Ground surface temperature history in southern Canada: Temperatures at the base of the Laurentide ice sheet and during the Holocene

We use temperature profiles from 7 deep (≈ 2000 m) boreholes located in southern Canada to infer ground surface temperature histories (GSTH) during the Last Glacial Maximum (LGM) and the Holocene. Visual inspection of the heat flow and of the reduced temperature depth profiles reveals significant regional differences with some sites showing conspicuous signs of post glacial warming, and other indicating only very small changes in ground surface temperature. These differences are confirmed by the inversions of the temperature profiles. The most prominent variations in GST are found at the Sudbury, Ontario, sites where the present ground surface temperature is high. With the exception of Sept-Iles, Quebec, the other sites only show moderate or no variation in GST. For all the sites, except possibly Sept-Iles, temperatures at the base of the ice sheet during the LGM were at or slightly below the melting point of ice. Temperatures might have been lower, a few degrees below 0 °C, at Sept-Iles. These results are consistent with field observations and model predictions suggesting high velocity basal flows in the ice sheet above the studied regions. These new data on basal temperatures will provide better quantitative constraints on glacier flow dynamics. The inversions give a chronology for the retreat of the ice sheet comparable to other proxies. Inversion and direct modeling show that, following the ice retreat, there was a warm period between 2 and 5 ka with temperatures 1–2 K higher than present. The inversion yields a time for this episode 1–2 kyr more recent than that inferred by other proxies for the Holocene climate optimum (HCO).     

Environmental isotopes as indicators for ground water recharge to fractured granite

To assess the contribution of accumulated winter precipitation and glacial meltwater to the recharge of deep ground water flow systems in fracture crystalline rocks, measurements of environmental isotope ratios, hydrochemical composition, and in situ parameters of ground water were performed in a deep tunnel. The measurements demonstrate the significance of these ground water recharge components for deep ground water flow systems in fractured granites of a high alpine catchment in the Central Alps, Switzerland. Hydrochemical and in situ parameters, as well as delta(18)O in ground water samples collected in the tunnel, show only small temporal variations. The precipitation record of delta(18)O shows seasonal variations of approximately 14% and a decrease of 0.23% +/- 0.03% per 100 m elevation gain. delta(2)H and delta(18)O in precipitation are well correlated and plot close to the meteoric water line, as well as delta(2)H and delta(18)O in ground water samples, reflecting the meteoric origin of the latter. The depletion of 18O in ground water compared to 18O content in precipitation during the ground water recharge period indicates significant contributions from accumulated depleted winter precipitation to ground water recharge. The hydrochemical composition of the encountered ground water, Na-Ca-HCO3-SO4(-F), reflects an evolution of the ground water along the flowpath through the granite body. Observed tritium concentrations in ground water range from 2.6 to 16.6 TU, with the lowest values associated with a local negative temperature anomaly and anomalous depleted 18O in ground water. This demonstrates the effect of local ground water recharge from meltwater of submodern glacial ice. Such localized recharge from glaciated areas occurs along preferential flowpaths within the granite body that are mainly controlled by observed hydraulic active shear fractures and cataclastic faults.     

Isotopes and sustainability of ground water resources, North China Plain

Ground water in deep confined aquifers is one of the major water resources for agricultural, industrial, and domestic uses in the North China Plain. Detailed information on ground water age and recharge is vital for the proper management of these water resources, and to this end, we used carbon 14 of dissolved inorganic carbon and tritium in water to measure the age and determine the recharge areas of ground water in the North China Plain. These isotopic data suggest that most ground water in the piedmont part of the North China Plain is <40 years old and is recharged locally. In contrast, ground water in the central and littoral portions of the North China Plain is 10,000 to 25,000 years old. The delta18O (deltaD) values of this ground water are 1.7 per thousand (11 per thousand) less than that in the piedmont plain ground water and possibly reflect water recharged during a cooler climate during the last glaciation. The temperature of this recharge, based on delta18O values, ranges from 3.7 degrees C to 8.4 degrees C, compared to 12 degrees C to 13 degrees C of modern recharge water. The isotopic data set combined indicates that ground water in the central and littoral part of the North China Plain is being mined under non-steady state conditions.     

