Biotite Reference Materials for Secondary Ion Mass Spectrometry 18O/16O Measurements

Five new biotite reference materials were calibrated at the SwissSIMS laboratory (University of Lausanne) for oxygen isotope determination by secondary ion mass spectrometry (SIMS) and are available to the scientific community. The oxygen isotope composition of the biotites, UNIL_B1 to B5, was determined by laser‐heating fluorination to be 11.4 ± 0.11‰, 8.6 ± 0.15‰, 6.1 ± 0.04‰, 7.1 ± 0.05‰ and 7.6 ± 0.04‰, respectively. SIMS analyses on spots smaller than 20 μm gave a measurement repeatability of 0.3‰ (2 standard deviation, 2s). The matrix effect due to solid solution in natural biotite could be expressed as a linear function of X_Mg and X_F for biotite. No effect was found for different crystallographic orientations. SIMS analysis allows the oxygen isotope composition of biotite to be measured with a measurement uncertainty of 0.3–0.4‰ (2s) for biotites with similar major element compositions. A measurement uncertainty of 0.5‰ (2s) is realistic when F poor biotites (lower than 0.2% m/m oxides) within the compositional range of X_Mg of 0.3–0.9 were compared from different sessions. The linear correlation with F content offers a reasonable working curve for F‐rich biotites, but additional reference materials are needed to confirm the model.     

Field experiment and numerical study on active vibration isolation by horizontal blocks in layered ground under vertical loading

In this paper, a series of field experiments were carried out to investigate the active vibration isolation for a surface foundation using horizontal wave impedance block (WIB) in a multilayered ground under vertical excitations. The velocity amplitude of ground vibration was measured and the root-mean-square (RMS) velocity is used to evaluate the vibration mitigation effect of the WIB. The influences of the size, the embedded depth and the shear modulus of the WIB on the vibration mitigation were also systematically examined under different loading conditions. The experimental results convincingly indicate that WIB is effective to reduce the ground vibration, especially at high excitation frequencies. The vibration mitigation effect of the WIB would be improved when its size and shear modulus increase or the embedded depth decreases. The results also showed that the WIB may amplify rather than reduce the ground vibration when its shear modulus is smaller or the embedded depth is larger than a threshold value. Meanwhile, an improved 3D semi-analytical boundary element method (BEM) combined with a thin layer method (TLM) was proposed to account for the rectangular shape of the used WIB and the laminated characteristics of the actual ground condition in analyzing the vibration mitigation of machine foundations. Comparisons between the field experiments and the numerical analyses were also made to validate the proposed BEM.     

黑海参脂肪酸的气相色谱／质谱法分析

黑海参（Holothuria atra）体壁经Folch法提取总脂,用HCl-甲醇进行甲酯化处理,以气相色谱／质谱法分析总脂中的脂肪酸组成。从黑海参中共分析出28种化合物,包括25种脂肪酸甲酯和3种脂肪醛二甲基缩醛。黑海参体壁中的饱和脂肪酸含量为22．93％,以C16：0（5．49％）和C18：0（4．38％）为主;不...     

Preservation of coal-waste geochemical markers in vegetation and soil on self-heating coal-waste dumps in Silesia,Poland

Occurrence and distributions of geochemical markers on vegetation and in soils covering two self-heating coal waste dumps were investigated with gas chromatography-mass spectrometry (GC–MS) and compared with those of bitumen expelled on the coal waste dump surface. Presence of biomarkers, alkyl aromatic hydrocarbons, polycyclic aromatic hydrocarbons (PAHs), and such polar compounds as phenols indicate that components of self-heating coal wastes indeed migrate to soils and plants surface and their characteristic fingerprints can be applied in passive monitoring to investigate migration of contaminants from self-heating coal wastes. Moreover, results allow to discriminate between the Upper- and Lower Silesian coal basins, notwithstanding value shifts caused by heating. Mechanisms enabling the migration of geochemical compounds into soils include mixing with weathered coal-waste material, transport in gases emitted due to self-heating and, indirectly, by deposition of biomass containing geochemical substances. Transport in gases involves mostly lighter compounds such as phenols, methylnaphthalenes, methylbiphenyls, etc. Distributions and values of geochemical ratios are related to differences in their boiling temperatures in the case of lighter compounds but preserve geochemical features in the case of heavier compounds such as pentacyclic trierpanes.     

敞开酸溶-电感耦合等离子体发射光谱法测定石煤钒矿中钒铁铝磷

石煤钒矿资源的勘探、研究和利用均需对其成分进行准确的分析测试,其中钒、铁、铝、磷等主要成分的测定尚未建立标准方法,当前所用的分析测试方法各有不足。采用碱熔电感耦合等离子体发射光谱法(ICP-OES)测定石煤钒矿样品时,高浓度的可溶性盐会导致高背景,干扰测定。酸溶法可避免上述问题,但由于常规的氢氟酸-盐酸-硝酸-高氯酸四酸体系不能消除碳和有机质对样品的吸附和包裹,待测成分无法完全释放,需先将样品高温灼烧除碳,过程繁琐。本文采用少量硫酸加四酸的五酸体系处理样品,电热板加热,盐酸浸提,利用硫酸的强氧化性将样品中大量的碳氧化成二氧化碳,免却了灼烧除碳流程,消除了含碳物质对样品的吸附和包裹,显著增强了消解效果。由此建立了ICP-OES测定石煤钒中钒、铁、铝、磷的分析方法,在称样量为0.1g、浓硫酸加入量为0.30mL时,样品消解率达到99%以上。方法检出限为17~51mg/kg,相对标准偏差(RSD, n=11)在1.7%~5.1%之间;相对误差为-4.6%~2.7%。该方法背景低、测定结果准确,可满足石煤钒矿石样品的检测要求。     

