浙江省连续运行卫星定位服务系统技术设计与试验

区域连续运行卫星定位服务系统可为用户提供包括实时高精度位置信息在内的多功能服务系统,近几年,在国内外得到迅速地发展。浙江省有十万多平方公里的陆地面积,如何在如此大的范围内建设连续运行卫星定位服务系统是本文的主要研究内容。本文在充分分析目前相关技术和设备的基础上,从浙江省的实际情况出发,制定科学合理的系统指标以及建设方案,满足系统的科学建设和正常运行的指导要求,并通过试验进行了验证。     

GPS单点测速的误差分析及精度评价 (英文)

Error sources which decrease the accuracy of GPS in absolute velocity determination have been changed since SA was turned off. Firstly, quantities of all kinds of error sources that influence velocity determination are analyzed. The potential accuracy of GPS absolute velocity determination is derived from both theory and field GPS data simulation. After that, two tests were carried out to evaluate the performance of GPS absolute velocity determination in the case of a static and an airborne GPS receiver and INS （Inertial Navigation System） instrument in kinematic mode. In static mode, the receiver velocity has been estimated to be several mm/s with the carrier-phase derived Doppler measurements, and several cm/s with the receiver generated Doppler measurements. In kinematic mode, GPS absolute velocity estimates are compared with the synchronized measurements from the high accuracy INS. The root mean square statistics of the velocity discrepancies between GPS and INS come up to dm/s. Moreover, it has a strong correlation with the acceleration or jerk of the aircraft.     

松散沉积物中天然气水合物生成、分解过程与声学特性的实验研究

为了解松散沉积物中天然气水合物的生成和分解规律以及水合物对沉积物声学特性的影响,在粒径为0.18~0.28mm天然沙中进行了甲烷水合物的生成和分解实验,并利用超声波探测技术和时域反射技术实时测量了反应体系的声学参数与含水量。结果表明:根据水合物的生成和分解速率,可将水合物的生成过程分为初始生长期、快速生长期和稳定期3个阶段,分解过程可分为初始分解期和样品表层水合物快速分解期以及样品内、外层水合物均快速分解期3个阶段;由温度和压力数据的分析,得出水合物先在沉积物表层生长,然后在沉积物内、外层迅速生成;由水合物分解过程3个阶段的平均分解率,得出水合物的分解是一个由慢到快的过程。对声学参数的研究表明:水合物在松散沉积物中先胶结骨架颗粒而生成,使纵波速度和声波衰减在饱和度0~1%之间陡然增大;随后水合物开始在沉积物孔隙中形成悬浮粒子,造成超声波信号在饱和度1%~90%间淬熄,声波速度无法获取。研究结果在揭示沉积物中水合物与颗粒间接触机制的同时,为海上地球物理勘探中地震信号的解释提供了新的思路。     

欧北地区深层三维地震采集技术

辽河盆地由于其特殊的地震地质条件,以往采集的深层地震资料信噪比和分辨率都较低,已经严重制约了油田的进一步勘探和开发.为了彻底摆脱地震资料品质对勘探工作的束缚,努力提高资料的信噪比和分辨率,辽河油田首先选择辽河盆地东部凹陷欧利坨子北为突破口,通过采取最佳岩性激发、有效弱信号保护和变观测系统施工等一系列的技术措施,取得了较好的效果.     

四川省九龙县娃娃沟泥石流运动特征与堵河成灾机制分析

2006年7月16日娃娃沟流域暴发的大规模泥石流,给下游3个电站造成巨大经济损失,是大渡河流域一次典型的灾害性泥石流。分析得出,娃娃沟泥石流重度高、搬运能力强,泥石流固体物质砂、石混杂,粗大砾石含量高;暴发频率低、规模大,流速及峰值流量分别高达10．78m／s及798．5m^3／s;在汇口处,泥石流堆积物堵塞河道是引起下游电站受灾的重要原因,高重度、粗颗粒、大流量的组合是此次泥石流堵江的重要原因。堵河判别计算结果显示在发生百年一遇泥石流时,该断面均有发生堵河的可能。娃娃沟泥石流表明：①在大渡河支流的泥石流沟周边的中小电站极有可能在泥石流暴发时受到破坏。因此,电站建设过程中应加强对周边泥石流沟的防灾减灾工作;②虽然娃娃沟流域植被良好,但仍然发生了大规模泥石流。表明植被不能完全避免泥石流的发生,对于此类泥石流沟不能疏忽大意。     

连续运行GPS定位服务系统的探讨

介绍了连续运行GPS定位服务的概念、实现模式及其在测绘行业中的应用。     

GPS RTK校准检测试验场建设的研究

叙述了GPSRTK接收机校准检测试验场建设的方法,介绍了GPSRTK接收机校准检测的步骤,提出了GPSRTK校准检测的项目和结果判定方法,为未来的GPSRTK国家检定规程的出台做了有益地探索。     

