Hydrogeochemistry and isotope techniques to determine water interactions in groundwater-dependent shallow lakes,Wet Pampa Plain,Argentina

This paper gives an account of the implementation of hydrochemical and isotopic techniques to identify and explain the processes that govern solute exchange in two groundwater-dependent shallow lakes in the Southeastern Pampa Plain of Argentina. Water samples (lakes, streams, spring water and groundwater) for hydrochemical and stable isotopic determination were collected and the main physical–chemical parameters were measured. The combination of stable isotope data with hydrogeochemical techniques was used for the identification of sources and preferential recharge areas to these aquatic ecosystems which allowed the explanation of the lake water origin. The hydrochemical processes which explain Los Padres Lake water chemistry are evaporation from groundwater, CO₂ input, calcite dissolution, Na⁺ release by Ca²⁺ and Mg²⁺ exchange, and sulfate reduction. The model that best aligns with La Brava Lake hydrochemical constraints includes: mixing, CO₂ and calcite dissolution, cationic exchange with Na⁺ release and Mg²⁺ adsorption, and to a lesser extent, Ca/Na exchange. This model suggests that the fractured aquifer contribution to this water body is greater than 50 %. An isotopic-specific fingerprint for each lake was identified, finding a higher evaporation rate for La Brava Lake compared to Los Padres Lake. Isotopic data demonstrate the importance of these shallow lakes as recharge areas to the regional aquifer, becoming areas of high groundwater vulnerability. The Tandilia Range System, considered in many hydrogeological studies as the impermeable bedrock of the Pampean aquifer, acts as a fissured aquifer in this area, contributing to low salinity waters and with a fingerprint similar to groundwater isotopic composition.     

Geochemical,isotopic and hydrological mass balance approaches to constrain the lake water–groundwater interaction in Dal Lake,Kashmir Valley

It is important to have qualitative as well as quantitative understanding of the hydraulic exchange between lake and groundwater for effective water resource management. Dal, a famous urban fresh water lake, plays a fundamental role in social, cultural and economic dynamics of the Kashmir Valley. In this paper geochemical, isotopic and hydrological mass balance approaches are used to constrain the lake water–groundwater interaction of Dal Lake and to identify the sources of lake water. Water samples of precipitation (n = 27), lake water (n = 18) and groundwater (n = 32) were collected across the lake and its catchment for the analysis of δ¹⁸O and δ²H. A total of 444 lake water samples and 440 groundwater samples (springs, tube wells and dug wells) were collected for the analysis of Ca²⁺, Mg²⁺, HCO₃ ^?, SO₄ ^2?, Cl^?, NO₃ ^?, Na⁺ and K⁺. Water table and lake water level were monitored at 40 observation locations in the catchment. Water table map including pH and EC values corroborate and verify the gaining nature of the Dal Lake. Stable isotopes of lake water in Boddal and Gagribal basins showed more deviation from the global meteoric water line than Hazratbal and Nigeen basins, indicating the evaporation of lake water. The isotopic and geochemical mass balance suggested that groundwater contributes a significant proportion (23–40%) to Dal Lake. The estimated average groundwater contribution to Dal Lake ranged from 31.2 × 10³ to 674 × 10³ m³ day^?1 with an average of 276 × 10³ m³ day^?1. The study will be useful to delineate the possible sources of nutrients and pollutants entering the lake and for the management of lake water resources for sustainable development.     

Stable isotopic compositions of Recent freshwater cyanobacterial carbonates from the British Isles: local and regional environmental controls

Recent (<50 years old) freshwater cyanobacterial carbonates from diverse environments (streams, lakes, waterfalls) throughout Britain and Ireland were analysed for their stable carbon and oxygen isotope compositions. The mean δ¹⁸O value of ?5–9‰ PDB for river and stream data represents calcite precipitation in equilibrium with the mean oxygen isotopic composition of precipitation in central Britain (?7–5‰SMOW) assuming a mean water temperature of 9°C. The mean δ¹⁸O of lake data, ?4–5‰ PDB, is statistically different, reflecting the effects of residence time and/or variations in the oxygen isotopic composition of rainfall. Carbon isotopes have wide variations in both fluviatile and lake data sets (+ 3 to ?12‰ PDB). These variations are principally controlled in the fluviatile samples by contribution of isotopically light ‘soil zone’ carbon relative to isotopically heavier carbon from limestone aquifer rock dissolution. Lake samples have the heaviest carbon isotope values, reflecting a trend toward isotopic equilibrium between atmospheric CO₂ and aqueous HCO^?₃. We infer that isotopic compositions of ancient cyanobacterial carbonates should also record environmental information, although the effects of stabilization and diagenesis on primary δ¹⁸O values will need careful consideration. Primary carbon isotope compositions should be well preserved, although in marine samples values will be buffered by the isotopic composition of aqueous marine bicarbonate.     

