Isotope geochemistry of the mafic dikes from the Vazante nonsulfide zinc deposit, Brazil

The Vazante Group, located in the northwestern part of Minas Gerais, hosts the most important zinc mine in Brazil, the Vazante Mine, which represents a major known example of a hypogene nonsulfide zinc deposit. The main zinc ore is represented by willemite and differs substantially from other deposits of the Vazante-Paracatu region, which are sulfide-dominated zinc-lead ore. The age of the Vazante Group and the hosted mineralization is disputable. Metamorphosed mafic dikes (metabasites) that cut the metasedimentary sequence and are affected by hydrothermal processes recently were found and may shed light on the geochronology of this important geological unit. Zircon crystals recovered from the metabasites are xenocrystic grains that yield U–Pb conventional ages ranging from 2.1 to 2.4 Ga, so the basement of the Vazante Group is Paleoproterozoic or has metasedimentary rocks whose source area was Paleoproterozoic. Pb isotopes determined for titanite separated from the metabasites have common, nonradiogenic Pb compositions, which prevents determination of their crystallization age. However, the Pb signatures observed for the titanite crystals are in agreement with those determined for galena from the carbonate-hosted Zn–Pb deposits hosted by the Vazante Group, including galena from minor sulfide ore bodies of the Vazante deposit. These similarities suggest that the metalliferous fluids that affected the metabasites may have been those responsible for galena formation, which could imply a similar lead source for both nonsulfide and sulfide zinc deposits in the Vazante–Paracatu district. This common source could be related to deep-seated, basin-derived, metalliferous fluids associated with a long-lived hydrothermal system related to diagenesis and deformation of the Vazante Group during the Neoproterozoic.     

Oxygen isotope fractionation in zinc oxides and implications for zinc mineralization in the Sterling Hill deposit, USA

Oxygen isotope fractionation in the zinc oxides has been calculated by means of the modified increment method. The results suggest that zincite is slightly enriched in ¹⁸O relative to the franklinite of the spinel-type structure but considerably depleted in ¹⁸O relative to the franklinite of the inverse spinel-type structure. The zinc oxides are significantly depleted in ¹⁸O relative to water under hydrothermal and metamorphic conditions. The oxygen isotope analyses of mineral pairs including the zinc oxides and the common gangue minerals such as calcite and quartz can constitute a sensitive isotope geothermometer. Application of oxygen isotope geothermometry to natural assemblages is attempted for the calcite-zinc ore mineral pairs from the Sterling Hill deposit in USA. The results indicate that the temperature of the zinc mineralization may be in the range from 410° to 630 °C and thus lower than the metamorphic temperatures of granulite facies. A metamorphic fluid could have been involved in the formation of the zinc ore minerals. Franklinite would structurally be an inverse spinel in the infancy of its formation, and thus could have originally evolved from Zn^{2 +} substitution to Fe^{2 +} of magnetite at the high temperatures.     

Calculation of equilibrium stable isotope partition function ratios for aqueous zinc complexes and metallic zinc

