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1.
Equilibrium isotope fractionation of thallium(Tl) includes the traditional mass-dependent isotope fractionation effect and the nuclear volume effect(NVE). The NVE dominates the overall isotope fractionation, especially at high temperatures. Heavy Tl isotopes tend to be enriched in oxidized Tl^3+-bearing species. Our NVE fractionation results of oxidizing Tl^+ to Tl^3+ can explain the positive enrichments observed in ferromanganese sediments. Experimental results indicate that there could be0.2–0.3 e-unit fractionation between sulfides and silicates at 1650 ℃. It is consistent with our calculation results,which are in the range of 0.17–0.38 e-unit. Importantly,Tl’s concentration in the bulk silicate Earth(BSE) can be used to constrain the amount of materials delivered to Earth during the late veneer accretion stage. Because the Tl concentration in BSE is very low and its Tl isotope composition is similar with that of chondrites, suggesting either no Tl isotope fractionation occurred during numerous evaporation events, or the Tl in current BSE was totally delivered by late veneer. If it is the latter, the Tl-contentbased estimation could challenge the magnitude of late veneer which had been constrained by the amount of highly siderophile elements in BSE. Our results show that the lateaccreted mass is at least five-times larger than the previously suggested magnitude, i.e., 0.5 wt% of current Earth’s mass. The slightly lighter 205 Tl composition of BSE relative to chondrites is probable a sign of occurrence of Tlbearing sulfides, which probably were removed from the mantle in the last accretion stage of the Earth.  相似文献   

2.
Equilibrium Si isotope fractionation factors among orthosilicic acid(i.e.,H4 Si O4(aq)), quartz and the adsorption complexes of H4 Si O4(aq)on Fe(III)-oxyhydroxide surface were calculated using the full-electron wave-function quantum chemistry methods [i.e., B3LYP/6-311G(2df,p)]with a new cluster-model-based treatment. Solvation effects were carefully included in our calculations via water-droplet method combined with implicit solvent models(e.g., PCM).The results revealed that, if it is under equilibrium conditions,heavy Si isotopes would be significantly enriched in quartz in comparison to H4 Si O4(aq). However, most of the field observations suggested that quartz would have identical or even depleted d30 Si values compared to that of H4 Si O4(aq). To explain this discrepancy between the equilibrium calculation results and the field observations, the kinetic isotope effect(KIE) associated with the formation of amorphous silica,which usually is the precursor of crystalline quartz, was investigated using quantum chemistry methods. The KIE results showed that amorphous silica would be significantly enriched in light Si isotopes during its formation. Our equilibrium fractionation results, however, matched a special type of quartz(i.e., Herkimer ‘‘diamond') very well, due to its nearly equilibrated precipitation condition. Opposite to the case of precipitated quartz, a large equilibrium Si isotope fractionation(i.e.,-3.0 %) was found between the absorbed bidentate Si surface complexes(i.e.,2C [ Fe2O2Si(OH)2) and H4 Si O4(aq). This calculated equilibrium Si isotope fractionation factor largely differed from a previous experimental result(ca.-1.08 %). We found that the formation of transient or temporary surface complexes [e.g.,1V [ Fe2OSi(OH)3] may have accounted for the smaller net fractionation observed.With the equilibrium and kinetic Si isotope fractionation factors provided here, the distributions and changes of Si isotope compositions in the Earth's surface systems can be better understood.  相似文献   

