Hydrogeochemistry and isotope analyses used to determine groundwater recharge and flow in low-gradient catchments of the province of Buenos Aires,Argentina   总被引：7，自引：3，他引：4  

O. M. Quiroz Londoño  D. E. Martínez  C. Dapeña  H. Massone 《Hydrogeology Journal》2008,16(6):1113-1127

The region known as Pampa Plain, in Argentina, is a vast area characterized by slopes of less than 0.05%. The surface sediment is silty sand, mainly Aeolian, referred to as Pampean Loess, which is a phreatic aquifer unit of utmost importance for the water supply of the region. On account of the slight gradient, hydrogeological analyses using only hydraulic measurements are difficult to perform, often leading to confusing results. Thus, the study presented relies on hydrochemical modeling and isotopic determinations as well. The study area comprises three catchments in the inter-mountainous area corresponding to El Moro, Tamangueyú and Seco creeks, and covering 2,570 km² in the province of Buenos Aires. Measurements of piezometric levels and samples of groundwater, surface water and rainwater were carried out between January and March 2005. Major ion results were analyzed by means of hydrochemical graphs and hydrogeochemical modelling using NETPATH. The resulting data show that it is possible to identify local changes in recharge, flow direction and stream/groundwater relationship by using hydrochemical and isotopic information, which may become a useful and more precise tool for the study of particularly flat landscapes.  相似文献   

Coalification in Carboniferous sediments from the Lötschberg base tunnel     

David J. A. Williams  Beda A. Hofmann  Ian G. Glasspool 《Swiss Journal of Geoscience》2008,101(3):651-658

Vitrinite reflectance (Rr), proximate analysis and carbon isotope composition (δ¹³C) have been used to characterise coal samples from two zones of Late Carboniferous sediments (Gastern and Ferden) in the Aar massif where they are penetrated by the Lötschberg base tunnel (constructed between 1999 and 2005). Samples are characterised by variable ash yields (21.7–93.9%; dry basis); those with ash yields of less than ~50% and with volatile matter content (V;dry ash-free basis) within the limits 2 < V% ≤ 8 are anthracite. Values of Rr range from 3.89% to 5.17% and indicate coalification to the rank of anthracite and meta-anthracite in both Gastern and Ferden Carboniferous zones. Samples of anthracite and shale from the Gastern Carboniferous exhibit a relatively small range in δ¹³C values (–24.52‰ to –23.38‰; mean: –23.86‰) and are lighter than anthracite samples from the Ferden Carboniferous (mean: –22.20‰). The degree of coalification in the Gastern and Ferden Carboniferous zones primarily depends on the maximum rock temperature (T) attained as a result of burial heating. Vitrinite reflectance based estimates of T range from ~290° –360 °C. For a proposed palaeogeothemal gradient of 25 ° C/km at the time of maximum coalification the required overburden is attributable to relatively thin autochtonous Mesozoic/Cenozoic sedimentary cover of the Aar massif and Gastern granite and deep tectonic burial beneath advancing Helvetic, Ultrahelvetic and Prealpine (Penninic) nappes in Early Oligocene to Miocene.  相似文献   

Composition-Induced Variations in SIMS Instrumental Mass Fractionation during Boron Isotope Ratio Measurements of Silicate Glasses     

Martin Rosner  Michael Wiedenbeck  Thomas Ludwig 《Geostandards and Geoanalytical Research》2008,32(1):27-38

An analytical artefact is reported here related to differences in instrumental mass fractionation between NIST SRM glasses and natural geological glasses during SIMS boron isotope determinations. The data presented demonstrated an average 3.4‰ difference between the NIST glasses and natural basaltic to rhyolitic glasses mainly in terms of their sputtering-induced fractionation of boron isotopes. As no matrix effect was found among basaltic to rhyolitic glasses, instrumental mass fractionation of most natural glass samples can be corrected by using appropriate glass reference materials. In order to confirm the existence of the compositionally induced variations in boron SIMS instrumental mass bias, the observed offset in SIMS instrumental mass bias has been independently reproduced in two laboratories and the phenomenon has been found to be stable over a period of more than one year. This study highlights the need for a close match between the chemical composition of the reference material and the samples being investigated.  相似文献   

