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1.
Microbial methane in sedimentary basins comprises approximately 20% of global natural gas resources, yet little is known about the environmental requirements and metabolic rates of these subsurface microbial communities. The Illinois Basin, located in the midcontinent of the United States, is an ideal location to investigate hydrogeochemical factors controlling methanogenesis as microbial methane accumulations occur: (1) in three organic-rich reservoirs of different geologic ages and organic matter types - Upper Devonian New Albany Shale (up to 900 m depth), Pennsylvanian coals (up to 600 m depth), and Quaternary glacial sediments (shallow aquifers); (2) across steep salinity gradients; and (3) with variable concentrations of . For all three organic-rich reservoirs aqueous geochemical conditions are favorable for microbial methanogenesis, with near neutral pH, concentrations <2 mM, and Cl− concentrations <3 M. Also, carbon isotopic fractionation of CH4, CO2, and DIC is consistent with microbial methanogenesis, and increased carbon isotopic fractionation with average reservoir depth corresponds to a decrease of groundwater flushing rates with average depth of reservoir. Plots of stable isotopes of water and Cl− show mixing between a brine endmember and freshwater, suggesting that meteoric groundwater recharge has affected all microbial methanogenic systems. Additionally, similar methanogenic communities are present in all three reservoirs with comparable cell counts (8.69E3-2.58E6 cells/mL). TRFLP results show low numbers of archaea species with only two dominant groups of base pairs in coals, shale, and limestone aquifers. These results compare favorably with other methanogen-containing deep subsurface environments. Individual hydrogeochemical parameters that have a Spearman correlation coefficient greater than 0.3 to variations in methanogenic species include stable isotopes of water (δ18O and δD), type of substrate (i.e. coals versus shale), pH, and Cl− concentration. The matching of variations between methanogenic TRFLP data and conservative tracers suggests that deep circulation of meteoric waters influenced archaeal communities in the Illinois Basin. In addition, coalification and burial estimates suggest that in the study area, coals and shale reservoirs were previously sterilized (>80 °C in nutrient poor environments), necessitating the re-introduction of microbes into the subsurface via groundwater transport.  相似文献   

2.
Changes in the climatic conditions during the Late Quaternary and Holocene greatly impacted the hydrology and geochemical evolution of groundwaters in the Great Lakes region. Increased hydraulic gradients from melting of kilometer-thick Pleistocene ice sheets reorganized regional-scale groundwater flow in Paleozoic aquifers in underlying intracratonic basins. Here, we present new elemental and isotopic analyses of 134 groundwaters from Silurian-Devonian carbonate and overlying glacial drift aquifers, along the margins of the Illinois and Michigan basins, to evaluate the paleohydrology, age distribution, and geochemical evolution of confined aquifer systems. This study significantly extends the spatial coverage of previously published groundwaters in carbonate and drift aquifers across the Midcontinent region, and extends into deeper portions of the Illinois and Michigan basins, focused on the freshwater-saline water mixing zones. In addition, the hydrogeochemical data from Silurian-Devonian aquifers were integrated with deeper basinal fluids, and brines in Upper Devonian black shales and underlying Cambrian-Ordovician aquifers to reveal a regionally extensive recharge system of Pleistocene-age waters in glaciated sedimentary basins. Elemental and isotope geochemistry of confined groundwaters in Silurian-Devonian carbonate and glacial drift aquifers show that they have been extensively altered by incongruent dissolution of carbonate minerals, dissolution of halite and anhydrite, cation exchange, microbial processes, and mixing with basinal brines. Carbon isotope values of dissolved inorganic carbon (DIC) range from −10 to −2‰, 87Sr/86Sr ratios range from 0.7080 to 0.7090, and δ34S-SO4 values range from +10 to 30‰. A few waters have elevated δ13CDIC values (>15‰) from microbial methanogenesis in adjacent organic-rich Upper Devonian shales. Radiocarbon ages and δ18O and δD values of confined groundwaters indicate they originated as subglacial recharge beneath the Laurentide Ice Sheet (14-50 ka BP, −15 to −13‰ δ18O). These paleowaters are isolated from shallow flow systems in overlying glacial drift aquifers by lake-bed clays and/or shales. The presence of isotopically depleted waters in Paleozoic aquifers at relatively shallow depths illustrates the importance of continental glaciation on regional-scale groundwater flow. Modern groundwater flow in the Great Lakes region is primarily restricted to shallow unconfined glacial drift aquifers. Recharge waters in Silurian-Devonian and unconfined drift aquifers have δ18O values within the range of Holocene precipitation: −11 to −8‰ and −7 to −4.5‰ for northern Michigan and northern Indiana/Ohio, respectively. Carbon and Sr isotope systematics indicate shallow groundwaters evolved through congruent dissolution of carbonate minerals under open and closed system conditions (δ13CDIC = −14.7 to−11.1‰ and 87Sr/86Sr = 0.7080-0.7103). The distinct elemental and isotope geochemistry of Pleistocene- versus Holocene-age waters further confirms that surficial flow systems are out of contact with the deeper basinal-scale flow systems. These results provide improved understanding of the effects of past climate change on groundwater flow and geochemical processes, which are important for determining the sustainability of present-day water resources and stability of saline fluids in sedimentary basins.  相似文献   

