CaCO3－CO2－H2O岩溶系统的平衡化学及其分析

在介绍了CaCO3- CO2 - H2O岩溶系统平衡化学的原理后,对平衡化学的控制因素,包括温度、CO2 分压、体系的开放程度、离子强度效应、同离子效应、酸效应、碱效应、离子对效应进行了分析,并与CaMg ( CO3 )2 - CO2 - H2O 岩溶系统平衡化学作了对比。结果显示,天然开放的岩溶系统的平衡pH值范围为6. 80～8. 40,在此pH值范围内,水中的碳组分主要以HCO-3 形式存在; 与开放系统相比,在其它条件相同情况下,封闭系统的平衡pH值较高,而平衡[ Ca2+ ]和平衡[ HCO-3 ]较低,特别是在低CO2 分压时,两者的差异更明显;在封闭系统条件下,两种不同的纯CaCO3 - CO2- H2O饱和溶液相混合,将导致溶液对CaCO3 重新具有侵蚀性;离子强度效应、酸效应和离子对效应使方解石的溶解度增加,而同离子效应和碱效应使方解石的溶解度降低; 与方解石溶解平衡相比,其它条件相同时,白云石溶解平衡pH较高,在温度< 70℃时溶解度较大,但在温度> 70℃时溶解度较小。      

东海DGKS96－03岩心中微体化石的古海洋学特点、δ18O曲线与AMS14C测年

运用微体化石的研究结果辨识岩心不同的沉积阶段的沉积特征及古海洋学特点,并辅以δ18O曲线及AMS14C测年去探讨岩心的沉积时代。该岩心是1996年5月中国、法国、韩国科学家一起利用法国L’ATAIANTE号海洋调查船在东海陆架获取的17个岩心中的一个,分别做了粒度、矿物、CaCo2、微体化石、δ18O、AMS14C测年等分析,初步分析认为：依据微体化石的冷、暖水种的丰度变化,可以辨识出该岩心气候的7个冷期(C1、C2、C3、C4-1、C4-2、C5、C6、C7),然后结合岩心中的矿物成份、CaCo3含量、粒度变化、AMS14C的测年数据把岩心划分为4个沉积阶段,1．晚更新世早玉木冰期沉积。2．玉木亚间冰期沉积。3．晚更新世玉木冰期沉积。4．全新世冰后期沉积。另外,利用浮游有孔虫壳体对不同的沉积阶段所做的AMS14C测年结果分别为9690aBP、12980aBP,26350aBP,27960aBP,37410aBP,41260aBP．。     

应用PIV系统研究横流中近壁水平圆柱绕流旋涡特性

应用粒子图像测速(PIV)系统对横流中近壁水平圆柱绕流进行了试验研究。介绍了试验原理及装置,讨论了试验参数的选取和粒子的跟随性问题。分析了上游来流的流动特性,显示了亚临界雷诺数下间隙比为0.5时圆柱后尾流区旋涡产生、发展和消亡的动态过程,比较了时均流场和瞬时流场旋涡结构。对圆柱尾迹的旋涡脱落特性进行了分析,得出在试验条件下斯特劳哈尔数保持为常数0.2的结论。     

新疆萨吾尔地区扎合岩体地球化学特征及构造意义

扎合岩体位于哈萨克斯坦-准噶尔板块北缘,属于萨吾尔晚古生代岛弧带,岩石类型以花岗闪长岩为主。笔者通过对该岩体的岩石地球化学、岩石类型、岩浆源区、构造背景研究表明,扎合岩体属于钙碱性系列侵入岩,在岩浆演化过程中没有明显的分离结晶作用且分异程度不高,暗示其原始岩浆的来源可能为上地幔,形成环境为后碰撞阶段的挤压环境;扎合岩体地球化学特征的确定为晚古生代西准噶尔地区地壳的垂向增生以及后碰撞岩浆活动的研究提供了新的证据。     

Metallogenic age and hydrothermal evolution of the Jidetun Mo deposit in central Jilin Province,northeast China: Evidence from fluid inclusions,isotope systematics,and geochronology

