无内标-多外标校正激光剥蚀等离子体质谱法测定磁铁矿微量元素组成

激光剥蚀电感耦合等离子体质谱(LA-ICP-MS)常用于磁铁矿原位微量元素分析,按照校正策略不同,主要分为内标法和无内标法。内标法需要用电子探针(EMPA)预先测定磁铁矿中内标元素Fe的含量,过程较繁琐,且待测元素含量会受到内标元素含量测定的影响。本文采用铁含量较高的玄武质玻璃BCR-2G、BIR-1G、BHVO-2G和GSE-1G作为外标,避免了内标元素含量的测定,建立了无内标-多外标校正LA-ICP-MS测定磁铁矿微量元素组成的分析方法。利用该方法测定了科马提岩玻璃GOR-128g和自然岩浆磁铁矿BC 28的微量元素组成以评估方法的可靠性。结果表明,科马提岩玻璃的测定结果与推荐值及前人内标法的测定值一致,多数元素的相对标准偏差RSD5%;自然岩浆磁铁矿的测定结果与推荐值相比,多数元素的RSD7%,低于前人内标法的RSD(15%)。由此说明无内标-多外标法可以实现富铁硅酸岩或磁铁矿微量元素含量的准确校正,克服了基体效应的影响。因此,无内标-多外标法是一种原位测定磁铁矿微量元素含量的快速、准确方法,具有一定的应用潜力。     

新疆北山小常山铁矿矿物电子探针分析及矿床成因探讨

小常山铁矿位于新疆北山裂谷带西段,矿体赋存于辉长岩、辉长岩和大理岩接触带中,部分赋存于花岗闪长岩和大理岩接触带。前人研究辉长岩年龄为276±1.2Ma,与坡北铜镍硫化物岩浆矿床形成年龄一致,同属早二叠世。小常山铁矿中可见有明显的岩浆贯入现象。矿体主要呈透镜状、块状、脉状、薄层状。金属矿物主要为磁铁矿,含极少量的褐铁矿和黄铁矿;近矿围岩蚀变较弱,主要有石榴子石化、绿帘石化、大理岩化。电子探针研究表明,磁铁矿FeOT含量范围较大,主要分布在85%范围以上,Al_2O_3含量相对较高,TiO_2-Al_2O_3-(MgO+MnO)图解、TiO_2-Al_2O_3-MgO图解均显示热液接触交代成因特点,表明小常山铁矿的形成和岩浆热液的交代作用有关。石榴子石属于钙铝榴石-钙铁榴石系列,与典型矽卡岩矿床的石榴子石端员组分组成有一定差别。结合小常山铁矿体地质特征以及电子探针分析测试等研究,认为小常山铁矿是多成因的复合型矿床,具有岩浆成因和热液成因特征,但后者是主要成因。     

Genesis and Metallogenic Process of the Lujing Uranium Deposit,Southwest Jiangxi Province,China: Constraints of Micropetrography and S–C–O Isotopes

The Lujing uranium deposit, located in the southeastern part of the Nanling metallogenic province, is one of the representative granite‐related hydrothermal uranium deposits in South China. Basic geology, geochemistry, and geochronology of the deposit have been extensively studied. However, there is still a chronic lack of systematic research on the genesis and metallogenic process of the deposit. Thus, we recently carried out an electron microprobe and stable isotopic analysis. The main research results and progresses are as follows: Uranium minerals in this deposit include coffinite, pitchblende, and uranothorite, and small amounts of uranium exist in accessory minerals in the form of isomorphism. Coffinite, which occurs predominantly as the pseudomorphs after pitchblende, also occurs as a primary mineral and is locally formed from the remobilization of uranium from adjacent uranium‐bearing minerals. The mineralizing fluid was originally composed of a magmatic fluid generated by late Yanshanian magmatism. The high As content of pyrite in ores may reflect the addition of meteoric water, or the formation water (or both), to the magmatic hydrothermal system. The δ³⁴S values vary from −14.4‰ to 13.9‰ (mean δ³⁴S = −3.9‰), showing a range that is similar to nearby Cambrian metamorphic strata and Indosinian granites, indicating that these host rocks represent the source of sulfur; however, the possibility of a mantle source cannot be completely ruled out. According to our new isotopic data and recent Pb isotopic data, we conclude that the uranium in ores was derived by leaching dominantly from the uranium‐rich host rocks, especially the Cambrian metamorphic strata. The δ¹³C_PDB values (−8.75‰ to 1.40‰; mean δ¹³C_PDB = −5.41‰) and δ¹⁸O_SMOW values (5.45–18.62‰; mean δ¹⁸O = 13.02‰) of reddish calcite from the ore‐forming stage suggest that the CO₂ in the mineralizing fluids was derived predominantly from the mantle, with a small component contributed by marine carbonates. Based on these new data and previous research results, this paper proposes that uranium metallogenesis in the Lujing deposit is closely associated with mafic magmatism resulting from crustal extension during the Cretaceous to Paleogene in South China.     

