Groundwater quality variations in glacial drift and bedrock aquifers,Barry County,Michigan, U.S.A.

Groundwater samples from 288 domestic wells in Barry County, Michigan, were analyzed for 33 inorganic chemical parameters. Variations in chemical composition were investigated by considering the possible effects of human impact, aquifer type (bedrock vs glacial drift), chemical evolution along groundwater flow paths, and glacial landform type (moraine vs outwash). Approximately 25 percent of the glacial drift wells were classified as degraded by human impact and were excluded from further analysis of chemical variation. Two-sample tests comparing individual concentrations from drift and bedrock aquifers suggest that groundwater in the Marshall Sandstone aquifer is derived from local recharge through the glacial drift. This conclusion is supported by generalized groundwater flow patterns recognized for the two aquifers.Concentrations in both aquifers were examined in relation to generalized flow paths derived from water level data and also by classification of wells as recharge, transition, and discharge. No spatial concentration trends in major ions were detected, although iron concentrations do appear to increase from recharge to discharge areas. Declining redox potential along groundwater flow paths may explain this trend.The possible influence of glacial landform type was investigated by comparing concentrations of wells in moraines with those in outwash deposits. Wells in moraines have significantly higher concentrations of most parameters, perhaps due to higher content of finer, more chemically reactive sediment grains.     

The impact of cattle pasturing on groundwater quality in bedrock aquifers having minimal overburden

Widespread agricultural activity may threaten water quality in fractured bedrock aquifers having little overburden protection. A study in Canada improves the understanding of the potential impact of agriculture on water quality in bedrock aquifers, focusing on spatial and temporal variability of nitrate and bacteria. A research site was developed in and adjacent to a hay field where a gneissic aquifer is overlain by a thin veneer of unconsolidated glacial material. Ten wells were installed, hydraulically tested and completed as multilevel piezometers. Results of monthly sampling for nitrate, dissolved organic carbon, and E. coli show significant temporal and spatial variation in concentrations. Intensive 5-day sampling rounds conducted during baseflow and recharge conditions indicate that bacterial concentrations vary daily, with higher concentrations during recharge periods. The location of the impacted monitoring wells is correlated to an upgradient cattle pasture that is used periodically each summer. It is evident that periodic upgradient sources, dilution from recharge, and heterogeneous flow systems lead to varied and unpredictable contaminant concentrations. The temporal and spatial variability of contaminants in bedrock aquifers with minimal overburden must be considered for the protection of human health, as annual or even monthly groundwater monitoring may not capture unsafe concentrations.     

Hydrogeochemical and multi-tracer investigations of arsenic-affected aquifers in semi-arid West Africa

The semi-arid Sahel regions of West Africa rely heavily on groundwater from shallow to moderately deep(100 m b.g.l.)crystalline bedrock aquifers for drinking water production.Groundwater quality may be affected by high geogenic arsenic(As)concentrations(10μg/L)stemming from the oxidation of sulphide minerals(pyrite,arsenopyrite)in mineralised zones.These aquifers are still little investigated,especially concerning groundwater residence times and the influence of the annual monsoon season on groundwater chemistry.To gain insights on the temporal aspects of As contamination,we have used isotope tracers(noble gases,~3H,stable water isotopes(~2 H,~(18)O))and performed hydrochemical analyses on groundwater abstracted from tube wells and dug wells in a small study area in southwestern Burkina Faso.Results revealed a great variability in groundwater properties(e.g.redox conditions,As concentrations,water level,residence time)over spatial scales of only a few hundred metres,characteristic of the highly heterogeneous fractured underground.Elevated As levels are found in oxic groundwater of circum-neutral pH and show little relation with any of the measured parameters.Arsenic concentrations are relatively stable over the course of the year,with little effect seen by the monsoon.Groundwater residence time does not seem to have an influence on As concentrations,as elevated As can be found both in groundwater with short(50 a)and long(10~3 a)residence times as indicated by ~3He/~4He ratios spanning three orders of magnitude.These results support the hypothesis that the proximity to mineralised zones is the most crucial factor controlling As concentrations in the observed redox/pH conditions.The existence of very old water portions with residence times10~3 years already at depths of50 m b.g.l.is a new finding for the shallow fractured bedrock aquifers of Burkina Faso,suggesting that overexploitation of these relatively low-yielding aquifers may be an issue in the future.     

