潮白河顺义段再生水补给区包气带理化参数相关性分析

土壤阳离子交换容量(CEC)、总有机碳(TOC)、粘土矿物总量和粘粒含量是影响再生水入渗过程中污染物在包气带及地下水含水层介质中迁移转化的四项重要指标,是反映包气带对污染物吸附性及生物作用的主要参数。本文选取北京市潮白河顺义段再生水补给区包气带作为对象,对CEC、TOC、粘土矿物总量及粘粒含量4项指标进行了两两相关性分析及函数拟合。结果表明,上述四项指标的大小均与埋深无关,只与介质本身特性有关,且两两之间存在着显著的相关性,相关系数均大于0.8。     

镉在蒙脱石等粘土矿物上的吸附行为研究

研究了土壤中主要硅酸盐粘土矿物蒙脱石、伊利石、高岭石、海泡石对重金属镉的吸附行为.结果表明:硅酸盐粘土矿物吸附镉受酸度和离子强度的影响;吸附反应是快反应,能很好地符合Lagergren二级吸附速度方程;优化条件下的高岭石对镉吸附很弱,蒙脱石、伊利石、海泡石对镉的实验饱和吸附容量分别为2.88、1.08、2.82 mg/g,蒙脱石吸附镉更适合Freundlich拟合,伊利石、海泡石对镉的吸附结果更适合Langmuir拟合;相关性分析表明,硅酸盐粘土矿物对镉的饱和吸附容量大小与其理化性质有关,其中矿物中氧化锰含量高低与其对镉饱和吸附容量大小的相关性达到极显著水平.     

2011年全球发现的新矿物种

在系统梳理2011年度全球发现并经国际矿物学协会(IMA)新矿物与矿物分类命名专业委员会(CNMNC)批准的122个新矿物种资料的基础上,从矿物名称、晶体化学式、晶系和空间群、晶胞参数、主要粉晶数据、物理性质、光学性质、产地与产状、与其他矿物种的关系、矿物名称来源、化学反应和光谱学特征等方面归纳总结了这些新矿物的重要矿物学特征。并按照中国新矿物及矿物命名专业委员会颁布的《矿物种汉名审订条例》,对122个新矿物种的中文名称进行了审订。通过适时公布国际新矿物工作的新进展和新成果,并逐步完善和规范矿物种中文译名体系,为我国新矿物的发现和研究提供有科学价值的参考和借鉴,不断推动矿物种中文译名规范化与标准化的进程。     

地质矿产数据资产管理利用探讨

目前,大部分地质矿产数据资产和信息资源分散在政府管理部门、事业单位和大型企业中,由于条块分割与标准不一,造成了资源不能共享。因此,需要开发并建立一个分布式数据管理及信息共享平台,逐步实现部门之间的信息交换和无缝连接,有效消除信息孤岛,提高数据资产的利用价值,为国家的经济建设和社会发展提供及时、适用、可靠的数据和信息保障。     

云南保山南红玛瑙矿物学特性及致色机理探究

通过光学显微镜、X射线粉晶衍射、X射线荧光光谱、电感耦合等离子体质谱、电子探针等测试分析手段对云南保山南红玛瑙的岩相学、矿物组成、化学成分等进行了系统研究,在此基础上进一步通过扫描电镜、X射线能谱元素面扫描、激光共聚焦显微拉曼分析了南红玛瑙致色矿物形貌、元素分布及矿物物相构成。研究结果表明,保山南红玛瑙主要矿物为石英(95%,质量分数),主要结构为粒状结构和纤维结构,次要矿物为斜硅石及方解石等,并含有吸附水和结构水两种状态水。致色矿物主要以小于1μm球状矿物颗粒、2~10μm絮状似球状集合体、针状矿物颗粒和不规则形态矿物集合体这4种类型存在,元素分析显示其为含铁矿物。显微拉曼进一步确认南红玛瑙的颜色是由含铁矿物所致,其中红色致色主要为赤铁矿,黄色致色主要为针铁矿,铁矿物的具体存在形式及其分布方式对南红玛瑙的价值具有决定性作用。本工作为南红玛瑙矿物学特性以及致色机理研究提供了有价值的参考信息,对完善其知识体系和推动南红玛瑙文化有重要意义,同时对借助共聚焦显微拉曼等微区表征技术推动宝玉石研究提供了新思路。     

Discrimination between wave‐ravinement surfaces and bedset boundaries in Pliocene shallow‐marine deposits,Crotone Basin,southern Italy: An integrated sedimentological,micropalaeontological and mineralogical approach

