Rising utilization of stable isotopes in tree rings for climate change and forest ecology

Analyses of stable isotopes(C,O,H)in tree rings are increasingly important cross-disciplinary programs.The rapid development in this field documented in an increasing number of publications requires a comprehensive review.This study includes a bibliometric analysis-based review to better understand research trends in tree ring stable isotope research.Overall,1475 publications were selected from the Web of Science Core Collection for 1974-2023.The findings are that:(1)numbers of annual publications and citations increased since 1974.From 1974 to 1980,there were around two relevant publications per year.However,from 2020 to 2022,this rose sharply to 109 publications per year.Likewise,average article citations were less than four per year before 1990,but were around four per article per year after 2000;(2)the major subjects using tree ring stable isotopes include forestry,geosciences,and environmental sciences,contributing to 42.5%of the total during 1974-2023;(3)the top three most productive institutions are the Chinese Academy of Sciences(423),the Swiss Federal Institute for Forest,Snow and Landscape Research(227),and the University of Arizona(204).These achievements result from strong collaborations;(4)review papers,for example,(Dawson et al.,Annu Rev Ecol Syst 33:507-559,2002)and(McCarroll and Loader,Quat Sci Rev 23:771-801,2004),are among the most cited,with more than 1000 citations;(5)tree ring stable isotope studies mainly focus on climatology and ecology,with atmospheric CO_(2) one of the most popular topics.Since 2010,precipitation and drought have received increasing attention.Based on this analysis,the research stages,key findings,debated issues,limitations and direc-tions for future research are summarized.This study serves as an important attempt to understand the progress on the use of stable isotopes in tree rings,providing scientific guid-ance for young researchers in this field.

Geochemistry, zircon U–Pb geochronology, and Hf isotopes of S-type granite in the Baoshan block, constraints on the age and evolution of the Proto-Tethys

Geochemistry, zircon U–Pb geochronology, and Hf isotope data for the Early Paleozoic granites in the Baoshan Block reveal the Early Paleozoic tectonic evolution of the Proto-Tethys. The samples are high-K, calcalkaline, strongly peraluminous rocks with A/CNK values of 1.37–1.46, are enriched in SiO2, K2O, and Rb, and are depleted in Nb, P, Ti, Eu, and heavy rare earth elements,which indicates the crystallization fractionation of the granitic magma. Zircon U–Pb dating indicates that they formed in ca. 480 Ma. The Nansa granites have εHf(t) values ranging from-16.04 to 4.36 with corresponding TC DMages of 2.10–0.81 Ga, which suggests the magmas derived from the partial melting of ancient metasedimentary with minor involvement of mantle-derived components. A synthesis of data for the Early Paleozoic igneous rocks in the Baoshan block and adjacent(Tengchong,Qiangtang, Sibumasu, Himalaya, etc.) blocks indicates that these blocks were all aligned along the proto-Tethyan margin of East Gondwana in the Early Paleozoic. The Early Paleozoic S-type granites from Nansa were generated in a high-temperature and low-pressure(HTLP) extensional tectonic setting, which resulted from Andean-type orogeny instead of the final assembly of Gondwana or crustal extension in a non-arc environment. In certain places, an expanding environment may exist in opposition to the tectonic backdrop of the lithosphere’s thickening and shortening, leading the crust to melt and decompress,mantle-derived materials to mix, and a small quantity of peraluminous granite to emerge.

Origin of the Dashuigou independent tellurium deposit at Qinghai–Xizang Plateau: constraints from the light stable isotopes C, O, and H

By studying the light isotopic compositions of carbon,oxygen,and hydrogen,combined with previous research results on the ore-forming source of the deposit,the authors try to uncover its metallogenic origin.The δ^(18)O and δ^(13)C isotope signatures of dolomite samples vary between 10.2 and 13.0‰,and between−7.2 and−5.2‰,respectively,implying that the carbon derives from the upper mantle.δD and δ^(18) O of quartz,biotite,and muscovite from diff erent ore veins of the deposit vary between−82 and−59‰,and between 11.6 and 12.4‰,respectively,implying that the metallogenic solutions are mainly magmatic.According to the relevant research results of many isotope geologists,the fractionation degree of hydrogen isotopes increases as the depth to the Earth’s core increases,and the more diff erentiated the hydrogen isotopes are,the lower their values will be.In other words,mantle-derived solutions can have extremely low hydrogen isotope values.This means that the δD‰ value−134 of the pyrrhotite sample numbered SD-34 in this article may indicate mantle-derived oreforming fl uid of the deposit.The formation of the Dashuigou tellurium deposit occurred between 91.71 and 80.19 Ma.