The goal of this study is to determine reduced partition function ratios for a variety of species of zinc, both as a metal and in aqueous solutions in order to calculate equilibrium stable isotope partitioning. We present calculations of the magnitude of Zn stable-isotope fractionation (^66,67,68Zn/⁶⁴Zn) between aqueous species and metallic zinc using measured vibrational spectra (fit from neutron scattering studies of metallic zinc) and a variety of electronic structure models. The results show that the reduced metal, Zn(0), will be light in equilibrium with oxidized Zn(II) aqueous species, with the best estimates for the Zn(II)-Zn(0) fractionation between hexaquo species and metallic zinc being Δ^66/64Zn_aq-metal ∼ 1.6‰ at 25 °C, and Δ^66/64Zn_aq-metal ∼ 0.8‰ between the tetrachloro zinc complex and metallic zinc at 25 °C using B3LYP/aug-cc-pVDZ level of theory and basis set. To examine the behavior of zinc in various aqueous solution chemistries, models for Zn(II) complex speciation were used to determine which species are thermodynamically favorable and abundant under a variety of different conditions relevant to natural waters, experimental and industrial solutions. The optimal molecular geometries for [Zn(H₂O)₆]²⁺, [Zn(H₂O)₆]·SO₄, [ZnCl₄]²⁻ and [Zn(H₂O)₃(C₃H₅O(COO)₃)]⁻ complexes in various states of solvation, protonation and coordination were calculated at various levels of electronic structure theory and basis set size. Isotopic reduced partition function ratios were calculated from frequency analyses of these optimized structures. Increasing the basis set size typically led to a decrease in the calculated reduced partition function ratios of ∼0.5‰ with values approaching a plateau using the aug-cc-pVDZ basis set or larger. The widest range of species were studied at the B3LYP/LAN2DZ/6-31G^∗ level of theory and basis-set size for comparison. Aqueous zinc complexes where oxygen is bound to the metal center tended to have the largest reduced partition function ratios, with estimated fractionations ranging from 2.2 to 2.9‰ (⁶⁶Zn/⁶⁴Zn) at 25 °C relative to metallic zinc. The tetrahedrally coordinated tetrachloro zinc complex, where zinc is bound exclusively to chloride, had the lowest reduced partition function ratio for a Zn(II) species (Δ^66/64Zn_aq-metal ∼ 1-1.3‰ at 25 °C). Increasing the number of waters in the second shell of solvation of the above complexes led to variable results, most commonly leading to a decrease of ∼0.2 to 0.3‰ in calculated Δ^66/64Zn_aq-metal at 25 °C.These estimates are useful in the interpretation of observed fractionations during the electrochemical deposition of zinc, where aqueous-metal fractionations of up to 5.5‰ are observed. The models show these are not caused by an equilibrium fractionation process. These results suggest that the redox cycle of zinc during industrial processing may be responsible for isotopically distinct reservoirs of zinc observed in polluted environments. The leaching of metallic zinc or zinc tailings from industrial sites could lead to the observed heavy signature in river systems, the magnitude of which will be reliant on the source material and the aqueous species that form.     

U-Pb SHRIMP geochronology of Th-poor, hydrothermal monazite: An example from the Llallagua tin-porphyry deposit, Bolivia

In situ U-Pb SHRIMP analysis of hydrothermal monazite virtually free of Th and poor in U (<0.2 ppm Th, 40-103 ppm U) from the world-class Llallagua tin porphyry deposit in Bolivia defines a mineralization age of 23.4 ± 2.2 Ma (MSWD 0.48) confirming earlier K-Ar sericite alteration age data. These ages are, however, in contrast with a weighted mean single crystal ²⁰⁷Pb/²⁰⁶Pb evaporation age of 39.3 ± 6.0 Ma, and a related Pb-Pb inverse isochron age of 42.4 ± 4.0 Ma (MSWD 0.66) on zircon from a post-porphyry dike, as well as with an earlier single crystal Sm-Nd apatite isochron age.Our data points to a significant time gap between emplacement of the ore-hosting porphyry intrusion (magmatism) and its hydrothermal overprint (tin mineralization), suggesting long-lived magmatic-hydrothermal activity in this part of the Andean back-arc crust. The decoupling of porphyry magmatism and hydrothermal activity may explain the unusual occurrence of relatively little fractionated felsic rocks together with extensive tin mineralization.Our study demonstrates the usefulness of the application of the U-Pb SHRIMP method to direct age determination of ore mineralization using Th-poor hydrothermal monazite even when dealing with geological young events. The common assumption of synchronous magmatism and hydrothermal ore formation in porphyry systems may not always be warranted.     

