mg L(-1) for NH4(+)-N) to lower reaches (higher than 4-5 mg L(-1) for TN and higher than 1.0 mg L(-1) for NH4(+)-N). However, the highest N contaminations (50-250 mg L(-1) for TN and 10-20 mg L(-1) for NH4(+)-N) was found in some tributaries, which was attributed as an effect of industrial wastewater and municipal sewage. Nitrogen concentrations from several monitoring sites were positively correlated with several regional socio-economic indices, such as population density, fertilization rates, livestock, industrial input and GDP. Depending on location, seasonal N concentrations contrasted among watersheds. Monitoring stations located in rural and agricultural areas showed higher N concentrations during the flood season while those located in areas with urban and industrial centers showed higher N concentration during the dry season. Mainstream flow and N concentrations showed a strong inverse relationship; with higher N concentrations as the river flow declined. Intensive water extraction for agricultural irrigation and increasing N input to the river from fertilized agricultural fields could explain the increasing N concentrations during extensive droughts.     

Pollution by oestrogenic endocrine disruptors and β-sitosterol in a south-western European river (Mira,Portugal)

The Mira River is a Portuguese water body widely known for its wilderness and is advertised as one of the less polluted European rivers. On this presumption, the levels of endocrine-disrupting compounds (EDCs) in Mira waters were never measured. However, because environmentalists have claimed that the Mira could be moderately polluted, a range of 17 EDCs were measured not only at the estuary but also along the river. The targeted EDCs included natural and pharmaceutical oestrogens (17β-oestradiol, oestrone and 17α-ethynylestradiol), industrial/household pollutants (octylphenols, nonylphenols and their monoethoxylates and diethoxylates and bisphenol A), phytoestrogens (formononetin, biochanin A, daidzein, genistein) and the phytosterol sitosterol (SITO). For this propose, waters from six sampling sites were taken every 2 months, over a 1-year period (2011), and analysed by gas chromatography–mass spectrometry. Unexpectedly high levels of oestrogens and of industrial/household pollutants were measured at all sampling sites, including those located inside natural protected areas. Indeed, the annual average sum of EDCs was ≈57 ng/L for oestrogens and ≈1.3 μg/L for industrial/household chemicals. In contrast, the global average levels of phytoestrogens (≈140 ng/L) and of SITO (≈295 ng/L) were lower than those reported worldwide. The EDC concentrations were normalised for ethynylestradiol equivalents (EE_2eq). In view of these, the oestrogenic load of the Mira River attained ≈47 ng/L EE_2eq. In addition, phosphates were above legal limits at both spring and summer (>1 mg/L). Overall, data show EDCs at toxicant relevant levels in the Mira and stress the need to monitor rivers that are allegedly less polluted.     

The role of forest type in the variability of DOC in atmospheric deposition at forest plots in Italy

Dissolved organic carbon (DOC) was studied in atmospheric deposition samples collected on a weekly basis in 2005-2009 at 10 forest plots in Italy. The plots covered a wide range of geographical attributes and were representative of the main forest types in Italy. Both spatial and temporal variations in DOC concentrations and fluxes are discussed, with the aim of identifying the main factors affecting DOC variability. DOC concentration increased from bulk to throughfall and stemflow water samples at all sites, as an effect of leaching from leaves and branches, going from 0.7-1.7 mg C L(-1) in bulk samples to 1.8-15.8 mg C L(-1) in throughfall and 4.2-10.7 mg C L(-1) in stemflow, with striking differences among the various plots. Low concentrations were found in runoff (0.5-2.0 mg C L(-1)), showing that the export of DOC via running waters was limited. The seasonality of DOC in throughfall samples was evident, with the highest concentration in summer when biological activity is at a maximum, and minima in winter due to limited DOC production and leaching. Statistical analysis revealed that DOC had a close relationship with organic and total nitrogen, and with nutrient ions, and a negative correlation with precipitation amount. Forest type proved to be a major factor affecting DOC variability: concentration and, to a lesser extent, fluxes were lower in stands dominated by deciduous species. The character of evergreens, and the size and shape of their leaves and needles, which regulate the interception mechanism of dry deposition, are mainly responsible for this.     

