考虑视觉传达效果的震后区域三维图像虚拟重建

传统二维震害图像方法对震后区域进行研究时,由于其拍摄角度具有局限性,震后区域图像的视觉效果不理想。提出基于三维激光扫描技术的震后区域三维虚拟重建方法,采用三维激光扫描仪测量震后区域,获取该区域的点云数据,采用Cyclone软件合并点云数据后,得到震后区域拼接后的整体点云图,将该图点云数据进行去体外孤点、去噪声点以及点云取样等处理后实施封装,在封装的点云数据上采用Sketch模型实施贴图操作,实现视觉传达效果理想的震后区域三维图形的虚拟重建。实验证明,所提方法对震后区域的三维图像虚拟重建结果精度高、视觉效果好。     

基于三维激光扫描技术的摩崖石刻数字化重建

三维激光扫描技术通过高速激光扫描测量的方法,可高效地获取被测对象表面的三维坐标数据,具有速度快、高采样率、无接触性等优点,为快速建立不规则物体的三维重建模型提供了一种全新的技术手段。本文以GLS-1500三维激光扫描仪为基础,介绍了三维激光扫描技术在柳州市龙潭公园摩崖石刻数字化重建中的应用,实现了对摩崖石刻对象的数字化重建,具有实际应用价值。     

Accurate U-Pb Age and Trace Element Determinations of Zircon by Laser Ablation-Inductively Coupled Plasma-Mass Spectrometry

Various zircons of Proterozoic to Oligocene ages (1060-31 Ma) were analysed by laser ablation-inductively coupled plasma-mass spectrometry. Calibration was performed using Harvard reference zircon 91500 or Australian National University reference zircon TEMORA 1 as external calibrant. The results agree with those obtained by SIMS within 2s error. Twenty-four trace and rare earth elements (P, Ti, Cr, Y, Nb, fourteen REE, Hf, Ta, Pb, Th and U) were analysed on four fragments of zircon 91500. NIST SRM 610 was used as the reference material and ²⁹Si was used as internal calibrant. Based on determinations of four fragments, this zircon shows significant intra-and inter-fragment variations in the range from 10% to 85% on a scale of 120 μm, with the variation of REE concentrations up to 38.7%, although the chondrite-normalised REE distributions are very similar. In contrast, the determined age values for zircon 91500 agree with TIMS data and are homogeneous within 8.7 Ma (2 s ). A two-stage ablation strategy was developed for optimising U-Pb age determinations with satisfactory trace element and REE results. The first cycle of ablation was used to collect data for age determination only, which was followed by continuous ablation on the same spot to determine REE and trace element concentrations. Based on this procedure, it was possible to measure zircon ages as low as 30.37 0.39 Ma (MSWD = 1.4; 2 s ). Other examples for older zircons are also given.     

Lidar Methods for Observing Mineral Dust

Lidar methods for observing mineral dust aerosols are reviewed.These methods include Mie scattering lidars,polarization lidars,Raman scattering lidars,high-spectral-resolution lidars,and fluorescence lidars.Some of the lidar systems developed by the authors and the results of the observations and applications are introduced.The largest advantage of the lidar methods is that they can observe vertical distribution of aerosols continuously with high temporal and spatial resolutions.Networks of ground-based lidars provide useful data for understanding the distribution and movement of mineral dust and other aerosols.The lidar network data are actually used for validation and assimilation of dust transport models,which can evaluate emission,transport,and deposition of mineral dust.The lidar methods are also useful for measuring the optical characteristics of aerosols that are essential to assess the radiative effects of aerosols.Evolution of the lidar data analysis methods for aerosol characterization is also reviewed.Observations from space and ground-based networks are two important approaches with the lidar methods in the studies of the effects of mineral dust and other aerosols on climate and the environment.Directions of the researches with lidar methods in the near future are discussed.     

Diamond in metasedimentary crustal rocks from Pohorje,Eastern Alps: a window to deep continental subduction

We report the first finding of diamond and moissanite in metasedimentary crustal rocks of Pohorje Mountains (Slovenia) in the Austroalpine ultrahigh‐pressure (UHP) metamorphic terrane of the Eastern Alps. Microscopic observations and Raman spectroscopy show that diamond occurs in situ as inclusions in garnet, being heterogeneously distributed. Under the optical microscope, diamond‐bearing inclusions are of cuboidal to rounded shape and of pinkish, yellow to brownish colour. The Raman spectra of the investigated diamond show a sharp, first order peak of sp³‐bonded carbon, in most cases centred between 1332 and 1330 cm^?1, with a full width at half maximum between 3 and 5 cm^?1. Several spectra show Raman bands typical for disordered graphitic (sp²‐bonded) carbon. Detailed observations show that diamond occurs either as a monomineralic, single‐crystal inclusion or it is associated with SiC (moissanite), CO₂ and CH₄ in polyphase inclusions_. This rare record of diamond occurring with moissanite as fluid‐inclusion daughter minerals implies the crystallization of diamond and moissanite from a supercritical fluid at reducing conditions. Thermodynamic modelling suggests that diamond‐bearing gneisses attained P–T conditions of ≥3.5 GPa and 800–850 °C, similar to eclogites and garnet peridotites. We argue that diamond formed when carbonaceous sediment underwent UHP metamorphism at mantle depth exceeding 100 km during continental subduction in the Late Cretaceous (c. 95–92 Ma). The finding of diamond confirms UHP metamorphism in the Pohorje Mountains, the most deeply subducted part of Austroalpine units.     