Defining trace-element alteration halos to skarn deposits hosted in heterogeneous carbonate rocks: Case study from the Cu–Zn Antamina skarn deposit,Peru

The presence of geochemical anomalies, defining haloes around hydrothermal ore deposits, can be used to vector towards mineralization, or identify ore bodies buried at depth. Several important types of ore deposits, including skarn deposits, are often hosted within carbonate-rich sedimentary rocks. Identifying anomalous trace-element concentrations in carbonate rocks is complicated by variable lithology (i.e. siliciclastic component) and volume loss during hydrothermal alteration. In this study of the world-class Antamina skarn deposit in Peru, we use the ratio of metals:immobile elements (e.g. La, Al₂O₃) to differentiate genuine and false geochemical anomalies in limestones and marbles surrounding the skarn deposit. Unaltered limestones are used to define threshold values for metal:immobile element ratios (through use of the median value ± 2 median absolute deviations). Genuine anomalies are identified when metal concentrations exceed those predicted using median + 2 median absolute deviations. In addition, comparison of “four acid” and lithium-borate fusion analytical techniques reveals that the lower cost four-acid techniques give reliable results. Our approach can be used to identify geochemical anomalies and halos related to hydrothermal alteration of carbonate-rich rocks, which have direct application to skarn deposits.     

K–Ar dating and δO–δD tracing of illitization within and outside the Shea Creek uranium prospect,Athabasca Basin,Canada

Isotope analyses (K–Ar, δ¹⁸O and δD) were performed on illite from both the sandstone cover and the underlying basement, close to and distant from Shea Creek, an unconformity-type U deposit (Athabasca Basin, Canada); the illite had previously been characterized crystallographically. In the barren areas away from deposit, illite is mainly of the cis-vacant 1M polytype occurring as relatively coarse-grained lath-shaped particles, while it occurs as fine-grained particles of the trans-vacant 1M type next to and in the U mineralized strata. The tectonic-induced hydrothermal system that favored illite crystallization was multi-episodic 1453 ± 2, 1330 ± 20 and probably about 1235 Ma ago. These illite-forming episodes appear to have occurred contemporaneously to those favoring the concentration of the associated U oxides, which were dated independently by the U–Pb method in the Shea Creek deposits and elsewhere in the Athabasca Basin.     

广西桂平市四德铅-锌-铜矿床地质特征及找矿潜力分析

通过对桂平市四德铅-锌-铜矿床的区域地质背景、矿床地质特征、矿物组合及结构构造、成矿物质来源等的研究,初步认为其矿床类型为热水沉积型铅-锌-铜矿床。通过对该矿床的成矿条件、地球物理、地球化学特征等的分析,认为该矿床具大型规模的成矿前景。     

Siderophile and chalcophile elemental constraints on the origin of the Jinchuan Ni-Cu-(PGE) sulfide deposit, NW China

The Jinchuan deposit, NW China, is one of the world’s most important Ni-Cu-(PGE) sulfide deposits related to a magma conduit system and is hosted in an ultramafic intrusion. The intrusion is composed of lherzolite and dunite with the two largest sulfide ore bodies (named as ore body 1 and 2) in its middle portion. The sulfide ores may be disseminated, net-textured, or massive. The disseminated and net-textured sulfide ores are characterized by variable but generally low PGE concentrations: 10-3200 ppb Pt, 240-9800 ppb Pd, 17-800 ppb Ir, 25-1500 ppb Ru, and 15-400 ppb Rh in 100% sulfides. The massive sulfide ores are extremely low in Pt (<30 ppb) on a 100% sulfides and have very high Cu/Pd ratios, ranging from 10⁴ to 4.5 × 10⁵. The low PGE contents suggest that the sulfide ores formed from the silicate magmas that had already experienced prior-sulfide separation.Our calculations indicate that if the first stage basaltic magmas had contained 6.3 ppb Pt, 6.2 ppb Pd, and 0.1 ppb Ir, 0.008% sulfide removal would result in PGE-depletion in the residual magma with 0.57 ppb Pt, 0.25 ppb Pd, and 0.009 ppb Ir. The Jinchuan sulfides were formed by a second stage of sulfide segregation from a PGE-depleted magma under silicate/sulfide liquid ratios (R-factor) ranging from 10³ to 10⁴ in a deep-seated staging chamber. The massive sulfide ores and some of the net-textured sulfide ores exhibit strong negative Pt-anomalies that cannot be explained by sulfide segregation under variable R-factors. Instead, the sulfide melts that formed the massive ores were segregated from magmas experienced prior fractionation of Pt-Fe alloy. Alternatively, the Pt may have been selectively leached by hydrothermal fluids during remobilization of the sulfide melts that produced the massive sulfides, which occur in cross-cutting veins. We propose that the Jinchuan intrusion and ore bodies were formed by injections of sulfide-free and sulfide-bearing olivine mushes from a deep-seated staging chamber.     

