Kirchhoff型反偏移场稳相分析(英文)

在文献中,Kirchhoff型反偏移场的稳相分析主要是在下列两个条件下进行的:(1)等时面和目标反射面相切;(2)深度偏移像场信号的长度接近于零。对于与目标反射面不相切的等时面和长度远大于零的深度偏移像场子波,已有的结果将不再成立。为了在等时面和目标反射面不相切和深度偏移像场的子波长度远大于零的条件(一般条件)下对Kirchhoff型反偏移场进行稳相分析,我推导了出现在二维稳相分析公式中的诸因子的计算公式,并从中发现:(1)对于不同的等时面,距离差函数的稳相点具有不同的水平坐标;(2)Kirchhoff型真振幅反偏移的输出场由两部分(真振幅反偏移信号与振幅畸变因子)的乘积组成。由此得到下列两个结论:(1)一个给定的反偏移信号由多个深度偏移信号上的采样点组装而成,反偏移信号上的采样点个数等于对于这种组装有贡献的偏移信号的个数。(2)振幅畸变效应是Kirchhoff型反偏移中的固有效应,靠反偏移本身无法消除。如果一定要消除这种振幅畸变效应,必须对反偏移结果进行振幅校正。     

Stationary phase approximation in the ambient noise method revisited

The method of extracting Green's function between stations from cross correlation has proven to be effective theoretically and experimentally.It has been widely applied to surface wave tomography of the crust and upmost mantle.However,there are still controversies about why this method works.Snieder employed stationary phase approximation in evaluating contribution to cross correlation function from scatterers in the whole space,and concluded that it is the constructive interference of waves emitted by the scatterers near the receiver line that leads to the emergence of Green's function.His derivation demonstrates that cross correlation function is just the convolution of noise power spectrum and the Green's function.However,his derivation ignores influence from the two stationary points at infinities,therefore it may fail when attenuation is absent.In order to obtain accurate noise-correlation function due to scatters over the whole space,we compute the total contribution with numerical integration in polar coordinates.Our numerical computation of cross correlation function indicates that the incomplete stationary phase approximation introduces remarkable errors to the cross correlation function,in both amplitude and phase,when the frequency is low with reasonable quality factor Q.Our results argue that the distance between stations has to be beyond several wavelengths in order to reduce the influence of this inaccuracy on the applications of ambient noise method,and only the station pairs whose distances are above several (5) wavelengths can be used.     

面向对象的极高海拔区水体及冰川信息提取——以珠穆朗玛峰国家级自然保护区核心区为例

极高海拔地区多为河流发源、冰川发育地,由于地形起伏强烈,且野外考察验证工作困难,传统的遥感信息提取方法很难保证该地区水体及冰川的提取精度。本文基于ASTER影像,运用面向对象的图像信息自动分析方法,对珠穆朗玛峰国家级自然保护区核心区的水体及冰川信息进行了提取研究。为保证信息提取的准确度,将数字高程模型(DEM)及其衍生数据(坡度、坡向),归一化植被指数(NDVI)数据,及有助于区分水体、冰川与其他地物的相关指数(冰雪指数NDSII)及波段运算结果(b1-b3)、(b3/b4)等,分别作为一个波段叠加到原始图像中,使之成为对目标地物光谱特征的有益补充。并对不同类型的水体及冰川进行多级、多尺度分割,以满足其对分割尺度的不同要求。分割完成后,综合考虑目标地物的光谱特征、纹理特征、空间结构特征,根据各特征指数的直方图信息,设定合适的阈值,建立了各水体及冰川类型信息提取的知识规则,并结合实地调查对信息提取的精度进行验证,改进了ASTER遥感影像自动快速提取极高海拔区水体及冰川信息的实用模型。     

元启发式搜索策略在构造模糊分类系统中的应用

论述了使用模拟退火元启发式搜索策略构造模糊分类系统的过程,目的是利用模拟退火原理研制一种精确的模糊分类器,改善与分类问题有关的搜索空间探索与发掘的性能,找到模糊if-then规则的优化集。算法可以从输入数据集中抽取精确的模糊分类规则,并在若干不同预定义类中将其应用于对新数据实例的分类。     

主应力轴循环旋转下高密实粉土稳定性影响研究

为研究主应力轴循环旋转对粉土性状影响,对长江入海口高密实饱和粉土进行了主应力轴180°转幅的循环旋转试验。试验发现,等向固结的高密实粉土在恒定动剪应力比的主应力轴循环旋转下能发生孔压达到初始围压水平的液化破坏,但液化前孔压开展会因动应力水平的不同而呈现以渐变相态点和激变相态点区分的3阶段变化形式,或仅以激变相态点区分的两阶段变化形式。试样应变开展则始终呈现由崩塌点区分的两阶段变化形式,且孔压激变相态点与应变崩塌点同步反映了土体结构崩塌状态,崩塌状态时主应变差双向幅值限制在0.2%～0.4%这一较小范围内。试样进行主应力轴旋转达到崩塌时的应力状态与频率无显著关系,可由 - 空间中一条准不稳定状态线归一化。而以崩塌状态为终点进行归一化的主应力轴循环旋转下孔压振次曲线,可用修正的Seed公式进行较好拟合     

