西藏冈底斯带石炭纪—二叠纪岛弧造山作用：火山岩及地球化学证据

系统研究了西藏冈底斯带石炭纪—二叠纪火山岩的时空分布、岩相学、元素及Sr、Nd、Pb 同位素地球化学和构造环境、源区性质,并与喜马拉雅带二叠纪火山岩进行了对比研究。冈底斯带石炭纪—二叠纪火山岩近东西向集中分布在冈底斯构造带中北部地带,空间上从东至西火山活动的强度和规模渐次减小,时间上从早至晚火山活动的强度和规模总体由弱到强。冈底斯带石炭纪—二叠纪火山岩形成于活动大陆边缘的岛弧构造环境,从早到晚岛弧造山作用经历了初始岛弧→早期岛弧→成熟岛弧的发展演变过程,火山岩浆来源于富集型地幔部分熔融作用,原始岩浆在形成和演化的过程中有俯冲洋壳及随带的深海沉积物和再循环进人地慢的地壳物质组分的强烈混染,明显不同于受地壳物质组分强烈混染的喜马拉雅带二叠纪陆缘裂陷型火山岩。综合研究冈底斯带及其邻区近年来的最新调查与研究成果,从北向南拟建了石炭纪—二叠纪冈底斯岛弧→雅鲁藏布江弧后裂谷盆地→喜马拉雅陆缘裂陷盆地的弧盆系时空结构演化模式,探讨了冈瓦纳大陆北缘石炭纪—二叠纪活动大陆边缘的岛弧造山作用与青藏高原古特提斯演化的耦合关系及其动力学机制,讨论了冈底斯带松多乡榴辉岩的形成过程。     

基于时空分配组合的消防设施服务范围计算方法探讨

基于时空分配组合方法,综合考虑服务时间在主干道路和街区内分配的各种情形,探讨了符合实际需求的消防站点服务范围计算方法.提出了基于多个独立指标的评价消防设施布局方案的方法,对消防规划方案进行评价.最后以武汉市武昌区为例对所提出方法进行了实验,实验结果也验证了该方法的可行性和合理性.     

胶东海阳所超镁铁岩中强亲铁元素的地球化学特征及其构造环境探讨

强亲铁元素与亲石元素具有不同的地球化学行为，因此能够从不同的角度为造山带中超镁铁岩的成因及演化提供重要信息。位于苏鲁造山带东北端的胶东海阳所超镁铁岩主要由橄榄岩和辉石岩组成，它们常以团块状赋存于花岗质片麻岩中。虽然前人对这些超镁铁岩已经开展大量岩石学研究，但关于其成因及构造属性仍存在较大争议。本文开展了海阳所超镁铁岩的全岩主微量元素、强亲铁元素及Re-Os同位素的分析工作，结果显示蛇纹石化橄榄岩具有较高的MgO和Fe₂O₃^T含量，较低的Al₂O₃、TiO₂和CaO含量，明显富集流体迁移元素（U、Pb），亏损高场强元素（Zr、Hf），强亲铁元素没有发生明显分异，但Ru显示正异常，表明海阳所蛇纹石化橄榄岩是经历了低-中等程度部分熔融及熔/流体交代作用影响的残余地幔橄榄岩。海阳所辉石岩的主量元素表现出明显的结晶分异特征，稀土元素较原始地幔富集，铂族元素（PGEs）含量较低且发生了明显的分异，表明辉石岩的地幔源区经历过高程度的部分熔融和硫化物的分离。海阳所蛇纹石化橄榄岩的Os同位素地球化学特征表现出大洋亲和性，与辉石岩不具有熔体-残留体的关系。由于该地区发育较深层次的韧性剪切带，蛇纹石化橄榄岩中的橄榄石与辉石表现出韧性变形的特征，同时有辉石岩侵入到橄榄岩的现象，表明该地区的蛇纹石化地幔橄榄岩与辉石岩既不同时，也不同源，因此，暗示了该套岩石组合可能形成于大洋核杂岩（OCC）与洋脊型蛇绿岩（MOR）堆晶岩交互发育环境。     

河北省唐山地区丰台—野鸡坨断裂第四纪活动性——来自14C和磁性地层年代学的证据

丰台—野鸡坨断裂为唐山地区主要断裂之一，西侧为鸦鸿桥凹陷，东侧为唐山凸起，断裂两侧第四系厚度之差巨大。本文依据该断层两侧钻孔对其第四纪以来活动性进行初步的探讨。通过对丰台—野鸡坨断裂上下两盘PZK14和PZK20孔磁性地层学研究，并结合钻孔岩石地层，及浅部光释光和¹⁴C测年结果，建立第四纪地层格架。结果表明：两孔底部“泥包砾”为新近纪沉积；PZK14孔下更新统底界埋深为387 m，中更新统底界埋深为114 m，上更新统底界埋深为71 m，全新统底界埋深为6 m；PZK20孔下更新统底界埋深为155 m，中更新统底界埋深为73 m，上更新统底界为36 m，无全新世地层。丰台—野鸡坨断裂活动在早更新世时表现为逐渐增强的特点，活动速率由早期的5.4 cm/ka增加到13.9 cm/ka。中更新世断裂活动基本处于停滞状态，活动速率为1.0 cm/ka。晚更新世以后，断裂重新活动，且更加剧烈，活动速率达到了54.5 cm/ka。     

