Evolution of Carbon Isotope Composition in Potential Global Stratotype Section and Point at Luoyixi, South China, for the Base of the Unnamed Global Seventh Stage of Cambrian System

This work deals with the evolution of carbon isotope composition in the Luoyixi （罗依溪） Section, a candidate of the Global Standard Stratotype-section and Point （GSSP）, defining the base of the as-yet-undefined seventh stage of Cambrian System at the first appearance of the cosmopolitan agnostoid Lejopyge iaevigata. This level is favored in a vote of International Subcommission on Cambrian Stratigraphy （ISCS） as the biohorizon for defining the base of a global stage. Two hundred and sixty-four samples for carbon and oxygen isotope analysis have been collected from the carbonate successions at an interval of 0.25 to 0.5 m in this section. Results of the carbon isotope data exhibit a remarkable disciplinarian trend. The pattern of the carbon isotope evolution is gently undulant with a relatively long period during the underlying Drumian Stage, and then the values of δ13C fluctuate sharply with a short period in provisional seventh stage. The onset of sharp fluctuation in the δ13C values begins at the proposed GSSP level, defining the base of the global seventh stage, where δ13C values change from a gentle trend to a sharp trend. Distinct covariant-relationships among δ13C,δ18O, and sea level fluctuations suggest that a warming change in paleoclimate took place during the early global seventh stage, which led to a positive shift in δ13C values.

Iron Isotope Compositions of Natural River and Lake Samples in the Karst Area,Guizhou Province,Southwest China

To better understand the Fe isotope characteristics of natural samples in the Karst area,the Fe isotope compositions of riverine suspended particulates,lake suspended particulates,lake sediments,porewaters,phytoplanktons,and aerosols in the watersheds of Lake Aha（a mineralized water system）and Lake Hongfeng（a mesotrophic water system）,which are located in the Karst area, southwest China,were investigated.The studied samples displayed a variable range betweenδ^（56）Fe=-2.03‰and 0.36‰.Aerosols and phytoplanktons have similar or slightly heavier Fe isotope compositions relative to the average of igneous rocks.Fe isotope compositions of riverine Suspended Particulate Matter（SPM）were mainly affected by the types of tributaries.Suspended particulates collected from tributaries seriously contaminated with coal mine drainages displayed negativeδ^（56）Fe values（-0.89‰to-0.31‰）during summer,and there were significant increases ofδ^（56）Fe values in winter,except AR2,which was polluted with both coal mine drainage and sewage effluent. Characteristics of lakes have important influences on Fe isotope compositions of suspended particulates,lake sediments,and porewaters.The epilimnetic particulate Fe of Lake Hongfeng hadδ^（56）Fe=-0.04‰to 0.13‰,while lighter Fe isotope compositions were measured for particulate Fe from Lake Aha,ranging from-0.42‰to-0.09‰.Sediments collected from Hou Wu（HW）station of Lake Hongfeng have an averageδ^（56）Fe value of 0.09‰and their corresponding porewaters have lighter Fe isotope compositions,ranging from-0.57‰to-0.31‰;no significant variations have been observed. For the Liang Jiang Kou（LJK）station of Lake Aha,the content of reactive Fe and the concentration of sulfate were all high.Due to the reactive Fe recycling,including dissimilatory Fe reduction,adsorption, and Fe-sulfide formation,porewaters sampled near the sediment surface have been found to have aδ^（56）Fe value as low as-2.03‰and an increase up to 0.12‰,with a burial depth of 10 cm.In contrast,an opposite variation trend was found for LJK sediments.Sediments sampled at 1-cm depth had a value ofδ^（56）Fe=-0.59‰and decrease as low as-1.75‰with burial depth.This investigation demonstrated that significant Fe isotope fractionations occur in surface environments.Fe isotope compositions of particulate Fe were seriously affected by Fe sources,and Fe biogeochemical recycling has an important influence on Fe isotope fractionations in lake sediments,especially when there are significant amounts of reactive Fe and sulfate.

