Differential response of radial growth and δ^(13)C in Qinghai spruce(Picea crassifolia) to climate change on the southern and northern slopes of the Qilian Mountains in Northwest China

Tree radial growth can have significantly differ-ent responses to climate change depending on the environ-ment.To elucidate the effects of climate on radial growth and stable carbon isotope(δ^(13)C)fractionation of Qing-hai spruce(Picea crassifolia),a widely distributed native conifer in northwestern China in different environments,we developed chronologies for tree-ring widths and δ^(13)C in trees on the southern and northern slopes of the Qilian Mountains,and analysed the relationship between these tree-ring variables and major climatic factors.Tree-ring widths were strongly influenced by climatic factors early in the growing season,and the radial growth in trees on the northern slopes was more sensitive to climate than in trees on the southern.Tree-ring δ^(13)C was more sensitive to climate than radial growth.δ^(13)C fractionation was mainly influenced by summer temperature and precipitation early in the growing season.Stomatal conductance more strongly limited stable carbon isotope fractionation in tree rings than photosynthetic rate did.The response between tree rings and climate in mountains gradually weakened as climate warmed.Changes in radial growth and stable carbon isotope fractionation of P.crassifolia in response to climate in the Qilian Mountains may be further complicated by continued climate change.

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.

Dynamics of soil organic carbon following land-use change:insights from stable C-isotope analysis in black soil of Northeast China

Intensive soil tillage is a significant factor in soil organic matter decline in cultivated soils. Both cultivation abandonment and foregoing tillage have been encouraged in the past 30 years to reduce greenhouse gas emissions and soil erosion. However, the dynamic processes of soil organic carbon (SOC) in areas of either continuous cultivation or abandonment remain unclear and inconsistent.Our aims were to assess and model the dynamic processes of SOC under continuous tillage and after cultivation abandonment in the black soil of Northeast China. Soil profiles were collected of cultivated or abandoned land with cultivation history of 0–100 years. An isotope mass balance equation was used to calculate the proportion of SOC derived from corn debris (C_4) and from natural vegetation (C_3) to deduce the dynamic process. Approximately 40% of SOC in the natural surface soil (0–10 cm) was eroded in the first 5 years of cultivation, increasing to about 75% within 40 years, before a slow recovery. C_4 above 30 cm soil depth increased by 4.5%–5% or 0.11–0.12 g·kg^(-1) on average per year under continuous cultivation, while it decreased by approximately 0.34% annually in the surface soil after cultivation abandonment.The increase in the percentage of C_4 was fitted to a linear equation with given intercepts in the upper 30 cm of soil in cultivated land. A significant relationship between the change of C_4 and time was found only in the surface soil after abandonment of cultivation. These results demonstrate the loss and accumulation of corn-derived SOC in surface black soil of Northeast China under continuous tillage or cultivation abandonment.

Nitrate isotope dynamics in the lower euphotic-upper mesopelagic zones of the western South China Sea

The dual isotopes(N and O)of nitrate were measured using a denitrifier bacterial method in the western South China Sea(WSCS)during September 2015 to elucidate key information during N transformation in the lower euphotic zone(LEZ)-upper mesopelagic zone(UMZ,down to 500 m in this study)continuum,which is a vital sub-environment for marine N cycle and sequestration of atmospheric CO_(2)as well.The N isotopic composition(δ^(15)N)of nitrate generally decreased from 500 m toward the base of the euphotic zone(∼100 m),reaching a value of∼4.6‰(vs.air N_(2))at the base of the LEZ,suggesting the imprint of remineralization(nitrification)of isotopically light N from atmospheric source.Theδ^(15)N andδ18O of nitrate only generally conform to a 1:1 line at 50 m and 75 m,suggesting that nitrate assimilation is a dominant process to shape nitrate isotope signature in this light-limited and relatively N-replete lower part of the euphotic zone.The fractionation factors of N and O isotopes during nitrate fractionation(15εASSIM,18εASSIM)using a steady-state model were estimated to be 4.0‰±0.3‰and 5.4‰±0.3‰,respectively.The occurrence of nitrification at the base of the LEZ and most of the UMZ is corroborated by the decoupling ofδ^(15)N and the oxygen isotopic composition(δ18O)of nitrate.Our results will provide insights for better understanding N cycle in the South China Sea from a perspective of present and past.