常压混酸溶矿一电感耦合等离子体发射光谱法测定铌钽

混酸溶解矿石样品,在酒石酸介质中,用电感耦合等离子体发生光谱法(ICP-AES)测定溶液中的铌钽。该方法ρ(Nb₂O₅)和ρ(Ta₂O₅)在0～20 μg/mL时,铌钽原子发射光谱强度与浓度呈良好的直线关系,Nb、Ta标准曲线相关系数尺分别为0.999 9和0.999 7。检出限分别为0.023 μg/mL和0.072 μg/mL。本方法测定标准样品,测定值与认定值相符。对实际样品分析,Nh、Ta的相对标准偏差(n=6)分别为0.42％～2.3％和1.8％～3.3％,加标回收率均为97％～103％,适合地质找矿、选冶等领域的样品测试。     

2010—2020年黄河下游河南典型灌区浅层地下水中砷和氟的演化特征及变化机制

黄河下游典型灌区河南段是豫北平原重要的农业种植区。该地区浅层水质整体较差,因常用于作物灌溉或家畜饮用,会对人体健康产生风险,因此对该地区地下水中砷与氟浓度变化特征和机制的研究将有助于提高对该地区地下水污染的认识水平。本文基于2010年和2020年在灌区范围内采集的327组浅层地下水样品,研究区内地下水砷和氟分布情况,并在此基础上对比研究十年间灌区浅层地下水中砷、氟的演化特征,探索分析砷与氟浓度及空间变化机制。研究结果表明：该地区浅层地下水中存在砷与氟超标问题,2020年浅层地下水中高砷（砷浓度大于10μg/L）和高氟（氟浓度大于1mg/L）的样品数量分别占总数的26.1%和26.06%。高砷水分布在太行山前洼地与黄河冲积平原等泥沙互层结构的沉积环境中,还原性较强,同时地下水径流不畅,较强的阳离子交换作用使得其所处环境中Ca2+浓度较高。近十年间砷浓度增加的水样占总数31.8%,砷浓度减少的水样占36.7%。砷浓度的增长（减少）是地下水还原性增强（减弱）使得锰氧化物溶解释放（吸附）导致。近十年间不同地区农业灌溉和水源置换等用水方式导致水位变化是引起砷浓度变化的潜在因素。高氟水主要分布在河南新乡与濮阳的黄河沿线,氟离子浓度受到沉积物中萤石等钙质矿物溶解影响,使得高氟地下水出现在低钙环境中。近十年间研究区中氟离子浓度减少的占总数60.2%,氟离子浓度增加的占32.1%,整体变化趋势向好,但是高氟区中氟离子浓度继续增加。氟浓度的变化同样受到Ca2+变化影响,在Ca2+浓度降低（升高）时氟浓度进一步升高（降低）。地下水中氟升高地区分布在黄河沿线,因此受到黄河水补给影响较大,地下水径流条件较好,阳离子交换作用减弱,使得Ca2+浓度降低,此时地下水中砷浓度受到环境影响而降低,因此研究区氟增加地区中砷与氟的分布和演化呈现反向关系。     

基于三维激光扫描的校园建筑物三维建模研究

"数字校园"建设是科技发展的必然趋势,为加快这一进程,本次研究将地面三维激光扫描技术应用到大学校园。本文以Z+F IM AGER 5010c地面三维激光扫描仪采集到的吉林建筑大学基础实验楼数据为基础,运用3ds max、Auto CAD、Point Cloud等建模软件建立三维模型。同时将依据点云数据建立的实体模型与实际测量数据进行对比和精度分析,验证了地面三维激光扫描仪在建筑物三维模型建立中的精度和可靠性。     

基于地面三维激光扫描的桥梁挠度变形测量

将地面三维激光扫描技术应用到桥梁挠度变形测量。针对桥底面点云的具体特点,采用点云拟合计算方法和重心计算方法,分别获取不同荷载情况下的桥底挠度变化,并进行对比分析,初步确定其变形测量精度,验证了该技术在桥梁挠度变形测量中的可行性。     

Determination of the REE in Geological Reference Materials DTS-1 (Dunite) and PCC-1 (Peridotite) by Ultrasonic and Microconcentric Desolvating Nebulisation ICP-MS

Inductively coupled plasma-mass spectrometry is well suited for the precise, accurate and rapid determination of rare earth elements in most geological samples. However, determination of rare earth elements in certain mantle-derived materials, without applying preconcentration techniques, remains problematical due to low natural concentrations (generally < 1 ng g⁻¹). Consequently, USGS reference materials DTS-1 (a dunite) and PCC-1 (a partially serpentinized harzburgite) have only suggested rather than recommended values for the rare earth elements in reference material compilations. We compared results obtained using two ICP-MS instruments: a U-5000AT ultrasonic nebuliser coupled to a PQ2+ quadrupole ICP-MS and an ELEMENT sector field ICP-MS equipped with a MCN-6000 microconcentric desolvating nebuliser, with the suggested literature values for these two reference materials. Precision and accuracy of analytical methods employed by both instruments were demonstrated by excellent relative standard deviations (< 2%) and inter-laboratory agreement (< 5%) for numerous analyses of BHVO-1 and BIR-1, which are well established with rare earth elements contents at the μg g⁻¹ level. Repeat analyses of DTS-1 and PCC-1 at each laboratory indicate that each method is generally precise to better than 5% at sub-g g⁻¹ levels. Furthermore, values from both instruments generally agree to within 10%. Our DTS-1 and PCC-1 values agree reasonably well with selected data reported in the literature (except for Ce and Sm in DTS-1) but exhibit poorer agreement with reported compilation values. With the demonstrated level of precision and accuracy, we contend that these new values for DTS-1 and PCC-1, generated by two different instruments, are the best estimates of the true whole-rock composition of these samples reported to date.