粤北诸广南部铀矿田流体包裹体的氦氩同位素组成及成矿流体来源示踪

粤北诸广南部铀矿田是我国重要的花岗岩型铀矿产地之一,有关诸广南部花岗岩型铀矿田的成因,多年来一直存在较大的争议。本文以诸广南部铀矿田典型铀矿床成矿期萤石、方解石和黄铁矿中流体包裹体为测试对象,研究了成矿流体的He、Ar同位素地球化学。研究表明,萤石流体包裹体的~3He/~4He比值为0. 021～0. 186Ra,~(40) Ar/~(36)比值为298. 4～2515. 7;方解石流体包裹体的3He/4He比值为0. 027～0. 209Ra,~(40) Ar/~(36)比值为295. 9～327. 2;黄铁矿流体包裹体的3He/4He比值为0. 021～1. 543Ra,~(40) Ar/~(36)比值为326. 9～1735. 1; He-Ar同位素系统显示成矿流体的3He/4He比值略高于地壳氦同位素特征值(0. 01～0. 05Ra),但低于幔源氦同位素特征值(6～9Ra),~(40) Ar/~(36)比值接近或高于大气氩的同位素组成(~(40) Ar/~(36)=295. 5),成矿流体为壳-幔混合来源。结合H-O、He-Ar、C和Sr等多元同位素证据表明,成矿流体由两个端元组成:一是含有一定放射性成因Ar的大气降水的地壳流体,二是含幔源He的地幔流体。进一步研究表明,受NNW向断裂控制的棉花坑、书楼丘、长排等铀矿床受地幔流体影响比较大,而受NE向断裂控制的蕉坪、东坑、烟筒岭铀矿床受大气降水影响比较大。     

Importance of mantle derived fluids during granite associated hydrothermal circulation: He and Ar isotopes of ore minerals from Panasqueira

Helium trapped in arsenopyrite and wolframite from the Panasqueira hydrothermal deposit in central Portugal is overwhelmingly—≈ 75%—derived from the mantle. This is surprising as the W-Cu(Ag)-Sn vein deposits are spatially and temporally associated with an S-type granite. It is difficult to reconcile ³He/⁴He ratios > 5Ra (where Ra is the atmospheric ³He/⁴He ratio) with a granite produced by crustal anatexis, therefore it seems likely that mantle derived fluids unrelated to the granite were the source of the magmatic component in the ore fluids.The mantle appears to transport ³He and heat to the surface in relatively constant proportions (³He/Q = 0.1-1 x10⁻¹² cm³ STP J⁻¹). However, the ³He/heat ratios in the Panasqueira fluids (1-10 x10⁻¹² cm³ STP J⁻¹, calculated using the ³He/³⁶Ar ratio) are considerably higher. Therefore, it does not seem likely that gradual cooling of the pluton supplied heat to the hydrothermal system (as this would result in low ³He/Q ratios). Therefore, both He and heat in this collision related, granite-associated hydrothermal deposit were supplied from the mantle.     

He-Ar Isotopic Systematics of Fluid Inclusions in Pyrites from PGEpolymetallic Deposits in Lower Cambrian Black Rock Series, South China

He-Ar isotopic compositions of fluid inclusions trapped in pyrites from some representative PGE-polymetallic deposits in Lower Cambrian black rock series in South China were analyzed by using an inert gas isotopic mass spectrometer. The results show that the ore-forming fluids possess a low 3He/4He ratio, varying from 0.43×10-8 to 26.39×10-8, with corresponding R/Ra value of 0.003-0.189. The 40Ar/36Ar ratios are 258-287, close to those of air saturated water (ASW). He-Ar isotopic indicator studies show that the ore-forming fluids were mainly derived from the formation water or basinal hot brine and sea water, while the content of mantle-derived fluid or deep-derived magmatic water might be negligible. The PGE-polymetallic mineralization might be related to the evolution of the Caledonian miogeosynclines distributed along the southern margin of the Yangtze Craton. During the Early Cambrian, the formation water or basinal hot brine trapped in Caledonian basins which accumulated giant thick sediments was     