Hydrogeochemical and isotopic assessment of the origin of NO_(3)^(−)and N-NH_(3)contents in the aquifer located in a closed lacustrine volcano-sedimentary basin in the metropolitan area of Mexico City

To explain the presence and spatial distribution of NO_(3)^(−)and N-NH_(3)in the Aquifer of the Metropolitan Area of Mexico City(AMAMC),a hydrogeochemical and isotopic analysis using^(13)C DIC(as well as the stable isotopes^(18)O and^(2)H)in groundwater was conducted.This aquifer is located in an old closed lacustrine volcano-sedimentary basin;some wells hosted in the semi-confined zone contain high N-NH_(3)concentrations,while others present NO_(3)^(−)contents in the recharge zones(hosted in an oxidizing environment).In this study,a change in the isotopic signature(primarily in^(18)O and^(2)H)was observed from the recharge zones to the basin center in some of the wells with high NO_(3)^(−)concentrations,this behavior can be attributed to evaporation during the incorporation of recently infiltrated water.In addition,the results for^(13)C(along with ^(2) H)in wells with the highest N-NH_(3)concentrations exhibited an atypically broad range of values.Results indicated the occurrence of hydrogeochemical and/or biochemical processes in the aquifer(in an oxidizing or reducing environment),such as organic degradation,bacterial decomposition(primarily in the ancient Lake Texcoco and which acts as a natural sink for carbon,nitrogen,sulfur,and phosphorus),besides rock weathering and dissolution,which may be responsible for a very marked isotopic modification of the^(13)C(and,to a lesser extent,2 H).Methanotrophic bacterial activity and methanogenic activity may be related to N-NH_(3)removal processes by oxidation and residual water incorporation respectively,whereas the increase in the NO_(3)^(−)content in some wells is due to the recent contribution of poor-quality water due to contamination.

Geochemistry of the Aptian bituminous limestones in Gümuü?hane area,Eastern Black Sea region:new insight into paleogeography and paleoclimate conditions

Aptian is characterized by widespread deposition of organic-rich sediment.The Aptian bitumen limestone horizon,which is thin decimetre-thick sequences,locally crops out in the Kircaova area,Eastern Black Sea Region(Eastern Pontides).They are well correlated with Aptian bitumen limestone in the other Tethys Reams.They are proposed as episodes of increased organic matter.However,background factors controlling organic matter enrichment are poorly known.In this study,we present new inorganic geochemistry,including trace elements,rare earth elements(REE),redox-sensitive elements(RSE),stable-isotopes(δ~(18)O andδ~(13)C),and total organic carbon(TOC).We integrated new geochemical data with existing stratigraphy,paleontology,and organic chemistry data to provide new insight into the depositional environment and paleoclimate conditions during Aptian.The lacustrine bitumen limestone(LBL)samples have variedδ~(13)C(ave.-1.45‰)andδ~(18)O(ave.-4.50‰).They possess distinct REE patterns,with an average of REE(ave.14.45 ppm)and Y/Ho(ave.35)ratios.In addition,they have variable Nd/YbN(0.28-0.81;ave.0.56)and Ce/Ce*(0.68-0.97;ave.0.86),and relatively high Eu^(*)/Eu(1.23-1.53;ave.1.35).They display seawater signatures with reduced oxygen conditions.The enrichment in RSE(Mo,Cu,Ni,and Zn)and the low Mo/TOC(0.70-3.69;ave.2.41)support a certain degree of water restriction.The high Sr/Ba,Sr/Cu,Ga/Rb,and K/Al records of the LBL facies suggest hot house climatic conditions.The sedimentary environment was probably an isolated basin that is transformed from the marine basin.In addition to depositional conditions,the regional parameters such as the climate,increased run-off period,nutrient levels,alkalinity level,and dominant carbonate producers favored the enrichment in organic matter of LBL facies.Thus,extreme greenhouse palaeoclimate conditions have an important role in organic matter enrichment in the isolated basin.Our results are conformable with the published data from marine,semi-restricted basin,and lacustrine settings in the different parts of the Tethys margin.Thus,this approach provides the first insight into the Aptian greenhouse paleo-climate conditions of the Eastern Black Sea Region,NE Turkey.