Investigating hydraulic connections and the origin of water in a mine tunnel using stable isotopes and hydrographs

Turquoise Lake is a water-supply reservoir located north of the historic Sugarloaf Mining district near Leadville, Colorado, USA. Elevated water levels in the reservoir may increase flow of low-quality water from abandoned mine tunnels in the Sugarloaf District and degrade water quality downstream. The objective of this study was to understand the sources of water to Dinero mine drainage tunnel and evaluate whether or not there was a direct hydrologic connection between Dinero mine tunnel and Turquoise Lake from late 2002 to early 2008. This study utilized hydrograph data from nearby draining mine tunnels and the lake, and stable isotope (δ¹⁸O and δ²H) data from the lake, nearby draining mine tunnels, imported water, and springs to characterize water sources in the study area. Hydrograph results indicate that flow from the Dinero mine tunnel decreased 26% (2006) and 10% (2007) when lake elevation (above mean sea level) decreased below approximately 3004 m (approximately 9855 feet). Results of isotope analysis delineated two meteoric water lines in the study area. One line characterizes surface water and water imported to the study area from the western side of the Continental Divide. The other line characterizes groundwater including draining mine tunnels, springs, and seeps. Isotope mixing calculations indicate that water from Turquoise Lake or seasonal groundwater recharge from snowmelt represents approximately 10% or less of the water in Dinero mine tunnel. However, most of the water in Dinero mine tunnel is from deep groundwater having minimal isotopic variation. The asymmetric shape of the Dinero mine tunnel hydrograph may indicate that a limited mine pool exists behind a collapse in the tunnel and attenutates seasonal recharge. Alternatively, a conceptual model is presented (and supported with MODFLOW simulations) that is consistent with current and previous data collected in the study area, and illustrates how fluctuating lake levels change the local water-table elevation which can affect discharge from the Dinero mine tunnel without physical transfer of water between the two locations.     

Thermal springs,fumaroles and gas vents of continental Yemen: Their relation with active tectonics,regional hydrology and the country’s geothermal potential

Most thermal springs of continental Yemen (about 65 emergences at 48 sampling sites) and a couple of fumaroles and boiling water pools have been sampled and analyzed for chemical and isotopic composition in the liquid phase and the associated free-gas phase. Whatever the emergence, all the water discharges have an isotopic signature of meteoric origin. Springs seeping out from high altitudes in the central volcanic plateau show a prevalent Na–HCO₃-composition, clearly affected by an anomalous flux of deep CO₂ deriving from active hydrothermal systems located in the Jurassic Amran Group limestone sequence and/or the Cretaceous Tawilah Group, likely underlying the 2000–3000 m thick volcanic suite. At lower elevations, CO₂ also affects the composition of some springs emerging at the borders of the central volcanic plateau.     

Volcanic degassing at Somma–Vesuvio (Italy) inferred by chemical and isotopic signatures of groundwater

A geochemical model is proposed for water evolution at Somma–Vesuvio, based on the chemical and isotopic composition of groundwaters, submarine gas emission and chemical composition of the dissolved gases. The active degassing processes, present in the highest part of the volcano edifice, strongly influence the groundwater evolution. The geological–volcanological setting of the volcano forces the waters infiltrating at Somma–Vesuvio caldera, enriched in volcanic gases, to flow towards the southern sector to an area of high pCO₂ groundwaters. Reaction path modelling applied to this conceptual model, involving gas–water–rock interaction, highlights an intense degassing process in the aquifer controlling the chemical and isotopic composition of dissolved gases, total dissolved inorganic C (TDIC) and submarine gas emission. Mapping of TDIC shows a unique area of high values situated SSE of Vesuvio volcano with an average TDIC value of 0.039 mol/L, i.e., one order of magnitude higher than groundwaters from other sectors of the volcano. On the basis of TDIC values, the amount of CO₂ transported by Vesuvio groundwaters was estimated at about 150 t/d. This estimate does not take into account the fraction of gas loss by degassing, however, it represents a relevant part of the CO₂ emitted in this quiescent period by the Vesuvio volcanic system, being of the same order of magnitude as the CO₂ diffusely degassed from the crater area.     

