首都减灾圈的思考与建议

首都减灾圈,系首都减轻自然灾害预测防治圈。1991年12月20—21日在北京召开了《首都圈自然灾害及其减灾对策研讨会》。本文根据这次会议所提供的材料,在从整体上实现减灾的思想指导下,就首都减灾圈的“成灾背景”、“首都减灾圈的组成”、“首都减灾圈的灾害预测与防治状况”、“首都减灾圈的灾害关联性分析”、“首都减灾圈的减灾实效预估”和“首都减灾圈的减灾对策与实施”等六个带有共同性的问题,进行了讨论。供制定首都圈减灾方案时参考。     

福建石炭纪岩相古地理分析

笔者总结了福建省石炭纪生物地层与岩石地层的研究成果,提出了生物地层与岩石地层的划分对比。在详尽的相分析基础上对该纪地层进行了相系、相、亚相及微相的划分,并按“优势相”的原则分期编制了林地期、黄龙期及船山期的岩相古地理图。笔者采用“相、层、位”控矿观点对石炭纪的矿产成因及成矿规律作了探讨。     

天然火山作用探测华北下地壳组成、结构及其形成过程

与中上地壳相比，对下地壳组成、结构的认识受限于样品的获取，然而天然火山作用携带的下地壳捕虏体可以为了解下地壳提供关键样品。华北克拉通是世界上最古老的克拉通之一，显生宙以来的火山作用携带有丰富的下地壳捕虏体，为探测华北下地壳组成、结构及其形成过程提供了可能。通过对这些捕虏体定深、定性及定年的综合研究，构建了以信阳，莒南，汉诺坝和女山等典型地区为代表的下地壳组成、结构剖面模型。这些剖面表明，华北克拉通下地壳具有分层的特点，且上老下新，暗示可能与底侵作用有关。其中捕虏体的锆石U- Pb年龄和Hf同位素的研究，揭示了该克拉通下地壳复杂的形成与演化过程：最古老的组成部分可能老至~4. 0 Ga冥古宙，此后经历了3. 80~3. 65 Ga古太古代的再造作用，2. 8~2. 5 Ga 新太古代和2. 3~1. 8 Ga 古元古代的增生与再造共存，同时还经历了显生宙以来包括462~220 Ma，140~90 Ma和47~45 Ma的增生与再造事件。     

雄安新区地热地质模型探究：来自地球物理的证据

雄安新区内地热资源丰富，区内有牛驼镇地热田、容城地热田和高阳地热田，地热资源开发利用较早，但是对其深部热源机制仍未形成统一观点。为了研究雄安新区内地热田深部热源机制，在新区及外围进行了深反射地震和长周期大地电磁探测，对取得的同剖面的深反射地震和大地电磁数据进行处理和综合解释，探明了研究区从地表至莫霍面范围内地质构造和电性结构。下地壳结构在深反射地震剖面与大地电磁剖面上有很好的对应关系。电阻率低值区对应着在深反射地震剖面上存在一系列反射同相轴，且同相轴可以延续到莫霍面，电阻率高值区对应着在深反射地震剖面上无明显连续反射同相轴，尤其是在莫霍面之上呈现地震反射近似"空白区"。结合区域地热资料构建了研究区深部地热地质模型，对新区内深部地热机制进行了解释。该模型为"二元"生热模型，其热源包含两个部分，深部地幔热源和地壳放射性元素衰变生热。放射性元素衰变生热占地表热流的接近30%，而幔源热流在地表热流中的占比可达约70%。在牛驼镇下方，莫霍面以上，由于地幔热物质上涌造成下地壳上隆，幔源岩浆底侵作用于下地壳形成了局部热异常，该热异常具有低速高导的地球物理特征，认为是牛驼镇地热田和容城地热田的深部热源；以区域断裂为热通道，大地热流由深部向上传导、扩散到牛驼镇凸起和容城凸起顶部，对碳酸盐岩储水层进行加热，形成地热储层；上覆新近系沉积地层是良好的热盖层。     

地震前兆含义,科学问题与研究途径的研讨

地震前兆的研究已经取得了很大的进展,地震前兆的复杂性引起了广泛的关注,对地震预报、有关科学问题和探索途径的研究现状及其前景有各种评价。文章认为由于一些科学问题没有解决,尽管对中缅边境１９９５年７月连７．３级地震作出了成功预报,经验性预报有一定的局限性,文中讨论了广义地震前兆和狭义地震前兆,广义地震前兆包含二类前兆：场兆和源兆;而狭义前兆仅指后者。大陆震例前兆的系统研究证实了广义地震前兆的存在,然而     

