Occurrence of nonylphenol an endocrine disrupter in Karun River,Khuzestan Province,Iran

The important Iranian Karun River has never been investigated for the presence of potentially endocrine-disrupting chemicals, nonylphenol (NP). In this study, concentrations of NP were measured in water from Karun River and five wastewater discharge points into this river, collected during April to July 2010. The analytes were extracted by solid-phase extraction, and quantitative analyses were performed by HPLC–FLD. NP was detected in water and wastewater samples with 0.17–1.83 and 15.27–21.79 μg/L, respectively. The results showed that the NP content of aqueous phase of all wastewater samples higher than particulate phase, which were detected in the aqueous and particulate phases with mean concentrations of 12.8 ± 2.4 and 5.2 ± 1.2 μg/L, respectively. These data suggest that the NP levels in Karun river water are likely attributable to untreated municipal wastewaters discharged directly into the river. To our knowledge; this is the first study to evaluate NP concentrations in water and wastewater in Iran.     

Health risk assessment of trace elements in drinking water from Najran City,southwestern Saudi Arabia

The concentrations of 16 trace elements (Ag, Al, As, B, Ba, Cd, Cr, Cu, Hg, Mn, Ni, Pb, Se, Ti, U, and Zn) in drinking water from Najran City, Saudi Arabia, were determined by inductively coupled plasma-mass spectrometry (ICP-MS) and compared with local, regional, and international guidelines. Water samples from 22 water treatment plants and 13 commercial bottled water brands were analyzed. Except for B and U, the trace element concentrations were below the permitted limits defined in SASO, GSO, and WHO drinking water quality guidelines. The B concentrations in three brands of bottled water were 533.19, 602.29, and 1471.96 μg/L, which were all higher than the GSO and SASO limit (500 μg/L). The U concentrations were higher than the SASO limits for drinking water in two samples; one in treatment plant (2.39 μg/L) and another in foreign bottled water (2.17 μg/L). The median As, Ba, Cu, Ni, U, and Zn concentrations were statistically significantly higher in the treatment plant water samples than those in the bottled water samples, and conversely, the B concentrations were higher in the bottled water samples. The Cd, Hg, and Ti concentrations were below the detection limits of ICP-MS in all of the water samples. Apart from few exceptions, trace element concentrations in drinking water of Najran City were all within limits permitted in the national, regional, and international drinking water quality guideline values.     

Arsenic and manganese in tube well waters of Prey Veng and Kandal Provinces,Cambodia

Twenty-eight tube well water samples were collected in February, 2006, from households in the Cambodian provinces of Prey Veng and Kandal. Concentrations of total As in both provinces ranged from not detectable (ND) up to about 900 μg/L, with about 54% of all the samples collected exceeding the WHO drinking water guide value of 10 μg/L. In addition, about 32% of all samples contained concentrations of Mn exceeding the WHO drinking water guide value of 400 μg/L. It is interesting to note that more than half (about 56%) of tube wells with Mn over 400 μg/L had the non-detectable As. Barium, Sr and Fe were also detected in most of tube well samples, which were typically circum-neutral and reducing. Arsenic speciation was dominated (80%) by dissolved inorganic As(III). The occurrence and composition of the well waters is consistent with the As being mobilized from aquifer sediments by natural processes in a highly reducing environment. The highest estimated cumulative As intake for individuals using the sampled well waters as drinking water is estimated to be around 400 mg As/a – this is comparable to intakes that have resulted elsewhere in the world in serious As-related illnesses and highlights the possibility that such adverse health impacts may arise in Cambodia unless appropriate remedial measures are taken.     

Geothermal spring causes arsenic contamination in river waters of the southern Tibetan Plateau,China

Large numbers of As-enriched geothermal springs are distributed at the southern Tibetan Plateau, and their influence on river water is still not clear. Lhasa River and its tributary, Duilong Qu located at downstream of the largest geothermal spring of the Tibetan Plateau, were selected for sampling during monsoon and non-monsoon seasons. Dissolved trace elements (B, Cr, Ni, Cu, Zn, As, Cs, Ba and U) were measured in river water samples by ICP-MS. The results show that due to contribution of geothermal spring, As levels of Duilong Qu (205.6 μg/L) and Lhasa River (12.7 μg/L) were higher during non-monsoon season than that of WHO guideline for drinking water (10 μg/L). Accordingly, As level of river water was lower during the monsoon season than that of the non-monsoon season due mainly to dilution process. Therefore, although Tibetan rivers are generally considered as free of contamination, geothermal springs cause As contamination of river water at some local regions and may harm the local residents. Further research is needed in other parts of the plateau to determine whether As level of groundwater of the related region is high.     

