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1.
The use of 14C (half-life?=?5,730 years) in modeling the evolution of the 36Cl/Cl ratios in groundwater is reported for the first time. The complexity of the Cl–36Cl system due to the occurrence of different Cl and 36Cl sources and the difficulty of the determination of the initial groundwater 36Cl/Cl ratios have raised concerns about the reliability of using 36Cl (half-life?=?301 thousand years, a) as a groundwater-dating tool. This work uses groundwater 14C age as a calibrating parameter of the Cl–36Cl/Cl decay-mixing models of three wells from the southwestern Great Artesian Basin (GAB), Australia. It aims to allow for the different sources of Cl and 36Cl in the southwestern GAB aquifer. The results show that the initial Cl concentrations range from 245 to 320 mg/l and stable Cl is added to groundwater along flowpaths at rates ranging from 1.4 to 3.5 mg/l/ka. The 36Cl content of the groundwater is assumed to be completely of atmospheric origin. The samples have different Cl–36Cl/Cl mixing-decay models reflecting recharge under different conditions as well as the heterogeneity of the aquifer.  相似文献   

2.
A number of chemical and physical processes inside and outside a sedimentary basin (e.g. evaporite dissolution and topographic drive, respectively) affect groundwater flow near the basin’s margin. Contrasting formations at the margin, typically basinal sedimentary rocks and basement, are host to the interplay between these processes so that groundwater flows and compositions change within a relatively small volume. To interpret how groundwater flow and geochemistry have evolved, interactions between these processes must be understood. Such interactions were investigated near the margin of the East Irish Sea Basin in NW England, by sampling deep groundwaters (to 1500 m below sea level) from Ordovician volcanic basement rocks and Carboniferous to Triassic sedimentary cover rocks. Variable Br/Cl ratios and Cl concentrations in deep saline waters and brines indicate mixing patterns. Variations in 36Cl/Cl constrain the timing of mixing. Relatively low Br/Cl ratios (ca. 1 × 10−3 by mass) characterise brine from the western sedimentary cover and reflect halite dissolution further west. Saline water with relatively high Br/Cl ratios (ca. 2 × 10−3 by mass) of uncertain origin occupies the eastern basement. These two waters mix across the area. However, mixing alone cannot explain variable 36Cl/Cl ratios, which partly reflect differing in situ36Cl production rates in different rock formations. Most 36Cl/Cl ratios in groundwater sampled from the eastern metavolcanic basement (mean = 25 × 10−15) and western sedimentary cover (mean = 10 × 10−15) are at or close to equilibrium with in situ36Cl production. These variations in 36Cl/Cl across the site possibly took >1.5 Ma to be attained, implying that deep groundwater flow responded only slowly to the Quaternary glaciation of the site. Interplay between varied processes in basin marginal settings does not necessarily imply flow instability.  相似文献   