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.

Geology and Isotope Geochemistry of the Yinchanggou-Qiluogou Pb-Zn Deposit,Sichuan Province,Southwest China

The Yinchanggou-Qiluogou Pb-Zn deposit,located in the western Yangtze Block,southwest China,is hosted by the Upper Sinian Dengying Formation dolostone.Ore bodies occur in the Qiluogou anticline and the NS-and NNW-trending faults.Sulfide ores mainly consist of sphalerite,pyrite,galena and calcite,with subordinate dolomite and quartz.Seventeen ore bodies have been discovered to date and they have a combined 1.0 million tons of sulfide ores with average grades of 2.27wt%Zn and 6.89wt%Pb.The δD（H2O-SMOW） and δ18O（H2O-SMOW） values of fluid inclusions in quartz and calcite samples range from-68.9‰ to-48.7‰ and 7.3‰ to 15.9‰,respectively,suggesting that H2O in the hydrothermal fluids sourced from metamorphic water.Calcite samples have δ13C（PDB） values ranging from-6.2‰ to-4.1‰ and δ18O（SMOW） values ranging from 15.1‰ to 17.4‰,indicating C and O in the hydrothermal fluids likely derived from a mixed source of metamorphic fluids and the host carbonates.The δ34S（CDT） values of sulfide minerals range from 5.5‰ to 20.3‰,suggesting that thermal chemical reduction of sulfate minerals in evaporates were the most probable source of S in the hydrothermal fluids.The 206Pb/204Pb,207Pb/204Pb and 208Pb/204Pb ratios of sulfide minerals fall in the range of 18.11 to 18.40,15.66 to 15.76 and 38.25 to 38.88,respectively.The Pb isotopic data of the studied deposit plot near the upper crust Pb evolution curve and overlap with the age-corrected Proterozoic basement rocks and the Upper Sinian Dengying Formation hosting dolostone.This indicates that the Pb originated from a mixed source of the basement metamorphic rocks and the ore-hosting carbonate rocks.The ore geology and C-H-O-S-Pb isotopic data suggest that the YinchanggouQiluogou deposit is an unusual carbonate-hosted,strata-bound and epigenetic deposit that derived ore-forming materials from a mixed source of the underlying Porterozoic basements and the Sinian hosting carbonates.

High resolution oxygen isotope and grayscale records of a medieval fossil giant clam(Tridacna gigas) in the South China Sea: physiological and paleoclimatic implications

Mollusks are well known for their detailed recording of paleoenvironmental and paleoclimatic changes in their carbonate shells. In this study, we constructed 18-year blue color intensity and oxygen isotope profiles of a14C dated （AD 990±40） fossil giant clam,Tridacna gigas, from Shidao Island, South China Sea. Theδ18O profile of theT. gigas specimen displayed regular annual cycles and was probably controlled by seasonal variations of the climatic parameters. The blue color intensity profile showed good agreement with theδ18O series, and both had 18 clear annual cycles in accordance with the 18 visually identified annual growth bands. The annual shell growth rate determined from the blue color intensity and oxygen isotope profiles indicated that the annual shell increment of theTridacna specimen was stable after the onset of sexual ma-turity. Spectral analysis of theδ18O and blue color intensity time series suggested that the El Ni？o-Southern Oscillation （ENSO） period observed in the instrumental temperature and precipitation records of the South China Sea during the past 50 years also existed in medieval times. Our results showed that fossil giant clams could provide a good archive of historical intra-seasonal to decadal climate variations.

