Future use of tritium in mapping pre-bomb groundwater volumes

The tritium input to groundwater, represented as volume-weighted mean tritium concentrations in precipitation, has been close to constant in Tucson and Albuquerque since 1992, and the decrease in tritium concentrations at the tail end of the bomb tritium pulse has ceased. To determine the future usefulness of tritium measurements in southwestern North America, volume-weighted mean tritium levels in seasonal aggregate precipitation samples have been gathered from 26 sites. The averages range from 2 to 9 tritium units (TU). Tritium concentrations increase with site latitude, and possibly with distance from the coast and with site altitude, reflecting local ratios of combination of low-tritium moisture advected from the oceans with high-tritium moisture originating near the tropopause. Tritium used alone as a tool for mapping aquifer volumes containing only pre-bomb recharge to groundwater will become ambiguous when the tritium in precipitation at the end of the bomb tritium pulse decays to levels close to the analytical detection limit. At such a time, tritium in precipitation from the last one to two decades of the bomb pulse will become indistinguishable from pre-bomb recharge. The threshold of ambiguity has already arrived in coastal areas with a mean of 2 TU in precipitation and will follow in the next three decades throughout the study region. Where the mean tritium level is near 5 TU, the threshold will occur between 2025 and 2030, given a detection limit of 0.6 TU. Similar thresholds of ambiguity, with different local timing possible, apply globally.     

Infiltration of river water to a shallow aquifer investigated with H/He, noble gases and CFCs

Noble gas isotopes (³He, ⁴He, Ne, Ar, Kr, Xe), tritium (³H), chlorofluorocarbons (CFCs) and dissolved oxygen (O₂) were seasonally measured in a small groundwater system recharged by infiltration of river water at Linsental, northeastern Switzerland. All Groundwater samples contained an excess of atmospheric noble gases (‘excess air’) usually with an elemental composition equal to air. The concentrations of atmospheric noble gases in the groundwater were used to calculate the excess air component and the water temperature at recharge. The noble gas temperatures (NGTs) in the boreholes close to the river vary seasonally, however, the average NGT of all samples lies close to the mean annual temperature of the river water. Groundwater ages were calculated using the tritium/helium-3 (³H/³He) dating method. The water ages of the samples obtained near the river depend on the amount of recently infiltrated river water and are young during times of active river discharge. In contrast, the mean water age of about 3 years of the deep aquifer remained nearly constant over the sampling period. The observed CFC-11 (CFCl₃) and CFC-12 (CF₂Cl₂) concentrations are significantly higher than the atmospheric equilibrium concentrations and therefore CFCs do not provide any direct information on the residence time of the groundwater. Nevertheless, the CFC excess in the groundwater shows a linear increase with the ³H/³He age. Additionally, both accumulation of radiogenic He (⁴He_rad) and O₂ consumption are strongly correlated with residence time. All these correlations can be interpreted either in terms of mixing of recently infiltrated river water with older groundwater or in terms of accumulation/consumption rates.     

Tritium in ground water of the georgia piedmont: Implications for recharge and flow paths

Environmental tritium was measured in 33 natural water samples representative of precipitation, stream runoff, and groundwater (derived principally from production wells) within the Georgia Piedmont Province. Major ion analyses were used to assist in the interpretation of the tritium results. Tritium concentrations were significantly greater within shallow groundwater derived from the regolith (28–34 TU) and stream runoff (25–30 TU) than within recent rainfall (4–17 TU). Based upon the decay-corrected tritium input function, this probably indicates that at least some of the shallow water is stored within the regolith for a period of approximately 25 years. A ‘post-bomb’ component of recharge was present in all groundwater derived from production wells in the study area. Groundwater sampled from the bedrock aquifers was commonly less tritiated than either stream runoff or shallow water stored in the regolith. the lower tritium concentrations May, have resulted from the mixing of ‘pre-bomb’ water stored within the fractures or the transitional zone directly above the bedrock and modern water stored in the shallow regolith. the preponderance of modern water provides evidence that groundwater flow paths are areally restricted within this setting, probably confined to local surface water drainage basins. the residence time of groundwater in the Piedmont is limited by the lack of deep, gravity-driven regional flow and the localized vertical flow induced by pumping. the results of this study indicate that relatively small tritium concentration variations (10-20 TU) May, have regional hydrological significance in the southeastern Piedmont Province and similar settings.     

