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1.
本文用铅、锌在花岗质硅酸盐熔体与流体间的分配实验确立了铅、锌的流-熔分配系数(D~(V/L))与氯化钠摩尔浓度[m_(NaCl)](0—6mol/L)间的3个线性关系式以及D~(V/L)与F/Cl、K/Na摩尔比值间的变化关系。这些结果被用来定量探讨花岗质岩浆-热液体系中铅、锌成矿的可能性和可能规模,以及碱质、挥发分相对含量对铅、锌成矿的不同影响等矿床成因方面的基本问题,得出了一些与前人不同的新认识。 相似文献
2.
本文提出了98个K-Ar法绝对年龄测定的新数据,样品是由中国科学院地质研究所和其他兄弟单位提供的。我们的试验条件大致与以往相同,但部分样品采用内加热法熔样。年龄计算常数仍采用:λK=5.57×10-11,λβ=4.72×10-10年-1,K40（克/克样品）=1.22×10-4K％。利用同位素铅法验证了集宁地区伟晶岩中云母以K-Ar 法测定的年龄值,并对同一岩石样品中所含云母、长石斑品及全岩分别进行了试验分析,得出其年龄相对偏差的范围。 相似文献
3.
本文利用作者首次设计改进的固液制样术、金管处理术及测试分析程序完成了铅、锌在花岗质硅酸盐熔体和共存含水流体间的分配实验,确定了一系列铅锌流-熔分配系数;并从分配模型和熔体地球化学等方面探讨了铅锌的流-熔分配规律和机理。实验结果和理论分析均表明,在含水花岗质岩浆体系中,氯(钠)有利于铅、锌的流-熔分离,而氟(钾)则相对地阻碍了这种分离。 相似文献
4.
今年六月图格林諾夫专家在科学院地貭所作了关于絕对年龄測定的报告。首先专家談到“粗铅法”测定古老岩浆（热液）成因的方鉛矿和近海沉积碳酸盐絕对年龄的可能性。粗鉛法测定年龄的依据是:在矿石和岩石中所谓普通鉛是由四种同位素所組成,即Pb204,Pb206,Pb207和Pb208,其中Pb204是非放射性成因的鉛,从地壳形成时起,它的含量从未发生任何变化;而Pb206,Pb207和Pb208是放射性成因的,由于U,Th的蛻变,它們的量一直在不断增长。 相似文献
5.
海南岛南岸的珊瑚礁,是我国全新世珊瑚岸礁最为发育的地区之一,仅次于台湾岛南端的恒春半岛沿岸。前人从生物学[1-5]、地貌学[6-8]和地质学[9-12]角度对海南岛南岸的珊瑚礁进行过较为广泛的研究。作者报道过崖县鹿回头水尾岭剖面珊瑚礁样品的C14年代测定结果[13,14]。1979年底至1980年初,作者在海南岛南岸东起小东海沿岸西至西瑁岛西岸地区进行了野外调查与采样。根据野外和室内分析资料,本文公布了一批新测试的C14年代数据,并进一步讨论了全新世珊瑚礁的发育历史及其与海岸变迁、海面变化和地壳运动的关系等问题。 相似文献
6.
稀土、钍、铀、锆、铌、钽、磷等元素的分离,以纸色层方法为简易快速[1,2]。但现有方法均采用沉淀或其它方法将稀土与大部份伴生元素分离后再进行色层分离,或经多次色层达到分离,失去纸色层方法的优越性。本文为适应微量矿物分析,利用各元素氟化物溶解度不同,一些离子的盐酸络合物可被酮类、醇类等有机溶剂萃取,及它们的分配系数各有差异,选用丁醇-氢氟酸-盐酸体系进行纸上分离,使稀土与其它伴生元素达到一次分离,然后分别进行测定。 相似文献
7.