Sources of organic matter and paleo-environmental implications inferred from carbon isotope compositions of lacustrine sediments at Inexpressible Island, Ross Sea, Antarctica

The carbon isotopic composition of organic matter （δ^13Corg） was determined in two sediment cores （IIL1 and IIL9） recovered from Inexpressible Island, Ross Sea, Antarctica, and analyzed to identify the sources of that organic matter. The δ^13Corg values of sediments of IIL9 were found to vary between -14.6‰ and -11.6‰, with a mean of-13.4‰ （n=48）. These values were significantly higher than those of IIL1 sediments which varied between -23.2‰ and -20.4‰, with a mean of-21.8%o （n=55）. The variation in δ^13Corg values in these two sediment cores indicate different sources of organic matter, The relatively high 6~3Corg values in IIL9 are in accordance with a source from algae, while the low δ^13Corg values in IIL1 evince significant influence from penguin guano with algae as the secondary source. Compared with the reference data from other high-latitude lake sediments and plants, the δ^13Corg values in IIL9 were extremely high, a result likely related to intense competition for CO2 assimilation among algal species during the growing season in this relatively shallow pond. These results indicate that sedimentary δ^13Corg is a reliable proxy for paleo-primary productivity in ponds at Inexpressible Island.

Sulphur and Lead Isotope Compositions of the Dajiangping Deposit in Western Guangdong Province

The Dajiangping pyrite deposit located in the middle sector of the Yunkai uplift in western Guangdong is a stratiform sulphide deposit occurring in Sinian marine clastic and fine clastic rocks. The formation of the deposit was related to submarine exhalation and hot brine deposition. A part of it was reformed by late-stage hydrothermal solution. The δ34S values of pyrite vary from - 25.55‰ to +21.07‰, which are inversely proportional to the content of organic carbon in ore and pyrite. Passing from striped fine-grained pyrite ore to massive coarse-grained pyrite ore, i.e. from south to north, the sulphur isotopic composition changes from the light sulphur-enriched one to the heavy sulphur-enriched one. The lead isotopic composition of striped ore is consistent with that of the country rocks of orebodies and the lead is radiogenic lead derived from the upper crust. The lead isotopic composition of massive ore is relatively homogeneous and its 206Pb/204Pb, 207Pb/204Pb and 208Pb/204Pb ratios are a bit lower than those of striped ore;the lead result from mixing of synsedimentary ore lead with that derived from basement migmatlte brought by late-stage hydrothermal solutions.

Correlations Between Foliar Stable Carbon Isotope Composition and Environmental Factors in Desert Plant Reaumuria soongorica （Pall.） Maxim.

Leaves of 407 individuals of Reaumuria soongorica （Pall.） Maxim. collected from the major distribution areas were measured to investigate the distribution characteristics of the stable carbon isotope in this desert plant, as well as correlations between δ^13C values and environmental factors. Results showed that δ^13C values in R. soongorica ranged from -22.77‰ to -29.85‰ and that the mean δ^13C value （-26.52‰） was higher than a previously reported δ^13C value for a different desert ecosystem. This indicates that R. soongorica belongs to the C3 photosynthetic pathway and has higher water use efficiency than other species. The correlations between δ^13C values and environmental factors demonstrated that the foliar δ^13C values in R. soongorica increased significantly with decreasing mean annual precipitation and mean relative humidity, and decreased with decreasing duration of sunshine and evaporation. The spatial distribution trend of δ^13C values in R. soongorica was not obvious and there was no significant correlation between the δ^13C values and mean annual temperature. We conclude that different distribution trends in δ^13C values for R. soongorica were likely caused by stomatal limitation rather than by nutrient-related changes in photosynthetic efficiency and that precipitation played an important role in the wide distribution range of R. soongorica. This pattern of δ^13C values for R. soongorica reinforced that it is a super-xerophil in terms of its adaptive strategies to a desert environment.

Integrating stable isotopes and factor analysis to delineate the groundwater provenance and pollution sources in the northwestern part of the Amman-Al Zarqa Basin, Jordan