Isotope hydrological study of mean transit times in an alpine basin (Wimbachtal, Germany)

Measurements of tritium and ¹⁸O concentrations in precipitation and runoff were used to provide further insight into the groundwater storage properties of the Wimbachtal Valley, a catchment area of 33.4 km², extending between 636 and 2713 m a.s.l. in the Berchtesgaden Alps. The catchment includes three aquifer types: a dominant porous aquifer; a fractured dolomite; a karstic limestone aquifer. Employing a simple hydrological model, information about mean transit times of environmental tracers is derived for the groundwater runoff component and several karst springs from the application of the exponential and dispersion flow models to the isotopic input and output data. The mean transit times calculated from a dispersion model with transit times of 4.1 years for ¹⁸O and 4.2 years for tritium, which agree well, allow calculation of total (mobile + stagnant) groundwater storage volume, which is equivalent to 6.6 m of water depth. Direct runoff appears negligible as in many other cases.     

用氚讨论中国西部新疆干旱区的水循环率

Tritium concentrations are used to trace water circulation in the Urumqi and Turfan basins in the Xinjiang, western China. Tritium analyses were made for 77 water samples of river waters, groundwaters, spring waters, lake waters and glacier ice collected in summers in 1992 and 1994. The tritium concentrations in the waters are in a wide range from 0 to 125 TU, most of which are considerably high compared with those of most waters in Japan, because tritium levels in precipitation in the area are over ten times as high as those in Japan. River waters originating in glacier regions contain melt glacier, the proportion of which is over 0.5 to river water. The mean resi-dence time of circulating meteoric water in the mountain regions is estimated to be about 15 years. Most groundwaters and spring waters in the flat regions are mainly derived from river waters originating in glacier regions. The groundwater of greatest tritium concentrations in wells in Urumqi City is derived from Urumqi River about 25 years ago. It takes several ten years for river water to pass the underground to many springs. Some groundwaters and spring waters have taken a long time more than 40 years to travel under the ground. Enrichment of tritium in lake water by evaporation is considered to estimate the contribution of groundwater flow to the recharge of lake. Various contributions of groundwater to lakes are inferred for the various type of salinity in closed or semi-closed lakes. The inflow rates of groundwater to salt lakes are small as against fresh water lakes.     

Chloride,hydrochemical and isotope methods of groundwater recharge estimation in eastern Mediterranean areas: a case study in Jordan

Jordan is classified as an arid to semi‐arid country with a population according to 1999 estimates of 4·8 millions inhabitants and a growth rate of 3·4%. Efficient use of Jordan's scarce water is becoming increasingly important as the urban population grows. This study was carried out within the framework of the joint European Research project ‘Groundwater recharge in the eastern Mediterranean’ and describes a combined methodology for groundwater recharge estimation in Jordan, the chloride method, as well as isotopic and hydrochemical approaches. Recharge estimations using the chloride method range from 14 mm year^?1 (mean annual precipitation of 500 mm) for a shallow and stony soil to values of 3·7 mm year^?1 for a thick desert soil (mean annual precipitation of 100 mm) and values of well below 1 mm year^?1 for thick alluvial deposits (mean annual rainfall of 250 mm). Isotopically, most of the groundwater in the Hammad basin, east Jordan, falls below the global meteoric water line and far away from the Mediterranean meteoric water line, suggesting that the waters are ancient and were recharged in a climate different than Mediterranean. Tritium levels in the groundwater of the Hammad basin are less than the detection limit (<1·3 TU). However, three samples in east Hammad, where the aquifer is unconfined, present tritium values between 1 and 4 TU. Copyright © 2007 John Wiley & Sons, Ltd.     