3.
The Canning Basin contains several Mississippi Valley‐type Zn‐Pb sulphide prospects and deposits in Devonian carbonate reef complexes on the northern edge of the Fitzroy Trough, and in Ordovician and Silurian marine sequences on the northern margin of the Willara Sub‐basin. This study uses the ionic composition and 5D, δ18O, δ34S, 87Sr/86Sr isotopic data on present‐day deep formation waters to determine their origin and possible relationship to the Zn‐Pb mineralizing palaeofluids.

The present‐day Canning Basin formation waters have salinity ranging from typically less than 5000 mg/L up to 250 000 mg/L locally. The brines are mixtures of highly saline water, formed by seawater which evaporated beyond halite saturation (bittern water), with meteoric water ranging in salinity from low (<5000 mg/L) to hypersaline water (up to about 50 000 mg/L) formed by re‐solution of halite and calcium sulphate minerals. The original marine chemical composition of the bittern‐dominated brines was changed to that of a Na‐Ca‐Cl water by addition of Ca and removal of Mg and SO4, initially by bacterial sulphate reduction and later by dolomitization of carbonate. Other reactions with terrigenous components of the sediment have provided additional Ca and Sr, including a small proportion of 87Sr‐rich material. The δ34S values of the bittern‐containing waters are within the range over which marine sulphate has fluctuated from the Ordovician to the Holocene, although one of the hypersaline waters has a value of +6.8%, indicating SO4 of non‐marine origin. The pH of the bittern‐containing waters is low (about 5) and they contain significant concentrations of dissolved Fe (up to 120 mg/L).

The Canning Basin bitterns appear similar in origin and chemical composition to highly saline marine brines in the Mississippi Salt Dome Basin, USA, which are known to be either metal or sulphide‐rich depending on the organic content of the host rock. In the Canning Basin, mixing of the bittern water with the various types of meteoric water has resulted in decreases in salinity, Na, Ca, Mg, K, Sr, Li and Fe, and increases in HCO3, SO4 and pH.

Mixing of the bitterns with other types of metalliferous fluids and/or with sulphate‐containing hypersaline meteoric waters formed from the same marine evaporite sequence should produce ore‐precipitating fluids which are relatively hot and saline, and the resulting ore deposit should be of high grade and contain abundant sulphate minerals. In the southern Canning Basin, this type of mixing and the corresponding style of ore deposit is evident in the evaporite‐associated areas of Zn‐Pb mineralization near the Admiral Bay Fault. If the bitterns mix with low salinity HCO3‐waters in near‐surface environments, then the ore‐precipitating fluids should have relatively low salinities and carbonate minerals would precipitate during later stages of mixing. In the Lennard Shelf, the present‐day formation waters, the style of the Zn‐Pb deposits, and range of salinity and temperature of the ore‐forming palaeofluids are consistent with this type of mixing.  相似文献   