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.     

Holocene estuarine sediments as a source of arsenic in Pleistocene groundwater in suburbs of Hanoi,Vietnam

Groundwater pollution by arsenic is a major health threat in suburban areas of Hanoi, Vietnam. The present study evaluates the effect of the sedimentary environments of the Pleistocene and Holocene deposits, and the recharge systems, on the groundwater arsenic pollution in Hanoi suburbs distant from the Red River. At two study sites (Linh Dam and Tai Mo communes), undisturbed soil cores identified a Pleistocene confined aquifer (PCA) and Holocene unconfined aquifer (HUA) as major aquifers, and Holocene estuarine and deltaic sediments as an aquitard layer between the two aquifers. The Holocene estuarine sediments (approximately 25–40 m depth, 9.6–4.8 cal ka BP) contained notably high concentrations of arsenic and organic matter, both likely to have been accumulated by mangroves during the Holocene sea-level highstand. The pore waters in these particular sediments exhibited elevated levels of arsenic and dissolved organic carbon. Arsenic in groundwater was higher in the PCA (25–94 μg/L) than in the HUA (5.2–42 μg/L), in both the monitoring wells and neighboring household tubewells. Elevated arsenic concentration in the PCA groundwater was likely due to vertical infiltration through the arsenic-rich and organic-matter-rich overlying Holocene estuarine sediments, caused by massive groundwater abstraction from the PCA. Countermeasures to prevent arsenic pollution of the PCA groundwater may include seeking alternative water resources, reducing water consumption, and/or appropriate choice of aquifers for groundwater supply.     

Geochemical indicators of interbasin groundwater flow within the southern Rio Grande Valley, southwestern USA

Increased groundwater withdrawals for the growing population in the Rio Grande Valley and likely alteration of recharge to local aquifers with climate change necessitates an understanding of the groundwater connection between the Jornada del Muerto Basin and the adjoining and more heavily used aquifer in the Mesilla Basin. Separating the Jornada and Mesilla aquifers is a buried bedrock high from Tertiary intrusions. This bedrock high or divide restricts and/or retards interbasin flow from the Jornada aquifer into the Mesilla aquifer. The potentiometric surface of the southern Jornada aquifer near part of the bedrock high indicates a flow direction away from the divide because of a previously identified damming effect, but a groundwater outlet from the southern Jornada aquifer is necessary to balance inputs from the overall Jornada aquifer. Differences in geochemical constituents (major ions, δD, δ¹⁸O, δ³⁴S, and ⁸⁷Sr/⁸⁶Sr) indicate a deeper connection between the two aquifers through the Tertiary intrusions where Jornada water is geochemically altered because of a geothermal influence. Jornada groundwater likely is migrating through the bedrock high in deeper pathways formed by faults of the Jornada Fault Zone, in addition to Jornada water that overtops the bedrock high as previously identified as the only connection between the two aquifers. Increased groundwater withdrawals and lowering of the potentiometric surface of the Jornada aquifer may alter this contribution ratio with less overtopping of the bedrock high and a continued deeper flowpath contribution that could potentially increase salinity values in the Mesilla Basin near the divide.     