Isotope tracers for deep-seated fluids and noble gases

The role of He and Ar isotopes in tracing the source of ore fluids has aroused great attention of the broad masses of the geological researchers. On the basis of lots of test and measurement of He and Ar isotopes in sulfides from Au, Ag polymetallic ore deposits in northern China, statistics has been made on the published He and Ar isotope data from 27 gold deposits, 13 silver polymetallic ore deposits, 8 polymetallic ore deposits, 1 rare-earth deposit, 3 oceanic incrustations, 3 volcanic springs and their wall rocks and granites. The statistical results indicate that the 3 He/ 4 Ar (×10-6 ) values of the Au, Ag polymetallic ore deposits are within the range of 0.24 9.39, with an average of 3.34×10-6 ; the He/Ar values, 0.007 6.01,with an average of 2.37; the 40 Ar/ 36 Ar values, 265.75 2361, with an average of 699.0; the 4 He/ 40 Ar values, 0.0020 643.86, with an average of 5.85, the 3 He/ 4 Ar (×10-6 ) values of gneiss and granite surrounding the mining area, 0.001 1.79, with an average of 1.00×10-6 , reflecting great differences in source. Mantle-source He in 48 Au, Ag polymetallic ore deposits accounts for 4.55% 83.06%, averaging 29.91%. It falls near the mantle-source region which can be seen in the He isotopic concentration diagram and the 3 He/ 4 He(R/Ra) 40 Ar/ 36 Ar plot. Studies suggested that the ore-forming materials for endogenic Au, Ag polymetallic ore deposits should be derived from the deep interior of the Earth, and with the multi-stage evolution of mantle plumes the deep-seated ore fluids would be transported from the deep interior of the Earth to the shallow levels. During this process the mixing of crust/mantle-source fluids would inevitably occur, therefore, the value range always lies between the mantle and the crust.     

广西栗木锡铌钽矿田成矿物质来源的惰性气体同位素示踪

文章利用黄铁矿流体包裹体惰性气体同位素,探讨了广西栗木锡铌钽矿田成矿流体的来源.黄铁矿流体包裹体的3He/4He比值为0.14～0.97 Ra,远远低于地幔流体的比值,接近饱和大气水的比值,并与地壳流体的比值处在相同的数量级上;40 Ar/36 Ar比值为555.98～ 855.11,平均705.55,显然偏离大气氩的同位素组成;40Ar*/4He比值为0.08～0.27,平均值为0.153,接近地壳值;20Ne/22 Ne=9.671～9.748和21Ne/22 Ne=0.0306～ 0.0330,具有饱和大气水的Ne同位素比值特征.结果表明,广西栗木锡铌钽矿田老虎头、牛栏岭和金竹源3个矿床的成矿流体是大气水和地壳流体的混合流体;水溪庙矿床的成矿流体也主要是大气水和地壳流体的混合流体,但可能有少量地幔流体的加入.     

Noble gas data from Goldfield and Tonopah epithermal Au-Ag deposits,ancestral Cascades Arc,USA: Evidence for a primitive mantle volatile source

The He, Ne, and Ar isotopic composition of fluid inclusions in ore and gangue minerals were analyzed to determine the source of volatiles in the high-grade Goldfield and Tonopah epithermal Au-Ag deposits in southwestern Nevada, USA. Ar and Ne are mainly atmospheric, whereas He has only a minor atmospheric component. Corrected ³He/⁴He ratios (with atmospheric He removed) range widely from 0.05 to 35.8 times the air ³He/⁴He ratio (R_A), with a median of 1.43 R_A. Forty-one percent of measured ³He/⁴He ratios are ≥4 R_A, corresponding to ≥50% mantle He assuming a mantle ratio of 8 R_A. These results suggest that mafic magmas were part of the magmatic-hydrothermal system underlying Goldfield and Tonopah, and that associated mantle-sourced volatiles may have played a role in ore formation. The three highest corrected ³He/⁴He ratios of 17.0, 23.7, and 35.8 R_A indicate a primitive mantle He source and are the highest yet reported for any epithermal-porphyry system and for the Cascades arc region. Compiled ³He/⁴He measurements from epithermal-porphyry systems in subduction-related magmatic arcs around the world (n = 209) display a statistically significant correlation between ³He/⁴He and Au-Ag grade. The correlation suggests that conditions which promote higher fluid inclusion ³He/⁴He ratios (abundance of mantle volatiles and focused upward volatile transport) have some relation to conditions that promote higher Au-Ag grades (focused flow of metal-bearing fluids and efficient chemical traps). Results of this and previous investigations of He isotopes in epithermal-porphyry systems are consistent with the hypothesis posed in recent studies that mafic magmas serve an important function in the formation of these deposits.     

