Fractionation mechanism of stable isotope in evaporating water body

Under Rayleigh equilibrium condition, stable isotopic ratio in residual water increases with the decrease of the residual water proportion f exponentially, and the fractionation rate of stable isotopes is inversely proportional to temperature. However, under kinetic evaporation condition, the fractionation of stable isotopes is not only related to the phase temperature but also influenced by the atmospheric humidity and the mass exchange between liquid and vapor phases. The ratio δ in residual water will not change with f after undergoing evaporation of a long time for great relative humidity. The rate that the evaporating water body reaches isotopic steady state is mainly dependent on the relative humidity in atmosphere. The analysis shows that the actual mean linear variety rates, about -30.0, of the δ18O in residual water versus the residual water proportion at Nagqu and Amdo stations are consistent with the simulated process under temperature of 20 oC and relative humidity of 50%. The distillation line simulated under Rayleigh equilibrium condition is analogous to the global meteoric water line (MWL) as the temperature is about 20 oC. Under non-equilibrium condition, the slope and constant values of distillation line are directly proportional to temperature and relative humidity. According to the basic data, the simulated distillation line is very consistent with the actual distillation line of Qinghai Lake.     

GGR Critical Review of Analytical Developments in 2003

The articles that comprise this critical review serve to draw attention to research papers published in specific fields of interest during 2003, provide critical comment on the relevance and importance of individual publications in these fields, and offer an overview of the comparative importance of advances in particular areas. In this way, these articles aim to assist experts in the field by keeping them informed of relevant recent publications, as well as providing an important resource for students or early career researchers who are embarking on studies in an area new to them. This year, five papers provide summaries of developments in bulk sample determinations employing (1) ICP-AES and ICP-MS (trace elements), (2) XRF and atomic absorption spectrometry and INAA, (3) isotope ratio measurements (TIMS, MC-ICP-MS, ICP-MS, ToF), as well as in situ measurements conducted using (4) secondary ion mass spectrometry and (5) laser ablation ICP-MS (trace element and isotope ratio determinations).     

Evolution of Hydrothermal System at the Dizon Porphyry Cu-Au Deposit, Zambales, Philippines

Abstract. Evolution of hydrothermal system from initial porphyry Cu mineralization to overlapping epithermal system at the Dizon porphyry Cu‐Au deposit in western central Luzon, Zambales, Philippines, is documented in terms of mineral paragen‐esis, fluid inclusion petrography and microthermometry, and sulfur isotope systematics. The paragenetic stages throughout the deposit are summarized as follows; 1) stockwork amethystic quartz veinlets associated with chalcopyrite, bornite, magnetite and Au enveloped by chlorite alteration overprinting biotite alteration, 2) stockwork quartz veinlets with chalcopyrite and pyrite associated with Au and chalcopyrite and pyrite stringers in sericite alteration, 3) stringer quartz veinlets associated with molybdenite in sericite alteration, and 4) WNW‐trending quartz veins associated with sphalerite and galena at deeper part, while enargite and stibnite at shallower levels associated with advanced argillic alteration. Chalcopyrite and bornite associated with magnetite in quartz veinlet stockwork (stage 1) have precipitated initially as intermediate solid solution (iss) and bornite solid solution (bnss), respectively. Fluid inclusions in the stockwork veinlet quartz consist of gas‐rich inclusions and polyphase inclusions. Halite in polyphase inclusions dissolves at temperatures ranging from 360d?C to >500d?C but liquid (brine) and gas (vapor) do not homogenize at <500d?C. The maximum pressure and minimum temperature during the deposition of iss and bnss with stockwork quartz veinlets are estimated to be 460 bars and 500d?C. Fluid inclusions in veinlet stockwork quartz enveloped in sericite alteration (stage 2) consist mainly of gas‐rich inclusions and polyphase inclusions. In addition to the possible presence of saturated NaCl crystals at the time of entrapment of fluid inclusions that exhibit the liquid‐vapor homogenization temperatures lower than the halite dissolution temperatures in some samples, wide range of temperatures of halite dissolution and liquid‐vapor homogenization of polyphase inclusions from 230d?C to >500d?C and from 270d?C to >500d?C, respectively, suggests heterogeneous entrapment of gaseous vapor and hypersaline brine. The minimum pressure and temperature are estimated to be about 25 bars and 245d?C. Fluid inclusions in veinlet quartz associated with molybdenite (stage 3) are dominated by gas‐rich inclusions accompanied with minor liquid‐rich inclusions that homogenize at temperatures between 350d?C and 490d?C. Fluid inclusions in vuggy veinlet quartz associated with stibnite (stage 4) consist mainly of gas‐rich inclusions with subordinate polyphase inclusions that do not homogenize below 500d?C. Fluid inclusions in veinlet quartz associated with galena and sphalerite (stage 4) are composed of liquid‐rich two‐phase inclusions, and they homogenize into liquid phase at temperatures ranging widely from 190d?C to 300d?C (suggesting boiling) and the salinity ranges from 1.0 wt% to 3.4 wt% NaCl equivalent. A pressure of about 15 bars is estimated for the dilute aqueous solution of 190d?C from which veinlet quartz associated with galena and sphalerite precipitated. In addition to a change in temperature‐pressure regime from lithostatic pressure during the deposition of iss and bnss with stockwork quartz veinlets to hydrostatic pressure during fracture‐controlled quartz veinlet associated with galena and sphalerite, a decrease in pressure is supposed to have occurred due to unroofing or removal of the overlying piles during the temperature decrease in the evolution of hydrothermal system. The majority of the sulfur isotopic composition of sulfides ranges from ±0 % to +5 %. Sulfur originated from an iso‐topically uniform and homogeneous source, and the mineralization occurred in a single hydrothermal system.     