石英颗粒表面结构类型以及它们和形成环境间的对应关系,国外已有初步总结[1,2,3]。对石英颗粒表面结构应用于历史环境分析,有着不同的意见[4-6]。多数研究者认为,对于松散的或未固结的沉积物(主要为第四纪的)中的石英颗粒表面结构,具有显著的环境分析意义,而对于地质年代久远、早已半固结或固结成岩的则看法不一,有的则予以否定。因为,地质年代愈老,成岩作用(包括浅变质作用)影响也就愈大。但也有些情况表明[7,8],虽已固结成岩,其物源区的搬运、沉积过程中产生的机械结构,仍然部分或大部分被保存下来,仍可以指示其环境。 相似文献
8.
9.
老挝某氧化铅锌矿中含Pb 2.87%、Zn 13.80%、Ag 143.90 g/t,矿石性质及结构较复杂,选别难度较大。为充分回收该矿石资源,对其进行了详细的浮选试验研究。通过对选别条件逐级优化,确定磨矿细度为-0.074mm占90.46%。选铅部分以Na2CO3为调整剂,水玻璃作为抑制剂,Na2S作为活化剂,丁基黄药和异戊基黄药为组合捕收剂,2#油为起泡剂;选锌部分以六偏磷酸钠为分散剂,Na2S为活化剂,KZF为捕收剂。通过选铅“二粗三精三扫”,选铅尾矿再选锌通过“一粗二精二扫”中矿循环返回的大开路小闭路流程,获得铅品位45.28%、回收率77.78%的铅精矿,锌品位34.13%、回收率89.38%的锌精矿。铅精矿中银品位为1016.38 g/t、回收率为34.82%;锌精矿中银品位为193.43 g/t、回收率为48.58%,较好地实现了对该矿石资源的综合回收利用。 相似文献
10.
矿物中的水分为结晶水,结构水(氢氧根)、层间水、沸石水和吸附水等几种结构状态。不同结构状态的水对矿物的性质应有不同的影响。但是著名矿物学家拉尔森[1](E.S.Larsen)给定矿物中水的比折射度k值(又称格拉斯顿-代尔常数),不论是对何种结构状态的水都适用。曾经有许多人对这一点产生过疑义,最近曼达利诺[2](J.A.Mandarino)修正k值时,对各种结构状态的水仍是同用一值。矿物中各种水的折射度是否变化呢?本文作者将列举大量数据来说明这一问题。 相似文献
11.
Peng Shenglin 《《地质学报》英文版》1989,63(2):189-196
Three logarithmic linear equations between D_(Me)~(V/L) and [m_(NaCl)], and the relationship of D_(Me)~(V/L) versus F/Cl or K/Na mole ratios have been established by the experiments of the partitioning of Pb and Zn between granitic silicate melt and aqueous fluid. These results have been used to quantitatively study some essential problems, such as the possibility and degree of Pb-Zn mineralization in the system of granitic magma and hydrothermal fluid, and the influence of the relative contents of alkali and volatiles on the Pb-Zn mineralization in the same system. Some new points have been put forward in this paper. 相似文献
12.