据花粉分析论许家窑遗址的时代和古环境

本文应用花粉分析,对许家窑遗址沉积物的地质时代和古环境进行了探讨。指出:遗址沉积期间的气候比较寒冷,气温比现今低;其时的植被面貌,为森林草原类型;遗址沉积物的地质时代为晚更新世     

丹池盆地热水成因硅岩的沉积地球化学特征

丹池盆地硅岩（D₃1）属于典型的热水成因沉积物。它的显著地球化学特征之一是Sb.As和Ag富集,而REE贫乏,并且从近热水喷口→远离热水喷口,即沿着类碧玉岩→纹理状硅岩→块状泥质硅岩→硅页岩方向,元素、元素组合及稀土元素特征出现规律性的变化。     

贵州南部“半边街式”铅锌矿床地质特征及其成因探讨

贵州省南部地区是全国重要的汞、锑资源分布区。2000年由于产于上泥盆统中铅锌矿的陆续发现,贵州省地矿局启动了以铅锌资源评价和成矿规律研究为主的地质工作,目标是总结铅锌矿产出的地质特征和成矿规律。通过三年的研究认为,该区处扬子准地台、华南褶皱带和右江造山带交汇部位,受晚古生代初期发生的陆内裂谷活动影响,产生了一个与桂中台陷相连的大型沉积凹陷区—黔南台陷沉积区,形成了巨厚碳酸盐和碎屑岩沉积,产生了与裂陷盆地边缘同沉积断层活动有关的低温成矿作用,造成了在晚泥盆纪以前的地层中汞、锑、砷、金、铅锌等矿床沿同沉积断层密集分布。本文通过矿床特征总结和矿床成因探讨,建立了准同生沉积成矿作用模式,旨在为该区寻找这类矿床提供参考和借鉴作用。     

Catalytic ozonation of phenol in water with natural brucite and magnesia

Catalytic ozonation has attracted much attention in treatment of wastewater for its mild conditions. Phenol and its ramifications are common components in a wide variety of wastewaters including those from coal conversion processes, coking plants, petroleum refineries and several chemical industries. In this paper, natural brucite and magnesia have been successfully used in catalytic ozonation of phenol. And the mechanisms of catalysis were also investigated. From Figs. 1 and 2, it can be found that both brucite and magnesia have remarkable catalysis on degradation of phenol and removal of Chemical Oxygen Demand （COD）. The pH of solutions on the process of ozonation alone, catalytic ozonation with brucites and with magnesia were 6.35-2.76, 10.18-8.52 and 10.58-10.83, respectively. It can be concluded that alkali environment plays a critical role for catalytic ozonation of phenol. We also found that the alkaline minerals reacted on the surface with oxalic acid and other low molecular-weight acids which are intermediate products in ozonation, but those intermediate products could be mineralized into carbon dioxide completely with enough ozonation time.     

XANES analysis of the mechanisms of arsenic removal in biological iron and manganese treatment unit

Biological iron and manganese removal utilizing indigenous iron and manganese oxidizing bacteria （IRB hereafter） in groundwater can also be applied to arsenic removal according to our pilot-scale test. The arsenic removal probably occurred through sorption and complexation of arsenic to iron and manganese oxides formed by enzymic action of IRB. We investigated the chemical properties of iron and manganese oxides in IRB floc and the valence state of arsenic sorbed to the floc to clarify the mechanisms of the arsenic [especially As （Ⅲ）] removal. The floc samples were collected from two drinking water plants using IRB （Jyoyo and Yamatokoriyama, Japan）, and our pilot - scale test site where arsenic and iron removal using IRB is under way （Mukoh, Japan）. The Jyoyo and Yamatokoriyama IRB floc samples were subjected to As （Ⅲ） and As（Ⅴ） sorption experiments. The elemental composition of the floc samples was measured. XANES spectra were collected on As, Fe and Mn K-edges at synchrotron radiation facility Spring 8 （Hyogo, Japan）. FT-IR and the X-ray diffraction spectra of the samples were also obtained. The IRB floc contained ca. 35 % Fe, 0.3%-3.5% Mn and 2%-6% P. The samples were highly amorphous and contained ferrihidrites and hydrated iron phosphate. According to XANES analyses of IRB, As associated with IRB was in ＋5 valence state when As （Ⅲ） （or As （Ⅴ）） was added in laboratory sorption test, Fe in ＋3 valence state, and Mn a mixture of＋3 and ＋4 valence states. Small shift was observed in the XANES spectra of IRB on As K-edge as the equilibration time of the sorption experiment was increased. Gradual oxidation of a small amount of As （Ⅲ） associated with IRB or change in arsenic binding with sorption site were the probable mechanism.     

青海热水柴达尔井田构造组合型式

柴达尔井田构造可分为压缩机制的推覆构造与伸展机制的断块体两类。南北F0为逆冲型的控制性边界断裂，井田内部一系列小型弧形构造为逆掩型浅层断裂；F1、F2、F17，是拉伸作用下的同沉积正断层，切断煤系基底T3地层。其动力机制为印度板块向北推移、西伯利亚板块向南运移发生对挤，脆一韧性剪切变形导致了井用现有的构造组合形式。