Genesis of the Jiajika superlarge lithium deposit,Sichuan,China:constraints from He–Ar–H–O isotopes

The Jiajika granitic-and pegmatite-type lithium deposit,which is in the Songpan-Garze Orogenic Belt in western Sichuan Province,China,is the largest in Asia.Previous studies have examined the geochemistry and mineralogy of pegmatites and their parental source rocks to determine the genesis of the deposit.However,the evolution of magmatic-hydrothermal fluids has received limited attention.We analyzed He–Ar–H–O isotopes to decipher the ore-fluid nature and identify the contribution of fluids to mineralization in the late stage of crystallization differentiation.In the Jiajika ore field,two-mica granites,pegmatites(including common pegmatites and spodumene pegmatites),metasandstones,and schists are the dominant rock types exposed.Common pegmatites derived from early differentiation of the two-mica granitic magmas before they evolved into spodumene pegmatites during the late stage of the magmatic evolution.Common pegmatites have~3He/~4He ratios that vary from 0.18 to 4.68 Ra(mean1.62 Ra),and their~(40)Ar/~(36)Ar ratios range from 426.70 to 1408.06(mean 761.81);spodumene pegmatites have~3He/~4He ratios that vary from 0.18 to 2.66 Ra(mean 0.87Ra)and their~(40)Ar/~(36)Ar ratios range from 402.13 to 1907.34(mean 801.65).These data indicate that the hydrothermal fluids were shown a mixture of crust-and mantle-derived materials,and the proportion of crustderived materials in spodumene pegmatites increases significantly in the late stage of the magmatic evolution.Theδ~(18)OH_(2)O–VSMOWvalues of common pegmatites range from 6.2‰to 10.9‰,with a mean value of 8.6‰,andδDV–SMOWvalues vary from-110‰to-72‰,with a mean o f-85‰.Theδ~(18)OH_(2)O–VSMOWvalues of spodumene pegmatites range from 5.3‰to 13.2‰,with a mean of 9.1‰,andδDV–SMOWvalues vary from-115‰to-77‰,with a mean of-91‰.These data suggest that the ore-forming fluids came from primary magmatic water gradually mixing with more meteoric water in the late stage of the magmatic evolution.Based on the He–Ar–H–O and other existing data,we propose that the oreforming metals are mainly derived from the upper continental crust with a minor contribution from the mantle,and the fluid exsolution and addition of meteoric water during the formation of pegmatite contributed to the formation of the Jiajika superlarge lithium deposit.

A Study of Sr, Nd and O Isotopes of the K-rich Melanocratic Dykes in the Late Mesozoic Gold Field in the Jiaodong Peninsula

Geologic, petrographic and petrochemical studies of the late Mesozoic K-rich melanocratic dykes, including lamprophyres, andesite porphyrites and dacite-porphyry in the gold field system in the Jiaodong Peninsula, China, have shown that these dykes are characterized by rich potassium and alkali but poor titanium. They belong to an ultra-high potassic, shoshonitic and high potassic calc-alkaline rock series. The parental magma has relatively high initial strontium ratios ((87Sr/86Sr),=0.70895-0.71140) and low (143Nd/144Nd)1 ratios (varying from 0.51135 to 0.51231); and its δ18Osmow, whole rock values vary from +5.8%c to +10.6%c with a mean of +7.1%c. These features suggest that the source region of the magma is an enriched mantle wedge transformed from a continental lithosphere mantle which has experienced metasomatism by mantle-derived fluids with H2O-dominated fluids that were provided during the underthrusting of an ocean crust. The initial magma was generated by low-degree partial melting of the enriched mantle in its mature stage in the back-arc spreading environment. The evolution of magmas is associated with two trends, i.e., fractional crystallization and mixing with or intensive contamination by palaeo-crust materials or metamorphic rocks. The former process is evident in the gold field system of quartz-vein type, whereas the latter is dominated in the gold field system of the altered-rock type. This conclusion is very important for more detailed study of petrogenesis and mineralization through the crust-mantle interaction (exchange) in the Mesozoic in this region.

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.