Globally,groundwater contamination by nitrate is one of the most widespread environmental problems,particularly in arid and semiarid areas,which are characterized by low amounts of rainfall and groundwater recharge.The stable isotope composition of groundwater(δ2H-H2O andδ18O-H2O)and dissolved nitrate(δ15N-NO3–andδ18O-NO3–)and factor analysis(FA)were applied to explore groundwater provenance,pollution,and chemistry evolution in the northwestern part of the Amman-Al Zarqa Basin,Jordan.In this study,we collected 23 samples from the Lower Ajloun aquifer in 2021,including 1 sample from a groundwater well and 22 samples from springs.These samples were tested for electrical conductivity,total dissolved solids,pH,temperature,dissolved oxygen,the concentration of major ions(Ca2+,Mg2+,Na+,K+,HCO3–,Cl–,SO42–,and NO3–),and the stable isotope composition of groundwater and dissolved nitrate.The results revealed that groundwater in the study area is mainly Ca–Mg–HCO3 type and can be classified as fresh water,hard water,and very hard water.The range and average concentration of NO3–were 3.5–230.8 and 50.9 mg/L,respectively.Approximately 33%of the sampling points showed NO3–levels above the maximum allowable concentration of 50.0 mg/L set by the World Health Organization(WHO)guidelines for drinking water quality.The values ofδ18O-H2O andδ2H-H2O showed that groundwater in the study area is part of the current water cycle,originating in the Mediterranean Sea,with significant evaporation,orographic,and amount effects.The values of the stable isotope composition of NO3–corresponded toδ15N-NO3–andδ18O-NO3–values produced by the nitrification process of manure or septic waste and soil NH4+.The FA performed on the hydrochemical parameters and isotope data resulted in three main factors,with Factor 1,Factor 2,and Factor 3,accounting for 50%,21%,and 11%of the total variance,respectively.Factor 1 was considered human-induced factor,named"pollution factor",whereas Factor 2,named"conservative fingerprint factor",and Factor 3,named"hardness factor",were considered natural factors.This study will help local researchers manage groundwater sustainably in the study area and other similar arid and semiarid areas in the world.

Carbon isotope composition and comparison of Lower Triassic marine carbonate rocks from Southern Longmenxia section in Guang＇an, Sichuan Basin

The Early Triassic was a period of ecological restoration for the earth's system after the end-Permian mass extinction.Geochemical records linked to the variations in marine ecosystems during this period have attracted the interest of geologists for many years.Based on petrographic analysis of samples and evaluations of their reliability as proxies for original seawater,this study investigated the carbon and oxygen isotopic compositions of 350 carbonate rock samples from the Lower Triassic(and adjacent strata)in the southern Longmenxia section of Guang'an,eastern Sichuan Basin.The results indicate that the Triassic carbonate rocks from the southern Longmenxia section favorably preserved the original seawater'sδ^(13)C signal.Furthermore,carbon and oxygen isotopic compositions are found to be poorly correlated,with a determination coefficient as low as 0.0205 and only 44 rock samples show results of Mn/Sr>2 and/orδ^(18)0<-6.5‰.The complete carbon isotopic curve for the Lower Triassic is established using the data from the remaining 306 samples with Mn/Sr<2 and/orδ^(18)O>-6.5‰.This curve presents favorable comparability on a global scale,specifically in theδ^(13)C minima near the Permian-Triassic boundary,at the top of the Jia1 and within the the Jia3,as well as in theδ^(13)C maxima at the tops of the Ye1 and Ye4,at the base of the Jia2 and at the top of the Ye3.The peaks and troughs corresponding to these maxima and minima all reflect global signals.By comparing these results to previous research on coeval carbon isotopic curves established within the chronostratigraphic framework,the ages of these critical evolution points are determined.The results show that the Ye1 roughly corresponds to the Griesbachian substage;the Ye2 through Ye4 correspond to the Dienerian substage;Jial corresponds to the Smithian substage;from the Jia2 to the lower part of the Jia4 correspond to the Spathian substage;and the middle and upper parts of the Jia4 belongs to the Aegean Substage of the Middle Triassic.Around the boundary between the Jial and Jia2(which represents the Smithian-Spathian boundary(SSB)),the value ofδ^(13)C increases rapidly from-0.911‰to 3.679‰.The span during which the seawater's carbon isotope experiences this drastic change may be less than36 kyr.The oxygen isotope,which is more sensitive to sedimentary environmental changes,exhibits changes prior to the carbon isotope near the SSB,indicating a significant increase in the salinity of the seawater before a sharp rise in the carbon isotope;this event leads to the formation of evaporites and dolomites.