Carbon and Oxygen Isotopic Composition of Surface‐Sediment Carbonate in Bosten Lake (Xinjiang,China) and its Controlling Factors

Bosten Lake is a mid-latitude lake with water mainly supplied by melting ice and snow in the Tianshan Mountains. The depositional environment of the lake is spatially not uniform due to the proximity of the major inlet and the single outlet in the western part of the lake. The analytical results show that the carbon and oxygen isotopic composition of recent lake sediments is related to this specific lacustrine depositional environment and to the resulting carbonate mineralogy. In the southwestern lake region between the Kaidu River inlet and the Kongqi River outlet, carbon isotope composition (δ13C) values of the carbonate sediment (?1‰ to ?2‰) have no relation to the oxygen isotope composition of the carbonate (δ18O) values (?7‰ to ?8‰), with both isotopes showing a low variability. The carbonate content is low (<20%). Carbonate minerals analyzed by X-ray diffraction are mainly composed of calcite, while aragonite was not recorded. The salinity of the lake water is low in the estuary region as a result of the Kaidu River inflow. In comparison, the carbon and oxygen isotope values are higher in the middle and eastern parts of the lake, with δ13C values between approximately +0.5‰ and +3‰, and δ18O values between ?1‰ and ?5‰. There is a moderate correlation between the stable oxygen and carbon isotopes, with a coefficient of correlation r of approximately 0.63. This implies that the lake water has a relatively short residence time. Carbonate minerals constitute calcite and aragonite in the middle and eastern region of the lake. Aragonite and Mg–calcite are formed at higher lake water salinity and temperatures, and larger evaporation effects. More saline lake water in the middle and eastern region of the lake and the enhanced isotopic equilibrium between water and atmospheric CO2 cause the correlating carbon and oxygen isotope values determined for aragonite and Mg–calcite. Evaporation and biological processes are the main reasons for the salinity and carbonate mineralogy influence of the surface-sediment carbonate in Bosten Lake. The lake water residence time and the CO2 exchange between the atmosphere and the water body control the carbon and oxygen isotope composition of the carbonate sediment. In addition, organic matter pollution and decomposition result in the abnormally low carbon isotope values of the lake surface-sediment carbonate.     

Quantification of the water balance and hydrogeological processes of groundwater–lake interactions in the Pampa Plain, Argentina

This paper gives an account of the assessment and quantification of the water balance and the hydrogeological processes related to lake–groundwater interaction in the Pampa Plain by using hydrogeochemical, isotopic and flow numerical modeling techniques. La Salada is a permanent shallow lake, with an area of 5.8 km², located on the SE of Buenos Aires Province. A total of 29 lake water samples and 15 groundwater samples were collected for both hydrochemical analysis and environmental stable isotope determination. Water table depths were measured in wells closed to the lake. Groundwater samples appear grouped on the Local Meteoric Water Line, suggesting a well-mixed system and that rainfall is the main recharge source to the aquifer. Water evaporation process within La Salada is also corroborated by its isotopic composition. The model that best adjusts to La Salada Lake hydrochemical processes includes evaporation from groundwater, calcite precipitation with CO₂ release and cationic exchange. The annual water balance terms for the lake basin indicates for each hydrological component the following values: 1.16 E⁰⁸ m³ rainfall, 8.15 E⁰⁷ m³ evapotranspiration, 1.90 E⁰⁶ m³ runoff, 1.55 E⁰⁷ m³ groundwater recharge, 6.01 E⁰⁶ m³ groundwater discharge to the lake, 9.54 E⁰⁶ m³ groundwater discharge to the river, 5.00 E⁰⁵ m³ urban extraction and 4.90 E⁰⁶ m³ lake evaporation. Integrated analysis of hydrochemical and isotopic information helped to calibrate the groundwater flow model, to validate the conceptual model and to quantitatively assess the basin water balance.     