珠江三角洲含N亚硝胺地下水与地区性癌症

肆虐我国南方局部区数百年以鼻咽癌和肝癌为主的恶性肿瘤病,为典型的地区性癌症。本文以珠江三角洲为例,应用流行病学与生态地球化学相结合的调查方法,检出了病区环境水和饮水中存在致癌物质N亚硝胺,研究了癌病区生态系统由地质构造背景、气候、水文和生态条件制约,自然形成水体N亚硝胺的机理。实验改进、优化了环境饮水微量亚硝胺测定方法,新建立的固相萃取气相色谱串联质谱(GC/El-MS/MS)测定纳克级N亚硝胺方法一次可测9种N亚硝胺化合物,检出限达到0.34~2.19 ng/L。在珠江三角洲癌病区环境饮水中首次发现9种亚硝胺化合物,含量为307~0.34 ng/L,总检出率为40%。四会等较低工业污染区古井水、手压井水和自来水的亚硝胺有相近似的含量统计特点:亚硝基二甲胺和亚硝基二正丁胺的均值和峰值为不高的超标值,均值分别为21.77和15.54 ng/L。这批水样大多采自0~20 m深度井水,属本区代表性特殊地质构造和气候生态环境中形成的地下水,也是研究区生产和生活开发最多的水源层;所含超标亚硝胺可能是本区数百年高发癌症的主因。近年工业发展带来的亚硝胺污染源的叠加,增高了该区环境饮水亚硝胺超标率及癌症发病率。文中分析了珠江三角洲土壤和地下水富氮营养化现象和区域氮的来源。     

Influence of hydrostratigraphy and structural setting on the arsenic occurrence in groundwater of the Cimino-Vico volcanic area (central Italy)

Arsenic occurrence in groundwater near the Cimino-Vico volcanoes (central Italy) was analysed considering the hydrostratigraphy and structural setting and the shallow and deep flows interacting within the Quaternary volcanics. Groundwater is the local source of drinking water. As documented in the past, arsenic in the groundwater has become a problem, and the European maximum allowable contaminant level was recently lowered to 10 μg/L. Chemical analyses of groundwater were conducted, sampled over an area of about 900 km², from 65 wells and springs representative of the volcanic aquifer and thermal waters. Considering the type of aquifer, the nature of the aquifer formation and its substratum, the hydrochemical data highlight that the arsenic content of the groundwater is mainly connected with the hydrothermal processes in the volcanic area. Thermal waters (54–60°C) fed from deep-rising fluids show higher arsenic concentrations (176–371 μg/L). Cold waters sampled from the volcanic aquifer are characterized by a wide variability in their arsenic concentration (1.6–195 μg/L), and about 62% exceed the limit of 10 μg/L. Where the shallow volcanic aquifer is open to deep-rising thermal fluids, relatively high arsenic concentrations (20–100 μg/L) are found. This occurs close to areas of the more recent volcano-tectonic structures.     

Survey of polycyclic aromatic hydrocarbons and nitrated polycyclic aromatic hydrocarbons in Jiaxing city, China

Polycyclic aromatic hydrocarbon (PAH) and nitrated PAH (NPAH) products are toxic. Thus, determination of their concentrations is of great interest to researchers of soil and water pollution control. In this work, soil samples, surface water samples, and groundwater samples were collected, and the concentrations of 16 priority PAHs and 15 NPAHs were determined using an HPLC-ultraviolet detector. Results showed that the total PAH concentrations ranged within 489.69–1,670.11 ng/g (average = 905.89 ng/g) in soil samples, 4.00–23.4 μg/l (average = 9.84 μg/l) in surface water samples, and 2.14–22.3 μg/l (average = 8.37 μg/l) in groundwater samples. The NPAH concentrations were one to two orders of magnitude lower than the PAH concentrations and ranged within 22.72–128.70 ng/g (average = 63.88 ng/g) in soil samples. 2-Nitropyrene and 6-nitrochrysene were the most abundant compounds, accounting for about 14.3 and 26.5 %, respectively. Source analysis revealed that most PAHs originated from coal combustion around the study area, whereas NPAH studies suggested that the primary emission of gasoline engines and daytime OH reactions were the dominant sources of these compounds.     

