Evaluating natural and anthropogenic trace element inputs along an alpine to urban gradient in the Provo River,Utah, USA

Numerous natural and anthropogenic processes in a watershed produce the geochemical composition of a river, which can be altered over time by snowmelt and rainfall events and by built infrastructure (i.e., dams and diversions). Trace element concentrations coupled with isotopic ratios offer valuable insights to disentangle the effects of these processes on water quality. In this study, we measured a suite of 40+ trace and major elements (including As, Cd, Ce, Cr, Cs, Fe, La, Li, Mo, Pb, Rb, Sb, Se, Sr, Ti, Tl, U, and Zn), Sr isotopes (⁸⁷Sr/⁸⁶Sr), and stable isotopes of H and O (δD and δ¹⁸O) to investigate natural and anthropogenic processes impacting the Provo River in northern Utah, USA. The river starts as a pristine mountain stream and passes through agricultural and urban areas, with two major reservoirs and several major diversions to and from the river. We sampled the entire 120 km length of the Provo River at 13 locations from the Uinta Mountains to Utah Valley, as well as two important tributaries, across the range of hydrologic conditions from low flow to snowmelt runoff during the 2013 water year. We also sampled the furthest downstream site in the Utah Valley urban area during a major flood event. Trace element concentrations indicate that a variety of factors potentially influence Provo River chemistry, including inputs from weathering of carbonate/siliciclastic rocks (Sr) and black shales (Se and U), geothermal groundwater (As, Cs, Li, and Rb), soil erosion during snowmelt runoff (Ce, Cr, Fe, La, Pb, and Ti), legacy mining operations (Mo, Sb, and Tl), and urban runoff (Cr, Pb, and Zn). Although specific elements overlap between different groups, the combination of different elements together with isotopic measurements and streamflow observations may act as diagnostic tools to identify sources. ⁸⁷Sr/⁸⁶Sr ratios indicate a strong influence of siliciclastic bedrock in the headwaters with values exceeding 0.714 and carbonate bedrock in the lower reaches of the river with values approaching 0.709. δD and δ¹⁸O changed little throughout the year in the Provo River, suggesting that the river is primarily fed by snowmelt during spring runoff and snowmelt-fed groundwater during baseflow. Based on nonmetric multidimensional scaling (NMS) water chemistry was unique across the upper, middle, and lower portions of the river, with high temporal variability above the first reservoir but minimal temporal variability below the reservoir. Thus, the results show that dams alter water chemistry by allowing for settling of particle-associated elements and also by homogenizing inflows throughout the year to minimize dilution during snowmelt runoff. Taken together, trace element concentrations and isotopic measurements can be used to evaluate the complex geochemical patterns of rivers and their variability in space and time. These measurements are critical for identifying natural and anthropogenic impacts on river systems.     

A hydrogeochemical survey of Kilimanjaro (Tanzania): implications for water sources and ages

Kilimanjaro, Tanzania, the highest mountain in Africa, has undergone extensive hydrologic changes over the past century in an area where water resources are critical. A hydrochemical and isotopic synoptic sampling program in January 2006 is used to characterize hydrogeology, hydrology, and water quality of the area. Samples were collected from the summit and southern side of Kilimanjaro and the Moshi region (Tanzania). Sample sources included four glaciers, seven groundwater wells, 12 rivers, 10 springs, precipitation, and a lake. Analyses included major ion chemistry, stable isotopes of water (¹⁸O and D); in addition, seven samples were analyzed for tritium. The samples generally have good water quality with the exception of three samples with elevated fluoride concentrations (>3 mg/L) and elevated nitrate concentrations (>2.5 mg/L NO₃ as N). There is a strong elevation control on stable isotopes, with an apparent elevation effect of – 0.1 ‰ δ¹⁸O per 100 m rise in elevation (R ² = 0.79). The results, including the tritium values, show that the hydrogeologic system is comprised of both local and regional flow systems, and that regional rivers are receiving significant inflow from shallow groundwater, and at very high elevations the hydrologic system is derived from groundwater, precipitation, and glacial melt water.     