The lower Pliocene Belvedere Formation, cropping out in the Crotone Basin, southern Italy, exhibits a metre‐scale to decametre‐scale shallow‐marine cyclicity that shares features of both high‐frequency sequences linked to shoreline shifts and controlled by minor relative sea‐level and/or sediment supply changes, and sedimentological cycles unrelated to shoreline shifts. In order to better understand the high‐frequency sequence stratigraphic framework of this succession, an integration of sedimentological, micropalaeontological (micro‐foraminifera assemblages) and mineralogical (heavy mineral abundance) data is used. From a sedimentological/stratigraphic point of view, wave‐ravinement surfaces bounding high‐frequency sequences, and associated substrate‐controlled ichnofacies, are prominent in outcrop and document environmental and water‐depth changes, whereas bedset boundaries separating sedimentological cycles have a more subtle field appearance and are only associated with changes of environmental energy. Moreover, condensed deposits are present only above wave‐ravinement surfaces, and the high‐frequency sequences bounded by these surfaces have a thickness that is an order of magnitude greater than that of the bedsets. Micro‐foraminifera assemblages may change, and the content of heavy minerals usually increases, across wave‐ravinement surfaces, whereas both parameters do not change significantly across bedset boundaries. The abundance of heavy minerals is systematically higher, with respect to the underlying and overlying deposits, in the condensed shell beds that overlie wave‐ravinement surfaces. An integrated sedimentological, micropalaeontological and mineralogical approach represents a powerful tool to discriminate between wave‐ravinement surfaces bounding high‐frequency sequences and bedset boundaries, and in general to investigate at the intra high‐frequency sequence scale. This integrated approach is expected to be very useful in the study of potentially all shallow‐marine successions composed of small‐scale cycles, in order to delineate a detailed sequence stratigraphic framework and understand the factors that controlled the cyclicity.     

Geochemistry of Mercury in the Permian Tectonically Deformed Coals from Peigou Mine, Xinmi Coalfield, China

As the mercury emitted from coal combustion can lead to serious environmental issues, researchers pay more attention to the content, distribution and occurrence of mercury in coal. In this paper, the content, distribution, and occurrence of mercury in the Permian tectonically deformed coals from Peigou Mine, Xinmi coalfield, Henan Province were investigated. A total of 18 bench samples were taken from No.2-1 coals seam in Peigou Mine, including 15 coal bench samples, two roofs and one floor. The mercury concentration, mineral composition, and main inorganic element content of 18 samples were determined by DMA-80 direct mercury analyzer, XRD, and XRF respectively. The results show that the mercury content ranges from 0.047 ppm to 0.643 ppm, with an average of 0.244 ppm. Though the coal seam has turned into typical tectonically deformed coal by the strong tectonic destruction and plastic deformation, the vertical distribution of mercury has remarkable heterogeneity in coal seam section. By the analysis of correlation between mercury and the main inorganic elements and the mineral composition in coal, we infer that majority of mercury mainly relates to pyrite or kaolinite.     

Petrogenesis and Metallogenesis of the Mazaertag Layered Intrusion in the Tarim Large Igneous Province, NW China

The Mazaertag layered intrusion is located in the northwestern part of the Tarim large igneous province where several early Permian layered mafic-ultramafic intrusions host important Fe-Ti oxide deposits. The intrusion covers an area of ～0.13 km~2 and has a vertical stratigraphic thickness of at least300 m. It consists chiefly of olivine clinopyroxenite, and is cut through by the nearby mafic-ultramafic dykes. In this paper, we report new mineral chemistry data and whole-rock chemical and isotopic compositions for the Mazaertag intrusion along with whole-rock isotopic compositions for the nearby mafic dykes. The averaged compositions of cumulus olivine, clinopyroxene and intercumulus plagioclase within individual samples range from Fo_(71-73),Mg~# = 76 to 79 and An_(65-75) but they do not define sustained reversals. The observed mineral compositions are consistent with the differentiation of a single batch of magma in a closed system. Rocks of the Mazaertag intrusion are characterized by enrichment in light REE relative to heavy REE, positive Nb and Ta anomalies and a small range of age-corrected ε_(Nd)(t)(-0.1 to +0.9) and initial ~(87)Sr/~(86)Sr values(0.7044 to 0.7068). The slightly lower ε_(Nd)(t), initial ~(206)Pb/~(204)Pb and higher initial ~(87)Sr/~(86)Sr values of the intrusion compared to those of the least contaminated dykes[ε_(Nd)(t) =+2.8 to +3.4;(~(206)Pb/~(204)Pb)_i = 18.516-18.521;(~(87)Sr/~(86)Sr)_i = 0.7038-0.7041] imply that the Mazaertag magma was subjected to small to modest degrees of contamination by the upper crust. The Sr-Nd isotopic compositions of the least contaminated dykes are consistent with derivation from a FOZO-like mantle source. The parental magma of the Mazaertag intrusion, estimated from clinopyroxene compositions using mineral-melt partition coefficients, has trace element compositions similar to some of the most primitive mafic dykes in the same area. This suggests that the Mazaertag intrusion and mafic dykes shared a similar mantle source. Therefore, the parental magma of the Mazaertag intrusion was interpreted to have originated from a mantle plume. Based on the Cr_2 O_3 contents in titanomagnetite and less-evolved characteristics of the Mazaertag intrusion compared to the Wajilitag Fe-Ti oxide deposit in Bachu, it is speculated that there might not be a potential to find economic Fe-Ti oxide mineralization in the intrusion.     