Isotopic characteristics of precipitation in Slovenia and Croatia: Comparison of continental and maritime stations

The stable isotopic composition of hydrogen and oxygen (δ²H and δ¹⁸O) and tritium activity (³H) were monitored in monthly precipitation at two continental stations (Ljubljana, Zagreb) and six stations along the eastern Adriatic coasts of Slovenia and Croatia in the period 2001–2003. Mean air temperatures and amount of precipitation were also recorded.

Distinct differences in both meteorological and isotopic data between the continental and maritime stations were observed. Seasonal variations in δ¹⁸O are smaller at the maritime stations than at the continental ones due to smaller seasonal temperature variations. A good correlation between δ¹⁸O and δ²H was obtained for each station, and the local meteoric water lines are close to the Global Meteoric Water Line, with a decreasing trend of slope for the south-Adriatic stations. Good correlations between δ¹⁸O in monthly precipitation and mean monthly air temperature were observed at all stations. The slope of δ¹⁸O vs. T varied between 0.37‰ °C⁻¹ and 0.15‰ °C⁻¹. Mean ³H activity and seasonal variation of ³H activity are smaller at maritime stations than at continental ones. Additionally, ³H activity decreases in the NW–SE direction of the Adriatic coast.

The study of spatial variations over this relatively small area rich in geographical and climatic diversities showed the complexity of the isotopic composition of precipitation and the isotopic data obtained for eight stations, most of them in the karstic area along the Adriatic coast, and gave valuable information for regional hydrological investigations and modelling of isotope variability over the Mediterranean basin.     

The water balance of a small lake using stable isotopes and tritium

A small maar lake, known as the Blue Lake, set in a karstic region of southeastern Australia, provides the municipal water supply for a population of 20,000. The lake has a volume of 3.6·10⁷m³, of which 10–15% is pumped from it each year. The lake is recharged almost entirely from groundwater and the main objective of this study was to estimate the total groundwater inflow and outflow rates. Estimation of groundwater throughflow in a lake is difficult to assess using classical hydrological techniques and an alternative method involving measurement of the concentrations of the environmental isotopes ³H, ¹⁸O, ²H and ¹⁴C in the lake water and in the recharging groundwater was used to establish the lake-water balance. The water-balance calculations indicated a total groundwater inflow to Blue Lake of between 5.0·10⁶ and 6.5·10⁶m³yr.⁻¹, corresponding to a residence time of water in the lake of 6 yr. It was not possible to derive the relative proportions of inflow to the lake from the two possible source aquifers, using these isotopes, because their concentrations did not show a sufficiently large contrast to distinguish the two water sources.     

Tritium in the Dead Sea

Tritium data in the Dead Sea for the period 1960–1979 are given. Tritium levels have increased until 1965 in the upper layers of the Dead Sea reaching a level of 170 TU, in response to the atmospheric buildup of tritium from thermonuclear testing. The levels have been decreasing ever since, both because of rapidly declining atmospheric concentrations of tritium and because of mixing of the surface layers with tritium deficient, deeper water masses. The depth of penetration of the tracer delineated the depth of meromictic stratification and successfully monitored the deepening of the pycnocline, until the overturn in 1979 homogenised the entire tritium profile. Modelling the changing tritium inventory over this period showed the predominance of the direct exchange across the air/sea interface, both in the buildup of tritium in the lake and also in its subsequent removal from it. The good fit between calculated and measured tritium inventories confirmed the evaporation estimate of 1.46 m/yr (the mean value for the period) with a precision unattained by other methods.     

Residence times in river basins as determined by analysis of long-term tritium records