内蒙拜仁达坝银铅锌多金属矿床地球化学异常分带模型研究

拜仁达坝银锌多金属矿床为岩浆热液矿床,通过分析该矿床不同中段微量元素和烃类组分的含量变化特征及其异常展布规律,建立了该矿床的地球化学异常分带模型。     

云南茂租铅-锌矿床地质特征及成因研究

阐述了茂祖铅．锌矿床的成矿地质背景、矿床地质特征，着重研究了赋矿地层、铅-锌矿体赋存及矿化特征，并通过该矿床的成矿时代、成矿物质来源、成矿温度方面的研究，综合分析后认为，茂祖铅-锌矿床的成因属同生断裂控矿的热水喷流-沉积改造型。     

Mineralogy and formation conditions of ores in the Bereznyakovskoe ore field,the Southern Urals,Russia

The Bereznyakovskoe ore field is situated in the Birgil’da-Tomino ore district of the East Ural volcanic zone. The ore field comprises several centers of hydrothermal mineralization, including the Central Bereznyakovskoe and Southeastern Bereznyakovskoe deposits, which are characterized in this paper. The disseminated and stringer-disseminated orebodies at these deposits are hosted in Upper Devonian-Lower Carboniferous dacitic-andesitic tuff and are accompanied by quartz-sericite hydrothermal alteration. Three ore stages are recognized: early ore (pyrite); main ore (telluride-base-metal, with enargite, fahlore-telluride, and gold telluride substages); and late ore (galena-sphalerite). The early and the main ore stages covered temperature intervals of 320–380 to 180°C and 280–300 to 170°C, respectively; the ore precipitated from fluids with a predominance of NaCl. The mineral zoning of the ore field is expressed in the following change of prevalent mineral assemblages from the Central Bereznyakovskoe deposit toward the Southeastern Bereznyakovskoe deposit: enargite, tennantite, native tellurium, tellurides, and selenides → tennantite-tetrahedrite, tellurides, and sulfoselenides (galenoclausthalite) → tetrahedrite, tellurides, native gold, galena, and sphalerite. The established trend of mineral assemblages was controlled by a decrease in $ f_{S_2 } $ f_{S_2 } , $ f_{Te_2 } $ f_{Te_2 } and $ f_{O_2 } $ f_{O_2 } and an increase in pH of mineral-forming fluids from early to late assemblages and from the Central Bereznyakovskoe deposit toward the Southeastern Bereznyakovskoe deposit. Thus, the Central Bereznyakovskoe deposit was located in the center of an epithermal high-sulfidation ore-forming system. As follows from widespread enargite and digenite, a high Au/Ag ratio, and Au-Cu specialization of this deposit, it is rather deeply eroded. The ore mineralization at the Southeastern Bereznyakovskoe deposit fits the intermediate- or low-sulfidation type and is distinguished by development of tennantite, a low Au/Ag ratio, and enrichment in base metals against a lowered copper content. In general, the Bereznyakovskoe ore field is a hydrothermal system with a wide spectrum of epithermal mineralization styles.     