3.
Several important equilibrium Si isotope fractionation factors among minerals,organic molecules and the H_4SiO_4 solution are complemented to facilitate the explanation of the distributions of Si isotopes in Earth's surface environments.The results reveal that,in comparison to aqueous H_4SiO_4,heavy Si isotopes will be significantly enriched in secondary silicate minerals.On the contrary,quadra-coordinated organosilicon complexes are enriched in light silicon isotope relative to the solution.The extent of ~(28)Si-enrichment in hyper-coordinated organosilicon complexes was found to be the largest.In addition,the large kinetic isotope effect associated with the polymerization of monosilicic acid and dimer was calculated,and the results support the previous statement that highly ~(28)Sienrichment in the formation of amorphous quartz precursor contributes to the discrepancy between theoretical calculations and field observations.With the equilibrium Si isotope fractionation factors provided here,Si isotope distributions in many of Earth's surface systems can be explained.For example,the change of bulk soil δ~(30)Si can be predicted as a concave pattern with respect to the weathering degree,with the minimum value where allophane completely dissolves and the total amount of sesquioxides and poorly crystalline minerals reaches their maximum.When,under equilibrium conditions,the well-crystallized clays start to precipitate from the pore solutions,the bulk soil δ~(30)Si will increase again and reach a constant value.Similarly,the precipitation of crystalline smectite and the dissolution of poorly crystalline kaolinite may explain the δ~(30)Si variations in the ground water profile.The equilibrium Si isotope fractionations among the quadracoordinated organosilicon complexes and the H_4SiO_4solution may also shed light on the Si isotope distributions in the Si-accumulating plants.  相似文献   

4.
Multiple sulfur and oxygen isotope compositions in Beijing aerosol   总被引：1，自引：0，他引：1  
Multiple sulfur isotopes(32S, 33 S, 34 S, 36S) and oxygen isotopes(16O, 18O) in Beijing aerosols were measured with MAT-253 isotope mass spectrometer. The δ34S values of Beijing aerosol samples range from 1.68‰ to 12.57‰ with an average value of 5.86‰, indicating that the major sulfur source is from direct emission during coal combustion. The δ18O values vary from 5.29‰ to 9.02‰ with an average value of 5.17‰, revealing that the sulfate in Beijing aerosols is mainly composed of the secondary sulfate. The main heterogeneous oxidation of SO2 in atmosphere is related to H2O2 in July and August, whereas H2O2 oxidation and Fe3+ catalytic oxidation with SO2 exist simultaneously in September and October. Remarkable sulfur isotope mass-independent fractionation effect is found in Beijing aerosols, which is commonly attributed to the photochemical oxidation of SO2 in the stratosphere. In addition, thermochemical reactions of sulfur-bearing compounds might be also a source of sulfur isotope anomalies based on the correlation between ?33S and CAPE.  相似文献   

5.
The establishment of geochemical-tracing system of gas generation and accumulation is helpful to re-elucidating the gas migration and accumulation in time and space. To deduce the complex process of gas accumulation, a ternary geochemical-tracing system is set up, according to stable isotope inheritance of source rocks, kinetic fractionation of stable isotopes, time-accumulating effect of noble gas isotopes, mantle-derived volatile inheritance, and organic molecule inheritance of light hydrocarbons and thermally kinetic fractionation in their generation, in combination with the previous achievements of gas geochemistry and geochemical parameters of gas-source correlation. There are tight interactions for the geochemical parameters with much information about parent inheritance and special biomarkers, in which they are confirmed each other, reciprocally associated and preferentially used for the requirement so that we can use these geochemical parameters to effectively demonstrate the sources of natural gas, sedimentary environments and thermal evolution of source rocks, migration and accumulation of natural gas, and rearrangement of natural gas reservoirs. It is necessary for the ternary geochemical-tracing system to predict the formation of high efficient gas reservoir and their distribution in time and space.  相似文献   