Ground water recharge and flow characterization using multiple isotopes

Stable isotopes of delta(18)O, delta(2)H, and (13)C, radiogenic isotopes of (14)C and (3)H, and ground water chemical compositions were used to distinguish ground water, recharge areas, and possible recharge processes in an arid zone, fault-bounded alluvial aquifer. Recharge mainly occurs through exposed stream channel beds as opposed to subsurface inflow along mountain fronts. This recharge distribution pattern may also occur in other fault-bounded aquifers, with important implications for conceptualization of ground water flow systems, development of ground water models, and ground water resource management. Ground water along the mountain front near the basin margins contains low delta(18)O, (14)C (percent modern carbon [pmC]), and (3)H (tritium units [TU]), suggesting older recharge. In addition, water levels lie at greater depths, and basin-bounding faults that locally act as a flow barrier may further reduce subsurface inflow into the aquifer along the mountain front. Chemical differences in ground water composition, attributed to varying aquifer mineralogy and recharge processes, further discriminate the basin-margin and the basin-center water. Direct recharge through the indurated sandstones and mudstones in the basin center is minimal. Modern recharge in the aquifer is mainly through the broad, exposed stream channel beds containing coarse sand and gravel where ground water contains higher delta(18)O, (14)C (pmC), and (3)H (TU). Spatial differences in delta(18)O, (14)C (pmC), and (3)H (TU) and occurrences of extensive mudstones in the basin center suggest sluggish ground water movement, including local compartmentalization of the flow system.     

Use of NADP archive samples to determine the isotope composition of precipitation: characterizing the meteoric input function for use in ground water studies

Stable oxygen and hydrogen isotopes have been used in ground water studies to investigate recharge, mixing, ground water/surface water interaction, advective-diffusive transport, paleohydrogeologic interactions and to estimate ground water ages. Such studies require that the isotopic composition of precipitation be known, as precipitation is a major input to ground water and surface water systems. As oxygen-18 and deuterium data for precipitation are lacking across much of the United States, there is need to establish additional local meteoric water lines as isotope input functions across the region, as well as to develop better understanding of the isotopic climate linkages that control oxygen and hydrogen isotope ratios in precipitation. In the absence of long-term monitoring stations, one possible solution to this problem is to determine the delta 18O and delta 2H values of precipitation using archive samples collected at monitoring stations managed by the National Atmospheric Deposition Program (NADP). This study describes and interprets the seasonal delta 18O and delta 2H composition of archived precipitation samples collected in eastern Nebraska near the town of Mead during the years 1992-1994. Values for delta 18O range from -23.6 to -0.7@1000. Values for delta 2H range from -172 to 0@1000. Yearly arithmetic mean delta 18O and delta 2H values for the Mead station are -8.1@1000 and -53@1000, respectively. Weighted yearly means for delta 18O and delta 2H were -7.4@1000 and -48@1000, respectively. Mead values show a strong isotopic enrichment between winter and summer precipitation, and a strong delta 18O-T correlation (r2 = 0.91) for mean monthly values of about 0.5@1000 per degree Celsius. The local meteoric water line for the Mead site is delta 2H = 7.40 delta 18O + 7.32. Deuterium excess values suggest that most of the moisture across the region is derived primarily from a Gulf of Mexico source. The results of this study demonstrate that in the absence of long-term monitoring stations such as those operated globally by the International Atomic Energy Association, NADP archive samples can be used to determine the isotopic composition of precipitation, to characterize the local meteoric water line and establish the various climatic relationships, and define the meteoric input function for use in ground water studies.     