The solubility of all possible Zn and Pb species in aqueous chloride fluids was evaluated by means of thermodynamic simulations in systems ZnO(PbO)-aqueous solution of NaCl (KCl, NaCl + HCl) within broad ranges of temperature (600–900°C), pressure (0.7–5 kbar), and chloride concentrations, under parameters corresponding to the crystallization and degassing of granitoid magmas in the Earth’s crust. Our simulation results demonstrate that the addition of Cl to the fluid phase in the form of Na(K)Cl and HCl significantly increases the concentrations of Cl-bearing Zn and Pb complexes and the total concentration of the metals in the solutions in equilibrium with the solid oxides. In Zn-bearing fluids, the Zn(OH) 2 0 , ZnOH+, and Zn(OH) 3 ? —hydroxyl complexes and the ZnCl 2 0 , and ZnCl+ chlorocomplexes, which are predominant at low Cl concentrations (CCl < 0.05–0.1 m) give way to ZnCl 4 2? with increasing CCl, which becomes the predominant Zn species of the fluid at CCl > 0.1–0.5 m throughout the whole temperature range in question and pressures higher than 1 kbar. For Pb-bearing fluids, the T-P-X region dominated by the Pb(OH) 2 0 , and Pb(OH) 3 ? hydroxyl complexes is remarkably wider than the analogous region for Zn, particularly at elevated temperatures (≥700°C) in alkaline solutions. An increase in CCl is associated with an increase in the concentration and changes in the speciation of Pb chlorocomplexes: PbCl 2 0 → PbCl 3 ? → PbCl 4 2? . The concentrations of Zn and Pb chlorocomplexes increase with increasing pressure, decreasing temperature, and decrease pH with the addition of HCl to the system. It is demonstrated that the solubility of ZnO at any given T-P-X in alkaline solutions with low chloride concentrations are lower than the solubility of PbO. The Zn concentration increases more significantly than with the Pb concentration with increasing CCl and decreasing pH, so that the Zn concentration in acidic solutions is higher than the Pb concentration over broad ranges of temperature, pressure, and Cl concentration. Chloride complexes of Zn (ZnCl 2 0 , and ZnCl 4 2? ) and Pb (PbCl 2 0 , and PbCl 3 ? are proved to be predominant within broad T-P-X-pH ranges corresponding to the parameters under which magmatic fluid are generated. Our simulation results confirm the hypothesis that chlorocomplexes play a leading role in Zn and Pb distribution between aqueous chloride fluids and granitic melts. These simulation results are consistent with experimental data on the Zn and Pb distribution coefficients (D(Zn)f/m and D(Pb)f/m, respectively) between aqueous chloride fluids and granitic melts that demonstrated that (1) D(Zn)f/m and D(Pb)f/m increase with increasing Na and K chloride concentrations in the aqueous fluid, (2) both D(Zn)f/m and D(Pb)f/m drastically increase when HCl is added to the fluid, and (3) (D(Zn)f/m is higher than D(Pb)f/m at any given T-P-X parameters. The experimentally established decrease in D(Zn)f/m and D(Pb)f/m with increasing pressure (at unchanging temperature and Cl concentration) is likely explained by an increase in the alkalinity of the aqueous chloride fluid in equilibrium with granite melt and, correspondingly, a decrease in the Zn and Pb solubility in this fluid. 相似文献
13.
Experiments on the partitioning of Cu between different granitic silicate melts and the respective coexisting aqueous fluids have been performed under conditions of 850 °C, 100 MPa and oxygen fugacity（f O2） buffered at approaching Ni–Ni O（NNO）. Partition coefficients of Cu（DCu= cfluid/cmelt） were varied with different alumina/alkali mole ratios [Al2O3/（Na2O·K2O）, abbreviated as Al/Alk], Na/K mole ratios, and Si O2 mole contents. The DCu increased from 1.28 ± 0.01 to 22.18 ± 0.22 with the increase of Al/Alk mole ratios（ranging from 0.64 to 1.20）and Na/K mole ratios（ranging from 0.58 to 2.56）. The experimental results also showed that DCuwas positively correlated with the HCl concentration of the starting fluid.The DCuwas independent of the Si O2 mole content in the range of Si O2 content considered. No DCuvalue was less than 1 in our experiments at 850 °C and 100 MPa, indicating that Cu preferred to enter the fluid phase rather than the coexisting melt phase under most conditions in the melt-fluid system, and thus a significant amount of Cu could be transported in the fluid phase in the magmatichydrothermal environment. The results indicated that Cu favored partitioning into the aqueous fluid rather than themelt phase if there was a high Na/K ratio, Na-rich, peraluminous granitic melt coexisting with the high Cl-fluid. 相似文献
14.