四川木里耳泽岩溶型金矿床形成条件和成矿机制

四川本里耳泽金-菱铁矿建造矿床,赋存于上二叠统海相碳酸盐岩层中,矿化受古岩溶的严格控制,组成矿石的基本矿物为菱铁矿,金不均匀地分布于菱铁矿矿体内。成矿溶液来自加热的循环地下水。成矿过程分为早阶段和中-晚阶段。成矿温度为156-210℃,成矿深度小于1km.成矿物质主要来自地层。成矿热液呈碱性和弱还原性,贫硫,含中等盐度。矿床形成时的地质构造环境较稳定。这是我国仅见的一种特殊金矿类型。     

“地理学公理”质疑——与楚义芳同志商榷

本文运用地理学和物理学的规律进行论证,认为楚义芳同志在《地理学的逻辑方法与基本法则》一文中提出的“地理学公理”不能成立。并在此基础上进一步阐明一个公理体系不适合于地理学,而经验假设则是绝对必要的。     

Sulfur Isotope Fractionation in Magmatic Systems：Models of Rayleigh Distillation and Selective Flux

The effect of Rayleigh distillation by outgassing of SO2 and H2S on the isotopic composition of sulfur remaining in silicate melts is quantitatively modelled.A threshold mole fraction of sulfur in sulfide component of the melts is reckoned to be of critical importance in shifting the δ^34S of the melts mith respect to the original magmas.The partial equilibrium fractionation in a magmatic system is evaluated by assuming that a non-equilibrium flux of sulfur occurs between magmatic volatiles and the melts,while an equilibrium fractionation is approached between sulfate and sulfide within the melts.The results show that under high fo2 conditions,the sulfate/sulfide ratio in a melt entds to increase,and the δ^34S value of sulfur in a solidified rock might then be shifted in the positive direction.This may either be due to Rayleigh outgassing in case the mole fraction of sulfide is less than the threshold,or due to a unidirectional increase in δ^34S value of the sulfate with decreaing temperature,Conversely,at low fo2,the sulfate/sulfide ratio tends to decrease and the δ^34S value of total sulfur could be driven in the negative direction,either because of the Rayleigh outgassing in case the mole fraction of sulfide is greater than the threshold,or because of a unidirectional decrease inδ^34S value of the sulfide.To establish isotopic equilibrium between sulfate and sulfide,the HM,QFM or WM buffers in the magmatic system are suggested to provide the redox couple that could simultaneously reduce the sulfate and oxidize the sulfide.CaO present in the silicatte Melts is also called upon to participate in the chemical equilibrium between sulfate and sulfide,Consequently,the δ^34S value of an igneous rock could considerably deviate from that of its original magma due to the influence of oxygen fugacity and temperature at the time of magma solidification.     

Carbon-oxygen isotopic covariation in hydrothermal calcite during degassing of CO2

The effect of the outgassing of CO₂ from a hydrothermal fluid on the C- and O-isotopic compositions of calcite, which is precipitated from this fluid, is quantitatively modelled in terms of batch and Rayleigh distillation equations. Both CO₂ degassing and calcite precipitation are considered to be the removal mechanisms for dissolved carbon species from the fluid. Combined degassing-precipitation models are then developed by taking H₂CO₃ and HCO ₃ ^– , respectively, as the dominant dissolved carbon species. A positive correlation array between ¹³C and ¹³O values of calcite can be yielded by the precipitation of calcite from a H₂CO ₃ ^– -dominant fluid, accompanied by a progressive decrease in temperature during CO₂ degassing, whereas calcite precipitated from a HCO ₃ ^– -dominant fluid under the same conditions tends to display much smaller variation in ¹³C values than in ¹⁸O values. The combined processes of CO₂ degassing and calcite precipitation result in lowering the ¹³C value of calcites with respect to those precipitated in a closed system simply due to temperature effect. Carbon and oxygen isotopic data for calcite from the Kushikino gold-mining area in Japan illustrate the application of quantitative modelling, and degassing of CO₂ is suggested as a more likely cause for the precipitation of the calcite and quartz in this mining area.