Petrogenesis and Tectonic Implications of the Early Triassic Nianzi Adakitic Granite Unit in the Yanshan Fold and Thrust Belt:New Constraints from U-Pb Geochronology and Sr-Nd-Hf Isotopes

The Nianzi granite unit,which includes the Nianzi,Xiaolianghou and Xiawopu granitic intrusions,is a significant component of the northern part of the North China Craton(NCC)and is situated in the Yanshan fold and thrust belt(YFTB).However,there is still debate regarding the tectonic evolutionary history of the YFTB during the late Permian to Triassic period,specifically regarding the timing of subduction and collision between the NCC and the Paleo-Asian Ocean.The Nianzi granite unit exhibits unique petrological,geochronological and geochemical signatures that shed light on the tectonic evolutionary history of the YFTB.This study presents detailed petrology,whole-rock geochemistry,together with Sr-Nd isotopic,zircon U-Pb dating and Lu-Hf isotopic data of the granites within the Nianzi granite unit.Our findings demonstrate that the granites primarily consist of subhedral K-feldspar,plagioclase,quartz,minor biotite and hornblende,with accessory titanite,apatite,magnetite and zircon.Zircon U-Pb dating indicates that the Xiaolianghou granite was emplaced at 247.5±0.62 Ma.Additionally,the adakitic characteristics of the Nianzi,Xiawopu and Xiaolianghou granitic intrusions,such as high Sr and Ba contents and high ratios of Sr/Y and(La/Yb)N,combined with negative Sr-Nd and Lu-Hf isotopes(87Sr/86Sr)i=0.705681–0.7057433,εNd(t)=−21.98 to−20.97,zirconεHf(t)=−20.26 to−9.92,as well as the I-type granite features of high SiO_(2),Na_(2)O and K_(2)O/Na_(2)O ratios,enriched Rb,K,Sr and Ba,along with depleted Th,U,Nb,Ta,P and Ti,suggest that the Nianzi granitic unit was mainly derived from the partial melting of a thickened lower crust containing hydrous,calc-alkaline to high-K calc-alkaline,mafic to intermediate metamorphic rocks.In light of these parameters,we further integrate our data with previous studies and conclude that the Nianzi granitic unit was generated in a post-collisional extensional environment during the Early Triassic.

A review of classical hydrogen isotopes storage materials

Hydrogen storage alloys(HSAs)are attracting widespread interest in the nuclear industry because of the generation of stable metal hydrides after tritium absorption,thus effectively preventing the leakage of radioactive tritium.Commonly used HSAs in the hydrogen isotopes field are Zr2M(M=Co,Ni,Fe)alloys,metallic Pd,depleted U,and ZrCo alloy.Specifically,Zr2M(M=Co,Ni,Fe)alloys are considered promising tritium-getter materials,and metallic Pd is utilized to separate and purify hydrogen isotopes.Furthermore,depleted U and ZrCo alloy are well suited for storing and delivering hydrogen isotopes.Notably,all the aforementioned HSAs need to modulate their hydrogen storage properties for complex operating conditions.In this review,we present a comprehensive overview of the reported modification methods applied to the above alloys.Alloying is an effective amelioration method that mainly modulates the properties of HSAs by altering their local geometrical/electronic structures.Besides,microstructural modifications such as nano-sizing and nanopores have been used to increase the specific surface area and active sites of metallic Pd and ZrCo alloys for enhancing de-/hydrogenation kinetics.The combination of metallic Pd with support materials can significantly reduce the cost and enhance the pulverization resistance.Moreover,the poisoning resistance of ZrCo alloy is improved by constructing active surfaces with selective permeability.Overall,the review is constructive for better understanding the properties and mechanisms of hydrogen isotope storage alloys and provides effective guidance for future modification research.

Linkage between precipitation isotopes and water vapor sources in the monsoon margin:Evidence from arid areas of Northwest China

The isotope composition in precipitation has been widely considered as a tracer of monsoon activity.Compared with the coastal region,the monsoon margin usually has limited precipitation with large fluctuation and is usually sensitive to climate change.The water resource management in the monsoon margin should be better planned by understanding the composition of precipitation isotope and its influencing factors.In this study,the precipitation samples were collected at five sampling sites(Baiyin City,Kongtong District,Maqu County,Wudu District,and Yinchuan City)of the monsoon margin in the northwest of China in 2022 to analyze the characteristics of stable hydrogen(δD)and oxygen(δ18O)isotopes.We analyzed the impact of meteorological factors(temperature,precipitation,and relative humidity)on the composition of precipitation isotope at daily level by regression analysis,utilized the Hybrid Single-Particle Lagrangian Integrated Trajectory(HYSPLIT)-based backward trajectory model to simulate the air mass trajectory of precipitation events,and adopted the potential source contribution function(PSCF)and concentration weighted trajectory(CWT)to analyze the water vapor sources.The results showed that compared with the global meteoric water line(GMWL),the slope of the local meteoric water line(LMWL;δD=7.34δ^(18)O-1.16)was lower,indicating the existence of strong regional evaporation in the study area.Temperature significantly contributed toδ18O value,while relative humidity had a significant negative effect onδ18O value.Through the backward trajectory analysis,we found eight primary locations that were responsible for the water vapor sources of precipitation in the study area,of which moisture from the Indian Ocean to South China Sea(ITSC)and the western continental(CW)had the greatest influence on precipitation in the study area.The hydrogen and oxygen isotopes in precipitation are significantly influenced by the sources and transportation paths of air mass.In addition,the results of PSCF and CWT analysis showed that the water vapor source areas were primarily distributed in the south and northwest direction of the study area.