Natural arsenic in Triassic rocks: A source of drinking-water contamination in Bavaria, Germany

 The aquifer system of the Upper Triassic Keuper Sandstone, an important source of drinking water in northern Bavaria, is affected by elevated arsenic concentrations. Within the study area of 8000 km², no evidence exists for any artificial source of arsenic. Data from about 500 deep water wells show that in approximately 160 wells arsenic concentrations are 10–150 μg/L. The regional distribution of arsenic in the groundwater shows that elevated arsenic concentrations are probably related to specific lithofacies of the aquifers that contain more sediments of terrestrial origin. Geochemical measurements on samples from four selected well cores show that arsenic has accumulated in the rocks. This indigenous arsenic is the source of arsenic in the groundwater of certain facies of the middle unit of the Keuper Sandstone. Received, June 1998 / Revised, January 1999, May 1999 / Accepted, June 1999     

Potential of groundwater contamination by polybrominated diphenyl ethers (PBDEs) in a sensitive bedrock aquifer (Canada)

It is necessary to understand the presence, movement, and persistence of contaminants in aquifers to develop adequate groundwater protection plans. Fractured bedrock aquifers with thin overburden cover are very sensitive to contamination, and little is known about transport processes from the ground surface to depth in this setting. This study was undertaken to investigate the potential of groundwater contamination by polybrominated diphenyl ethers (PBDEs), which are flame retardants, in a natural fractured bedrock aquifer in Canada proven to be sensitive to contamination. PBDEs, which had not been previously measured in groundwater in detail, were detected in the study aquifer at concentrations greater than those observed in surface-water bodies. Potential sources include manure, septic tanks, and the atmosphere. From this scoping study, it is evident that additional surveys of PBDE concentrations in groundwater are warranted, especially in settings with high potential source concentrations coupled with sensitive aquifers.     

Evaluating salinity sources of groundwater and implications for sustainable reverse osmosis desalination in coastal North Carolina, USA

The natural and pumping-induced controls on groundwater salinization in the coastal aquifers of North Carolina, USA, and the implications for the performance of a reverse osmosis (RO) desalination plant have been investigated. Since installation of the well field in the Yorktown aquifer in Kill Devil Hills of Dare County during the late 1980s, the groundwater level has declined and salinity of groundwater has increased from ??1,000 to ??2,500 mg/L. Geochemical and boron isotope analyses suggest that the salinity increase is derived from an upflow of underlying saline groundwater and not from modern seawater intrusion. In the groundwater of four wells supplying the plant, elevated boron and arsenic concentrations were observed (1.3?C1.4 mg/L and 8?C53 ??g/L, respectively). Major ions are effectively rejected by the RO membrane (96?C99% removal), while boron and arsenic are not removed as effectively (16?C42% and 54?C75%, respectively). In coming decades, the expected rise of salinity will be associated with higher boron content in the groundwater and consequently also in the RO-produced water. In contrast, there is no expectation of an increase in the arsenic content of the salinized groundwater due to the lack of increase of arsenic with depth and salinity in Yorktown aquifer groundwater.     

Groundwater mining of bedrock aquifers in the Denver Basin – past,present, and future

The Denver Basin bedrock aquifer system is an important source of water for municipal and agricultural uses in the Denver and Colorado Springs metropolitan areas. The Denver area is one of the fastest growing areas in the United States with a population of 1.2 million in 1960 that has increased to over 2.4 million by 2000. This rapid population growth has produced a corresponding increase in demand for potable water. Historically, the Denver area has relied on surface water, however, in the past 10 years new housing and recreation developments have begun to rely on groundwater from the bedrock aquifers as the surface water is fully appropriated and in short supply.The Denver Basin bedrock aquifer system consists of Tertiary and Cretaceous age sedimentary rocks known as the Dawson, Denver, Arapahoe and Laramie-Fox Hills Aquifers. The number of bedrock wells has increased from 12,000 in 1985 to 33,700 in 2001 and the withdrawal of groundwater has caused water level declines of 76 m. Water level declines for the past 10 years have ranged from 3 to 12 m per year. The groundwater supplies were once thought to last 100 years but there is concern that the groundwater supplies may be essentially depleted in 10 to 15 years in areas on the west side of the basin.Extensive development of the aquifer system has occurred in the last 25 years especially near the center of the basin in Douglas and El Paso Counties where rapid urban growth continues and surface water is lacking. Groundwater is being mined from the aquifer system because the discharge by wells exceeds the rate of recharge. Concern is mounting that increased groundwater withdrawal will cause water level declines, increased costs to withdraw groundwater, reduced well yield, and reduced groundwater storage. As the long-term sustainability of the groundwater resource is in doubt, water managers believe that the life of the Denver Basin aquifers can be extended with artificial recharge, water reuse, restrictions on lawn watering, well permit restrictions and conservation measures.     