Geodynamic Background of Intracontinental Cenozoic Alkaline Volcanic Rocks in Laojiezi, Western Yangtze Craton: Constraints from Sr-Nd-Hf-O Isotopes

The Laojiezi alkaline volcanic rocks, which are located in the intraplate region of the Yangtze craton, coincide with the formation of the Jinshajiang-Ailaoshan-Red River alkaline rock belt. Although this belt has been widely studied by geologists because of its porphyry-related Pb-Ag-Au polymetallic deposit and geotectonic location, the material sources of this belt are still debate. Whole-rock analyses show that these rocks have high total alkali contents(3.73–11.08 wt%), and their aluminum saturation index(ASI) values widely vary from 0.82 to 3.07, which comprise a metaluminous-peraluminous magma series. These rocks are characterized by high K(K2 O/Na2 O>1) and low Ti and Mg contents; enrichment in large-ion lithophile elements, such as Rb, Ba, K and light rare earth elements; and depletion in high field strength elements, such as Ta, Nb, P, and Ti. These rocks exhibit moderate Eu(Eu/Eu*=0.86–1.04) and Ce(Ce/Ce*=0.63–0.96) anomalies. Their(87 Sr/86 Sr)i, εNd(t), zircon εHf(t) and δ18 O values range from 0.70839 to 0.71013, from-10.16 to-12.45, from-19.6 to-5.8, and from 5.69‰ to 8.54‰, respectively, and their Nd and Hf two-stage model ages(TDM2) are 1.67–1.86 Ga and 1.27–2.02 Ga, respectively. These data reflect the primary partial melting of Paleoproterozoic to Mesoproterozoic lower crust with minor residual continental lithospheric mantle and supracrustal metasediments. The lithosphere was likely thickened along the southeastern margin of the Tibetan Plateau following the Indian-Asian continentcontinent collision(65–41 Ma). During the post-collision phase(36–16 Ma), the transition from a compressional to extensional setting triggered the convective removal of the over-thickened CLM beneath the Yangtze craton, which led to the upwelling of asthenospheric materials. This process created alkali-rich and high-K magma through the partial melting of the thickened lower crust. Magma that carried Cu-Au-Pb-Ag minerals was emplaced by strike-slip motion along the E-to W-or ENE-to WSWtrending tectonically weak zone, finally forming an alkaline porphyry Cu-Au-Pb-Ag polymetallic deposit.

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.

Isotopes (¹³C and ¹⁸O) Geochemistry of Lower Triassic Montney Formation, Northeastern British Columbia, Western Canada

Oxygen isotope (δ18O) serves as paleothermometer, and provides paleotemperature for carbonates. δ18O signature was used to estimate the temperature of fractionation of dolomite and calcite in Montney Formation, empirically calculated to have precipitated, between approximately 13°C to ±33°C during Triassic time in northeastern British Columbia, Western Canada Sedimentary Basin (WCSB). Measurements of stable isotopes (δ13C and δ18O) fractionation, supported by quantitative X-ray diffraction evidence, and whole-rock geochemical characterization of the Triassic Montney Formation indicates the presence of calcite, dolomite, magnesium, carbon and other elements. Results from isotopic signature obtained from bulk calcite and bulk dolomite from this study indicates depleted δ13CPDB (-2.18‰ to -8.46‰) and depleted δ18OPDB (-3.54‰ to -16.15‰), which is interpreted in relation to oxidation of organic matter during diagenesis. Diagenetic modification of dolomitized very fine-grained, silty-sandstone of the Montney Formation may have occurred in stages of progressive oxidation and reduction reactions involving chemical elements such as Fe, which manifest in mineral form as pyrite, particularly, during early burial diagenesis. Such mineralogical changes evident in this study from petrography and SEM, includes cementation, authigenic quartz overgrowth and mineral replacement involving calcite and dolomite, which are typical of diagenesis. High concentration of chemical elements in the Montney Formation?-Ca and Mg indicates dolomitization. It is interpreted herein, that calcite may have been precipitated into the interstitial pore space of the intergranular matrix of very fine-grained silty-sandstone of the Montney Formation as cement by a complex mechanism resulting in the interlocking of grains.