Environmental isotopes (18O, 2H, and 87Sr/86Sr) as a tool in groundwater investigations in the Keta Basin, Ghana

Analyses of environmental isotopes (¹⁸O, ²H, and ⁸⁷Sr/⁸⁶Sr) are applied to groundwater studies with emphasis on saline groundwater in aquifers in the Keta Basin, Ghana. The ⁸⁷Sr/⁸⁶Sr ratios of groundwater and surface water of the Keta Basin primarily reflect the geology and the mineralogical composition of the formations in the catchments and recharge areas. The isotopic compositions of ¹⁸O and ²H of deep groundwater have small variations and plot close to the global meteoric water line. Shallow groundwater and surface water have considerably larger variations in isotopic compositions, which reflect evaporation and preservation of seasonal fluctuations. A significant excess of chloride in shallow groundwater in comparison to the calculated evaporation loss is the result of a combination of evaporation and marine sources. Groundwaters from deep wells and dug wells in near-coastal aquifers are characterized by relatively high chloride contents, and the significance of marine influence is evidenced by well-defined mixing lines for strontium isotopes, and hydrogen and oxygen stable isotopes, with isotopic compositions of seawater as one end member. The results derived from environmental isotopes in this study demonstrate that a multi-isotope approach is a useful tool to identify the origin and sources of saline groundwater. Electronic Publication     

Behavior and budget of dissolved uranium in the lower reaches of the Yellow (Huanghe) River: Impact of Water–Sediment Regulation Scheme

The Water–Sediment Regulation Scheme (WSRS) is an important water conservancy project in the Yellow River basin, which is usually operated annually from June to July to control water and sediment release from the Xiaolangdi Reservoir in the middle reaches. As a greatly concentrated period of delivering terrigenous materials from the Yellow River to the sea, the WSRS can serve as a natural laboratory to examine the geochemical behavior of elements during their transport along the river. Uranium isotopes (²³⁴U and ²³⁸U) were measured in Yellow River waters at stations Xiaolangdi (located in the middle reaches of the Yellow River) and Lijin (the last hydrologic station near the Yellow River estuary) during the WSRS 2012. Compared with station Xiaolangdi, dissolved uranium concentration at station Lijin was markedly higher, showing a significant impact from the WSRS. Budget calculation for dissolved uranium during the WSRS indicated that two major sources of new added dissolved uranium in the section of the Yellow River between Xiaolangdi and Lijin: suspended particles (46%) and porewater of bottom sediment (45%). The flux of dissolved uranium from the Yellow River to the sea was estimated to be 2.40 × 10⁷ g during the WSRS 2012.     

First data on the uranium content in water of the Yenisei River basin in the area affected by the operation of Rosatom plants

This study is devoted to investigating the content of uranium isotopes in water of the Yenisei River and its tributaries within the territories affected by the operation of Rosatom plants (mining chemical combine, and electrochemical plant). Long-term monitoring of the ²³⁸U content by mass spectrometry carried out in two institutes of the Siberian Branch of the Russian Academy of Sciences first revealed the multiple excess of ²³⁸U over the background content in different areas of the Yenisei River basin, such as the region of the Yenisei River near the effluents of the mining and chemical combine (MCC), and the territories of the Bol’shaya Tel’ and Kan rivers. In these regions, the ²³⁸U content in water reaches 2.1–4.0 μg/l, which exceeds its content upstream from the MCC (0.3–0.6 μg/l) by almost an order of magnitude. The studies of the isotopic composition of uranium in water samples, which were carried out at the Institute of Inorganic Chemistry, Siberian Branch, Russian Academy of Sciences, showed the presence of a technogenic isotope of uranium ²³⁶U in the samples from the Bolshaya Tel’ River and revealed the deviation of the isotope ratio ²³⁸U/²³⁵U (167 ± 3 and 177 ± 3) from the equilibrium natural ratio (²³⁸U/²³⁵U = 138). These facts attest to the technogenic origin of part of the uranium in water of the Bol’shaya Tel’ River connected with the activity of MCC. The excess uranium content in the Kan River requires additional studies to ascertain the fraction of uranium of technogenic origin connected with the activity of the electrochemical plant (ECP) (Fig. 1, Table 4).     