Chemistry and Sulfur Isotopes in a Chert-dominant Sequence around the Stratiform Manganese Deposit of the Noda-Tamagawa Mine, Northern Kitakami Terrane, Northeast Japan: Implication for Paleoceanographic Environmental Setting

Abstract. Chemistry and sulfur isotopes are analyzed for a series of rocks in the chert‐dominant sequence around the stratiform manganese ore deposit of the Noda‐Tamagawa mine in the northern Kitakami Terrane, northeast Japan. The sequence is litholog‐ically classified into six units in ascending order: lower bedded chert, lower black shale, massive chert, manganese ore, upper black shale, and upper bedded chert. The rocks around the manganese ore deposit exhibit anomalous enrichment in Ni (max. 337 ppm), Zn (102) and U (30) in the upper part of lower bedded chert, Mo (122), Tl (79) and Pb (33) in the lower black shale, MnO, Cu (786) and Co (62) in the manganese ore, and As (247) and Sb (17) in the upper black shale. The aluminum‐normalized profiles reveal zonal enrichment of redox‐sensitive elements around the manganese bed: Zn‐Ni‐Fe‐Mo‐U(‐Co), Tl‐Pb(‐Mo), Mn‐Fe‐Cu‐V‐Cr‐Co(‐Zn) and As‐Sb in ascending order. The uppermost part of the lower bedded chert and black shale exhibit negative Ce/Ce* values, whereas the massive chert, manganese ore and lower part of the upper bedded chert display positive values. The isotopic δ³⁴S values are 0±6 % in the lower part of the lower bedded chert, ‐19 to ‐42 % in the upper part of the lower bedded chert, ‐36 to ‐42 % in the lower black shale, ‐28 to ‐35 % in the massive chert, manganese ore and upper black shale, and ‐23±5 % in the upper bedded chert. Thus, there is a marked negative shift in δ³⁴S values in the lower bedded chert, and an upward‐increasing trend in δ³⁴S through the manganese ore horizon. The present data provide evidence for a change in the paleoceanographic environmental resulting from inflow of oxic deepwater into the stagnant anoxic ocean floor below the manganese ore horizon. This event is likely to have triggered the precipitation of manganese oxyhydroxides. The redistribution of redox‐sensitive elements through the formation of metalliferous black shale and manganese carbonate ore may have occurred in association with bacterial decomposition of organic matter during early diagenesis of initial manganese oxyhydroxides.     

沙坡头没蒿和柠条叶片δ13C 和 N 含量的季节变化特征

通过对腾格里沙漠东南缘沙坡头人工固沙区油蒿和柠条叶片稳定碳同位素分辨率（△）和N 含量的测定，研究了不同种植方式下油蒿和柠条叶片△ 和 N 含量的季节变化及其关系。结果表明：在不同种植方式下，两种植物的△ 与 N 含量在不同月份之间均存在显著差异。油蒿叶片 △ 极显著高于柠条的：在不同种植方式下，油蒿单种下 △ 显著高于混种，柠条则反之。 油蒿叶片 N 含量极显著低于柠条的：不同种植方式下柠条叶片 N 含量无显著差异，而单种油蒿叶片 N 含量则显著低于混种。在 △ 与 N 含量的关系中，柠条叶片 △ 与 N 在两种生境、单种和混种下均极显著正相关，雨明柠条叶片 N 含量可以作为其 △ 与 N 含量的季节变化及其关系在不同微生境有所差异。     

华北地块东部晚中生代至新生代岩石圈不均一减薄与改造模式

本文综合运用不同时代幔源包体平衡温压对比、玄武岩地球化学性质对岩石圈厚度的反演以及不同时代岩石圈地幔地球化学性质的对比的方法，把华北地块东部岩石圈的减薄时间限定在晚中生代至新生代之间。减薄的机制可能是华北东部地区晚白垩世以来大陆岩石圈的拉张作用。由于机械性拉薄和热、机械和化学侵蚀作用，岩石圈厚度最终减薄到70km以下。但古老的岩石圈地幔并没有完全因减薄而消失，残留部分受到了来自软流圈物质的强烈改造，使其Sr、Nd同位素组成类似于软流圈，但Os同位素没有受到明显的改变。改造后的岩石圈地幔成为华北地块东部新生代岩石圈地幔的主体。在时空上，岩石圈的减薄具有不均一的性质。     