Holocene climate reconstructions of Ulungur Lake (Xinjiang,China) inferred from ostracod species assemblages and stable isotopes     

Qingfeng JIANG  Ji SHEN  Xingqi LIU  Enlou ZHANG 《Frontiers of Earth Science》2008,2(1):31-40

In this paper, the data on the paleoclimatic and paleoenvironmental changes during the Holocene are presented and a discussion is made on a 225-cm-long sediment core from Ulungur Lake, located in Northwest China. The chronology is constructed from six AMS radiocarbon dates on the bulk organic matter. On the basis of the analysis of ostracod assemblages and the shell stable isotopes, the core is divided into three paleoclimatic and paleoenvironmental evolution stages: 9 985–5 250 cal.aB.P. stage is the wettest phase of the core section. The climate changed from moderate-dry to cool-wet, and then to warm-wet in turn, and the lake level rose accordingly, showing the characteristic of a high lake level. 5 250–1 255 cal.aB.P. stage was the driest phase of the core sediment. The climate turned from the early warm-dry to the late warm-wet and the lake level fell and rose again. Finally, the 1 255 cal.aB.P. stage was the medium stage of the section. The temperature was low and then increased after the 1920s and the climate was dry. The whole climatic and environmental evolution records of Lake Ulungur were not only in agreement with the sporopollen record of the same core but also in agreement with the record of environmental changes of adjacent areas. It responded to regional environmental changes and global abrupt climate events, following the westerly climate change mode on 100-year-scale, primarily with cold-wet and warmdry characteristics. __________ Translated from Quaternary Sciences, 2007, 27(3):382–391 [译自:第四纪研究]  相似文献   

Oxygen isotopes in the Cretaceous-Paleogene granites of Primorye and some problems of their genesis     

G. A. Valui  E. Yu. Moskalenko  A. A. Strizhkova  G. R. Sayadyan 《Russian Journal of Pacific Geology》2008,2(2):150-157

The Cretaceous-Paleogene granites of the Eastern Sikhote Alin volcanic belt (ESAVB) and Late Cretaceous granitoids of the Tatibin Series (Central Sikhote Alin) are subdivided into three groups according to their oxygen isotope composition: group I with δ¹⁸O from +5.5 to +6.5‰, group II with δ¹⁸O from +7.6 to +10.2‰, and group III with less than +4.5‰. Group I rocks are similar in oxygen isotope composition to that of oceanic basalts and can be derived by melting of basaltic crust. Group II (rocks of the Tatibin Series) have higher δ¹⁸O, which suggests that their parental melts were contaminated by sedimentary material. The low ¹⁸O composition of group III rocks can be explained by their derivation from ¹⁸O-depleted rocks or by subsolidus isotopic exchange with low-¹⁸O fluid or meteoric waters. The relatively low δ¹⁸O and ⁸⁷Sr/⁸⁶Sr in the granitoids of Primorye suggest their derivation from rocks with a short-lived crustal history and can result from the following: (1) melting of sedimentary rocks enriched in young volcanic material that was accumulated in the trench along the transform continental margin (granites of the Tatibin Series) and (2) melting of a mixture of abyssal sediments, ocean floor basalts, and upper mantle in the lithospheric plate that subsided beneath the continent in the subduction zone (granites of the ESAVB).  相似文献   

Dike rock generation and magma interactions in the Bir Safsaf igneous complex,south-west Egypt: Implications for the Pan-African evolution in north-east Africa     

D. Pudlo  G. Franz 《International Journal of Earth Sciences》1994,83(3):523-536

The geological setting, ages, petrography and geochemistry of late Pan-African ( 580 Ma) calc-alkaline and tholeiitic dike rocks in the Bir Safsaf igneous complex of south-west Egypt are discussed. These basaltic to rhyolitic dikes intruded contemporaneously and shortly after the intrusion of granitoids. The major and trace element data, Sr and Nd isotope relations, in combination with textural observations, confirm complex interactions between most of the intermediate calcalkaline dike melts and plutonic melts, with different degrees of mixing, assimilation, replenishment and tapping of magma chambers. Trachytic and rhyolitic dikes are strongly differentiated melts from the granitic pluton. The tholeiitic dikes evolved dominantly by fractional crystallization processes. It is inferred that open system and closed system processes operated in calc-alkaline magma chambers, and that the calc-alkaline melts came from a garnet-and amphibole-bearing mantle, modified by a subduction component. Tholeiitic rocks were formed later by fractional crystallization and assimilation processes. Magma ascent of both dike types took place in an extensional environment and the presumed subduction zone has to be seen in connection with the Atmur-Delgo suture zone.  相似文献   

