High Resolution ID-TIMS Redefines the Distribution and Age of the Main Mesozoic Lacustrine Hydrocarbon Source Rocks in the Ordos Basin,China

Using high-precision zircon U-Pb ID-TIMS geochronology, tuffs from the Chang 9 shale and the Chang 7 shale were dated. The tuff in the Chang 9 shale is 241.47 ± 0.17 Ma, which falls between the top tuff age of 241.06 ± 0.12 Ma and the bottom tuff age of 241.558 ± 0.093 Ma in the Chang 7 shale. These reveal that the Chang 9 and Chang 7 shales are contemporaneous, belonging to the Ladinian stage of the Middle Triassic. This insight expands the region of the main source rock of Chang 7 to the north...     

Genesis of Fibrous Calcite in the Chang 7 Member of the Yanchang Formation, Ordos Basin, China

To explore the genesis of the laminated calcite veins developed in the black shale of Chang 73 submember of the Ordos Basin, the petrology, microstructure and geochemistry of calcite veins are studied using thin sections, fluid inclusions, trace elements and isotopic geochemistry. The source, the time of formation, the mechanism of formation, and the dynamic background of the veins are discussed. The veins are mostly made up of calcite, mixed with lenticular or spindle-shape solid wall rock inclusions. Three structures are identified in the calcite minerals: fibrous, rhombic cleavage, and wedge-like structure. Trace elements and isotopes of carbon and oxygen confirm that the calcite veins were formed from a high density hydrothermal fluid. It is assumed that calcite veins formed prior to wall rock consolidation during the formation of the Qinling Orogenic Belt in the Middle and Late Triassic. The results show that the sedimentary sources of Chang 73 submember were influenced by hydrothermal materials besides terrigenous detritus. The fibrous calcite is different from the fibrous calcite reported in the morphology and mechanism of formation. In this way, the research complements and improves the morphology and the mechanism of formation of fibrous calcite.     

Perihelion motion of small irregular dust particles due to radiation forces

Perihelion motion, i.e. a secular change of longitude of perihelion, of interplanetary dust particles is investigated under the action of solar gravity and solar electromagnetic radiation. As for spherical particle [Kla?ka, J., 2004. Electromagnetic radiation and motion of a particle. Cel. Mech. Dynam. Astron. 89, 1-61]: (i) perihelion motion is of the order ( is heliocentric velocity of the meteoroid and c is the speed of light in vacuum), if a component of electromagnetic radiation acceleration is considered as a part of central acceleration; (ii) perihelion motion is of the first order in if the total electromagnetic radiation force is considered as a disturbing force. The new facts presented in this paper concern irregular dust particles. Detailed numerical calculations were performed for the grains ejected at aphelion of comet Encke. Perihelion motion for irregular interplanetary dust particles exists already in the first order in for both cases of central accelerations. Moreover, perihelion motion of irregular particles exhibits both positive and negative directions during the particle orbital motion. Irregularity of the grains causes not only perihelion motion, but also dispersion of the dust in various directions, also normal to the orbital plane of the parent body.     

兴隆庄井田奥灰水单孔小口径抽水降距问题分析

针对岩溶发育的大水矿区,在进行小孔径抽水试验工作时,现有的国产压风机虽然尽了最大机械能力,但水位的降低值仍然达不到规范的质量要求,不得不将小孔径抽水试验改为大口径或孔组抽水的情况,采取了加长风管长度,用进口在压风机的方法,完成了兴隆庄井田O2-7号水文孔的小孔径抽水试验工作。从抽水试验的曲线来看,该方法切实可行,有一定推广价值。     

“礼炮”号遥感图像在于桥水库流域土壤侵蚀调查及治理规划中的应用

本文论述了采用前苏联“礼炮”号航天遥感图像作信息源开展天津市于桥水库流域1:10万比例尺土壤侵蚀现状调查与制图、面积量算、分区治理规划措施等项研究工作的方法和结果。并在典型样区初步探讨了遥感调查土壤侵蚀与氮、磷元素流失关系,为天津市人民生活和工农业用水水质富营养化问题的解决提供了科学依据。     

DCS－偶氮胂光度法测定钛酸锶烧结物中游离的氧化锶

ＤＣＳ－偶氮胂光度法测定钛酸锶烧结物中游离的氧化锶胡浩，周宏实江苏海安磷肥厂２２６６００ＤＣＳ－偶氮肿［２－（２－胂酸基苯偶氮）－７－（２，６－二氯－４－磺酸基苯偶氮）－１，８－二羟基－３，６－二磺酸萘］属双偶氮变色酸类显色剂，主要用于稀土元素的高灵...     