The Jidetun deposit is a large porphyry Mo deposit that is located in central Jilin Province, northeast China. The Mo mineralization occurs mainly at the edge of porphyritic granodiorite, as well as the adjacent monzogranite. Field investigations, cross-cutting relationships, and mineral paragenetic associations indicate four stages of hydrothermal activity. To determine the relationships between mineralization and associated magmatism, and better understand the metallogenic processes in ore district, we have undertaken a series of studies incluiding molybdenite Re–Os and zircon U–Pb geochronology, fluid inclusions microthermometry, and C–H–O–S–Pb isotope compositions. The molybdenite Re–Os dating yielded a well-defined isochron age of 168.9 ± 1.9 Ma (MSWD = 0.34) that is similar to the weighted mean ²⁰⁶Pb/²³⁸U age of 173.5 ± 1.5 Ma (MSWD = 1.8) obtained from zircons from the porphyritic granodiorite. The results lead to the conclusion that Mo mineralization, occurred in the Middle Jurassic (168.9 ± 1.9 Ma), was spatially, temporally, and genetically related to the porphyritic granodiorite (173.5 ± 1.5 Ma) rather than the older monzogranite (180.1 ± 0.6 Ma). Fluid inclusion and stable (C–H–O) isotope data indicate that the initial H₂O–NaCl fluids of mineralization stage I were of high-temperature and high-salinity affinity and exsolved from the granodiorite magma as a result of cooling and fractional crystallization. The fluids then evolved during mineralization stage II into immiscible H₂O–CO₂–NaCl fluids that facilitated the transport of metals (Mo, Cu, and Fe) and their separation from the ore-bearing magmas due to the influx of abundant external CO₂ and heated meteoric water. Subsequently, during mineralization stage III and IV, increase of pH in residual ore-forming fluids on account of CO₂ escape, and continuous decrease of ore-forming temperatures caused by the large accession of the meteoric water into the fluid system, reduced solubility and stability of metal clathrates, thus facilitating the deposition of polymetallic sulfides.     

Rb‐Sr geochronology and Sr isotopic composition of Devonian granitoids,eastern Tasmania

Biotite igneous ages and well‐defined isochron ages of plutons from the composite Blue Tier Batholith and the Coles Bay area in northeastern Tasmania range from 395 to 370 Ma. The older limit of this range, for the George River granodiorite, is considerably older than any age previously recorded for NE Tasmania. The ages of the youngest plutons (Mt Paris and Anchor granites), which host cassiterite ores, record pervasive hydrothermal alteration events. The initial ⁸⁷Sr/⁸⁰Sr ratios of the granitoids range from 0.7061 to 0.7136 and suggest different protolith compositions, consistent with mineralogical and geochemical characteristics of each pluton. The S‐type garnetbiotite granites (Ansons Bay and Booby alia granites) have initial ratios greater than 0.7119, indicative of enriched, high Rb/Sr ratio, crustal source‐rocks of Proterozoic age (1700–800 Ma). The S‐type biotite granites (Poimena and Pearson granites) have relatively high initial ⁸⁷Sr/⁸⁶Sr ratios (0.7070, 0.7105) but overlap with those of the I‐type granodiorites (George River, Scamander Tier, Pyengana and Coles Bay granodiorites) which are in the range of 0.7061 to 0.7073. The initial ratios of the enriched altered plutons are poorly constrained, and on both hand‐specimen and thin‐section scales, reveal open‐system Sr isotopic patterns.

Isochron ages for the arenite‐lutite and lutite sedimentary associations of the Mathinna Beds, which are intruded by the granitoids, reflect an approach to Sr isotopic equilibrium during regional metamorphism. The metamorphic age (401 ± 7 Ma) of the early Pragian arenite‐lutite association indicates a relatively small time interval between deposition, regional metamorphism and granitoid intrusion. The isotopic age for the lutite sedimentary association (423 ± 22 Ma) is tentatively correlated with a Benambran‐age burial metamorphic event that has not previously been recorded in Tasmania.     

The origin of the Maozu carbonate-hosted Pb–Zn deposit,southwest China: Constrained by C–O–S–Pb isotopic compositions and Sm–Nd isotopic age

The Maozu Pb–Zn deposit, located on the western margin of the Yangtze Block, southwest China, is a typical carbonate-hosted deposit in the Sichuan–Yunnan–Guizhou Pb–Zn metallogenic province with Pb + Zn reserves of about 2.0 million tonnes grading 4.15 wt.% Pb and 7.25 wt.% Zn. Its ore bodies are hosted in Sinian (635–541 Ma) Dengying Formation dolostone and show stratiform, vein and irregular textures. Ores are composed of sphalerite, galena, pyrite, calcite, dolomite, quartz and fluorite with massive, banded, disseminated and veined structures. The C–O–Sm–Nd isotopic compositions of hydrothermal calcites and S–Pb isotopic compositions of sulfides were analyzed to constrain the origin of the Maozu deposit. δ¹³C_PDB and δ¹⁸O_SMOW values of hydrothermal calcites range from −3.7‰ to −2.0‰ and +13.8‰ to +17.5‰, respectively, and plot near the marine carbonate rocks field in a plot of δ¹³C_PDB vs. δ¹⁸O_SMOW, with a negative correlation. It suggests that CO₂ in the hydrothermal fluids was mainly originated from marine carbonate rocks, with limited influence from sedimentary organic matter. δ³⁴S_CDT values of sulfides range from +9.9‰ to +19.2‰, similar to that of Cambrian to Triassic seawater sulfate (+15‰ to +35‰) and evaporate (+15‰ to +30‰) in the Cambrian to Triassic sedimentary strata. It suggests that reduced sulfur was derived from evaporate in sedimentary strata by thermo chemical sulfate reduction. Sulfides have low radiogenic Pb isotope compositions (²⁰⁶Pb/²⁰⁴Pb = 18.129–18.375, ²⁰⁷Pb/²⁰⁴Pb = 15.640–15.686 and ²⁰⁸Pb/²⁰⁴Pb = 38.220–38.577) that plot in the field between upper crust and the orogenic belt evolution curve in the plot of ²⁰⁷Pb/²⁰⁴Pb vs. ²⁰⁶Pb/²⁰⁴Pb, and similar to that of age corrected Proterozoic basement rocks (Dongchuan and Kunyang Groups). This indicates that ore-forming metals were mainly derived from basement rocks. Hydrothermal calcite yields a Sm–Nd isotopic age of 196 ± 13 Ma, possibly reflecting the timing of Pb–Zn mineralization in the SYG province, younger than the Permian Emeishan mantle plume (∼260 Ma). All data combined suggests that hydrothermal fluids circulated through basement rocks where they picked up metals and migrated to surface, mixed with reduced sulfur-bearing fluids and precipitated metals. Ore genesis of the Maozu deposit is different from known magmatic–hydrothermal, Sedimentary Exhalative or Mississippi Valley-types, which maybe represent a unique ore deposit type, named as the SYG-type.     

