太古宙克拉通型下地壳剖面：华北怀安－丰镇－尚义的麻粒岩－角闪岩系

华北克拉通北缘晋冀内蒙交界地区有变质程度连续变化、从高压基性麻粒岩、麻粒岩到角闪岩相的变质岩系出露。它们的古变质压力由＞１．４ＧＰａ（５０ｋｍ）变化到０．５ＧＰａ（１５ｋｍ）；岩石类型从变辉长岩、中酸性正片麻岩到表壳岩变化；变质矿物组合由不含水的耐火组合变为富含云母和角闪石的组合；地球化学性质表现出从贫Ｓｉ和Ａｌ、轻度亏损生热元素到具有正常的化学成分的连续变化；包裹体流体性质在轻度亏损生热元素的麻粒岩中均为ＣＯ２流体，而在麻粒岩相的表壳岩和角闪岩系中Ｈ２Ｏ流体逐渐增加。上述变质岩系剖面的组成和特点符合大陆下地壳的定义，可能代表了包括最下部地壳在内的华北地块太古宙克拉通型大陆下地壳。据此本文建立了我国第一条克拉通型大陆下地壳剖面，并讨论其地质意义以及相关的问题     

榴辉岩的化学分类

以山东荣成地区的榴辉岩为例,把榴辉岩分为镁一榴辉岩、铁一榴辉岩和钙一榴辉岩三类。三类榴辉岩的岩石化学,主要造岩矿物成分都有明显差别,石榴石分别是镁铝榴石、铁铝榴石和钙铝榴石。绿辉石的硬玉分子也有不同。三类榴辉岩的化学成分限制是Mg-榴辉岩MgO>10%,石榴石以镁铝榴分子占优势,Fe-榴辉岩的MgO<10,石榴石以铁铝榴石分子占优势。Ca-榴辉岩CaO>19%,石榴石以钙铝榴石分子优势。     

吉林省地质灾害类型及防治对策探讨

本文针对吉林省的地质灾害类型及各类地质灾害的成因，分布及其危害进行了论述。对其防治对策进行了探讨，提出了切合本省实际的五项防治措施。     

岩质高边坡岩体变形参数及松弛带厚度研究

预测岩质高边坡开挖后岩体变形模量的变化及松弛带厚度，是分析岩质高边坡在开挖后变形（位移）和作好防护设计的重要资料，运用波动力学关于平均应力与体积模量、岩体纵波速度与弹性模量、变形模量间的关系，通过部分实测资料及边坡应力场有限元分析的资料，分别建立了纵波速度与岩体变形模、岩体应力间的关系，研究了开挖边坡岩体变形模量的变化，预测了岩体松弛带的厚度。     

天津盛夏降水趋势与初夏华北高压的统计分析

根据初夏(6月)的天气气候演变，预测盛夏(7～8月)的短期气候趋势，一直是急需解决的难题。文章揭示了自1958年以来天津盛夏降水趋势与初夏时节临近地区上空的环流特征之间的统计关系。结果表明，初夏华北高压强时盛夏天津降水偏少，反之盛夏天津降水偏多，不仅逐年的对应关系显著，而且变化趋势相反，转折时期也一致。初步解释了20世纪70年代以前天津(华北)盛夏多雨和80年代至今天津(华北)少雨的物理原因。以此为主要根据建立了初夏对于盛夏天津降水的短期气候预测方法，1998～2003年连续6年预报正确。     

青藏高原影响亚洲夏季气候研究的最新进展

文中回顾了近 10a来吴国雄等在青藏高原影响亚洲夏季气候研究方面的最新进展。通过分析东西风交界面的演变证明 ,由于青藏高原的春季加热 ,亚洲季风区对流层低层冬季盛行偏东风转变为夏季偏西南风最早发生在孟加拉湾东部 ,与其相伴随的激烈对流降水出现在其东面。因此孟加拉湾东部至中印半岛西部是亚洲季风最早爆发的地区。同时也指出盛夏伊朗高原和青藏高原加热所激发的同相环流嵌套在欧亚大陆尺度的热力环流中 ,从而加强了东亚的夏季风 ,加剧了中西亚的干旱 ;并通过其所激发的波动对夏季东亚的气候格局产生重要影响。文中还比较了夏季南亚高压的伊朗模态和青藏模态性质的异同及其对亚洲夏季降水异常分布的不同影响。     

Analytical methods Of assessing the image quality associated with digital and photographic imaging systems

The introduction of digital cameras for aerial survey photography and use of scanners with processed aerial film present a number of technical questions concerning the way photography is to be acquired in the future. Among the questions to be addressed are the comparative metric properties of images acquired by each system and the associated image quality characteristics. The new digital camera systems will require very careful appraisal, using well-established methods of assessing metric quality already available to survey organisations. The questions concerning image quality are more difficult to answer, as they require very specialised instrumentation if measurements are to be made directly in practice. Over the course of the past several decades a more analytical approach to assessing image quality has emerged, and one that may be used by individuals. The method is particularly effective where information on the micro-image characteristics of products is made available by the manufacturers concerned. An outline is given of some considerations that need to be taken into account when using an analytical approach, with references given for further reading.     

