Soil carbon stock of the Central-East Asia in the climate warming

Water samples from the Wujiang River, a typical karst river system, were analyzed for major ion concentrations and δ^34S values of dissolved sulfate in order to identify the sources of sulfate, quantify the sulfate export flux and understand the role of sulfur cycling in chemical weathering rate of carbonate. Spatial variations in sulfate concentration and sulfur isotopic composition of tributaries over the catchment area are obvious, allowing to decipher S sources between rocks and atmosphere. According to the variations in sulfate concentration and isotopic composition, it is inferred that sulfate ions in the upper-reach river waters may have three sources, rain water, sulfate resultant from oxidation of pyrite in coal, and sulfate from sulfide deposits. In the lower reaches, the S isotopic composition of the samples lies mainly on a mixing trend between evaporite sulfate and rainwater sulfate, the contribution of sulfate from oxidation of pyrite being lesser. A pronounced seasonal variation in both content and isotopic composition of sulfate characterizes the Wujiang River. The average sulfate concentration of the waters is 0.65 mmol/L in winter, 0.17 mmol/L higher than that in summer. River water δ^34S values range from -15.7‰ to 18.9‰ in winter, while the δ^34S values of river waters in summer vary to a lesser extent than in winter, from -11.5‰ to 8.3‰. The δ^34S values of the main stream range from -6.7‰ to -3.9‰ in summer, averaging 3‰ lower than in winter. This indicates that in summer, when the discharge increases, the contribution of a source enriched in light isotopes to the atmosphere or the oxidation of pyrite in coal is more important.     

Analysis of water vapor characteristics in snowstorm process on the northern slope of Tianshan Mountains北大核心CSCD

Based on the daily precipitation data of 16 national meteorological observation stations on the north⁃ ern slope of Tianshan Mountains from 2000 to 2020（September to April the following year）,28 blizzard weath⁃ er processes were screened out. Then NCEP/NCAR reanalysis data and HYSPLIT model were used to simulate backward tracking of the water vapor during the snowstorm,analysis of the circulation background of the snow⁃ storm process on the northern slope of the Tianshan Mountains,as well as the main sources and transport of wa⁃ ter vapor and its contribution to the snowstorm. The research showed that the snowstorm area in the northern slope of the Tianshan Mountains was located on the right side of the axis of the southwest jet at 300 hPa high,the southwest airflow in front of the West Siberia trough at 500 hPa,the front convergence of the exit area of the southwest jet at low level at 700 hPa,and the convergence area of water vapor flux divergence and the overlap near the ground cold front area. The water vapor affecting the blizzard on the northern slope of the Tianshan Mountains mainly came from the Mediterranean Sea,the Black Sea and its vicinity,Southwest Asia,Central Asia,the Atlantic Ocean and its coasts,as well as the 850 hPa water vapor in Europe and northern Xinjiang. The water vapor from North America and other places had a relatively small contribution to the blizzard;after each water vapor source reaches the key area with the westerly airflow,under suitable circulation conditions. It mainly entered the blizzard area along the westward（southwest）and the northwest paths. But there were some differences between the layers. Based on the above characteristics,the structure of the source and transport of wa⁃ ter vapor in the snowstorm process on the northern slope of the Tianshan Mountains was established and the char⁃ acteristics of vapor transport at various heights were revealed. © 2023 The Author(s).     

Seasonal variations in sulfur isotopic composition of dissolved SO<Subscript>4</Subscript><Superscript>2−</Superscript> in the Aha Lake,Guiyang and their implications