The US Geological Survey has maintained a network of stations to collect samples for the measurement of tritium concentrations in precipitation and streamflow since the early 1960s. Tritium data from outflow waters of river basins draining 4500–75000 km² are used to determine average residence times of water within the basins. The basins studied are the Colorado River above Cisco, Utah; the Kissimmee River above Lake Okeechobee, Florida; the Mississippi River above Anoka, Minnesota; the Neuse River above Streets Ferry Bridge near Vanceboro, North Carolina; the Potomac River above Point of Rocks, Maryland; the Sacramento River above Sacramento, California; the Susquehanna River above Harrisburg, Pennsylvania. The basins are modeled with the assumption that the outflow in the river comes from two sources—prompt (within-year) runoff from precipitation, and flow from the long-term reservoirs of the basin. Tritium concentration in the outflow water of the basin is dependent on three factors: (1) tritium concentration in runoff from the long-term reservoir, which depends on the residence time for the reservoir and historical tritium concentrations in precipitation; (2) tritium concentrations in precipitation (the within-year runoff component); (3) relative contributions of flow from the long-term and within-year components. Predicted tritium concentrations for the outflow water in the river basins were calculated for different residence times and for different relative contributions from the two reservoirs. A box model was used to calculate tritium concentrations in the long-term reservoir. Calculated values of outflow tritium concentrations for the basin were regressed against the measured data to obtain a slope as close as possible to 1. These regressions assumed an intercept of zero and were carried out for different values of residence time and reservoir contribution to maximize the fit of modeled versus actual data for all the above rivers. The final slopes of the fitted regression lines ranged from 0.95 to 1.01 (correlation coefficient > 0.96) for the basins studied. Values for the residence time of waters within the basins and average relative contributions of the within-year and long-term reservoirs to outflow were obtained. Values for river basin residence times ranged from 2 years for the Kissimmee River basin to 20 years for the Potomac River basin. The residence times indicate the time scale in which the basin responds to anthropogenic inputs. The modeled tritium concentrations for the basins also furnish input data for urban and agricultural settings where these river waters are used.     

Tracing anthropogenically driven groundwater discharge into a coastal lagoon from southern Brazil

We investigated the distribution of naturally occurring geochemical tracers (²²²Rn, ²²³Ra, ²²⁴Ra, ²²⁶Ra, CH₄, δ¹⁸O, and δ²H) in the water column and adjacent groundwater of Mangueira Lagoon as proxies of groundwater discharge. Mangueira Lagoon is a large (90 km long), shallow (4–5 m deep), fresh, and non-tidal coastal lagoon in southern Brazil surrounded by extensively irrigated rice plantations and numerous irrigation canals. We hypothesized that the annual, intense irrigation for rice agriculture creates extreme conditions that seasonally change groundwater discharge patterns in the adjacent lagoon. We further supposed that dredging of irrigation canals alters groundwater fluxes.

While the activities of ²²²Rn in shallow groundwater were 2–3 orders of magnitude higher than in surface water, CH₄ and radium isotopes were only 1 order of magnitude higher. Therefore, ²²²Rn appears to be the preferred groundwater tracer in this system. Radon concentrations and conductivities were dramatically higher near the pump house of rice irrigation canals, consistent with a groundwater source. Modeling of radon inventories accounting for total inputs (groundwater advection, diffusion from sediments, and decay of ²²⁶Ra) and losses (atmospheric evasion, horizontal mixing and decay) indicated that groundwater advection rates in the irrigation canals (25 cm/d) are over 2 orders of magnitude higher than along the shoreline (0.1 cm/d). Nearly 75% of the total area of the canals is found in the southern half of the lagoon, where groundwater inputs seem to be higher as also indicated by methane and stable isotope trends. In spite of the relatively small area of the canals, we estimate that they contribute nearly 70% of the total (57,000 m³/d) groundwater input into the entire Mangueira Lagoon. We suggest that the dredging of these canals cut through aquitards which previously restricted upward advection from the underlying permeable strata. The irrigation channels may therefore represent an important but previously overlooked source of nutrients and other dissolved chemicals derived from agricultural practices into the lagoon.     

Deduction of groundwater flow regime in a basaltic aquifer using geochemical and isotopic data: The Golan Heights, Israel case study

Groundwater flow-paths through shallow-perch and deep-regional basaltic aquifers at the Golan Heights, Israel, are reconstructed by using groundwater chemical and isotopic compositions. Groundwater chemical composition, which changes gradually along flow-paths due to mineral dissolution and water–rock interaction, is used to distinguish between shallow-perched and deep-regional aquifers. Groundwater replenishment areas of several springs are identified based on the regional depletion in rainwater δ¹⁸O values as a function of elevation (−0.25‰ per 100 m). Tritium concentrations assist in distinguishing between pre-bomb and post-bomb recharged rainwater.

