一种符合ISO 14651语义的藏文排序实现方法

本文介绍了一种实现藏文字典序排序的方法,它针对藏文"大字丁字符集"编码方案.通过引入有(无)前加基字符的概念,它把待排序的藏字预处理为有(无)前加基字符、前加字符、基字(基字符或者字丁)、后加字符、再后加字符串后,再行比较,从而避免拆分字丁.本实现方法符合ISO/IEC14651标准语义.

ISO 2022的有限状态机描述

ISO 2022编码体系对字符集国家标准的制订有很大影响,然而标准条款存在不确定性,有时难于理解。本文引入有限状态机(FSM)模型来形式化地刻画ISO 2022的特征。针对FSM五元组,详细说明了其状态空间的构成,提出了输入字母表的等效分类方法,给出了初始状态以及终结状态集合,分析了状态转移函数的规模,并采用FSM描述方法分析了ISO-2022-CN、EUC-CN、复合文本等标准,揭示了这些标准与ISO 2022的内在联系。这些工作有助于ISO 2022标准符合性检测、扩展标准的制订与系统实现复杂度评估。鉴于形式化描述方法在编码字符集标准领域未得到广泛应用,本文工作为该类研究引入了新的思路和方法。

基于ISO/IEC10646标准的藏文操作系统若干问题研究

长期以来尚未有完整的藏文操作系统,原因是藏文文字的特性要求特定的文字处理。本文基于ISO/IEC10646的藏文字符集标准,结合藏文正字法要求,详细分析了藏文操作系统实现中的关键问题:(1)藏文字符集方案比较与藏文存储;(2)藏文输入;(3)藏文显现。藏文显现是公认的“瓶颈”问题。对此,本文提出基于音节划分、使用OpenType字体及相应的文本引擎来解决藏文“叠加”字符的显现。此方案应用于Qt库的实验及相关测试证明基于ISO/IEC10646标准的藏文操作系统实现是较合理的方案。

陕西省汉台区1978年至2006年耕地数量变化及驱动力分析

汉台区是陕西省农业产业结构调整典型示范区,近年来,由于农业产业结构调整、退耕还林还草和建设占用耕地,汉台区耕地数量大量减少,耕地供需矛盾突出。本文利用1978年以来汉台区耕地长序列统计资料和近9年的土地详查与变更数据,研究汉台区土地利用现状及其结构变化、分析汉台区耕地数量变化的基本过程及空间差异、探讨耕地数量变化的主要驱动力。研究结果表明:①1978年～2006年全区耕地共减少5600hm2,平均每年减少200hm2,人均耕地减少0.027hm2,耕地递减率曲线与人均耕地递减率曲线走势基本一致;②建设占用耕地、退耕还林还草和农业结构调整等直接影响因子在4种类型区影响耕地变化差异明显;总体上,农业产业结构调整是全区耕地减少的主导因素,经济发展较快的城镇,建设占用耕地较多;③耕地面积与社会经济发展各因素间的相关系数约低于累计耕地面积与各因素之间的相关系数,说明全区耕地减少与社会经济发展存在时间上的错位性,即经济和社会发展滞后于对耕地资源的占用。

Solvent extraction study of protactinium(V) with methyl-iso-butyl carbinol and methyl-iso-butyl ketone

In order to study the extraction pattern of protactinium in different types of extracting agents and compare the similarity of patterns of extraction with dubnium and thereby unraveling its chemistry, solvent extraction of protactinium(V) with methyl-iso-butyl carbinol (MIBC) and methyl-iso-butyl ketone (MIBK) was studied using Pa-233 as a radiotracer. The extraction efficiencies of Pa were determined as a function of shaking time, concentrations of mineral acids, and extractant concentrations using the two extractants. The results show that MIBK is more suitable for the extraction of protactinium than MIBC in benzene. Furthermore, the effect of the F anion is also discussed.

