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1.
《Geochimica et cosmochimica acta》1986,50(3):419-433
δD and δ18O values have been determined for fluid inclusions in 45 samples of Permian halite. The inclusions are enriched in 18O relative to the meteoric water line but are depleted in D relative to ocean water. Inclusions with the more positive δ-values coincide with the isotopic composition expected for evaporating sea water which follows a hooked trajectory on a δD-δ18O diagram. Inclusions with more negative δ-values may represent more highly evaporated sea water but probably reflect synsedimentary or diagenetic mixing of meteoric water with evaporite brines. The isotope systematics in these inclusions are sufficiently similar to those of a modern evaporite pan to indicate that Permian sea water was isotopically similar to modern sea water.Connate evaporite brines can have negative δ-values because of the probable hooked isotope trajectory of evaporating sea water and/or synsedimentary mixing of evaporite brines with meteoric waters. Subsurface formation waters composed of mixtures of remnant primary evaporite brines and later meteoric waters may be more common than previous isotopic evidence has suggested. 相似文献
2.
成矿热液的氢、氧同位素组成与其水的类型、水/岩交换的岩石成分和同位素组成、水/岩交换时的温度及水/岩交换程度(W/R比值大小)等诸多因素有关,微生物和有机质也对其有一定的影响。因此,仅通过简单投影的方法将成矿热液的氢、氧同位素值与一些所谓的标准值进行类比,由此就推断出热液中水的来源,这种方法是不可取的;尤其当成矿热液的氢、氧同位素值介于大气降水和岩浆水的值之间时,切忌滥用两种水混合成矿模式,因为实际情况往往并不是这样。本文以胶东乳山金矿床为例,展开了这方面的讨论。 相似文献
3.
Hydrogen and oxygen isotopic compositions of cherts (δD for hydroxyl hydrogen in the chert, δ18O for the total oxygen) have been determined for a suite of samples from the central and western United States. When plotted on a δD-δ18O diagram, Phanerozoic cherts define domains parallel to the meteoric water line which are different for different periods of geologic time. The elongation parallel to the meteoric water line suggests that meteoric waters were involved in the formation of many cherts.The existence of different chert δ-values for different geologic times indicates that once the granular microcrystalline quartz of cherts crystallizes its isotopic composition is preserved with time. An explanation for the change with time of the isotopic composition of cherts involving large changes with time in the isotopic composition of ocean water is unlikely since δ18O of the ocean would have had to decrease by about 3‰between Carboniferous and Triassic time and then increase about 5%.` from Triassic to Cretaceous time. Such isotopic changes cannot be accounted for by extensive glaciation, sedimentation of hydrous minerals, or input of water from the mantle into the oceans.The variation with time of the chert δ-values can be satisfactorily explained in terms of past climatic temperature fluctuations if the chert-water isotope fractionation with temperature is approximated by 1000 lnα = 3.09 × 106T?2 – 3.29. Crystallization temperatures so inferred suggest that the average climatic temperatures for the central and western U.S. decreased from about 34 to 20°C through the Paleozoic, increased to 35–40°C in the Triassic, and then decreased through the Mesozoic to Tertiary values of about 17°C. A few data for the Precambrian suggest the possibility that Earth surface temperatures may have reached about 52°C at 1.3 b.y. and about 70°C at 3 b.y. 相似文献
4.
