河南省洛阳—三门峡铝土矿地质特征及其勘查开发前景

河南省洛阳-三门峡的铝土矿，是赋存于中石炭统本溪组的一水硬铝石型沉积铝土矿。本区不仅蕴藏量多，而且有相当数量的富铝土矿，勘查开发潜力大，前景广阔。     

东南极Lambert冰川-Amery冰架系统平衡通量分布的计算

通过对Lambert冰川盆地(LGB)考察路线上约1 700 km长的LGB剖面和距冰架末端约50 km、长150 km的A剖面, 分别利用GPS冰流速值及雷达测厚值进行冰通量的计算得出:每年流过LGB剖面的冰通量为43.95 Gta-1, 而通过A剖面的冰通量仅为26. 42 Gt*a-1, Amery冰架底部净融化量为7.8 Gt*a-1. 整个Lambert冰川-Amery冰架系统(LAS)地区的表面净物质平衡总量约为90 Gt*a-1; LGB地区的表面净物质平衡总量为46 Gt*a-1. 通过分析得出, 整个LAS地区及LGB地区均处于物质正平衡状态, 而LAS流域的上游区域S'则处于物质负平衡状态.     

天山奎屯河哈希勒根51号冰川表面运动特征分析

奎屯河哈希勒根51号冰川位于新疆奎屯市以南的天山依连哈比尔尕山北坡, 奎屯河上游支沟哈希勒根河源区. 1999年8月, 在该冰川上布设了用于冰川运动和冰川物质平衡观测研究的测杆18根, 并进行了冰川表面运动、冰川物质平衡和冰川末端变化的首次观测. 根据2000年8月和2001年8月的冰川运动观测资料, 分析了奎屯河哈希勒根51号冰川的运动特征和冰舌末端的变化状况. 结果表明: 奎屯河51号冰川应属于亚大陆型冰川; 1999/2000年度和2000/2001年度的表面运动值不大, 最大流速点的年运动速度为3.15 ma-1; 运动速度垂直分量UZ的变化规律同乌鲁木齐河源1号冰川的变化规律相同, 即消融区的显出流作用和积累区的显入流作用. 该冰川的冰舌末端处于相对稳定的退缩状态, 1964-1999年间平均退缩量约为1.4 m*a-1, 而1999-2001年间的平均退缩量为5.0 m*a-1, 反映出冰川退缩增大的趋势.     

利用ERS-2 SAR图像纹理分析方法揭示长白山天池火山近代喷发物空间分布特征

简单介绍了SAR图像的纹理特征以及正交小波变换纹理提取方法。论述了SAR图像的纹理特征参与分类的重要性。以长白山天池火山为例,通过对ERS2SAR图像进行纹理分析,提取了SAR图像两个层次的尺度变化、时频局部化和方向性纹理特征。并将SAR纹理特征与TM图像及DEM进行复合,利用多源信息各自的优势,进行了BP神经元网络分类,从较大范围对长白山天池火山735±15aB.P.大喷发的喷发物空间分布进行评价。获取了长白山天池火山近代喷发物的空间分布及规模。这对长白山天池火山未来喷发危险性初步评价、火山地质制图及火山灾害预测有重要意义。     

渤海湾盆地北部奥陶纪岩相古地理

渤海湾盆地北部主要包括黄骅坳陷、沧县隆起、冀中坳陷和下辽河坳陷,区内奥陶系厚 6 0 0～ 80 0m,主要由石灰岩和白云岩组成。下奥陶统分为冶里组和亮甲山组,中奥陶统分为下马家沟组、上马家沟组和峰峰组,上统缺失。其中下马家沟组、上马家沟组和峰峰组又进一步划分为下段和上段。早奥陶世冶里期和亮甲山期,本区以局限海环境为主,其内散布着一些潮坪和滩。中奥陶世,本区岩相古地理面貌变化旋回极为明显,下马家沟期早期潮坪广布,晚期以局限海为主;上马家沟期早期又是潮坪广布,晚期以开阔海为主;峰峰期早期潮坪广布,晚期又以开阔海为主。在奥陶纪,本区经历了 4个大的海侵-海退旋回,其中上马家沟期晚期是本区乃至整个华北地台的最大海侵期。     

