Accuracy assessment of digital elevation models by means of robust statistical methods

Measures for the accuracy assessment of Digital Elevation Models (DEMs) are discussed and characteristics of DEMs derived from laser scanning and automated photogrammetry are presented. Such DEMs are very dense and relatively accurate in open terrain. Built-up and wooded areas, however, need automated filtering and classification in order to generate terrain (bare earth) data when Digital Terrain Models (DTMs) have to be produced. Automated processing of the raw data is not always successful. Systematic errors and many outliers at both methods (laser scanning and digital photogrammetry) may therefore be present in the data sets. We discuss requirements for the reference data with respect to accuracy and propose robust statistical methods as accuracy measures. Their use is illustrated by application at four practical examples. It is concluded that measures such as median, normalized median absolute deviation, and sample quantiles should be used in the accuracy assessment of such DEMs. Furthermore, the question is discussed how large a sample size is needed in order to obtain sufficiently precise estimates of the new accuracy measures and relevant formulae are presented.     

卫星激光测距的新进展

扼要综述了近几年国际上卫星激光测距的进展，介绍了国内激光测距网的现状，展望了未来卫星激光测距的发展。     

激光天文动力学弱光锁相的研究

近年来激光物理与应用的进展促成了激光天文动力学空间任务概念的提出。在激光天文动力学任务概念研究方面 ,必须对由远程航天器上传回的激光进行讯号的测量与处理。激光经过长距离的传输后 ,功率大幅下降 ,因此在空间任务概念的考虑上 ,弱光锁相是计划中关键性的技术。由航天器射来的激光 ,经过望远镜聚光后与本地激光进行锁相 ,由本地激光承载及传达太空激光的相位信息。实验中 ,我们使用 2支半导体激光泵浦非平面环形共振腔钇镏石激光 (Diodelaserpumpednon -planarringcavityNd :YAGlaser) ,分别代表远程的弱光及代表本地的强光 ,建立弱光锁相环路系统 (weak -lightphase -lockedloopsystem)。以中性光强度滤光器 (ND -filter;neutraldensityfilter)减弱光讯号来仿真远程激光传来的弱光。在相位探测部分使用均衡探测法 ,消除激光强度噪声 ,以提高讯噪比。同时配合适当的环路滤波器 ,控制激光频率 ,提高锁相的能力。对 2nW的弱光与 2mW的强光可长时间锁相 ,其均方根相位误差为 57mrad。 2 0 0pW的弱光与 2 0 0 μW的强光锁相时间可达 2h以上 ,其相位误差为 2 0 0mrad。 2 0pW的弱光与 2 0 0 μW的强光锁相时间亦可达 2h以上 ,其相位误差为 1 60mrad。最后 ,我们对 2pW的弱光与 2 0 0 μW的强光锁相 ,     

Sulfur isotope measurement of sulfate and sulfide by high-resolution MC-ICP-MS

We have developed a technique for the accurate and precise determination of ³⁴S/³²S isotope ratios (δ³⁴S) in sulfur-bearing minerals using solution and laser ablation multiple-collector inductively coupled plasma mass spectrometry (MC-ICP-MS). We have examined and determined rigorous corrections for analytical difficulties such as instrumental mass bias, unresolved isobaric interferences, blanks, and laser ablation- and matrix-induced isotopic fractionation. Use of high resolution sector-field mass spectrometry removes major isobaric interferences from O₂⁺. Standard-sample bracketing is used to correct for the instrumental mass bias of unknown samples. Background on sulfur masses arising from memory effects and residual oxygen-tailing are typically minor (< 0.2‰, within analytical error), and are mathematically removed by on-peak zero subtraction and by bracketing of samples with standards determined at the same signal intensity (within 20%). Matrix effects are significant (up to 0.7‰) for matrix compositions relevant to many natural sulfur-bearing minerals. For solution analysis, sulfur isotope compositions are best determined using purified (matrix-clean) sulfur standards and sample solutions using the chemical purification protocol we present. For in situ analysis, where the complex matrix cannot be removed prior to analysis, appropriately matrix-matching standards and samples removes matrix artifacts and yields sulfur isotope ratios consistent with conventional techniques using matrix-clean analytes. Our method enables solid samples to be calibrated against aqueous standards; a consideration that is important when certified, isotopically-homogeneous and appropriately matrix-matched solid standards do not exist. Further, bulk and in situ analyses can be performed interchangeably in a single analytical session because the instrumental setup is identical for both. We validated the robustness of our analytical method through multiple isotope analyses of a range of reference materials and have compared these with isotope ratios determined using independent techniques. Long-term reproducibility of S isotope compositions is typically 0.20‰ and 0.45‰ (2σ) for solution and laser analysis, respectively. Our method affords the opportunity to make accurate and relatively precise S isotope measurement for a wide range of sulfur-bearing materials, and is particularly appropriate for geologic samples with complex matrix and for which high-resolution in situ analysis is critical.     