Metallogenic Age and Ore-forming Material Sources of the Dahongshan Fe-Cu Deposit,Yunnan Province:Insights from Molybdenite Re-Os Dating and H-O-S-Pb Isotopes

The Dahongshan Fe-Cu(-Au)deposit is a superlarge deposit in the Kangdian metallogenic belt,southwestern China,comprising approximately 458 Mt of Fe ores(40%Fe)and 1.35 Mt Cu.Two main types of Fe-Cu(-Au)mineralization are present in the Dahongshan deposit:(1)early submarine volcanic exhalation and sedimentary mineralization characterized by strata-bound fine-grained magnetite and banded Fe-Cu sulfide(pyrite and chalcopyrite)hosted in the Na-rich metavolcanic rocks;(2)late hydrothermal(-vein)type mineralization characterized by Fe-Cu sulfide veins in the hosted strata or massive coarse-grained magnetite orebodies controlled by faults.While previous studies have focused primarily on the early submarine volcanic and sedimentary mineralization of the deposit,data related to late hydrothermal mineralization is lacking.In order to establish the metallogenic age and ore-forming material source of the late hydrothermal(-vein)type mineralization,this paper reports the Re-Os dating of molybdenite from the late hydrothermal vein Fe-Cu orebody and H,O,S,and Pb isotopic compositions of the hydrothermal quartz-sulfide veins.The primary aim of this study was to establish the metallogenic age and ore-forming material source of the hydrothermal type orebody.Results show that the molybdenite separated from quartz-sulfide veins has a Re-Os isochron age of 831±11 Ma,indicating that the Dahongshan Fe-Cu deposit experienced hydrothermal superimposed mineralization in Neoproterozoic.The molybdenite has a Re concentration of 99.7-382.4 ppm,indicating that the Re of the hydrothermal vein ores were primarily derived from the mantle.The δ^(34)S values of sulfides from the hydrothermal ores are 2‰-8‰ showing multi-peak tower distribution,suggesting that S in the ore-forming period was primarily derived from magma and partially from calcareous sedimentary rock.Furthermore,the abundance of radioactive Pb increased significantly from ore-bearing strata to layered and hydrothermal vein ores,which may be related to the later hydrothermal transformation.The composition of H and O isotopes within the hydrothermal quartz indicates that the ore-forming fluid is a mixture of magmatic water and a small quantity of water.These results further indicate that the late hydrothermal orebodies were formed by the Neoproterozoic magmatic hydrothermal event,which might be related to the breakup of the Rodinia supercontinent.Mantle derived magmatic hydrothermal fluid extracted ore-forming materials from the metavolcanic rocks of Dahongshan Group and formed the hydrothermal(-vein)type Fe-Cu orebodies by filling and metasomatism.

Origin of ore-forming fluids in Qinggouzi stibnite deposit,NE China:Constraints from fluid inclusions and H-O-S isotopes

The Qinggouzi stibnite deposit is located in Huashan Town,Jilin Province,in the northeastern margin of North China Craton(NCC).It is controlled by fault structures,hosted within structurally controlled felsic dykes,predominantly surrounded by phyllite,schist and quartzite.This study presents the results of fluid inclusions studies,intending to determine the source of the fluid responsible for ore-formation,hence exploring its metallogenesis.The aqueous biphase inclusions are identified in the stibnite-bearing quartz veins of the deposit.Moreover,aqueous biphase inclusions are further classified into(1)biphase liquid-rich inclusions(1 a)and(2)biphase gas-rich inclusions(1 b)depending upon liquid to gas ratio trapped within the fluid inclusions.Homogenization temperatures for(1 a)and(1 b)range between 114.8℃to 422℃and 128.3℃to 267.5℃,respectively.1 a and 1 b have salinities of 0.18%to 16.14%NaCleqv and 1.22%to 12.88%NaCleqv,and density range from 0.43 to 1.02 g/cm^(3) and 0.81 to 0.98 g/cm^(3),respectively.Sulfur isotopic analysis indicatesδ34SV-CDT from 4.4×10-3 to 6.5×10^(-3),with an average of 5.2×10^(-3),whereas H isotopes values onδDV-SMOW standard are-100.8×10^(-3) and-107.5×10^(-3),while O isotopes data onδ18OV-SMOW standard range between 20.1×10^(-3) and 20.4×10-3.Fluid inclusions study,combining with sulfur and H-O isotopic data reveal that the ore-forming fluids originated from deep source and were subsequently contaminated by meteoric water.Hydrostatic pressure calculation shows that the minimum and maximum pressures are 11.65 and 42.33 MPa,and relevant depths of deposit are estimated to be 1.16 and 4.23 km.Finally,we inferred that Qinggouzi stibnite deposit is a medium-low temperature,low salinity hydrothermal deposit,which is formed by deep source and later contaminated by meteoric water,and is classified as epizonal deposit in terms of orogenic series.