GONG Xiaodong YAN Guangsheng YE Tianzhu ZHU Xinyou LI Yongsheng ZHANG Zhihui JIA Wenbin YAO Xiaofeng 《《地质学报》英文版》2015,89(3):822-835
The Dahutang tungsten polymetallic ore field is located north of the Nanling W-Sn polymetallic metallogenic belt and south of the Middle—Lower Yangtze River Valley Cu-Mo-Au-Fe porphyry-skarn belt.It is a newly discovered ore field,and probably represents the largest tungsten mineralization district in the world.The Shimensi deposit is one of the mineral deposits in the Dahutang ore field,and is associated with Yanshanian granites intruding into a Neoproterozoic granodiorite batholith.On the basis of geologic studies,this paper presents new petrographic,microthermometric,laser Raman spectroscopic and hydrogen and oxygen isotopic studies of fluid inclusions from the Shimensi deposit.The results show that there are three types of fluid inclusions in quartz from various mineralization stages:liquid-rich two-phase fluid inclusions,vapor-rich two-phase fluid inclusions,and three-phase fluid inclusions containing a solid crystal,with the vast majority being liquid-rich two-phase fluid inclusions.In addition,melt and melt-fluid inclusions were also found in quartz from pegmatoid bodies in the margin of the Yanshanian intrusion.The homogenization temperatures of liquid-rich two-phase fluid inclusions in quartz range from 162 to 363℃ and salinities are 0.5wt%-9.5wt%NaCI equivalent.From the early to late mineralization stages,with the decreasing of the homogenization temperature,the salinity also shows a decreasing trend.The ore-forming fluids can be approximated by a NaCl-H_2O fluid system,with small amounts of volatile components including CO_2,CH_4 and N_2,as suggested by Laser Raman spectroscopic analyses.The hydrogen and oxygen isotope data show that δ5D_(V-smow) values of bulk fluid inclusions in quartz from various mineralization stages vary from-63.8‰ to-108.4‰,and the δ~(18)O_(H2O) values calculated from the δ~(18)O_(V-)smow values of quartz vary from-2.28‰ to 7.21‰.These H-O isotopic data are interpreted to indicate that the ore-forming fluids are mainly composed of magmatic water in the early stage,and meteoric water was added and participated in mineralization in the late stage.Integrating the geological characteristics and analytical data,we propose that the ore-forming fluids of the Shimensi deposit were mainly derived from Yanshanian granitic magma,the evolution of which resulted in highly differentiated melt,as recorded by melt and melt-fluid inclusions in pegmatoid quartz,and high concentrations of metals in the fluids.Cooling of the ore-forming fluids and mixing with meteoric water may be the key factors that led to mineralization in the Dahutang tungsten polymetallic ore field. 相似文献
15.
The Cangyuan Pb-Zn-Ag polymetallic deposit is located in the Baoshan Block, southern Sanjiang Orogen. The orebodies are hosted in low-grade metamorphic rocks and skarn in contact with Cenozoic granitic rocks. Studies on fluid inclusions (FIs) of the deposit indicate that the ore-forming fluids are CO2-bearing, NaCl-H2O. The initial fluids evolved from high temperatures (462–498 °C) and high salinities (54.5–58.4 wt% NaCl equiv) during the skarn stage into mesothermal (260–397 °C) and low salinities (1.2–9.5 wt% NaCl equiv) during the sulfide stage. The oxygen and hydrogen isotopic compositions (δ18OH2O: 2.7–8.8‰; δD: −82 to −120‰) suggest that the ore-forming fluids are mixture of magmatic fluids and meteoric water. Sulfur isotopic compositions of the sulfides yield δ34S values of −2.3 to 3.2‰; lead isotopic compositions of ore sulfides are similar to those of granitic rocks, indicating that the sulfur and ore-metals are derived from the granitic magma. We propose that the Cangyuan Pb-Zn-Ag deposit formed from magmatic hydrothermal fluids. These Cenozoic deposits situated in the west of Lanping-Changdu Basin share many similarities with the Cangyuan in isotopic compositions, including the Laochang, Lanuoma and Jinman deposits. This reveals that the Cenozoic granites could have contributed to Pb-Zn-Cu mineralization in the Sanjiang region despite the abundance of Cenozoic Pb-Zn deposits in the region, such as the Jingding Pb-Zn deposit, that is thought to be of basin brine origin. 相似文献
16.