4.
《Applied Geochemistry》1999,14(3):333-363
The hydrochemical, radiochemical, stable isotope, 14C and dissolved noble gas composition of groundwaters has been determined along two profiles across the confined, fissured Chalk aquifer of the London Basin of southern England, and for selected sites in the adjacent Berkshire Basin. During downgradient flow in the London Basin aquifer, the groundwater chemistry is modified by water–rock interactions: congruent and incongruent reaction of the carbonate lithology resulting in enhanced Mg/Ca and Sr/Ca ratios and 13C contents with increased residence times; redox and ion exchange reactions; and towards the centre of the Basin, mixing with a residual saline connate water stored in the Chalk matrix. There is evidence from anomalous water chemistries for a component of vertical leakage from overlying Tertiary beds into the confined aquifer as a result of historical dewatering of the aquifer. Dissolved noble gas contents indicate the climate was up to 4.5°C cooler than at present during recharge of the waters now found in the centres of both Basins; stable isotope (2H and 18O) depletions correspond to this recharge temperature change. For evolved waters having δ13C > −8‰ PDB a negative linear correlation is demonstrated between derived recharge temperatures and δ13C values, which is interpreted as mixing between relatively warm, light isotopic, fracture-borne waters and cooler stored waters of the matrix having a 13C signature more or less equilibrated with the Chalk. From geochemical (14C, 4He) age estimates, the abstracted water is interpreted as being either of wholly Holocene/post-Devensian glacial origin, or an admixture of Holocene and Late Pleistocene pre-glacial (cold stage interstadial) recharge. Devensian pleniglacial stage waters of the Last Glacial Maximum are not represented.  相似文献   

5.
Zhangye Basin, in arid northwestern China, has recently been repeatedly flooded by rising groundwater. Isotope signatures of sampled waters gained insight into the recharge source of the groundwater. The summer Heihe River water and most of the spring water in Zhangye and Yongchang basins plotted above the global meteoric water line (GMWL) on the δ18O-δD plot. The spring water had R/Ra ratio >1, low TDS and high tritium, which indicates origin from Qilian Mountain glacier meltwater. The groundwater of Qilian Mountains was transported to the Hexi Corridor (in which Zhangye Basin is located) through underground fault zones. Additionally, some of the groundwater in the alluvial plain, and all spring water surrounding Zhangye Basin, plotted below the GMWL on the δ18O-δD plot along an evaporation line, and had R/Ra ratio?<?1 and high TDS. It is proposed that the Tibetan rivers or lakes source the Hexi Corridor groundwater through either the NE-trending or NW-trending buried fault zones. The isotopic signatures presented as part of this study rule out the conventional viewpoint that groundwater of the Zhangye Basin was recharged by local precipitation and infiltration of Heihe River water on the alluvial plain.  相似文献   

6.
Stable isotope data for the Hueco Bolson aquifer (Texas, USA and Chihuahua, Mexico) distinguish four water types. Two types relate to recharge from the Rio Grande: pre-dam (pre-1916) river water with oxygen-18 and deuterium (δ18O, δD, ‰) from (?11.9, ?90) to (?10.1, ?82), contrasts with present-day river water (?8.5, ?74) to (?5.3, ?56). Pre-dam water is found beneath the Rio Grande floodplain and Ciudad Juárez, and is mixed with post-dam river water beneath the floodplain. Two other types relate to recharge of local precipitation; evidence of temporal change of precipitation isotopes is present in both types. Recharge from the Franklin and Organ Mountains plots between (?10.9, ?76) and (?8.5, ?60) on the global meteoric water line (GMWL), and is found along the western side of the Hueco Bolson, north of the Rio Grande. Recharge from the Diablo Plateau plots on an evaporation trend originating on the GMWL near (?8.5, ?58). This water is found in the southeastern Hueco Bolson, north of the river; evaporation may be related to slow recharge through fine-grained sediment. Pre-dam water, recognizable by isotope composition, provides information on groundwater residence times in this and other dammed river basins.  相似文献   