Carbon and Oxygen Isotopic Composition of Surface-Sediment Carbonate in Bosten Lake (Xinjiang,China) and its Controlling Factors

Bosten Lake is a mid-latitude lake with water mainly supplied by melting ice and snow in the Tianshan Mountains. The depositional environment of the lake is spatially not uniform due to the proximity of the major inlet and the single outlet in the western part of the lake. The analytical results show that the carbon and oxygen isotopic composition of recent lake sediments is related to this specific lacustrine depositional environment and to the resulting carbonate mineralogy. In the southwestern lake region between the Kaidu River inlet and the Kongqi River outlet, carbon isotope composition （δ^13C） values of the carbonate sediment （-1‰ to -2‰） have no relation to the oxygen isotope composition of the carbonate （δ^18O） values （-7‰ to -8‰）, with both isotopes showing a low variability. The carbonate content is low （〈20%）. Carbonate minerals analyzed by X-ray diffraction are mainly composed of calcite, while aragonite was not recorded. The salinity of the lake water is low in the estuary region as a result of the Kaidu River inflow. In comparison, the carbon and oxygen isotope values are higher in the middle and eastern parts of the lake, with δ^13C values between approximately ＋0.5‰ and ＋3‰, and δ^18O values between -1‰ and -5‰. There is a moderate correlation between the stable oxygen and carbon isotopes, with a coefficient of correlation r of approximately 0.63. This implies that the lake water has a relatively short residence time. Carbonate minerals constitute calcite and aragonite in the middle and eastern region of the lake. Aragonite and Mg-calcite are formed at higher lake water salinity and temperatures, and larger evaporation effects. More saline lake water in the middle and eastern region of the lake and the enhanced isotopic equilibrium between water and atmospheric CO2 cause the correlating carbon and oxygen isotope values determined for aragonite and Mg-calcite. Evaporation and biological processes are the main reasons for the salinity and carbonate mineralogy influence of the surface-sediment carbonate in Bosten Lake. The lake water residence time and the CO2 exchange between the atmosphere and the water body control the carbon and oxygen isotope composition of the carbonate sediment. In addition, organic matter pollution and decomposition result in the abnormally low carbon isotope values of the lake surface-sediment carbonate.

Evaluation of boron isotopes in halite as an indicator of the salinity of Qarhan paleolake water in the eastern Qaidam Basin, western China

In this study, nineteen brine samples from the Qarhan Salt Lake(QSL) in western China were collected and analyzed for boron(B) and chlorine(Cl) concentrations, total dissolved solids(TDS), pH values and stable B isotopic compositions. The B concentrations and δ^(11) B values of brines in the QSL range from 51.6 mg/L to138.4 mg/L, and from +9.32& to +13.08&, respectively. By comparison of B concentrations and TDS of brines in QSL with evaporation paths of brackish water, we found that B enrichment of brines primarily results from strong evaporation and concentration of Qarhan lake water. Combining with comparisons of B concentrations, TDS, p H values and δ^(11) B values of brines, previously elemental ratios(K/Cl, Mg/Cl, Ca/Cl, B/Cl) and δ^(11) B values of halite from a sediment core(ISL1 A), we observe good correlations between B concentrations and TDS, TDS and pH values, pH and δ^(11) B values of brines, which demonstrate that higher B concentrations and more positive δ^(11) B values of halite indicate higher salinity of the Qarhan paleolake water as well as drier paleoclimatic conditions. Based on this interpretation of the δ^(11) B values of halite in core ISL1 A, higher salinity of the Qarhan paleolake occurred during two intervals, around 46-34 ka and26-9 ka, which are almost coincident with the upper and lower halite-dominated salt layers in core ISL1 A,drier climate phases documented from the δ^(18) O record of carbonate in core ISL1 A and the paleomoisture record in monsoonal central Asia, and a higher solar insolation at 30°N. These results demonstrate that the δ^(11) B values of halite in the arid Qaidam Basin could be regarded as a new proxy for reconstructing the salinity record of paleolake water as well as paleoclimate conditions.

The late Early-Paleozoic granitic magmatism in Northwestern Fujian, China: constraints on intraplate orogeny in the South China block