老柞山金矿田鸡爪沟金矿床地质特征及成因探讨

分析了鸡爪沟金矿床地质特征和成因 ,并对形成过程进行理论推导 ,认为该矿床为与火山作用有关的中温岩浆热液充填型矿床。     

熊耳山地区太古宙超镁铁质岩的地球化学特征及成因探讨

熊耳山地区太古宙超镁铁质岩在空间分布上具有不均一性、成带性和多方向性特征 ,岩石以橄榄岩、辉石岩、角闪石岩为主 ,蚀变强烈。岩石贫钙、镁 ,低铝、K2 O Na2 O,稀土总量较高 ,轻重稀土分馏显著。地球化学特征表明大部分超镁铁质岩体为岩浆侵入成因     

富碱斑岩中超镁铁深源包体岩石的矿物学特征

在云南省鹤庆县六合乡富碱斑岩体中找到超镁铁深源岩石包体，这对于研究富碱斑岩的起源和演化及其成岩成矿作用具有重要意义。本文较系统地研究了深源包体岩石的矿物学特征，揭示该深源包体具有原始上地幔岩在地幔条件下受到一定程度富集地幔流体交代作用改造的特征，具有富集地幔低程度部分熔融属性，为富碱斑岩的成岩成矿演化提供了重要的矿物学依据。     

An experimental study of grain scale melt segregation mechanisms in two common crustal rock types

Creation of pathways for melt to migrate from its source is the necessary first step for transport of magma to the upper crust. To test the role of different dehydration‐melting reactions in the development of permeability during partial melting and deformation in the crust, we experimentally deformed two common crustal rock types. A muscovite‐biotite metapelite and a biotite gneiss were deformed at conditions below, at and above their fluid‐absent solidus. For the metapelite, temperatures ranged between 650 and 800 °C at P_c=700 MPa to investigate the muscovite‐dehydration melting reaction. For the biotite gneiss, temperatures ranged between 850 and 950 °C at P_c=1000 MPa to explore biotite dehydration‐melting under lower crustal conditions. Deformation for both sets of experiments was performed at the same strain rate (ε.) 1.37×10^?5 s^?1. In the presence of deformation, the positive ΔV and associated high dilational strain of the muscovite dehydration‐melting reaction produces an increase in melt pore pressure with partial melting of the metapelite. In contrast, the biotite dehydration‐melting reaction is not associated with a large dilational strain and during deformation and partial melting of the biotite gneiss melt pore pressure builds more gradually. Due to the different rates in pore pressure increase, melt‐enhanced deformation microstructures reflect the different dehydration melting reactions themselves. Permeability development in the two rocks differs because grain boundaries control melt distribution to a greater extent in the gneiss. Muscovite‐dehydration melting may develop melt pathways at low melt fractions due to a larger volume of melt, in comparison with biotite‐dehydration melting, generated at the solidus. This may be a viable physical mechanism in which rapid melt segregation from a metapelitic source rock can occur. Alternatively, the results from the gneiss experiments suggest continual draining of biotite‐derived magma from the lower crust with melt migration paths controlled by structural anisotropies in the protolith.     

Cation distribution and structure modelling of spinel solid solutions

 This paper presents an improved generalisation of cation distribution determination based on an accurate fit of all crystal-chemical parameters. Cations are assigned to the tetrahedral and octahedral sites of the structure according to their scattering power and a set of bond distances optimised for spinel structure. A database of 295 spinels was prepared from the literature and unpublished data. Selected compositions include the following cations: Mg²⁺, Al³⁺, Si⁴⁺, Ti⁴⁺, V³⁺, Cr³⁺, Mn²⁺, Mn³⁺, Fe²⁺, Fe³⁺, Co²⁺, Ni²⁺, Zn²⁺ and vacancies. Bond distance optimisation reveals a definite lengthening in tetrahedral distance when large amounts of Fe³⁺ or Ni²⁺ are present in the octahedral site. This means that these cations modify the octahedral angle and hence the shared octahedral edge, causing an increase in the tetrahedral distance with respect to the size of the cations entering it. Some applications to published data are discussed, showing the capacity and limitations of the method for calculating cation distribution, and for identifying inconsistencies and inaccuracies in experimental data. Received: 19 February 2001 / Accepted: 1 June 2001