7.
The isotopic composition of Sr has been measured in 73 formation-water samples from Paleozoic strata in the Illinois basin; 87Sr/86Sr ratios range from 0.7079 to 0.7108. With the exception of four samples, the waters are more radiogenic than corresponding Paleozoic sea-water values. The relatively narrow range of slightly elevated 87Sr/86Sr rations is uniformly distributed in waters throughout the stratigraphic column and in Silurian waters across the basin. Isotopic analyses of core samples from reservoir rocks show an absence of water-rock Sr isotopic equilibration. Basin lithology and analyses of detrital rock units indicate that clay minerals in shales and in quartz sandstone matrices represent the only significant source of radiogenic Sr for the waters. Silurian and Devonian water show a two-component mixing relation which suggests that they comprise a single hydrogeological system that evolved when radiogenic water from New Albany shales entered Silurian-Devonian carbonate rocks and mixed with marine interstitial water. Regional migration of the waters and associated petroleum within the Silurian-Devonian strata, proposed in other studies, is consistent with the Sr isotopic data. Under favorable circumstances subsurface waters are capable of retaining a Sr isotopic recor of their evolution.  相似文献   

8.
The major ion hydrochemistry, sodium absorption ratio (SAR), sodium percentage, and isotopic signatures of Hammamet-Nabeul groundwaters were used to identify the processes that control the mineralization, irrigation suitability, and origin of different water bodies. This investigation highlights that groundwater mineralization is mainly influenced by water-rock interaction and pollution by the return flow of irrigation water. The comparison of groundwater quality with irrigation suitability standards proves that most parts of groundwater are unacceptable for irrigation and this long-term practice may result in a significant increase of the salinity and alkalinity in the soils. Based on isotopic signatures, the shallow aquifer groundwater samples were classified into (i) waters with depleted δ18O and δ2H contents, highlighting recharge by modern precipitation, and (ii) waters with enriched stable isotope contents, reflecting the significance of recharge by contaminated water derived from the return flow of evaporated irrigation waters. The deep-aquifer groundwater samples were also classified into (i) waters with relatively enriched isotope contents derived from modern recharge and mixed with shallow-aquifer groundwater and (ii) waters with depleted stable isotope contents reflecting a paleoclimatic origin. Tritium data permit to identify three origins of recharge, i.e., contemporaneous, post-nuclear, and pre-nuclear. Carbon-14 activities demonstrate the existence of old paleoclimatic recharge related to the Holocene and Late Pleistocene humid periods.  相似文献   

9.
Ayadi  Rahma  Trabelsi  Rim  Zouari  Kamel  Saibi  Hakim  Itoi  Ryuichi  Khanfir  Hafedh 《Hydrogeology Journal》2018,26(4):983-1007

Major element concentrations and stable (δ18O and δ2H) and radiogenic (3H and 14C) isotopes in groundwater have proved useful tracers for understanding the geochemical processes that control groundwater mineralization and for identifying recharge sources in the semi-arid region of Sfax (southeastern Tunisia). Major-ion chemical data indicate that the origins of the salinity in the groundwater are the water–rock interactions, mainly the dissolution of evaporitic minerals, as well as the cation exchange with clay minerals. The δ18O and δ2H relationships suggest variations in groundwater recharge mechanisms. Strong evaporation during recharge with limited rapid water infiltration is evident in the groundwater of the intermediate aquifer. The mixing with old groundwater in some areas explains the low stable isotope values of some groundwater samples. Groundwaters from the intermediate aquifer are classified into two main water types: Ca-Na-SO4 and Ca-Na-Cl-SO4. The high nitrate concentrations suggest an anthropogenic source of nitrogen contamination caused by intensive agricultural activities in the area. The stable isotopic signatures reveal three water groups: non-evaporated waters that indicate recharge by recent infiltrated water; evaporated waters that are characterized by relatively enriched δ18O and δ2H contents; and mixed groundwater (old/recent) or ancient groundwater, characterized by their depleted isotopic composition. Tritium data support the existence of recent limited recharge; however, other low tritium values are indicative of pre-nuclear recharge and/or mixing between pre-nuclear and contemporaneous recharge. The carbon-14 activities indicate that the groundwaters were mostly recharged under different climatic conditions during the cooler periods of the late Pleistocene and Holocene.