3.
When using 36Cl to date very old groundwater in regional aquifer systems, knowledge of the subsurface 36Cl input into the aquifer system is essential. Although 36Cl can be produced through nuclear reactions in the subsurface, in many situations, the input of 36Cl into sedimentary aquifer systems by this avenue of production can be neglected. This is a valid assumption when investigating long-flowpath groundwater systems composed of sandstones, limestones, and shales of typical composition. These rock types are not sufficiently enriched in radioactive elements to produce significant 36Cl in the deep subsurface. Carbonaceous shales, on the other hand, can concentrate the radioactive elements necessary to produce significant 36Cl in the deep subsurface. Chlorine-36 ratios (36Cl/Cl) for a suite of Late Devonian and Pennsylvanian carbonaceous shales were calculated from bulk-rock chemistry as well as measured using accelerator mass spectrometry. The poor agreement between calculated and measured ratios is the result of the assumption of chemical homogeneity used by the calculation algorithm, an assumption that was not satisfied by the carbonaceous shales. In these shales, organic matter, clay minerals, and accessory minerals are heterogeneously distributed and are physically distinct on a micron-order scale. Although organic matter and clay minerals constitute the overwhelming bulk of the shales, it is the phosphate minerals that are most important in enhancing, and suppressing, 36Cl production. Minerals such as apatite and carbonate-apatite (francolite)—by including uranium, rare earth elements (REEs), and halogens—have an important impact on both neutron production and thermal neutron absorption. By incorporating both uranium and fluorine, phosphate minerals act as neutron production centers in the shale, increasing the probability of 36Cl production. By incorporating REEs and chlorine, phosphate minerals also act to shield 35Cl from the thermal neutron flux, effectively suppressing the production of 36Cl. To reconcile the measured 36Cl ratios with the ratios calculated assuming chemical homogeneity, the shales were artificially split into three fractions: organic, clay mineral, and phosphate mineral. Neutron production was calculated separately for each fraction, and the calculation results demonstrated that the phosphate fraction exerted much more control on the 36Cl ratio than the organic or clay mineral fractions. By varying the uranium and chlorine contents in the phosphate fraction, a new, heterogeneous 36Cl ratio was calculated that agreed with the measured ratio for the overwhelming majority of the carbonaceous shales. When using rock chemistry to calculate the 36Cl ratio, rock types that show mineralogical heterogeneity on a micron scale can be divided into bulk fractions and accessory fractions for separate calculations of neutron production and neutron absorption. In this manner, a more accurate, heterogeneous 36Cl ratio can be calculated for the rock as a whole.  相似文献   

4.
《Applied Geochemistry》1991,6(4):435-445
The36Cl/Cl ratios of 12 groundwater samples from the Milk River aquifer were determined by accelerator mass spectrometry. Using known Cl concentrations,36Cl concentrations were deduced. Approximately linear relations were observed between the logarithm of the36Cl concentration, the Cl concentration, and the distance from the recharge area along two flow paths. The results are discussed in two approaches:
  • (1)in an interpretation of the linear relation between logarithm of the36Cl concentration and Cl concentration excluding and includingin situ production of36Cl;
  • (2)in a diffusion model. The increase of the Cl concentration with the distance from the recharge area is considered to be due to diffusion of Cl from the underlying confining Colorado shale to the aquifer.
Flow velocities ranging between 0.04 and 0.14 m/a, and ages of the groundwater between 0.6 and 2 Ma are obtained at a distance of 80 km from the recharge area.  相似文献   

5.
The gravel aquifer within the Szigetköz Plain in northern Hungary is mainly fed by the infiltration of the Danube River. This infiltration process can be identified using the tritium/helium method to a distance of about 30 km away from the infiltration area of the Danube. In this study, chlorine-36 analyses are used as additional method. This natural radioisotope was also produced by nuclear bomb tests in the atmosphere. It is an ideal, stable constituent for this particular study due to its very long half-life (300,000 years), and consequently acts as an independent check of the established model of aquifer recharge. The chlorine-36 data of the analysed selected groundwater samples of this area clearly show the effect of the atmospheric nuclear bomb tests, with enhanced 36Cl/Cl ratios of up to a factor 10 higher than the unaffected groundwater of the pre-bomb period within the study area. Finally, the observed 36Cl values were introduced into a transport model with dispersion/advection-type flow of groundwater to deduce the transport parameters.  相似文献   

6.
《Applied Geochemistry》2005,20(3):599-609
36Cl produced by thermonuclear bomb testing has been proposed as an additional tool to date or at least to identify recent groundwater components. In order to investigate the behaviour of 36Cl in shallow groundwater a multi-tracer approach (3H/3He, SF6, CFC-12 and 85Kr) was used to characterise and date the groundwater of a quaternary sands aquifer which is located on the Island of Funen near the city of Odense, Denmark. Recharge to the semi-confined shallow aquifer occurs through permeable sand windows and fractured tills at the surface. Locally, however, mixing with older pre-bomb water from the underlying limestone aquifer may occur. The integrated analyses of the available tracer data allowed a well constrained age structure determination of the investigated water system.The 36Cl/Cl ratios measured in groundwater were used to reconstruct the fallout rates for radioactive 36Cl at Odense. The calculated fallout values exceeded the fallout estimated based on data from the Dye-3 ice core in Greenland. Recycling of the bomb peak fallout seems to be the most probable reason of the high values measured. The local extent of this process is difficult to quantify, which impedes the use of 36Cl for dating.  相似文献   