Stable isotopic records of the glacial deep-water properties in the South China Sea

Based on the oxygen and carbon stable isotopic records of benthic foraminifera in nine deep-sea cores of the South China Sea (SCS), the bathymetric profiles of δ¹⁸O and δ¹³C since the last glacial maximum (LGM) are preliminarily established. The bathymetric gradients of deep-water δ¹⁸O and δ¹³C in the SCS are obviously greater during the LGM than during the Holocene, showing the existence of the deep thermocline and nutricline at water depth of about 2 000 m. Particularly, the differences in δ¹⁸O and δ¹³C between the LGM and Holocene, from which the ice-volume effect and the global mean shift have been subtracted respectively, are positive values at water depths of 1 000–2 500 m in the SCS. This indicates the existence of deep-water mass with relatively cool temperature or higher salinity, better ventilation and more δ¹³C within the water depth range of the SCS during the LGM, which is distinctly different from that at present. These changes further confirm the existence of the glacial “North Pacific Deep Water” which, however, is possibly confined to the water depth range of 1 000–2 500 m. Project supported by the National Natural Science Foundation of China (Grant Nos. 49576286 and 49732060).     

Implications of ground water chemistry and flow patterns for earthquake studies

Ground water can facilitate earthquake development and respond physically and chemically to tectonism. Thus, an understanding of ground water circulation in seismically active regions is important for earthquake prediction. To investigate the roles of ground water in the development and prediction of earthquakes, geological and hydrogeological monitoring was conducted in a seismogenic area in the Yanhuai Basin, China. This study used isotopic and hydrogeochemical methods to characterize ground water samples from six hot springs and two cold springs. The hydrochemical data and associated geological and geophysical data were used to identify possible relations between ground water circulation and seismically active structural features. The data for delta18O, deltaD, tritium, and 14C indicate ground water from hot springs is of meteoric origin with subsurface residence times of 50 to 30,320 years. The reservoir temperature and circulation depths of the hot ground water are 57 degrees C to 160 degrees C and 1600 to 5000 m, respectively, as estimated by quartz and chalcedony geothermometers and the geothermal gradient. Various possible origins of noble gases dissolved in the ground water also were evaluated, indicating mantle and deep crust sources consistent with tectonically active segments. A hard intercalated stratum, where small to moderate earthquakes frequently originate, is present between a deep (10 to 20 km), high-electrical conductivity layer and the zone of active ground water circulation. The ground water anomalies are closely related to the structural peculiarity of each monitoring point. These results could have implications for ground water and seismic studies in other seismogenic areas.     

Dynamics and stable isotope composition of gaseous and dissolved oxygen

The vadose zone and ground water environments are a sink for atmospheric O(2). The pathways and rates of O(2) consumption are primarily related to the availability and rate of oxidation of key reductants (e.g., organics, sulfides), through a combination of biological or abiotic reactions. The range in delta(18)O of O(2) in the subsurface is large, from +20 per thousand to +39 per thousand (Vienna Standard Mean Ocean Water) in the vadose zone and from +12 per thousand to +46 per thousand in ground water. The aggregated O(2) isotope fractionation by consumption (alpha(k)) was found to range from 0.970 to 1.300 and 0.980 to 1.030 in vadose zones and aquifers, respectively. These data suggest the delta(18)O patterns in both unsaturated zones and aquifers can be attributed to microbially mediated reactions (alpha(k)= range from 0.975 to 1.000), but there are apparently other inverse isotope fractionating processes (alpha(k) > 1.000). Circumstantial evidence suggested O(2) processed during the sulfide oxidation and precipitation of Fe-oxyhydroxides process (or other unidentified processes) could be the cause of the significant (18)O depletions. Overall, delta(18)O data from vadose zones and ground water revealed that isotope fractionation by consumption of gaseous and dissolved O(2) in the subsurface and ground water environments is more complicated than what has classically been attributed solely to geomicrobial respiration. Given the questions and inexplicable data arising from this study, further detailed research on O(2) consuming processes in the Earth's subsurface and ground water is warranted.     