Antibacterial mechanism of kojic acid and tea polyphenols against Escherichia coli O157:H7 through transcriptomic analysis

Escherichia coli O157:H7 is one of the major foodborne pathogenic bacterial that cause infectious diseases in humans.The previous found that a combination of kojic acid and tea polyphenols exhibited better activity against E.coli O157:H7 than using either alone.This study aimed to explore responses underlying the antibacterial mechanisms of kojic acid and tea polyphenols from the gene level.The functional enrichment analysis by comparing kojic acid and tea polyphenols individually or synergistically against E.coli O157:H7 found that acid resistance systems in kojic acid were activated,and the cell membrane and genomic DNA were destructed in the cells,resulting in“oxygen starvation”.The oxidative stress response triggered by tea polyphenols inhibited both sulfur uptake and the synthesis of ATP,which affected the bacteria's life metabolic process.Interestingly,we found that kojic acid combined with tea polyphenols hindered the uptake of iron that played an essential role in the synthesis of DNA,respiration,tricarboxylic acid cycle.The results suggested that the iron uptake pathways may represent a novel approach for kojic acid and tea polyphenols synergistically against E.coli O157:H7 and provided a theoretical basis for bacterial pathogen control in the food industry.

Ground State of ^4-7H Considering Internal Collective Rotation

The g.s. of heavy and superheavy hydrogen isotopes, namely 4-7 H, are successfully examined by applying the Isomorphic Shell Model. Properties examined are binding energies and effective radii. The novelty of the present work is that, due to the small number of nucleons involved and the subsequently large deformation, an internal collective rotation appears which is inseparable from the usual internal motion even in the ground states of these nuclei, i.e., for such nuclei the adiabatic approximation is not valid. This extra degree of freedom leads to a reduction of binding energies, an increase of effective radii, and an increase of level widths.

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.

[(NH_2CH_2CH_2NH_3)_2W^(Ⅵ)O_2(NHC_6H_4NH)_2]_2(NH_2CH_2CH_2NH_2)·H_2O配合物的合成与晶体结构

Cis-dioxo-tungsten(Ⅵ ) complex, (NH2CH2CH2NH2)[(NH2CH2CH2NH3)2WⅥO2(NHC6H4NH)2]2·H2O is synthesized at room temperature by the reaction of sodium tungstate with o-phenylenediamine. The crystal structure of complex was determined by X-ray diffraction structural analysis. The results show that complex belongs to monoclinic system with space group P21 / c, a=0.712 8(2) nm, b=3.081 1(10) nm, c=0.981 9(3) nm, β=102.615(4)°, V=2.104 4(11) nm3, Z=2, μ=55.26 cm-1, F(000)=1 176. Compared the complex with its analogous biomimetic complexes of the cofactor of molybdoenzymes and tungstoenzymses, it is found that the variance of the coordination atoms and the metal ions center have no influence on the coordination feature, and exhibits distored octahedral coordination with cis-dioxo o-phenylenediamine. CCDC: 252834.

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。

电生H_2O_2协同电解絮凝法处理餐饮废水实验研究

采用电生H2O2协同电解絮凝法处理餐饮废水,研究了废水初始浓度、电解时间、电压、电极材料、pH等因素对降解餐饮废水的影响.结果表明,进水CODCr在1200mg/L以内、pH值为中性的餐饮废水,在10V电压、电磁搅拌、曝气条件下,电解15min后,COD去除率在80%以上.该法利用了铝阳极反应生成的絮凝剂Al(OH)3和阴极上电合成的H2O2对有机物的去除作用,同时阳极产生的H+与阴极产生的OH-中和又促进了两极的反应,使有机物降解更彻底.

The ROCK pathway inhibitor Y-27632 mitigates hypoxia and oxidative stress-induced injury to retinal Müller cells

Rho kinase （ROCK） was the first downstream Rho effector found to mediate RhoA-induced actin cytoskeletal changes through effects on myosin light chain phosphorylation. There is abundant evidence that the ROCK pathway participates in the pathogenesis of retinal endothelial injury and proliferative epiretinal membrane traction. In this study, we investigated the effect of the ROCK pathway inhibitor Y-27632 on retinal Müller cells subjected to hypoxia or oxidative stress. Müller cells were subjected to hypoxia or oxidative stress by exposure to CoCl2 or H2O2. After a 24-hour treatment with Y-27632, the 3-（4,5-dimethylthiazol-2-yl）-2,5-diphenyl tetrazolium bromide assay was used to assess the survival of Müller cells. Hoechst 33258 was used to detect apoptosis, while 2′,7′-dichlorodihydrofluorescein diacetate was used to measure reactive oxygen species generation. A transwell chamber system was used to examine the migration ability of Müller cells. Western blot assay was used to detect the expression levels of α-smooth muscle actin, glutamine synthetase and vimentin. After treatment with Y-27632, Müller cells subjected to hypoxia or oxidative stress exhibited a morphology similar to control cells. Y-27632 reduced apoptosis, α-smooth muscle actin expression and reactive oxygen species generation under oxidative stress, and it reduced cell migration under hypoxia. Y-27632 also upregulated glutamine synthetase expression under hypoxia but did not impact vimentin expression. These findings suggest that Y-27632 protects Müller cells against cellular injury caused by oxidative stress and hypoxia by inhibiting the ROCK pathway.