7.
Fifty-three samples, including brines associated with oil and natural gas reservoirs and groundwater samples from deep boreholes, were collected from the Pacific and Japan Sea coastal regions in Japan. The 129I/127I and 36Cl/Cl ratios, and stable isotopes (δD and δ18O) are compared to investigate differences related to the geotectonic settings of the two regions. The δD and δ18O data indicate that brine and groundwater from the Pacific coastal region reflect mixing of meteoric water with connate seawater in the pores of sedimentary rocks. On the other hand, brine and groundwater from the Japan Sea coastal region have been hydrothermally altered. In particular, brines associated with petroleum accumulations at Niigata and Akita showed the same isotopic characteristics as fluids found in the Kuroko deposits of the Green Tuff region in northeastern Japan. There is little difference in the 36Cl/Cl ratios in brine and groundwater from the Pacific and Japan Sea coasts. Most brine and some deep groundwater, except those from the Pleistocene Kazusa Group, have already reached the average secular equilibrium ratio of 9.9 ± 2.7 × 10−15 for their mudstone and sandstone reservoirs. There was no correlation between the 36Cl/Cl ratios and differences in geotectonic setting between the Pacific and the Japan Sea coast. The molar I/Br ratio suggests that the I in all of water samples was of biogenic origin. The average 129I/127I ratio was 290 ± 130 × 10−15 to 294 ± 105 × 10−15 in both regions, showing no relationship to the different geotectonic settings. The uncontaminated brine and groundwater samples are likely to have retained the original 129I/127I ratios of marine I released from the old organic matter stored in sedimentary rock.  相似文献   

8.
《Applied Geochemistry》1993,8(6):643-647
Mazor (1992) has reinterpreted several previous 36Cl studies. The studies he revised used extensive physical hydrogeological data to aid in interpretation of the 36Cl measurements. Major ion chemistry and other isotope tracers were considered in order to evaluate the groundwater geochemistry. The studies then used simple geochemical models to account for Cl behavior in the subsurface. The result of these 36Cl dating studies was in reasonable agreement with both numerical models of the aquifer systems and with independent geochemical studies.Mazor (1992) has reinterpreted these studies based on the assumption that spatial variation in chemical and isotope data should be attributed to unspecified “discontinuities” in the flow regime. The conceptual models of aquifer hydrodynamics resulting from this approach differ radically not only from the previous 36Cl interpretations, but also from the findings of virtually all previous hydrogeological and geochemical investigations. Although Mazor's “reinterpretations” are provocative, he does not show how they explain the data of the numerous previous studies better than the conceptual models presented by the authors of those studies, nor has he demonstrated that his new models are consistent with the fundamental physical laws governing groundwater flow. Until this is satisfactorily accomplished I will continue to prefer the original 36Cl interpretations.  相似文献   

9.
 Chlorine-36 is a radionuclide with a half-life of 3.01×105a. Most 36Cl in the hydrosphere originates from cosmic radiation interacting with atmospheric gases. Large amounts were also produced by testing thermonuclear devices during 1952–58. Because the monovalent anion, chloride, is the most common form of chlorine found in the hydrosphere and because it is extremely mobile in aqueous systems, analyses of both total Cl– as well as 36Cl have been important in numerous hydrologic studies. In almost all applications of 36Cl, a knowledge of the initial, or pre-anthropogenic, levels of 36Cl is useful, as well as essential in some cases. Standard approaches to the determination of initial values have been to: (a) calculate the theoretical cosmogenic production and fallout, which varies according to latitude; (b) measure 36Cl in present-day precipitation and assume that anthropogenic components can be neglected; (c) assume that shallow groundwater retains a record of the initial concentration; (d) extract 36Cl from vertical depth profiles in desert soils; (e) recover 36Cl from cores of glacial ice; and (f) calculate subsurface production of 36Cl for water that has been isolated from the atmosphere for more than one million years. The initial value from soil profiles and ice cores is taken as the value that occurs directly below the depth of the easily defined bomb peak. All six methods have serious weaknesses. Complicating factors include 36Cl concentrations not related to cosmogenic sources, changes in cosmogenic production with time, mixed sources of chloride in groundwater, melting and refreezing of water in glaciers, and seasonal groundwater recharge that does not contain average year-long concentrations of 36Cl. Received, December 1996 · Revised, August 1997 · Accepted, August 1997  相似文献   