Interaction between zinc and freshwater and marine diatom species: Surface complexation and Zn isotope fractionation

This work is devoted to characterization of zinc interaction in aqueous solution with two marine planktonic (Thalassiosira weissflogii = TW, Skeletonema costatum = SC) and two freshwater periphytic species (Achnanthidium minutissimum = AMIN, Navicula minima = NMIN) by combining adsorption and electrophoretic measurements with surface complexation modeling and by assessing Zn isotopes fractionation during both long term uptake and short term adsorption on diatom cells and their frustules. Reversible adsorption experiments were performed at 25 and 5 °C as a function of exposure time (5 min to 140 h), pH (2 to 10), zinc concentration in solution (10 nM to 1 mM), ionic strength (I = 0.001 to 1.0 M) and the presence of light. While the shape of pH-dependent adsorption edge is almost the same for all four species, the constant-pH adsorption isotherm and maximal Zn binding capacities differ by an order of magnitude. The extent of adsorption increases with temperature from 5 to 25 °C and does not depend on light intensity. Zinc adsorption decreases with increase of ionic strength suggesting competition with sodium for surface sites. Cell number-normalized concentrations of sorbed zinc on whole cells and their silica frustules demonstrated only weak contribution of the latter (10-20%) to overall zinc binding by diatom cell wall. Measurements of electrophoretic mobilities (μ) revealed negative diatoms surface potential in the full range of zinc concentrations investigated (0.15-760 μmol/L), however, the absolute value of μ decreases at [Zn] > 15 μmol/L suggesting a change in surface speciation. These observations allowed us to construct a surface complexation model for Zn binding by diatom surfaces that postulates the constant capacitance of the electric double layer and considers Zn complexation with carboxylate and silanol groups. Thermodynamic and structural parameters of this model are based on previous acid-base titration and spectroscopic results and allow quantitative reproduction of all adsorption experiments. Although Zn adsorption constants on carboxylate groups are almost the same, Zn surface adsorption capacities are very different among diatom species which is related to the systematic differences in their cell wall composition and thickness. Measurements of Zn isotopic composition (⁶⁶Zn/(⁶⁴Zn)) performed using a multicollector ICP MS demonstrated that irreversible incorporation of Zn in cultured diatom cells produces enrichment in heavy isotope compared to growth media (Δ⁶⁶Zn(solid-solution) = 0.27 ± 0.05, 0.08 ± 0.05, 0.21 ± 0.05, and 0.19 ± 0.05‰ for TW, SC, NMIN, and AMIN species, respectively). Accordingly, an enrichment of cells in heavy isotopes (Δ⁶⁶Zn(solid-solution) = 0.43 ± 0.1 and 0.27 ± 0.1‰ for NMIN and AMIN, respectively) is observed following short-term Zn sorption on freshwater cells in nutrient media at pH ∼ 7.8. Finally, diatoms frustules are enriched in heavy isotopes compared to solution during Zn adsorption on silica shells at pH ∼ 5.5 (Δ⁶⁶Zn(solid-solution) = 0.35 ± 0.10‰). Measured isotopes fractionation can be related to the structure and stability of Zn complexes formed and they provide a firm basis for using Zn isotopes for biogeochemical tracing.     

广东省清新县辣菜水锌矿床特征及成因分析

辣菜水锌矿床产于海西-印支期盆地边缘,矿体严格受石炭系下统石磴子组下亚段白云岩控制,呈层-似层状,具层控型特征。矿床成矿具有多期性,早期沉积为矿胚层,受断裂构造热动力改造成矿体,后期岩浆热液叠加,矿体进一步富集,形成富闪锌矿体。通过成矿环境及矿床特征研究分析,认为该矿床成因属于沉积-改造-叠加的复控型矿床。     