Exposure assessment for methyl and total mercury from seafood consumption in Korea, 2005 to 2008

Reports on the occurrence and intake assessment of mercury for Korean seafood are currently not available. This is the first report to estimate the intake of methyl (Me-Hg) and total mercury (T-Hg) from seafood consumption in Korea. The concentrations of Me-Hg and T-Hg in seafood ranged from 1.02 to 780 (mean: 55.6) ng g(-1) wet weight and 4.89 to 1008 (mean: 100) ng g(-1) wet weight, respectively. The residue levels of Me-Hg and T-Hg in Korean seafood were moderate compared with those found in other countries. The methylation ratios of fish, cephalopods and crustaceans were similar, but shellfish had lower values compared with other species. The intakes of Me-Hg and T-Hg from seafood consumption for the general population were estimated to be 38.8 and 73.8 ng kg(-1) body weight per day, respectively. Mackerel, tuna and squid made the highest contributions to the total intake of these contaminants. Among eight age groups, 30-49 year and 3-6 year age groups had the highest exposure to Me-Hg and T-Hg. The concentrations and intakes of Me-Hg and T-Hg from Korean seafood were less than the allowable residue levels and threshold intake levels suggested by Korean and international authorities. The present study may be useful for risk management of mercury in Korean seafood.     

Sources and distribution of hexabromocyclododecanes (HBCDs) in Japanese river sediment

The distribution of hexabromocyclododecane (HBCD) in the sediment of three Japanese rivers with different characteristics (i.e., population and potential source in the catchment) was investigated and compared with the results estimated using a multimedia fate model (ChemCAN). High concentrations of HBCD in sediments in the range of 134-2060 ng g(-1) were found in a river receiving textile wastewater. This contrasted with the much lower concentrations (0.8-4.8 ng g(-1)) observed for an urban river (with a surrounding population of 1.8 million). The medians of observed HBCD concentrations in each river were close to those estimated based on the assumed input source (e.g., 1810 ng g(-1) for the observed median concentration, and 1436 ng g(-1) for the estimation, in the Kuzuryu River). These results demonstrated the importance of considering source contributions of HBCD, including both industrial and consumer sources, to aquatic environments, for reliable risk management.     

Changes in the sorption and rate of 17β-estradiol biodegradation by dissolved organic matter collected from different water sources

The potential biodegradation and subsequent transformation of 17β-estradiol (E2) to estrone (E1) were examined in the presence of various dissolved organic matter (DOM) isolated from effluent, river and lake waters. In addition, estrogenicity was estimated in association with the removal of E2 via its sorption onto DOM and biodegradation. The more biodegradable lake-derived DOM promoted more extensive transformation of E2 into E1 than the effluent organic matter through a biodegradation process. Overall, under all conditions, biodegradation dominated the removal of E2 in water. The increased dissolved organic carbon (DOC) concentrations in river and lake-derived DOM (e.g. 6.5 mg C L(-1)) reduced the removal of E2 by decreasing its biodegradation due to the moderate sorption of E2 onto DOM. The effluent organic matter showed greater removal of E2 via biodegradation, as well as significantly high sorption. This was associated with a large amount of hydrophobic fulvic acid (FA)- and humic acid (HA)-like organic components, as shown by the small increase in the specific UV absorbance at 254 nm (SUVA(254)). An increase in the DOC concentration reduced the removal of E2, resulting in high estrogenicity. The present study suggests that both organic composition and DOC concentration influenced the removal of E2 and, therefore, should be fully considered when assessing estrogenicity and its impacts on the aquatic environment.     

Distribution and partition of polycyclic aromatic hydrocarbon in surface water of the Pearl River Estuary, South China

Water samples were collected in the Pearl River Estuary in July 2002 and April 2003. The particulate and dissolved phase polycyclic aromatic hydrocarbons (PAHs) were determined. Total PAH concentrations in water samples were higher in April of 2003 (C (p): 4.0-39.1 ng/L or 445.1-1,089.9 ng/g; C (w): 15.9-184.2 ng/L) than in July of 2002 (C (p): 2.6-26.6 ng/L or 297.7-1,336.6 ng/g; C (w): 12.9-28.3 ng/L). It was found that 5, 6-ring PAHs enrich in the inner estuary samples and so did 3-ring PAHs in the July samples. Compositional differences in the suspended particulate matter (SPM) might be responsible for this observation. The partition coefficient (K (p)) increased with the increasing of the particular organic carbon content of suspended particles as well as the salinity of water, decreased with the increase of the total suspended particles content of samples. A linear correlation between logK (OC) and logK (OW) was found in two sampling periods. The observed values of logK (OC) exceed their predicted values derived form linear free energy relationship between logK (oc) and logK (ow), which could be attributed to the nonlinear sorption of soot-like carbons in suspended particles.     