10.
Mazor (1992) has reinterpreted several previous 36Cl studies. The studies he revised used extensive physical hydrogeological data to aid in interpretation of the 36Cl measurements. Major ion chemistry and other isotope tracers were considered in order to evaluate the groundwater geochemistry. The studies then used simple geochemical models to account for Cl behavior in the subsurface. The result of these 36Cl dating studies was in reasonable agreement with both numerical models of the aquifer systems and with independent geochemical studies.Mazor (1992) has reinterpreted these studies based on the assumption that spatial variation in chemical and isotope data should be attributed to unspecified “discontinuities” in the flow regime. The conceptual models of aquifer hydrodynamics resulting from this approach differ radically not only from the previous 36Cl interpretations, but also from the findings of virtually all previous hydrogeological and geochemical investigations. Although Mazor's “reinterpretations” are provocative, he does not show how they explain the data of the numerous previous studies better than the conceptual models presented by the authors of those studies, nor has he demonstrated that his new models are consistent with the fundamental physical laws governing groundwater flow. Until this is satisfactorily accomplished I will continue to prefer the original 36Cl interpretations.  相似文献   

11.
Tunnel excavation at Äspö Island, Sweden, has caused severe groundwater disturbance, gradually extending deeper into the tunnel as present-day Baltic seawater intrudes through fractures connecting to the surface. However, the paleo-hydrogeochemical conditions have remained in the deep highly saline waters that have avoided mixing. A correlation has been observed between dissolved 4He concentration and Cl− ion concentration, measured every two years from 1995 to 2001 at Äspö. Groundwater mixing conditions can be examined by the correlations between 1/Cl, 36Cl/Cl, and 3H concentrations. Subsurface production is responsible for the majority of the 36Cl and excess dissolved 4He of interstitial groundwater in fractures. The secular equilibrium ratio of 36Cl/Cl in rock was theoretically estimated to be (5.05 ± 0.82) × 10−14 based on the neutron flux intensity, a value comparable to the measured 36Cl/Cl ratio in rock and groundwater. The degassing crustal 4He flux was estimated to be 2.9 × 10−8  1.3 × 10−6 (ccSTP/cm2a) using the HTO diffusion coefficient for the Äspö diorite. The 4He accumulation rate ranges from 6.8 × 10−10 (for the in situ accumulation rate) to 7.0 × 10−9 (ccSTP/(gwater · a) considering both 4He in situ production and the degassing flux, assuming 4He is accumulated constantly in groundwater. By comparing the subsurface 36Cl increase with 4He concentrations in groundwater, the 4He accumulation rate was determined from data for groundwater arriving at the secular equilibrium of 36Cl/Cl. The 4He accumulation rate was found to be (1.83 ± 0.72) × 10−8 ccSTP/(gwater · a) without determining the magnitude of degassing 4He flux.  相似文献   

12.
《Applied Geochemistry》2001,16(3):291-315
Hydraulic changes caused by tunneling at the Aspo Hard Rock Laboratory (HRL) in Sweden have been investigated over a period of 2a using different hydrochemical approaches, i.e. noble gas content, isotopic measurements and major ion concentrations. The dissolved noble gases (4He and Ne contents, and the ratio of 3He/4He, 40Ar/36Ar), stable isotopes, chemical concentrations of major ions, and 36Cl/Cl ratios, were determined in groundwater samples collected in the tunnel from borehole sections isolated by inflated packers. Groundwater was categorized into 3 groups based on 4He and Cl− contents: undisturbed groundwater (i.e. prior to tunnel construction) with high 4He and Cl− contents, groundwater that has been gradually changed by mixing with Baltic seawater and whose 4He and Cl− contents have gradually increased with increasing depth, and groundwater that has been totally changed due to a rapid mixing of Baltic seawater and/or shallow groundwater and whose 4He and Cl− contents are extremely low compared with other samples collected at the same surrounding depth. The oldest groundwater with a high salinity of more than 14,000 mg l−1 of Cl− is estimated to be more than 1.8 Ma old. The groundwater residence time ranges from 0.9 to 900 Ka in the mixing-zone. Groundwater in the disturbed zone where rapid mixing has occurred is hard to date reliably and its primary hydrochemical character has already been lost.  相似文献   