湖北凹子岗锌矿床Rb-Sr同位素测年及其地质意义

凹子岗锌矿床位于黄陵背斜东部,是近年来在湘西鄂西地区发现的代表性矿床。锌矿体呈似层状-透镜状产出,赋存于灯影组二段,含矿岩性为一套角砾状泥粉晶云岩,严格受地层层位及岩性控制。文章运用闪锌矿Rb-Sr同位素测年方法,测得凹子岗锌矿床成矿年龄为431~434 Ma,相当于早志留世,代表了矿床的主成矿阶段年龄。闪锌矿具有较高的Sr同位素初始比值(0.71119~0.71136),反映成矿物质或成矿流体由基底岩石和震旦系碳酸盐岩地层共同提供。凹子岗锌矿床早期成矿作用与早志留世的裂谷盆地伸展运动关系密切,晚期成矿作用与加里东运动关系密切,是伸展环境盆地流体运移的产物。加里期运动与黄陵周缘铅锌矿的成矿作用关系密切。凹子岗锌矿床成因类型为热液喀斯特成因,可分为深埋藏成岩成矿阶段和热液喀斯特化成矿阶段。     

铁米尔特——恰夏——萨热阔布多金属金矿床系列矿床地质地球化学研究

铁米尔特－－恰夏－－萨热阔布多金属金矿田已发现铁米尔特铜铅锌矿床、恰夏铜矿床、萨热阔布金矿床，组成了矿田的矿床系列。早泥盆世火山活动于近火山口附近形成了与火山喷气热液有关的恰夏黄铁矿型铜矿床；于火山洼地中形成与火山沉积作用有关的铁米尔特铜铅锌多金属矿床，褶皱期构造破碎带中形成构造蚀变岩型萨热阔布金矿床。     

Effects of hydrothermal alteration on Pb in the active PACMANUS hydrothermal field, ODP Leg 193, Manus Basin, Papua New Guinea: A LA-ICP-MS study

The conventional model of leaching volcanic rocks as a source of metals in a seafloor hydrothermal systems has been tested by examining the behavior of Pb and other trace elements during hydrothermal alteration. ODP Leg 193 drill sites 1188 (Snowcap) and 1189 (Roman Ruins) on Pual Ridge in the eastern Manus Basin offshore eastern Papua New Guinea provide a unique three-dimensional window into an active back-arc hydrothermal system. We investigate by means of a LA-ICP-MS microbeam technique the capacity of Pb to be leached from a host volcanic rock exposed to various types and intensities of alteration. Our results are in general agreement with previous studies that utilized bulk analytical techniques but provide a more detailed explanation of the processes.Fresh representative dacitic lavas from the Pual Ridge have an average whole rock Pb content of 5.2 ppm, an average interstitial glass Pb content of 5.6 ppm and an average plagioclase Pb content of 1.0 ppm. Altered matrix samples have highly variable Pb values ranging from 0 to 52.4 ppm. High Pb values in altered samples are associated with a low temperature chlorite and clay mineral assemblage, in some cases overprinted by a high temperature (up to 350 °C) silica-rich “bleaching” alteration. Only the most highly altered matrix samples have REE patterns that differ from the fresh Pual Ridge dacite. This may represent either different lava histories or alteration characteristics that have affected normally immobile REEs. Altered samples with the highest Pb values have similar REE patterns to those of the local unaltered lavas. They are compositionally similar to typical Pual Ridge dacites indicating a genetic relationship between the main regional volcanic suite and the subseafloor hydrothermally altered, Pb-enriched material.Relative loss/gain for Pb between the analyzed altered samples and a calculated precursor show a maximum relative gain of 901%. Samples with relative Pb gain from both drill sites are associated with lower temperature alteration mineral assemblages characterized by pervasive chloritization. The related lower temperature (220-250 °C) neutral to slightly acidic fluids have been ascribed by others to return circulation of hydrothermal fluids that did not interact with seawater. Because altered samples have a higher Pb content than the fresh precursor, leaching of fresh volcanic rocks cannot be the source of Pb in the hydrothermal systems.     