The production of iron oxide during peridotite serpentinization: Influence of pyroxene

Serpentinization produces molecular hydrogen(H2)that can support communities of microorganisms in hydrothermal fields;H2 results from the oxidation of ferrous iron in olivine and pyroxene into ferric iron,and consequently iron oxide(magnetite or hematite)forms.However,the mechanisms that control H2 and iron oxide formation are poorly constrained.In this study,we performed serpentinization experiments at 311℃ and 3.0 kbar on olivine(with 5% pyroxene),orthopyroxene,and peridotite.The results show that serpentine and iron oxide formed when olivine and orthopyroxene individually reacted with a saline starting solution.Olivine-derived serpentine had a significantly lower FeO content(6.57±1.30 wt.%)than primary olivine(9.86 wt.%),whereas orthopyroxene-derived serpentine had a comparable FeO content(6.26±0.58 wt.%)to that of primary orthopyroxene(6.24 wt.%).In experiments on peridotite,olivine was replaced by serpentine and iron oxide.However,pyroxene transformed solely to serpentine.After 20 days,olivine-derived serpentine had a FeO content of 8.18±1.56 wt.%,which was significantly higher than that of serpentine produced in olivine-only experiments.By contrast,serpentine after orthopyroxene had a slightly higher FeO content(6.53±1.01 wt.%)than primary orthopyroxene.Clinopyroxene-derived serpentine contained a significantly higher FeO content than its parent mineral.After 120 days,the FeO content of olivine-derived serpentine decreased significantly(5.71±0.35 wt.%),whereas the FeO content of orthopyroxene-derived serpentine increased(6.85±0.63 wt.%)over the same period.This suggests that iron oxide preferentially formed after olivine serpentinization.Pyroxene in peridotite gained some Fe from olivine during the serpentinization process,which may have led to a decrease in iron oxide production.The correlation between FeO content and SiO_2 or AI_2 O_3 content in olivine-and orthopyroxene-derived serpentine indicates that aluminum and silica greatly control the production of iron oxide.Based on our results and data from natural serpentinites reported by other workers,we propose that aluminum may be more influential at the early stages of peridotite serpentinization when the production of iron oxide is very low,whereas silica may have a greater control on iron oxide production during the late stages instead.     

广西典型近岸海域表层沉积物碎屑矿物分布及其物源意义

基于“我国重点海岸带滨海环境地质调查与评价”项目,分析了广西典型岸段20 m以浅的海域表层沉积物和地貌类型及其分布特征,并在此基础上探讨了碎屑矿物含量和种类的分布、变化以及组合。研究结果表明: 研究区水动力较强,作用方式多样,有近30种碎屑矿物,其中主要有石英、长石、钛铁矿、云母、锆石、黄铁矿以及海绿石等,重矿物较为丰富; 自全新世早期海侵以来,研究区先后进入了浅海海湾相沉积环境,但碎屑矿物种类与之前基本相似,其含量变化是由于气候和海平面的波动而致; 研究区碎屑矿物在以沉积物和地貌类型为单位的各类地质单元中,其含量和种类均有所不同,尤以重矿物的变异性最为突出; 各研究区重矿物组合可分为2~3个亚分区,均反映出与沉积环境关系密切。结果表明,研究区碎屑物质主要源于周缘陆区风化剥蚀、海岸侵蚀和河流输入,碎屑物质具有陆源性。