渭北东部奥陶系岩溶地下水环境同位素特征分

本文通过对渭北东部岩溶地下水环境同位素组成特征的研究，分析了大气降水、地表水、地下水三者之间的转化关系，并对研究区岩溶地下水的形成进行了初步探讨，认为大气降水是研究区岩溶地下水的补给源，地表水与地下水之间存在水力联系，地表水对地下水的补给占补给水源的74.3％。西部岩溶裸露区为岩溶水的直接补给区，其周边浅埋区为岩溶水的间接补给区，东南部的岩溶中-深埋区为岩溶水的径流排泄区。     

多接收等离子质谱（MC-ICP-MS )测定Mg同位素初步研究

常量元素Mg的同位素比值，应用在地球化学上有重要意义。笔者采用“样品-标准”交叉技术，以国际标准SRM980,AIdrich, Romil和实验室标准GSB作为实验材料，探讨浓度和基质效应影响，尝试建立高精度多接收等离子质谱(MC-ICP-MS)测定Mg同位素方法。相对于国际标准物质SRM980，本研究测得的国际标准物质Aldrich的δ26Mg和δ25Mg值分别为（2.64±0.15)‰(2σ）和（1.34±0.09)‰(2σ); Romil的δ26Mg和δ25Mg值分别为（2.46±0.15)‰(2σ）和（1.27±0.08)%(2σ)；国土资源部同位素地质重点实验室的实验室标准GSB的δ26Mg和δ25Mg值分别为（4.05±0.03)‰(2σ)和(2.05±0.03)‰(2σ)。     

Assimilation and Fractional Crystallization Controlled by Transport Process of Crustal Melt: Implications from an Alkali Basalt-Dacite Suite from Rishiri Volcano, Japan

Mechanisms of fractional crystallization with simultaneous crustalassimilation (AFC) are examined for the Kutsugata and Tanetomilavas, an alkali basalt–dacite suite erupted sequentiallyfrom Rishiri Volcano, northern Japan. The major element variationswithin the suite can be explained by boundary layer fractionation;that is, mixing of a magma in the main part of the magma bodywith a fractionated interstitial melt transported from the mushyboundary layer at the floor. Systematic variations in SiO₂ correlatewith variations in the Pb, Sr and Nd isotopic compositions ofthe lavas. The geochemical variations of the lavas are explainedby a constant and relatively low ratio of assimilated mass tocrystallized mass (‘r value’). In the magma chamberin which the Kutsugata and Tanetomi magmas evolved, a strongthermal gradient was present and it is suggested that the marginalpart of the reservoir was completely solidified. The assimilantwas transported by crack flow from the partially fused floorcrust to the partially crystallized floor mush zone throughfractures in the solidified margin, formed mainly by thermalstresses resulting from cooling of the solidified margin andheating of the crust. The crustal melt was then mixed with thefractionated interstitial melt in the mushy zone, and the mixedmelt was further transported by compositional convection tothe main magma, causing its geochemical evolution to be characteristicof AFC. The volume flux of the assimilant from the crust tothe magma chamber is suggested to have decreased progressivelywith time (proportional to t^–1/2), and was about 3 x 10^–2m/year at t = 10 years and 1 x 10^–2 m/year at t = 100years. It has been commonly considered that the heat balancebetween magmas and the surrounding crust controls the couplingof assimilation and fractional crystallization processes (i.e.absolute value of r). However, it is inferred from this studythat the ratio of assimilated mass to crystallized mass canbe controlled by the transport process of the assimilant fromthe crust to magma chambers. KEY WORDS: assimilation and fractional crystallization; mass balance model; magma chamber; melt transport; Pb isotope     

青藏高原腹地植物碳同位素组成对环境条件的响应

现代植物碳同位素组成是特定环境影响的结果,通过对植物碳同位素组成的研究可以揭示植物生长期环境信息。针对青藏高原腹地高寒草甸~高寒草原过渡区植被碳同位素组成进行研究;该区高山嵩草样δ13C值在-25.63‰~-27.95‰间,平均值-26.63‰;高寒草原区混合样δ13C值于-26.29‰~-27.73‰间,平均值-27.04‰。高山嵩草样δ13C值总体呈现由南东往北西方向正偏趋势,研究区北部高寒草原区混合植物样也呈现出由南向北富重碳同位素趋势。这些变化规律被认为是主要受降水环境影响的结果,而区域内降水条件的展布规律则是受高原夏季风运移方式的控制。对植物δ13C值与地理位置的回归分析表明,该区植被碳同位素组成与地理位置相关,高山嵩草样(r=0.44603,n=29,p<0.05)和混合样(r=0.8112,n=5,p<0.1)均表现出对区域降水环境条件的良好响应。据此,以该区植物δ13C值为背景,进行合理推算,拟定了研究区内干旱区和湿润区界限的位置。