The Aha Lake is a seasonal anoxic water system in the southwest of Guiyang City, Guizhou Province, China. Seasonal variations in SO42- concentrations and their isotopic compositions in lake water as well as in the tributaries were investigated in this study. The results showed that sulfate concentrations in river water range from 0.94 to 6.52 mmol/L and their δ34S values range from -14.9‰ and 0.9‰, while lake water has sulfate concentrations ranging from 1.91 to 2.79 mmol/L, and δ34S values from -9.8‰ to -5.9‰. It is suggested that coal mining drainage is the major source of SO42- in the Aha Lake. Rainfall, sewage discharge, sulfide oxidation and gypsum dissolution have made only limited contributions. Different depth-dependent distributions of dissolved SO42- and δ34S were de-veloped for both DB and LJK in summer and winter. Due to water overturn, δ34S values display homogenous vertical distributions in winter and spring. While in summer and autumn, significant positive shifts of δ34S were clearly ob-served in epilimnion and bottom strata as a result of water stratification. High δ34S values in epilimnion may result from the retention of rainwater during water stratification. Dissimilatory sulfate reduction by bacteria was thought to be responsible for the increase of δ34S value in hypolimnion.     

Origin of Ore-Forming Fluids of Mississippi Valley-Type （MVT） Pb-Zn Deposits in Kangdian Area, China

Analyses of fluid-inclusion leachates from ore deposits show that Na/Br ratios are within the range of 75 - 358 and Cl/Br 67 - 394, respectively, and this variation trend coincides with the seawater evaporation trajectory on the basis of the Na/Br and Cl/Br ratios. The average Cl/Br and Na/Br ratios of mineralizing fluids are 185 and 173 respectively, which are very close to the ratios ( 120 and 233 ) of the residual evaporated seawater past the point of halite precipitation. It is suggested that the original mineralizing brine was derived from highly evapo-rated seawater with a high salinity. However, the inclusion fluids have absolute Na values of 69.9—2606.2 mmol kg^-1 and Cl values of 106.7 — 1995.5 mmol kg^-1. Most of the values are much less than those of seawater: Na, 485 mmol kg^-1 and Cl, 566 mmol kg^-1 , respectively; the salinity measured from fluid inclusions of the deposits ranges from 2.47 wt% to 15.78 wt% NaCl equiv. The mineralizing brine has been diluted. The δ ^18O and δD values of ore-forming fluids vary from -8.21‰ to 9.51‰ and from -40.3‰ to -94.3‰, respectively. The δD values of meteoric water in this region varied from - 80‰ to - 100‰ during the Jurassic. This evidenced that the ore-forming fluids are the mixture of seawater and meteoric water. Highly evaporated seawater was responsible for leaching and extracting Pb, Zn and Fe, and mixed with and diluted by descending meteoric water, which resulted in the formation of ores.     

Genesis of Neogene Formation Waters in the Central Qaidam Basin: Clues from Hydrochemistry and Stable D-O-S-Sr Isotopes

Geological explorations have revealed plentiful Neogene formation waters in anticlines in the central Qaidam Basin (QB). However, the hydrochemistry and origin of these waters are obscure. In this study, the hydrochemistry and D-O-S-Sr isotopes of these formation waters were determined to study their origin and evolution. The formation waters are enriched in Na-Ca-Cl, and depleted in Mg-K-SO4-HCO3 ions with elevated Li-B-Br-Sr elements. The D-O isotopes prove that the formation waters originated from weak-evaporated meteoric waters, and experienced water-rock interactions. Ion comparisons and Caexcess–Nadeficit diagrams suggest that solute sources of these waters include evaporite dissolution, water-rock interaction, and minor residual lake brines. Bacterial sulfate reduction and water-rock interactions are supported by the high S-Sr isotopes. The enriched Li-B-Br-Sr concentrations of these waters are in accord with the high geochemical background values of the QB. Regarding the genesis of the formation waters, it can be concluded that meteoric waters from the southern Kunlun Mountains were discharged into the basin, weakly evaporated, and then infiltrated into the Neogene strata through faults leaching the soluble ions and mixing with residual lake brines, and all experienced water–rock interactions and a sulphate reduction process.     