Use of water quality index and multivariate statistical techniques for the assessment of spatial variations in water quality of a small river

Rapid urban development has led to a critical negative impact on water bodies flowing in and around urban areas. In the present study, 25 physiochemical and biological parameters have been studied on water samples collected from the entire section of a small river originating and ending within an urban area. This study envisaged to assess the water quality status of river body and explore probable sources of pollution in the river. Weighted arithmetic water quality index (WQI) was employed to evaluate the water quality status of the river. Multivariate statistical techniques namely cluster analysis (CA) and principal component analysis (PCA) were applied to differentiate the sources of variation in water quality and to determine the cause of pollution in the river. WQI values indicated high pollution levels in the studied water body, rendering it unsuitable for any practical purpose. Cluster analysis results showed that the river samples can be divided into four groups. Use of PCA identified four important factors describing the types of pollution in the river, namely (1) mineral and nutrient pollution, (2) heavy metal pollution, (3) organic pollution, and (4) fecal contamination. The deteriorating water quality of the river was demonstrated to originate from wide sources of anthropogenic activities, especially municipal sewage discharge from unplanned housing areas, wastewater discharge from small industrial units, livestock activities, and indiscriminate dumping of solid wastes in the river. Thus, the present study effectively demonstrates the use of WQI and multivariate statistical techniques for gaining simpler and meaningful information about the water quality of a lotic water body as well as to identify of the pollution sources.     

Perfluorooctane sulfonate (PFOS) distribution and effect factors in the water and sediment of the Yellow River Estuary, China

The distribution of perfluorooctane sulfonate (PFOS) was investigated in a total of 15 water and sediment samples from the Yellow River Estuary, China in April 2011. The results indicated that the concentrations of PFOS in the water and sediment samples averaged 157.5 ng/L and 198.8 ng/g and ranged from 82.30 to 261.8 ng/L and 75.48 to 457.0 ng/g, respectively. The concentrations of PFOS in the sediment column increased from 45.32 to 379.98 ng/g with the decrease of the sampling depth, which showed that the increased PFOS pollution in the sediment appeared in this region in over recent years. The distribution coefficient (K _d) of PFOS between water and sediment linearly increased from 0.37 to 4.80 L/g as the salinity (S‰) increased from 0.18 to 4.47. Correlation analysis revealed that K _d was significantly and positively correlated to the contents of total organic carbon and clay of the sediment, and salinity. Therefore, salinity was an important parameter in controlling the sediment–water interactions and the fate or transport of PFOS in the aquatic environment. The results of this study showed that the estuary was an important sink for PFOS and suggested that PFOS might be carried with the river water and transported for long distances before it reached to the sea and largely scavenged to the sediment in the estuaries due to the change in salinity.     

溶解性有机碳对微库仑法测定水中可吸附有机卤素的影响

微库仑法测水样中可吸附有机卤素(AOX)受多种因素影响,其中溶解性有机碳(DOC)的影响非常显著。DOC对微库仑法2种前处理方法(双柱法和振荡法)的影响差异很大。双柱法受DOC影响较小,当DOC浓度小于1 000 mg/L时,AOX加标回收率范围为94.0%~104%。振荡法受DOC影响较明显,随着DOC浓度的升高,AOX回收率持续下降,当DOC浓度达到1 000 mg/L时,AOX加标回收率下降至72.1%,但DOC浓度小于100 mg/L时,AOX加标回收满足方法要求。进一步研究发现,DOC对振荡法的影响主要由于竞争吸附降低了活性炭对AOX的吸附容量,而非吸附速率,虽然增大活性炭用量可在一定程度上减小DOC对AOX测定的影响,但对样品进行稀释是减少DOC影响的最简单高效的办法。同时,DOC对不同类型的有机卤代物影响不同,有机溴受DOC影响程度小于有机氯。     

Phytoplankton abundance and pigment biomarkers in the oligotrophic, eastern Adriatic estuary