胶东盘子涧金矿床成矿流体特征--来自包裹体、H-O同位素证据

盘子涧金矿床地处华北板块胶辽隆起区,栖霞—蓬莱金成矿带上。金矿的形成主要与区内控矿断裂——盘子涧断裂和中生代岩浆岩有关。为研究该矿床成矿流体性质及演化,并控讨矿床成因,对该矿床不同阶段的包裹体进行岩相学、显微测温、包裹体激光拉曼及H—O同位素分析研究。盘子涧金矿床成矿热液期可划分为4个成矿阶段,从早到晚分别是黄铁矿—石英阶段(Ⅰ阶段)、石英—黄铁矿(绢云母)阶段(Ⅱ阶段)、金—石英—多金属硫化物阶段(Ⅲ阶段)和石英—碳酸盐阶段(Ⅳ阶段)。其中Ⅱ、III阶段为主成矿阶段。不同成矿阶段的流体包裹体有3种类型,分别是富液气液两相盐水包裹体、含CO_(2)三相包裹体和纯液相包裹体。显微测温结果显示,成矿流体的完全均一温度介于142~348℃,主要集中于200~300℃,盐度介于4.44%~10.98%NaCl_(eqv)。石英的δD_(V-SMOW)值为-74.6‰~-68.5‰,δ^(18)O_(V-SMOW)值为+11.65‰~+13.92‰。显示成矿流体为中低温、低盐度的CO_(2)—H_(2)O—NaCl体系,来源于地幔,以岩浆热液为主,并伴有部分大气降水加入。矿床成因类型属石英脉型金矿。

Response to the Lomagundi-Jatuli Event in the southwestern margin of the Yangtze Plate:Evidence from the carbon and oxygen isotopes of the Paleoproterozoic Yongjingshao Formation

The Lomagundi-Jatuli Event(LJE)refers to the significant positive carbon isotope excursion in seawater constituents that occurred immediately after the increase in atmospheric oxygen content during the Paleoproterozoic(2.22-2.06 Ga).Theδ^(13)C values of 46 dolostone samples collected from the Paleoproterozoic Yongjingshao Formation varied in the range of 0.05‰-4.95‰(V-PDB;maximum:4.95‰)in this study,which may be related to the multicellular eukaryotes in the Liangshan Formation in the Yimen Group.They are much higher than theδ^(13)C values of marine carbonates(-1.16‰on average).Theδ^(13)C values of other formations in the Paleoproterozoic Yimen Group are negative.The notable positive carbon isotope anomalies of the Yongjingshao Formation indicate the response to the LJE at the southwestern margin of the Yangtze Block,which is reported for the first time.Furthermore,they are comparable to theδ^(13)C values of carbonates in the Dashiling Formation of the Hutuo Group in the Wutaishan area in the North China Craton,the Wuzhiling Formation of the Songshan Group in the Xiong'er area,Henan Province,and the Dashiqiao Formation of the Liaohe Group in the Guanmenshan area,Liaoning Province.Therefore,it can be further concluded that the LJE is a global event.This study reveals that LJE occurred in Central Yunnan at 2.15-2.10 Ga,lasting for about 50 Ma.The macro-columnar,bean-shaped,and microfilament fossils and reticular ultramicrofossils of multicellular eukaryotes in this period were discovered in the Liangshan Formation of the Yimen Group.They are the direct cause for the LJE and are also the oldest paleontological fossils ever found.The major events successively occurring in the early stage of the Earth include the Great Oxygenation Event(first occurrence),the global Superiortype banded iron formations(BIFs),the Huronian glaciation,the Great Oxygenation Event(second occurrence),the explosion of multicellular eukaryotes,the positive carbon isotope excursion,and the global anoxic and selenium-rich sedimentary event.The authors think that the North China Craton and the Yangtze Craton were possibly in different tectonic locations of the same continental block during the Proterozoic.