Occurrence,distribution and source of arsenic in deep groundwater wells in Maydavood area,southwestern Iran

Groundwater in some deep wells of Maydavood aquifer, southwestern Iran, contains relatively high concentrations of arsenic. Detailed hydrochemical analysis of these groundwaters (with ICP-OES instrument) showed that concentrations of iron, manganese, nickel, and vanadium are also high in them and concentrations of total arsenic in 81% of deep wells are greater than World Health Organization’s permissible value (10 ppb). XRF analysis of surrounding geological formations and aquifer sediments proposed that original source of arsenic in aquifer material can be attributed to minerals from Asmari Formation. It appears that a key mechanism for arsenic mobilizing to deep wells is microbial biodegradation of petroleum related organic matters (PROMs), which exist in aquifer sediments and originates from the bedrock of the aquifer (Gachsaran Formation). This process is followed by microbially mediated reductive dissolution of arsenic-bearing iron/manganese oxyhydroxides/oxides and further by nickel and vanadium mobilizing to groundwater. According to hydrogeochemical conditions and cluster analysis, water wells in Maydavood aquifer are divided to four subgroups: the wells with mildly reducing condition (subgroup I), moderately reducing condition (subgroup II), reducing condition (subgroup III), and high reducing condition (subgroup IV). Affected wells to arsenic are belonged to subgroups III and IV.     

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.     

天鹅洲长江故道湿地地下水砷的时空分布特征及控制机理

高砷地下水不仅直接危害供水安全,还可通过与湿地之间的交互作用,影响湿地水质进而威胁湿地生态安全.长江中游河湖平原已被报道广泛分布有高砷地下水,而位于长江中游故道区域的天鹅洲湿地地下水中砷的空间分布特征尚不明确,湿地与地下水的交互作用对地下水中砷季节性动态的控制机理尚不明确.本研究在天鹅洲湿地采集2个水文地质钻孔的35件沉积物样品、12个分层监测井不同季节的共72组地下水样和18组地表水样,通过水位-水化学监测、沉积物地球化学组成分析和砷、铁形态表征探究天鹅洲湿地地下水中砷的时空分布规律及控制机理.研究发现天鹅洲湿地地下水砷含量为1.08~147 μg/L,牛轭湖外侧浅井（10 m）地下水砷含量普遍高于深井（25 m）和牛轭湖内侧浅井（10 m）、深井（25 m）地下水,枯水期和平水期的砷含量高于丰水期.牛轭湖外侧浅层地下水系统具有更厚的粘土、亚粘土沉积,沉积物中总砷、强吸附态砷和易还原的铁氧化物的含量更多,吸附砷的水铁矿等无定形铁氧化物还原性溶解导致砷释放进入地下水中.枯水期天鹅洲湿地底部向牛轭湖外侧浅层含水层输送不稳定的有机质,使天鹅洲湿地地下水-地表水界面成为砷释放的热点区域.丰水期时牛轭湖外侧含水层受长江补给的影响,还原环境发生改变使地下水中的砷和铁被氧化固定从而不利于砷向地下水释放.      