Rapid Alkalization in Lake Inawashiro, Fukushima, Japan: Implications for Future Changes in the Carbonate System of Terrestrial Waters

The global carbon cycle, one of the important biogeochemical cycles controlling the surface environment of the Earth, has been greatly affected by human activity. Anthropogenic nutrient loading from urban sewage and agricultural runoff has caused eutrophication of aquatic systems. The impact of this eutrophication and consequent photosynthetic activity on CO₂ exchange between freshwater systems and the atmosphere is unclear. In this study, we focused on how nutrient loading to lakes affects their carbonate system. Here, we report results of surveys of lakes in Japan at different stages of eutrophication. Alkalization due to photosynthetic activity and decreases in PCO₂ had occurred in eutrophic lakes (e.g., Lake Kasumigaura), whereas in an acidotrophic lake (Lake Inawashiro) that was impacted by volcanic hot springs, nutrient loading was changing the pH and carbon cycling. When the influence of volcanic activity was stronger in the past in Lake Inawashiro, precipitation of volcanic-derived iron and aluminum had removed nutrients by co-precipitation. During the last three decades, volcanic activity has weakened and the lake water has become alkalized. We inferred that this rapid alkalization did not result just from the reduction in acid inputs but was also strongly affected by increased photosynthetic activity during this period. Human activities affect many lakes in the world. These lakes may play an important part in the global carbon cycle through their influence on CO₂ exchange between freshwater and the atmosphere. Biogeochemical changes and processes in these systems have important implications for future changes in aquatic carbonate systems on land.     

Estimating groundwater inflow and leakage outflow for an intermontane lake with a structurally complex geology: Georgetown Lake in Montana,USA

Stable isotopes of the water molecule (δ¹⁸O and δD) for groundwater, lake water, streams, and precipitation were coupled with physical flux measurements to investigate groundwater–lake interactions and to establish a water balance for a structurally complex lake. Georgetown Lake, a shallow high-latitude high-elevation lake, is located in southwestern Montana, USA. The lake is situated between two mountain ranges with highlands primarily to the east and south of the lake and a lower valley to the west. An annual water balance and (δ¹⁸O and δD) isotope balance were used to quantify annual groundwater inflows of 2.5?×?10⁷ m³/year and lake leakage outflows of 1.6?×?10⁷ m³/year. Roughly, 57% of total inflow to the lake is from groundwater, and 37% of total outflow at Georgetown Lake is groundwater. Stable isotopes of groundwater and springs around the lake and surrounding region show that the east side of the lake contains meteoric water recharged annually from higher mountain sources, and groundwater discharge to the lake occurs through this region. However, springs located in the lower western valley and some of the surrounding domestic wells west of the lake show isotopic enrichment indicative of strong to moderate evaporation similar to Georgetown Lake water. This indicates that some outflowing lake water recharges groundwater through the underlying west-dipping bedrock in the region.     

Terrestrial and freshwater carbonates in Hoxnian interglacial deposits, UK: micromorphology, stable isotopic composition and palaeoenvironmental significance

MIS 11 is often considered to be the best climatic analogue for the Holocene. Many studies have suggested, however, that it is a period of extreme climate warmth comparable in temperatures to the Middle and Late Pliocene. In Britain deposits of the Hoxnian interglacial are correlated to MIS 11 and multi-proxy techniques can be used to reconstruct the climate of this interglacial. Soil, groundwater and freshwater carbonates are common in Hoxnian deposits and the stable isotopic composition of these precipitates can be used to increase our understanding of MIS 11 environments in Britain. Carbonates from Marks Tey, Clacton, Swanscombe, Elveden and West Stow are studied, the stratigraphic context of which indicates that their formation is broadly synchronous (in the mid-Hoxnian, pollen zones Ho II to Ho III). The carbon isotopic composition of groundwater and pedogenic carbonates is typically depleted with respect to δ¹³C (ca −9 to −8‰ VPDB) reflecting uptake of plant respired CO₂ during water migration/recharge. The carbon isotopic composition of lacustrine carbonate is more enriched with respect to δ¹³C (ca 0-1‰VPDB) reflecting the equilibration of lake waters with atmospheric CO₂. The δ¹⁸O of groundwater and pedogenic carbonates is slightly more enriched than modern soil carbonates but not as enriched as soil carbonates formed under interglacials that were warmer than the Holocene (i.e. the Cromerian). The stable isotopic composition of Hoxnian carbonates does not, therefore, indicate that this interglacial was characterised by uniquely warm climates in the context of other Middle Pleistocene interglacials and the Holocene. This is contrary to many marine and littoral records from around the world but consistent with environmental records from Britain and Europe.     