挪威山地冰川上雪和粒雪中δ18O的解释及对区域气候的指示意义

Variations of δ18O in the snow which accumulates at a Nordic temperate glacier during the win-ter are not entirely eliminated after a few months of ablation in the following summer. Survive of isotopicsignals closely relates to the re-freezing capacity of snow accumulated in winter when its temperature wasbelow 0 ℃. The melt-water re-freezing ice layers formed in winter hindered subsequent melt-water percolation in summer when snow temperature was at melting point and, therefore, varied isotopic record wasreserved between these ice layers. The isotopic record in snow pack can provide an estimate of the ap-proximate trend of the most recent winter season temperatures. The relationship between regional tem-perature changes and δ18O values in the snow pack is affected by many natural factors, but 1989-1990 (aglacier balance year) winter air temperatures were reflected in the snow which remained on the glacierAustre Okstindbreen at an altitude of 1 350 m in July 1990. There was larger amplitude of variations ofδ18O values in the 4. 1 m of snow above the 1989 summer surface, but variations in the underlying firnwere relatively small. Melt water percolation modifies the initial variations of δ18O values in the snowpack. At a site below the mean equilibrium line altitude on Austre Okstindbreen, increased isotopic bom-ogenization within a ten-day period in July accompanied an increase of the mean δ18O value. Although theisotopic record at a temperate glacier is likely to be influenced by more factors than is that at polar glac-iers, it can provide an estimate of the approximate trend of recent local temperature variations.     

Carbon and Oxygen Isotopic Composition of Surface-Sediment Carbonate in Bosten Lake (Xinjiang, China) and its Controlling Factors

Bosten Lake is a mid-latitude lake with water mainly supplied by melting ice and snow in the Tianshan Mountains. The depositional environment of the lake is spatially not uniform due to the proximity of the major inlet and the single outlet in the western part of the lake. The analytical results show that the carbon and oxygen isotopic composition of recent lake sediments is related to this specific lacustrine depositional environment and to the resulting carbonate mineralogy. In the southwestern lake region between the Kaidu River inlet and the Kongqi River outlet, carbon isotope composition (δ13C) values of the carbonate sediment (-1‰ to -2‰) have no relation to the oxygen isotope composition of the carbonate (δ18O) values (-7‰ to -8‰), with both isotopes showing a low variability. The carbonate content is low (<20%). Carbonate minerals analyzed by X-ray diffraction are mainly composed of calcite, while aragonite was not recorded. The salinity of the lake water is low in the estuary region as a result of the Kaidu River inflow. In comparison, the carbon and oxygen isotope values are higher in the middle and eastern parts of the lake, with δ13C values between approximately +0.5‰ and +3‰, and δ18O values between -1‰ and -5‰. There is a moderate correlation between the stable oxygen and carbon isotopes, with a coefficient of correlation r of approximately 0.63. This implies that the lake water has a relatively short residence time. Carbonate minerals constitute calcite and aragonite in the middle and eastern region of the lake. Aragonite and Mg-calcite are formed at higher lake water salinity and temperatures, and larger evaporation effects. More saline lake water in the middle and eastern region of the lake and the enhanced isotopic equilibrium between water and atmospheric CO2 cause the correlating carbon and oxygen isotope values determined for aragonite and Mg-calcite. Evaporation and biological processes are the main reasons for the salinity and carbonate mineralogy influence of the surface-sediment carbonate in Bosten Lake. The lake water residence time and the CO2 exchange between the atmosphere and the water body control the carbon and oxygen isotope composition of the carbonate sediment. In addition, organic matter pollution and decomposition result in the abnormally low carbon isotope values of the lake surface-sediment carbonate.     

Oxygen and Hydrogen Isotopes of Waters in the Ordos Basin,China: Implications for Recharge of Groundwater in the North of Cretaceous Groundwater Basin