Phytoplankton distribution and environmental characteristics were determined in a shallow, highly stratified and oligotrophic estuary (Zrmanja, eastern Adriatic). Samples were collected in two contrasting seasons; winter (February 2000), when river discharge was high, and in summer (July 2003), a period of drought. Phytoplankton distribution was closely related to salinity gradients, nutrient levels, and water residence time. Microscopic analysis revealed that phytoplankton was composed mainly of marine diatoms, dinoflagellates, cryptophytes, green flagellates, and coccolithophorids. The dominant biomarker pigments were fucoxanthin, alloxanthin and 19'-hexanoyloxyfucoxanthin, while lower, but indicative contributions of peridinin and chlorophyll b were also noted. Maximum abundance and biomass were found in the middle estuary in winter and in the upper estuary in summer. The estuary is mostly P-limited. Development of chain-forming marine diatoms was evident in winter. Due to the reduced nutrient input in summer, the biomass accumulated in the upper estuary (1,000 ng chlorophyll a l(-1)) was composed mostly of nanoplanktonic unicellular diatoms, nanoplanktonic marine dinoflagellates, cryptophytes, and chlorophytes. The concentrations of about 200 ng l(-1) hex-fuco, suggested that the contribution of prymnesiophytes to total biomass was comparable to that of diatoms and dinoflagellates. In the middle estuary and coastal sea, PO(4) and TIN were 3.5 times lower, resulting in a fivefold decrease in biomass (<100 ng chlorophyll a l(-1)). The oligotrophic Zrmanja and other karstic rivers discharging in the eastern Adriatic Sea, provide insufficient source of nutrients and low productivity of the eastern Adriatic Sea.     

东江下游污染源和纳污水体的雌激素效应水平

利用重组双杂交酵母快速检测技术分析了东江下游两个污水厂、8个工业废水排放口和6条受纳河流水体共16个样品中的雌激素效应物质浓度,并按照雌二醇当量(EEQ)计算了水中雌激素效应水平。在被检测废水样品中,排水的EEQ值处于0.3~2.8ng/L之间,其中造纸厂与纸制品厂排水具有明显雌激素效应。采自河涌的6个样品有4个样品检出雌激素活性,雌激素效应水平在1.9~8.8ng EEQ/L之间。结果表明,东江下游行业废水处理厂出水中的EEQ浓度应与河涌水体中的EEQ在相同数量级, 与国内报道的其他地区河流及工厂排水污染水平类似。污染较为严重的河涌水体雌激素水平明显高于污水处理厂及工厂排水,推断污染河涌水体中的雌激素效应物质应来自未经处理的污染源。     

CDOM fluorescence as a proxy of DOC concentration in natural waters: a comparison of four contrasting tropical systems

Chromophoric dissolved organic matter (CDOM) fluorescence or absorption is often proposed as a rapid alternative to chemical methods for the estimation of bulk dissolved organic carbon (DOC) concentration in natural waters. However, the robustness of this method across a wide range of systems remains to be shown. We measured CDOM fluorescence and DOC concentration in four tropical freshwater and coastal environments (estuary and coastal, tropical shallow lakes, water from the freshwater lens of two small islands, and soil leachates). We found that although this method can provide an estimation of DOC concentration in sites with low variability in DOC and CDOM sources in systems where the variability of DOC and CDOM sources are high, this method should not be used as it will lead to errors in the estimation of the bulk DOC concentration.     

Polycyclic musks in the Ruhr catchment area--transport, discharges of waste water, and transformations of HHCB, AHTN and HHCB-lactone

The polycyclic musk fragrance compounds HHCB (1,3,4,6,7,8-hexahydro-4,6,6,7,8,8-hexamethylcyclopenta-(g)-2-benzopyran; trade name, e.g. galaxolide) and AHTN (7-acetyl-1,1,3,4,4,6-hexamethyl-1,2,3,4-tetrahydronaphthalene, trade name, e.g. tonalide) and the transformation product of HHCB (HHCB-lactone) were analysed in surface water samples and sewage treatment plants (STP) effluents in the Ruhr megalopolis. The STPs were the dominant source for these pollutants. In the part of the river where the drinking water is extracted from the river, about 60 ng L(-1) HHCB, 10 ng L(-1) AHTN and 20-30 ng L(-1) HHCB-lactone were found as typical riverine concentrations, while none of the compounds were detected near the spring of the river. On the other hand sewage treatment plant effluents exhibited concentrations up to 600 ng L(-1). The STP's effluent resulted in elevated concentrations in some parts of the river and in the lakes into which they discharge. As some of the plants emit HHCB-lactone with a significantly changed enantiomeric pattern, biotransformation of HHCB to HHCB-lactone occurs in some waste water treatment plants operating with activated sludge. In those parts of the river where no relevant discharges of waste water or fresh water takes place neither the concentration nor the pattern changes significantly. This holds true especially for the HHCB versus HHCB-lactone ratios which indicates degradation less than 15% of the HHCB inventory in the river Ruhr itself. In other rivers, such as the Rhine, higher levels of HHCB-lactone in comparison to HHCB were detected (ratio 1 : 1).     