Inferring groundwater contributions and pathways to streamflow during snowmelt over multiple years in a discontinuous permafrost subarctic environment (Yukon, Canada)

Research on large northern rivers suggests that as permafrost thaws, deeper groundwater flowpaths become active, resulting in greater baseflow, increased concentrations of weathering ions and reduced concentrations of dissolved organic carbon in the streamflow. In contrast, at the headwater-catchment scale, where understanding of groundwater/surface-water interactions is developed, inter-annual variability in climate and hydrology result in complex hydrological and chemical responses to change. This paper reports on a 4-year runoff investigation in an alpine discontinuous permafrost environment in Yukon, Canada, using stable isotopes, major dissolved ions and hydrometric data, to provide enhanced insight into the inter-annual-variability runoff-generation processes. Stable isotope results suggest that pre-event (old) water stored within the catchment dominates the snowmelt hydrograph, and dissolved ion results reveal that groundwater pathways occur predominantly in the near-surface during freshet. Dissolved organic carbon varies inter-annually, reflecting changing melt patterns, whereas weathering ions generated from deeper flowpaths become diluted. The total snow-water equivalent does not have a major influence on the fraction of snowmelt water reaching the stream or the runoff ratio. Results from multiple years highlight the considerable variability over short time scales, limiting our ability to detect climate-change influences on groundwater at the headwater scale.     

A study of the interrelation between surface water and groundwater using isotopes and chlorofluorocarbons in Sanjiang plain,Northeast China

Surface water and groundwater are the main water resources used for drinking and production. Assessments of the relationship between surface water and groundwater provide information for water resource management in Sanjiang plain, Northeast China. The surface water (river, lake, and wetland) and groundwater were sampled and analyzed for stable isotopic (δD, δ ¹⁸O) composition, tritium, and chlorofluorocarbons concentrations. The local meteoric water line is δD = 7.3δ ¹⁸O–6.7. The tritium (T) and chlorofluorocarbon (CFC) contents in groundwater were analyzed to determine the groundwater ages. Most groundwater were modern water with the ages <50 years. The groundwaters in mountain area and near rivers were younger than in the central plain. The oxygen isotope (δ ¹⁸O) was used to quantify the relationship between surface water and groundwater. The Songhua, Heilongjiang, and Wusuli rivers were gaining rivers, but the shallow groundwater recharged from rivers at the confluence area of rivers. At the confluence of Songhua and Heilongjiang rivers, 88 % of the shallow groundwater recharged from Songhua river. The combination of stable isotopes, tritium, and CFCs was an effectively method to study the groundwater ages and interrelation between surface water and groundwater. Practically, the farmlands near the river and under foot of the mountain could be cultivated, but the farmlands in the central plain should be controlled.     

The deuterium and oxygen-18 isotopic composition of the groundwater in Khan Younis City,southern Gaza Strip (Palestine)

The environmental isotopes such as deuterium and oxygen-18 and the deuterium excess values have been used to assess groundwater recharge sources and their dynamics in Khan Younis City in the Gaza Strip in Palestine. Three isotopic lines for the relationship between δ²H and δ¹⁸O were used in the assessment. These lines are the global meteoric water line, the local meteoric water line and the groundwater evaporation line. The δ²H, δ¹⁸O and D-excess values indicate that deuterium and oxygen-18 isotopes originated in the groundwater from groundwater mixing with rainfall and other water sources; the groundwater in the area recharged from rainfall from a distant source that came from the Mediterranean Sea and from other sources such as wastewater, irrigation return flow and saline water.     

A study of234U/238U ratios in groundwaters of Taiyuan area,Shanxi Province

Uranium contents and²³⁴U/²³⁸U ratios have been determined on 29 water samples from the Taiyuan area, Shanxi Province. The results show that the same artesian aquifer has similar uranium contents and²³⁴U/²³⁸U activity ratios, and the deeper aquifers have higher A. R. values but lower uranium contents. The A. R. values increase slightly towards groundwater flow in the artesian aquifers dominated by oxidizing ground waters. The Lancun Spring and the famous Jinci Spring belong to two different karst groundwater systems, i.e., the east and west karst groundwater systems. The recharge area of the Lancun Spring should cover the wide limestone outcrops of middle Ordovician in the northeast. The Ordovician fissure-karst ground water to the Jinci Spring is extensively mixed with fissure water in Carboniferous-Jurassic formations and seepage water from the Fenhe River.     