Noble Gas and Stable Isotopic Constraints on the Origin of the Ag–Cu Polymetallic Ore Deposits in the Baiyangping Area,Yunnan Province,SW China

The Lanping basin, Yunnan province, SW China, is located at the juncture of the Eurasian and Indian Plates in the eastern part of the Tibetan Plateau. The Lanping basin, in the Sanjiang Tethyan metallogenic province, is a significant Cu–Ag–Zn–Pb mineralized belt in China that includes the largest sandstone‐hosted Zn–Pb deposit in the world, the Jinding deposit, as well as several Ag–Cu deposits (the Baiyangping and Jinman deposits). These deposits, with total reserves of over 16.0 Mt Pb + Zn, 0.6 Mt Cu, and 7,000 t Ag, are mainly hosted in Meso‐Cenozoic clastic rocks and are dominantly controlled by two Cenozoic thrust systems developed in the western and eastern segments of the basin. The Baiyangping, Babaoshan, and Hetaoqing ore deposits are representative of the epithermal base metal deposits in the Lanping basin. The microthermometric data show that the ore‐forming fluids for these deposits were low temperature (110–180 °C) and had bimodal distribution of salinity at moderate and mid to high salinities (approximately 2–8 wt.% and 18–26 wt.% NaCl equivalent). The C and O isotope data indicate that the ore‐forming fluids were related to hot basin brines. We present new He and Ar isotope data on volatiles released from fluid inclusions contained in sulfides and in barite in these three deposits. ³He/⁴He ratios of the ore‐forming fluids are 0.01 to 0.14 R/Ra with a mean of 0.07 Ra (where R is the ³He/⁴He ratio and Ra is the ratio for atmospheric helium). This mean value is intermediate to typical ³He/⁴He ratios for the crust (R/Ra = 0.01 to 0.05) and the ratio for air‐saturated water (R/Ra = 1). The mean ratio is also significantly lower than the ratios found for mantle‐derived fluids (R/Ra = 6 to 9). The ⁴⁰Ar/³⁶Ar ratios of the ore‐forming fluids range from 298 to 382 with a mean of 323. This value is slightly higher than that for the air‐saturated water (295.5). The ³He/⁴He ratios of fluids from the fluid inclusions imply that the ore‐forming fluid for the Baiyangping, Babaoshan, and Hetaoqing deposits was derived from the crust and that any mantle‐derived He was negligible. The content of the radiogenic Ar ranges between 0.2 to 20.4%, and the proportion of air‐derived ⁴⁰Ar averages 94.1%. This indicates that atmospheric Ar was important in the formation of these deposits but that some radiogenic ⁴⁰Ar was derived from crustal rocks. Based on these observations coupled with other geochemical evidence, we suggest that the ore‐forming fluids responsible for the formation of the Ag–Cu–Pb–Zn polymetallic ore deposits in the Baiyangping area of the Lanping basin were mainly derived from crustal fluids. The fluids may have mixed with some amount of air‐saturated water, but there was no significant involvement of mantle‐derived fluids.     