内蒙古自治区翁牛特旗姚家店铅锌矿地质特征

内蒙古自治区翁牛特旗姚家店铅锌矿矿床为一受NW向断裂带构造控制的中低温岩浆热液充填交代型铅锌矿床,形成于燕山晚期,矿体呈脉状产于二叠世额里图组安山质凝灰岩之构造破碎带内,形态产状严格受断裂构造控制。矿石为硅化、黄铁矿化碎裂岩型铅锌矿石。     

Low temperature volatile production at the Lost City Hydrothermal Field, evidence from a hydrogen stable isotope geothermometer

Although commonly utilized in continental geothermal work, the water-hydrogen and methane-hydrogen isotope geothermometers have been neglected in hydrothermal studies. Here we report δD-CH₄ and δD-H₂ values from high-temperature, black smoker-type hydrothermal vents and low-temperature carbonate-hosted samples from the recently discovered Lost City Hydrothermal Field. Methane deuterium content is uniform across the dataset at − 120 ± 12‰. Hydrogen δD values vary from − 420‰ to − 330‰ at high-temperature vents to − 700‰ to − 600‰ at Lost City. The application of several geothermometer equations to a suite of hydrothermal vent volatile samples reveals that predicted temperatures are similar to measured vent temperatures at high-temperature vents, and 20-60 °C higher than those measured at the Lost City vents. We conclude that the overestimation of temperature at Lost City reflects 1) that methane and hydrogen are produced by serpentinization at > 110 °C, and 2) that isotopic equilibrium at temperatures < 70 °C is mediated by microbial sulfate reduction. The successful application of hydrogen isotope geothermometers to low-temperature Lost City hydrothermal samples encourages its employment with low-temperature diffuse hydrothermal fluids.     

Atmospheric deposition and isotope biogeochemistry of zinc in ombrotrophic peat

Zinc isotope ratios were measured in the top sections of dated ombrotrophic peat cores in Finland to investigate their potential as proxies for atmospheric sources and to constrain post depositional processes affecting the geochemical record. The peat deposits were located in Hietajärvi, a background site well away from any point pollution source and representing ‘background’ conditions, in Outokumpu, next to a mining site, and in Harjavalta, next to a smelter. Measured total concentrations, calculated excess concentrations and mass balance considerations suggest that zinc is subjected to important biogeochemical cycling within the peat. Significant isotopic variability was found in all three peat bogs, with heavier zinc in the deeper and lighter zinc in the upper sections. Isotope ratios and concentrations correlated in the two peats located next to dominant point sources, i.e. the smelting and mining site, suggesting that zinc isotopes trace pollution sources. Concentration and isotope peaks were offset from the period of mining and smelting activity, supporting migration of zinc down the profile. The δ⁶⁶Zn_JMC (where δ⁶⁶Zn = [(⁶⁶Zn/⁶⁴Zn)_sample/(⁶⁶Zn/⁶⁴Zn)_JMC-standard − 1] × 10³) of the top section sample at the remote Hietajärvi site was 0.9‰ and we suggest this represents the regional background isotope signature of atmospheric zinc. The deeper sections of the peat cores show isotopically heavier zinc than any potential atmospheric source, indicating that post depositional processes affected the isotopic records. The large variations encountered (up to 1.05‰ for δ⁶⁶Zn) and Rayleigh modelling imply that multiple fractionation of zinc during diagenetic alterations occurs and nutrient recycling alone cannot explain the fractionation pattern.We propose that zinc isotopes are amenable to identify different atmospheric zinc sources, including zinc derived from anthropogenic activities such as mining and smelting, but multiple biogeochemical processes seriously affect the record and they need to be evaluated and assessed carefully if zinc isotopes are used in terrestrial paleorecords.     

广西陆川县下水铅锌矿地质地球化学特征

研究认为下水铅锌矿床为喷流沉积 区域变质 部分岩浆热液迭加的多因复成铅锌矿床 ,查明了矿床的控矿因素 ,确定了矿床的找矿标志和找矿方向