Hundreds of precipitation samples collected from meteorological stations in the Ordos Basin from January 1988 to December 2005 were used to set up a local meteoric water line and to calculate weighted average isotopic compositions of modern precipitation. Oxygen and hydrogen isotopes, with averages of ?7.8‰ and ?53.0‰ for δ18O and δD, respectively, are depleted in winter and rich in spring, and gradually decrease in summer and fall, illustrating that the seasonal effect is considerable. They also show that the isotopic difference between south portion and north portion of the Ordos Basin are not obvious, and the isotope in the middle portion is normally depleted. The isotope compositions of 32 samples collected from shallow groundwater (less than a depth of 150 m) in desert plateau range from ?10.6‰ to ?6.0‰ with an average of ?8.4‰ for δ18O and from ?85‰ to ?46‰ with an average of ?63‰ for δD. Most of them are identical with modern precipitation. The isotope compositions of 22 middle and deep groundwaters (greater than a depth of 275 m) fall in ranges from ?11.6‰ to ?8.8‰ with an average of ?10.2‰ for δ18O and from ?89‰ to ?63‰ with an average of ?76‰ for δD. The average values are significantly less than those of modern precipitation, illustrating that the middle and deep groundwaters were recharged at comparatively lower air temperatures. Primary analysis of 14C shows that the recharge of the middle and deep groundwaters started at late Pleistocene. The isotopes of 13 lake water samples collected from eight lakes define a local evaporation trend, with a relatively flat slope of 3.77, and show that the lake waters were mainly fed by modern precipitation and shallow groundwater.     

Isotopic effect of runoff in the Yarlung Zangbo River

This paper mainly analyzed the isotopic effect of precipitation in the Yarlung Zangbo River.On the whole,the isotopic compositions of most water samples fall on the upper right of the global meteoric water line.According to δD and δ18O data of the samples,the precipitation equation is figured out as δD=8 δ18O+10,showing that they are derived from precipitation but have experienced intensive evaporation.With obvious region-continental effect(a continuous depletion in heavy isotopes in water bodies occurs with increasing distance from the coast),the water presents a reducing trend of δD and δ18O westwards and southwards.Altitudinal effect is evident here,occur-ring in both trunk stream and main branches of the Yarlung Zangbo River.The distribution of water isotopic compo-sitions is concerned with the movement of precipitation clouds from the Bay of Bengal and the Nujiang River and is affected by the topographic and climatic conditions of the Tibetan Plateau.     

Carbon and Oxygen Isotopic Composition of Surface‐Sediment Carbonate in Bosten Lake (Xinjiang,China) and its Controlling Factors

Bosten Lake is a mid-latitude lake with water mainly supplied by melting ice and snow in the Tianshan Mountains. The depositional environment of the lake is spatially not uniform due to the proximity of the major inlet and the single outlet in the western part of the lake. The analytical results show that the carbon and oxygen isotopic composition of recent lake sediments is related to this specific lacustrine depositional environment and to the resulting carbonate mineralogy. In the southwestern lake region between the Kaidu River inlet and the Kongqi River outlet, carbon isotope composition (δ13C) values of the carbonate sediment (?1‰ to ?2‰) have no relation to the oxygen isotope composition of the carbonate (δ18O) values (?7‰ to ?8‰), with both isotopes showing a low variability. The carbonate content is low (<20%). Carbonate minerals analyzed by X-ray diffraction are mainly composed of calcite, while aragonite was not recorded. The salinity of the lake water is low in the estuary region as a result of the Kaidu River inflow. In comparison, the carbon and oxygen isotope values are higher in the middle and eastern parts of the lake, with δ13C values between approximately +0.5‰ and +3‰, and δ18O values between ?1‰ and ?5‰. There is a moderate correlation between the stable oxygen and carbon isotopes, with a coefficient of correlation r of approximately 0.63. This implies that the lake water has a relatively short residence time. Carbonate minerals constitute calcite and aragonite in the middle and eastern region of the lake. Aragonite and Mg–calcite are formed at higher lake water salinity and temperatures, and larger evaporation effects. More saline lake water in the middle and eastern region of the lake and the enhanced isotopic equilibrium between water and atmospheric CO2 cause the correlating carbon and oxygen isotope values determined for aragonite and Mg–calcite. Evaporation and biological processes are the main reasons for the salinity and carbonate mineralogy influence of the surface-sediment carbonate in Bosten Lake. The lake water residence time and the CO2 exchange between the atmosphere and the water body control the carbon and oxygen isotope composition of the carbonate sediment. In addition, organic matter pollution and decomposition result in the abnormally low carbon isotope values of the lake surface-sediment carbonate.     