利用U—1000型激光拉曼探针测定流体包裹体气体成分的研究

本文利用U－1000型激光拉曼探针成功地测量出单个流体包裹体中H2S、CH4、CO2气体成分，并讨论了包裹体中这些气体的拉曼谱峰位移与包裹体内压的关系，分析了影响激光拉曼探针定量测定包裹体气相成分的取面积和拉曼定量因子因素。     

由电子探针分析数据估算角闪石、黑云母中的Fe~（3＋）、Fe~（2＋）

待定矿物化学式中阳离子数法是由电子探针分析值求矿物中Ｆｅ￣（３＋）、Ｆｅ￣（２＋）的新方法。在该方法中，矿物化学式中的阴离子数是唯一已知条件，阳离子数未知，通过本文给出的一系列步骤可以得出实际阳离子数的可能估计。进而求出Ｆｅ＿２Ｏ＿２、ＦｅＯ。该法对Ｆｅ＿２Ｏ＿３、ＦｅＯ的计算结果避免了出现负值，在总体上，该方法的计算结果较其它方法更接近其化学分析值。     

A FORTRAN Program for tabulating and naming amphibole analyses according to the International Mineralogical Association Scheme

Summary Amphibole analyses input to program AMPHTAB (optionally with H₂O, F, Cl, minor elements and one or both of Fe₂O₃, FeO), are output in conventional column tables, with formula units, complete IMA names, and extensive messages indicating the quality of each analysis. AMPHTAB accepts data-files ranging from a single amphibole analysis to (in principle) unlimited batched data-e.g., multiple analyses from each of numerous probe sections. Options are provided to reallocate total Fe in probe data between Fe³ and Fe², to allow for common analytical problems (e.g., low H₂O values), and to enable the number of oxygens in the formula unit to be either preset or assigned automatically. Results for 57 probe analyses are compared with an unpublished BASIC program, which uses a different Fe-reallocation method. Three-quarters of the IMA names resulting from the two programs are essentially identical, despite somewhat different estimated formula units. The remainder are borderline cases, where incidental changes in formula units effect disproportionate differences in name.

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Ein FORTRAN-Programm zum tabellieren und benennen von amphibolanalysen entsprechend dem Schema der International Mineralogical Association

Zusammenfassung In das Programm eingegebene Amphibolanalysen (wahlweise mit H₂O, F, Cl, Spurenelementen und Fe₂O₃, und/oder FeO), werden in Form herkömmlicher Spaltentabellen mit den Formeleinheiten, vollständigen IMA-Namen und ausführlichen Bemerkungen bezüglich der Analysenqualität ausgegeben. Das AMPHTAB-Programm verarbeitet Datensätze von einer einzigen Amphibolanalyse bis zu (im Prinzip) unbegrenzten Datenblöcken; z. B. Mehrfachanalysen eines Probenabschnittes von mehreren. Es sind die Möglichkeiten vorgesehen, das Gesamteisen in einer Analyse in die Fe³ und Fe²-Anteile umzurechnen, allgemeine analytische Probleme (z. B. niedrige H₂O-Gehalte) zu lösen und die Anzahl der Sauerstoffatome in der Formeleinheit entweder vorzugeben oder automatisch setzen zu lassen. Die Resultate von 57 Mikrosonden-Analysen sind mit einem unveröffentlichten BASICProgramm, das eine andere Methode zur Aufteilung des Fe-Gehaltes benutzt, verglichen worden. Drei Viertel der von den beiden Programmen vorgeschlagenen Mineralnamen sind identisch, trotz einiger unterschiedlich berechneter Formeleinheiten. Die übrigen 25% sind Grenzfälle, bei denen zufällige Veränderungen in den Formeleinheiten unverhältnismäßige Unterschiede in der Benennung bewirkten.

     

罕见的蓝色饵-纳透闪石研究

尽管角闪石在地壳中大量存在 ,但是蓝色钾 钠透闪石却是角闪石中的稀有品种。本文采用X射粉晶线衍射和晶胞参数计算 ,确定该矿物为蓝色的钾 钠透闪石 ,用电子探针 (EMPA)精确分析了它的化学成分 ,确定为钾 钠透闪石 ,而不是蓝色软玉 (即不是透闪石或阳起石 )。     

激光探针质谱分析碳酸盐碳、氧同位素技术

用激光显微装置和MAT 2 5 1质谱计原位分析碳酸盐的碳、氧同位素 ,与常规酸解法有同样的分析精度(标准偏差 0 .0 6‰～ 0 .0 8‰ ) ,δ1 3 C值无明显差异 ,而δ1 8O值比酸解法偏负约 1.11‰～ 1.2 3‰ ,可能是温度效应的结果 ,可以进行系统校正。     

汉诺坝幔源单斜辉石巨晶氢同位素组成的离子探针分析：微尺度不均一性

运用离子探针技术测定了河北汉诺坝新生代玄武岩中3个单斜辉石巨晶的氢同位素组成，结果显示同一颗粒内部表现出微尺度的不均一性，2mm范围内δD的变化达到60‰。δD和氢含量之间不存在同步的变化，巨晶内部的化学成分均一，因此我们认为巨晶的氢同位素不均一性继续自母岩浆。母岩浆的氢同位素变化可能是去气过程中气相与熔体之间的分馏引起的。单斜辉石巨晶形成后很短的时间内即被寄主岩浆带至地表并经历了快速淬火。