大气干湿沉降: 地下河多环芳烃的重要来源——以广西清水泉地下河为例

为证实大气干湿沉降物是岩溶地下河中多环芳烃(PAHs)的来源,研究选择了某城市典型的岩溶地下河水源地作为研究地点,采用大气干湿采样器、聚氨酯泡沫(PUF)大气被动采样器分别采集大气及其干湿沉降物样品,同时采集地下河水样和分层采集流域土壤,利用气相色谱-质谱联用仪(GC-MS)测定了16种PAHs优先控制污染物。结果表明,地下河流域大气干湿沉降中PAHs的干湿沉降通量为147.26 ng·(m2·d)-1,流域PAHs沉降量为1943.8 g;大气中的PAHs浓度为45.33 ng·m-3;地下河水中PAHs浓度平均值为220.98 ng·L-1;土壤中PAHs浓度为38.72 ng·g-1;大气、降雨和土壤中PAHs组成以2~3环的萘、芴、菲、荧蒽、芘5种为主,地下河水中以芴、菲、荧蒽、芘、苯并[a]蒽、苯并[a]芘6种为主。利用地下河多介质中的16种PAHs成分谱、特征比值结合它们的物理化学性质进行PAHs的源解析,研究显示大气干湿沉降是岩溶地下河水中多环芳烃的主要污染源之一,这归因于岩溶地区防污性能的脆弱性。     

Hydrogeochemistry and arsenic contamination of groundwater in the Rayen area, southeastern Iran

High As contents in groundwater were found in Rayen area and chosen for a detailed hydrogeochemical study. A total of 121 groundwater samples were collected from existing tube wells in the study areas in January 2012 and analyzed. Hydrogeochemical data of samples suggested that the groundwater is mostly Na–Cl type; also nearly 25.62 % of samples have arsenic concentrations above WHO permissible value (10 μg/l) for drinking waters with maximum concentration of aqueous arsenic up to 25,000 μg/l. The reducing conditions prevailing in the area and high arsenic concentration correlated with high bicarbonate and pH. Results show that arsenic is released into groundwater by two major phenomena: (1) through reduction of arsenic-bearing iron oxides/oxyhydroxides and Fe may be precipitated as iron sulfide when anoxic conditions prevail in the aquifer sediments and (2) transferring of As into the water system during water–acidic volcanic rock interactions.     

Findings on water quality in Upper Mustang (Nepal) from a preliminary geochemical and geological survey

The major ion and trace element chemistry of water samples, including springs, rivers and irrigation ditches, collected during a survey on August 2016 in the Upper Mustang region of the Mustang District of Dhawalagiri Zone (Nepal) has been investigated. The Upper Mustang region, a cold desert, represents a hot-spot for climate change: indeed, violent hailstorms and rainstorms have been recently observed, consequently exposing land to erosion. Results of this study indicate that waters in the region belong to the Ca–HCO₃, Ca–Mg–Cl–SO₄ and Na–K–Cl-types, reflecting different hydrochemical regimes. Uranium is widespread in waters, with concentrations up to 19 µg/L recorded in a potable water supply. Locally, anoxic conditions affect uranium mobility due to the low solubility of U(IV) minerals. Highly toxic thallium was detected in a thermal spring at an elevated concentration (45 µg/L Tl). The association of thallium with high concentrations of iron suggests that these elements are derived from pyrite oxidation. Detectable levels of thallium were also measured in the water of an irrigation ditch. Lithium concentrations ranged from 7 µg/L to 12 mg/L in the thermal water and showed a strong association with chloride ions. Arsenic concentrations up to 4.7 µg/L were measured in tributaries of the Kali Gandaki river. The data provide evidence that solutes in water have originated from an array of input sources, including carbonate dissolution, the dissolution of soluble salts, silicate weathering and localized sulfide oxidation. In particular, chemical weathering of granitic rocks is likely the primary source for metals and metalloids in waters. Since the erosion rate is a factor affecting lithological weathering, high-intensity rainfalls due to climate change are expected to influence the release and fate of potentially harmful elements in the in the Upper Mustang Valley.     

