GIS技术在旅游业中的应用——兼谈旅游地理信息系统及其研究进展与展望   总被引：1，自引：0，他引：1  

刘德辉 《测绘与空间地理信息》2008,31(1):90-92

本文对地理信息系统的组成与功能做了简单的概述,在此基础上介绍了GIS在旅游业发展中的主要作用及应用现状,并就旅游地理信息系统的结构与功能及其研究进展和发展趋势做了探讨。  相似文献   

河南板厂银多金属矿床钾长石氩-氩年龄及其地质意义   总被引：4，自引：0，他引：4  

李厚民  王登红  郭保健  陈毓川  白凤军  仇建军 《地球学报》2008,29(2):154-160

河南内乡板厂矿床通过近年来的勘查工作,为一大型斑岩-热液型银铜铅锌(钼)矿床.本文对该矿床斑岩型铜矿石中钾长石进行了Ar-Ar定年,获得两个年龄坪:900～1150℃年龄坪包括了43.4%的39Ar,坪年龄为(148.1±1.6)Ma,反等时线年龄为(145.7±2.3)Ma;1200～1450℃年龄坪包括了48.8%的39Ar,坪年龄为(161.0±1.6)Ma,反等时线年龄(159.0±14.0)Ma.前者代表了该矿床的成矿年龄,后者代表了含矿斑岩的成岩年龄.该二阶段年龄谱特征反映了板厂矿床成岩成矿的阶段性.在我国不少矿区的Ar-Ar法年龄谱上均有多坪显示,这与我国许多矿区成矿作用和构造事件的多期多阶段特征一致.  相似文献   

氧化锰矿物的生物成因及其性质的研究进展   总被引：5，自引：0，他引：5  

刘凡  冯雄汉  陈秀华  邱国红  谭文峰  贺纪正 《地学前缘》2008,15(6):66

土壤中的氧化锰矿物是原生矿物风化和成土过程的产物,是最具反应活性的一类矿物,决定着环境中许多物质的形态、迁移和转化,在元素生物地球化学循环中起着重要的作用,其形成机制和环境效应备受关注。已有的研究表明,环境中氧化锰的形成与微生物作用紧密相关,微生物作用可使自然环境中的Mn(Ⅱ)氧化速率提高105倍。参与Mn(Ⅱ)氧化的微生物在环境中广泛存在,已知的典型锰氧化细菌分布在变形菌门、放线菌门或厚壁菌门,它们均通过胞外聚合物中的多铜氧化酶来催化氧化Mn(Ⅱ)。细菌氧化Mn(II)成Mn(Ⅳ)是酶催化的两个连续的快速单电子传递过程,Mn(Ⅲ)在溶液中以与酶结合的瞬时中间态出现。生物形成氧化锰的最初形态为层状锰矿物,与δ-MnO2或酸性水钠锰矿很类似,且结晶弱,粒径小,锰氧化度高,结构中的八面体空穴多,因而比化学形成的氧化锰具有更强的吸附、氧化等表面活性。环境中Mn(Ⅱ)微生物氧化及形成的Mn(Ⅲ)中间体与碳、氮、硫等生命元素的地球化学循环的关系令人关注。  相似文献   

谈测绘项目管理   总被引：4，自引：0，他引：4  

周萌萌  黄鑫雄 《现代测绘》2008,31(4)

本文从工程项目管理学的观点,结合测绘项目的特殊性,阐述了测绘项目管理的基本方法和要求,内容包括测绘项目组织与程序、计划、质量、进度与合同管理等。  相似文献   

Actinic flux and photolysis frequency comparison computations using the model PHOTOGT     

Carsten Blindauer  Vladimir Rozanov  John Philip Burrows 《Journal of Atmospheric Chemistry》1996,24(1):1-21

The accurate radiative transfer model GOMETRAN, initially designed to yield radiances at TOA in the wavelength range 240–790 nm, has been extended to allow for the computation of actinic fluxes down to 175 nm and for the calculation of photolysis frequencies in the atmosphere. The capability of the extended model PHOTOGT (PHOTOGOMETRAN) is demonstrated in a number of successful comparison studies both with recent experiments (ground-based, balloonborne, airborne) and model calculations of radiances, actinic fluxes and photolysis frequencies in the stratosphere and troposphere. In an atmospheric case study, the impact of new quantum yield data for the O₃ » O₂+O(¹ d) photodissociation channel on the photolytic production of O(¹ d) atoms in the lower atmosphere has been quantified.  相似文献   

RATIONAL UTILIZATION OF MOUNTAIN SOILS IN SOUTHEAST QINGHAI-XIZANG (TIBETAN)PLATEAU     

Li Mingsen 《地理学报(英文版)》1996,(4)

ISoil-fo~gEnvironmentandMainSoilTrocsThesoLItheastQinghai-Xizang(Tibetan)PlateauwheretheHengduanMoUnains,eastempartoftheThmalayanandNyainqentanglhamoUnainsarelocatedextendsfrom25'to34"Nand92'to1O5'Ewithanareaof5OO,OOOkm',oraboutone-fiffooftheentireQinghai-XiZangPlateau.ItisatransitionalzoneofdeePdisseCtedmoUntainseXtendingsoutheastWardpenpherallowlandsandwichedin-betWeenSichuanBasinandcentralYunnanPlateau.Whletheterrainofthesmponinclinestosoutheast,thealtitudeofthevaIleysraises…  相似文献   