Geochemistry and stable isotope composition of the Berkeley pit lake and surrounding mine waters,Butte, Montana

Samples of mine water from Butte, Montana were collected for paired geochemical and stable isotopic analysis. The samples included two sets of depth profiles from the acidic Berkeley pit lake, deep groundwater from several mine shafts in the adjacent flooded underground mine workings, and the acidic Horseshoe Bend Spring. Beginning in July-2000, the spring was a major surface water input into the Berkeley pit lake. Vertical trends in major ions and heavy metals in the pit lake show major changes across a chemocline at 10–20 m depth. The chemocline most likely represents the boundary between pre-2000 and post-2000 lake water, with lower salinity, modified Horseshoe Bend Spring water on top of higher salinity lake water below. Based on stable isotope results, the deep pit lake has lost approximately 12% of its initial water to evaporation, while the shallow lake is up to 25% evaporated. The stable isotopic composition of SO₄ in the pit lake is similar to that of Horseshoe Bend Spring, but differs markedly from SO₄ in the surrounding flooded mine shafts. The latter is heavier in both δ³⁴S and δ¹⁸O, which may be due to dissolution of hypogene SO₄ minerals (anhydrite, gypsum, barite) in the ore deposit. The isotopic and geochemical evidence suggests that much of the SO₄ and dissolved heavy metals in the deep Berkeley pit lake were generated in situ, either by leaching of soluble salts from the weathered pit walls as the lake waters rose, or by subaqueous oxidation of pyrite on the submerged mine walls by dissolved Fe(III). Laboratory experiments were performed to contrast the isotopic composition of SO₄ formed by aerobic leaching of weathered wallrock vs. SO₄ from anaerobic pyrite oxidation. The results suggest that both processes were likely important in the evolution of the Berkeley pit lake.     

洞庭湖湖区降水-地表水-地下水同位素特征

为探明洞庭湖湖区水体稳定同位素时间和空间上的变化规律,弄清各水体间的相互关系,分别在2012年4月和8月对区域内具有代表性的采样点进行了地表水和地下水的采样。通过对样品进行D、18O同位素分析,结合全球大气降水同位素监测网（GNIP）公布的1988—1992年间长沙降水同位素数据,发现湖区年内受不同盛行风影响,降水及地表水的同位素存在较大的季节性差异,4月份同位素富集,8月份贫化。此外,河水、湖水同位素也呈现明显的空间差异。两个时期地表水的水线斜率均小于当地降水线,地表水在两个时期均存在蒸发作用。虽然地表水和地下水的来源均为大气降水,但与地表水相比,地下水同位素季节变化较小,地下水接受地表水补给是一个较为长期的过程。     

Using Mg Isotopes to Trace Cyanobacterially Mediated Magnesium Carbonate Precipitation in Alkaline Lakes

This study assesses the potential use of Mg isotopes to trace Mg carbonate precipitation in natural waters. Salda Lake (SW Turkey) was chosen for this study because it is one of the few modern environments where hydrous Mg carbonates are the dominant precipitating minerals. Stromatolites, consisting mainly of hydromagnesite, are abundant in this lake. The Mg isotope composition of incoming streams, groundwaters, lake waters, stromatolites, and hydromagnesite-rich sediments were measured. Because Salda Lake is located in a closed basin, mass balance requires that the Mg isotopic offset between Lake Salda water and precipitated hydromagnesite be comparable to the corresponding offset between Salda Lake and its water inputs. This is consistent with observations; a ??²⁶Mg offset of 0.8?C1.4??? is observed between Salda Lake water and it is the incoming streams and groundwaters, and precipitated hydromagnesite has a ??²⁶Mg 0.9?C1.1??? more negative than its corresponding fluid phase. This isotopic offset also matches closely that measured in the laboratory during both biotic and abiotic hydrous Mg carbonate precipitation by cyanobacteria (Mavromatis, V., Pearce, C., Shirokova, L. S., Bundeleva, I. A., Pokrovsky, O. S., Benezeth, P. and Oelkers, E.H.: Magnesium isotope fractionation during inorganic and cyanobacteria-induced hydrous magnesium carbonate precipitation, Geochim. Cosmochim. Acta, 2012a. 76, 161?C174). Batch reactor experiments performed in the presence of Salda Lake cyanobacteria and stromatolites resulted in the precipitation of dypingite (Mg₅(CO₃)₄(OH)₂·5(H₂O)) and hydromagnesite (Mg₅(CO₃)₄(OH)₂·4H₂O) with morphological features similar to those of natural samples. Concurrent abiotic control experiments did not exhibit carbonate precipitation demonstrating the critical role of cyanobacteria in the precipitation process.     