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.

Evolution of the 3.65-2.58 Ga Mairi Gneiss Complex,Brazil:Implications for growth of the continental crust in the São Francisco Craton

The composition and formation of the Earth’s primitive continental crust and mantle differentiation are key issues to understand and reconstruct the geodynamic terrestrial evolution,especially during the Archean.However,the scarcity of exposure to these rocks,the complexity of lithological relationships,and the high degree of superimposed deformation,especially with long-lived magmatism,make it difficult to study ancient rocks.Despite this complexity,exposures of the Archean Mairi Gneiss Complex basement unit in the São Francisco Craton offer important information about the evolution of South America’s primitive crust.Therefore,here we present field relationships,LA-ICP-SFMS zircon U-Pb ages,and LA-ICP-MCMS Lu-Hf isotope data for the recently identified Eoarchean to Neoarchean gneisses of the Mairi Complex.The Complex is composed of massive and banded gneisses with mafic members ranging from dioritic to tonalitic,and felsic members ranging from TTG(Tonalite-Trondhjemite-Granodiorite)to granitic composition.Our new data point to several magmatic episodes in the formation of the Mairi Gneiss Complex:Eoarchean(ca.3.65–3.60 Ga),early Paleoarchean(ca.3.55–3.52 Ga),middle-late Paleoarchean(ca.3.49–3.33 Ga)and Neoarchean(ca.2.74–2.58 Ga),with no records of Mesoarchean rocks.Lu-Hf data unveiled a progressive evolution of mantle differentiation and crustal recycling over time.In the Eoarchean,rocks are probably formed by the interaction between the pre-existing crust and juvenile contribution from chondritic to weakly depleted mantle sources,whereas mantle depletion played a role in the Paleoarchean,followed by greater differentiation of the crust with thickening and recycling in the middle–late Paleoarchean.A different stage of crustal growth and recycling dominated the Neoarchean,probably owing to the thickening of the continental crust by collision,continental arc growth,and mantle differentiation.

Fourth-Order Compact Formulation for the Resolution of Heat Transfer in Natural Convection of Water-Cu Nanofluid in a Square Cavity with a Sinusoidal Boundary Thermal Condition

In the present work, we numerically study the laminar natural convection of a nanofluid confined in a square cavity. The vertical walls are assumed to be insulated, non-conducting, and impermeable to mass transfer. The horizontal walls are differentially heated, and the low is maintained at hot condition (sinusoidal) when the high one is cold. The objective of this work is to develop a new height accurate method for solving heat transfer equations. The new method is a Fourth Order Compact (F.O.C). This work aims to show the interest of the method and understand the effect of the presence of nanofluids in closed square systems on the natural convection mechanism. The numerical simulations are performed for Prandtl number ( ), the Rayleigh numbers varying between and for different volume fractions varies between 0% and 10% for the nanofluid (water + Cu).

Copper-Catalyzed C-C(O)C Bond Cleavage of Monoalkylated β-Diketone: Synthesis of α,β-Unsaturated Ketones

A new and simple route for the synthesis of α,β-unsaturated ketones via cleavage of the C-C(O)C single bond of monoalkylated β-diketone has been described. The reaction was catalyzed by copper, a cheap transition metal in a weakly basic medium (K3PO4) at room temperature. To carry out this study, we first had to synthesize the monoalkylated β-diketones 1. Afterwards, α,β-unsaturated ketones 2 were obtained with high yields around 80%. Finally, all the products were characterized by 1H NMR, 13C NMR, and HRMS spectra. .