6.
Compared with the measureable but limited K isotope variation in geological samples,biological samples have much larger variations in δ~(41)K values:from-1.3‰ to+1.1‰ relative to the international K standard NIST SRM 3141a.Notably,higher plants generally have δ~(41)K values that are lower than igneous rocks,whereas sea plants(algae)have δ~(41)K values that are higher than seawater;the range in δ~(41)K values of plants encompasses the δ~(41)K values of both igneous rocks and seawater.Plant cells utilize different K uptake mechanisms in response to highand low-K conditions.In a low-K environment,plant cells use energy-consuming ion pumps for active uptake of K;plant cells in high-K environments use non-energy-consuming ion channels.Based on these facts and on K isotope data from sea and land plants,it is hypothesized that the different K uptake mechanisms are accompanied by distinct K isotope fractionation behaviors or vital effects.The enrichment of light K isotopes in terrestrial plants could be attributed to preferential transport of isotopically light K in the energy-consuming active uptake process by K ion pumps in the membranes of plant root cells.On the other hand,the enrichment of heavy K isotopes in algae may be caused by a combination of the lack of K isotope fractionation during K uptake from seawater via ion channels and the preferential efflux of light K isotopes across the cell membrane back to the seawater.The large variation of K isotope compositions in biological samples therefore may reflect the diversity of isotopic vital effects for K in organisms,which implies the great potential of K isotopes in biogeochemical studies.  相似文献   

7.
Shallow gas reservoirs are distributed widely in Chinese heavy oil-bearing basins.At present,shallow gas resources have opened up giant potentials.The previous researches indicate the intimate genetic relationship between shallow gas and heavy oil.Shallow gas resources are generated from crude oil degraded by anaerobic microscopic organism,it belongs to biogenic gas family of secondary genesis, namely heavy oil degraded gas.Shallow gas resources are usually distributed in the upward position or the vicinity of heavy oil reservoirs.They are mainly of dry gas,which are composed of methane and only tiny C2 heavy hydrocarbon and relatively higher contents of nitrogen gas.Generally,methane isotopes are light,whose values are between biogenic gas and thermal cracking gas.Ethane isotopes are heavy,which mixed possibly with thermogenic gas.Carbon dioxide bear the characteristics of very heavy carbon isotope,so carbon isotopic fractionation effects are very obvious on the process of microscopic organism degradation crude oil.The heavy oil degraded gas formation,a very complex geological,geochemical and microbiological geochemical process,is the result of a series of reactions of organic matter-microbes and water-hydrocarbon,which is controlled by many factors.  相似文献   

8.
The kinetic fractionation of open-water evaporation against the stable water isotope H_2 ~(18)O is an important mechanism underlying many hydrologic studies that use ~(18)O as an isotopic tracer. A recent in-situ measurement of the isotopic water vapor flux over a lake indicates that the kinetic effect is much weaker(kinetic factor 6.2‰) than assumed previously(kinetic factor14.2‰) by lake isotopic budget studies. This study investigates the implications of the weak kinetic effect for studies of deuterium excess-humidity relationships, regional moisture recycling, and global evapotranspiration partitioning. The results indicate that the low kinetic factor is consistent with the deuterium excess-humidity relationships observed over open oceans.The moisture recycling rate in the Great Lakes region derived from the isotopic tracer method with the low kinetic factor is a much better agreement with those from atmospheric modeling studies than if the default kinetic factor of 14.2‰ is used. The ratio of transpiration to evapotranspiration at global scale decreases from 84±9%(with the default kinetic factor) to 76±19%(with the low kinetic factor), the latter of which is in slightly better agreement with other non-isotopic partitioning results.  相似文献   