Variation in the composition of Lake Bonneville marl: a potential key to lake-level fluctuations and paleoclimate     

Charles G. Oviatt  Geoff D. Habiger  James E. Hay 《Journal of Paleolimnology》1994,11(1):19-30

Lake Bonneville marl provides a stratigraphic record of lake history preserved in its carbonate minerals and stable isotopes. We have analyzed the marl in shallow cores taken at three localities in the Bonneville basin. Chronology for the cores is provided by dated volcanic ashes, ostracode biostratigraphy, and a distinctive lithologic unit believed to have been deposited during and immediately after the Bonneville Flood.A core taken at Monument Point at the north shore of Great Salt Lake encompasses virtually the entire Bonneville lake cycle, including the 26.5 ka Thiokol basaltic ash at the base and deposits representing the overflowing stage at the Provo shoreline at the top of the core. Two cores from the Old River Bed area near the threshold between the Sevier basin and the Great Salt Lake basin (the main body of Lake Bonneville) represent deposition from the end of the Stansbury oscillation ( 20 ka) to post-Provo time ( 13 ka), and one core from near Sunstone Knoll in the Sevier basin provides a nearly complete record of the period when Lake Bonneville flooded the Sevier basin (20–13 ka).In all cores, percent calcium carbonate, the aragonite to calcite ratio, and percent sand were measured at approximately 2-cm intervals, and ¹⁸O and ¹³C were determined in one core from the Old River Bed area. The transgressive period from about 20 ka to 15 ka is represented in all cores, but the general trends and the details of the records are different, probably as a result of water chemistry and water balance differences between the main body and the Sevier basin because they were fed by different rivers and had different hypsometries. The Old River Bed marl sections are intermediate in position and composition between the Monument Point and Sunstone Knoll sections. Variations in marl composition at the Old River Bed, which are correlated with lake-level changes, were probably caused by changes in the relative proportions of water from the two basins, which were caused by shifts in water balance in the lake.This is the second paper in a series of papers published in this issue on Climatic and Tectonic Rhythms in Lake Deposits.  相似文献   

Paleohydrology and paleochemistry of Lake Manitoba,Canada: the isotope and ostracode records   总被引：1，自引：1，他引：0  

William M. Last  James T. Teller  Richard M. Forester 《Journal of Paleolimnology》1994,12(3):269-282

Lake Manitoba, the largest lake in the Prairie region of North America, contains a fine-grained sequence of late Pleistocene and Holocene sediment that documents a complex postglacial history. This record indicates that differential isostatic rebound and changing climate have interacted with varying drainage basin size and hydrologic budget to create significant variations in lake level and limnological conditions. During the initial depositional period in the basin, the Lake Agassiz phase (12–9 ka), ¹⁸O of ostracodes ranged from –16 to –5 (PDB), implying the lake was variously dominated by cold, dilute glacial meltwater and warm to cold, slightly saline water.Candona subtriangulata, which prefers cold, dilute water, dominates the most negative ¹⁸O intervals, when the basin was part of proglacial Lake Agassiz. At times during this early phase, the ¹⁸O of the lake abruptly shifted to higher values; euryhaline taxa such asC. rawsoni orLimnocythere ceriotuberosa, and halobiont taxa such asL. staplini orL. sappaensis are dominant in these intervals. This positive covariance of isotope and ostracode records implies that the lake level episodically fell, isolating the Lake Manitoba basin from the main glacial lake.¹⁸O values from inorganic endogenic Mg-calcite in the post-Agassiz phase of Lake Manitoba trend from –4 at 8 ka to –11 at 4.5 ka. We interpret that this trend indicates a gradually increasing influence of isotopically low (–20 SMOW) Paleozoic groundwater inflow, although periods of increased evaporation during this time may account for zones of less negative isotopic values. The ¹⁸O of this inorganic calcite abruptly shifts to higher values (–6) after 4.5 ka due to the combined effects of increased evaporative enrichment in a closed basin lake and the increased contribution of isotopically high surface water inflow on the hydrologic budget. After 2 ka, the ¹⁸O of the Mg-calcite fluctuates between –13 and –7, implying short-term variability in the lake's hydrologic budget, with values indicating the lake varied from outflow-dominated to evaporation-dominated. The ¹³C values of Mg-calcite remain nearly constant from 8 to 4.5 ka and then trend to higher values upward in the section. This pattern suggests primary productivity in the lake was initially constant but gradually increased after 4.5 ka.This is the sixth in a series of papers published in this issue on the paleolimnology of arid regions. These papers were presented at the Sixth International Palaeolimnology Symposium held 19–21 April, 1993 at the Australian National University, Canberra, Australia. Dr A. R. Chivas served as guest editor for these papers.  相似文献   