The Early Paleozoic tectono-thermal event was a significant orogenic activity during the Phanerozoic era,which had a profound impact on the early crust of the South China Block(SCB) and established the foundation for later tectonic activity.The Wuyi-Yunkai orogenic belt in Southeastern China was extensively exposed to Early Paleozoic magmatism,the genetic mechanism of which remains controversial.To shed light on this issue,detailed petrological,geochemical,and zircon U-Pb-Hf isotopic studies were carried out on two granitoids,namely the Yuntongshan pluton and the Gaoqiao pluton,identified in the central Wuyishan.Zircon U-Pb chronology of the Yuntongshan and Gaoqiao bodies yielded ages of437±4 Ma(MSWD=2.2) and 404±2 Ma(MSWD=12),respectively,indicating that they were emplaced during the Early Silurian and Early Devonian periods.These granitoids are primarily composed of biotite-granite and biotite-monzonitic-granites,with high concentrations of S_(i)O_(2)(73.59-75.91 wt%),K_(2)O+Na_(2)O(8.31-8.73wt%),and low contents of MgO,CaO,Cr,Ni.They are classified as high-K calc-alkaline and weakly metaluminous-strongly peraluminous S-type granites.These granitoids are enriched in light rare earth elements(LREEs) and large ion lithophile elements(LILEs) and depleted in heavy rare earth elements(HREEs) and high field strength elements(HFSEs) with arc affinity.The εHf(t) values of-3.3 to-15.4 with two-stage Hf model ages ranging from 2829 to 1644 Ma,combined with the presence of Neoproterozoic inherited zircons,suggest that the primary magma of these granitoids was derived from the partial melting of Neoproterozoic crust with a Paleoproterozoic crustal model age.These findings,combined with the spatio-temporal distribution of regional magmatism,reveal that the late Early-Paleozoic granitoids formed in the intraplate orogenic background originating from the subduction of the proto-Tethys Ocean and proto-Pacific Ocean around the margin of the east Gondwana supercontinent.

Temporal and spatial variations of carbon isotope signature reveal substantial contribution of bracts and internode assimilates to grain filling of japonica rice

Carbon isotope composition(δ^(13)C)of a plant organ is an inherent signature reflecting its physiological property,and thus is used as an integrative index in crop breeding.It is also a non-intrusive method for quantifying the relative contribution of different source organs to grain filling in cereals.Using the samples collected from two-year field and pot experiments with two nitrogen(N)fertilization treatments,we investigated the temporal and spatial variations of δ^(13)C in source organs of leaf,sheath,internode,and bracts,and in sink organ grain.Constitutive nature of δ^(13)C was uncovered,with an order of leaf(−27.84‰)<grain(−27.82‰)<sheath(−27.24‰)<bracts(−26.81‰)<internode(−25.67‰).For different positions of individual organs within the plant,δ^(13)C of the leaf and sheath presented a diminishing trend from the top(flag leaf and its sheath)to the bottom(the last leaf in reverse order and its sheath).No obvious pattern was found for the internode.For temporal variations, δ^(13)C of the leaf and sheath had a peak(the most negative)at 10 days after anthesis(DAA),whereas that of the bracts showed a marked increase at the time point of anthesis,implying a transformation from sink to source organ.By comparing the δ^(13)C in its natural abundance in the water-soluble fractions of the sheath,internode,and bracts with the δ^(13)C in mature grains,the relative contribution of these organs to grain filling was assessed.With reference to the leaf,the internode accounted for as high as 32.64%and 42.56%at 10 DAA and 20 DAA,respectively.Meanwhile,bracts presented a larger contribution than the internode,with superior bracts being higher than inferior bracts.In addition,N topdressing reduced the contribution of the internode and bracts.Our findings clearly proved the actual significance of non-foliar organs of the internode and bracts for rice yield formation,thus extending our basic knowledge of source and sink relations.

Characteristics of Stable Isotopes in an Inland Lake and Their Implications for Water Management in Northwestern China

Bosten Lake is the largest inland freshwater lake in China, functioning as a critical control and allocation facility for agricultural, industrial, ecological and social development in southern Xinjiang in northwestern China. The distribution of stable isotopes, spatial and temporal variations of δ18O, and hydrograph separation of Bosten Lake and its principal recharge rivers—the Kaidu River and the Huangshuigou River—were analyzed using isotope composition. Hydrograph separation indicated that Bosten lake water comprised four components as follows: river runoff, groundwater, agricultural and industrial drainage, and local precipitation. Their contributions were 31%, 35%, 25%, and 9%, respectively. Irrigation drainage and industrial wastewater, enriched high TDS, were the main factors affecting the water quality of Bosten Lake. The δ18O of lake water, which was significantly reduced compared with river water, remained below the local meteoric water line (LMWL), indicating strong evaporation in the lake, especially during summer. The spatial and temporal distribution of δ18O exhibited slow water circulation in the lake. Both the Kaidu River and the Huangshuigou River depend on alpine precipitation and glacier snow, especially the Kaidu River, where ice-snow-melt water accounts for 43% of the river runoff. These rivers are sensitive to climate change. The Bosten Lake inflows would be reduced by the decrease in river runoff and groundwater under future climate change. To improve water quality and reduce evaporative loss, the amount of wastewater should be strictly restricted by local government, and water diversions from Bosten Lake should be concentrated between May and September.