13.
The natural distribution of 36Cl/Cl in groundwater across the continental United States has recently been reported by Davis et al. (2003). In this paper, the large-scale processes and atmospheric sources of 36Cl and chloride responsible for controlling the observed 36Cl/Cl distribution are discussed.The dominant process that affects 36Cl/Cl in meteoric groundwater at the continental scale is the fallout of stable chloride from the atmosphere, which is mainly derived from oceanic sources. Atmospheric circulation transports marine chloride to the continental interior, where distance from the coast, topography, and wind patterns define the chloride distribution. The only major deviation from this pattern is observed in northern Utah and southern Idaho where it is inferred that a continental source of chloride exists in the Bonneville Salt Flats, Utah.In contrast to previous studies, the atmospheric flux of 36Cl to the land surface was found to be approximately constant over the United States, without a strong correlation between local 36Cl fallout and annual precipitation. However, the correlation between these variables was significantly improved (R 2=0.15 to R 2=0.55) when data from the southeastern USA, which presumably have lower than average atmospheric 36Cl concentrations, were excluded. The total mean flux of 36Cl over the continental United States and total global mean flux of 36Cl are calculated to be 30.5±7.0 and 19.6±4.5 atoms m–2 s–1, respectively.The 36Cl/Cl distribution calculated by Bentley et al. (1986) underestimates the magnitude and variability observed for the measured 36Cl/Cl distribution across the continental United States. The model proposed by Hainsworth (1994) provides the best overall fit to the observed 36Cl/Cl distribution in this study. A process-oriented model by Phillips (2000) generally overestimates 36Cl/Cl in most parts of the country and has several significant local departures from the empirical data.
Resumen Davis et al. (2003) han informado de la distribución natural de la proporción 36Cl/Cl en las aguas subterráneas de la parte continental de los Estados Unidos de América [EUA]. En este artículo, se discute cuáles son los procesos a gran escala y las fuentes atmosféricas del 36Cl y del cloruro que dan lugar a la distribución observada de 36Cl/Cl.El proceso dominante que afecta a la relación 36Cl/Cl en las aguas subterráneas de origen meteórico a escala continental es el aporte de cloruro estable desde la atmósfera, que procede principalmente de los océanos. La circulación atmosférica transporta el cloruro marino hacia el interior, donde la distancia a la costa, topografía y corrientes del viento definen la distribución del cloruro. La única desviación principal de este esquema tiene lugar al norte de Utah y en el sur de Idaho, donde se deduce que existe una fuente continental de cloruro en los Rellanos Salados de Bonneville (Salt Flats).En contraste con estudios previos (Knies et al. 1994; Phillips 2000), se ha descubierto que el flujo atmosférico de 36Cl hacia la superficie terrestre es aproximadamente constante en todos los estados, sin deducirse una correlación fuerte entre el aporte de 36Cl y la precipitación anual. Sin embargo, la