Zoltán Zajacz Werner E. Halter Marcel Guillong 《Geochimica et cosmochimica acta》2008,72(8):2169-2197
Analyses of co-existing silicate melt and fluid inclusions, entrapped in quartz crystals in volatile saturated magmatic systems, allowed direct quantitative determination of fluid/melt partition coefficients. Investigations of various granitic systems (peralkaline to peraluminous in composition, log fO2 = NNO−1.7 to NNO+4.5) exsolving fluids with various chlorinities (1-14 mol/kg) allowed us to assess the effect of these variables on the fluid/melt partition coefficients (D). Partition coefficients for Pb, Zn, Ag and Fe show a nearly linear increase with the chlorinity of these fluid (DPb ∼ 6 ∗ mCl, DZn ∼ 8 ∗ mCl, DAg ∼ 4 ∗ mCl, DFe ∼ 1.4 ∗ mCl, where mCl is the molinity of Cl). This suggests that these metals are dissolved primarily as Cl-complexes and neither oxygen fugacity nor the composition of the melt affects significantly their fluid/melt partitioning. By contrast, partition coefficients for Mo, B, As, Sb and Bi are highest in low salinity (1-2 mol/kg Cl) fluids with maximum values of DMo ∼ 20, DB ∼ 15, DAs ∼ 13, DSb ∼ 8, DBi ∼ 15 indicating dissolution as non-chloride (e.g., hydroxy) complexes. Fluid/melt partition coefficients of copper are highly variable, but highest between vapor like fluids and silicate melt (DCu ? 2700), indicating an important role for ligands other than Cl. Partition coefficients for W generally increase with increasing chlorinity, but are exceptionally low in some of the studied brines which may indicate an effect of other parameters. Fluid/melt partition coefficients of Sn show a high variability but likely increase with the chlorinity of the fluid (DSn = 0.3-42, DW = 0.8-60), and decrease with decreasing oxygen fugacity or melt peraluminosity. 相似文献
17.
Shigang DUAN Chunji XUE Guoxiang CHI Guoyin LIU Changhai YAN Qiwei FENG Yaowu SONG 《Resource Geology》2011,61(3):224-240
The Chitudian Zn‐Pb ore deposit, Luanchuan, Henan province, was recently discovered in the southern margin of the North China Craton. The Zn‐Pb orebodies are hosted in the Proterozoic Guandaokou and Luanchuan Groups, occurring as veins in interbedding fracture zones mainly in a WNW‐ and partially in a NS‐direction. The Zn‐Pb ores are characterized by banded, massive, and breccia structures, coarse crystal grains, and a simple mineral composition mainly of galena, sphalerite, pyrite, quartz, dolomite, and calcite. In addition to the vein type orebodies, there are Mo‐ and Zn‐bearing skarn orebodies in the northwest of the Chitudian ore field. Four types of primary fluid inclusions in quartz and calcite were recognized in the Chitudian Zn‐Pb ores, including aqueous, aqueous‐CO2, daughter‐mineral‐bearing aqueous, and daughter‐mineral‐bearing aqueous‐CO2 inclusions, with aqueous inclusion being most common. The homogenization temperatures of the fluid inclusions from the main mineralization stage are from 290°C to 340°C, and the salinities mainly from 3.7 to 14.8 wt% NaCl equivalent. In addition to CO2, CH4 and H2S were detected in the vapor phase and HS‐ in the liquid phase of the fluid inclusions by Laser Raman spectroscopy. The δ34SV‐CDT values of ore sulfides from the Chitudian deposit range from ?0.32‰ to 8.30‰, and show two modal peaks in the histogram, one from 1‰ to 4‰, and the other from 5‰ to 7‰. The former peak is similar to that of porphyry‐type Mo‐W deposits in the area, whereas the latter is relatively close to the sulfur in the strata. The ore sulfur may have been derived from both the magma and the strata. The Pb‐isotopic compositions of the ore minerals from Chitudian, with 206Pb/204Pb from 17.005 to l7.953, 207Pb/204Pb from 15.414 to 15.587, and 208Pb/204Pb from 37.948 to 39.036, are similar to those of Mesozoic porphyries in the Chitudian ore field, suggesting that the ore‐forming metals were mainly derived from the Mesozoic magmatic intrusions. The Chitudian Zn‐Pb deposit is interpreted to be a distal hydrothermal vein‐type deposit, which was genetically related to the proximal, skarn‐type Mo ore deposits in the region. 相似文献
18.