High-Resolution Records of the Holocene Paleoenvironmental Variation Reflected by Carbonate and Its Isotopic Compositions in Bosten Lake and Response to Glacial Activities

The Early Holocene paleoclimate in Bosten Lake on the northern margin of the Tarim Basin, southern Xinjiang, is reconstructed through an analysis of a 953 cm long core （BSTC2000） taken from Bosten Lake. Multiple proxies of this core, including the mineral components of carbonate, carbonate content, stable isotopic compositions of carbonate, Ca/Sr, TOC and C/N and C/S of organic matter, are used to reconstruct the climatic change since 8500 a B.P. The chronology model is made by nine AMS 14C ages of leaves, seeds and organic matter contained in two parallel cores. The climate was cold and wet during 8500 to 8100 a B.P. Temperature increased from 8100 to 6400 a B.P., the climate was warm and humid, and the lake expanded. The lake level was highest during this stage. Then from 6400 to 5100 a B.P., the climate became cold and the lake level decreased slightly. During the late mid-Holocene, the climate was hot and dry from 5100 to 3100 a B.P., but there was a short cold period during 4400 to 3800 a B.P. At this temporal interval, a mass of ice and snow melting water supplied the lake at the early time and made the lake level rise. The second highest lake level stage occurred during 5200 to 3800 a B.P. The climate was cool and wet during 3100 to 2200 a B.P., when the lake expanded with decreasing evaporation. The lake had the last short-term high level during 3100 to 2800 a B.P. After this short high lake level period, the lake shrank because of the long-term lower temperature and reduced water supply. From 2200 to 1200 a B.P., the climate was hot and dry, and the lake shrank greatly. Although the temperature decreased somewhat from 1200 a B.P. to the present, the climate was warm and dry. The lake level began to rise a little again, but it did not reach the river bed altitude of the Konqi River, an outflow river of the Bosten Lake.

Isotopic Compositions of Sulfur in the Jinshachang Lead–Zinc Deposit, Yunnan, China, and its Implication on the Formation of Sulfur-Bearing Minerals

The Jinshachang lead-zinc deposit is mainly hosted in the Upper Neoproterozoic carbonate rocks of the Dengying Group and located in the Sichuan-Yunnan-Guizhou （SYG） Pb-Zn-Ag multi- metal mineralization area in China. Sulfides minerals including sphalerite, galena and pyrite postdate or coprecipitate with gangue mainly consisting of fluorite, quartz, and barite, making this deposit distinct from most lead-zinc deposits in the SYG. This deposit is controlled by tectonic structures, and most mineralization is located along or near faults zones. Emeishan basalts near the ore district might have contributed to the formation of orebodies. The j34S values of sphalerite, galena, pyrite and barite were estimated to be 3.6‰-13.4‰, 3.7‰-9.0‰, -6.4‰ to 29.2‰ and 32.1‰34.7‰, respectively. In view of the similar δ34S values of barite and sulfates being from the Cambrian strata, the sulfur of barite was likely derived from the Cambrian strata. The homogenization temperatures （T ≈ 134--383℃） of fluid inclusions were not suitable for reducing bacteria, therefore, the bacterial sulfate reduction could not have been an efficient path to generate reduced sulfur in this district. Although thermochemical sulfate reduction process had contributed to the production of reduced sulfur, it was not the main mechanism. Considering other aspects, it can be suggested that sulfur of sulfides should have been derived from magmatic activities. The δ34S values of sphalerite were found to be higher than those of coexisting galena. The equilibrium temperatures calculated by using the sulfur isotopic composition of mineral pairs matched well with the homogenization temperature of fluid inclusions, suggesting that the sulfur isotopic composition in ore-forming fluids had reached a partial equilibrium.