Behaviour of lithium and its isotopes during weathering in the Mackenzie Basin, Canada

We report Li isotopic compositions, for river waters and suspended sediments, of about 40 rivers sampled within the Mackenzie River Basin in northwestern Canada. The aim of this study is to characterize the behaviour of Li and its isotopes during weathering at the scale of a large mixed lithology basin. The Mackenzie River waters display systematically heavier Li isotopic compositions relative to source rocks and suspended sediments. The range in δ⁷Li is larger in dissolved load (from +9.3‰ to +29.0‰) compared to suspended sediments (from −1.7‰ to +3.2‰), which are not significantly different from δ⁷Li values in bedrocks. Our study shows that dissolved Li is essentially derived from the weathering of silicates and that its isotopic composition in the dissolved load is inversely correlated with its relative mobility when compared to Na. The highest enrichment of ⁷Li in the dissolved load is reported when Li is not or poorly incorporated in secondary phases after its release into solution by mineral dissolution. This counterintuitive observation is interpreted by the mixing of water types derived from two different weathering regimes producing different Li isotopic compositions within the Mackenzie River Basin. The incipient weathering regime characterizing the Rocky Mountains and the Shield areas produces ⁷Li enrichment in the fluid phase that is most simply explained by the precipitation of oxyhydroxide phases fractionating Li isotopes. The second weathering regime is found in the lowland area and produces the lower δ⁷Li waters (but still enriched in ⁷Li compared to bedrocks) and the most Li-depleted waters (compared to Na). Fractionation factors suggest that the incorporation of Li in clay minerals is the mechanism that explains the isotopic composition of the lowland rivers. The correlation of boron and lithium concentrations found in the dissolved load of the Mackenzie Rivers suggests that precipitation of clay minerals is favoured by the relatively high residence time of water in groundwater. In the Shield and Rocky Mountains, Li isotopes suggest that clay minerals are not forming and that secondary minerals with stronger affinity for ⁷Li appear.Although the weathering mechanisms operating in the Mackenzie Basin need to be characterized more precisely, the Li isotope data reported here clearly show the control of Li isotopes by the weathering intensity. The spatial diversity of weathering regimes, resulting from a complex combination of factors such as topography, geology, climate and hydrology explains, in fine, the spatial distribution of Li isotopic ratios in the large drainage basin of the Mackenzie River. There is no simple relationship between Li isotopic composition and chemical denudation fluxes in the Mackenzie River Basin.     

Snowmelt runoff and groundwater discharge in Himalayan rivers: a case study of the Satluj River,NW India

The Himalayas are one of the largest cryospheric systems outside the Polar Regions, and include more than 12,000 glaciers spread over an area of about 33,000 km². The Himalayan glaciers and snow packs retreating at an accelerating rate, thereby creating an alarming situation for the huge population that resides in northwestern India and southeastern Pakistan, as they depend on surface water resources in the region and rivers emanating from the Himalayas. This work attempts to quantify the contribution of different sources such as glacial/ice/snow melt and groundwater discharge to the Satluj River using the stable isotopes based hydrograph separation method at Ropar (foot hill) and Yusufpur in plain of Punjab, India. A mass balance model of three-component mixing has been engaged using the values of δ¹⁸O and electrical conductivity of the river water, and its discharge fraction, to estimate the time-varying relative proportion of each component from July 2013 to January 2014. The proportion of glacier melt was found to peak up to ~?64% at Ropar and ~?15% at Yusufpur during the wet summer months. The fraction of groundwater discharge was found to vary between 10–20% at Ropar and 25–35% at Yusufpur (Punjab plain) over time. The observed trend of d-excess (deuterium excess) values of river water also suggests that the glaciers and snow packs at higher altitudes contain a significant fraction of snow derived from vapor originating in the Mediterranean region, driven by the mid-latitude westerlies known as western disturbances.     