MEN Lanjing SUN Jinggui ZHANG Zengjie LI Yixin XING Shuwen CUI Peilong 《《地质学报》英文版》2011,85(1):175-188
An isotopic study was systemically carried out on the granitic complex, diorite-porphyrite, ores and ore minerals of the 103 Ma Xiaoxinancha gold-rich copper deposit in Jilin province to determine the geodynamic model of diagenesis and metallogenesis. Results show that the initial Nd and Sr isotopic compositions of the granitic complex are in the range of 0.70425–0.70505 for (87Sr/86Sr)i , 0.51243–0.51264 for INd, and –1.31 to +2.64 for εNd(t); those of the diorite-porphyrite are in the range from 0.70438–0.70448 for (87Sr/86Sr)i, 0.51259–0.51261 for INd, and +1.56 to +2.09 for εNd(t). For ores and sulfides, the (87Sr/86Sr)i , INd, and εNd(t) values are in the range from 0.70440–0.70805, 0.51259–0.51279 and +1.72 to +5.56, respectively. The Pb isotopic ratios of the granitic complex range from 18.2992–18.6636 for 206Pb/204Pb, from 15.5343–15.5660 for 207Pb/204Pb, and from 38.1640–38.5657 for 208Pb/204Pb. For diorite-porphyrite, the isotopic ratios of 206Pb/204Pb, 207Pb/204Pb and 208Pb/204Pb are 18.3919, 15.5794 and 38.3566, respectively, whereas those of the ores and ore sulfides vary from 18.2275–18.3770 for 206Pb/204Pb, from 15.5555–15.5934 for 207Pb/204Pb and from 38.1318–38.3131 for 208Pb/204Pb. The results indicate that the mineralization was correlated to the formation and evolution of the granitic complex and the diorite-porphyrite. Combining with the reported data in petrologic characteristics, elemental geochemistry and chronology, conclusions can be drawn that the geodynamic settings of diagenesis and metallogenesis of this deposit were consistent with the subduction of the Izanagi oceanic plate during the Early Cretaceous. The diorite-porphyrite was formed by the emplacement of the adakitic magma triggered by partial melting of the enriched mantle, which originated from the derivative continental lithospheric mantle metasomatized by dehydration fluids from the subducting oceanic crust. The granitic complex was produced by fractional crystallization of the mixture between the adakitic magma and the high-K calc-alkaline acidic magma, which were generated by the remelting of the lower crust in the course of intraplate upwelling of the adakitic magma. The ore-bearing fluid reservoir convened in a late stage of the evolution of the mixed magma chamber. 相似文献
19.