Mechanism of mineralization in the Changjiang uranium ore field,South China: Evidence from fluid inclusions,hydrothermal alteration,and H–O isotopes

The Changjiang uranium ore field, which contains >10,000 tonnes of recoverable U with a grade of 0.1–0.5%, is hosted by Triassic two-mica and Jurassic biotite granites, and is one of the most important uranium ore fields in South China. The minerals associated with alteration and mineralization can be divided into two stages, namely syn-ore and post-ore. The syn-ore minerals are primarily quartz, pitchblende, hematite, hydromica, chlorite, fluorite, and pyrite; the post-ore minerals include quartz, calcite, fluorite, pyrite, and hematite. The fluid inclusions of the early syn-ore stage characteristically contain O₂, and those of the late syn-ore and post-ore stage contain H₂ and CH₄. The fluid inclusions in quartz of the syn-ore stage include H₂O, H₂O–CO₂, and CO₂ types, and they occur in clusters or along trails. Homogenization temperatures (T_h) for the H₂O–CO₂ and two-phase H₂O inclusions range from 106 °C to >350 °C and cluster in two distinct groups for each type; salinities are lower than 10 wt% NaCl equiv. The ore-forming fluids underwent CO₂ effervescence or phase separation at ∼250 °C under a pressure of 1000–1100 bar. The U/Th values of the altered granites are lowest close to the ore, increase outwards, but subsequently decrease close to unaltered granites. From the unaltered granites to the ore, the lowest Fe₂O₃/FeO values become lower and the highest values higher. The REE patterns of the altered granites and the ores are similar to each other. The U contents of the ores show a positive correlation with total REE contents but a negative correlation with LREE/HREE ratios, indicating the pitchblende is REE-bearing and selectively HREE-rich. The δEu values of the ore show a positive correlation with U contents, indicating the early syn-ore fluids were oxidizing. The δCe values show a negative correlation, indicating the later mineralization environment became reducing. The water–rock interactions of the early syn-ore stage resulted in oxidization of altered granites and reduction of the ore-forming fluids, and it was this reduction that led to the uranium mineralization. During alteration in the early syn-ore stage, the oxidizing fluids leached uranium from granites close to faults, and Fe₂O₃/FeO ratios increased in the alteration zones. The late syn-ore and post-ore alteration decreased the Fe₂O₃/FeO ratios in the alteration zones. The δ¹⁸O_W–SMOW values of the ore-forming fluids range from −1.8‰ to 5.4‰, and the δD_W–SMOW values range from −104.4‰ to −51.6‰, suggesting meteoric water. The meteoric water underwent at least two stages of water–rock interaction: the first caused the fluids to become uranium-bearing, and the second stage, which was primarily associated with ore-bearing faults, led to uranium deposition as pitchblende, accompanied by CO₂ effervescence.     

黔中地区含铝岩系中钪的分布及丰度研究

黔中地区含铝岩系是重要的含钪层,其铝土矿体和伴生硬质粘土岩中含有较为丰富的Sc2O3研究表明：铝土矿品位越高的区域,其含铝岩系中硬质粘土岩中钪的含量更高。铝土矿的Al2O3和A／S能直接反映Sc2O3质量和规模。Sc2O3与SiO2关系较为密切,与TFe2O3呈弱相关性,Fe203异常值时Sc2O3含量异常较明显。     

几个天然矿物中某些阳离子近邻结构的EXAFS研究

本文利用EXAFS方法对镁铝榴石、几种锰矿和不同铁含量的闪锌矿中有关阳离子的近邻结构进行了研究,得到了有关阳离子在相应矿物中的近邻结构参数.对闪锌矿的研究,得到了杂质Fe绝大部分以六配位的形式存在的结果,这与传统的观点不同;提出了闪锌矿不仅可作为地质温度计,还可能作为地质温度、压力变化记录仪的设想。