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10.
鄂尔多斯盆地中南部发育有侏罗系延安组第二段和第三段陆相暗色厚层泥岩层系,矿物成分以石英、黏土为主,石英43%~56%,黏土矿物29%~33%。总有机碳(TOC)1.63%~3.89%,有机质成熟度Ro为0.59%~0.60%,含气量(CH4)0.25~0.85 m3/t,等温吸附实验表明延安组泥岩的甲烷吸附能力与总有机碳含量呈正相关关系。泥岩处于生物成因气阶段,具备页岩气形成的基本地质条件,并可对比美国密歇根盆地Antrim页岩和伊利诺斯盆地的New Albany页岩的地质条件。为查清黄陵北部侏罗系延安组页岩气的勘探潜力,通过分析勘查和化验测试资料,对其页岩气勘探潜力进一步评价认为:黄陵北部延安组泥岩分布范围和厚度较大,已进入生物成因气和热催化生气的中间阶段,有机质丰度较高,具备形成页岩气的成藏条件,页岩气潜力巨大。   相似文献   

11.
The Sacramento Mountains and the adjacent Roswell Artesian Basin, in south-central New Mexico (USA), comprise a regional hydrologic system, wherein recharge in the mountains ultimately supplies water to the confined basin aquifer. Geologic, hydrologic, geochemical, and climatologic data were used to delineate the area of recharge in the southern Sacramento Mountains. The water-table fluctuation and chloride mass-balance methods were used to quantify recharge over a range of spatial and temporal scales. Extrapolation of the quantitative recharge estimates to the entire Sacramento Mountains region allowed comparison with previous recharge estimates for the northern Sacramento Mountains and the Roswell Artesian Basin. Recharge in the Sacramento Mountains is estimated to range from 159.86?×?106 to 209.42?×?106 m3/year. Both the location of recharge and range in estimates is consistent with previous work that suggests that ~75 % of the recharge to the confined aquifer in the Roswell Artesian Basin has moved downgradient through the Yeso Formation from distal recharge areas in the Sacramento Mountains. A smaller recharge component is derived from infiltration of streamflow beneath the major drainages that cross the Pecos Slope, but in the southern Sacramento Mountains much of this water is ultimately derived from spring discharge. Direct recharge across the Pecos Slope between the mountains and the confined basin aquifer is much smaller than either of the other two components.  相似文献   

12.
Spring and Snake valleys, western USA, are scheduled for development and groundwater export to Las Vegas, Nevada (USA). New work, compared to published studies, illustrates the critical role of conceptual models to underpin water withdrawals in arid regions. Interbasin flow studies suggest that 30–55?% of recharge to Snake Valley arrives from adjacent Spring Valley. This study, however, suggest little or no interbasin flow; rather, Spring and Snake valleys comprise separate systems. Contrary to expectation, δD and δ18O contours are perpendicular to proposed interbasin flow paths. 14C age gradients up to 10?ka along interbasin flow paths indicate that old waters are not displaced by such fluxes. 14C and 3H patterns indicate local recharge occurs in adjacent mountain ranges and is transferred to basin-fill by losing streams, mountain front recharge, and upward leakage from carbonate bedrock beneath basins. The choice of conceptual models is critical for groundwater development. Simple analyses of water withdrawals indicate that monitoring discharges at desert springs is an inadequate protective measure. Once flows decline, recovery is lengthy even if pumping is stopped. The conceptual framework behind quantitative evaluations of sustainable yield is critical to determine the ability of a groundwater system to deliver sustained withdrawals.  相似文献   