Arsenic Distribution Pattern in Different Sources of Drinking Water and their Geological Background in Guanzhong Basin,Shaanxi, China

To study arsenic(As) content and distribution patterns as well as the genesis of different kinds of water, especially the different sources of drinking water in Guanzhong Basin, Shaanxi province, China, 139 water samples were collected at 62 sampling points from wells of different depths, from hot springs, and rivers. The As content of these samples was measured by the intermittent flowhydride generation atomic fluorescence spectrometry method(HG-AFS). The As concentrations in the drinking water in Guanzhong Basin vary greatly(0.00–68.08 μg/L), and the As concentration of groundwater in southern Guanzhong Basin is different from that in the northern Guanzhong Basin. Even within the same location in southern Guanzhong Basin, the As concentrations at different depths vary greatly. As concentration of groundwater from the shallow wells(50 m deep, 0.56–3.87 μg/L) is much lower than from deep wells(110–360 m deep, 19.34–62.91 μg/L), whereas As concentration in water of any depth in northern Guanzhong Basin is 10 μg/L. Southern Guanzhong Basin is a newly discovered high-As groundwater area in China. The high-As groundwater is mainly distributed in areas between the Qinling Mountains and Weihe River; it has only been found at depths ranging from 110 to 360 m in confined aquifers, which store water in the Lishi and Wucheng Loess(Lower and Middle Pleistocene) in the southern Guanzhong Basin. As concentration of hot spring water is 6.47–11.94 μg/L; that of geothermal water between 1000 and 1500 m deep is 43.68–68.08 μg/L. The high-As well water at depths from 110 to 360 m in southern Guanzhong Basin has a very low fluorine(F) value, which is generally 0.10 mg/L. Otherwise, the hot springs of Lintong and Tangyu and the geothermal water in southern Guanzhong Basin have very high F values(8.07–14.96 mg/L). The results indicate that highAs groundwater in depths from 110 to 360 m is unlikely to have a direct relationship with the geothermal water in the same area. As concentration of all reservoirs and rivers(both contaminated and uncontaminated) in the Guanzhong Basin is 10 μg/L. This shows that pollution in the surface water is not the source of the high-As in the southern Guanzhong Basin. The partition boundaries of the high- and low-As groundwater area corresponds to the partition boundaries of the tectonic units in the Guanzhong Basin. This probably indicates that the high-As groundwater areas can be correlated to their geological underpinning and structural framework. In southern Guanzhong Basin, the main sources of drinking water for villages and small towns today are wells between 110–360 m deep. All of their As contents exceed the limit of the Chinese National Standard and the International Standard(10 μg/L) and so local residents should use other sources of clean water that are 50 m deep, instead of deep groundwater(110 to 360 m) for their drinking water supply.     

Hydrogeologic framework of the Maku area basalts, northwestern Iran

The Maku area in northwestern Iran is characterized by young lava flows which erupted from Mount Ararat in Turkey. These fractured volcanic rocks overlie alluvium associated with pre-existing rivers and form a good basalt-alluvium aquifer over an area of 650 km². Groundwater discharge occurs from 12 large springs, ranging from 20 to 4,000 L s^?1, and from some extraction wells. Permian and Oligo-Miocene age limestones along the northern boundary of the Bazargan and Poldasht Plains basalts are intensively karstified and groundwater from these high lands easily enters the basalt-alluvium aquifers. The transmissivity of the basalt-alluvium aquifer ranges from 24 to 870 m² d^?1, indicating heterogeneity. Groundwater of the aquifer is a sodium-bicarbonate and mixed cation-bicarbonate type and the concentration of fluoride is higher than the universal maximum admissible concentrations for drinking. In order to determine the chemical composition and identify the source of the high fluoride concentrations in the groundwater of the basaltic area, water samples from the springs, wells and rivers were analyzed. The results indicate that the high fluoride water enters the study area from the Sari Su River.     