It was found that waters emerging through the larger springs are lower in δ¹⁸O than surrounding meteoric water and poor in tritium; thus, they are inferred to originate in high-elevation regions up to 20 km away from their discharge points and at least several decades ago. These results verify the numerically simulated groundwater flow field proposed in a previous study, which considered the geological configuration, water mass balance and hydraulic head spatial distribution.     

Hydrochemical and stable isotope evidence for the extent and nature of the effective Chalk aquifer of north Norfolk, UK

In eastern England the Chalk aquifer is covered by extensive Pleistocene deposits which influence the hydraulic conditions and hydrochemical nature of the underlying aquifer. In this study, the results of geophysical borehole logging of groundwater temperature and electrical conductivity and depth sampling for major ion concentrations and stable isotope compositions (δ¹⁸O and δ²H) are interpreted to reveal the extent and nature of the effective Chalk aquifer of north Norfolk. It is found that the Chalk aquifer can be divided into an upper region of fresh groundwater, with a Cl concentration of typically less than 100 mg l⁻¹, and a lower region of increasingly saline water. The transition between the two regions is approximately 50 m below sea-level, and results in an effective aquifer thickness of 50–60 m in the west of the area, but less than 25 m where the Eocene London Clay boundary is met in the east of the area. Hydrochemical variations in the effective aquifer are related to different hydraulic conditions developed in the Chalk. Where the Chalk is confined by low-permeability Chalky Boulder Clay, isotopically depleted groundwater (δ¹⁸O less than −7.5‰) is present, in contrast to those areas of unconfined Chalk where glacial deposits are thin or absent (δ¹⁸O about −7.0‰). The isotopically depleted groundwater is evidence for groundwater recharge during the late Pleistocene under conditions when mean surface air temperatures are estimated to have been 4.5°C cooler than at the present day, and suggests long groundwater residence times in the confined aquifer. Elevated molar Mg:Ca ratios of more than 0.2 resulting from progressive rock-water interaction in the confined aquifer also indicate long residence times. A conceptual hydrochemical model for the present situation proposes that isotopically depleted groundwater, occupying areas where confined groundwater dates from the late Pleistocene, is being slowly modified by both diffusion and downward infiltration of modem meteoric water and diffusive mixing from below with an old saline water body.     

The rates of tritium input to the world oceans

Mean annual rates of tritium input into the ocean averaged over 5° latitude bands are presented for the major oceans, for the period 1952–1975. The rates are obtained by converting tritium concentrations in marine precipitation into net oceanic tritium input, by means of a hydrological model. The tropospheric tritium pattern is specified on the basis of available observations, and climatological means from the literature are used for the rates of evaporation and precipitation and for the relative humidity in ship's height, that enter the model. Tritium input by water vapor exchange exceeds that by precipitation about three-fold. Tritium input by river runoff and by net tropospheric tritium outflow from the continents is also accounted for. This contribution is small except for the northern Indian Ocean and the North Atlantic.The inputs have hemispheric maxima near 50° latitude. The northern hemisphere inputs were strongly peaked in 1963–1964, whereas temporal changes in the southern hemisphere were much more gradual. By 1972, about 75% of the total oceanic input had been received by the northern ocean. For the Pacific, the computed total input agrees with the actual tritium inventory within the limits of uncertainty (about ±20%). The global tritium inventory is estimated at 1.9 GCi in 1972, which corresponds to an average tritium yield of 0.9 kg tritium per megaton TNT equivalent of nuclear fusion.     