垃圾填埋场衬垫系统穿刺性能评价

垃圾中含有铁、玻璃和陶瓷等尖锐物,在荷载作用下极有可能使衬垫系统发生破坏,导致渗滤液流入地下污染周边环境,如何正确评价衬垫系统的穿刺性能很重要。考虑材料的抗拉强度、厚度以及穿刺棒的直径提出了衬垫系统穿刺力的评价公式,并与试验结果进行了比较。结果表明,单层土工膜的抗穿刺力试验结果与评价值比较吻合,但由土工膜与无纺布组成的衬垫系统抗穿刺力的试验值与评价结果有一定偏差;土工膜与无纺布一起使用能大幅度提高衬垫系统的抗穿刺能力,因此土工膜上应铺设无纺布有利于保护衬垫系统;土工膜的抗拉强度越大,抗穿刺能力越强;基础的存在能在一定程度上提高衬垫系统的抗穿刺性能。所得结果对垃圾填埋场衬垫系统的设计具有一定的指导意义     

基于迭代法的同轴法X射线相衬成像的相位复原

相位复原问题是指在只有强度可以测量的情况下,从强度数据中提取出物体的相位信息。相位复原是同轴法X射线相衬成像的关键问题之一。本文采用误差递减法,通过限制物体的空间大小,结合测量到的强度数据,在物体的空域和频域都进行约束。通过反复迭代,进行带宽外推,最终实现物面和像面的相位复原。仿真实验证明了此迭代算法的收敛性,并且以塑料管为样品,在上海光源采集到同轴法X射线相衬成像的实验数据,对上述算法进行了验证。     

Selective Solid Phase Extraction for Separation and Preconcentration of Palladium from Gold Ore and Anode Slime after Complexation with a N4O2 Mixed Donor Ligand Derivative

A selective and sensitive method for the preconcentration, separation, and determination of palladium with flame atomic absorption spectrometry using 4,15‐bis[(4‐methylphenyl)sulfonyl]‐20,21‐dinitro‐2,3,4,5,6,7,9,10,12,13,14,15,16,17‐tetradecahydro‐8,11‐ethano‐1,18,4,8,11,15‐benzodioxa tetraaza cycloicosine (TNACIN) on XAD‐2010 was developed. TNACIN–Pd(II) complex formed acidic aqueous solution (0.075–0.100 M HNO₃) was accumulated on XAD‐2010 and then eluted with 1 M HCl in acetone. The effects of some analytical parameters including pH, TNACIN amount, sample volume, eluent type, and concentration, sample flow rate and matrix ions were studied for optimization of the method. Detection limit and precision were calculated for Pd(II). This method was also verified with CRM and internal standard, and satisfactory results were obtained.     

Metal Ion Extraction with Bipyridine Derivatives as Chelating Ligands in Supercritical Carbon Dioxide

Three fluorinated bipyridine ligands have been designed and synthesized as chelating agents for the extraction of metal ions in supercritical CO₂ (sc‐CO₂). The ligand solubilities in sc‐CO₂ were investigated at different temperatures and pressures, and the measured data have been correlated using a semiempirical model. The calculated results showed satisfactory agreement with the experimental data. Based on these data, metal ion extraction with the three compounds as chelating agents in sc‐CO₂ was performed from spiked filter paper, whereby ligand 1 showed the highest extraction efficiency, especially for Ni²⁺ and Cu²⁺. The extraction constants, K_ex, of the three chelating ligands were seen to increase with increasing extraction efficiency for the same metal ion in the same extraction system.     

Application of the Response Surface Method for Optimization of Headspace Liquid Phase Microextraction of Trihalomethanes in Drinking Water

An optimized analysis method based on headspace liquid phase microextraction (HS‐LPME) and gas chromatography coupled with mass spectrometry was proposed for the determination of trihalomethanes (THMs) in drinking water. The response surface method (RSM) was used to optimize the extraction of THMs for analysis by HS‐LPME. The temperature, extraction time and NaCl concentration were found to be important extraction parameters. The coefficient of determination (R²) for the model was 94.97%. A high probability value (P < 0.0001) for the regression indicated that the model had a high level of significance. The optimum conditions were seen to be: temperature 42.0°C, NaCl concentration 0.30 g/mL, and extraction time 28 min. The response variable was the summation of the THMs chromatography peak areas and the reproducibility of this was investigated in five replicate experiments under the optimized conditions. The relative standard deviations (RSD%) of the THMs ranged from 8.0–11.6%. The limits of detection (LODs), based on a signal‐to‐noise ratio (S/N) of three ranged from 0.42–0.78 μg/L, and were lower than the maximum limits for THMs in drinking water established by the WHO.