Helium and argon isotopic compositions of the Longquanzhan gold deposit in the Yishu fault zone and their geological implications

The Longquanzhan gold deposit hosted in granitic cataclasites with mylontization of the foot wall of the main Yishui-Tangtou fault. 3He/4He ratios in fluid inclusions range from 0. 14 to 0. 24 R/Ra,close to those of the crust-source helium. 40Ar/36Ar ratios were measured to be 289-1811, slightly higher than those of atmospheric argon. The results of analysis of helium and argon isotopes suggested that ore-forming fluids were derived chiefly from the crust. The δ18O values of fluid inclusions from vein quartz range from -1.78‰ to 4.07‰, and the δD values of the fluid inclusions vary between -74‰ and -77‰. The hydrogen and oxygen isotope data indicated that the ore-forming fluid for the Longquanzhan gold deposit had mixed with meteoric water in the process of mineralization. This is consistent with the conclusion from the helium and argon isotope data.     

Geochemical and Isotopic Techniques Constraints on the Origin, Evolution, and Residence Time of Low-enthalpy Geothermal Water in Western Wugongshan, SE China

Geothermal resources are increasingly gaining attention as a competitive, clean energy source to address the energy crisis and mitigate climate change. The Wugongshan area, situated in the southeast coast geothermal belt of China, is a typical geothermal anomaly and contains abundant medium- and low-temperature geothermal resources. This study employed hydrogeochemical and isotopic techniques to explore the cyclic evolution of geothermal water in the western Wugongshan region, encompassing the recharge origin, water–rock interaction mechanisms, and residence time. The results show that the geothermal water in the western region of Wugongshan is weakly alkaline, with low enthalpy and mineralization levels. The hydrochemistry of geothermal waters is dominated by Na-HCO3 and Na-SO4, while the hydrochemistry types of cold springs are all Na-HCO3. The hydrochemistry types of surface waters and rain waters are Na-HCO3 or Ca-HCO3. The δD and δ18O values reveal that the geothermal waters are recharged by atmospheric precipitation at an altitude between 550.0 and 1218.6 m. Molar ratios of major solutes and isotopic compositions of 87Sr/86Sr underscore the significant role of silicate weathering, dissolution, and cation exchange in controlling geothermal water chemistry. Additionally, geothermal waters experienced varying degrees of mixing with cold water during their ascent. The δ13C values suggest that the primary sources of carbon in the geothermal waters were biogenic and organic. The δ34S value suggests that the sulfates in geothermal water originate from sulfide minerals in the surrounding rock. Age dating using 3H and 14C isotopes suggests that geothermal waters have a residence time exceeding 1 kaBP and undergo a long-distance cycling process.     

Study of Metallogenic Fluid Sources of Five Gold Deposits in Zhangjiakou,China

It is very important to define the type and composition of metallogenic fluid in terms of the hydrogen and oxygen isotope data in the study of ore-forming mechanism.In the long past,the method to discriminate metallogenic fluid sources by comparing the δD-δ^18 O diagram with the standard values in not valid when the hydrogen and oxygen isotope values are plotted between the meteoric water line and the magmatic water area.Based on their hydrogen and oxygen isotope information of five gold deposits(Shuijingtun,Xiaoyingpan,Dongping, Zhongshangou and Jinjiazhuang)in the Zhangjiakou area,this paper details the metallogenic fluid sources and presents water/rock ratios in the vie gold deposits and the principle of water/rock exchange.     

Stable isotope geochemical characteristics of dissolved inorganic carbon in the Jiulong River Estuary,Fujian Province,China

The isotopic composition of dissolved inorganic carbon （DIC） in estuarine environments has been studied for its significant role in determining the isotopic composition of inorganic/organic matter and its applications to the study of various natural processes. In this paper, based on the stable isotope geochemical characteristics of dis- solved inorganic carbon in the Jiulong River Estuary, the following conclusions are drawn： （1） δ13CDIC values are mainly controlled by the mixing ratio of fresh water and sea water; （2）δ13Cphytoplankton values are linearly related to the δ13CDIC values; （3） δ13CpoM values for the Jiulong River Estuary are affected by anthropogenic pollution signifi- cantly; and （4） the comprehensive analysis of δ13Cphytoplankton, δ13CpoM and δ13CDIc shows that along with increasing salinity, the proportion of POM derived from the degradation of phytoplanktons gradually increases.     