Sources of ground water salinity on islands using 18O, 2H, and 34S

Stable isotopes of 18O and 2H in water, and 34S and 18O in dissolved SO4, are used to verify the interpretation of the chemical evolution and proposed sources of salinity for two islands that have undergone postglacial rebound. Results for delta18O and delta34S in dissolved SO4 on the Gulf Islands, southwest British Columbia, Canada, suggest a three-component mixing between (1) atmospheric SO4 derived largely from recharge of meteoric origin, (2) modern marine SO4 associated with either modern-day salt water intrusion or Pleistocene age sea water, and (3) terrestrial SO4. The age of the marine SO4 is uncertain based on the geochemistry and SO4 isotopes alone. Two options for mixing of saline ground waters are proposed--either between current-day marine SO4 and atmospheric SO4, or between older (Pleistocene age) marine SO4 and atmospheric SO4, delta18O and delta2H compositions are relatively consistent between both islands, with a few samples showing evidence of mixing with water that is a hybrid mixture of Fraser River water and ocean water. The isotopic composition of this hybrid water is approximately delta18O = 10 per thousand. delta18O and delta2H values for many saline ground waters plot close to the global meteoric water line, which is distinctly different from the local meteoric water line. This suggests a meteoric origin for ground waters that is different from the current isotopic composition of meteoric waters. It is proposed these waters may be late Pleistocene in age and were recharged when the island was submerged below sea level and prior to rebound at the end of the last glaciation.     

Oxidation of fugitive methane in ground water linked to bacterial sulfate reduction

When fugitive methane migrates upward along boreholes of oil and gas wells, it may migrate into shallow ground water or pass through overlying soil to the atmosphere. Prior to this study, there was little information on the fate of fugitive methane that migrates into ground water. In a field study near Lloydminster, Alberta, Canada, we found hydrogeochemical evidence that fugitive methane from an oil well migrated into a shallow aquifer but has been attenuated by dissimilatory bacterial sulfate reduction at low temperature ( approximately 5 degrees C) under anaerobic conditions. Evidence includes spatial and temporal trends in concentrations of methane and sulfate in ground water and associated trends in concentrations of bicarbonate and sulfide. Within 10 m of the oil well, sulfate concentrations were low, and sulfate was enriched in both 34S and 18O. Sulfate concentrations had a strong positive correlation with delta13C values of bicarbonate, and sulfide was depleted in 34S compared to sulfate. These data indicate that bacterial sulfate reduction occurred near the production well. Near the oil well, elevated concentrations of bicarbonate were observed, and the bicarbonate was depleted in 13C. Modeling indicates that the main source of this excess 13C-depleted bicarbonate is oxidized methane. In concert with the sulfate concentration and isotope data, these results support an interpretation that in situ bacterial oxidation of methane has occurred, linked to bacterial sulfate reduction. Bacterial sulfate reduction may play a major role in bioattenuation of fugitive natural gas in ground water in western Canada.     

Spatial and temporal variability of ground water recharge in central Australia: a tracer approach

Two environmental tracer methods are applied to the Ti-Tree Basin in central Australia to shed light on the importance of recharge from floodouts of ephemeral rivers in this arid environment. Ground water carbon-14 concentrations from boreholes are used to estimate the average recharge rate over the interval between where the ground water sample first entered the saturated zone and the bore. Environmental chloride concentrations in ground water samples provide estimates of the recharge rate at the exact point in the landscape where the sample entered the saturated zone. The results of the two tracer approaches indicate that recharge rates around one of the rivers and an extensive floodplain are generally higher than rates of diffuse recharge that occurs in areas of lower topographic relief. Ground water 2H/1H and 18O/16O compositions are all depleted in the heavier isotopes (delta2H = -67 per thousand to -50 per thousand; delta18O = -9.2 per thousand to -5.7%o) compared with the long-term, amount-weighted mean isotopic composition of rainfall in the area (delta2H = -33.8 per thousand; delta18O = -6.3 per thousand). This indicates that recharge throughout the basin occurs only after intense rainfall events of at least 150 to 200 mm/month. Finally, a recharge map is developed to highlight the spatial extent of the two recharge mechanisms. Floodout recharge to the freshest ground water (TDS <1,000 mg/L) is approximately 1.9 mm/year compared with a mean recharge rate of approximately 0.2 mm/year to the remainder of the basin. These findings have important implications for management of the ground water resource.     