9.
The stable carbon isotope values of coalbed methane range widely, and also are gener- ally lighter than that of gases in normal coal-formed gas fields with similar coal rank. There exists strong carbon isotope fractionation in coalbed methane and it makes the carbon isotope value lighter. The correlation between the carbon isotope value and Ro in coalbed methane is less obvious. The coaly source rock maturity cannot be judged by coalbed methane carbon isotope value. The carbon isotopes of coalbed methane become lighter in much different degree due to the hydrodynamics. The stronger the hydrodynamics is, the lighter the CBM carbon isotopic value becomes. Many previous investigations indicated that the desorption-diffusion effects make the carbon isotope value of coalbed methane lighter. However, the explanation has encountered many problems. The authors of this arti- cle suggest that the flowing groundwater dissolution to free methane in coal seams and the free methane exchange with absorbed one is the carbon isotope fractionation mechanism in coalbed methane. The flowing groundwater in coal can easily take more 13CH4 away from free gas and com- paratively leave more 12CH4. This will make 12CH4 density in free gas comparatively higher than that in absorbed gas. The remaining 12CH4 in free gas then exchanges with the adsorbed methane in coal matrix. Some absorbed 13CH4 can be replaced and become free gas. Some free 12CH4 can be ab- sorbed again into coal matrix and become absorbed gas. Part of the newly replaced 13CH4 in free gas will also be taken away by water, leaving preferentially more 12CH4. The remaining 12CH4 in free gas will exchange again with adsorbed methane in the coal matrix. These processes occur all the time. Through accumulative effect, the 12CH4 will be greatly concentrated in coal. Thus, the stable carbon isotope of coalbed methane becomes dramatically lighter. Through simulation experiment on wa- ter-dissolved methane, it had been proved that the flowing water could fractionate the carbon isotope of methane, and easily take heavy carbon isotope away through dissolution.  相似文献   

10.
The Rayleigh distillation isotope fractionation(RDIF) model is one of the most popular methods used in isotope geochemistry. Numerous isotope signals observed in geologic processes have been interpreted with this model. The RDIF model provides a simple mathematic solution for the reservoir-limited equilibrium isotope fractionation effect. Due to the reservoir effect, tremendously large isotope fractionations will always be produced if the reservoir is close to being depleted. However, in real si...  相似文献   

11.
In this study, we performed an integrated investigation of K and Mg isotopes in hydrothermally altered rocks from the giant Dexing porphyry Cu deposit in China. Both the altered porphyry intrusion and the surrounding wall rocks exhibit large variations in K and Mg isotope compositions, with δ41K values ranging between-1.02‰ and 0.38‰, and δ26Mg values ranging between-0.49‰ and 0.32‰. The δ41K and δ26Mg values of the majority of altered samples are higher than the isotopic baseline values for upper continental crust. We attribute the general increase in δ41 K and δ26Mg in altered rocks to hydrothermal alteration,which caused preferential incorporation of heavy K and Mg isotopes in alteration products, particularly phyllosilicates. However,a few altered samples show anomalously low δ41K and δ26Mg values. The δ41K and δ26Mg values do not correlate with K and Mg concentrations, or mineralogy of altered samples. The variable K-Mg isotope data likely reflect fluids of different physicalchemical properties, or different isotopic compositions. Based on the combined K-Mg isotope data, at least three groups of hydrothermal fluids are distinguished from the Dexing porphyry deposit. Therefore, K-Mg isotopes are potentially a novel tracer for fingerprinting fluids in complex hydrothermal systems.  相似文献   

12.
Hydrogen isotopes in lipid biomarkers can trace past changes in the hydrologic cycle. Recent studies have revealed the potential of hydrogen isotopes in microalgal lipids for quantitatively reconstructing water δ~2H(δD) values and salinity. In this study we collected suspended particles along a salinity gradient from the Changjiang River Estuary(CRE), and measured δD values in fatty acids in these particles. The results indicated that δD values of water were correlated highly with salinity from the CRE, in agreement with the results from other estuaries. δD values in palmitic acid and stearic acid had a positive correlation with δD values of water from the CRE. Nevertheless, in the CRE, hydrogen isotope fractionation in fatty acids relative to water increased as salinity increased, opposite the trend in hydrogen isotope fractionation with salinity found in microalgal culture and field studies. We attribute the increase in hydrogen isotope fractionation as salinity increased to light availability, which was likely lower in the particle rich mixing zone at the end of the estuary, and potentially as well to multiple sources of fatty acids in the CRE.  相似文献   