Influence of Structural Non-Stationarity of Surface Roughness on Morphological Characterization and Mechanical Deformation of Rock Joints

Summary Structural non-stationarity of surface roughness affects accurate morphological characterization as well as mechanical behaviour of rock joints at the laboratory scale using samples with a size below the stationarity threshold. In this paper, the effect of structural non-stationarity of surface roughness is investigated by studying the scale dependence of surface roughness and mechanical behaviour of rock joints. The results show that the structural non-stationarity mainly affects the accurate characterization of the surface roughness of the fracture samples. It also controls the amount and location of the contact areas during shear tests, which in turn affects the mechanical properties and asperity degradation of the samples. It is concluded that for accurate determination of the morphological and mechanical properties of rock joints at laboratory and field scales, samples with size equal to or larger than the stationarity threshold are required. Author’s address: Nader Fardin, Rock Mechanics Group, Department of Mining Engineering, Faculty of Engineering, University of Tehran, P.O. Box: 11365/4563, Tehran, Iran     

新甘交界红柳河地区二叠纪玄武岩年代学、地球化学及构造意义

新甘交界红柳河地区二叠系剖面中发育有块状和枕状玄武岩,激光ArAr定年确定的玄武岩形成时间在280～300Ma之间;玄武岩SiO_2含量为44.71%～49.27%,Mg~#为42.4～52.4,(~(87)Sr/~(86)Sr)_i为0.703834～0.706819,(~(143)Nd/~(144)Nd)_i为0.518861～0.5121220,ε_(Nd)(t)为-3.01～3.67。玄武岩微量元素、稀土元素和Sr-Nd同位素均显示出与OIB性质相似的特征。其弱富集的不相容元素和轻稀土元素,显示出源区富集的特点。而Zr/Nb(14.63)和Th/U(2.83)则指示岩浆中可能有少量循环原始地幔和亏损地幔物质的加入。综合对比北山南部柳园地区二叠纪玄武岩源区特征,提出红柳河地区早二叠世OIB型玄武岩主要来源于北山地区晚古生代裂谷带下伏已被不同程度改造的富集地幔。     

Shallow Water Bathymetry Derived from Green Wavelength Terrestrial Laser Scanner

Abstract

Shallow water bathymetry has proved to be a challenging task for remote sensing applications. In this work, Green-Wavelength Terrestrial Laser Scanning (GWTLS) is employed to survey nearshore bathymetry under clear atmospheric and water conditions. First, the obtained seabed points were corrected for refraction and then geo-registration, and filtering processes were exerted to obtain an accurate bathymetric surface. Terrain analysis was performed with respect to a reference surface derived from classical surveying techniques. The overall analysis has shown that the best results stem from 35° to 50° incident angles, whereas for angles higher than 65° measurements are not acceptable, although for the same angle in front and close to the instrument accuracy is considered acceptable due to the high laser power. Also, high resolution micro-topography, shallower than 1?m water depth, was managed to be captured. Systematic experimental approaches are expected to improve the GWTLS technique to detect bathymetry, which is anticipated to assist in mapping very shallow foreshore, tidal, and deltaic environments, to contribute conceptual into developing hybrid observation systems for coastal monitoring, and also to be applied in various maritime applications.     