Preliminary results of the close-off depth and the stable isotopic records along a 109.91 m ice core from Dome A,Antarctica

A 109.91 m ice core was recovered from Dome A (or Dome Argus), the highest ice feature in Antarctica, during the 2004/05 austral summer by the 21st Chinese National Antarctic Research Expedition (CHINARE-21). Both methane profile along the core and firn densification model calculation suggest that the close-off depth is at about 102.0 m with an ice age about 4200 a. Stable isotopes (δ18O and δD) of the chips samples produced during each run of ice core drilling at Dome A, together with those of the other co...     

Effects of hydrogeological and climate change on the subsurface thermal regime in the Sendai Plain

We estimated the effects of hydrogeological and surface temperature warming on subsurface thermal regime from the temperature-depth profiles and hydrological data of groundwater quality both in the quaternary and tertiary systems in the Sendai Plain as a preliminary step toward reconstruction of climate changes.Annual mean air temperature in the plain has increased about 1.5 °C in the last 70 years and this surface warming resulted in low or negative thermal gradient. However, anomaly of thermal gradient was recognized in not all temperature-depth profiles. Groundwater chemical compositions and stable isotope data (δD and δ¹⁸O) show that the groundwater flow system has marked difference between those of tertiary and quaternary systems. Calculated results of three dimensional groundwater flow and heat transport model ensure the above hypothesis and shows that thermal gradient changes at close to basement of the quaternary system. The differences in groundwater flow systems are expressed as subsurface thermal gradient anomalies in the temperature-depth profiles in the Sendai Plain. Furthermore, one-dimensional numerical analyze including the effect of surface warming indicates that calculated profile has departure from steady state line at depths in 60-80 m agree well with observed one.     

Rock-magnetic proxies of climate change from loess -paleosol sediments of the Czech Republic

Summary Rock-magnetic characteristics of late Pleistocene loess-paleosol sequences in the Czech Republic show patterns of variation that reflect climate-related depositional and diagenetic processes which acted on the sedimentary profiles. Mass-normalized magnetic susceptibility is high in interglacial and interstadial paleosols, while uniformly low values are measured in unweathered loess horizons. Normalized ferrimagnetic susceptibility and anhysteretic remanent magnetization show an enhancement of ultrafine (superparamagnetic, SP) and fine (single-domain, SD, and pseudo-single-domain, PSD) grains in chernozem paleosols correlated with δ¹⁸O substages 5c and 5a as well as in the Holocene soil. The parabraunerde paleosol associated with peak interglacial conditions, correlated with δ¹⁸O substage 5e, shows evidence of diagenetic loss of fine grained magnetic minerals, although coarse (multidomain, MD) grains appear to be preserved. Low temperature remanence behavior plus high temperature susceptibility measurements of representative samples from each lithologic unit indicate that magnetite and maghemite are the dominant magnetic minerals within the sediments. Variations in concentration-independent rock-magnetic parameters are therefore primarily a function of grain size variations through the profile. It is anticipated that with additional magnetic and non-magnetic sedimentological and geochemical tests, a quantitative rock-magnetic — paleoclimate model can be developed for the central European loess region.     

