Assessment of groundwater quality with special reference to arsenic in Nawalparasi district,Nepal using multivariate statistical techniques

Groundwater is a precious resource for humankind not only in Nepal but also across the globe due to its diverse functions. A total of 48 groundwater samples were collected from three villages of Nawalparasi district, Nepal, during pre-monsoon and monsoon to estimate the overall groundwater quality and to identify the sources of contamination with emphasis on arsenic (As). The average concentrations of all tested groundwater quality parameters (temp., pH, EC, ORP, Ca²⁺, Mg²⁺, Na⁺, K⁺, Cl^?, F^?,SO₄ ^2?, PO₄ ^3?, HCO₃ ^?, NO₃ ^?, Cu, Ni, Mn, Cd, Pb, Fe, Zn, Cr, and As) were well within permissible limits of WHO for drinking water, except for Ni, Cd, Pb, Cr, and As. Concentration of As ranged from 60 to 3,100 μg L^?1 and 155 to 1,338 μg L^?1 in pre-monsoon and monsoon, respectively. The Piper diagram of the groundwater chemistry showed groundwater of Nawalparasi belongs to Ca–Mg–HCO₃ and Mg–HCO₃ water type with HCO₃ ^? as dominant ions. As content in the study area was negatively correlated with Fe in pre-monsoon, while it was positively correlated in monsoon. Furthermore, As was negatively correlated with oxidation reduction potential suggesting reducing condition of groundwater. Principal component analysis revealed seven major factors that explained 81.996 and 83.763 % of total variance in water quality in pre-monsoon and monsoon, respectively. The variance of water quality was related mainly with the degree of water–rock interaction, mineralization, and anthropogenic inputs.     

Geological and geochemical examination of arsenic contamination in groundwater in the Holocene Terai Basin, Nepal

Geological and geochemical study has been carried out to investigate arsenic contamination in groundwater in Nawalparasi, the western Terai district of Nepal. The work carried out includes analyses of core sediments, provenance study by rare earth elements analyses, ¹⁴C dating, and water analyses. Results showed that distribution of the major and trace elements are not homogeneous in different grain size sediments. Geochemical characteristics and sediment assemblages of the arsenic contaminated (Nawalparasi) and uncontaminated (Bhairahawa) area have been compared. Geochemical compositions of sediments from both the areas are similar; however, water chemistry and sedimentary facies vary significantly. Extraction test of sediment samples showed significant leaching of arsenic and iron. Chemical reduction and contribution from organic matter could be a plausible explanation for the arsenic release in groundwater from the Terai sediments.     

Salinization and arsenic contamination of surface water in southwest Bangladesh

To identify the causes of salinization and arsenic contamination of surface water on an embanked island (i.e., polder) in the tidal delta plain of SW Bangladesh we collected and analyzed water samples in the dry (May) and wet (October) seasons in 2012–2013. Samples were collected from rice paddies (wet season), saltwater ponds used for brine shrimp aquaculture (dry season), freshwater ponds and tidal channels (both wet and dry season), and rainwater collectors. Continuous measurements of salinity from March 2012 to February 2013 show that tidal channel water increases from ~0.15 ppt in the wet season up to ~20 ppt in the dry season. On the polder, surface water exceeds the World Health Organization drinking water guideline of 10 μg As/L in 78% of shrimp ponds and 27% of rice paddies, raising concerns that produced shrimp and rice could have unsafe levels of As. Drinking water sources also often have unsafe As levels, with 83% of tubewell and 43% of freshwater pond samples having >10 μg As/L. Water compositions and field observations are consistent with shrimp pond water being sourced from tidal channels during the dry season, rather than the locally saline groundwater from tubewells. Irrigation water for rice paddies is also obtained from the tidal channels, but during the wet season when surface waters are fresh. Salts become concentrated in irrigation water through evaporation, with average salinity increasing from 0.43 ppt in the tidal channel source to 0.91 ppt in the rice paddies. Our observations suggest that the practice of seasonally alternating rice and shrimp farming in a field has a negligible effect on rice paddy water salinity. Also, shrimp ponds do not significantly affect the salinity of adjacent surface water bodies or subjacent groundwater because impermeable shallow surface deposits of silt and clay mostly isolate surface water bodies from each other and from the shallow groundwater aquifer. Bivariate plots of conservative element concentrations show that all surface water types lie on mixing lines between dry season tidal channel water and rainwater, i.e., all are related by varying degrees of salinization. High As concentrations in dry season tidal channel water and shrimp ponds likely result from groundwater exfiltration and upstream irrigation in the dry season. Arsenic is transferred from tidal channels to rice paddies through irrigation. Including groundwater samples from the same area (Ayers et al. in Geochem Trans 17:1–22, 2016), principal components analysis and correlation analysis reveal that salinization explains most variation in surface water compositions, whereas progressive reduction of buried surface water by dissolved organic carbon is responsible for the nonconservative behavior of S, Fe, and As and changes in Eh and alkalinity of groundwater.     