River water quality and pollution sources in the Pearl River Delta, China

Some physicochemical parameters were determined for thirty field water samples collected from different water channels in the Pearl River Delta Economic Zone river system. The analytical results were compared with the environmental quality standards for surface water. Using the SPSS software, statistical analyses were performed to determine the main pollutants of the river water. The main purpose of the present research is to investigate the river water quality and to determine the main pollutants and pollution sources. Furthermore, the research provides some approaches for protecting and improving river water quality. The results indicate that the predominant pollutants are ammonium, phosphorus, and organic compounds. The wastewater discharged from households in urban and rural areas, industrial facilities, and non-point sources from agricultural areas are the main sources of pollution in river water in the Pearl River Delta Economic Zone.     

Intertidal macrofaunal communities in an intensely polluted estuary

The Bilbao estuary (northern Spain) has suffered a serious environmental deterioration due to industrial and domestic discharges during decades. A total of 21 sampling stations were selected in order to: (1) study the intertidal fauna distribution on both hard and soft bottoms; (2) link this information with the prevalence of certain environmental variables at the sampling sites; and (3) define distinct biological zones with all the information gathered. Up to 50 taxa were identified mainly in the outer estuary with an abrupt decrease upstream. In general, fauna on hard substrates was more diverse, while soft bottom communities exhibited a more consistent structure. Sporadic hypoxic events were recorded in the water column of all the sites studied, which affects the distribution of species. Three major biotic zones are proposed in the estuary. This provides a reliable biomonitoring tool for assessing the effectiveness of a sewerage and remediation scheme ongoing on the river and evaluating the future use of each area in the urban development of the city of Bilbao and conurbation.     

Spatial–temporal variation and comparative assessment of water qualities of urban river system: a case study of the river Bagmati (Nepal)

The study presents the assessment of variation of water qualities, classification of monitoring networks and detection of pollution sources along the Bagmati River and its tributaries in the Kathmandu valley of Nepal. Seventeen stations, monitored for 23 physical and chemical parameters in pre-monsoon, monsoon, post-monsoon and winter seasons, during the period 1999-2003, were selected for the purpose of this study. The study revealed that the upstream river water qualities in the rural areas were increasingly affected from human sewage and chemical fertilizers. In downstream urban areas, the river was heavily polluted with untreated municipal sewage. The contribution of industries to pollute the river was minimal. The higher ratio of COD to BOD (3.74 in the rural and 2.06 in the urban) confirmed the increased industrial activities in the rural areas. An increasing trend of nitrate was found in the rural areas. In the urban areas, increasing trend of phosphorus was detected. The water quality measurement in the study period showed that DO was below 4 mg/l and BOD, COD, TIN, TP and TSS above 39.1, 59.2, 10.1, 0.84 and 199 mg/l, respectively, in the urban areas. In the rural areas, DO was above 6.2 mg/l and BOD, COD, TIN, TP and TSS below 15.9, 31, 5.24, 0.41 and 134.5 mg/l, respectively. The analysis for data from 1988 to 2003 at a key station in the river revealed that BOD was increasing at a rate of 1.8 mg/l in the Bagmati River. A comparative study for the water quality variables in the urban areas showed that the main river and its tributaries were equally polluted. The other comparison showed the urban water qualities were significantly poor as compared with rural. The cluster analysis detected three distinct monitoring groups: (1) low water pollution region, (2) medium water pollution region, (3) heavy water pollution region. For rapid assessment of water qualities using the representative sites could serve to optimize cost and time without loosing any significance of the outcome. The factor analysis revealed distinct groups of sources and pollutions (organics, nutrients, solutes and physicochemical).