Chloride contamination in construction aggregates due to periodic saline water intrusion: a case study in the Kaluganga River Estuary, Sri Lanka

The Kaluganga River Estuary is one of the main sources of construction sand in Sri Lanka. Salt water intrusion along this estuary due to extensive sand mining has increased over the years. Thus, the focus of the current research is to understand the relationship between river sand mining, salt water intrusion, and the resultant effects on construction sand. Two surveys were conducted along the Kaluganga Estuary along an 11 km stretch from the river mouth at predetermined intervals to measure depth water quality profiles, and to collect sediment samples. These surveys were carried out during maximum spring tide; first in a dry period and then in a wet period, to understand hydrographic effects on the quality of river sands. Sand samples were analysed for absolute chloride content and grain size distribution. Results showed significant salt water intrusion during the dry period, averaging 2,307 μS cm^?1 in surface waters throughout the surveyed 11 km stretch along with 3,818 μS cm^?1 (average) in bottom waters up to 5.6 km upstream from the river mouth causing above normal chloride content in the bottom sandy sediments. The high chloride content in bottom sands was recorded up to 5.5 km from the river mouth making them unsuitable for construction purposes. However, during wet period, salt water intrusion levels in the bottom waters were insignificant (average 61 μS cm^?1) and the chloride content in bottom sediments was very low. This study highlighted the requirement for regulations on river estuary sandmining for construction purposes.     

Sources and transports of organochlorine pesticides in the Nanshan underground river,China

Karst areas have much higher ecological vulnerability and are prone to be contaminated. Organochlorine pesticides (OCPs) were detected in waters and sediment from the two sites of the karst Nanshan underground river system, China, to understand the sources and transport of OCPs in the underground river systems. Obviously, seasonal variations were found both in the waters and the sediments. Detected OCPs ranged from 61 to 936 ng L^?1 in the groundwaters and 51–3,842.0 ng g^?1 in the underground sediments, respectively. OCPs in groundwaters were mixture of younger and older residues from commercial sources. The maximum OCPs in the sediments of the underground river were historically older residues from commercial sources. The sources of OCPs in the waters and sediments of the underground river indicated that the surface systems play an important role in OCPs transport and pollution in the underground river. Karst features were liable for the transport behavior.     

高效液相色谱-串联质谱法测定黄河河口段水中全氟化合物的初步研究

以近年来备受关注的持久性有机污染物———全氟化合物为研究目标物,黄河河口段为目标研究区域,应用高效液相色谱-串联质谱法测定黄河河口段河水、自来水和浅层地下水中的19种全氟化合物含量,描述研究该区域水体中全氟化合物的污染水平和分布规律,并探讨水体中全氟化合物的来源。结果表明,全氟丁酸和全氟辛酸是黄河河口段水体中最主要的全氟化合物,黄河水中的全氟丁酸和全氟辛酸浓度分别为1.61～4.20ng/L和2.04～3.36 ng/L。浅层地下水中各待测物检出率都很低;自来水中全氟丁酸和全氟辛酸的浓度分别为1.62～3.24 ng/L和4.66～9.34 ng/L;自来水与黄河水中全氟化合物的组成特征明显不同。东营地区黄河水中全氟辛烷磺酸的浓度与国内其他北方城市相比浓度相当,明显低于长江水和珠三角地表水;全氟辛酸的浓度与呼和浩特市周边河水以及北京官厅水库中浓度相当,相比国内其他地区处于较低水平。     

Arsenic and antimony contamination of waters,stream sediments and soils in the vicinity of abandoned antimony mines in the Western Carpathians,Slovakia

Environmental contamination with As and Sb caused by past mining activities at Sb mines is a significant problem in Slovakia. This study is focused on the environmental effects of the 5 abandoned Sb mines on water, stream sediment and soil since the mines are situated in the close vicinity of residential areas. Samples of mine wastes, various types of waters, stream sediments, soils, and leachates of the mine wastes, stream sediments and selected soils were analyzed for As and Sb to evaluate their geochemical dispersion from the mines. Mine wastes collected at the mine sites contained up to 5166 mg/kg As and 9861 mg/kg Sb. Arsenic in mine wastes was associated mostly with Fe oxides, whereas Sb was present frequently in the form of individual Sb, Sb(Fe) and Fe(Sb) oxides. Waters of different types such as groundwater, surface waters and mine waters, all contained elevated concentrations of As and Sb, reaching up to 2150 μg/L As and 9300 μg/L Sb, and had circum-neutral pH values because of the buffering capacity of abundant Ca- and Mg-carbonates. The concentrations of Sb in several household wells are a cause for concern, exceeding the Sb drinking water limit of 5 μg/L by as much as 25 times. Some attenuation of the As and Sb concentrations in mine and impoundment waters was expected because of the deposition of metalloids onto hydrous ferric oxides built up below adit entrances and impoundment discharges. These HFOs contained >20 wt.% As and 1.5 wt.% Sb. Stream sediments and soils have also been contaminated by As and Sb with the peak concentrations generally found near open adits and mine wastes. In addition to the discharged waters from open adits, the significant source of As and Sb contamination are waste-rock dumps and tailings impoundments. Leachates from mine wastes contained as much as 8400 μg/L As and 4060 μg/L Sb, suggesting that the mine wastes would have a great potential to contaminate the downstream environment. Moreover, the results of water leaching tests showed that Sb was released from the solids more efficiently than As under oxidizing conditions. This might partly explain the predominance of Sb over As in most water samples.     