Identifying groundwater arsenic contamination mechanisms in relation to arsenic concentrations in water and host rocks

Leaching and oxidation of high arsenic (As) host rocks tend to be induced by circulation of deep geothermal waters, which increase As concentration in shallow groundwater. The purpose of this study is to identify the mechanism of groundwater As contamination in relation to leaching and oxidation along the border between the South Minahasa and Bolaang Mongondow districts, North Sulawesi, Indonesia. This region contains Miocene sedimentary rock-hosted disseminated gold deposits associated with hydrothermal alteration in a fault zone. Abnormally high As concentrations were observed in hot and cold springs and in surrounding shallow groundwater for a total mineralization area of 8 × 10 km². Two methods were adopted in this study: (1) microscopic and spectroscopic analyses of rock samples for mineral identification and (2) geostatistics for spatial modeling of As concentrations in groundwater. Jarosite was identified as the chief fill mineral in rock defects (cracks and pores). The presence of this mineral may indicate release of As into the environment, as can occur as an alteration product derived from oxidation and leaching of pyrite, As-rich pyrite or sulfide minerals by geothermal waters. Moreover, As concentrations in groundwater were estimated using geostatistics for spatial modeling. The co-kriging map identified local anomalies in groundwater As concentrations over the permissible limit (10 ppb). Such anomalies did not appear through ordinary kriging. Integration of the results indicates that As contamination in shallow groundwater probably is controlled by heterogeneous distributions of jarosite and variations in intensity and extent of hydrothermal activities.     

Geochemical distribution of arsenic in waters,sediments and weathered gold mineralized rocks from Iron Quadrangle,Brazil

The Iron Quadrangle has been the scenery of the most important gold production in Brazil. It is estimated that during the three centuries of gold mining in the Iron Quadrangle, at least 390,000 t of arsenic was discharged into the drainage system. This study presents geochemical data for the three river basins in the region, with focus on surface water and stream sediment monitoring. Samples of primary and oxidized sulfide ores as well as of tailings and groundwater from the major gold mines were also studied. The highest As concentrations in water and stream sediments occur in the vicinity of mining areas. In surface water, up to 300 g As/l were found whereas the As contents in stream sediments were in the range of 20 to 4,000 mg/kg. The As³⁺/As⁵⁺ concentration ratios obtained for some water samples range from 1.10^у to 4.10^ф. The As mobility associated with ore-deposit weathering could be traced in some closed gold mines by observation of in-situ pyrite and arsenopyrite oxidation, precipitation of scorodite and gippsite, As adsorption onto goethite, and final liberation of As into underground and surface waters. This process is likely to produce large volumes of mine effluents containing total As and trivalent As up to 1,960 and 60 g/l, respectively. River sediments and tailings pile samples were submitted to a leaching procedure showing maximal arsenic release from 1 to 4% of the original total As in the samples. There are potential risks for As hazards in some areas induced by, for instance, the dispersion of old tailings by flooding, occupation of poisoned soils for settlements, and occasional consumption of contaminated surface and groundwater.     

Geochemical controls on lead concentrations in stream water and sediments

The equilibrium distribution of lead in solution and adsorbed on cation exchange sites in sediment theoretically may be calculated from equations representing selectivities of substrate for lead over H⁺, Ca²⁺ and Na⁺, and the stabilities of lead solute species. Such calculations include consideration of total concentrations of major ions, cation exchange capacity (CEC) of substrate, and pH, at values expected in various natural systems. Measurements of CEC and selectivity coefficients were made for synthetic halloysite, a finely divided amorphous 1:1 clay prepared by precipitation from a mixture of solutions of aluminum and silica. Where suspended sediment having the same properties is present in concentrations of 10-1,000 mg/1 at pH 6–8, more than 90% of the lead present can be adsorbed on sediment surfaces. The cation exchange behavior of lead and other minor cationic species in natural systems could be predicted by this type of model if enough other supporting information were available. Information of the type needed describing natural stream sediments, however, is presently inadequate for accurate predictions.     