13.
The Sinian Dengying Formation in China hosts one of the oldest gas-bearing reservoirs in the world.With a long geological history,it has developed into the reservoir rocks,whose quality depends on chemical dissolution and cementation.Despite presence of cavities and pores in the algal dolomites of the Dengying Formation,they were mostly filled with various forms of dolomite cements.Therefore,the investigation of these dolomites and their evolution is significant for analyzing the mechanism of pore space preservation.There are five types of cements in the Dengying Formation,which were well sampled for lab measurements such as thin section,cathodeluminescence,minor elements,isotope analysis of carbon,oxygen and strontium,in attempt to explore the fillers’ geochemical characteristics and the diagenetic fluids.They are characterized as follows:firstly,fibrous rim dolomite cement is a typical product formed at sea bottom,and geochemically very similar to the matrix(micrite and microcrystalline dolomite),which could be a reflection of the geochemical characteristics of water at that time;secondly,the diagenetic fluids of the foliated dolomite cements tend to be inheriting,derived from the shallow burial "imprisoned" seawater;thirdly,fine-to medium-grained dolomite cements with fairly high strontium isotopes and low carbon and oxygen isotopes were precipitated chiefly in freshwater during the period of uplifting caused by Tongwan tectonic movement;fourthly,coarse-grained dolomite cements bear a relatively high percentage of Mn element,but low in Fe and Sr,with carbon and oxygen isotopes remarkably shifted to negative values,which all show that they are related to hydrocarbon maturation and migration,and corresponding Thermochemical Sulfate Reduction;lastly,saddle-shaped dolomite cements are hydrothermally associated,and they were formed in high-temperature brine,which had passed through the areas rich in radioactive strontium isotopes.  相似文献   

14.
Geochemistry, zircon U–Pb geochronology, and Hf isotope data for the Early Paleozoic granites in the Baoshan Block reveal the Early Paleozoic tectonic evolution of the Proto-Tethys. The samples are high-K, calcalkaline, strongly peraluminous rocks with A/CNK values of 1.37–1.46, are enriched in SiO2, K2O, and Rb, and are depleted in Nb, P, Ti, Eu, and heavy rare earth elements,which indicates the crystallization fractionation of the granitic magma. Zircon U–Pb dating indica...  相似文献   

15.
Natural nitrogen isotope composition(δ~(15)N) is an indicator of nitrogen sources and is useful in the investigation of nitrogen cycling in organisms and ecosystems. δ~(15)N is also used to study assimilation of inorganic nitrogen. However, the foliar δ~(15)N of intact plants, which is a consequence of nitrate assimilation occurring in the roots and shoots, is not suited for studying nitrate assimilation in cases where nitrate is the sole nitrogen source. In this study, Orychophragmus violaceus(Ov) and Brassica napus(Bn) plantlets, in which nitrate assimilation occurred in the leaves, were used to study the relationship between foliar δ~(15)N and nitrate assimilation.The plantlets were grown in vitro in culture media with different nitrate concentrations, and no root formation occurred for the plantlets during the multiplication stage.Nitrogen isotope fractionation occurred in both the Ov and the Bn plantlets under all treatments. Furthermore, the foliar nitrogen content of both the Ov and Bn plantlets increased with increasing nitrate concentration. Foliar nitrogen isotope fractionation was negatively correlated with foliar nitrogen content for both the Ov and Bn plantlets. Our results suggest that the foliar nitrogen isotope fractionation value could be employed to evaluate nitrate assimilation ability and leaf nitrate reductase activity.Moreover, high external nitrate concentrations couldcontribute to improved foliar nitrogen content and enhanced nitrate assimilation ability.  相似文献   

