跨国公司地区总部职能与亚洲地区总部的区位研究

跨国公司建立地区总部制度是跨国公司应对经营“全球化”和“本地化”的要求而进行的一项组织变革。由于跨国公司地区总部承担着制定区域性经营战略和协调区域内众多子公司生产、销售、物流、研究与开发、资金筹供、人力资源培养等经营活动的职能，它的区位对东道国及其所在城市经济带来广泛影响。本文从跨国公司和地区总部职能特点入手，分析了该职能的区位因素，并探讨了跨国公司亚洲地区总部的区位特点，最后对中国大陆的国际商务职能建设提出了若干建议。     

三维变分同化雷达资料暴雨个例试验

采用中国新一代数值预报模式及其同化系统开展雷达资料的三维变分同化和数值模拟研究.通过一次暴雨个例的对比试验,结果表明:不考虑垂直运动影响的情况下,仅同化多普勒雷达径向风资料可以增加初始场中的中小尺度系统信息,并在一定程度上改善预报开始阶段的降水;同化由反射率因子导出的垂直速度、雨水混合比并令上升区饱和,可以较大改善降水预报结果;联合同化径向速度和反射率因子资料将得到它们的共同影响.模拟的β中尺度对流系统6 h的演变过程与观测十分一致,基本消除了旋转加强现象.发展旺盛阶段的对流单体南北方向范围约50 km,最大上升速度位于500 hPa附近,超过3.0 m/s;雨水最大含量在400 hPa附近,超过5.0 g/kg;云水最大值位于600 hPa,约0.5 g/kg;造成的降水强度可达30 mm/h,具有明显的β中尺度系统的特征.初始场中水汽是否达到β中尺度降水维持所需条件是至关重要的,如果初始场中水汽条件较差,即使含有云水、雨水、垂直速度的信息,这些信息也会很快消亡,难以维持下去;此外,雷达资料的质量控制也是十分重要的.     

乌鲁木齐国际机场一次强东南大风天气分析

对乌鲁木齐国际机场2003年11月12日出现的强东南大风天气过程,利用常规天气资料和机场跑道自动观测系统(AWOS)采集的实时观测资料,对机场东南大风天气形势、机场跑道附近气象要素和水平风切变演变特征、高空风垂直分布特征等方面进行了分析,给出了东南大风的成因。     

火山岩与地形联合约束下海岛土壤稀土元素地球化学空间分布异质性——以广西涠洲岛为例

海岛土壤地球化学特征的研究对于认识海岛表生地质环境有重要意义。本研究以我国最大的第四纪火山海岛——涠洲岛为案例,重点研究亚热带海岛环境下火山岩风化土壤的稀土元素（REE）地球化学特征,并探讨影响其空间分布的关键因素。结果表明,涠洲岛土壤REE总量（ΣREE）自然变化范围较大,介于59.07~575.30 mg/kg,平均值为285.53 mg/kg,高于中国大陆土壤背景值（163.86 mg/kg）,指示火山岩风化海岛具有较高的土壤REE丰度。反距离权重插值法（IDW）分析指示,岛内土壤的REE含量高低变化呈现出以带状和斑块状为主体形态的空间分布不均一性,推断其成因与母质岩石类型和地形位置等因素密切相关。3种不同岩性的成土母岩的ΣREE含量变化序列为：玄武岩（236.66 mg/kg）>火山碎屑岩（215.58 mg/kg）>含生物碎屑海滩沉积物（18.99 mg/kg）,对应的土壤ΣREE含量具有类似变化规律,即玄武岩土壤（307.20 mg/kg）>火山碎屑岩土壤（297.46 mg/kg）>含生物碎屑海滩沉积物土壤（89.73 mg/kg）。该证据指示母岩是控制岛内土壤REE含量变化的首位因素,玄武岩整体上易形成具有较高REE丰度的土壤,火山碎屑岩次之,而含生物碎屑海滩沉积物反之。此外,本研究还发现火山碎屑岩单一岩性区内,发育的土壤REE含量也会随地形地貌差异而出现显著变化,其原因是地形地貌制约了土壤矿物和化学风化程度,海蚀丘陵比海积平原更利于海岛土壤中REE次生富集作用的发生。

     

Origin of the Breno and Esino dolomites in the western Southern Alps (Italy): Implications for a volcanic influence

The Esino Limestone of the western Southern Alps represents a differentiated Ladinian-Lower Carnian (?) carbonate platform comprised of margin, slope and peritidal inner platform facies up to 1000 m thick. A major regional subaerial exposure event lead to coverage by another peritidal Lower Carnian carbonate platform (Breno Formation). Multiphase dolomitization affected the carbonate sediments. Petrographic examinations identified at least three main generations of dolomites (D1, D2, and D3) that occur as both replacement and fracture-filling cements. These phases have crystal-size ranges of 3–35 μm (dolomicrite D1), 40–600 μm (eu-to subhedral crystals D2), and 200 μm to 5 mm (cavity- and fracture-filling anhedral to subhedral saddle dolomite D3), respectively.The fabric retentive near-micritic grain size coupled with low mean Sr concentration (76 ± 37 ppm) and estimated δ¹⁸O of the parent dolomitizing fluids of D1 suggest formation in shallow burial setting at temperature ∼ 45–50 °C with possible contributions from volcanic-related fluids (basinal fluids circulated in volcaniclastics or related to volcanic activity), which is consistent with its abnormally high Fe (4438 ± 4393 ppm) and Mn (1219 ± 1418 ppm) contents. The larger crystal sizes, homogenization temperatures (D2, 108 ± 9 °C; D3, 111 ± 14 °C) of primary two-phase fluid inclusions, and calculated salinity estimates (D2, 23 ± 2 eq wt% NaCl; D3, 20 ± 4 eq wt% NaCl) of D2 and D3 suggest that they formed at later stages under mid-to deeper burial settings at higher temperatures from dolomitizing fluids of higher salinity, which is supported by higher estimated δ¹⁸O values of their parent dolomitizing fluids. This is also consistent with their high Fe (4462 ± 4888 ppm; and 1091 ± 1183 ppm, respectively) and Mn (556 ± 289 ppm and 1091 ± 1183 ppm) contents, and low Sr concentrations (53 ± 31 ppm and 57 ± 24 ppm, respectively).The similarity in shale-normalized (SN) REE patterns and Ce (Ce/Ce*)_SN and La (Pr/Pr*)_SN anomalies of the investigated carbonates support the genetic relationship between the dolomite generations and their calcite precursor. Positive Eu anomalies, coupled with fluid-inclusion gas ratios (N₂/Ar, CO₂/CH₄, Ar/He), high F⁻ concentration, high F/Cl and high Cl/Br molar ratios suggest an origin from diagenetic fluids circulated through volcanic rocks, which is consistent with the co-occurrence of volcaniclastic lenses in the investigated sequence.     