Liquid-liquid extraction of protactinium(V) using tri-iso-octylamine

Solvent extraction of protactinium with tri-iso-octyl-amine (TIOA) in xylene, benzene, carbon tetrachloride and chloroform from HCl, HF, HNO3, HClO4 and H2SO4 media was studied using Pa-233 as a radiotracer. The extraction efficiencies of protactinium were determined as a function of shaking time, concentrations of mineral acids in aqueous phase, extractant concentrations and diluents in organic phase. The extraction mechanism was discussed. The results show that the extracted species in the organic phase is [(R3N-H)(n)Pa(OH)(x)Cl-y(5-x-y)].

Theoretical study on the formation mechanism of Iso-CH2I-Cl

The dissociation and isomerization reaction mechanism on the ground-state potential energy surface for CH2ClI are investigated by ab initio calculations. It is found that the isomer iso-CH2I-Cl can be produced from either the recombination of the photodissociation. fragments or the isomerization reaction of CH2ClI, rather than from isomerization reaction of iso-CH2Cl-I. Further explanations of experimental results are also presented. (C) 2003 Wiley Periodicals, Inc.

The temporal and spatial evaluation on China's agricultural policy output since 1978

Since reform and opening up, how much contribution has China's implementation of new agricultural policy made to agricultural output? This paper is trying to establish an agricultural policy output econometric model for doing a quantitative analysis of China's new agricultural policy. The results show that China's agricultural policies on agricultural output have an average contribution rate of about 7% since 1978, which is consistent with the OECD's basic forecast. There are obvious temporal and spatial differences. Generally speaking, we can divide the contribution of agricultural policy into three periods, which are the start-up phase from 1978 to 1991 (14 years), the stationary phase from 1992 to 2002 (11 years) and the rising phase from 2003 to 2008 (6 years). In space, the contribution of agricultural policy underwent a process from the all-low in the start-up phase, the gradual increase in the stationary phase to the all-high in the rising phase. Northern and western regions are more sensitive to policies. There are three major factors that can affect the contribution of regional agricultural policies, which are the process of national industrialization strategy, terrain and the level of local finance.

Surface-enhanced resonance Raman spectroscopic study of yeast iso-1-cytochrome c and its mutant

The structural stability and redox properties of yeast iso-1-cytochrome c and its mutant, F82H, were studied by surface-enhanced resonance Raman scattering (SERRS) spectroscopy. Phenylalanine, which exists at the position-82 in yeast iso-1-cytochrome c, is replaced by histidine in the mutant. The SERRS spectra of the proteins on the bare silver electrodes indicate that the mutant possesses a more stable global structure with regard to the adsorption-induced conformational alteration. The redox potential of the mutant negatively shifts by about 400 mV, relative to that of yeast iso-1-cytochrome c. This is ascribed to axial ligand switching and higher solvent accessibility of the heme iron in the mutant during the redox reactions.

X-ray crystal structure and molecular mechanics calculations of (2,6-iso-dipropyl-phenylamide) dimethyl (tetra-methylcyclopenta-dienyl) silane titanium dichloride

Crystal and molecular structure of (2.6-dipropylphenylamide) dimethyl (tetra-methyl cyclopentadienyl) silane titanium dichloride (I) was fully characterized by X-ray diffraction. The crystal is obtained from a mixture of ether/hexane as orthorhombic. with a = 12.658 (3) Angstrom. b = 16.62 (3) Angstrom. c = 11.760 (2) Angstrom. V = 2474.2 (9) Angstrom(3). Z = 4, space group Pnma. R = 0.0399; Componud I compose of the pi-bounded ring with its dimethylsilyl-dipropyl phenyl amido group and the two terminal chloride atoms coordinated to central metal to form a so-called constrained geometry catalyst (CGC) structure. The result of molecular mechanics (MM) calculations on compound I shows that bond lengths and bond angles from the MM calculation are comparable to the data obtained from the X-ray diffraction study. The relation of the structure of CGCs and their catalytic activity by MM calculations is also discussed.