Molecular and bulk isotopic analyses of organic matter in marls of the Mulhouse Basin (Tertiary, Alsace, France)     

Hollander DJ  Sinninghe Damste JS  Hayes JM  de Leeuw JW  Huc AY 《Organic Geochemistry》1993,20(8):1253-1263

Contents of 13C in kerogens and carbonates in 21 samples from a core of the MAX borehole, Mulhouse Evaporite Basin, range from -27.3 to -23.5 and -3.7 to -1.8% vs PDB, respectively. Organic nitrogen in the same samples is enriched in 15N relative to atmospheric N2 by 12.2-15.7%. Hydrogen indices and delta values for kerogens vary systematically with facies, averaging 493 mg HC/g Corg and -25.7% in the most saline facies (dominated by inputs from aquatic sources) and 267 mg HC/g Corg and -23.7% in the least saline facies (50/50 aquatic/terrigenous). Values of delta were measured for individual aliphatic hydrocarbons from three samples representing three different organic facies. For all samples, terrigenous inputs were unusually rich in 13C, the estimated delta value for bulk terrigenous debris, apparently derived partly from CAM plants, being -22.5%. In the most saline facies, isotopic evidence indicates the mixing of 13C-depleted products of photosynthetic bacteria with 13C-enriched products of halotolerant eukaryotic algae. At lower salinities, a change in the producer community is marked by a decrease in the 13C content of algal lipids. The content of 13C in algal lipids increases in the least saline facies, due either to succession of different organisms or to decreased concentrations of dissolved CO2.  相似文献   

Boron isotope variations in nature: a synthesis   总被引：9，自引：0，他引：9  

S. Barth 《International Journal of Earth Sciences》1993,82(4):640-651

The large relative mass difference between the two stable isotopes of boron, ¹⁰B and ¹¹B, and the high geochemical reactivity of boron lead to significant isotope fractionation by natural processes. Published ¹¹B values (relative to the NBS SRM-951 standard) span a wide range of 90. The lowest ¹¹B values around — 30 are reported for non-marine evaporite minerals and certain tourmalines. The most ¹¹B-enriched reservoir known to date are brines from Australian salt lakes and the Dead Sea of Israel with ¹¹B values up to +59. Dissolved boron in present-day seawater has a constant world-wide ¹¹B value of + 39.5. In this paper, available ¹¹B data of a variety of natural fluid and solid samples from different geological environments are compiled and some of the most relevant aspects, including possible tracer applications of boron-isotope geochemistry, are summarized.

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Résumé La grande différence relative de masse entre les isotopes stables du bore, ¹⁰B et ¹¹B, et la grande réactivité geochimique du bore ont pour conséquence un fractionnement isotopique naturel important. Les valeurs de ¹¹B publiées (par rapport au standard NBS SRM-951) varient de 90. Les valeurs de ¹¹B les plus basses (–30) correspondent aux evaporites non-marines et à certaines tourmalines. Le réservoir le plus enrichi en ¹¹B est représenté par les saumures des lacs salés d' Australie et par la Mer Morte en Israël, qui ont des valuers de ¹¹B allent jusqu'à + 59. L'eau de mer a une valeur de ¹¹B mondialement constante de + 39.5. Des valeurs de ¹¹B des solutions naturelles ainsi que des roches et minéraux de différentes origines, publiées jusqu'à présent, sont présentées ici. En outre quelques aspects importants concernant la géochimie des isotopes du bore y compris quelques applications sont exposés.

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