The influence of irrigation and Wuliangsuhai Lake on groundwater quality in eastern Hetao Basin,Inner Mongolia,China

Geochemical and isotopic characterization of groundwater and lake-water samples were combined with water and total dissolved solids balances to evaluate sources of groundwater quality deterioration in eastern Hetao Basin, Inner Mongolia, China. Groundwater quality is poor; 11 of 13 wells exceed drinking-water guidelines for at least one health-based parameter and all wells exceed aesthetic guidelines. The well water is largely derived from Yellow River irrigation water. Notably high uranium concentrations in the Yellow River, relative to world rivers, suggest groundwater uranium and other trace elements may originate in the river-derived irrigation water. Complex hydrostratigraphy and spatial variation in groundwater recharge result in spatially complex groundwater flow and geochemistry. Evapotranspiration of irrigation water causes chloride concentration increases of up to two orders of magnitude in the basin, notably in shallow groundwater around Wuliangsuhai Lake. In addition to evapotranspiration, groundwater quality is affected by mineral precipitation and dissolution, silicate weathering, and redox processes. The lake-water and TDS balances suggest that a small amount of discharge to groundwater (but associated with very high solute concentrations) contributes to groundwater salinization in this region. Increasing salinity in the groundwater and Wuliangsuhai Lake will continue to deteriorate water quality unless irrigation management practices improve.     

Seasonal and Annual Fluxes of Nutrients and Organic Matter from Large Rivers to the Arctic Ocean and Surrounding Seas

River inputs of nutrients and organic matter impact the biogeochemistry of arctic estuaries and the Arctic Ocean as a whole, yet there is considerable uncertainty about the magnitude of fluvial fluxes at the pan-Arctic scale. Samples from the six largest arctic rivers, with a combined watershed area of 11.3?×?10⁶?km², have revealed strong seasonal variations in constituent concentrations and fluxes within rivers as well as large differences among the rivers. Specifically, we investigate fluxes of dissolved organic carbon, dissolved organic nitrogen, total dissolved phosphorus, dissolved inorganic nitrogen, nitrate, and silica. This is the first time that seasonal and annual constituent fluxes have been determined using consistent sampling and analytical methods at the pan-Arctic scale and consequently provide the best available estimates for constituent flux from land to the Arctic Ocean and surrounding seas. Given the large inputs of river water to the relatively small Arctic Ocean and the dramatic impacts that climate change is having in the Arctic, it is particularly urgent that we establish the contemporary river fluxes so that we will be able to detect future changes and evaluate the impact of the changes on the biogeochemistry of the receiving coastal and ocean systems.     

Preliminary research on hydrogen and oxygen stable isotope characteristics of different water bodies in the Qilian Mountains,northwestern Tibetan Plateau

Hydrogen and oxygen stable isotope in water bodies is a widely used tracer in hydrological process studies. In order to provide a basis for stable isotopic characteristics in different water bodies at the high mountainous area of northwestern Tibetan Plateau, samples for river water, groundwater, soil water, and plant water were collected from 10 sites in the Qilian Mountains during July and August 2015, and then analyzed for δ¹⁸O and δD, respectively. Results indicated that the stable isotope values of soil water were mostly plotted below the global meteoric water line (GMWL), which suggested that evaporation made heavy isotope in soil water enriched. The stable isotope values of soil water were quite different in the top soil layer, but tended to be uniform in the deep soil layer. Furthermore, the stable isotope difference of plant water is related to climatic conditions, water isotopes utilized by plant, plant species, growing season, and so on. Additionally, the variation of δ¹⁸O values for river water and groundwater relatively coincided with each other, and this showed the recharge sources of above two water bodies may be consistent. The stable isotope values of river water and groundwater were mainly plotted on the upper left of GMWL, and the lower level of isotopic fractionation due to weak evaporation may accountable for this.     