Low Temperature Heat Capacities and Thermodynamic Properties of Zinc L-Threonate Zn(C_4H_7O_5)_2(s) by Adiabatic Calorimetry

Low-temperature heat capacities of the solid compound Zn（C4H7O5）2（s） were measured in a temperature range from 78 to 374 K, with an automated adiabatic calorimeter. A solid-to-solid phase transition occurred in the temperature range of 295？322 K. The peak temperature, the enthalpy, and entropy of the phase transition were determined to be （316.269±1.039） K, （11.194±0.335） kJ？mol-1, and （35.391±0.654） J？K-1？mol-1, respectively. The experimental values of the molar heat capacities in the temperature regions of 78？295 K and 322？374 K were fitted to two polynomial equations of heat capacities（Cp,m） with reduced temperatures（X） and [X = f（T）], with the help of the least squares method, respectively. The smoothed molar heat capacities and thermodynamic functions of the compound, relative to that of the standard reference temperature 293.15 K, were calculated on the basis of the fitted polynomials and tabulated with an interval of 5 K. In addition, the possible mechanism of thermal decomposition of the compound was inferred by the result of TG-DTG analysis.

Factors Controlling Precipitation of Barite and Witherite and Genesis of the Ankang-Xunyang Barium Deposits,Shaanxi,China

The barium deposits in Ankang and Xunyang counties,Shaanxi Province,China,occur in the northernmost part of the world-class barium metallogenic belt in south Qinling.The deposits are hosted by the Lower Silurian carbonaceous siliceous rocks,with a unique combination of barite and witherite.The homogenization temperatures of fluid inclusions in the barite are mainly concentrated between 135 and 155 ℃,whereas those from the witherite have two peaks of 165-175 ℃,and 215-225℃,respectively.Laser Raman analysis of fluid inclusions indicates that the vapor phase of fluid inclusions in barite is dominated by H_2O,although some contains N_2,H_2S,and CH_4.The compositions of the vapor and liquid phases of fluid inclusions in witherite can be divided into two end-members,one dominated by H_2O without other volatiles,and the other containing CH_4,C_2H_6,C_3H_8,C_2H_4,and C_6H_6 in addition to H_2O.CO_2,H_2S,and some CH_4 are interpreted as products of chemical reactions during mineralization.Organic gases（CH_4,C_2H_6,C_3H_8,C_2H_4,and C_6H_6） in the fluids were critical in the formation of barium sulfate versus carbonate.The δ^（34）S values of barite range from 38.26‰ to54.23‰（CDT）,the δ^（34）S values of sulfides coexisting with barium minerals vary from 22.44‰ to25.11‰（CDT）,and those in the wall rock from 11.60‰ to 19.06‰（CDT）.We propose that the SO_4^（2-）generally experienced bacterial sulfate reduction in seawater before mineralization,and some SO_4^（2-）also experienced thermochemical sulfate reduction in hydrothermal system during mineralization.The δ^（13）C values of witherite range from-27.30‰ to-11.80‰（PDB）,suggesting that carbon was sourced from organic substances（like CH_4,C_2H_4,and C_2H_6）.The formation of witherite was possibly associated with thermochemical sulfate reduction,which caused the consumption of the organic gases and SO_4^（2-） in the hydrothermal solutions,consequently inhibiting barite formation.The important conditions for forming witherite include high fluid temperatures,high Ba^（2＋） concentrations,CO_2 in the fluids,low HS^- concentrations,and the subsequent rapid diffusion of H_2S during thermochemical sulfate reduction of the fluids.

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.

C-H-O Stable Isotope, Elements and Fluid Geochemistry of Uraniferous Leucogranites in Gaudeanmus Area, Southern Central Zone, Damara Orogen, Namibia

This paper focuses on the effect of the later hydrotherm on uraniferous leucogranites and the stages of uranium mineralization. Here, we review C-H-O stable isotope, elements and fluid geochemistry of uraniferous leucogranites in Gaudeanmus, Namibia. The results show that there is significant increasing amount of rare earth element from non-mineralized to uraniferous leucogra-nites, indicating the synchronization of REE enrichment and uranium mineralization. Uranium enrichment may have close relations with Pb, Th, Co, Ni, REE in this region, so REE and U evidently exist homology. There are at least two stages of uranium mineralization by later hydrothermal alteration: firstly, due to magnatic residual high temperature and low salinity fluid, the temperature of main metallogenetic epoch ranges from 470°C to 530°C, salinity ranges from 3.55% to 9.60% NaCleq, and C, H, O stable isotope is -23‰ - -13.6‰, -53.3‰ - -46.4‰, 7.71‰ - 8.81‰, respectively. Secondly, due to superim-posed hydrothermal fluid, the temperature, salinity, and C, H, O stable isotope is 150°C - 220°C, 4.65% - 19.05% NaCleq, -20.3‰ -?-3.7‰, -64.7‰ - -53.6‰, 1.49‰ - 1.99‰, respectively. The fluid for reformation is derived from postmagmatic fluid, mixed with a number of meteoric water.