Geochemical tracers to evaluate hydrogeologic controls on river salinization

The salinization of rivers, as indicated by salinity increases in the downstream direction, is characteristic of arid and semiarid regions throughout the world. Historically, salinity increases have been attributed to various mechanisms, including (1) evaporation and concentration during reservoir storage, irrigation, and subsequent reuse; (2) displacement of shallow saline ground water during irrigation; (3) erosion and dissolution of natural deposits; and/or (4) inflow of deep saline and/or geothermal ground water (ground water with elevated water temperature). In this study, investigation of salinity issues focused on identification of relative salinity contributions from anthropogenic and natural sources in the Lower Rio Grande in the New Mexico-Texas border region. Based on the conceptual model of the system, the various sources of water and, therefore, salinity to the Lower Rio Grande were identified, and a sampling plan was designed to characterize these sources. Analysis results for boron (delta(11)B), sulfur (delta(34)S), oxygen (delta(18)O), hydrogen (delta(2)H), and strontium ((87)Sr/(86)Sr) isotopes, as well as basic chemical data, confirmed the hypothesis that the dominant salinity contributions are from deep ground water inflow to the Rio Grande. The stable isotopic ratios identified the deep ground water inflow as distinctive, with characteristic isotopic signatures. These analyses indicate that it is not possible to reproduce the observed salinization by evapotranspiration and agricultural processes alone. This investigation further confirms that proper application of multiple isotopic and geochemical tracers can be used to identify and constrain multiple sources of solutes in complex river systems.     

Development of saline ground water through transpiration of sea water

As vegetation usually excludes salt during water uptake, transpiration will increase the salinity of the residual water. If the source water is sea water, then the residual water may become highly saline. In the unconfined coastal aquifer of the tropical Burdekin River delta, northeastern Australia, areas of highly saline ground water with chloride concentrations up to almost three times that of sea water occur up to 15 km from the present coastline, and are attributed to transpiration by mangrove vegetation during periods of high sea level. Radiogenic ((14)C) carbon isotope analyses indicate that ground water with chloride concentrations between 15,000 and 35,000 mg/L is mostly between 4000 and 6000 years old, at which time sea level was 2 to 3 m higher than present. Stable isotope analyses of oxygen-18 and deuterium show no evidence for evaporative enrichment of this water. Oxygen-18, deuterium, and stable (delta(13)C) carbon isotope analyses of ground water and soil water point to a recharge environment beneath the mangrove forests during this postglacial sea level high stand. During that period, transpiration of the mangrove forests would have led to high chloride concentrations in the residual ground water, without inducing isotopic fractionation. Due to the higher density, this hypersaline water moved downward through the aquifer by gravity and has formed lenses of highly saline ground water at the bottom of the unconfined aquifer.     

Forensic isotope analysis to refine a hydrologic conceptual model

Water resources in the arid southwestern United States are frequently the subject of conflict from competing private and public interests. Legal remedies may remove impasses, but the technical analysis of the problem often determines the future success of legal solutions. In Owens Valley, California, the source of water for the Los Angeles Aqueduct (LAA) is flow diverted from the Owens River and its tributaries and ground water from valley aquifers. Future management of ground water delivered to the LAA needs technical support regarding quantity available, interconnection of shallow and confined aquifers, impact on local springs, and rate of recharge. Ground water flow models and ground water composition are tools already in use, but these have large uncertainty for local interpretations. This study conducted targeted sampling of springs and wells to evaluate the hydrologic system to corroborate conceptual and numerical models. The effort included measurement of intrinsic isotopic composition at key locations in the aquifers. The stable isotopic data of boron (delta(11)B), sulfur (delta(34)S), oxygen (delta(18)O), hydrogen (delta D), and tritium ((3)H) supported by basic chemical data provided rules for characterizing the upper and the lower aquifer system, confirmed the interpretation of ground water flow near faults and flow barriers, and detected hydraulic connections between the LAA and the perennial springs at key locations along the unlined reach of the LAA. This study exemplifies the use of forensic isotopic approaches as independent checks on the consistency of interpretations of conceptual models of a ground water system and the numerical hydrologic simulations.     