Stable isotopes （S, Cl） and hydrochemical variations in a karstic ground water system, Guiyang, SW China

A groundwater system in a karstic terrain is easily subject to pollution and its remediation is difficult once contaminated by human activities. The groundwater samples collected in both winter and summer seasons at Guiyang, SW China, show a wide range of variations in chemical composition and dominance of Ca^2＋, Mg^2＋, SO4^2-, and HCO3^- ions. The anthropogenic inputs include Cl^-, NO3^-, SO4^2-, Na^＋, and K^＋, as judged from the relationships between different elemental ratios and sewage samples. Cl^- concentrations of all water samples in the study area vary from 0 to 3.9 mmol/L in winter and are higher than in summer. In most of the samples, SO4^2- concentrations are high, ranging from 0.1 to 11 mmol/U The studies show that the cycling of sulfur plays an important role in controlling water chemistry and fate of contaminants in groundwater. In order to understand the source of SO4^2- and the geochemical cycling of some elements in the karstic groundwater environment, we have carried out a study on the variations of S and Cl isotope compositions, in addition to other isotopic tracers such as ^87Sr/^86Sr and δ^13C studied previously. The δ^37Cl values of the groundwater samples present a seasonal variation, ranging from 0.00‰ to ＋2.03‰ in winter and from -1.46‰ to ＋0.29‰ in summer. The surface water samples show a similar range of variations as observed for groundwater. Two rainwater samples collected at Guiyang have a distinct isotopic signature （mean value is -3‰） compared to the δ^37Cl values reported in literature. These results indicate that ground water is mainly derived from precipitation and suggest a fast recharge of the karst system by surface water.     

B, Sr, O and H Isotopic Compositions of Formation Waters from the Bachu Bulge in the Tarim Basin

In order to elucidate the origin and migration of basinal brines in the Bachu Bulge, Tarim Basin, we have carried out analyses on chemical composition, and boron, hydrogen and oxygen isotopes of formation waters together with the XRD of clay minerals from the Paleozoic strata. The waters show Ca, B, Li and Sr enrichment and SO4 depletion in the Carboniferous and Ordovician and K enrichment in part of the Ordovician relative to seawater. The relationship between δD and δ^18O shows that all the data of the waters decline towards the Global Meteoric Water Line with the intersection of them close to the present-day local meteoric water, suggesting that modern meteoric water has mixed with evaporated seawater. The ^87Sr/^86Sr ratios range from 0.7090 to 0.7011, significantly higher than those of the contemporary seawater. The δ^11B values range from ＋19.7 to ＋32.3‰, showing a decrease with the depth and B concentrations. The results suggest that isotopically distinct B and Sr were derived from external sources. However, since the percentages of illite are shown to increase with depth among clay minerals in the study area, i.e., illite is due to precipitation rather than leaching during deeper burial, it is unlikely for illite to have contributed a significant amount of B to the waters. Thus, B with low δ^11B values is interpreted to have been added mainly from thermal degradation of kerogen or the basalts in the Cambrian and Lower Ordovician.     