Petrogenesis and Tectonic Significance of the Xiuwacu Two-Period Magmatism in Geza Arc of Yunnan Province： Constraints from Lithogeochemistry, Zircon U-Pb Geochronology and Hf isotopic Compositions

Objective The Late Cretaceous Xiuwacu ore-bearing porphyry is located in the Geza area of southern Yidun arc, SW China. In this area, the rock mass is mainly composed of three lithofacies： biotite granite porphyry, monzonitic granite and light alkali feldspar granite. As a part of the Yidun arc, the Geza arc has common structure and temporal- spatial evolution with the ~idun arc, which has experienced three stages of oceanic crust subduction, collision orogeny and intracontinent convergence stages. The molybdenite ores in the area are mainly hosted in monzonitic granite-porphyry and structural fracture zone, and the ore bodies are strictly controlled by faults. In recent years, great geological prospecting results have been achieved in Xiuwacu, and the deposit has reached a medium scale. However, there are few researches on the metallogenic porphyry. Based on the previous research, we determined the rock-forming and ore-forming age of the porphyry, and found that there were two stages of magmatism intrusion in Xiuwacu： Indosinian and Yanshanian. We also discussed the geochemical characteristics and source area of the rocks in the area.

Lead Isotopic Composition and Lead Source of the Huogeqi Cu-Pb-Zn Deposit,Inner Mongolia,China

The Huogeqi orefield located on the northern side of Mt. Langshan, Inner Mongolia occurs in the Middle Proterozoic Langshan Group metamorphic rocks, and the orebodies arc stratiform. In the past twenty years, many Chinese geologists have conducted researches on the Huogeqi Cu-Pb-Zn deposit, but there has been still a controversy on its origin. Some advocate that the deposit is of sedimentary-metamorphic rcworking origin, some hold that it is of sea-floor SEDEX origin, and others have a preference for magmatic superimposition origin. The crux of the controversy is that there is no common understanding about the source of ore-forming materials. In this paper, the Pb isotopic compositions of regional Achaean-Early Proterozoic basement rocks, various types of sedimentary- metamorphic rocks and volcanic rocks in the mining district, Late Proterozoic and Hercynian magmatic rocks arc introduced and compared with the orc-lead composition, so as to constrain the source of the ore lead. The result indicates that （1） sulfides in the ores have homogeneous Pb isotopic compositions, showing a narrow variation range. Their ^206pb/^204pb ratios arc within a range of 17.027- 17.317; ^207Pb/^204pb ratios, 15.451-15.786 and ^208Pb/^204pb ratios, 36.747-37.669; （2） the Pb isotopic compositions of the regional Achaean-Early Proterozoic basement rocks arc characteristic of the old Pb isotopic composition at the early-stage evolution of the Earth, which varies over a wider range, reflecting significant differences in Pb isotopic compositions of the ores. All this indicates that the source of ore lead has no bearing on the basement rocks; （3） the sedimentary-metamorphic rocks in the mining district arc characterized by highly variable and more radiogenic Pb isotopic compositions and their Pb isotopic ratios arc obviously higher than those of ores, demonstrating that ore lead did not result from metamorphic rcworking of these rocks; （4） Pb isotopic compositions of Late Proterozoic diorite-gabbro and Hercynian granite are higher than those of ores. Meanwhile, the Pb isotopic compositions of sulfides in the small-sized strata-penetrating mineralized veinlets formed at later stages arc completely consistent with that of sulfides in stratiform-banded ores, suggesting that these veiniets arc the product of autochthonous rcworking of the stratiform-banded ores during the period of metamorphism and the late magmatic superimposition-mineralization can be excluded; （5） amphibolite, whose protolith is basic volcanic rocks, has the same Pb isotopic compositions as ores, implying that ore lead was derived probably from basic volcanism. So, the source of ore-forming materials for the Huogeqi deposit is like that of the volcanic massive sulfide （VMS） deposits. However, the orebodies do not occur directly within the volcanic rocks, and instead they overlie the volcanic rocks, showing some differences from those typical VMS-type deposits.

Noble Gas Isotopic Compositions of Cobalt-rich Ferromanganese Crusts from the Western Pacific Ocean and Their Geological Implications