Hydrogen isotope ratios of recent lacustrine sedimentary n-alkanes record modern climate variability
Hydrogen isotope ratios were measured on n-alkanes (n-C12 to n-C31) extracted from recent lake surface sediments along a N-S European transect to test if modern climate variability is recorded in these biomarkers. δD values of the n-alkanes are compared to δD values of meteoric water from the IAEA-GNIP database spanning a range from −119‰ in northern Sweden to −41‰ in southern Italy, to lake water δD values, and to mean annual temperatures, varying between −2.0°C in the north and 13.7°C in the south.δD values of the short-chained n-alkanes n-C12 to n-C20, excluding algal derived n-C17 and n-C19, are higher in the north and lower in the south. The isotopic fractionation ε for hydrogen between meteoric water and the short-chained n-alkanes is increasing from N to S by more than 100‰ and is significantly correlated to mean annual temperature for n-C16 and n-C18. This suggests that these n-alkanes may originate from a different source in the northern lakes, possibly due to petroleum contamination, or are synthesized using a different biochemical pathway.The n-C17 and n-C19 alkanes of algal origin, the n-C21 and n-C23 alkanes originating from water plants, and the long-chain n-alkanes n-C25, n-C27, n-C29, and n-C31 of terrestrial origin, clearly correlate with δD values of meteoric water, lake water, and mean annual temperature, indicating that they excellently record the δD value of meteoric water. The mean hydrogen isotope fractionation εC17/w of −157‰ (SD = 13) between n-C17 and meteoric water is fairly constant over the wide range of different climates and lake environments, suggesting only minor influence of environmental factors on this biochemical fractionation. This suggests that δD values of n-C17 are suitable to reconstruct the isotopic composition of source water. The mean fractionation between the long-chain n-alkanes and water is −128‰ (SD = 12). The mean difference of 31‰ between both ε values is likely due to evaporative enrichment of deuterium in the leaf water. If this is the only influence on the enrichment, the difference between the δD values of terrestrial and aquatic compounds might be suitable to reconstruct terrestrial evapotranspiration of the lake environment. 相似文献
5.
Mostafa Fayek Lawrence M. Anovitz Debra A. Bostick 《Geochimica et cosmochimica acta》2011,75(13):3677-3686
Diffusion coefficients for oxygen and hydrogen were determined from a series of natural uraninite-H2O experiments between 50 and 700 °C. Under hydrous conditions there are two diffusion mechanisms: (1) an initial extremely fast-path diffusion mechanism that overprinted the oxygen isotopic composition of the entire crystals regardless of temperature and (2) a slower volume-diffusive mechanism dominated by defect clusters that displace or eject nearest neighbor oxygen atoms to form two interstitial sites and two partial vacancies, and by vacancy migration. Using the volume diffusion coefficients in the temperature range of 400-600 °C, diffusion coefficients for oxygen can be represented by D = 1.90e−5 exp (−123,382 J/RT) cm2/s and for temperatures between 100 and 300 °C the diffusion coefficients can be represented by D = 1.95e−10 exp (−62484 J/RT) cm2/s, where the activation energies for uraninite are 123.4 and 62.5 kJ/mol, respectively. Hydrogen diffusion in uraninite appears to be controlled by similar mechanisms as oxygen. Using the volume diffusion coefficients for temperatures between 50 and 700 °C, diffusion coefficients for hydrogen can be represented by D = 9.28e−6 exp (−156,528 J/RT) cm2/s for temperatures between 450 and 700 °C and D = 1.39e−14 exp (−34518 J/RT) cm2/s for temperatures between 50 and 400 °C, where the activation energies for uraninite are 156.5 and 34.5 kJ/mol, respectively.Results from these new experiments have implications for isotopic exchange during natural UO2-water interactions. The exceptionally low δ18O values of natural uraninites (i.e. −32‰ to −19.5‰) from unconformity-type uranium deposits in Saskatchewan, in conjunction with theoretical and experimental uraninite-water and UO3-water fractionation factors, suggest that primary uranium mineralization is not in oxygen isotopic equilibrium with coeval clay and silicate minerals. The low δ18O values have been interpreted as resulting from the low temperature overprinting of primary uranium mineralization in the presence of relatively modern meteoric fluids having δ18O values of ca. −18‰, despite petrographic and U-Pb isotope data that indicate limited alteration. Our data show that the anomalously low oxygen isotopic composition of the uraninite from the Athabasca Basin can be due to meteoric water overprinting under reducing conditions, and meteoric water or groundwater can significantly affect the oxygen isotopic composition of spent nuclear fuel in a geologic repository, with minimal change to the chemical composition or texture. Moreover, the rather fast oxygen and hydrogen diffusion coefficients for uraninite, especially at low temperatures, suggest that oxygen and hydrogen diffusion may impart characteristic isotopic signals that can be used to track the route of fissile material. 相似文献
6.