金属矿床的成矿流体成分和流体包裹体

自然界中的成矿流体按其主要成分,可分为:(1)岩浆,即形成岩浆矿床的岩浆;(2)以H2O为主的流体(含Na Cl);(3)以CO2为主的流体。地壳中的流体类型很多,只有含一定金属元素含量的,并且达到一定浓度时才称为金属矿床的成矿流体。基于对矿床中流体包裹体和天然成矿流体中金属种类和含量的测定,这些金属矿床的成矿流体按金属元素含量可以分为五组,成矿流体可以来自岩浆、岩浆热液、大气降水、盆地卤水和变质流体等地质环境。     

The Daduhe gold field at the eastern margin of the Tibetan Plateau: He, Ar, S, O, and H isotopic data and their metallogenic implications

The Daduhe gold field comprises several shear-zone-controlled Tertiary lode gold deposits distributed at the eastern margin of the Tibetan Plateau. The deposits are hosted in a Precambrian granite–greenstone terrane within the Yangtze Craton. The gold mineralization occurs mainly as auriferous quartz veins with minor sulphide minerals. Fluid inclusions in pyrite have ³He/⁴He ratios of 0.16 to 0.86 R_a, whereas their ⁴⁰Ar/³⁶Ar ratios range from 298 to 3288, indicating a mixing of fluids of mantle and crust origins. The δ³⁴S values of pyrite are of 0.7–4.2‰ (n = 12), suggesting a mantle source or leaching from the mafic country rocks. δ¹⁸O values calculated from hydrothermal quartz are between − 1.5‰ and + 6.0‰ and δD values of the fluids in the fluid inclusions in quartz are − 39‰ and − 108‰. These ranges demonstrate a mixing of magmatic/metamorphic and meteoric fluids. The noble gas isotopic data, along with the stable isotopic data suggest that the ore-forming fluids have a dominantly crustal source with a significant mantle component.     

A geochemical traverse across the Eastern Carpathians (Romania): constraints on the origin and evolution of the mineral water and gas discharges

The inner sector of the Eastern Carpathians displays a large number of Na–HCO₃, CO₂-rich, meteoric-originated cold springs (soda springs) and bore wells, as well as dry mofettes. They border the southern part of the Pliocene–Quaternary Calimani–Gurghiu–Harghita (CGH) calc-alkaline volcanic chain. Both volcanic rocks and CO₂-rich emissions are situated between the eastern part of the Transylvanian Basin and the main east Carpathian Range, where active compression tectonics caused diapiric intrusions of Miocene halite deposits and associated saline, CO₂-rich waters along active faults. The regional patterns of the distribution of CO₂ in spring waters (as calculated pCO₂) and the distribution pattern of the ³He/⁴He ratio in the free gas phases (up to 4.5 R_m/R_a) show their maximum values in coincidence with both the maximum heat-flow measurements and the more recent volcanic edifices. Moving towards the eastern external foredeep areas, where oil fields and associated brines are present, natural gas emissions become CH₄-dominated. Such a change in the composition of gas emissions at surface is also recorded by the ³He/⁴He ratios that, in this area, assume ‘typical’ crustal values (R_m/R_a=0.02).In spite of the fact that thermal springs are rare in the Harghita volcanic area and that equilibrium temperature estimates based on geothermometric techniques on gas and liquid phases at surface do not suggest the presence of shallow active hydrothermal systems, a large circulation of fluids (gases) is likely triggered by the presence of mantle magmas stored inside the crust. If total ³He comes from the mantle or from the degassing of magmas stored in the crust, CO₂ might be associated to both volcanic degassing and thermometamorphism of recently subducted limestones.     

He–Ar isotope geochemistry of iron and gold deposits reveals heterogeneous lithospheric destruction in the North China Craton