Noble gas isotopic compositions of various layers in three-layered （outer, porous and compact layers） cobalt-rich ferromanganese crusts and their basaltic and phosphorite substrates from the western Pacific Ocean were analyzed by using a high vacuum gas mass spectrum. The analytical results show that the noble gases in the Co-rich crusts have derived mainly from the ambient seawater, extraterrestrial grains such as interplanetary dust particles （IDPs） and wind-borne continental dust grains, and locally formation water in the submarine sediments, but different noble gases have different sources. He in the crusts derives predominantly from the extraterrestrial grains, with a negligible amount of radiogenic He from the eolian dust grains. Ar is sourced mainly from the dissolved air in the seawater and insignificantly from radiogenic Ar in the eolian continental dust grains or the formation water. Xe and Ne derive mainly from the seawater, with minor amounts of extraterrestrial Xe and Ne in the IDPs. Compared with the porous and outer layers, the compact layer has a relatively high 4He content and lower 3He/4He ratios, suggesting that marine phosphatization might have greatly modified the noble gas isotopic compositions of the crusts. Besides, the 3He/4He values of the basaltic substrates of the cobalt-rich crusts are very low and their R/R. ratios are mostly 〈0.1 R., which are similar to that of phosphorite substrates （0.087 R.）, but much lower than that of fresh submarine MORB （8.75±14 Ra） or seamount basalts （3-43 Ra）, implying that the basaltic substrates have suffered strong water/rock interaction and reacted with radiogenic ^4He and P-rich upwelling marine currents during phosphatization. The trace elements released in the basalt/seawater interaction might favor the growth of cobalt-rich crusts. The relatively low ^3He/^4He values in the seamount basalts may be used as an important exploration criterion for the cobalt-rich ferromanganese crusts.

Sulfur isotopic composition of seafloor hydrothermal sediment from the Jade hydrothermal field in the central Okinawa Trough and its geological significance

Eighteen samples of hydrothermal sediments from the Jade hydrothermal field in the central Okinawa Trough have been analyzed. Sulfur isotopic values for 10 sulfide samples vary from 5.2× 10^(-3)to 7.2× 10^(-3), δ^(34)S values for 7 sulfate samples vary from 16.3 × 10^(-3) to 22.3 × 10^(-3), and 1 native sulphur sample has a δ^(34)S value of 8.2 × 10^(-3). The major sources of sulfur for hydrothermal sediment are intermediate to acid volcanic rocks and sea water sulfate, and it is possible that the partial sulfur of hydrothermal sediment is from the pelagic sediment by the interaction between hydrothermal fluid and sediment. The reasons of causing the distinct differences in sulfur isotopic values for sulfide samples from hydrothermal sediment ( compared with other hydrothermal fields), are the differences in the sources of sulfur, the magmatic activity and the tectonic evolution in different hydrothermal fields. The sulfur evolution is a long and complex process in the seafloor hydrothermal system, involving the ascending of heating sea water, the interaction between fluid and volcanic rocks, the mixing of sea water sulfate and sulfur from intermediate to acid volcanic rocks, and the fluid/pelagic-sediment interaction. And the interaction between sea water and intermediate to acid volcanic rocks is an important mechanism for the sulfur evolution in the Jade hydrothermal field.

Stable Carbon Isotopic Compositions of Methylated-MTTC in Crude Oils from Saline Lacustrine Depositional Environment:Source Implications

Significantly high abundant methyl-Methyl Trimethyl Tridecyl Chromans （MTTCs） have been detected in aromatic hydrocarbon fractions in crude oils from the Jizhong Depression and Jianghan Basin. The distribution of these compounds is dominated by methyl-MTTC and dimethyl- MTTC series, which indicate diagenetic products of a hypersaline depositional environment in the early stage and show a low degree of methylation. The occurrence of significantly high abundant methyl-MTTC depends mainly on good preservation conditions with a strongly reductive, hypersaline and water-columned depositional environment and subsequent non-intensive diagenetic transformations. The stable carbon isotopic compositions of the methyl-MTTCs and dimethyl-MTTCs in two samples are far different from the stable carbon isotopic composition of C30 hopane of apparent bacteria biogenesis （up to 4.11‰ and 5.75‰, respectively）. This obviously demonstrates that the methyl-MTTC and dimethyl-MTTCs cannot be of bacteria origin, which is different from the previous point of view about non-photosynthetic bacteria products or possible bacteria-reworked products. On the contrary, the stable carbon isotopic compositions of methyl-MTTC and dimethyl-MTTCs in the two samples were similar to that of the same carbon-numbered n-alkanes （nC27-nC28-nC29）, which indicates that they share the same source origin. Especially in the crude oil from the Zhao61 well, stable carbon isotopic compositions are also similar to that of the same carbon-numbered steranes with ααα- 20R isomer （mostly less than 0.4‰）. In consideration of the results of previous studies on saline lake ecological sedimentation, the authors hold that the methyl-MTTC and dimethyl-MTTCs in the saline lake sediments should be of algal biogenesis origin.