Isotope geochemistry of the Tieluping silver-lead deposit, Henan, China: A case study of orogenic silver-dominated deposits and related tectonic setting

The Tieluping silver deposit, which is sited along NE-trending faults within the high-grade metamorphic basement of the Xionger Terrane in the Qinling orogenic belt, is part of an important, recently discovered Mesozoic orogenic-type Ag-Pb belt. Ore formation includes three stages: an early barren quartz-pyrite stage (E), an intermediate polymetallic sulfide ore stage (M), and a late barren carbonate stage (L). Carbon, sulfur and lead isotope systematics indicate that the E-stage fluids are deeply sourced; the L-stage fluids are shallow-sourced meteoric water; whereas the M-stage fluids are a mix of deep-sourced and shallow-sourced fluids. Sulfur and lead isotope data show that the ore-forming fluids must have originated from a source with elevated radiogenic lead and low ³⁴S values, that differs significantly from exposed geologic units in the Xionger Terrane, the lower crust and the mantle. This supports the view that the carbonate-shale-chert sequences of the Guandaokou and Luanchuan Groups south of the Machaoying fault might be the favorable sources, although little is known about their isotopic compositions. A tectonic model that combines collisional orogeny, metallogeny and hydrothermal fluid flow is proposed to explain the formation of the Tieluping silver deposit. During the Mesozoic collision between the North China Craton and South China Block (Early-Mid Triassic Indosinian Orogeny), crustal slabs containing the carbonate-shale-chert sequences of the Guandaokou and Luanchuan Groups, locally rich in organic matter (carbonaceous shale), were thrust northwards beneath the Xionger Terrane along the Machaoying fault. Metamorphic devolatilisation of this underthrust slab probably provided the ore-forming fluids to develop the Ag-Pb ore belt, which includes the Tieluping silver deposit. Fluids and magmas were emplaced during extensional stages related to the Jurassic-Cretaceous Yanshanian Orogeny.Editorial Handling: B. Lehmann     

Elastic and thermoelastic properties of synthetic Ca<Subscript>2</Subscript>MgSi<Subscript>2</Subscript>O<Subscript>7</Subscript> (åkermanite) and Ca<Subscript>2</Subscript>ZnSi<Subscript>2</Subscript>O<Subscript>7</Subscript> (hardystonite)

Elastic and thermoelastic constants of large single crystals of Ca₂MgSi₂O₇ and Ca₂ZnSi₂O₇ have been derived from ultrasonic resonance frequencies of plane-parallel plates and their shift upon variation of temperature, respectively. In addition, coefficients of thermal expansion and dielectric constants were determined. Both species possess quite similar properties. As observed in other isotypic magnesium and zinc compounds, the mean elastic stiffness and the deviation from the Cauchy relations are significantly larger in the zinc compound, due to a covalent contribution of the Zn–O bond. Positive thermoelastic constants T₄₄ and T₆₆ in Ca₂MgSi₂O₇ allow temperature-independent ultrasonic generators and oscillators to be manufactured.     

Static compression of α-Fe<Subscript>2</Subscript>O<Subscript>3</Subscript>: linear incompressibility of lattice parameters and high-pressure transformations

The high-pressure behavior of -Fe₂O₃ has been studied under static compression up to 60 GPa, using a laser-heated diamond anvil cell. Synchrotron-based angular-dispersive X-ray diffraction shows that the sample remains in the corundum structure up to 50 GPa, but with the appearance of coexisting diffraction lines from a high-pressure phase at pressures above 45 GPa. A least-squares fit of low-pressure phase data to an Eulerian finite-strain equation of state yields linear incompressibilities of K _{a 0}=749.5 (± 18.4) GPa and K _{c 0}= 455.7 (± 21.4) GPa, differing by a factor of 1.6 along the two directions. The enhanced compressibility of the c axis may lead to breaking of vertex- or edge-sharing bonds between octahedra, inducing the high-pressure phase transformation at 50 GPa. Analysis of linear compressibilities suggests that the high-pressure phase above 50 GPa is of the Rh₂O₃ (II) structure. Continuous laser heating reveals a new structural phase transformation of -Fe₂O₃ at 22 GPa, to an orthorhombic structure with a=7.305(3) Å, b=7.850(3) Å, and c=12.877(14) Å, different from the Rh₂O₃ (II) structure.