The North China Craton (NCC) provides a classic example for extensive destruction of the cratonic lithosphere. The Mesozoic magmatism which contributed to the decratonization of the NCC was also accompanied by the formation of a variety of mineral deposits. In order to gain further insights into the cratonic destruction process, typical iron and gold deposits are investigated here. Helium–argon isotopic data on pyrite, from typical skarn iron deposits of the Beiminghe and Fushan in the Han-Xing district of the central NCC, and the Linglong and Canzhuang gold deposits in the Jiaodong district in the eastern NCC, are presented in this paper. The ³He/⁴He, ⁴⁰Ar/³⁶Ar and ⁴⁰Ar/⁴He ratios show generally uniform patterns within the individual deposits and reveal a complex evolutionary history of the ore-forming fluids with varying degree of crust–mantle interaction. The ore-forming fluids associated with the gold mineralization at the Jiaodong mine have higher content of fluids of mantle origin with mantle helium ranging from 1.24% to 18.02% (average 6.73%; N = 18). In contrast, the ore-forming fluids related to the iron ore deposits contain less mantle contribution with mantle helium ranging from 0.12% to 4.96% (average 1.29%; N = 10). Our results suggest complex and heterogeneous crust–mantle processes associated with the magmatism and metallogeny, where the lithosphere of the eastern NCC was subjected to more extensive thinning and destruction as compared with that in the western part, consistent with the observations from geophysical studies in the region. Our study demonstrates that fluids associated with the Mesozoic metallogenic processes in the NCC provide useful insights into the geodynamics of destruction and refertilization of the cratonic lithosphere.     

Apparent decoupling of the He and Ne isotope systematics of the Icelandic mantle: The role of He depletion, melt mixing, degassing fractionation and air interaction

We present new He-Ne data for geothermal fluids and He-Ne-Ar data for basalts from throughout the Icelandic neovolcanic zones and older parts of the Icelandic crust. Geothermal fluids, subglacial glasses, and mafic phenocrysts are characterized by a wide range in helium isotope ratios (³He/⁴He) encompassing typical MORB-like ratios through values as high as 36.8 R_A (where R_A = air ³He/⁴He). Although neon in geothermal fluids is dominated by an atmospheric component, samples from the northwest peninsula show a small excess of nucleogenic ²¹Ne, likely produced in-situ and released to circulating fluids. In contrast, geothermal fluids from the neovolcanic zones show evidence of a contribution of mantle-derived neon, as indicated by ²⁰Ne enrichments up to 3% compared to air. The neon isotope composition of subglacial glasses reveals that mantle neon is derived from both depleted MORB-mantle and a primordial, ‘solar’ mantle component. However, binary mixing between these two endmembers can account for the He-Ne isotope characteristics of the basalts only if the ³He/²²Ne ratio of the primordial mantle endmember is lower than in the MORB component. Indeed, the helium to neon elemental ratios (⁴He/²¹Ne∗ and ³He/²²Ne_s where ²¹Ne∗ = nucleogenic ²¹Ne and ²²Ne_s = ‘solar’-derived ²²Ne) of the majority of Icelandic subglacial glasses are lower than theoretical values for Earth’s mantle, as observed previously for other OIB samples. Helium may be depleted relative to neon in high-³He/⁴He ratio parental melts due to either more compatible behavior during low-degree partial melting or more extensive diffusive loss relative to the heavier noble gases. However, Icelandic glasses show higher ⁴He/⁴⁰Ar∗ (⁴⁰Ar∗ = radiogenic Ar) values for a given ⁴He/²¹Ne∗ value compared to the majority of other OIB samples: this observation is consistent with extensive open-system equilibrium degassing, likely promoted by lower confining pressures during subglacial eruptions of Icelandic lavas. Taken together, the He-Ne-Ar systematics of Icelandic subglacial glasses are imprinted with the overlapping effects of helium depletion in the high-³He/⁴He ratio parental melt, binary mixing of two distinct mantle components, degassing fractionation and interaction with atmospheric noble gases. However, it is still possible to discern differences in the noble gas characteristics of the Icelandic mantle source beneath the neovolcanic zones, with MORB-like He-Ne isotope features prevalent in the Northern Rift Zone and a sharp transition to more primitive ‘solar-like’ characteristics in central and southern Iceland.     

Geochemical/isotopic evolution of Pb–Zn deposits in the Central and Eastern Taurides,Turkey

The Central and Eastern Taurides contain numerous carbonate-hosted Pb–Zn deposits, mainly in Devonian and Permian dolomitized reefal–stramatolitic limestones, and in massive Jurassic limestones. We present and compare new fluid inclusion and isotopic data from these ore deposits, and propose for the first time a Mississippi Valley-type (MVT) mode of origin for them.