Isotope geochemistry of ore fluids for the Dongsheng sandstone-type uranium deposit, China

The Dongsheng sandstone-type uranium deposit is one of the large-sized sandstone-type uranium deposits discovered in the northern part of the Ordos Basin of China in recent years. Geochemical characteristics of the Dongsheng uranium deposit are significantly different from those of the typical interlayered oxidized sandstone-type uranium ore deposits in the region of Middle Asia. Fluid inclusion studies of the uranium deposit showed that the uranium ore-forming temperatures are within the range of 150–160℃. Their 3He/4He ratios are within the range of 0.02–1.00 R/Ra, about 5–40 times those of the crust. Their 40Ar/36Ar ratios vary from 584 to 1243, much higher than the values of atmospheric argon. The δ18OH2O and δD values of fluid inclusions from the uranium deposit are -3.0‰– -8.75‰ and -55.8‰– -71.3‰, respectively, reflecting the characteristics of mixed fluid of meteoric water and magmatic water. The δ18OH2O and δD values of kaolinite layer at the bottom of the uranium ore deposit are 6.1‰ and -77‰, respectively, showing the characteristics of magmatic water. The δ13CV-PDB and δ18OH2O values of calcite veins in uranium ores are -8.0‰ and 5.76‰, respectively, showing the characteristics of mantle source. Geochemical characteristics of fluid inclusions indicated that the ore-formation fluid for the Dongsheng uranium deposit was a mixed fluid of meteoric water and deep-source fluid from the crust. It was proposed that the Jurassic-Cretaceous U-rich metamorphic rocks and granites widespread in the northern uplift area of the Ordos Basin had been weathered and denudated and the ore-forming elements, mainly uranium, were transported by meteoric waters to the Dongsheng region, where uranium ores were formed. Tectonothermal events and magmatic activities in the Ordos Basin during the Mesozoic made fluids in the deep interior and oil/gas at shallow levels upwarp along the fault zone and activated fractures, filling into U-bearing clastic sandstones, thus providing necessary energy for the formation of uranium ores.     

Geochemical characteristics and source analysis of inflow of mine water in Wang’ershan Gold Mine, Shandong

Through a systematic observation of water level and temperature, and a comprehensive analysis of the data on major/trace elements, nitrite, hydrogen-oxygen isotopes, the conclusion has been drawn that there are two relatively independent groundwater systems (cool water and hot water), and the geochemical indicators of hot/cool waters are described. The cool water system is relatively enriched in Ca2 , Mg2 and HCO3-. Its TDS is relatively low, about 1400–1800 mg/L. The hot water system is relatively enriched in K , Na , Cl- and SO42-. Its TDS is relatively high, about 2200–2300 mg/L. The cool water system is enriched in Ba, Ga, Cd, and the hot water system is enriched in B, Ti, Cr, Ni, Cu, Mo, Rb, and Cs, relatively. Especially, the contents of Rb and Cs in the hot water system are more than five times as high as those in the cool water system. The NO3- contents of cool water discharged from the gold mine are relatively high, and those of hot water are extremely low. The δD and δ18O values follow an increasing order of surface water>mine cool water>mine hot water. The cool water comes mainly from the lateral supply of phreatic water, while the hot water comes mainly from the vertical supply of deeply circulating structure-fracture water. The ratio of cool water over hot water was estimated to be about 1:1 by a water quality model..     

西藏东部大气降水氧同位素组成特征

The Xizang Plateau, with a common altitude of more than 4000 m sbove sea level,has long been celebrated as “The Roof of the World”. In order to study oxygen isotopic composition of meteoric water in the Xizang Plateau Region and its relationship with the attitude, we made an investigation tour to the Xizang Plateau, starting from Guizhow, during 1979 from July to October, and 79 meteoric Water samples were collected, including brook, well, lake, snow, firn, spring and running waters, at different altitudes. Oxygen isotope analyses indicate that the isotopie composition of meteoric water in the areas more than 4000g and in the western parts of SichuanGaizhow shows remarkable altitude effect. There is a negative correlation between δ^28O and altitude, which is reflected by --δ^18O = 0.0026H 7.75. The average δ^18O value for metcoric water in the areas: more than 4000m above sea level turns out to be --18.15‰ is evident that δ^18O value for lake water on the plateau is related to its water supply. δ^18O value for lake water, in which the evaporation is greater than supply,is approximately three or four times higher than that of supplied water, averaging -5.74‰. Oxygen isotopic compasition of geothermal water can be compared with that of local meteoric water, but shows certain δ^18O-shift, suggesting that the main water-supply source seems to be meteoric water in the same area.