Geochemical constraints on the distribution of trace elements and volatiles in fluorapatite from the Panasqueira tin-tungsten deposit (Portugal)

A large, euhedral crystal of fluorapatite (ca. 19.5 × 20.0 mm) from the Panasqueira tin-tungsten deposit (Portugal) was investigated in terms of the distribution of trace elements by using several microanalytical techniques. The studied material represents almost pure fluorapatite with minor amounts of other cations (mainly Sr, Mn, REE and Fe), OH and Cl. Particular interest was given to the distribution of rare earth elements with respect to the crystallographic orientation. A broad range of analytical techniques were used, including optical microscopy coupled with cathodoluminescence imaging, electron probe microanalysis (EPMA), laser ablation – inductively coupled plasma mass spectrometry (LA-ICPMS), Raman microspectroscopy, and simultaneous thermal analysis coupled with mass spectrometry. The investigated crystal consists of the main crystal with a distinct core and rim (Ap_2core and Ap_2rim, respectively), which grew on a previous, euhedral crystal (Ap₁). The fluorapatite demonstrates various types of zoning: regular oscillatory, irregular, and internal sectoring, which is also reflected in trace elements concentrations. The rim Ap_2rim has lower concentrations of Mn, Sr and Fe, and significantly higher concentrations of REE compared to the core Ap_2core and older crystal Ap₁. Furthermore, the rim Ap_2rim is strongly depleted in Th, U and Pb. The entire crystal shows elevated Eu contents, expressed as a strong positive anomaly in chondrite-normalized REE patterns. With regards to the volatiles, F concentrations are constant in Ap₁, Ap_2core and Ap_2rim, whereas Cl is below the EPMA detection limit. The Ap_2rim was the only part of the investigated material containing OH and CO₃, which were observed in the Raman spectra. Furthermore, part of the crystal Ap_2core is extensively altered, likely due to fluid-induced metasomatic processes. LA-ICPMS U-Pb dating yielded highly discordant dates due to common Pb content. A lower intercept age of 297 ± 13 Ma (MSWD = 0.13) indicates the age of the fluorapatite crystallization. The overall analytical data constrain growth and post-growth processes, including crystallization of Ap₁ and Ap_2core, which both have typical hydrothermal Sn-W deposit characteristics, whereas Ap_2rim is related to a carbonate stage of the mineralization in the Panasqueira deposit.     

浙江省衢州市上方镇重钙方解石矿工艺指标影响因素

重质碳酸钙的白度和色相值(Lab)是最重要的工业指标,但影响因素尚不清楚.本文通过扫描电镜、粉晶X射线衍射(XRD)和电感耦合等离子体发射光谱(ICP-OES)等分析手段,对浙江衢州上方镇的重钙方解矿石进行了研究,以期阐明重质碳酸钙白度和色相的影响因素.结果表明,矿石随研磨粒度的减小白度逐渐增加,在100～400目,白...     

银川盆地第四纪地球化学元素特征及沉积环境

通过分析银川盆地Ｙ１孔地球化学元素含量及其分布规律,参考地层岩性等因素,确定了该盆地第四系地层地球化学元素的分带。依据地球化学元素分布,结合孢娄分析成果探讨了银川盆地第四纪中、晚期以来的沉积环境和古气候及其演化规律。     

安徽女山单斜辉石巨晶的地球化学

本文研究了安徽女山14个单斜辉石巨晶。它们属于铝普通辉石、透辉石和铁钠造辉石。主要元素、稀土和微量元素及同位素特征表明：它们是同一碱性玄武岩浆在幔源条件下不同程度结晶分异的产物，相对于寄主岩均属捕虏晶，可能自中生代即已开始形成。     

Gold and Platinum-Group Element Analysis of Geochemical and Platinum Reference Materials Using Fluoroxidation Decomposition

A novel method is described for the rapid dissolution of various geological, geochemical and related reference samples for the determination of Au and the platinum-group elements. The decomposition procedure is based on reaction with the fluoroxidants, liquid bromine trifluoride or molten potassium tetrafluorobromate. Results by this novel procedure are compared with data obtained by traditional methods of sample decomposition, including fire assay, autoclave techniques and an aqua regia leach. The oxidative fluorination procedure with the subsequent conversion of fluorocomplexes into the chloride form was found to be an effective and rapid method for the quantification of all the precious metals in a range of sample types.