Fluid inclusion studies reveal that the ore fluids were highly saline (13–26% NaCl equiv.), chloride-rich (CaCl₂) brines, and have average homogenization temperatures of 112°C, 174.5°C, and 211°C for the Celal Da?, Delikkaya, and Ayrakl? deposits, respectively. Furthermore, the δ³⁴S values of carbonate-hosted Pb–Zn deposits in the Central and Eastern Taurides vary between –5.4‰ and?+13.70‰. This indicates a possible source of sulphur from both organic compounds and crustal materials. In contrast, stable sulphur isotope data (average δ³⁴S –0.15‰) for the Çad?rkaya deposit, which is related to a late Eocene–Oligocene (?) granodioritic intrusion, indicates a magmatic source. The lead isotope ratios of galena for all investigated deposits are heterogeneous. In particular, with the exception of the Suçat? district, all deposits in the Eastern (Delikkaya, Ayrakl?, Denizovas?, Çad?rkaya) and Central (Katranba??, Küçüksu) Taurides have high radiogenic lead isotope values (²⁰⁶Pb/²⁰⁴Pb between 19.058 and 18.622; ²⁰⁷Pb/²⁰⁴Pb between 16.058 and 15.568; and ²⁰⁸Pb/²⁰⁴Pb between 39.869 and 38.748), typical of the upper continental crust and orogenic belts.

Fluid inclusion, stable sulphur, and radiogenic lead isotope studies indicate that carbonate-hosted metal deposits in the Eastern (except for the Çad?rkaya deposit) and the Central Taurides are similar to MVT Pb–Zn deposits described elsewhere. The primary MVT deposits are associated with the Late Cretaceous–Palaeocene closure of the Tethyan Ocean, and formed during the transition from an extensional to a compressional regime. Palaeogene nappes that typically limit the exposure of ore bodies indicate a pre-Palaeocene age of ore formation. Host rock lithology, ore mineralogy, fluid inclusion, and sulphur?+?lead isotope data indicate that the metals were most probably leached from a crustal source such as clastic rocks or a crystalline massif, and transported by chloride-rich hydrothermal solutions to the site of deposition. Localization of the ore deposits on autochthonous basement highs indicates long-term basinal fluid migration, characteristic of MVT depositional processes. The primary MVT ores were oxidized in the Miocene, resulting in deposition of Zn-carbonate and Pb-sulphate–carbonate during karstification. The ores underwent multiple cycles of oxidation and, in places, were re-deposited to form clastic deposits. Modified deposits resemble the ‘wall-rock replacement’ and the ‘residual and karst fill’ of non-sulphide zinc deposits and are predominantly composed of smithsonite.     

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.     

赣南淘锡坑钨矿床He-Ar同位素地球化学研究

华南石英脉型黑钨矿的形成一直被认为是与地壳沉积物质重熔形成的S型花岗岩有关。然而,近年来对南岭中生代成岩成矿机制的研究发现,地幔组分可能参与了钨、锡成矿作用。本文对淘锡坑石英脉型钨多金属矿床与黑钨矿共生的黄铁矿和毒砂中流体包裹体的He、Ar同位素进行了研究。结果显示,上述矿物中流体包裹体的~3He/~4He值为0. 37～2. 11Ra(Ra为空气的~3He/~4He值,1Ra=1. 39×10~(-6)),介于地幔与地壳的~3He/~4He值之间;~(40)Ar/~(36)Ar值为309. 5～383. 6,平均335. 4,略高于大气的~(40)Ar/~(36)Ar比值(295. 5)。研究表明,成矿流体具有壳-幔两端元混合的特征。其中,地壳端元的流体为经过地下循环的低温饱和大气水,地幔端元的流体为矿区隐伏花岗岩体成岩过程中分异出的岩浆流体。结合前人研究成果,认为该矿床的形成与华南中生代燕山期发生的软流圈上涌、岩石圈减薄、地壳伸展等地球动力学作用有密切联系。这种动力学过程为地幔组分带来的热引起地壳沉积物质重熔形成钨多金属成矿花岗岩浆提供了条件。     

Identification of He sources and estimation of He ages in groundwater of the North China Plain