山东省东部地区土壤地球化学特征及污染评价

以山东省东部地区农业生态地球化学调查取得的区域土壤地球化学数据为依据,研究了区内54种元素或指标的土壤地球化学基准值和背景值与全国土壤的差异。通过对比区内土壤基准值与背景值的变化,认为本区大部分元素或指标在表层土壤中的含量继承了成土母质,后期人类活动对其影响较小,Zn、Pb、Cu、Se、Cd、S、P、Hg、N、OrgC等元素或指标在表生作用或人类活动等因素影响下,其分布分配特征产生明显变化。本文通过对表层和深层土壤元素相关系数的研究,认为深层土壤元素地球化学含量可表征表层土壤原始沉积的地球化学含量;讨论了人为活动导致土壤污染的评价方法,莱州—招远—烟台和牟平—乳山金矿集中区以及人口密集的城镇地带表层土壤中Hg、Cd、Pb、As、Zn、Se、S等元素污染严重。地质背景和人类活动(采金污染、工业生产、城市人口密集生活等)的共同作用,是造成环境中有害元素含量较高的主要原因。     

Geochemical mobility of arsenic in the surficial waters from Argentina

The presence of arsenic (As) in surface water constitutes an important environmental risk, where mobility and adsorption processes are responsible for its behavior in the sediment–water interface. Therefore, the assessment of adsorption, mobility and water availability of arsenic in freshwater sediments, with agricultural, livestock and urban soil uses was performed. Arsenic concentrations in sediments ranged from 5.4 to 15.9 mg kg^?1 (total) and 2.8 to 6.5 mg kg^?1 (labile), and those of iron and manganese were 11,563–23,500 and 140.6–662.1 mg kg^?1, respectively. The As levels in water were significantly lower than those of sediments. Results would suggest that As co-precipitation and adsorption on Fe oxides are probably the major route of immobilization, determining its low lability. Manganese did not present an outstanding contribution to the retention, and cation-exchange capacity, pH and organic matter of sediments did not show an influence on the mobility of As.     

An assessment of selected heavy metal contamination in the surface sediments from the South China Sea before 1998

Rapid economic development in East Asian countries has inevitably resulted in environmental degradation in the surrounding seas, and concern for both the environment and protection against pollutants is increasing. Identification of sources of contaminants and evaluation of current environmental status are essential to environmental pollution management, but relatively little has been done in the South China Sea (SCS). In order to investigate the metal pollution status and source within the SCS, a total of 52 surface sediment samples were collected in 1998 from the SCS for the selected heavy metal measurements such as Pb, Zn, Cu, V, Cr, Cd and Sc. The total concentrations (in mg kg^− 1 dry weight) in sediments ranged and averaged (mean ± S.D.): Pb, 4.18 to 58.7 (23.6 ± 8.93); Zn, 10.7 to 346 (87.4 ± 47.7); Cu, 5.29 to 122 (38.1 ± 24.6); V, 0.03 to 148 (78.0 ± 37.0); Cr, 4.48 to 589 (105 ± 86); Cd, 0.08 to 2.14 (0.40 ± 0.40) and Sc, 0.33 to 20.6 (10.6 ± 4.4), respectively. Enrichment factor (EF) values and geoaccumulation indexes (I_geo) suggest that Cu, Pb, Zn and V contamination exists only in few localized areas, but Cr and Cd contamination can be found in large-scale area of the SCS before 1998. Further studies are needed to reconstruct deposition history and for trend analysis.     

Hydrocarbons in the water and bottom sediments of a region with continuous petroleum contamination

The abundances and compositions of aliphatic hydrocarbons (AHC) and polyaromatic hydrocarbons (PAH) were investigated in the water and bottom sediments of the southwestern Amur Bay in the Sea of Japan. The water contained from 0 to 129 μg/1AHC (averaging 42.2 μg/l) and from 5 to 85 ng/l PAH (averaging 18 ng/l). The bottom sediments contained 168–2098 μg/g AHC and 7.2–1100 ng/g dry mass PAH. It was shown that the input of anthropogenic HC is better recorded by molecular markers than the distribution of AHC and PAH concentrations. The discovery of elevated HC concentrations in the bottom water layer suggests that the bottom sediments induced secondary contamination of the water body.     

Application of pyrolysis-GC/MS for rapid assessment of organic contamination in sediments from Barcelona harbor

Pyrolysis-GC/MS is advantageous as a tool for rapid sediment contamination assessment because of the small sample size required, minimal sample preparation and its ability to detect a wide variety of organic pollutants as well as naturally-occurring biological materials. Py-GC/MS was applied, together with determination of organic carbon, and major and minor element concentrations, to evaluate potentially contaminated sediments in the port of Barcelona (Spain) and the adjacent Llobregat River delta. Detected contaminant markers, most evident in the Old Port (Port Vell) area, included hopanes and alkylated PAHs (petroleum), sterenes (sewage), C₁₆–C₁₉ phenylalkanes (detergents) and parent PAHs (combusted fuels).     