Zircon U-Pb geochronology,Hf isotopes,and geochemistry constraints on the age and tectonic affinity of the basement granitoids from the Qiongdongnan Basin,northern South China Sea

Studies in the northern South China Sea(SCS)basement remain important for understanding the evolution of the Southeast Asian continental margin.Due to a thick cover of sediments and scarce borehole penetration,little is known about the age and tectonic affinity of this basement.In this study,an integrated study of zircon U-Pb geochronology,Hf isotopes,and whole-rock major and trace elements on seven basement granitoids from seven boreholes of Qiongdongnan Basin has been carried out.New zircon U-Pb results for these granitoids present middle-late Permian((270.0±1.2)Ma;(253±3.4)Ma),middle to late Triassic((246.2±3.4)Ma;(239.3±0.96)Ma;(237.9±0.99)Ma;(228.9±1.0)Ma)and Late Cretaceous ages((120.6±0.6)Ma).New data from this study,in combination with the previous dataset,indicates that granitoid ages in northern SCS basement vary from 270 Ma to 70.5 Ma,with three age groups of 270–196 Ma,162–142 Ma,and 137–71 Ma,respectively.Except for the late Paleozoic-Mesozoic rocks in the basement of the northern SCS,a few old zircon grains with the age of(2708.1±17)Ma to(2166.6±19)Ma provide clues to the existence of the pre-Proterozoic components.The geochemical signatures indicate that the middle Permian-early Cretaceous granitoids from the Qiongdongnan Basin are I-type granites formed in a volcanic arc environment,which were probably related to the subduction of the Paleo-Pacific Plate.

Trace-element geochemistry and S–O isotopes in the fluorite-barite mineralization of Merguechoum,Moroccan eastern Meseta:insights into ore genesis to the Pangea rifting

The Merguechoum fluorite-barite mineralization,located in the Eastern Meseta of Morocco,is hosted in the Late Hercynian granite.The ore consists of fine crystals of fluorite 1,massive barite 1,euhedral crystals of fluorite 2,and barite 2 with calcite and minor quartz and sulfides.The Merguechoum ore deposits have never been investigated.This study was the first contribution that studied the genesis of fluorite and barite.The ore occurs as dissemination within granite intrusion and also fills the NE-SWtrending meter-sized fractures and faults.The values of the total Rare Earth Elements and Yttrium(REY)and the ratios of LREY/HREY,Y/Ho,Tb/Ca,and Tb/La indicate that the Merguechoum fluorite precipitated from hydrothermal fluids,likely basinal brines,which interacted with the Hercynian granite.The REY data indicate that the ore-forming fluids of the early stage have intensely interacted with the Hercynian granite compared to those of the late ore stage.The gradual decrease in the europium(Eu/Eu^(*)),yttrium(Y/Y^(*)),and cerium(Ce/Ce^(*))anomalies and a low concentration ofΣREY observed in the second ore stage compared to the first ore stage suggest an increase in p H and fO_(2)and by inference a decrease in temperature during the evolution of the hydrothermal system.This evolution could be explained by fluid mixing between the ascending basinal hydrothermal fluids and the diluted sulfate-rich meteoric water barite separates from selected samples reveal that the dissolved sulfates(SO_(4)^(2-))were derived from Permian–Triassic sulfates and/or coeval poreseawater sulfates.The proposed fluid mixing triggered the precipitation of an early-stage F-Ba assemblage followed by the second-stage F-Ba mineralization.Geologic fieldwork,REY inventories,and isotope data point to the ore genesis during the Permian–Triassic extensional tectonic activity concerning the Pangea rifting.This extensional tectonic environment is likely the driving force that mobilized a large amount of the ore-forming basinal brines along the available faults and fractures to the loci of ore deposition.

Genesis of the Huoshenmiao Mo deposit in the Luanchuan ore district, China: Constraints from geochronology, ?uid inclusion, and H-O-Sisotopes