correlación entre estas variables se ve mejorada de forma significativa, con coeficientes de regresión comprendidos entre 0,15 y 0,55, cuando se excluyen los datos recogidos en el sudeste de los EUA, que tienen concentraciones de 36Cl atmosférico presuntamente inferiores a la media. El flujo medio total de 36Cl calculado en la zona continental de los Estados Unidos vale 30,5±7,0 átomos por metro cuadrado y segundo, mientras que el flujo total global de 36Cl es de 19,6±4,5 átomos por metro cuadrado y segundo.La distribución de 36Cl/Cl calculada por Bentley et al. (1986) infravalora la magnitud y variabilidad observada en los valores medidos a lo largo de los Estados Unidos. El modelo propuesto por Hainsworth (1994) proporciona el mejor ajuste conjunto a la distribución observada de 36Cl/Cl en este estudio. El modelo orientado a procesos de Phillips (2000) sobreestima por lo general la distribución de 36Cl/Cl en la mayoría del país y difiere significativamente de algunos valores locales empíricos.
Résumé La distribution naturelle du rapport 36Cl/Cl dans les eaux souterraines des États-Unis a été récemment présentée par Davis et al. (2003). Dans ce travail, les processus à grande échelle et les sources atmosphériques de 36Cl et de chlorure responsables du contrôle de la distribution observée du rapport 36Cl/Cl sont discutés. Le processus dominant qui affecte le rapport 36Cl/Cl dans les eaux souterraines dorigine météorique à léchelle continentale est lapport atmosphérique de chlorure stable, qui provient pour lessentiel de sources océaniques. La circulation atmosphérique transporte des chlorures marins vers lintérieur des continents, où la distribution de chlorure est définie par la distance à la côte, la topographie et les régimes des vents. La seule exception majeure à ce schéma est observée dans le nord de lUtah et le sud de lIdaho où lon suppose quil existe une source continentale de chlorure dans les bas-fonds salés de Bonneville. Au contraire de précédentes études (Knies et al. 1994; Phillips 2000), on trouve que le flux atmosphérique de 36Cl vers le sol est approximativement constant sur lensemble des États-Unis, sans forte corrélation entre la retombée locale de 36Cl et les précipitations annuelles. Cependant, la corrélation entre ces variables devient significative (R 2=0.15 à 0.55) lorsquon supprime les données du sud-est des États-Unis, dont on pense quelles présentent des concentrations en 36Cl atmosphérique inférieures à la moyenne. Le flux total moyen de 36Cl sur les États-Unis continentaux et le flux moyen global de 36Cl sont respectivement évalués à 30.5 ± 7.0 et 19.6 ± 4.5 atomes.m–2.s–1. La distribution du rapport 36Cl/Cl calculée par Bentley et al. (1986) sous-estime lordre de grandeur et la variabilité observés pour la distribution mesurée du rapport 36Cl/Cl sur les États-Unis continentaux. Le modèle proposé par Hainsworth (1994) fournit le meilleur ajustement densemble à la distribution du rapport 36Cl/Cl observée dans cette étude. Un modèle orienté vers les processus proposé par Phillips (2000) surestime dans lensemble le rapport 36Cl/Cl dans la plupart des régions du pays et présente plusieurs désaccords locaux avec les données empiriques.
  相似文献   