13.
This paper will discuss the use of chemical proxies in coral skeletons to reconstruct the history of salinity (from the δ18O of the skeleton) and nutrients in the water (from the δ13C) in Florida Bay between 1824 and 1994. Monthly salinity and water temperature data collected since 1989 were used to establish a correlation between salinity, temperature, and the δ18O of the skeleton of the coralSolenastrea bournoni from Lignumvitae Basin in Florida Bay. This relationship explains over 50% of the variance in the δ18O of the skeleton. Assuming that interannual variations in the temperature of the water are small, we have applied this relationship to the δ18O measured in the coral skeleton collected from Lignumvitae Basin which has a record between 1824 and 1993. These data provide a revised estimate of salinity variation in Lignumvitae Basin for the period when historical records for salinity were not available, and show that the highest salinity events occurred in the past 30 yr. Using the relationships between the salinity in Lignumvitate Basin and other basins, obtained using a modern dataset, we are able to estimate ranges in salinity for other portions of Florida Bay. Skeletons of specimens of the coral speciesSiderastrea radians collected from other areas of Florida Bay show similar patterns in the δ18O over the past 10 yr, indicating that corals in most portions of Florida Bay are recording salinity variations in their skeletons and therefore support the idea that salinity variations in different portions of Florida Bay can be related. Fluorescence analysis of the coral from Lignumvitae Basin shows a large change in the magnitude of the 10-yr signal coincident with the construction of the railway, confirming that this event had a significant impact upon Florida Bay. The δ13C of the coral skeletons reveals a long-term history of the oxidation of organic material, fixation of carbon by photosynthesis (algal blooms), and the intrusion of marine water into the bay. Since the construction of the railway from Miami to Key West there has been a long-term decrease in the δ13C of the coral skeleton from Lignumvitae Basin, suggesting the increased oxidation of organic material in this area. This decrease in δ13C appears to have reached a minimum value around 1984 and has increased since this time in the western portions of Florida Bay. The increase may be related to the algal blooms prevalent in the area or alternatively could result from intrusion of more marine water. In the eastern areas, a small increase in the δ18C between 1984 and 1988 was followed by further decline suggesting more oxidation of organic material. We have also attempted to use the concentration of barium in the coral skeleton as a proxy indicator of the nutrient status in Florida Bay.  相似文献   

14.
Groundwater recharge and evolution in the Quaternary aquifer beneath the Dunhuang Basin was investigated using chemical indicators, stable isotopes, and radiocarbon data to provide guidance for regional water management. The quality of groundwater and surface water is generally good with low salinity and it is unpolluted. The dissolution of halite and sylvite from fine-grained sediments controls concentrations of Na+ and K+ in the groundwater, but Na+/Cl− molar ratios >1 in all samples are also indicative of weathering of feldspar contributing to excess Na+. The dissolution of carbonate minerals yields Ca2+ to the groundwater, thereby exerting a strong influence on groundwater salinity. The δ18O and δ2H values in unconfined groundwater are enriched along the groundwater flow path from SW to NE. In contrast, confined groundwater was depleted in heavy isotopes, with mean values of −10.4‰ δ18O and −74.4‰ δ2H. Compared with the precipitation values, all of the groundwater samples were strongly depleted in heavy isotopes, indicating that modern direct recharge to the groundwater aquifers in the plains area is quite limited. The unconfined water is generally young with radiocarbon values of 64.9–79.6 pmc. In the northern basin, radiocarbon content in the confined groundwater is less than 15 pmc and an uncorrected age of ∼15 ka, indicates that this groundwater was recharged during a humid climatic phases of the late Pleistocence or early Holocene. The results have important implications for inter-basin water allocation programmes and groundwater management in the Dunhuang Basin.  相似文献   