Information from a database, which was compiled and continuously updated by the authors of this paper and now includes information from 19500 publication on fluid and melt inclusions in minerals, is used to summarize results on the physicochemical formation parameters of hydrothermal Au, Ag, Pb, and Zn deposits. The database provides information on fluid inclusions in minerals from 970 Pb-Zn, 220 Au-Ag-Pb-Zn, and 825 Au-Ag deposits in various settings worldwide. Histograms for the homogenization temperatures of fluid inclusion are presented for the most typical minerals of the deposits. In sphalerite, most homogenization temperatures (1327 measurements) of fluid inclusions lie within the range of 50–200°C with a maximum at 100–200°C for this mineral from Pb-Zn deposits and within the range of 100–350°C (802 measurements) with a maximum at 200–300°C for this mineral from Au deposits. Data are presented on fluid pressures at Au (1495 measurements) and Pb-Zn (180 measurements) deposits. The pressure during the preore, ore-forming, and postore stages at these deposits ranged from 4–10 to 6000 bar. The reason for the high pressures during preore stages at the deposits is the relations of the fluids to acid magmatic and metamorphic processes. More than 70% of the fluid pressures values measured at Pb-Zn deposits lie within the range of 1–1500 bar. Au-Ag deposits are characterized by higher fluid pressures of 500–2000 bar (61% of the measurements). The overall ranges of the salinity and temperature of the mineral-forming fluid at Au-Ag (6778 measurements) and Pb-Zn (3395 measurements) deposits are 0.1–80 wt % equiv. NaCl and 20–800°C. Most measurements (～64%) for Au-Ag deposits yield fluid salinity <10 wt % equiv. NaCl and temperatures of 200–400°C (63%). Fluids at Pb-Zn deposits are typically more saline (10–25 wt % equiv. NaCl, 51% measurements) and lower temperature (100–300°C, 74% measurements). Several measurements of the fluid density fall within the range of 0.8–1.2 g/cm3. The average composition of volatile components of the fluids was evaluated by various techniques. The average composition of volatile components of fluid inclusions in minerals is calculated for hydrothermal W, Au, Ag, Sn, and Pb-Zn deposits, metamorphic rocks, and all geological objects. The Au, Ag, Pb, and Zn concentrations in magmatic melts and mineral-forming fluids is evaluated based on analyses of individual inclusions. 相似文献
20.
The Hetaoping skarn type Pb–Zn deposit is located in the Baoshan–Narong–Dongzhi block metallogenic belt (BND belt), a belt between the Tengchong terrane and the Lanping basin. The deposit is hosted by marble of the upper Cambrian Hetaoping Formation and there are no outcrops of plutonic rocks present. This deposit is one of two large Pb–Zn deposits recently discovered in the BND belt. The Hetaoping deposit is a high Mn skarn. Four types of fluid inclusions were recognized in quartz from the deposit: vapor-rich inclusions (Type I), liquid-rich inclusions (Type II), pure vapor inclusions (Type III), and pure fluid inclusions (Type IV). The coexistence of Type I and Type III inclusions in Stage I (pre-ore stage) and Stage II (main ore stage) shows evidence of fluid boiling. Quartz-hosted fluid inclusions (Stage I and Stage II) display high homogenization temperatures and salinities (134–315 °C; 3.7–18.6 wt% NaCl equivalent) but calcite-hosted fluid inclusions in Stage III (post-ore stage) record lower homogenization temperatures and salinities (85–214 °C; 0.5–5.4 wt% NaCl equivalent). These data suggest a possible mixing between primary magmatic water and meteoric water. Based on chromatography data, the fluid inclusions in quartz contain abundant CO2 and O2 and subordinate CO, CH4 and C2H2 + C2H4, suggesting an oxidizing environment. Based on their Na/K and Cl/SO4 ratios, fluids contained in fluid inclusions are similar to volcanic spring waters. The low Na/K ratios (0.40–1.34) of the ore-forming fluids may have resulted from interaction with a deep alkaline intermediate-acid intrusion. Hydrogen and oxygen isotope determinations on quartz from different ore stages show low δ18O and δD values relative to VSMOW (−4.3‰ to 2.3‰; −109‰ to −91‰), indicating that the ore-forming fluids were diluted by external fluid sources as the skarn system cooled. Overall, geological and geochemical interpretations suggest that the Hetaoping deposit is a distal manganese skarn Pb–Zn deposit related to concealed intrusions. 相似文献