L. V. Zamana 《Doklady Earth Sciences》2012,442(1):81-85
The negative correlation between values δD and δ18O and concentrations of dissolved silicon in nitrogen hot springs is ascertained, which attests to the directed alteration
of their hydroisotopic composition towards being depleted in heavy isotopes during interaction in the water-rock system. This
fact can be allowed for the cases of the lighter isotopic composition of the hot springs of meteogenic origin relative to
that of local atmospheric precipitation. The shifts in points of isotopic composition of hot springs from the global meteoric
water line can be caused by alterations in either oxygen or hydrogen composition. 相似文献
7.
稳定同位素分析已日益广泛用于对古环境的研究，成为一种十分重要的手段。本文从洛川离石黄土古土壤中钙结核的氧同位素组分分析结果，探讨了将钙结核δ１８Ｏ值转化为古土壤形成时古温度的途径。指出此方法有良好的应用前景，但需要积累大量资料，用统计的方法才能获得可靠的结果。洛川离石黄土中各种古土壤形成时的地表年平均温度都比当地现在的温度要高。发育最好的Ｓ,形成时高出约５℃。用氧同位素组分推算的古温度与其他方法得出的结果可互相比较，但也略有差异。 相似文献
8.
The long-lived halogen radioisotopes 129I and 36Cl provide valuable information regarding the source of fluids in hydrocarbon systems and in localized areas where infiltration of younger meteoric water has occurred. Despite the utility of these two isotopes in providing time-signatures for fluid end-members, considerable uncertainty remains regarding the interpretation of “intermediate-age” waters in hydrologic systems. These waters are likely the result of the combination of two or more halogen sources at some time in the past, each with its own characteristic concentration and isotopic composition. In order to unravel the evolution of these “intermediate-age” waters, the effect that infiltration of meteoric water has on the isotopic composition of older formation waters is modeled. Also evaluated is the effect that the timing of dilution has on 129I and 36Cl signatures observed in the present, specifically, the hypothesis that halogen isotopic signatures imparted by the mixing of brine and meteoric waters early in the development of a sedimentary basin are quantitatively different from those imparted by the mixing of old brines with recent meteoric waters. 相似文献
9.
10.
The oxygen isotopic composition of carbonate in lakes has been used as a useful indicator in Palaeolimnological research, and has made some important contributions to our understanding of lacustrine systems. For modern lakes in arid or cold areas, however, there are few data available to test the effect of lake salinity and temperature on the oxygen isotopic composition of various carbonate sources such as ostracod, bulk carbonate, and fine-grained carbonate (< 60 μm). Here we examined the oxygen isotopic composition of ostracods, bulk carbonate, and fine-grained carbonates, as well as that of coexisting water from Lake Qinghai and the smaller surrounding lakes and ponds on the Qinghai–Tibet Plateau. Our investigation highlights three key effects. First, the oxygen isotopic composition of ostracods, bulk carbonate, and fine-grained carbonate in the lakes and ponds shows a clear response to lake water δ18O values, and these vary with water salinity. The relationship between lake water δ18O and salinity is not only dominated by the evaporation/freshwater input ratios, but is also controlled by the distance to the mouth of the major rivers supplying to the lake. Second, the ostracod, bulk carbonate, and fine-grained carbonate show similar isotopic change trends in the study area, and oxygen isotopic differences between ostracods and authigenic carbonate may be explained by the different water temperatures and very small ‘vital offsets’ of ostracods. Finally, the effect of water depth on temperature leads to increasing δ18O values in carbonates as water depth increases, both in benthic ostracods living on the lake bottom, as well as in bulk carbonate precipitated at the water surface.For arid, high-altitude Lake Qinghai, our results suggest that variations in the δ18O values of carbonate in Lake Qinghai are mainly controlled by the oxygen-isotope ratio of the lake water changing with water salinity. As a secondary effect, increasing water depth leads to cooler bottom and surface water, which may result in more positive δ18O values of ostracod and bulk carbonate. 相似文献
11.