Zircon M257 ‐ a Homogeneous Natural Reference Material for the Ion Microprobe U‐Pb Analysis of Zircon

We introduce and propose zircon M257 as a future reference material for the determination of zircon U‐Pb ages by means of secondary ion mass spectrometry. This light brownish, flawless, cut gemstone specimen from Sri Lanka weighed 5.14 g (25.7 carats). Zircon M257 has TIMS‐determined, mean isotopic ratios (2s uncertainties) of 0.09100 ± 0.00003 for ²⁰⁶pb/²³⁸U and 0.7392 ± 0.0003 for ²⁰⁷pb/²³⁵U. Its ²⁰⁶pb/²³⁸U age is 561.3 ± 0.3 Ma (unweighted mean, uncertainty quoted at the 95% confidence level); the U‐Pb system is concordant within uncertainty of decay constants. Zircon M257 contains ～ 840 μg g^?1 U (Th/U ～ 0.27). The material exhibits remarkably low heterogeneity, with a virtual absence of any internal textures even in cathodoluminescence images. The uniform, moderate degree of radiation damage (estimated from the expansion of unit‐cell parameters, broadening of Raman spectral parameters and density) corresponds well, within the “Sri Lankan trends”, with actinide concentrations, U‐Pb age, and the calculated alpha fluence of 1.66 × 10¹⁸ g^?1. This, and a (U+Th)/He age of 419 ± 9 Ma (2s), enables us to exclude any unusual thermal history or heat treatment, which could potentially have affected the retention of radiogenic Pb. The oxygen isotope ratio of this zircon is 13.9%o VSMOW suggesting a metamorphic genesis in a marble or calc‐silicate skarn.     

Composition-Induced Variations in SIMS Instrumental Mass Fractionation during Boron Isotope Ratio Measurements of Silicate Glasses

An analytical artefact is reported here related to differences in instrumental mass fractionation between NIST SRM glasses and natural geological glasses during SIMS boron isotope determinations. The data presented demonstrated an average 3.4‰ difference between the NIST glasses and natural basaltic to rhyolitic glasses mainly in terms of their sputtering-induced fractionation of boron isotopes. As no matrix effect was found among basaltic to rhyolitic glasses, instrumental mass fractionation of most natural glass samples can be corrected by using appropriate glass reference materials. In order to confirm the existence of the compositionally induced variations in boron SIMS instrumental mass bias, the observed offset in SIMS instrumental mass bias has been independently reproduced in two laboratories and the phenomenon has been found to be stable over a period of more than one year. This study highlights the need for a close match between the chemical composition of the reference material and the samples being investigated.     

Recommended Values of 239Pu, 240Pu and 239+240Pu Concentrations in Reference Material IAEA-315 (Marine Sediment) Estimated by Thermal Ionisation Mass Spectrometry, Inductively Coupled Plasma-Mass Spectrometry and Alpha Spectrometry

The recommended concentrations of ²³⁹Pu, ²⁴⁰Pu and ^239+240Pu in reference material IAEA‐315 (marine sediment) were estimated by three analytical methods: isotope dilution thermal ionisation mass spectrometry (TIMS), isotope dilution inductively coupled plasma‐mass spectrometry (ICP‐MS) and alpha spectrometry. The determination of ²³⁹Pu and ²⁴⁰Pu (^239+240Pu by alpha spectrometry) was carried out with samples from randomly selected bottles using each method. Plutonium‐238 was also measured by alpha spectrometry. A plutonium‐242 reference material was used as a spike for the quantitative analysis. The influence of ²⁴²Pu in the samples was therefore calculated; however, this contribution was less than the range of uncertainty and did not influence the final results. The obtained data were statistically analysed using variance component analysis and paired comparison. The combined standard uncertainties from “method/measurement”, “bottle” and “sub‐sample” were in the order of 3 to 6%. The main contributions to the uncertainty were from the material heterogeneity and from systematic differences between methods. Based on this study with twenty‐seven analyses using 10–14 g sample mass, concentrations of (38 ± 3) Bq kg^?1, (28 ± 3) Bq kg^?1 and (66 ± 4) Bq kg^?1 are proposed as recommended values for ²³⁹Pu, ²⁴⁰Pu and ^239+240Pu, respectively, and (9.5 ± 0.4) Bq kg^?1 for ²³⁸Pu as an information value in reference material IAEA‐315. In mass concentration units, these amount to (16.4 ± 1.2) ng kg^?1, (3.3 ± 0.4) ng kg^?1 and (0.015 ± 0.003) ng kg^?1 for ²³⁹Pu, ²⁴⁰Pu and ²³⁸Pu, respectively. The certified reference materials NIST 4350B and NIST 4354 were also analysed by TIMS for quality assurance of the method used in this study.