14.
Chlorine-36 data for groundwater from the Death Valley regional flow system is interpreted in the context of existing conceptual models for regional groundwater flow in southern Nevada. Chlorine-36 end member compositions are defined for both recharge and chemically evolved groundwater components. The geochemical evolution of 36Cl is strongly controlled by water-rock interaction with Paleozoic carbonate rocks that comprise the regional aquifer system, resulting in chemically evolved groundwater that is characteristically low in 36Cl/Cl and high in Cl. Groundwater from alluvial and volcanic aquifers that overlie the regional carbonate aquifer are generally characterized by high 36Cl/Cl and low Cl signatures, and are chemically distinct from water in the regional carbonate aquifer. This difference provides a means of examining vertical transport and groundwater mixing processes. In combination with other geochemical and hydrogeologic data, the end members defined here provide constraints on aquifer residence times and mixing ratios.  相似文献   

15.
New cosmogenic surface-exposure ages of moraine-crest boulders from southwestern Colorado are compared with published surface-exposure ages of boulders from moraine complexes in north-central Colorado and in west-central (Fremont Lake basin) Wyoming. 10Be data sets from the three areas were scaled to a single 10Be production rate of 5.4 at/g/yr at sea level and high latitude (SLHL), which represents the average 10Be production rate for two high-altitude, mid-latitude sites in the western United States (US) and Austria. Multiple nuclide ages on single boulders indicate that this 10Be production rate yields ages comparable to those calculated with a commonly used 36Cl production scheme. The average age and age range of moraine-crest boulders on terminal moraines at the southwestern Colorado and Wyoming sites are similar, indicating a retreat from their positions ∼16.8 36Cl ka (Cosmogenic ages in this paper are labeled 10Be or 36Cl ka or just ka when both 10Be or 36Cl ages are being discussed; radiocarbon ages are labeled 14C ka, calibrated radiocarbon are labeled cal ka, and calendar ages are labeled calendar ka. Errors (±1σ) associated with ages are shown in tables. Radiocarbon ages were calibrated using the data of Hughen et al. (Science 303 (2004) 202). This suggests a near-synchronous retreat of Pinedale glaciers across a 470-km latitudinal range in the Middle and Southern Rocky Mountains. Hypothetical corrections for snow shielding and rock-surface erosion shifts the time of retreat to between 17.2 and 17.5 10Be ka at Pinedale, Wyoming, and between 16.3 and 17.3 36Cl ka at Hogback Mountain, Colorado.  相似文献   

16.
《Applied Geochemistry》1991,6(4):447-464
Analytical data are presented for Cl, Br and I on a regional scale for the Milk River aquifer. The three halides show strikingly similar spatial distributions and are highly correlated. Concentrations are low in the freshwater portions of the aquifer but increase by as much as two orders of magnitude along the margins. However, halide ratios reach nearly constant values moving down-gradient, suggesting the dominance of a common subsurface source for these ions. Ratios of Cl/I and Cl/Br are less than those of seawater and fit an origin derived from the diagenesis of organic matter in the sediments. Halide ratios rule out leakage and/or diffusion from the underlying Colorado Group as a major influence on the chemistry; the favored hypothesis is altered connate seawater diffusing from low-permeability units within the Milk River Formation as the primary source of salts. This hypothesis of an internal source has important implications for solute sources in other aquifers affected by saline waters because it does not require the importation of a distant fluid.The129I/I ratio has a meteoric value in groundwater collected near the recharge area, but ratios for downflow waters are only 8–70% of this value. Due to the 16 Ma half-life of129I, these data indicate that most of the increase in dissolved I cannot derive from concentration of a meteoric source by ion filtration, but must have a subsurface origin. Concentrations of129I producedin situ by spontaneous fission of238U attain measurable levels only in the oldest waters sampled (ages≥ 105a), in which it may account for nearly 90% of the total dissolved129I concentration.Water ages based upon36Cl/Cl data range up to 2 Ma if uncorrected for any dilution by subsurface sources of dead Cl. If one assumes that the subsurface contributions of Cl contribute at least 90% of total Cl in the distal portion, then the36Cl-based ages are reduced to ∼ 1Ma, somewhat greater than those estimated by hydrodynamic modeling.  相似文献   

17.
The radioactive isotope 36Cl, with a half-life of 301 ka, is a valuable chronometer for estimation of groundwater residence time up to 2 millions of years. Aerial thermonuclear fission bomb tests, performed during the late 1950s, injected a massive amount of this isotope into the atmosphere, which exceeded the natural fallout signal. Since this bomb pulse, atmospheric 36Cl deposition tends to return to natural fallout rate. The monitoring of this attenuation can provide a good opportunity to extend the use of this chronometer to shorter time spans. Venice’s lagoon alimentation zone shows groundwaters with residence times distributed over last fifty years. This permits the estimation of a continuous 36Cl deposition curve, free from latitudinal and seasonal variations of the signal. Three old groundwater samples, with residence times comprised in the range −900 to −8000 BP, allow the estimation of a mean natural deposition of 49 at m−2 s−1 and are in good agreement with 36Cl fallout observed for the last 40,000 years by (Plummer et al., 1997). For the bomb pulse period, a fallout of 5300 at m−2 s−1 was calculated. This was followed by a strong attenuation period, taking place until the 1980s, during which the fallout reached values ranging between 167 and 354 at m−2 s−1. The attenuation reached then a plateau: it experienced a slower lowering until the actual deposition, with fallout values calculated between 124 and 252 at m−2 s−1. This persistence of high deposition rate was classically attributed to biological and atmospherical recycling processes or underestimation of the natural atmospheric production of the 36Cl. Additional source of 36Cl production has been envisaged through the activation of chlorine radicals from stratospherical CFCs, leading to a 36Cl production rate comparable with that of Ar spallation from the first approximation. Lastly, the latitudinal factor of the attenuation of the fallout rate is discussed and the impact of the jet streams is proposed as an explanation for the discrepancies in the attenuation rate.  相似文献   