Iron isotope composition of the suspended matter along depth and lateral profiles in the Amazon River and its tributaries

Samples of suspended matter were collected at different locations, seasons, depths and lateral profiles in the Amazon River and three of its main tributaries, the Madeira, the Solimões and the Negro rivers. Their iron isotope compositions were studied in order to understand the iron cycle and investigate the level of isotopic homogeneity at the river cross-section scale. Samples from four depth profiles and three lateral profiles analyzed show suspended matter δ⁵⁷Fe values (relative to IRMM-14) between −0.501 ± 0.075‰ and 0.196 ± 0.083‰ (2SE). Samples from the Negro River, a blackwater river, yield the negative values. Samples from other stations (whitewater rivers, the Madeira, the Solimões and the Amazon) show positive values, which are indistinguishable from the average composition of the continental crust (δ⁵⁷Fe_IRMM-14 ∼ 0.1‰). Individual analyses of the depth and lateral profiles show no significant variation in iron isotope signatures, indicating that, in contrast to certain chemical or other isotopic tracers, one individual subsurface sample is representative of river deeper waters. This also suggests that, instead of providing detailed information on the riverine iron cycling, iron isotopes of particulate matter in rivers will rather yield a general picture of the iron sources.     

The interaction between surface water and groundwater and its effect on water quality in the Second Songhua River basin,northeast China

The relationship between surface water and groundwater not only influences the water quantity, but also affects the water quality. The stable isotopes (δD, δ ¹⁸O) and hydrochemical compositions in water samples were analysed in the Second Songhua River basin. The deep groundwater is mainly recharged from shallow groundwater in the middle and upper reaches. The shallow groundwater is discharged to rivers in the downstream. The runoff from upper reaches mainly contributed the river flow in the downstream. The CCME WQI indicated that the quality of surface water and groundwater was ‘Fair’. The mixing process between surface water and groundwater was simulated by the PHREEQC code with the results from the stable isotopes. The interaction between surface water and groundwater influences the composition of ions in the mixing water, and further affects the water quality with other factors.     

Stable isotope systematics and geochemical signatures constraining groundwater hydraulics in the mining environment of the Korba Coalfield,Central India

The present study explores the use of stable isotopes and major ion chemistry of various water sources such as mine water, groundwater, river water, and rainwater to identify the dominant hydrogeochemical process that controls the water quality in the active opencast coal mining area of the Korba Coalfield, India. Different hydrochemical models have revealed that the study area is mostly characterized by two facies alongside a dominance by ion exchange: i.e., a slightly mineralized Ca²⁺–Mg²⁺–Cl^? and a meteorically derived Ca²⁺–HCO₃^? fresh water facies. In the isotope bivariate plot, the samples plot to the right of the LMWL and slopes observed in pre (4.94) and post-monsoon (5.85) seasons are not as steep as the LMWL (7.95) and this warrants the suggestion that meteoric water is the major source that replenishes the dynamic groundwater resource in the study area after being subjected to evaporation. The negative d-excess values (<?0) and enrichment of the δ¹⁸O ratio observed at some locations suggests a non-equilibrium process and a “mechanism of mixing”. A noteworthy fact is that isotopically river water is in tandem with the mine water samples for both seasons and testifies to a hydraulic connectivity between Hasdeo River water and mine water through a major fault. It is substantiated by mine inflows assessed by the sump test for Kusmunda and Gevra, which is two times higher than the predicted values by Darcy’s law. The wide variation in the isotopic composition is attributed to different vapor sources viz., southwest monsoon (SW) that originates in the Arabian Sea and locally driven air moisture from surface water bodies.     

Use of 234U and 238U isotopes to evaluate contamination of near-surface groundwater with uranium-mill effluent: a case study in south-central Colorado, U.S.A.