Deuterium composition and flow path analysis as additional calibration targets to calibrate groundwater flow simulation in a coastal wetlands system

A conceptual model of the Lake Warden coastal wetlands system, Western Australia, was developed using hydraulic, chemical and stable isotopic data, and formed the basis for a groundwater flow model using the finite element numerical code (FEFLOW). The system to be modeled is complex. The surface water and groundwater within the wetlands system show varying salinity and isotopic composition over short distances and time frames. As a first step, the flow model was calibrated to observed groundwater levels measured since 2001 for both steady state and transient stresses. Particle tracking analysis was conducted to test the source areas of water discharging to the lakes within the wetlands system. The analysis was able to delineate the connectivity between the lakes in the wetland and the flow path. Enrichment of isotopic concentration is evident along a NE–SW transect and the data set provides a means for calibrating a detailed transport model. The study incorporates the varying deuterium composition of the water bodies directly into a transport model and a good match between observed and simulated temporal variations along the transect indicates that the model closely simulated the dynamics of water exchange between the lakes and groundwater within the system.     

The combined use of Sr/Sr and carbon and water isotopes to study the hydrochemical interaction between groundwater and lakewater in mantled karst

The hydrochemical interaction between groundwater and lakewater influences the composition of water that percolates downward from the surficial aquifer system through the underlying intermediate confining unit and recharges the Upper Floridan aquifer along highlands in Florida. The ⁸⁷Sr/⁸⁶Sr ratio along with the stable isotopes, D, ¹⁸O, and ¹³C were used as tracers to study the interaction between groundwater, lakewater, and aquifer minerals near Lake Barco, a seepage lake in the mantled karst terrane of northern Florida. Upgradient from the lake, the ⁸⁷Sr/⁸⁶Sr ratio of groundwater decreases with depth (mean values of 0.71004, 0.70890, and 0.70852 for water from the surficial aquifer system, intermediate confining unit, and Upper Floridan aquifer, respectively), resulting from the interaction of dilute oxygenated recharge water with aquifer minerals that are less radiogenic with depth. The concentrations of Sr²⁺ generally increase with depth, and higher concentrations of Sr²⁺ in water from the Upper Floridan aquifer (20–35 μg/L), relative to water from the surficial aquifer system and the intermediate confining unit, result from the dissolution of Sr-bearing calcite and dolomite in the Eocene limestone. Dissolution of calcite [δ¹³C = −1.6 permil (%o)] is also indicated by an enriched δ¹³C_DIC(-8.8 to -11.4% o) in water from the Upper Floridan aquifer, relative to the overlying hydrogeologic units (δ¹³C_DIC < -16%o).

Groundwater downgradient from Lake Barco was enriched in ¹⁸O and D relative to groundwater upgradient from the lake, indicating mixing of lakewater leakage and groundwater. Downgradient from the lake, the ⁸⁷Sr/⁸⁶Sr ratio of groundwater and aquifer material become less radiogenic and the Sr²⁺ concentrations generally increase with depth. However, Sr²⁺ concentrations are substantially less than in upgradient groundwaters at similar depths. The lower Sr²⁺ concentrations result from the influence of anoxic lakewater leakage on the mobility of Sr²⁺ from clays. Based on results from mass-balance modeling, it is probable that cation exchange plays the dominant role in controlling the ⁸⁷Sr/⁸⁶Sr ratio of groundwater, both upgradient and downgradient from Lake Barco. Even though groundwater from the three distinct hydrogeologic units displays considerable variability in Sr concentration and isotopic composition, the dominant processes associated with the mixing of lakewater leakage with groundwater, as well as the effects of mineral-water interaction, can be ascertained by integrating the use of stable and radiogenic isotopic measurements of groundwater, lakewater, and aquifer minerals.     