15.
Oxygen and hydrogen isotope analysis was performed to study the processes of distribution of water masses and modification of their salinity in the Russian Arctic seas. A wealth of new isotopic data was obtained for freshwater (river runoff, Novaya Zemlya glaciers) and seawater samples collected along a set of extended 2D profiles in the Barents, Kara, and Laptev Seas. The study presents the first δD values measured for the Northeast Atlantic Deep Water NEADW dominated the water column of the Barents Sea (S = 34.90 ± 0.05, δD = +1.55 ± 0.4‰, δ18O = +0.26 ± 0.1‰, n = 44). This water mass is present in the Kara Sea and western Laptev Sea. The relationship between δD, δ18О, and salinity data was used to calculate the fractions of waters of different origin, including the fractions of continental runoff in waters of the Barents, Kara, and Laptev Seas. It was shown that the relationships between the isotopic parameters (δD, δ18О) and salinity in waters of the Kara and Laptev Seas is controlled by the intensity of continental runoff and sea ice processes. Sea ice formation is the main factor controlling the formation of the water column on the Laptev Sea shelf, whereas the surface waters of the middle Kara Sea are dominated by the contribution of river runoff. A very strong stratification in the Kara Sea is caused by the presence of a relatively fresh surface layer mostly contributed by estuarine water inputs from the Ob and Yenisei Rivers. The contribution of river waters reaches 40–60% in the surface layer in the central part of the sea and decreases to a few percent down 100 m water depth. Stratification in the western part of the Laptev Sea is controlled by the contribution of freshwater input from the Lena River and modification of salinity by sea ice formation.  相似文献   

16.
Major element concentrations, stable (δ18O and δ2H) and radiogenic (3H, 14C) isotopes determined in groundwater provided useful initial tracers for understanding the processes that control groundwater mineralization and identifying recharge sources in semi-arid Cherichira basin (central Tunisia).Chemical data based on the chemistry of several major ions has revealed that the main sources of salinity in the groundwaters are related to the water–rock interaction such as the dissolution of evaporitic and carbonate minerals and some reactions with silicate and feldspar minerals.The stable isotope compositions provide evidence that groundwaters are derived from recent recharge. The δ18O and δ2H relationships implied rapid infiltration during recharge to both the Oligocene and Quaternary aquifers, with only limited evaporation occurring in the Quaternary aquifer.Chemical and isotopic signatures of the reservoir waters show large seasonal evolution and differ clearly from those of groundwaters.Tritium data support the existence of recent recharge in Quaternary groundwaters. But, the low tritium values in Oligocene groundwaters are justified by the existence of clay lenses which limit the infiltration of meteoric water in the unsaturated zone and prolong the groundwater residence time.Carbon-14 activities confirm that groundwaters are recharged from the surface runoff coming from precipitation.  相似文献   

17.
In the arid sub-Saharan of southern Morocco, groundwater salinization poses a direct threat for agricultural production in six oases’ basins that are irrigated by water imported from the High Atlas Mountains. Here the geospatial distribution of salinity is evaluated in shallow groundwater, springs and surface waters in the Drâa Basin, integrating major and trace element geochemistry and isotopic tracers (O, H, Sr and B). The data show that water discharge from the High Atlas Mountains to the Upper section of the Drâa Basin is characterized by both low and high salinity, a distinctive low δ18O and δ2H composition (as low as −9‰ and −66‰, respectively), typical for meteoric water from high elevation, a 87Sr/86Sr range of 0.7078–0.7094, and δ11B of 12–17‰. The Ca–Mg–HCO3, Na–Cl–SO4, and Ca–SO4 compositions as well as the Br/Cl, 87Sr/86Sr, and δ11B values of the saline water suggest dissolution of Lower Jurassic carbonates and evaporite rocks in the High Atlas Mountain catchment. Storage and evaporation of the imported water in a man-made open reservoir causes an enrichment of the stable isotope ratios with a δ18O/δ2H slope of <8 but no change in the Sr and B isotope fingerprints. Downstream from the reservoir, large salinity variations were documented in the shallow groundwater from the six Drâa oases, with systematically higher salinity in the three southern oases, up to 12,000 mg/L. The increase of the salinity is systematically associated with a decrease of the Br/Cl ratio, indicating that the main mechanism of groundwater salinization in the shallow aquifers in the Drâa oases is via salt dissolution (gypsum, halite) in the unsaturated zone. Investigation of shallow groundwater that flows to the northern Drâa oases revealed lower salinity (TDS of 500–4225) water that is characterized by depleted 18O and 2H (as low as −9‰ and −66‰, respectively) and higher 87Sr/86Sr ratios (∼0.7107–0.7115) relative to irrigation water and groundwater flow from the Upper Drâa Basin. This newly-discovered low-saline groundwater with a different isotopic imprint flows from the northeastern Anti-Atlas Jabel Saghro Mountains to the northern oases of the Lower Drâa Basin. This adjacent subsurface flow results in a wide range of Sr isotope ratios in the shallow oases groundwater (0.7084–0.7131) and appears to mitigate salinization in the three northern Drâa oases. In contrast, in the southern oases, the higher salinity suggests that this mitigation is not as affective and increasing salinization through cycles of water irrigation and salt dissolution appears inevitable.  相似文献   