16.
Shales are a major sink for K into seawater delivered from continental weathering,and are potential recorders of K cycling.High precision K isotope analyses reveal a[0.6%variation in δ^41K values(41K/39K relative to NIST SRM 3141a)from a set of well characterized postArchean Australian shale(PAAS)samples.By contrast,loess samples have relatively homogenous δ^41K values(-0.5±0.1%),which may represent the average K composition of upper continental crust.Most of the shales analyzed in this study have experienced K enrichment relative to average continental crust,and the majority of them define a trend of decreasing δ^41K value(from-0.5to-0.7%)with increasing K content and K/Na ratio,indicating cation exchange in clays minerals is accompanied by K isotope fractionation.Several shale samples do not follow the trend and have elevated δ^41K values up to-0.1%,and these samples are characterized by variable Fe isotope compositions,which reflect post-depositional processes.The K isotope variability observed in shales,in combination with recent findings about K isotope fractionation during continental weathering,indicates that K isotopes fractionate during cycling of K between different reservoirs,and K isotopes in sediments may be used to trace geological cycling of K.  相似文献   

17.
Tectonically deformed coal(TDC)develops because of the superimposed deformation and metamorphism of a coal seam by tectonic movements.The migration and accumulation of trace elements in TDC is largely in response to stress-strain conditions.To develop a law governing the migration and aggregation of sensitive elements and investigate the geological controls on TDC,coal samples from different deformation sequences were collected from the Haizi mine,in the Huaibei coalfield in Anhui Province,China,and the concentrations of 49 elements were determined by XRF and ICP-MS,and then microscopically analyzed.The results show that the distribution and morphology of minerals in coal is related to the deformation degree of TDC.The evolutionary process runs from orderly distribution of minerals in a weak brittle deformed coal to disordered distributions in ductile deformed coal.According to the elemental distribution characteristics in TDC,four types of element migration can be identified:stable,aggregate,declining,and undulate types,which are closely related to the deformation degree of TDC.Present data indicate that the overall distribution of rare earth elements(REE)does not change with metamorphism and deformation,but it shows obvious dynamic differentiation phenomena along with the deformation of TDC.Tectonic action after coal-formation,brittle or ductile deformation,and the metamorphic mechanism and its accompanying dynamic thermal effects are the main factors that influence the redistribution of elements in TDC.We conclude that tectonic movements provide the motivation and basis for the redistribution of elements and the paths and modes of element migration are controlled by brittle and ductile deformation metamorphic processes.The dynamic thermal effect has the most significant effect on coal metamorphism and tectonic-stress-accelerated element migration and accumulation.These factors then induce the tectonic-dynamic differentiation phenomenon of element migration.  相似文献   

18.
The surface water and groundwater are important components of water cycle, and the interaction between surface water and groundwater is the important part in water cycle research. As the effective tracers in water cycle research, environmental isotope and hydrochemistry can reveal the interrelationships between surface water and groundwater effectively. The study area is the Huaisha River basin, which is located in Huairou district, Beijing. The field surveying and sampling for spring, river and well water were finished in 2002 and 2003. The hydrogen and oxygen isotopes and water quality were measured at the laboratory. The spatial characteristics in isotope and evolution of water quality along river lines at the different area were analyzed. The altitude effect of oxygen isotope in springs was revealed, and then using this equation, theory foundation for deducing recharge source of spring was estimated. By applying the mass balance method, the annual mean groundwater recharge rate at the catchment was estimated. Based on the groundwater recharge analysis, combining the hydrogeological condition analysis, and comparing the rainfall-runoff coefficients from the 1960s to 1990s in the Huaisha River basin and those in the Chaobai River basin, part of the runoff in the Huaisha River basin is recharged outside of this basin, in other words, this basin is an un-enclosed basin. On the basis of synthetically analyses, combining the compositions of hydrogen and oxygen isotopes and hydrochemistry, geomorphology, geology, and watershed systems characteristics, the relative contributions between surface water and groundwater flow at the different areas at the catchments were evaluated, and the interaction between surface water and groundwater was re- vealed lastly.  相似文献   