Using multiple environmental methods to estimate groundwater discharge into an arid lake (Dakebo Lake,Inner Mongolia,China)

It is important to have both a qualitative and quantitative understanding of the hydraulic exchange between groundwater and surface water to support the development of effective management plans for sustainable use of water resources. Groundwater is a major source of surface-water recharge and plays an important role in maintaining the integrity of ecosystems, especially within wetlands in semi-arid regions. The Ordos Desert Plateau of Inner Mongolia (China) is a vulnerable ecosystem that suffers from an extreme lack of water. The hydraulic exchange between groundwater and lake water in Dakebo Lake (the largest of hundreds of lakes on the Ordos Desert Plateau) was evaluated using multiple environmental methods. Continuous monitoring of the groundwater and lake-water levels indicated that the lake was recharged vertically by groundwater. Application of hydrodynamic and temperature tracing methods to the western side of the lake indicated that the rate of groundwater discharge to the lake was about 2?×?10^?6 to 3?×?10^?6 m/s in spring, summer, and autumn, but that there was no recharge in winter because the hypolentic zone (HZ) was frozen. Mixing ratios of groundwater and lake water in the HZ, estimated from the ¹⁸O and ²H ratios, showed that there were spatial variations in the hydrodynamic exchange between groundwater and lake water within the HZ.     

云南程海富营养化过程的碳氧稳定同位素示踪

近500年来程海生物成因碳酸盐δ¹⁸O和δ¹³C及其有机质δ¹³C同位素记录了程海湖泊环境由贫营养到中富营养的演化过程.碳酸盐δ¹⁸O记录显示,大约1690年程海成为封闭湖泊后,当时湖泊贫营养环境并没有发生变化,但造成了湖泊水体交换周期加长,碳酸盐δ¹³C、有机质δ¹³C及其色素含量、碳酸盐含量变化指示湖泊生产力开始增高.1911～1942年碳酸盐δ¹⁸O和δ¹³C及有机质δ¹³C突然显著偏负,表明湖泊生物种群结构发生转变,湖泊初级生产力迅速增加,湖泊由贫营养向中营养转化.湖泊沉积物色素含量及碳酸盐含量变化也记录了这一湖泊环境的转换过程.约1986年以来,随着藻类养殖业及其农业耕作方式的转变,程海水环境渐渐转变成目前的中富营养化状态.     

The impact of gravel extraction on groundwater dependent wetlands and lakes in the Boreal Plains, Canada

The impact of gravel excavation on a groundwater dependent ecosystem (GDE) in a glacial outwash plain was determined using a combination of time-series stable isotopic measurements (??²H and ??¹⁸O) and a numerical flow model of lake?Cgroundwater interaction. Isotopic analyses of the lake and groundwater indicated a shift from a dominance of evaporative enrichment to more meteoric conditions, confirming the hypothesis of increased recharge following forest clearing and gravel extraction from an esker on the outwash plain. The effect of these land-use changes on source water for the GDE was quantified by simulating the lake water budget, seepage, and groundwater conditions for a period spanning pre- and post-mining activity. Enhanced cycling of shallow groundwater, driven by increased recharge in the gravel excavation area, was predicted to cause annual groundwater discharge pulses greater than baseline conditions for the groundwater-fed lake. The additional groundwater discharge represents approximately 4% of the annual lake budget, increasing the flushing rate of the lake. The influence of regional groundwater conditions, represented by variation of water table gradient and outwash hydraulic conductivity, and an alternative excavation location were investigated in a sensitivity analysis. Simulation results illustrate that a simple groundwater capture zone analysis for the GDE could be used to determine a location for gravel excavation that would reduce impact on GDE water source.     

The Correlation of Inorganic C,O Isotopic Values for Lake Chenghai Sediments and Its Environmental Implications

As one of the lakes on the Yunnan-Guizhou plateau, Lake Chenghai, which is a typical closed lake with the precipitation accounting for one-third or more of the annual water input, has a high total salinity (almost like a saline lake). The inorganic C, O isotopic composition of lake sediments bears much sensitive information about environmental change in the catchment, while their correlations revealed the hydrological conditions under which the lake was closed. Their compositional variations are controlled by temperature, precipitation, photosynthesis, dissolving equilibrium of the carbonate system and hydrological condition. According to our research on inorganic C, O isotopic composition of Lake Chenghai sediments, we investigated the environmental change of this catchment several decades ago. The results showed that Lake Chenghai has kept good hydrological closing conditions in the past several decades, as indicated by the good correlation of inorganic C, O isotopic composition of sediments; and that the environmental change in this catchment shows a tendency of periodical evolution on a 10⁻¹¹-years scale, although the signal noise is relatively high at the bottom of the sediment core. And we also can extend C, O isotopes, a sensitive environmental indicator, to nearly saline lake environments with a high degree of mineralization.