The Huoshenmiao δeposit is Mo skarn δeposit, located in the western part of the Luanchuan ore δistrict.Mineralization process can be δivided into a skarn and a quartz-sulfide episodes with six stages: prograde(I), retrograde(II), quartz-K-feldspar(III), quartz-molybdenite(IV), quartz-pyrite(V), and quartzcalcite(VI). A combined study of geochronology, fluid inclusion(FI), and stable isotopes was conducted to constrain the mineralization age, source of ore materials, as well as the origin and evolution of the ore-forming fluids. Molybdenite Ree Os δating indicates that the δeposit was formed in the Late Jurassic(~145 Ma). The δ^(34)S values of sulfides range from 3.0‰ to 7.1‰, implying that the ore materials in the δeposit are magmatic in origin. Three types and six subtypes of FIs are δistinguished, namely, aqueous two-phase(W_1-and W_2-type), δaughter mineral-bearing multiphase(S_1-and S_2-type), and CO_2-bearing three-phase(C_1-and C_2-type). In stages I and II, the W_1-type FIs δisplay homogenization temperatures(Th) from 496°C to >600°C, with salinities of 14.9-18.3 wt.% NaCl eqv. The FIs in stages III, IV and early stage V composed of coeval S-, C-and W-types, respectively homogenize at similar Th, suggesting the occurrence of boiling. The W1-type FIs in late stage V and stage VI, yield Th of 102-406°C and salinities of 0-4.7 wt.% NaCl eqv. The δD_(H_2O)and δ^(18) O(H_2O)values of the ore-forming fluids in quartz-sulfide episode vary from-112‰ to-76‰, and 11.0‰ to 1.0‰, respectively. All these above observations reveal that the early ore-forming fluids are magmatic in origin, and characterized by high temperature and moderate to high salinity, and gradually evolve to low temperature, low salinity meteoric water. The Huoshenmiao Mo δeposit is associated with the magmatism event induced by the protracted subduction of the Izanagi plate beneath the eastern China continent. The δecrease in temperature, salinity and f(O_2), as well as change of p H δue to boiling and fluid-rock interaction, are the main factors controlling Mo δeposition.

Origin and evolution of ore-forming fluid for the Gaosongshan gold deposit, Lesser Xing’an Range:Evidence from fluid inclusions,H-O-S-Pb isotopes

Epithermal gold deposits are typical precious metal deposits related to volcanic and subvolcanic magmatism.Due to the lack of direct geological and petrographic evidences,the origin of the ore-forming fluid is deduced from the spatial diagenesis-mineralization relationship,chronological data,physicochemical characteristics of mineral fluid inclusions,mineral or rock elements and isotopic geochemical characteristics.By objectively examining this scientific problem via a geological field survey and petrographic analysis of the Gaosongshan epithermal gold deposit,we recently discovered and verified the following points:(1) Pyrite-bearing spherical quartz aggregates (PSQA) occur in the rhyolitic porphyry;(2) the mineralization is structurally dominated by WNW- and ENE-trending systems and occurs mostly in hydrothermal breccias and pyrite-quartz veins,and the ore types are mainly hematite-crusted quartz,hydrothermal breccia,massive pyrite-quartz,etc.;(3) the alteration types consist of prevalent silicification,sericitization,propylitization and carbonation,with local adularization and illitization.The ore minerals are mainly pyrite,primary hematite,native gold,and electrum,with lesser amounts of chalcopyrite,magnetite,sphalerite,and galena,indicating a characteristic epithermal low-sulfidation deposit.The ore-forming fluid may have been primarily derived from magmatic fluid exsolved from a crystallizing rhyolitic porphyry magma.Further zircon U-Pb geochronology,fluid inclusion,physicochemical and isotopic geochemical analyses revealed that (1) rhyolitic porphyry magmatism occurred at 104.6 ± 1.0 Ma,whereas the crystallization of the PSQA occurred at 100.8 ± 2.1 Ma;(2) the hydrothermal fluid of the pre-ore stage was an exsolved CO2-bearing H2O-NaCl magmatic fluid that produced inclusions mainly composed of pure vapor (PV),vapor-rich (WV) and liquid-rich (WL) inclusions with a small number of melt-(M) and solid-bearing (S) inclusions;mineralization-stage quartz contains WL and rare PV,WV and pure liquid (PL) inclusions characterized by the H2O-NaCl system with low formation temperatures and low salinities;(3) the characteristics of hydrogen,oxygen,sulfur,and lead isotopes and those of rare earth elements (REEs) provide insight into the affinity between PSQA and orebodies resulting from juvenile crust or enriched mantle.Combined with previous research on the mineralogenetic epoch (99.32 ± 0.01 Ma),we further confirm that the mineralization of the deposit occurred in the late Early Cretaceous,which coincides with the extension of the continental margin induced by subduction of the Pacific Plate beneath the Eurasian Plate.The formation of the ore deposit was proceeded by a series of magmatic and hydrothermal events,including melting of enriched juvenile crust,upwelling,the eruption and emplacement of the rhyolitic magma,the exsolution and accumulation of magmatic hydrothermal fluid,decompression,the cooling and immiscibility/boiling of the fluid,and mixing of the magmatic fluid with meteoric water,in association with water-rock interaction.