The impact of freshwater and wastewater irrigation on the chemistry of shallow groundwater: a case study from the Israeli Coastal Aquifer

Differences in the impact of irrigation with freshwater versus wastewater on the underlying shallow groundwater quality were investigated in the Coastal Aquifer of Israel. Seven research boreholes were drilled to the top-most 3–5 m of the saturated zone (the water table region-WTR) in the agricultural fields. The unsaturated zone and the WTR below the irrigated fields consist mainly of clayey sands, while the main aquifer comprises mainly of calcareous sandstones and sands. We show that the salinity and composition of the groundwater at the WTR are highly variable over a distance of less than 1 km and are controlled by the irrigating water and the processes in the overlying unsaturated zone. Tritium data in this groundwater (4.6 tritium units (TU)) support that these water are modern recharge. The water at the WTR is more saline and has a different chemical composition relative to the overlying irrigation water. High SAR values (sodium adsorption ratio) in wastewater irrigation lead to absorption of Na⁺ onto the clay and release of Ca²⁺ into the recharging water, resulting in low Na/Cl (0.4 compared to 1.2 in the wastewater) and high Ca/Cl ratios. In contrast, in the freshwater-irrigated field the irrigation water pumped from the aquifer (Na/Cl=0.9; SAR=0.6) is modified into Na-rich groundwater (Na/Cl=2.0) due to reverse base-exchange reactions. The high NO₃ concentration (>100 mg/l) in the WTR below both fields is derived from the agricultural activities. In the freshwater field, the source of NO₃ is fertilizer leachates, whereas in the wastewater field, where less fertilizers are applied, nitrate is probably derived from nitrification of the NH₄ in the wastewater. Some of the original inorganic nitrogen in the wastewater is consumed by the agricultural plants, resulting in a lower inorganic-N/Cl ratio in the WTR as compared to that in the wastewater. This study demonstrates the important role of the composition of irrigation water, combined with lithology and land use, in determining the quality of the water that recharge the aquifer below agricultural fields.     

BIBLIOGRAPHY / BIBLIOGRAPHIE

Summary

In 1958 the U.S. Geological Survey and the U.S. Weather Bureau jointly conducted a study of tritium fallout distribution over the continental United States, Alaska, and Puerto Rico. The observation period extended from early April to late July in most areas. While this was insufficient to cover the decay side of the curve, it was sufficiently long to establish general trends of tritium activity contours. Tritium activities were found to be maximum in the north central part of the country and minimum in coastal areas. The tritium activities show an inverse correlation with chloride concentrations in precipitation. Tritium activities in precipitation appear to be influenced by several “low altitude effects” particularly in storms of brief duration. Ground level tritium activity measurements are not directly representative of tritium in cloud moisture because of these effects.     

Environmental tracer transport (H and SF6) in the saturated and unsaturated zones and its use in nitrate pollution management

An important quantity in groundwater protection is the residence time of water in an aquifer. It relates to both the travel time of a pollutant to arrive at a well and the time span required for self-purification of a polluted aquifer after removal of pollutant inputs. Time scales for aquifers can be gained from artificial tracer experiments or from environmental tracer data, the latter offering the only realistic alternative if time scales of years or decades have to be taken into account.

Different tracers show different time scales due to their different transport mechanisms especially in the unsaturated zone. While solute tracers are moved advectively with the seepage water, gas tracers pass the unsaturated zone diffusively through the air phase. Depending on the properties of the unsaturated zone (hydraulic properties, thickness) this difference in behavior can be used to separate the subsurface transport process into the unsaturated and the saturated parts.

In a field study in Germany, SF₆ and ³H were used as environmental tracers. Both have a relatively well-known input function. Interpretation of data from observation wells by a box model approach led to spatially and temporally varying residence times. This was an indication that the influence of the unsaturated zone could not be neglected. While the gas tracer SF₆ shows only residence times in the saturated zone, the tracer ³H reflects the whole travel time of water including both the unsaturated and saturated zones. Using a one-dimensional plug-flow model for the unsaturated zone combined with a detailed two-dimensional flow and transport model for the saturated zone leads to a holistic and consistent interpretation of the measured tracer concentrations. The observed pattern of old water under thick loess cover and younger water under areas where the fractured basalt aquifer crops out is reproduced after adjusting only two parameters: the effective porosity of the saturated aquifer and the product of field capacity and thickness of the unsaturated zone. While the effective porosity of the saturated zone is adjusted by means of the SF₆ data, the field capacity of the loess layer is adjusted by means of the ³H observations. The thickness of the unsaturated zone is deduced from geological and pedological maps. All flow data are obtained from a calibrated flow model, which is based on geological data, observed heads and pumping tests only.