18.
The geochemical and isotopic composition of surface waters and groundwater in the Velenje Basin, Slovenia, was investigated seasonally to determine the relationship between major aquifers and surface waters, water–rock reactions, relative ages of groundwater, and biogeochemical processes. Groundwater in the Triassic aquifer is dominated by HCO3 –, Ca2+, Mg2+ and δ13CDIC indicating degradation of soil organic matter and dissolution of carbonate minerals, similar to surface waters. In addition, groundwater in the Triassic aquifer has δ18O and δD values that plot near surface waters on the local and global meteoric water lines, and detectable tritium, likely reflecting recent (<50 years) recharge. In contrast, groundwater in the Pliocene aquifers is enriched in Mg2+, Na+, Ca2+, K+, and Si, and has high alkalinity and δ13CDIC values, with low SO4 2– and NO3 – concentrations. These waters have likely been influenced by sulfate reduction and microbial methanogenesis associated with coal seams and dissolution of feldspars and Mg-rich clay minerals. Pliocene aquifer waters are also depleted in 18O and 2H, and have 3H concentrations near the detection limit, suggesting these waters are older, had a different recharge source, and have not mixed extensively with groundwater in the Triassic aquifer.  相似文献   

19.
Glendonites, calcite pseudomorphs after the metastable mineral ikaite (CaCO3 · 6H2O), occur in the Late Aptian interval of the Bulldog Shale in the Eromanga Basin, Australia and in other Early Cretaceous basins at high paleolatitudes. Ikaite precipitation in the marine environment requires near-freezing temperatures (not higher than 4°C), high alkalinity, increased levels of orthophosphate, and high PCO2. The rapid and complete transformation of ikaite to calcite at temperatures between 5 and 8°C provides an upper limit on the oxygen isotopic composition of the pore waters: −2.6 <δw <−3.4‰SMOW. If it is assumed that these pore waters are representative of the shallow Eromanga Basin, the calculated δw can be used to reassess belemnite fossil oxygen isotopic paleotemperatures—temperature recorded by fauna living in the basin at the time of ikaite precipitation. Data previously reported as 11 to 16°C (assuming δw = 0.0‰SMOW) yield paleotemperatures ranging from −1 to 5°C, squarely in the range of ikaite stability. The low δw indicates hyposaline conditions, most likely caused by mixing high latitude meteoric waters with seawater. The 18O depleted, low temperature waters suggest that the region was at least seasonally colder than previously accepted.  相似文献   

20.
Benzene extractable aliphatic hydrocarbons from the New Albany Shale in the Illinois Basin were characterized by gas chromatography and mass spectrometry, and the total organic matter of the shale was characterized by solid state carbon-13 cross polarization magic angle spinning nuclear magnetic resonance. Core samples from a northwest-trending cross-section of the Illinois Basin were studied. Gas chromatography (GC) and gas chromatography-mass spectrometric analysis (GC/MS) data indicate a regional variation of the aliphatic composition of the shale extracts. A positive, linear relationship between the two ratios, pristane/n-C17 and phytane/n-C18, is indicated. The NMR results indicated that organic matter deposited in northwestern Illinois shale is relatively high in aliphatic hydrocarbon content while, in contrast, organic matter found in southeastern Illinois shale is relatively low in aliphatic hydrocarbon content. Our findings suggest that the organic variation of the shale is mainly due to the differences in thermal maturity of the shale organic matter and the use of pristane/n-C17 ratio as a thermal parameter in the study of oil may be extended to the study of the ancient sediments.  相似文献   

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