吉林烟筒砬子铂铜矿床矿物特征及成因浅析

烟筒砬子矿床是吉林省东部新发现的铂铜矿床之一,其矿床特征国内外研究鲜有提及。通过对吉林省烟筒砬子铂铜矿床的地质特征、矿物学、矿相学以及电子探针分析发现,矿体主要赋存在辉长岩与五道沟群浅变质岩的内接触带,热液交代作用形成的石榴石化辉长岩是其主要赋矿围岩,由此认为热液交代对铂族元素富集成矿起到了决定性作用。     

吉林省桦甸地区太古宙花岗质片麻岩的侵位与变形研究

根据岩石组合，分布，接触，包裹关系以及结构和构造，吉林省桦甸地区太古宙花岗质林岩为角闪英云闪长质片麻岩类和黑云母花岗闪长质片麻岩类，角闪英云闪长质片麻岩类为变形前侵入体，黑云母花岗闪长质片麻岩类为同变形侵入体，两类花岗质片麻岩的侵位是晚太古宙近东西向构造变形相伴生的岩浆活动事件。     

吉林露水河硅藻土在煅烧中的结构及性能的变化

应用X射线衍射、红外光谱分析、扫描电镜及化学分析方法对吉林露水河硅藻土在煅烧中的结构及性能的变化进行研究，结果表明：高温时蛋白石转变成方英石，激烈的相变温度为1160℃左右；当温度在1100℃～1200℃时，硅藻的微孔开始阻塞或消失，并出现开裂现象，硅藻的结构变得模糊，但硅藻仍保持其外形；室温～600℃，比表面积逐渐增加，600℃～1200℃比表面积则减少；室温～700℃时，pH值逐渐减小，700℃～1200℃时，pH值则逐渐增加。     

吉林省辽源市主要环境地质问题及其防治对策研究

以辽源市为例,阐述了其主要的环境地质问题.据此,对辽源市进行了地质环境质量分区.根据分区结果并结合一些重点工程有针对性地研究了辽源市主要环境地质问题的防治对策,以期能对辽源市的下一步发展规划有所意义.     

吉林松江河金矿床流体包裹体特征及矿床成因

松江河金矿位于夹皮沟—海沟成矿带的东南段,矿床受一韧性剪切带控制,矿体主要赋存于SN向断裂中。按矿石自然类型,可进一步划分为蚀变岩型与石英脉型。矿化类型主要为浸染状和细脉状。依据矿物共生组合、交代与穿插关系,可将松江河金矿成矿过程划分为3个阶段:黄铁矿--石英阶段、多金属硫化物--石英阶段及石英--碳酸盐阶段。研究结果表明,包裹体类型主要为气液两相包裹体及CO2三相包裹体。成矿流体均一温度范围为138℃~355℃,盐度范围为2.23%~11.60%NaCl,密度范围为0.59~0.99 g/cm3,成矿压力为64~92 MPa,成矿深度为6.45~7.88 km。主成矿阶段含CO2三相包裹体与气液两相包裹体共存,且两种类型包裹体的均一温度相近,盐度差别较大,CO2/H2O比值降低,表明成矿流体发生了以CO2逸失为特征的不混溶或沸腾,残余流体盐度升高。成矿流体的气相成分为CO2与CH4,显示出幔源的特征。综合研究表明,松江河金矿床成因类型属于中成造山型金矿。     

吉林东南部早寒武含铜层及其形成的古地理分析

吉林省东南部早寒武世晚期地层中含有数层含铜层，它们主要赋存在红色岩层所夹的灰绿黄绿色岩层之中。本区含铜层的形成与当时富氧阶段中的缺氧时期息息相关；而且该类型含铜层主要产自滨海或滨浅海地带，受当时古地理严格控制     

吉林省海沟金矿断裂地球化学预测研究

在总结海沟矿区控矿断裂构造几何形态学，动力学，运动学和地球化学特征基础上，应用数学模拟和GIS图层分析技术，综合分析研究断裂构造控矿规律和金矿成矿地球化学行为，初步建立了断裂构造地球化学定位预测模型。并对矿区主要赋矿构造-28号矿体深部及外围进行打矿预测。     

吉林集安金厂沟矿田岩石化学及地球化学特征

金厂沟矿田以金矿床为主，矿体与矿化点分布于燕山期中酸性杂岩体的内外接触带上。岩石化学及地球化学特征表明集安变质岩系遭受中级变质，含有较高的金等金属成矿元素； 中酸性杂岩体是地幔熔浆与壳源物质混杂形成，各成矿物质为幔源，同时汲取壳源，金来源于变质岩系和中酸性岩浆岩。     

吉林红旗岭铜镍硫化物矿床的成矿时代讨论

通过对红旗岭铜镍硫化物矿床1号含矿超镁铁质岩体和8号不含矿镁铁-超镁铁质岩体进行单矿物40Ar-39Ar法测年,得到与铜镍硫化物矿床相关的角闪石与黑云母结晶年龄分别为250 Ma和225 Ma,这一结果与前人所报道的K-Ar法年龄有明显的差异.结合与热液矿化相关的斜长伟晶岩锆石SHRIMP法年龄216 Ma,认为镁铁-超镁铁质岩形成于250 Ma左右的印支早期,铜镍硫化物矿床的形成时间晚于含矿岩体,大约为225 Ma前后的印支中期.216 Ma前后的岩浆期后热液叠加对成矿具有积极作用.     

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.