Sources and transformations of nitrite in the Amundsen Sea in summer 2019 and 2020 as revealed by nitrogen and oxygen isotopes

In this study,the nitrogen and oxygen isotope compositions of nitrite in the upper 150 m water column of the Amundsen Sea in the summer of 2019 and 2020 were measured to reveal the distribution and transformation of nitrite in the euphotic zone of the Southern Ocean.We found that primary nitrite maxima(PNMs)are widely present in the Amundsen Sea,where the depth of occurrence deepens from east to west and nitrite concentrations increases.Evidence from dual isotopes suggests that the formation of PNMs in all regions of the Amundsen Sea is dominated by ammonia oxidation.More importantly,the nitrogen and oxygen isotope compositions of nitrite in the Amundsen Sea mixed layer are abnormal,and their depth profiles are mirror symmetrical.Isotopic anomalies exhibit spatial variations,with central surface water having the lowest nitrogen isotope composition(−89.9‰±0.2‰)and western surface water having the highest oxygen isotope composition(63.3‰±0.3‰).Isotopic exchange reaction between nitrate and nitrite is responsible for these isotope anomalies,as both nitrogen and oxygen isotopes have large isotopic fractionation and opposite enrichment effects.This proves that isotopic exchange reaction operates extensively in different regions of the Amundsen Sea.Our study highlights the unique role of dual isotopes of nitrite in deepening the understanding of nitrogen cycle.Further studies on ammonia oxidation and isotopic exchange between nitrate and nitrite are warranted in the future to understand their roles in the nitrogen cycle in the Southern Ocean.

青藏高原西北部班公湖流域夏季主要水体H-O同位素组成及其影响因素

作为高寒内陆区的青藏高原西北部班公湖流域水文数据资料较为匮乏,导致对区域水循环过程和气候环境的认识不够深入,氢氧稳定同位素示踪技术可为解决该问题提供理想途径。本文系统分析班公湖流域夏季含湖水、河水、冰川融水和地下水4种不同类型的水体中氢氧同位素的组成,阐释水体氢氧同位素、氘盈余参数沿程变化的特征及其与水体矿化度、高程、经纬度和全球大气降雨线之间的关系,并进一步剖析同位素组成变化的控制因素。结果显示,水体中δ^(2)H和δ^(18)O的波动范围分别为-112.37‰~-24.90‰和-14.84‰~2.01‰,平均值及标准差分别为-76.73‰±26.49‰和-8.43‰±5.24‰。湖水δ^(2)H和δ^(18)O相对其他水体富集,测定结果更偏正值,冰川融水δ^(2)H和δ^(18)O相对其他水体更为贫化。流域水体氢氧同位素的大陆效应总体不明显,部分水体有一定高程效应体现。水体氢氧同位素演化趋势表明,冰川融水与全球大气水线接近,易受大气降雨影响。同时其他水体线的较小截距和斜率值,表明大气降雨不是这些水体的直接补给源。河流沿程的水体δ^(2)H和δ^(18)O呈递增趋势,越远离冰川融水补给端的河水和湖水值越偏正,反映强蒸发的特点。水体氘盈余参数及其与矿化度之间的关系也指示蒸发作用是影响该区域水体氢氧同位素变化的主要因素。

Metallogenesis and hydrothermal evolution of the Tonggou Cu deposit in the Eastern Tianshan:Evidence from fluid inclusions,H-O-S isotopes,and Re-Os geochronology

The Tonggou Cu polymetallic deposit in the Bogda Orogenic Belt,Eastern Tianshan shows evidence for three stages of hydrothermal mineralization:early pyrite veins(Stage 1),polymetallic sulfide±epidote-quartz(Stage 2),and late-stage pyrite-calcite veins(Stage 3).Fluid inclusion petrography and microthermometry analyses indicate that the liquid-rich aqueous inclusions(L),vapour-rich aqueous inclusions(V),and NaCl daughter mineral-bearing three phase inclusions(S)formed during the main stage of mineralization,and that the ore fluids represent high-temperature and high-salinity H20-NaCl hydrothermal fluids that underwent boiling.Stable isotope(H,O)data indicate that the ore fluids of the Tonggou deposit were originally derived from magmatic water in Stage 2 and subsequently mixed with local meteoric water during Stage 3.Sulphur isotope compositions(6.7‰to 10.9‰)are consistent with theδ^34 S values of pyrite from the Qijiaojing Formation sandstone,indicating the primary source of the sulphur ore.Furthermore,chalcopyrite grains separated from the chalcopyrite-rich ore samples yield an isochron age of 303±12 Ma(MSWD=1.2).These results indicate that the Tonggou deposit is a transition between high-sulfidation and porphyry deposits which formed in the Late Carboniferous.It also suggests an increased likelihood for the occurrence of Cu(Au,Mo)in the Bogda Orogenic Belt,especially at locations where the Cu-Zn deposits are thicker;further deep drilling and exploration are encouraged in these areas.