X…H_2O(X=Li,Na,K)非线性光学性质的从头算研究

在MP2水平上采用6-311G基组计算了van der Waals复合物X…H2O(X=Li,Na,K)的非线性光学性质(μα,β),讨论了基组效应和电子相关效应对计算结果的贡献．在MP2／6-311++G(2df,2pd)水平上计算得到的三个复合物分子X(X=Li,Na,K)…H2O的非线性光学性质．结果表明,三种复合物分子均具有巨大的一阶超极化率,其中最外层电子的弥散特性对一阶超极化率有很大的影响．

华南燕山期佛冈–南昆山花岗岩石成因:来自锆石微量元素、H_(2)O含量及Hf-O同位素的约束

华南地区发育大规模与稀有金属成矿相关的燕山期花岗岩,其岩石类型与成因存在诸多争议,厘清这些争议有助于理解华南地区的成矿作用。锆石是花岗岩中常见的副矿物,具有非常稳定的物理化学性质,不容易受后期地质作用影响,可以很好地保存其形成时母岩浆的地球化学信息,从而避免全岩地球化学分析的不足。本研究选取华南地区佛冈–南昆山花岗岩中的锆石进行LA-ICP-MS微量元素和Hf同位素研究,结合SIMS氧同位素和H_(2)O含量等数据,探讨佛冈岩体和南昆山岩体的岩石类型和成因。两个岩体的锆石都呈现LREE亏损、HREE富集、Eu负异常、Ce正异常,以及Zr/Hf>55、Eu/Eu~*>0.005、Hf含量低(<1.2%)等特点,明显不同于高分异I型花岗岩,指示母岩浆分异程度较低。同时,锆石的REE+Y与P含量之间的关系表明它们也不是S型花岗岩。佛冈岩体锆石较高的δ18O值(7.97‰~10.29‰)、富集的εHf(t)值(-13.6~-5.7)、较低的H_(2)O含量(核密度峰值317~412μg/g)以及较高的锆饱和温度(799~800℃)表明,佛冈花岗岩可能是源区有高比例沉积物加入的A型花岗岩。南昆山岩体也具有类似的、但变化范围更大的锆石δ18O值(6.34‰~11.11‰)、εHf(t)值(-11.1~1.1)和H_(2)O含量(297~1253μg/g)。锆石Hf-O同位素和H_(2)O含量分析结果显示,二者均具有壳幔混合的特点,其中南昆山花岗岩源区地幔物质加入比例更大。

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.

Non-isothermal kinetic analysis of thermal dehydration of La_2(CO_3)_3·3.4H_2O in air

The single phase La2（CO3）3·3.4H2 O was synthesized by hydrothermal method. The thermal decomposition and intermediates and final solid products of La2（CO3）3·3.4H2O from 30 to 1000 °C were characterized by XRD, FTIR and DTA-TG. The kinetics of dehydration of La2（CO3）3·3.4H2O in the temperature range of 30-366 °C was investigated under non-isothermal conditions. Flynn-Wall-Ozawa and Friedman isoconversion methods were used to calculate the activation energy and analyze the reaction steps; multivariate non-linear regression program was applied to determine the most probable mechanism and the kinetic parameters. The results show that the thermal dehydration of La2（CO3）3·3.4H2O is a kind of three-step competitive reaction, and controlled by an n-order initial reaction followed by n-order competitive reaction（FnFnFn model）. The activation energy matching with the most probable model is close to value obtained by Friedman method. The fitting curves match the original TG-DTG curves very well.