The transport model for the saturated zone was calibrated by fitting the porosity by means of gaseous tracer concentrations (SF₆). The combined saturated–unsaturated zone model was then calibrated by fitting the field capacity of the unsaturated zone by means of ³H concentrations. With this model it was possible to verify the observed NO₃ concentrations at the drinking water wells and to develop predictions for their future development under various scenarios of fertilizer input reduction in specific areas.     

Tritium in the Arctic Ocean and East Greenland Current

High concentrations of tritium are found in the surface water of the Arctic Ocean (up to 50 TU) and in the East Greenland Current (up to 70 TU). These high tritium values are a direct result of atmospheric testing of nuclear weapons in the early 1960's. A box model with a time-dependent input of highly tritiated precipitation predicts that high tritium concentrations are to be expected in the surface layer of the Arctic Ocean and its various outflows. We suggest that a few tritium stations in the Arctic Ocean would provide a powerful analytical tool for assigning time scales to exchange processes.     

Using chlorofluorocarbons (CFCs) and tritium to improve conceptual model of groundwater flow in the South Coast Aquifers of Laizhou Bay,China

The southern coastal plain of Laizhou Bay, which is the area most seriously affected by salt water intrusion in north China, is a large alluvial depression, which represents one of the most important hydrogeological units in the coastal region of northern China. Chlorofluorocarbons (CFCs, including CFC‐11, CFC‐12 and CFC‐113) and tritium were used together for dating groundwater up to 50 years old in the study area. There are two cones of depression, caused by intensive over‐exploitation of fresh groundwater in the south and brine water in the north. The assigned CFC apparent ages for shallow groundwater range from 8 a to >50 a. A binary mixing model based on CFC‐113 and CFC‐12 concentrations in groundwater was used to estimate fractions of young and pre‐modern water in shallow aquifers and to identify groundwater mixing processes during saltwater intrusion. Discordance between concentrations of different CFC compounds indicate that shallow groundwater around the Changyi cone of depression is vulnerable to contamination. Pumping activities, CFC contamination, mixing and/or a large unsaturated zone thickness (e.g. >20 m) may be reasons for some groundwater containing CFCs without tritium. Saline intrusion mainly occurs because of large head gradients between fresh groundwater in the south and saline water bodies in the north, forming a wedge of saline water below/within fresh aquifer layers. Both CFC and tritium dates indicate that the majority of the saline water is from >50 a, with little or no modern seawater component. Based on the distribution of CFC apparent ages, tritium contents plus chemical and physical data, a conceptual model of groundwater flow along the investigated Changyi‐Xiaying transect has been developed to describe the hydrogeological processes. Three regimes are identified from south to north: (i) fresh groundwater zone, with a mixing fraction of 0.80–0.65 ‘young’ water calculated with the CFC binary mixing model (groundwater ages <34 a) and 1.9–7.8TU of tritium; (ii) mixing zone characterized by a mixing fraction of 0.05–0.65 young groundwater (ages of 23–44 a), accompanied by local vertical recharge and upward leakage of older groundwater; and (iii) salt water zone, mostly comprising waters with ages beyond the dating range of both CFCs and tritium. Some shallow groundwater in the north of the Changyi groundwater depression belongs to the >50a water group (iii), indicating slow velocity of groundwater circulation and possible drawing in of saline or deep groundwater that is tracer‐free. Copyright © 2012 John Wiley & Sons, Ltd.     

Isotopic study of alluvial groundwaters,south-west lockyer valley,queensland, australia

The isotopic chemistry of alluvial groundwaters from two adjacent valleys are described and hydrological processes within related aquifers are identified as evidenced by oxygen-¹⁸, deuterium, tritium and chloride data. A plot of δ¹⁸O against δD values reveals isotopic enrichment of the groundwater by the recycling of spray irrigation water. A plot of tritium versus chloride concentrations displays separate linear correlations for alluvial groundwaters within the two valleys. The salinity has a common source, therefore the separate correlations are interpreted as the past transfer of low salinity groundwater from the alluvial aquifers in one valley to the underlying sandstone aquifers.