Procedure for determining the number of thermal diffusion columns in square cascade for separation of Ne stable isotopes

The thermal diffusion column represents one method of separating stable isotopes.This method is advantageous for smallscale operations because of the simplicity of the apparatus and small inventory,especially in gas-phase operations.Consequently,it has attracted attention for its applicability in tritium and noble gas separation systems.In this study,the R cascade was used to design and determine the number of columns.A square cascade was adopted for the final design because of its flexibility,and calculations were performed to separate 20Ne and 22Ne isotopes.All the R cascades that enriched the Ne isotopes by more than 99%were investigated,the number of columns was determined,and the square cascade parameters were optimized using the specified columns.Additionally,a calculation code“RSQ_CASCADE”was developed.A unit separation factor of three was considered,and the number of studied stages ranged from 10 to 20.The results showed that the column separation power,relative total flow rate,and required number of columns were linearly related to the number of stages.The separation power and relative total flow decreased and the number of columns increased as the stage number increased.Therefore,a cascade of 85 columns is recommended to separate the stable Ne isotopes.These calculations yielded a 17-stage square cascade with five columns in each stage.By changing the stage cut,feed point,and cascade feed flow rate,the best parameters for the square cascade were determined according to the cascade and column separation powers.As the column separation power had a maximum value in cascade feed 50,it was selected for separating Ne isotopes.

Features and factors of radium isotopes in Tianjin’s typical estuaries

In order to characterize the features of radium isotopes in estuaries of Tianjin,a continuous survey and sampling of typical estuaries were conducted from 2013 to 2017 in this study.The activities of natural radioactive radium isotopes(^(223)Ra,^(224)Ra,and ^(228)Ra)in groundwater and surface water were measured by the radium-delayed coincidence counting(RaDeCC)system.The non-conservative behavior of the radium isotopes was investigated under hydrogeochemical conditions and urbanization.The results indicated that in terms of horizontal distribution,the activities of radium in groundwater(Hangu,Tanggu,and Dagang)showed an upward trend from north to south and demonstrated a higher figure than surface water(Haihe River and Duliujian River).Concerning the vertical distribution,the activitives of radium at a 15 m burial depth was higher than that at a 30 m burial depth in all measurements.The activities of radium isotopes in the study area increased with the increase of total dissolved solids,and their desorption behavior on Fe-Mn oxides was constrained by the redox intensity.Different hydrogeological conditions resulted in variations in the vertical profile of radium activities.The activity of radium was regulated by seasonal variation and precipitation in groundwater and surface water.In addition,the rapid urbanization has caused a significant impact on the features of radium isotopes in typical estuaries of Tianjin.Meanwhile,radium isotopes can be applied to reflect the impact of urbanization on surface watergroundwater systems.Clarifying and cleverly utilizing the relationship between behavior of radium isotopes and urbanization will promote the development of the Tianjin Binhai New Area in a healthy way.

Geochemistry,Fluid Inclusions and Sulfur Isotopes of the Goshgarchay Cu-Au Deposit(Western Azerbaijan)in Lesser Caucasus:Implications for the Origins of Ore-forming Fluids

The Goshgarchay Cu-Au deposit is located in the central part of the northwest flank of the Murovdagh region in the Lesser Caucasus.The Goshgarchay Cu-Au deposit is associated with Middle Jurassic volcanic and Late Jurassic-Early Cretaceous high-K calc-alkaline intrusive rocks.The Cu-Au mineralization is commonly related to quartz-sericite-chlorite alteration dominantly composed of chalcopyrite,gold,sphalerite,pyrite,bornite,hematite,covellite,chalcocite,malachite,and azurite.The Goshgarchay copper-gold deposit,which is 600 m wide and approximately 1.2 km long,is seen as a faultcontrolled and vein-,stockwork-and disseminated type deposit.The Goshgarchay Cu-Au deposit predominantly comprises Cu(max.64500 ppm)and Au(max.11.3 ppm),while it comprises relatively less amounts Zn(max.437 ppm),Mo(max.47.5 ppm),Pb(max.134 ppm),and Ag(max.21 ppm).The homogenization temperatures and salinities of fluid inclusions in quartz for stage Ⅰ range from 380℃ to 327℃,and 6.9 wt% to 2.6 wt% NaCl eq.,respectively.Thand salinities in quartz for stage Ⅱ range from 304℃ to 253℃,and 7.6 wt% to 3.2 wt% NaCl eq.,respectively.The calculated δ^(34)S_(h2s)values(-1.5‰ to 5.5‰)of sulfides and especially the narrow range of δ^(34)S_(h2s) values of chalcopyrite and bornite(between -0.07‰ and +0.7‰)indicate that the source of the Goshgarchay Cu-Au mineralization is magmatic.Based on the mineralogical,geochemical,fluid inclusion,and sulfur isotopic data,the Goshgarchay Cu-Au deposit represents a late stage peripheral magmatic-hydrothermal mineralization probably underlain by a concealed porphyry deposit.