Geochemical behavior of arsenic in reducing sulfidic sediments of reservoir contaminated by acid mine drainage

The sediment from an acid mine drainage affected reservoir of Guizhou province of China has the iron and arsenic concentration of about 400 and 2.6 g/kg, respectively. Sediment cores were collected, and were used to study the arsenic behavior in the seriously acidified reservoir from the viewpoint of chemical thermodynamics. The limestone neutralization and ferric iron hydrolysis regulated the porewater pH from about 2.9–5.8. The reductive dissolution of As–Fe-rich (hydr)oxides under the mild acidic conditions was the main mechanism for the release of absorbed arsenic into porewater. The maximum concentrations of iron, sulfate and arsenic reached to about 2,800, 9,000 and 1 mg/l, respectively. Arsenic speciation transformation and hydrous ferric oxide (HFO) crystallization enhanced the arsenic mobility in sediment. In addition, the iron sulfide minerals diagenesis could play a role in removing the dissolved arsenic from porewater. The actual distribution of arsenic concentration in porewater was well simulated using the model of surface complexation of arsenic to HFO. Although arsenic concentration in porewater could be above 100 times higher than that of reservoir water, it was not easy to release into the reservoir water through diffusion, because the shallow sediment had relatively strong arsenic adsorption capacity, and new HFO could be generated continuously at the sediment water interface.     

Erratum to: Geochemical and environmental magnetic characteristics of high arsenic aquifer sediments from Datong Basin,northern China

Geochemical and environmental magnetic studies were carried out to identify the effect of iron oxyhydroxides on arsenic mobilization in high arsenic aquifer system. Using high arsenic sediment samples from two boreholes, specifically drilled for this study, chemical composition and magnetic properties including magnetic susceptibility, saturation remnant magnetization, and isothermal remnant magnetization were measured. Results of correlation analysis of element contents show that arsenic and iron are closely associated with each other (r ² = 0.40, α = 0.05, n = 21). In contrast, the correlation of phosphorus with iron (r = 0.11, α = 0.05, n = 21) and arsenic (r ² = 0.18, α = 0.05, n = 21) was poor, which might result from competitive adsorption of phosphorus and arsenic on the surface of Fe-oxyhydroxides. The high correlation coefficients between arsenic contents and magnetic parameters suggest that the ferrimagnetic minerals including maghemite and hematite are the dominant carrier of arsenic in aquifer sediments. The results of sequential extraction experiments also revealed the association of arsenic with reducible iron oxides, such as maghemite and hematite in aquifer sediments. Therefore, under reducing conditions, reductive dissolution and desorption of arsenic from Fe-oxyhydroxides into the aqueous phase should be the dominant geochemical processes for its enrichment in groundwater at Datong. An erratum to this article can be found at     

Geochemical assessment of an arsenic mine adjacent to a water reservoir (León, Spain)

A water reservoir constructed for production of hydraulic energy and drinking water in the Riaño valley (León, northern Spain) receives leachates from polluted soils and spoil heaps from a site where small-scale As mining and smelting operations have been developed in the first half of the twentieth century. Water of the upper catchments of the Esla, Yuso and Orza Rivers is stored in this reservoir. The location of these abandoned mine works within the reservoir drainage basin suggested that the stored water could contain high As concentrations. In order to evaluate possible environmental risks, a preliminary soil and surface water geochemical survey has been carried out downstream of the Santa Águeda Mine. Total As concentrations in soils reach 23,800 mg kg^?1 in soils and increase with depth, at least up to a depth of 80 cm. Total As concentrations in surface waters reach 890 μg l^?1. Despite the fact that there is an important As input to the water reservoir, the water flow from the mine catchment is a negligible contribution when compared with the total volume of water inside the dam (0.07%). This fact considerably decreases the environmental risk associated with the presence of untreated spoil heaps containing As-rich minerals at Santa Águeda mine site.     