Dissolved helium concentrations and ³He/⁴He ratios were measured for 18 groundwater samples collected from the Quaternary confined aquifers in the North China Plain (NCP). The dissolved helium concentrations ranged from 1 × 10⁻⁷ to 1 × 10⁻⁶ cm³STP·g⁻¹ in the 14 samples from the central plain, but was approximately two orders of magnitude higher, between 6 × 10⁻⁶ and 9 × 10⁻⁵ cm³STP·g⁻¹, in 4 samples from the coastal plain. Based on these concentrations and the corresponding ³He/⁴He ratios varying from 0.09 to 0.55 R_a (where R_a is the ³He/⁴He ratio of air), the dissolved helium in groundwater in the central plain was identified to be primarily a mixture of atmospheric helium with radiogenic helium and a representative radiogenic helium ratio was estimated to be 0.035 R_a. Despite the high fraction of terrigenic ⁴He in the samples from the coastal plain, their ³He/⁴He ratios were found to be significantly above this radiogenic value, ranging between 0.20 and 0.37 R_a, indicating the presence of a mantle-derived He component in this area. About 2–4% mantle helium was estimated to be present in the groundwater of the coastal plain, which probably is associated with the regional Cangdong fault and tectonic activities. Based on the radiogenic He component, ⁴He ages of the groundwater in the central plain were calculated by assuming either pure in situ production or an external helium flux J₀ of 4.7 × 10⁻⁸ cm³STPcm⁻²a⁻¹. The estimated ⁴He ages fall between 9.5 and 51.4 ka and are comparable to the ¹⁴C ages, suggesting that the results of ⁴He dating are reasonable and can be an effective tool to estimate groundwater residence times under suitable conditions.     

Noble gas isotopic compositions and water/gas chemistry of soda springs from the islands of Bioko,São Tomé and Annobon,along with Cameroon Volcanic Line,West Africa

Chemical and isotopic compositions are reported for water, and CO₂ and noble gases in groundwater and soda springs from Bioko, Principé, São Tomé and Annobon, all islands located in the off-shore part of the Cameroon Volcanic Line in West Africa. The soda spring waters are of Ca–Mg–HCO₃ type, with δD and δ¹⁸O values that range from −20 to −8‰ and −5.4 to −2.7‰ respectively, indicative of a meteoric origin. CO₂ is the main gas species in the springs. δ¹³C–CO₂ values vary from −2.8 to −5.0‰, overlapping the observed mantle C range (−3 to −8‰). CO₂/³He ratios (3–9×10⁹) suggest that most C (∼90%) in the samples is derived from the mantle. Neon has atmospheric isotopic compositions, while Ar is slightly enriched in radiogenic ⁴⁰Ar. ³He/⁴He ratios (3.0 to 10.1×10⁻⁶ or 2.1 to 7.2R_a, where R_a is the atmospheric ratio of 1.4×10⁻⁶) are much higher than those for typical crustal fluids (∼10⁻⁸) but lower than those expected for fluids derived from ‘high-³He/⁴He’ hotspots like Loihi and Iceland. This precludes significant contributions of such fluids in the source regions of the gases, and by inference, in the magmatism of these oceanic islands. Alternatively, approximately 90% of the He in São Tomé gases is inferred to be derived from a source similar to the MORB source. The ³He/⁴He ratio for the Bioko gas (6.6×10⁻⁶) may be derived from a source with a higher time integrated (U+Th)/³He ratio than the MORB source.     

Shale basins,sulfur-deficient ore brines and the formation of exhalative base metal deposits