High-pressure experimental growth of diamond using C–K2CO3–KCl as an analogue for Cl-bearing carbonate fluid

High-pressure, high-temperature diamond growth experiments have been conducted in the system C–K₂CO₃–KCl at 1050–1420 °C, 7.0–7.7 GPa. KCl is of interest because of the strong effect of halogens on the phase relations of carbonate-rich systems [Geophys. Res. Lett. 30 (2003) 1022] and because of the occurrence of KCl coexisting with alkali silicate–carbonate fluids in natural-coated diamond [Geochim. Cosmochim. Acta 64 (2000) 717]. We have used system C–K₂CO₃–KCl as an analogue for these mantle fluids in diamond growth experiments. The presence of KCl reduces the potassium carbonate liquidus to ≤1000 °C at 7.7 GPa, allowing it to act as a solvent catalyst for diamond growth at temperatures below the continental geotherm. This is a reduction on the minimum diamond growth temperature reported in the alkali-carbonate–C–O–H system [Lithos 60 (2002) 145]. Diamond growth using carbonate solvent catalysts is characterised by a relatively long induction period. However, the addition of KCl also reduced the period for diamond growth in carbonate to 5 min; no such induction period appears to be necessary. It is suggested that KCl destabilises carbonate, allowing greater solubility and diffusion of carbon.     

Experimental and theoretical study of stability of dense hydrous magnesium silicates in the deep upper mantle

Fluid-undersaturated experiments were conducted to determine the phase relations in the simplified peridotite system MgO-SiO₂-H₂O (MSH) at 11.0-14.5 GPa and 800-1400 °C. Stability relations of dense hydrous magnesium silicates (DHMSs) under fluid-undersaturated conditions were experimentally examined. From the fluid-absent experimental results, we retrieved thermodynamic data for clinohumite, phase A, phase E, and hydrous wadsleyite, consistent with the published data set for dry mantle minerals. With this new data set, we have calculated phase equilibria in the MSH system including dehydration reactions. The dehydration reactions calculated with lower water activities of 0.68-0.60 match the fluid-present experiments of this study above 11.0 GPa and 1000 °C, indicating that considerable amounts of silicate component were dissolved into the fluid phase. The calculated phase equilibria illustrate the stability of the post-antigorite phase A-bearing assemblages. In the cold subducting slab peridotite, phase A + enstatite assemblage survives into the transition zone, whereas phase A + forsterite + enstatite assemblage forms hydrous wadsleyite at a much shallower depth of about 360-km. The slab is subducted with no dehydration reactions occurring when entering the transition zone. The phase equilibria also show the high temperature stability of phase E. Phase E is stable up to 1200 °C at 13.5 GPa, a plausible condition in the mantle of relatively low temperature, i.e., beneath subduction zones. Phase E is a possible water reservoir in the mantle as well as wadsleyite and ringwoodite.     

Polymorphic phase transition in Superhydrous Phase B

We synthesized superhydrous phase B (shy-B) at 22 GPa and two different temperatures: 1200°C (LT) and 1400°C (HT) using a multi-anvil apparatus. The samples were investigated by transmission electron microscopy (TEM), single crystal X-ray diffraction, Raman and IR spectroscopy. The IR spectra were collected on polycrystalline thin-films and single crystals using synchrotron radiation, as well as a conventional IR source at ambient conditions and in situ at various pressures (up to 15 GPa) and temperatures (down to −180°C). Our studies show that shy-B exists in two polymorphic forms. As expected from crystal chemistry, the LT polymorph crystallizes in a lower symmetry space group (Pnn2), whereas the HT polymorph assumes a higher symmetry space group (Pnnm). TEM shows that both modifications consist of nearly perfect crystals with almost no lattice defects or inclusions of additional phases. IR spectra taken on polycrystalline thin films exhibit just one symmetric OH band and 29 lattice modes for the HT polymorph in contrast to two intense but asymmetric OH stretching bands and at least 48 lattice modes for the LT sample. The IR spectra differ not only in the number of bands, but also in the response of the bands to changes in pressure. The pressure derivatives for the IR bands are higher for the HT polymorph indicating that the high symmetry form is more compressible than the low symmetry form. Polarized, low-temperature single-crystal IR spectra indicate that in the LT-polymorph extensive ordering occurs not only at the Mg sites but also at the hydrogen sites.