氮气、氧气和空气水合物的合成及其拉曼光谱特征

在-20℃和不同的压力下,在实验室内分别合成了氮气水合物(16MPa)、氧气水合物(13MPa)和空气水合物(15MPa),并对其N—N和O—O键伸缩振动的拉曼光谱特征进行了研究。结果表明,人工合成的水合物中的N—N和O—O键的拉曼位移与天然的空气水合物中的数据十分接近。在氮气水合物和空气水合物中,N—N键的拉曼峰值均为2322.4cm-1;O—O键的拉曼峰值在氧气水合物和空气水合物保持一致,均为1547.8cm-1。空气水合物分解的拉曼谱图表明,它不是氮气水合物和氧气水合物组成的混合物,而是由氮分子和氧分子共同生成的单一水合物,氮分子和氧分子同时进入水合物的大笼和小笼中。与空气中的氮、氧比例相比,水合物中氧分子明显富集,氮分子和氧分子的比例为2.4∶1。     

Laser ablation coupled with ICP-MS applied to U–Pb zircon geochronology: A review of recent advances

Improvements in the technology of laser ablation and ICP-MS instruments make LA-MC-ICPMS a rapid, precise and accurate method for U–Pb zircon geochronology. In this review we describe the main stages of the evolution of this in situ approach from the early 1990s to the present time. Some key points have been progressively improved. The crater size has been reduced to achieve real in situ measurements. The laser wavelength has been reduced as well as the duration of each pulse in order to lower inter-element fractionation. The blank from the gas has to be lowered as far as possible. Double focusing instruments and magnetic field sectors allow flat-topped peaks required for precise isotope ratio measurement to be obtained. The use of a multi-ion counting system significantly improves the sensitivity of the method and the static mode of integration favours the precision of measurement of the transient signal originating from a noisy laser ablated particle beam.Combining the use of a 213 nm UV laser and a MC-ICPMS equipped with a multi-ion counting system operating in static mode, the common precisions achieved for the key ratios ²⁰⁷Pb/²⁰⁶Pb and ²⁰⁶Pb/²³⁸U are better than 1% and 3% (2σ) respectively, including error propagation associated with standard normalization. Until now, the use of a zircon standard has remained necessary to ensure the accuracy of the calculated age. A strategy for common-Pb correction is proposed according to the age of the zircon and according to the Th/U ratio of the grains. After recording sixteen to twenty spot analyses the precision usually achieved on the age is about 1% and even significantly better for Proterozoic samples.In order to show the performance achieved by modern LA-MC-ICPMS geochronology, we tested four zircon samples covering a wide age range from 290 to 2440 Ma. These new age determinations can be compared in term of precision and accuracy since they have already been dated by reference methods (ID-TIMS and SHRIMP). Further developments in the technology of ion counters equipping modern MC-ICPMS and in laser systems will certainly be applied to a large field of geochronology studies in the near future as an alternative to SIMS for in situ age determination.     

Laser probe Ar/Ar dating: History and development from a technical perspective

The ⁴⁰Ar/³⁹Ar method using a laser probe opened the door to microscale measurements and diffusion profiles frozen in samples. In the first decade since the initial application of a laser for ⁴⁰Ar/³⁹Ar dating in 1973, practical applications have been few. This is due not only to the fact that the laser and vacuum technologies were immature but that mass spectrometry was also in its infancy. In those days, the sensitivity of a mass spectrometer was generally insufficient to measure the small amount of argon degassed from a geological sample by a laser. These problems have subsequently been solved by new technologies. To understand their current status, a brief history of their development is outlined. This outline focuses on the required detection limit in micro scale measurement, practical approaches for accurate measurement are explained through examples in our laboratory specifically relating to the technical aspects of ⁴⁰Ar/³⁹Ar dating.