Assessment of naturally occurring arsenic contamination in the groundwater of Sarkisla Plain (Sivas/Turkey)

High arsenic levels in groundwater of the aquifers, belonging to the Pliocene terrestrial layers and Quaternary alluvial sediments, have become a significant problem for the inhabitants living in Sarkisla (Turkey). The main objective of this study was to determine the origin and arsenic contamination mechanisms of the Sarkisla drinking water aquifer systems. The highest arsenic concentrations were found in Pliocene layers and alluvial sediments with concentrations ranging from 2.1 to 155 mg/kg. These rocks are the main aquifers in the study area, and most of the drinking groundwater demand is met by these aquifers. Groundwater from the Pliocene aquifer is mainly Ca-HCO₃ and Ca-SO₄ water type with high EC values reaching up to 3,270 μS/cm, which is due to the sulfate dissolution in some parts of the alluvial aquifer. Stable isotope values showed that the groundwater was of meteoric origin. Tritium values for the groundwater were between 8.31 and 14.06 TU, representing a fast circulation in the aquifer. Arsenic concentrations in the aquifers were between 0.5 and 345 μg/L. The highest arsenic concentrations detected in the Pliocene aquifer system reached up to 345 μg/L with an average value of 60.38 μg/L. The arsenic concentrations of the wells were high, while the springs had lower arsenic concentrations. These springs are located in the upper parts of the study area where the rocks are less weathered. The hydrogeochemical properties demonstrated that the water–rock interaction processes in sulfide-bearing rocks were responsible for the remarkably high groundwater arsenic contamination in the study area. In the study area, the arsenic levels determined in groundwater exceeded the levels recommended by the WHO. Therefore, it is suggested that this water should not be used for drinking purposes and new water sources should be investigated.     

A survey of the inorganic chemistry of bottled mineral waters from the British Isles

The inorganic chemistry of 85 samples of bottled natural mineral waters and spring waters has been investigated from 67 sources across the British Isles (England, Wales, Scotland, Northern Ireland, Republic of Ireland). Sources include boreholes, springs and wells. Waters are from a diverse range of aquifer lithologies and are disproportionately derived from comparatively minor aquifers, the most represented being Lower Palaeozoic (10 sources), Devonian Sandstone (10 sources) and Carboniferous Limestone (9 sources). The waters show correspondingly variable major-ion compositions, ranging from Ca–HCO₃, through mixed-cation–mixed-anion to Na–HCO₃ types. Concentrations of total dissolved solids are mostly low to very low (range 58–800 mg/L). All samples analysed in the study had concentrations of inorganic constituents well within the limits for compliance with European and national standards for bottled waters. Concentrations of NO₃–N reached up to half the limit of 11.3 mg/L, although 62% of samples had concentrations <1 mg/L. Concentrations of Ba were high (up to 1010 μg/L) in two spring water samples. Such concentrations would have been non-compliant had they been classed as natural mineral waters, although no limit exists for Ba in European bottled spring water. In addition, though no European limit exists for U in bottled water, should a limit commensurate with the current WHO provisional guideline value for U in drinking water (15 μg/L) be introduced in the future, a small number of groundwater sources would have concentrations close to this value. Two sources had groundwater U concentrations > 10 μg/L, both being from the Welsh Devonian Sandstone. The highest observed U concentration was 13.6 μg/L.     