Low-temperature opal-CT precipitation in Antarctic deep-sea sediments: evidence from oxygen isotopes

Porcellanite has been found in Antarctic deep-sea sediments of shallow burial depth at four different sites in host sediments younger than 4 Ma. Oxygen isotope analysis shows that the opal-CT samples are extremely rich in¹⁸O (δ¹⁸O= 41.2to44.7‰ rel. SMOW). According to the quartz/water fractionation the calculated isotopic opal-CT formation temperature is in the range of 0 to 4°C. This agrees well with sediment temperature measurements. The low opal-CT precipitation temperature contrasts with current ideas about later diagenetic formation of opal-CT at higher temperatures of 18 to 56°C.     

Characterization of lake water and ground water movement in the littoral zone of Williams Lake,a closed‐basin lake in north central Minnesota

Williams Lake, Minnesota is a closed‐basin lake that is a flow‐through system with respect to ground water. Ground‐water input represents half of the annual water input and most of the chemical input to the lake. Chemical budgets indicate that the lake is a sink for calcium, yet surficial sediments contain little calcium carbonate. Sediment pore‐water samplers (peepers) were used to characterize solute fluxes at the lake‐water–ground‐water interface in the littoral zone and resolve the apparent disparity between the chemical budget and sediment data. Pore‐water depth profiles of the stable isotopes δ¹⁸O and δ²H were non‐linear where ground water seeped into the lake, with a sharp transition from lake‐water values to ground‐water values in the top 10 cm of sediment. These data indicate that advective inflow to the lake is the primary mechanism for solute flux from ground water. Linear interstitial velocities determined from δ²H profiles (316 to 528 cm/yr) were consistent with velocities determined independently from water budget data and sediment porosity (366 cm/yr). Stable isotope profiles were generally linear where water flowed out of the lake into ground water. However, calcium profiles were not linear in the same area and varied in response to input of calcium carbonate from the littoral zone and subsequent dissolution. The comparison of pore‐water calcium profiles to pore‐water stable isotope profiles indicate calcium is not conservative. Based on the previous understanding that 40–50 % of the calcium in Williams Lake is retained, the pore‐water profiles indicate aquatic plants in the littoral zone are recycling the retained portion of calcium. The difference between the pore‐water depth profiles of calcium and δ¹⁸O and δ²H demonstrate the importance of using stable isotopes to evaluate flow direction and source through the lake‐water–ground‐water interface and evaluate mechanisms controlling the chemical balance of lakes. Published in 2003 by John Wiley & Sons, Ltd.     

Carbon biogeochemistry of ground water, Guiyang, southwest China

Variations in the concentrations and isotopic compositions (delta13C(DIC)) of dissolved inorganic carbon (DIC) reflect contamination and biogeochemical cycling of the carbon in ground water. In order to understand contamination and biogeochemical cycling of DIC, we carried out research on the geochemistry of ground water of Guiyang, the capital city of Guizhou Province, China. Results show that ground water is mainly characterized by SO4.HCO3-Ca.Mg and HCO3-Ca.Mg chemical compositions. The hydrochemical characteristics of these types of water are mainly controlled by lithology of the aquifers. HCO3- is the dominant species of DIC in ground water and has lower concentrations and more negative values of delta13C(DIC) in the high-flow (summer monsoon) season, as compared to the low-flow season. This indicates that DIC is relatively enriched in carbon of biological origin in the high-flow season as compared to the low-flow season and that biological activities are the predominant control on shifts of stable carbon isotope values. The evidence that the delta13C(DIC) values of ground water decrease with increasing concentrations of anthropogenic species shows that the carbon isotopic composition of DIC can be a useful tracer of contamination, in addition to biogeochemical cycling of inorganic carbon in ground water. Results from this study show that ground water is impacted by significant levels of contamination from human activities, especially in the urban areas, as well as the northeast and west suburbs, in Guiyang city, southwest China.