磁暴期间极光椭圆与极盖区电离层效应比较研究--F区负暴

联合利用EISCAT和E-Svalbard非相干散射雷达数据,研究l997年5月强磁暴期间向阳侧极盖与极光椭圆区电离层F区负暴.发现在磁暴主相和恢复相初期,极光椭圆和极盖区电离层都在大约l90km高度出现类似F1的峰,F2主峰完全消失,F区电子密度大幅度下降.但离子温度的变化在两个区域很不相同,在极光椭圆区大幅度升高,而在极盖区没有显著变化,反映出引起F区负暴的主要机制在两个区域不尽相同.强对流电场引起大气焦耳加热与离子增温而使O+离子消失的化学反应速率增大所导致的电离损失,对极光椭圆区负暴起主要作用;而输运过程,特别是持续长达数小时的沿场上行离子流,对极盖区负暴起重要作用.磁暴主相期间,当EISCAT雷达位于等离子体对流涡旋转换区下方时,在无焦耳加热与离子摩擦增温的情况下,观测到由顶部电离层O+离子沿场高速外流引起的F区电子密度耗空.     

Structure of the earth's crust in Jordan from potential field data

Gravity and magnetic data were collected and used to study the crustal structure of Jordan. Three new geophysical maps of Jordan were created: a Moho discontinuity map, a crystalline basement surface map, and a map showing the lowest limit of magnetic blocks. Depths of the Curie Isotherm were also calculated. Results indicate that the depth to the Moho discontinuity in Jordan varies from 32 to 33 km in the northwest to 38 km in the southeast. The basement complex rocks outcrop on the surface in the southwest but lie at about 8 km in the northeast. The Curie Isotherm (585 °C) lies at a depth of about 10 km in the area east of the Dead Sea and dips southeastward towards the Al-Sirhan (Wadi Sirhan), southeast Jordan, where it is located at 35 km depth. Local isostasy of rock masses (blocks) in Jordan does not occur. Nevertheless, this does not rule out the possible existence of isostasy in a regional scale at greater depths within the mantle.     

Rapid cooling and geospeedometry of granitic rocks exhumation within a volcanic arc: A case study from the Central Slovakian Neovolcanic Field (Western Carpathians)

U–Pb Sensitive High‐Resolution Ion MicroProbe (SHRIMP) dating of zircon in combination with (U–Th)/He dating of zircon and apatite is applied to constrain the emplacement and exhumation history of the youngest granitic rocks in the Western Carpathians collected in the Central Slovakian Neovolcanic Field. Two samples of diorite from the locality Banky, and granodiorite from Banská Hodru?a yield the U–Pb zircon concordia ages of 15.21 ±0.19 Ma and 12.92 ±0.27 Ma, respectively, recording the time of zircon crystallization and the intrusions’ emplacement. Zircon (U–Th)/He ages of 14.70 ±0.94 (Banky) and 12.65 ±0.61 Ma (Banská Hodru?a), and apatite (U–Th)/He ages of 14.45 ±0.70 Ma (diorite) and 12.26 ±0.77 Ma (granodiorite) are less than 1 Myr younger than the corresponding zircon U–Pb ages. For both diorite and granodiorite rocks their chronological data thus document a simple cooling process from magmatic crystallization/solidification temperatures to near‐surface temperatures in the Middle Miocene, without subsequent reheating. Geospeedometry data suggest for rapid cooling at an average rate of 678 ±158 °C/Myr, and the exhumation rate of 5 mm/year corresponding to active tectonic‐forced exhumation. The quick cooling is interpreted to record the exhumation of the studied granitic rocks complex that closely followed its emplacement, and was likely accompanied by a drop in the paleo‐geothermal gradient due to cessation of volcanic activity in the area.     

流动注射-氢化物发生原子荧光法测定海洋沉积物样品中痕量铅

铅是一种具有累积性的有害元素,是海洋监测调查中沉积物介质的必测元素之一,常用测定方法有双硫腙分光光度法、火焰原子吸收光谱法、无火焰原子吸收光谱法等[1],前两种方法灵敏度较低,测定时一般需要预富集,操作较繁琐;后一种方法虽然灵敏度高,但仪器昂贵,对操作人员要求高.氢化物发生原子荧光法由于灵敏度高、检出限低且线性范围宽,在铅的分析中日益被重视.     

乙醇增强—电感耦合等离子体质谱法直接测定地质样品中碲

建立了HF—HN03密封酸溶以及Na2O2熔融处理样品,乙醇增强灵敏度,电感耦合等离子体质谱直接测定地质样品中微量和超痕量碲的方法。样品溶液中加入乙醇(φ＝4％),在0．85L/min的载气流速下,碲信号可增强2．5倍以上。碲的方法检出限(100,DF＝1000)为0．02μg/g。用土壤和水系沉积物国家一级标准物质验证了方法的准确度,标准物质的绝大多数分析结果与标准值的误差在允许范围内。分析了大洋多金属结核样品及深海沉积物样品中的微量碲,结果与其他方法相符,精密度试验RSD(n＝3)＜10％。