19.
The Baiyangping Cu-Ag polymetallic ore district is located in the northern part of the Lanping-Simao foreland fold belt,between the Jinshajiang-Ailaoshan and Lancangjiang faults,and the deposit can be divided into eastern and western ore zones.Based upon microscope observation of ore minerals and analysis of zinc,copper,and strontium isotope composition,we conclude that:(1)the zinc isotopic compositions of sphalerite from the eastern and western ore belt of the Baiyangping polymetallic ore deposits are enriched in both the heavy(-0.09‰ to+0.15‰) and light(-0.19‰ to-0.01‰)zinc isotopes.Rayleigh fractionation is likely the additional factor controlling the observed temporal and spatial variations in zinc isotopes in the two studied ore zones.The zinc isotopic composition in the Baiyangping polymetallic Pb-Zn deposits may have the same fractionation as that of magmatic-hydrothermal,VHMS,SEDEX,and MVT deposits,as demonstrated by geological and other geochemical evidence;(2) the range of δ~(65)Cu in massive tetrahedrite is from-0.06‰ to+0.12 ‰ that relates to the early stages of ore-formation,which are higher than that of venial chalcopyrite(from-0.72‰ to-0.07‰)formed at a late ore-forming stage in the western ore belt.Different ore-forming stages and alteration or leaching processes are likely the main factors controlling the observed variations in copper isotopes in the western ore zone;(3) the ~(87)Sr/~(86)Sr value of hydrothermal calcite in eastern(0.7080-0.7093) and western(0.7085-0.7113) ore belt suggested that mineralization of early calcite,with~(87)Sr/~(86)Sr values much higher than in ancient Late Triassic seawater,may be related to recrystallization from a radiogenic Sr-rich or silicifying fluid,either from the strata that the ore-forming fluid flows through or from other fluids.  相似文献   

20.
Discovered in S15 and some other wells, the Lower Ordovician in the northern Tarim Basin consists mainly of brown gray-dark gray very fine-fine crystalline dolomite, with a minor portion of locally light gray-white medium-coarse crystalline dolomite. Silicification can be observed in the medium-coarse dolomite, and some euhedral drusy quartz can also be found in pores and fractures of the dolomite. The homogenization temperature of the fluid inclusions in the medium-coarse dolomite is between 110 and 200°C with maximum between 140 and 190°C, and the salinity is between 10.7 and 18.5 wt.% NaCl Eq. The homogenization temperature and salinity of the fluid inclusions in the medium-coarse dolomite are similar to those in the drusy quartz. Compared with the very fine-fine dolomite, the medium-coarse phase contains relatively high Fe and Mn. The average concentration of FeO and MnO in the medium-coarse dolomite is 1.917% and 0.323%, respectively. The medium-coarse dolomite has a remarkable negative Eu anomaly, consistent with the REE pattern of the intermediate-felsic igneous rocks in the Tarim Basin. The oxygen isotopic composition of the medium-coarse dolomite is relatively lighter than that of the very fine-fine dolomite. The δ18OPDB values of the medium-coarse dolomite are between -10.35‰ and -7.31‰. The δ18OSMOW values of the fluid associated with the medium-coarse dolomite can be calculated according to homogenization temperature and oxygen isotope fractionation factor between dolomite and fluid, and the calculated values are between +4‰ and +10‰, consistent with those of the hydrothermal fluid. The medium-coarse dolomite has relatively high 87Sr/86Sr ratios as well, indi- cating an origin associated with intermediate-felsic igneous rock. The homogenization temperature, element composition, REE pattern, oxygen and strontium isotopes demonstrate that the medium-coarse dolomite is the result of recrystallization of very fine-fine dolomite under hydrothermal environment. The hydrothermal dolomite recrystallization is a special event but exists extensively in the Tarim Basin. The recrystallized dolomite becomes well reservoir bed for many intercrystalline pores and dissolution pores are produced in this event, so that more attention should be paid to the altered dolomite during the petroleum exploration in the lower Paleozoic in the Tarim Basin.  相似文献   

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