DFT Studies on Thermal Stabilities,Electronic Structures,and ^(13)C Chemical Shifts of C_(24)O_2 Based on Fullerene C_(24)(D_6)

Quantum chemical calculations on some possible equilibrium geometries of C24O2 isomers derived from C24 （D6） and C24O have been performed using density functional theory （DFT） method. The geometric and electronic structures as well as the relative energies and thermal stabilities of various C24O2 isomers at the ground state have been calculated at the B3LYP/6-31G（d） level of theory. And the 1,4,2,5-C24O2 isomer was found to be the most stable geometry where two oxygen atoms were added to the longest carbon-carbon bonds in the same pentagon from a thermodynamic point of view. Based on the optimized neutral geometries, the vertical ionization potential and vertical electron affinity have been obtained. Meanwhile, the vibrational frequencies, IR spectrum, and 13C chemical shifts of various C24O2 isomers have been calculated and analyzed.

Pretreatment of Alumina and Its Influence on the Properties of Co/Alumina Catalysts for Fischer-Tropsch Synthesis

16.6%Co/γ-Al2O3 catalysts prepared by incipient wetness impregnation method were used for Fischer-Tropsch synthesis. The support was pre-treated with different concentration of NH4NO3 aqueous solution. The effect of support pre-treatment on the properties of support and performance of supportedcobalt-based catalysts was investigated. To treat the support with NH4NO3 aqueous solution enlarged the pore of γ-Al2O3, decreased the impurity Na2O content, and weakened the surface acidity of γ-Al2O3. The change in the properties of the support decreased the interaction between cobalt species and support, enhanced the CO hydrogenation rate and the C5＋ selectivity. For all catalysts, increasing the reaction temperature increased the CO hydrogenation rate or the CO conversion, slightly decreased the total hydrocarbon selectivity, and favored the formation of methane and light hydrocarbons, while the chain growth probability decreased. For 16.6%Co/γ-Al2O3 catalysts, prepared with the support treated with 100 g/L NH4NO3 aqueous solution, the CO conversion, the CH4 selectivity, and the C5＋ selectivity were 83.13%, 6.86% and 82.75% respectively, and the chain growth probability was 0.83 under the condition of 493 K, 1.5 MPa, 500 h-1 and the molar ratio of H2 to CO being 2.0 in feed.

Density Functional Study of the C Atom Adsorption on the α-Fe_2O_3 (001) Surface

The adsorption of C atoms on the α-Fe2O3（001） surface was studied based on density function theory（DFT） ,in which the exchange-correlation potential was chosen as the PBE（Perdew,Burke and Ernzerhof） generalized gradient approximation（GGA） with a plane wave basis set. Upon the optimization on different adsorption sites with coverage of 1/20 and 1/5 ML,it was found that the adsorption of C atoms on the α-Fe2O3（001） surface was chemical adsorption. The coverage can affect the adsorption behavior greatly. Under low coverage,the most stable adsorption geometry lied on the bridged site with the adsorption energy of about 3.22 eV; however,under high coverage,it located at the top site with the energy change of 8.79 eV. Strong chemical reaction has occurred between the C and O atoms at this site. The density of states and population analysis showed that the s,p orbitals of C and p orbital of O give the most contribution to the adsorption bonding. During the adsorption process,O atom shares the electrons with C,and C can only affect the outermost and subsurface layers of α-Fe2O3; the third layer can not be affected obviously.