张家口南部地区温泉形成的氢氧稳定同位素及气体组成证据 总被引：5，自引：0，他引：5
本文研究了张家口南部地区温泉（井）水的氢氧稳定同位素组成及溶解气体组分特征。结果表明,大气降水是该区温泉（井）水的补给来源。大气降水在深循环过程中,受地热增温,岩浆残余热的影响,使水温增高并在适当的构造部位涌出地表形成温泉． 相似文献
12.
《Quaternary Research》1986,25(1):63-78
The isotopic composition of paleosol carbonates from Olduvai Gorge can be used to give estimates of the paleoclimatic history of East Africa during the Plio-Pleistocene. Oxygen isotopes are indicative of major changes in the isotopic composition of meteoric water, while carbon isotopes are indicative of major changes in the fraction of biomass using the Hatch-Slack (C4) photosynthetic pathway. Three major periods of climatic change in this terrestrial setting occurred at about 1.67, 1.3, and 0.6 myr. These involved major changes in flora as well as major changes in the isotopic composition of meteoric water. Overall, the climate has become warmer and more arid over the past 2.2 myr. 相似文献
13.
The isotopic composition of meteoric water in Sicily, Italy was investigated from May 2004 until June 2006. Samples were sampled monthly from a network of 50 rain gauges. During the same period 580 groundwater samples were collected from springs and wells to obtain insight into the isotopic composition of the water circulating in the main aquifers of the area. The mean weighted precipitation values were used to define the weighted local meteoric water line for five different sectors of Sicily. The use of Geographical Information System tools, coupled with isotopic vertical gradients, allowed designing an isotopic contour map of precipitation in Sicily. The defined meteoric compositions were highly consistent with most of the groundwater samples in each sector. However, in some areas fractionation processes occurring during and after rainfall slightly modify the isotopic composition of the groundwater. The obtained data set defines the present day isotopic composition of meteoric water in the central Mediterranean area and provides baseline values for future climatic and/or isotope-based hydrology studies. 相似文献
14.
The present work was conducted in the Sinai Peninsula (1) to identify the recharge and flow characteristics and to evaluate
the continuity of the Lower Cretaceous Nubian Sandstone aquifer; and (2) to provide information for the aquifer's rational
appraisal. Isotopic and hydrochemical compositions combined with the geological and hydrogeological settings were used for
this purpose.
A considerable depletion in isotopic content (oxygen-18 and deuterium) and low d-excess values exist in the studied groundwater,
reflecting the contribution of old meteoric water that recharged the aquifer in pluvial times. Modern recharge also occurs
from precipitation that falls on the aquifer outcrops. The wide scatter of the data points around the two meteoric lines,
the global meteoric water line (GMWL) and Mediterranean meteoric water line (MMWL), in the δ18O–δD diagram indicates considerable variation in recharge conditions (amount, altitude, temperature, air masses, distances
from catchment, overland flow, etc.). The isotopic composition in the El-Bruk area is minimum (18O=–9.53‰), very close to the average value of the Western Desert Nubian Sandstone (18O=–10‰), where the local structural and lithologic conditions retard groundwater flow and the main bulk of water becomes noncyclic.
The continuity of the aquifer in northern and central Sinai is evidenced by the isotopic similarity between samples taken
from above and below the central Sinai Ragabet El-Naam fault, the distribution of potentiometric head, and hydrogeological
cross sections.
The combination of isotopic composition in terms of 18O and chemical composition in terms of TDS and salt contents is the basis for separating the studied groundwater into groups
that reflect the recharge sources and isotopic and chemical modifications during flow.
Electronic Publication 相似文献
15.