长江中游河湖平原浅层地下水中砷空间异质性的同位素指示

近年来陆续有报道发现长江中游河湖平原广泛分布着高砷地下水,鄱阳湖平原与江北平原（古彭蠡泽）作为长江中游南北两岸典型的河湖平原,其地下水资源丰富,但砷的空间分布规律尚不清楚,区域供水安全存在风险.本研究在两个区域系统采集98个浅层地下水（< 40 m）样品和8个地表水样品,通过水化学、氢氧稳定同位素分析,查明地下水中砷的空间分布异质性及其影响因素.研究发现江北平原浅层地下水砷含量为0.65~956.72 μg/L（平均值210.78 μg/L）,高砷地下水集中分布于长江古河道;鄱阳湖平原浅层地下水砷含量为0.09~267.45 μg/L（平均值11.85 μg/L）,高砷地下水仅分布于赣江三角洲局部地区.江北平原地下水δD与δ18O值相对鄱阳湖平原更偏负,且与地表水的差异更大.地下水化学及主成分分析结果表明物源和含水层结构差异是影响鄱阳湖平原和江北平原砷空间分布异质性的关键因素,来自长江物源的古彭蠡泽区域沉积物为高砷含水层的形成提供了物质来源,湖相含水层中含砷铁氧化物的还原性溶解是地下水砷富集的主要过程.地下水氢氧稳定同位素指示江北平原较鄱阳湖平原地下水赋存环境更封闭,地下水循环交替速度缓慢,有利于砷的富集.      

Heterogeneous redox conditions, arsenic mobility, and groundwater flow in a fractured-rock aquifer near a waste repository site in New Hampshire, USA

Anthropogenic sources of carbon from landfill or waste leachate can promote reductive dissolution of in situ arsenic (As) and enhance the mobility of As in groundwater. Groundwater from residential-supply wells in a fractured crystalline-rock aquifer adjacent to a Superfund site in Raymond, New Hampshire, USA, showed evidence of locally enhanced As mobilization in relatively reducing (mixed oxic-anoxic to anoxic) conditions as determined by redox classification and other lines of evidence. Redox classification was determined from geochemical indicators based on threshold concentrations of dissolved oxygen (DO), nitrate (NO ₃ ^– ), iron (Fe²⁺), manganese (Mn²⁺), and sulfate (SO ₄ ^2– ). Redox conditions were evaluated also based on methane (CH₄), excess nitrogen gas (N₂) from denitrification, the oxidation state of dissolved As speciation (As(III) and As(V)), and several stable isotope ratios. Samples from the residential-supply wells primarily exhibit mixed redox conditions, as most have long open boreholes (typically 50–100?m) that receive water from multiple discrete fractures with contrasting groundwater chemistry and redox conditions. The methods employed in this study can be used at other sites to gauge redox conditions and the potential for As mobilization in complex fractured crystalline-rock aquifers where multiple lines of evidence are likely needed to understand As occurrence, mobility, and transport.     

Arsenic enrichment in unconfined sections of the southern Gulf Coast aquifer system, Texas

Groundwater arsenic concentrations exceeding the federal drinking water standard are common in the southern Gulf Coast aquifer system in Texas, including in aerobic, unconfined groundwater which provides much of the municipal and domestic water supplies for the region. The objective of this study was to determine geochemical factors affecting the occurrence and distribution of groundwater As in unconfined portions of the southern Gulf Coast aquifer system through a comparative transect study of groundwater across three major hydrostratigraphic units (the Catahoula Formation, Jasper aquifer and Evangeline aquifer) and analysis of regional water quality data. Results show that As concentrations decrease with increasing distance from the Catahoula Formation, which is consistent with Miocene volcanic ash as the main source of As to groundwater in the region. Arsenic concentrations correlate with V, SiO₂ and K, all of which were released during weathering of volcanic sediments and their degradation products. In all three units, carbonate weathering and active recharge in the unconfined zones result in circum-neutral pH and oxidizing groundwater, which are typically amenable to As immobilization by adsorption of arsenate onto mineral oxides and clays. However, As concentrations exceed 10 μg/L in approximately 30% of wells. Silica that was co-released with As may compete for sorption sites and reduce the capacity for arsenate adsorption.     