18.
 The sustainability of community water supplies drawn from shallow aquifers in the arid southwest of the Northern Territory has been evaluated using the radioactive isotope chlorine-36 (36Cl). These aquifers include fractured sandstones of the Ngalia Basin, fractured metamorphic rocks and Cainozoic sands and gravels. 36Cl/Cl ratios for these shallow, regional groundwaters exhibit a bimodal distribution with peaks at 205 (±7) and 170 (±7)×10–15. The higher ratio probably represents modern (Holocene) recharge, diluted with windblown salts from local playa lakes, and occurs mostly around the margin of the basin. The lower ratio corresponds to a 36Cl "age", or mean residence time, of 80–100 ka, implying that the last major recharge occurred during the last interglacial interval (Oxygen Isotope Stage 5). These values are mainly observed in the interior of the Ngalia Basin. Lower values of the 36Cl/Cl ratio measured near playa lakes are affected by addition of chloride from remobilised salts. Finite carbon-14 (14C) data for the groundwaters are at variance with the 36Cl results, but a depth profile suggests low recharge, allowing diffusion of recent atmospheric carbon to the water table. The 36Cl results have important implications for groundwater management in this region, with substantial recharge only occurring during favourable, wet, interglacial climatic regimes; most community water supplies are dependent on these "old" waters. Received, September 1997 · Revised, August 1998, March 1999 · Accepted, March 1999  相似文献   

19.
《Applied Geochemistry》1999,14(7):917-925
The origin of salinity within the Äspö groundwater system is investigated by combining interpretations of conservative dissolved ions and of stable isotope ratios in water. The interpretation concludes that the groundwater salinity results from a mixing between Baltic Sea water intrusion and a deep seated saline groundwater of marine origin. This conclusion supports the geochemical model developed for the Äspö site. The residence time of the deep salinity is assessed by comparing the 36Cl content of dissolved salt at different depths and the secular equilibrium value of the host rock. The 36Cl of deepest levels corresponding to the highest salinity, is in equilibrium with rock, suggesting a penetration of the deep salinity into the host rock more than 1.5 Ma ago.  相似文献   

20.
The need for more agricultural or residential land has encouraged reclamation at the coastal areas of Korea since 1200 ad (approximately). The groundwaters of these reclaimed areas could be expected to reveal hydrogeochemical properties different from those of areas directly affected by seawater intrusion. The purpose of this study, therefore, was to examine the salinization of shallow groundwater in a coastal reclaimed area and to identify the effect of land reclamation on groundwater quality. Major cations and anions, iodide, total organic carbon, δD, δ 18O and δ 13C were measured to assist the hydrogeochemical analysis. Chloride, δD and δ 18O data clearly show that the Na–Cl type water results from mixing of groundwater with seawater. In particular, the δD and δ 18O of Ca+Mg–Cl+NO3 type groundwaters are close to the meteoric water line, but Na–Cl type waters enriched in chloride are 18O-enriched with respect to the meteoric water line. Meanwhile, carbon isotopic data and I/Cl ratios strongly suggest that there are various sources of salinity. The δ 13C values of Na–Cl type groundwaters are generally similar to those of Ca+Mg–Cl+NO3 type waters, which are depleted in 13C with respect to seawater. I/Cl ratios of Na–Cl type groundwater are 10–100 times higher than that of seawater. Because the reclamation has incorporated a large amount of organic matter, it provides optimum conditions for the occurrence of redox processes in the groundwater system. Therefore, the salinization of groundwater in the study area seems to be controlled not only by saltwater intrusion but also by other effects, such as those caused by residual salts and organic matter in the reclaimed sediments.  相似文献   

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