Indication of hydrogen and oxygen stable isotopes on the characteristics and circulation patterns of medium-low temperature geothermal resources in the Guanzhong Basin,China 
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下载免费PDF全文 Guanzhong Basin is a typical medium-low temperature geothermal field mainly controlled by geo-pressure in the west of China.The characteristics of hydrogen and oxygen isotopes were used to analyze the flow and storage modes of geothermal resources in the basin.In this paper,the basin was divided into six geotectonic units,where a total of 121 samples were collected from geothermal wells and surface water bodies for the analysis of hydrogen-oxygen isotopes.Analytical results show that the isotopic signatures of hydrogen and oxygen throughout Guanzhong Basin reveal a trend of gradual increase from the basin edge areas to the basin center.In terms of recharge systems,the area in the south edge belongs to the geothermal system of Qinling Mountain piedmont,while to the north of Weihe fault is the geothermal system of North mountain piedmont,where the atmospheric temperature is about 0.2℃-1.8℃in the recharge areas.The main factors that affect the geothermal waterδ18O drifting include the depth of geothermal reservoir and temperature of geothermal reservoir,lithological characteristics,water-rock interaction,geothermal reservoir environment and residence time.Theδ18O-δD relation shows that the main source is the meteoric water,together with some sedimentary water,but there are no deep magmatic water and mantle water which recharge the geothermal water in the basin.Through examining the distribution pattern of hydrogen-oxygen isotopic signatures,the groundwater circulation model of this basin can be divided into open circulation type,semi-open type,closed type and sedimentary type.This provides some important information for rational exploitation of the geothermal resources. 相似文献
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17.
Coastal salt marsh ecosystems contain strong environmental gradients that are anticipated to influence the D/H ratios recorded in the leaf waxes of salt-tolerant plants. We characterized the molecular and hydrogen isotopic composition of alkanes in plant and sediment samples as well as the D/H ratios of environmental and plant waters across an elevation and inundation gradient in a southern Californian, coastal salt marsh. We sampled the dominant salt marsh plant species: Salicornia virginica, Arthrocnemum subterminale and Jamuea carnosa (all succulents), as well as Monanthochloe littoralis and Limonium californicum (nonsucculents). Plant xylem water hydrogen isotopic compositions indicate a shift in source waters from meteoric influences at upland sites (δD value −20‰) to seawater dominated values (0‰) at lowland areas. We found leaf water D enrichment relative to xylem water ranging from mean δD values of +54‰ (upland) to +28‰ (lowland), interpreted as a reduction of transpiration with increasing inundation time. This has the effect of increasing the net fractionation between source water and leaf wax product across the environmental gradient from mean values of −101‰ (upland) to −134‰ (lowland), with an attenuated signal recorded in the δD values of plant leaf wax n-alkanes (−122‰ to −136‰). These results constrain the hydrogen isotopic composition of salt marsh organic matter that may contribute to marine carbon budgets of the Santa Barbara Basin, and further indicate the potential for plant leaf waxes to resolve paleoenvironmental change, including sea level change, in sediment cores from salt marsh ecosystems. 相似文献
18.
The chemistry of water in the Cambrian-Ordovician aquifer in six midwestern states has been studied as part of the Northern Midwest Regional Aquifer-System Analysis of the U.S. Geological Survey. Dissolved-solids concentrations generally increase perpendicular to the direction of regional groundwater flow, from less than 400 mg/liter in southeast Minnesota, southwest Wisconsin, and northeast Iowa to more than 10,000 mg/liter in northwest Missouri. Isotopic ratios of hydrogen and oxygen are significantly depleted from north to south, with an areal distribution approximately parallel to the distribution of dissolved solids. For example, δ18O in southern Iowa and northern Missouri is about 6 parts per thousand lighter than δ18O of modern recharge water in Minnesota and Wisconsin. Covariance between δ18O and δD of the groundwater, similar to that of modern precipitation, suggests that the differences in isotopic ratios between groundwater and modern recharge water reflect meteoric signatures of water during past recharge events rather than geochemical processes such as isotopic exchange with aquifer materials. The pronounced parallelism between the distribution of isotopes and dissolved solids over large areas probably reflects largescale recharge of Pleistocene glacial meltwater into the aquifer system, which probably had a paleoflow system with a gradient from northeast to southwest rather than from northwest to southeast. 相似文献
19.