Sub-arcsec 10 μm imaging of β pictoris and other star disk candidates     

P. O. Lagage  E. Pantin 《Experimental Astronomy》1994,3(1-4):57-60

We have used the ESO 10 m camera, TIMMI, to image with a very high angular resolution (PFoV: 0.3; FWHM:0.9) several main-sequence star disk candidates. Information on the -Pictoris dust disk has been obtained in a region largely inaccessible to previous observations: 0–80 AU, with a resolution of about 5 AU after deconvolution. Another promising target for 10 m imaging, 51 Ophiuchi, appears point-like.based on data collected at the European Southern Observatory (ESO), La Silla, Chile  相似文献   

Laboratory study of the rates and products of the phototransformations of naphthalene adsorbed on samples of titanium dioxide,ferric oxide,muscovite, and fly ash     

Chantal Guillard  Hervé Delprat  Can Hoang-van  Pierre Pichat 《Journal of Atmospheric Chemistry》1993,16(1):47-59

The photodegradation of naphthalene (NPH), chosen as a model of polynuclear aromatic pollutants, has been studied in the presence of a layer of four water-insoluble inorganic solids which can be found in the troposphere (TiO₂, Fe₂O₃, muscovite, and a fly ash sample). Direct photolysis of NPH is negligible at >340 nm. Dark adsorption of NPH on TiO₂ (mainly anatase, nonporous, 50 m² g^–1) at 293 K corresponds to a surface coverage ofca. 50% at equilibrium. Under these conditions (saturated surface), the stationary-state photocatalytic degradation reaches 0.4 molecule nm^–2 h^–1 (>340 nm, radiant fluxca. 22 mW cm^–2). Dioxygen is required and its partial pressure in air is such that the degradation is zero order in O₂. Water vapor markedly increases the rate. The other particulates have also an effect, less important than that of TiO₂, however quite noticeable with respect to surface area unit for the fly ash sample which contains 3.2% Fe₂O₃. Apart from 1,4-naphthoquinone, which is the main intermediate product in all cases, 2-naphthol, phthalide, phthaldialdehyde, phthalic acid, acetophenone, benzaldehyde, benzoic acid are also formed on dry TiO₂. Depending on their volatility, these compounds are transferred to the gas phase or remain principally adsorbed on the solid particles where they are further transformed. For instance, phthalic acid (or anhydride) and benzoic acid are generated from 1,4-naphthoquinone. Degradation mechanisms are briefly discussed.  相似文献   

On the pH-dependent formation constants of iron(III)-sulfur(IV) transient complexes     

Eric A. Betterton 《Journal of Atmospheric Chemistry》1993,17(4):307-324

An experimental study is described of Fe(III)-S(IV) formation constants measured as a function of pH (1–3), ionic strength (0.2–0.5 M) and [Fe(III)] _T (2.5–5.0×10^–4 M) using a continuous-flow spectrophotometric technique to make observations 160 ms after mixing. Preliminary experiments using pulse-accelerated-flow (PAF) spectrophotometry to measure rate constants on a microsecond timescale are also described. The conditional formation constant at 25 °C can be modeled with the following equation: {ie307-1} where {ie307-2}K ₇ andK ₈ can be interpreted as intrinsic constants for the coordination of HSO ₃ ^– by FeOH²⁺ and Fe³⁺, respectively, but until further evidence is obtained they should be regarded as fitting constants. PAF spectrophotometry showed that the initial reaction of Fe(III) with S(IV) (pH 2.0) is characterized by a second-order rate constant of 4×10⁶ M^–1 s^–1 which is comparable to rate of reaction of FeOH²⁺ with SO ₄ ^2– . However, the PAF results should be regarded as preliminary since unexpected features in the initial data indicate that the reaction may be more complex than expected.  相似文献   

Kinetics of redox cycling of iron coupled with fulvic acid     

Yiwei Deng  Werner Stumm 《Aquatic Sciences - Research Across Boundaries》1993,55(2):103-111

The kinetics of conversion of iron(III) (hydr)oxides to ferrous iron mediated by fulvic acid have been investigated in order to improve the understanding of the redox cycling of iron at the oxic-anoxic boundary in natural waters. Under the conditions similar to natural waters, fulvic acid is able to reduce the iron(III) (hydr)oxide. The kinetics of the reaction depend on the reactivity of iron(III) (hydr)oxides and the reducing power of the fulvic acid. The rate of reaction is 60 nm/h obtained under following conditions: total concentration of Fe(III) 1.0 × 10^–4 M, pH 7.5, fulvic acid 5 mg/L. The rate is considered as a net result of reduction and oxidation in the > Fe^III-OH/Fe(II) wheel coupled with fulvic acid. In a real natural water system, reductants other than fulvic acid may be of importance. The results obtained in the laboratory, however, provide evidence that the Fe(OH)₃(s)/Fe(II) redox couple is able to act as an electron-transfer mediator for the oxidation of natural organic substances, such as fulvic acid by molecular oxygen either in the absence of microorganisms or as a supplement to microbial activity.  相似文献