西南典型地下河系统无机-有机指标特征及健康风险评价

岩溶地下水为全球约25%的人口提供饮用水源,地下河作为主要岩溶地下水类型,是中国西南岩溶区重要供水水源,掌握其水质污染状况及人体健康风险,对岩溶区水资源保护与安全用水具有重要意义。本文以广西桂林会仙狮子岩地下河系统为例,采集地下河水样品22组(无机和有机样品各11组),采用电感耦合等离子体质谱、离子色谱、气相色谱-质谱等方法测定11项无机离子、10项金属元素及41项有机指标的质量浓度,运用单指标污染标准指数法、健康风险评价模型揭示了研究区无机与有机指标分布、污染及健康风险。结果表明：(1)狮子岩地下河水中无机超标指标有NH~+₄(1.33倍)、Fe(1.2倍)、Al(1.5倍)和Mn(1.01倍),超标点多位于地下河排泄区;检出18项有机物,其中挥发性有机物(VOCs)、半挥发性有机物(SVOCs)和有机氯农药(OCPs)检出率分别为18.75%、30.77%和91.67%,研究区存在普遍的农药残留(49.14～109.83ng/L)。(2)与地下水对照值相比,研究区受到10项无机指标的轻度～中度污染、14项有机指标的轻度污染,个别采样点受到NO~-_3<...     

Ionic sources and water quality assessment around a reservoir in Tehri, Uttarakhand, Garhwal Himalaya

The paper discusses the ionic sources and chemical quality of the waters (surface and groundwater) around the Tehri reservoir in Uttarakhand, Garhwal, Himalaya, for drinking and irrigation purposes. The main Bhagirathi river, tributary streams and springs and groundwater are the main sources of water for the reservoir and inhabitant living around it. Fifty-two water samples were collected from springs, handpumps (borewell) and streams and were analysed for major ions. The pH is varying from 6.8 to 8.6 and EC from 28 to 820 μS/cm. The chemical composition of water is dominated by Ca, Mg and HCO₃. The high ratio of Ca + Mg/Na + K and low ratio of Na + K/TZ indicate dominance of carbonate dissolution as the main solute acquisition process in this part of Lesser Himalaya. The trilinear and X–Y plots suggest less contribution from silicate weathering and anthropogenic activities. The excess of Na over Cl indicating much of the alkalis in the waters of Tehri area have source other than precipitation possibly from silicate weathering. Recharged by meteoric water, the quality of water in the study area is controlled essentially by chemical processes occurring between water and lithology and locally altered by human activities. Among the trace metals the concentration of Fe at few locations has marginally exceeded the WHO and BIS standards of drinking water. The analytical result computed from various water quality indices indicate fairly good quality of water for both drinking and irrigation purposes. The factor analysis performed on the major ion data indicate two factors are the most important affecting the water quality of the area.     

Organic compounds in produced waters from coalbed natural gas wells in the Powder River Basin,Wyoming, USA

The organic composition of produced water samples from coalbed natural gas (CBNG) wells in the Powder River Basin, WY, sampled in 2001 and 2002 are reported as part of a larger study of the potential health and environmental effects of organic compounds derived from coal. The quality of CBNG produced waters is a potential environmental concern and disposal problem for CBNG producers, and no previous studies of organic compounds in CBNG produced water have been published. Organic compounds identified in the produced water samples included: phenols, biphenyls, N-, O-, and S-containing heterocyclic compounds, polycyclic aromatic hydrocarbons (PAHs), aromatic amines, various non-aromatic compounds, and phthalates. Many of the identified organic compounds (phenols, heterocyclic compounds, PAHs) are probably coal-derived. PAHs represented the group of organic compounds most commonly observed. Concentrations of total PAHs ranged up to 23 μg/L. Concentrations of individual compounds ranged from about 18 to <0.01 μg/L. Temporal variability of organic compound concentrations was documented, as two wells with relatively high organic compound contents in produced water in 2001 had much lower concentrations in 2002.     

Polychlorinated biphenyls in the Nanshan Underground River, China

Abstract Karst areas have much higher ecological vulnerability and are easy to be contaminated by polychlorinated biphenyls(PCBs) which are introduced as health risk pollutants.PCBs concentrations were used to understand the transport behavior of PCBs conducted in the karst Nanshan Underground River,China.Water and sediments from the underground river water,and sediments and soil from the surface of the corresponding watershed were collected monthly in 2011 and 2012 and PCBs were analyzed.Seasonal variations were found in concentrations of PCBs both in the waters and sediments.PCBs concentrations varied from 0.3 to 29.9 ng·L-1 in the groundwater,while from 0.1 to 366.1 ng·g-1 in the underground sediments.Correlations were found in concentrations of PCBs in waters and sediments between the underground river and surface systems which indicate that the surface systems play a major role for the transport of PCBs and contamination in the underground river systems.Karst features are liable for the transport behavior.The underground river waters transport PCBs at mean 3 g·day-1.