The ²³⁴U/²³⁸U alpha activity ratio (AR) was determined in 47 samples of variably uraniferous groundwater from the vicinity of a uranium mill near Cañon City, Colorado. The results illustrate that uranium isotopes can be used to determine the distribution of uranium contamination in groundwater and to indicate processes such as mixing and chemical precipitation that affect uranium concentrations. Highly to moderately contaminated groundwater samples collected from the mill site and land immediately downgradient from the mill site contain more than 100?μg/l of dissolved uranium and typically have AR values in the narrow range of 1.0–1.06. Other samples from the shallow alluvial aquifer farther downgradient from the mill contain 10–100?μg/l uranium and plot along a broad trend of increasing AR (1.06–1.46) with decreasing uranium concentration. The results are consistent with mixing of liquid mill waste (AR≈1.0) with alluvial groundwater of small, but variable, uranium concentrations and AR of 1.3–1.5. In the alluvial aquifer, the spatial distribution of wells with AR values less than 1.3 is consistent with previous estimates of the probable distribution of contamination, based on water chemistry and hydrology. Wells more distant from the area of probable contamination have AR values that are consistently greater than 1.3 and are indicative of little or no contamination. The methodology of this study can be extended usefully to similar sites of uranium mining, milling, or processing provided that local geohydrologic settings promote uranium mobility and that introduced uranium contamination is isotopically distinct from that of local groundwater.     

Isotope evidence for quantifying river evaporation and recharge processes in the lower reaches of the Yellow River

Evaporation and recharge are important hydrological processes in the water cycle. However, accurately quantifying these two processes of river remains to be difficult due to their spatial heterogeneity and the limitations of traditional methods. In this study, a more reliable method of stable isotopes of δ ¹⁸O and δ ²H based on the Rayleigh distillation equation and mass conservation was used to estimate the evaporation and recharge of the rivers in the lower reaches of the Yellow River, North China Plain. Comprehensive sampling campaigns including 30 surface water samples from 10 rivers, 33 groundwater samples from domestic and observation wells, and two Yellow River water samples were conducted. The results showed that the evaporation proportion of the rivers based on δ ¹⁸O and δ ²H both averaged 14.4%. The evaporation proportions in each river did not completely follow a linear increasing trend along the flow path. This phenomenon could be mainly explained by the different proportions of recharge from groundwater and Yellow River water. With closer to the Yellow river, evaporation of the rivers decreased while the recharge by the Yellow River increased. Regression equations based on δ ¹⁸O, δ ²H, and their average revealed that the evaporation proportion respectively increased by 1.02, 0.79, and 0.90% with the increase in the distance to the Yellow River per 10 km. On the contrary, the recharge proportion decreased by 7.68, 5.51, and 6.59%, respectively. In addition, using δ ¹⁸O rather than δ ²H was more reliable in studying the spatial influence of the Yellow River on evaporation and recharge. Sensitivity analysis showed that the evaporation model was most sensitive to isotopic composition, rather than to air temperature or relative humidity. The results of this study provide insights into the determination of river hydrological processes and the management of water resources.     

Isotope hydrology of the Chalk River Laboratories site,Ontario, Canada

This paper presents results of hydrochemical and isotopic analyses of groundwater (fracture water) and porewater, and physical property and water content measurements of bedrock core at the Chalk River Laboratories (CRL) site in Ontario. Density and water contents were determined and water-loss porosity values were calculated for core samples. Average and standard deviations of density and water-loss porosity of 50 core samples from four boreholes are 2.73 ± 12 g/cc and 1.32 ± 1.24 percent. Respective median values are 2.68 and 0.83 indicating a positive skewness in the distributions. Groundwater samples from four deep boreholes were analyzed for strontium (⁸⁷Sr/⁸⁶Sr) and uranium (²³⁴U/²³⁸U) isotope ratios. Oxygen and hydrogen isotope analyses and selected solute concentrations determined by CRL are included for comparison. Groundwater from borehole CRG-1 in a zone between approximately +60 and −240 m elevation is relatively depleted in δ¹⁸O and δ²H perhaps reflecting a slug of water recharged during colder climatic conditions. Porewater was extracted from core samples by centrifugation and analyzed for major dissolved ions and for strontium and uranium isotopes. On average, the extracted water contains 15 times larger concentration of solutes than the groundwater. ²³⁴U/²³⁸U and correlation of ⁸⁷Sr/⁸⁶Sr with Rb/Sr values indicate that the porewater may be substantially older than the groundwater. Results of this study show that the Precambrian gneisses at Chalk River are similar in physical properties and hydrochemical aspects to crystalline rocks being considered for the construction of nuclear waste repositories in other regions.