The massive sulfide deposits of the Iberian Pyrite Belt are interbedded with felsic volcanic rocks and shale, and underlain by several thousand meters of siliciclastic sedimentary rocks known as the PQ Group. Isotope geochemistry and regional geology are both consistent with equilibration of the ore-forming fluids with the PQ Group, prior to ore deposition near the former seafloor. The average Cu:Zn:Pb ratio of the PQ Group rocks (ca. 26:55:19) is similar to the weighted average of all the massive sulfide orebodies combined (ca. 25:52:23).The genetic relationship between massive sulfide deposits and a siliciclastic sedimentary metal source is explained here by a thermodynamic model, proposing that mildly reducing redox conditions imposed by equilibration with the sedimentary rocks are most critical for the formation of an effective ore-forming fluid. Relatively metal-rich but organic-poor pyrite-bearing shale undergoing dewatering of saline pore fluids is an effective source for the generation of sulfur-deficient but relatively iron and base metal-rich brines. Thus, we propose that the giant deposits of the Iberian Pyrite Belt owe their existence not to exceptionally metal-enriched (e.g., magmatic) fluids, but to the existence of a fairly ordinary but large metal source in reactive siliciclastic sediments, combined with an underlying igneous heat source and a particularly efficient mechanism of sulfide precipitation by mixing with H₂S-rich fluids at or near the seafloor.Essentially similar mineral equilibria are imposed when saline fluids are buffered by typical continental basement rocks. Leaching of retrograde minerals and possibly residual salts from their magmatic or metamorphic prehistory is expected to generate similar, variably metal-rich but relatively sulfide-deficient fluids. Thus, the existence of mildly reducing rocks can be the dominant chemical control in the source of fluids generating many volcanogenic, Irish-type or sedex deposits, many of which are known to precipitate their metal load in response to biogenic sulfide addition at the ore deposition site.     

贵州晴隆锑矿床成矿流体He-Ar同位素地球化学

晴隆锑矿床是华南中生代低温成矿域右江盆地Au-Sb-As-Hg矿集区内的大型锑矿床,成矿时代约150Ma。本文以该矿床矿石矿物辉锑矿中的流体包裹体为测试对象,研究了成矿流体的He和Ar同位素地球化学。研究表明,成矿流体的~3He/~4He为0.13~0.46Ra(Ra为空气的3He/4He值,1.4×10~(-6)),~(40)Ar/~(36)Ar为305~327,He、Ar同位素组成具有一定程度的正相关;成矿流体由两个端元组成:一是含地壳He的低温饱和空气的雨水,二是含地幔He的高温流体。含地幔He的高温流体可能来自右江盆地下部的侏罗纪壳幔混合成因花岗岩浆,这种岩浆的形成机制与华夏地块侏罗纪与钨锡成矿有关的花岗岩具有相似性。晴隆锑矿床以大气降水为主的成矿流体的加热、循环并浸取矿床围岩"大厂层"下伏地层中的成矿元素而成矿,受深部壳幔混合成因花岗岩浆释放出的含幔源He和岩浆S的热流所驱动。     

Origin of ore fluids in the Muruntau gold system: Constraints from noble gas, carbon isotope and halogen data

Hydrothermal vein minerals directly associated with native gold mineralization in the Muruntau vein system (Uzbekistan) have been studied for noble gas, carbon isotope and halogen chemistry of the trapped ore-related fluids. Helium trapped in early arsenopyrite 1, which has preserved the original fluid signature better than associated scheelite and quartz, indicates a small input from a mantle source (?5% of total He). However, the overwhelming majority of the He in the fluid (∼95%) is from crustal sources. The noble gases Ne, Kr and Xe in the sample fluids are dominated by gases of atmospheric origin. The carbon isotope (δ¹³C: −2.1‰ to −5.3‰) and halogen characteristics of the fluids (log Br/Cl: −2.64 to −3.23) lend further support for the activity of juvenile fluids during the main ore stage. The high proportion of crustal components in the ore-forming fluids may be explained by intense fluid-rock interaction and is also supported by previous Nd and Sr isotope studies. The involvement of a juvenile fluid component during the main stage of hydrothermal activity at Muruntau (∼275 Ma) can be linked to the emplacement of lamprophyric dikes at Muruntau, due to apparently overlapping ages for high-temperature alteration, related ore vein formation and intrusion of the dikes. The input of mantle-derived fluids, possibly related to the Hercynian collisional event in the western Tien Shan, stimulated intense fluid-rock interaction in the crust. In this context, the mantle-derived fluid should be considered as one possible carrier of metals. Significant amounts of external meteoric fluids circulating in fracture systems are interpreted to have modified the noble gas signature of fluid in quartz, mostly during late, low temperature fluid circulation.