Geochemical and hydrogeological contrasts between shallow and deeper aquifers in two villages of Araihazar, Bangladesh: Implications for deeper aquifers as drinking water sources

Sediment and groundwater profiles were compared in two villages of Bangladesh to understand the geochemical and hydrogeological factors that regulate dissolved As concentrations in groundwater. In both villages, fine-grained sediment layers separate shallow aquifers (< 28 m) high in As from deeper aquifers (40-90 m) containing < 10 μg/L As. In one village (Dari), radiocarbon dating indicates deposition of the deeper aquifer sediments > 50 ka ago and a groundwater age of thousands of years. In the other village (Bay), the sediment is < 20 ka old down to 90 m and the deeper aquifer groundwater is younger, on the order of hundreds of years. The shallow aquifers in both villages that are high in As contain bomb-³H and bomb-¹⁴C, indicating recent recharge. The major and minor ion compositions of the shallow and deeper aquifers also differ significantly. Deeper aquifer water is of the Na⁺-HCO₃^- type, with relatively little dissolved NH₄⁺ (76 ± 192 μmol/L), Fe (27 ± 43 μmol/L) and Mn (3 ± 2 μmol/L). In contrast, shallow aquifer water is of the Ca²⁺-Mg²⁺-HCO₃^- type, with elevated concentrations of dissolved NH₄⁺ (306 ± 355 μmol/L), Fe (191 ± 73 μmol/L), and Mn (27 ± 43 μmol/L). In both villages, the quantity of As extractable from deeper aquifer sands with a 1 mol/L phosphate solution (0.2 ± 0.3 mg/kg, n = 12; 0.1 ± 0.1 mg/kg, n = 5) is 1 order of magnitude lower than P-extractable As from shallow deposits (1.7 ± 1.2 mg/kg, n = 9; 1.4 ± 2.0 mg/kg, n = 11). The differences suggest that the concentration of P-extractable As in the sediment is a factor controlling the concentration of As in groundwater. Low P-extractable As levels are observed in both deeper aquifers that are low in As, even though there is a large difference in the time of deposition of these aquifers in the two villages. The geochemical data and hydrographs presented in this study suggest that both Holocene and Pleistocene deeper aquifers that are low in As should be a viable source of drinking water as long as withdrawals do not exceed recharge rates of ∼1 cm/yr.     

Virus occurrence in private and public wells in a fractured dolostone aquifer in Canada

Groundwater samples from 22 wells completed in a regional fractured dolostone aquifer in the Guelph region of southern Ontario, Canada, were collected over an 8-month period and analyzed for viruses and Campylobacter jejuni. Only 8% of the 118 samples exhibited viruses at extremely low concentrations, but of the 22 wells sampled, 10 (45%) were positive for human enteric viruses (polyomavirus, adenovirus A, and GII norovirus) including 5 of the 8 public supply wells (62.5%) and 5 of the 11 private wells (45%). Each virus-positive well had only one virus occurrence with six sampling events during the 8-month sampling campaign and only one virus type was detected in each well. The probability of virus detection was positively associated with well open-interval length. Virus concentration (in the wells that were virus-positive) was negatively associated with well depth and open-interval length and positively associated with overburden thickness (i.e., the thickness of unconsolidated materials overlying bedrock facies) and the amount of precipitation 8–14 and 15–21 days prior to the sampling date. The ephemeral nature of the virus detections and the low detection rate on a per sample basis were consistent with previous studies. The percentage of virus-positive wells, however, was much higher than previous studies, but consistent with the fact that the hydrogeologic conditions of fractured bedrock aquifers create wide capture zones and short groundwater travel times to wells making them more vulnerable to contamination occurrence but at very low concentrations.