Hsueh-Yu Lu Tsung-Ren Peng Tsung-Kwei Liu Chung-Ho Wang Chih-Chao Huang 《Environmental Geology》2006,50(6):885-898
This study was based on the analysis of isotopic compositions of hydrogen and oxygen in samples from precipitation, groundwater and stream water. In addition, parts of groundwater samples were dated by carbon-14 and tritium. These data are integrated to provide other views of the hydrologic cycle in the Hsinchu-Miaoli groundwater district. The groundwater district is principally composed of Pleistocene and Holocene aquifers. The Pleistocene aquifers are highly deformed by folding and faults into small sub-districts with areas of only tens of square kilometers. These aquifers are exclusively recharged by local precipitation. The Holocene aquifers cover narrow creek valleys, only tens of meters in thickness. The local meteoric water line (LMWL), constructed from rainfall samples in the Hsinchu Science Park, is described by the equation δD=8.02δ18O+10.16, which agrees with the global meteoric water line. In addition, the precipitation isotopic compositions can be categorized into two distinct end members: typhoon type and monsoon type. The groundwater isotopic compositions are perfectly located on an LMWL and can be considered a mixture of precipitations. Based on the mass balance of isotopic compositions of oxygen and hydrogen, infiltration is more active in the rainy season with depleted isotopic compositions. The amount of infiltration during May–September is roughly estimated to comprise at least 55% of the whole year’s recharge. The isotopic compositions of stream water are expressed by a regression equation: δD=7.61δ18O+9.62, which is similar to the LMWL. Although precipitation isotopic compositions are depleted during summer time, the isotopic compositions contrarily show an enriched trend in the upstream area. This is explained by the opposite altitude effect on isotopic compositions for typhoon-related precipitations. 相似文献
20.
Mark J. Abruzzese 《Geochimica et cosmochimica acta》2005,69(6):1377-1390
The oxygen and hydrogen isotopic composition of Eocene and Miocene freshwater cherts in the western United States records regional climatic variation in the Cenozoic. Here, we present isotopic measurements of 47 freshwater cherts of Eocene and Miocene age from the Great Basin of the western United States at two different sites and interpret them in light of regional climatic and tectonic history. The large range of δ18O of terrestrial cherts measured in this study, from 11.2‰ to 31.2‰ (SMOW: Standard Mean Ocean), is shown to be primarily the result of variations in δ18O of surface water. The following trends and patterns are recognized within this range of δ18O values. First, in Cenozoic rocks of northern Nevada, chert δ18O records the same shift observed in authigenic calcite between the Eocene and Miocene that has been attributed to regional surface uplift. The consistent covariation of proxies suggests that chert reliably records and retains a signal of ancient meteoric water isotopic composition, even though our analyses show that chert formed from warmer waters (40°C) than coexisting calcite (20°C). Second, there is a strong positive correlation between δ18O and δD in Eocene age chert from Elko, Nevada and Salina, Utah that suggests large changes in lake water isotopic composition due to evaporation. Evaporative effects on lake water isotopic composition, rather than surface temperature, exert the primary control on the isotopic composition of chert, accounting for 10‰ of the 16‰ range in δ18O measured in Eocene cherts. From authigenic mineral data, we calculate a range in isotopic composition of Eocene precipitation in the north-central Great Basin of −10 to −14‰ for δ18O and −70 to −100‰ for δD, which is in agreement with previous estimates for Eocene basins of the western United States. Due to its resistance to alteration and record of variations in both δ18O and δD of water, chert has the potential to corroborate and constrain the cause of variations in isotope stratigraphies. 相似文献