Poisoning the well: neoliberalism and the contamination of municipal water in Walkerton, Ontario

In May of 2000, thousands of residents of the town of Walkerton, Ontario became ill from drinking municipal water contaminated by Escherichia coli and Campylobacter jejuni bacteria. Seven people died, while many suffered debilitating injuries. A highly unusual and risk prone local hydrological regime, coupled with manure spreading on farms near municipal wells, and lax oversight by municipal water utility officials, were quickly blamed by Ontario government figures, including then premier Mike Harris. However, the scandal surrounding Walkerton's tragedy and a subsequent public inquiry into the incident also implicated neoliberal reforms of environmental governance introduced by Harris's government subsequent to its election in 1995. This paper examines the Walkerton incident as an important example of a “normal accident” of neoliberalism, one that can be expected from neoliberal environmental regulatory reforms arising from systematic irresponsibility in environmental governance. This irresponsibility is promulgated by an overarching hostility to any regulatory interference with free markets, as well as specific regulatory gaps that produce environmental risks. The paper also serves as a case study of the extent to which neoliberalism is constituted by environmental governance reform, and conversely, how environmental governance reform is reconfigured as part of the emergent neoliberal mode of social regulation.     

Characterization of arsenic occurrence in the water and sediments of the Okavango Delta,NW Botswana

Detailed chemical analyses were performed on surface water, groundwater and sediment samples collected from the Okavango Delta between February and November 2003 in order to examine the distribution and geochemistry of naturally occurring As in the area. Surface water in the Okavango Delta, which is neutral to slightly acidic and has high dissolved organic C (DOC), was found to be slightly enriched in As when compared to a global value for stream water. Of the 20 new borehole analyses from this project, six were found to have values exceeding 10 μg/L, the current World Health Organization provisional guideline value for As. The results from field speciation indicate that As(III) is slightly more predominant than As(V). There is a positive correlation between As and pH and between As and DOC in the groundwater samples. For the sediment samples, there is a positive correlation between As and Co, As and Fe, As and loss on ignition (LOI) and between As and the percent fines in the sample. Reductive dissolution of oxides and hydroxides in the sediments with organic C as an electron acceptor is the likely mechanism for the release of As from the sediments into the groundwater.     

Geochemical characteristics of heavy metals in coastal sediments from the northern Beibu Gulf (SW China): the background levels and recent contamination

Four sediment cores and one hundred surface sediments were collected from the intertidal zone of the northern Beibu Gulf (SW China). In order to detect the intensity of metal contamination recently, the background levels were successfully established for Pb, Zn, Cd and Cr, based on the linear regression of deeper sediments (pre-industrial). Aluminum is a better geochemical normalizer than Fe and it is commonly used to describe the natural metal variability of the coastal sediments. The evident enrichment of Zn and Cd is recorded in the surface sediments of the eastern side of the Guangxi coast and the central part of the Qinzhou Bay, but it does not exceed the effects range-low values, due to a low percentage of fine-grained sediments in the region. Although the Pb and Cr concentrations are mainly of natural origin, 3 and 6% sites exceed the effects range-low values, respectively; indicating the potential for adverse ecological effects of metals on the benthic communities.     

Geochemical study of arsenic and other trace elements in groundwater and sediments of the Old Brahmaputra River Plain,Bangladesh

The geochemical study of groundwaters and core sediments from the Old Brahmaputra plain of Bangladesh was conducted to investigate the distribution of arsenic and related trace elements. Groundwaters from tube wells are characterized by pH of 6.4–7.4, dissolved oxygen (DO) of 0.8–1.8 mg/l, Ca contents of 5–50 mg/l, and Fe contents of 0.2–12.9 mg/l. Arsenic concentrations ranged from 8 to 251 μg/l, with an average value of 63 μg/l. A strong positive correlation exists between As and Fe (r ² = 0.802; p = 0.001) concentrations in groundwater. The stratigraphic sequences in the cores consist of yellowish silty clays at top, passing downward into grayish to yellowish clays and sands. The uppermost 3 m and lower parts (from 13 to 31 m) of the core sediments are oxidized (average oxidation reduction potential (ORP) +170 and +220 mV, respectively), and the ORP values gradually become negative from 3 to 13 m depths (−35 to −180 mV), indicating that anoxic conditions prevail in the shallow aquifers of the Brahmaputra plain. Age determinations suggest that clay horizons at ~10 m depth were deposited at around 2,000 and 5,000 years BP (¹⁴C ages) during the transgressive phase of sea-level change. Elevated concentrations of As, Pb, Zn, Cu, Ni, Cr, and V are present in the silts and clays, probably due to adsorption onto clay particles. Significant concentrations of As occur in black peat and peaty sediments at depths between 9 and 13 m. A strong positive correlation between As and Fe was found in the sediments, indicating As may be adsorbed onto Fe oxides in aquifer sediments.