新型复合物Li…HF,Li…FH,Li…H_2O和Li…NH_3的一阶超极化率的从头算理论研究

在MP2/6-311++G(2df,2pd)水平上优化得到了几种小型碱金属—极性分子复合物的结构,利用有限场方法[HF,MP2,MP3,MP4(SDQ)]在15种基组上分别计算了它们的偶极矩(μ),极化率(α0),各向异性极化率(Δα)和一阶超极化率(β0).在MP4(SDQ)/6-311++G(2df,2pd)理论水平上,各复合物分子一阶超极化率分别为:Li…HF,β0=3957.575 a.u.;Li…FH,β0=12939.614 a.u.;Li…NH3,β0=34881.899a.u.;Li…H2O,β0=39820.410 a.u..而分子HF,NH3,H2O的一阶超极化率的值分别为1.224 a.u.,35.560 a.u.,20.130 a.u..结果表明,复合物分子中的额外电子对分子非线性光学性质有巨大的贡献.

宁芜矿集区多阶段火山作用岩浆源区的转变:来自侵入岩锆石Hf-O同位素特征的记录

宁芜玢岩型铁矿矿集区是中国东部重要的铁矿矿集区之一。宁芜矿集区在早白垩世135~126 Ma间连续发育了成分和源区相似的4组火山作用旋回,并伴随有两大类侵入岩发育:一类为辉石闪长玢岩-闪长玢岩,与玢岩型铁矿床的形成密切相关,主要发育于大王山火山旋回晚期(约131 Ma);另一类为花岗岩类侵入岩,形成于铁矿化之后,成岩时代与姑山和娘娘山火山旋回相近(130~126 Ma)。两类侵入岩源区的差异与联系目前尚未揭露。本次研究通过对两类侵入岩锆石年代学、Hf-O同位素特征的研究,区分了不同侵入岩源区差异。结果表明,与成矿母岩同旋回侵入岩锆石的δ^(18)O集中于6.0‰~6.5‰,εHf(t)集中于-6.0~-5.0;成矿后形成的花岗岩类侵入岩锆石的δ18O集中于7.0‰至8.0‰,ε_(Hf)(t)分布于-8.7~-1.2。结合前人研究,区内岩浆活动存在有富集地幔、太古代地壳和新元古代地壳3个岩浆源区,4个火山作用旋回的岩浆源区在130 Ma左右发生了改变。130 Ma之前的龙王山和大王山火山旋回的岩浆岩源区主要为受太古代地壳混染的富集地幔,而130 Ma之后的姑山和娘娘山火山作用旋回的岩浆岩源区主要为受新元古代地壳混染的富集地幔。多阶段火山作用中只有大王山旋回的闪长玢岩与玢岩型铁矿的形成有关。相比较其他火山旋回,大王山旋回具有更高的富集地幔组分以及更少的新元古代地壳的混染。因而,岩浆中较高比例的富集地幔含量是控制玢岩型铁矿形成的关键因素之一。

Carbon isotopes of graphite:Implications on fluid history

Stable carbon isotope geochemistry provides important information for the recognition of funda- mental isotope exchange processes related to the movement of carbon in the lithosphere and permits the elab- oration of models for the global carbon cycle. Carbon isotope ratios in fluid-deposited graphite are powerful tools for unravelling the ultimate origin of carbon （organic matter, mantle, or carbonates） and help to constrain the fluid history and the mechanisms involved in graphite deposition. Graphite precipitation in fluid-deposited occurrences results from C02- and/or CH4-bearing aqueous fluids. Fluid flow can be considered as both a closed （without replenishment of the fluid） or an open system （with renewal of the fluid by successive fluid batches）. In closed systems, carbon isotope systematics in graphite is mainly governed by Rayleigh precipi- tation and/or by changes in temperature affecting the fractionation factor between fluid and graphite. Such processes result in zoned graphite crystals or in successive graphite generations showing, in both cases, isotopic variation towards progressive 13C or 12C enrichment （depending upon the dominant carbon phase in the fluid, C02 or CH4, respectively）. In open systems, in which carbon is episodically introduced along the fracture systems, the carbon systematics is more complex and individual graphite crystals may display oscillatory zoning because of Rayleigh precipitation or heterogeneous variations of 613C values when mixing of fluids or changes in the composition of the fluids are the mechanisms responsible for graphite precipitation.