海南琼海烟塘梅岭铜钼矿床地质特征

琼海烟塘梅岭铜钼矿床位于海南五指山隆起东北侧的一个“角砾岩筒”中，该“角砾岩筒”的形成受南北向、东西向构造一岩浆岩带控制，与燕山期花岗闪长岩、花岗闪长斑岩关系密切。工业矿体主要集中在岩筒边缘接触带附近，共发现大小铜、钼矿体23个，矿体多呈透镜状、脉状，全为盲矿体，埋深数十米至400余米。矿石为细脉浸染状，Cu品位0．4％～0．9％，Mo品位0．01％～0．1％。蚀变带可粗略划分为钾化带、石英-绢云母化带和青盘岩化带，可能属斑岩型矿床。     

高寒富水地区-西藏那曲镇给水管道的安装及维修

西藏那曲镇是全世界海拔最高、含氧量最稀薄、最后一个安装自来水的地级城市。那曲镇海拔高度为4500m，冻土层深达2．8m，地下水丰富，基础开挖超过lm时就有地下水渗出，且土质多为流沙型，施工时容易引起塌方，施工环境恶劣。本文就那曲镇的具体情况介绍一下给水管道的安装及维修。     

马来西亚沙捞越邦达、什兰江控矿角砾岩筒构造对比研究及其找矿意义

马来西亚沙捞越邦达、什兰江控矿角砾岩筒构造均为典型的浅成—半浅成角砾岩筒构造，角砾岩及控矿类型具有明显的垂向分带特点。邦达控矿角砾岩筒构造发育角砾岩筒上段的塌陷角砾岩，角砾岩筒剥蚀深度较浅，控制典型的高硫化型浅成低温金铜矿床，且其深部具有较大的找矿潜力。什兰江控矿角砾岩筒构造发育角砾岩筒下段的爆发角砾岩和中段的流化角砾岩，分别控制斑岩型金矿化和低硫化型浅成低温热液型金矿化，角砾岩筒剥蚀深度较大，对矿床的保存和找矿极为不利。     

振动沉模大直径现浇薄壁管桩技术及其应用 (Ⅰ):开发研制与设计

振动沉模现浇混凝土薄壁管桩（PCC桩）技术是河海大学自主开发研制的用于地基加固处理的专利技术，是一种适合于软土地区的新型高效优质桩型，可有效地提高地基承载力和减小地基沉降。笔者介绍了振动沉模现浇混凝土薄壁管桩的技术原理、加固机理、施工设备、施工工艺及其设计与质量检测方法。该桩型具有承载力高、质量可靠和工程造价低等优点，具有较大的推广应用价值。     

地下管线源数据处理方法的研究

为了保障顺利建设上海市地下管线数据库．需要对现存的地下管线的源数据进行一些技术处理，以满足数据入库的要求。本文主要个绍：笔者在从事地下管线源数据处理工作中，碰到的现存的上海市地下管线源数据对于建设上海市地下管线数据库所存在的一些问题：以及笔者利用Autodesk公司的AutoCAD二次开发工具开发的应用程序来处理这些问题的方法。     

深基坑复合喷锚支护技术探讨

工程实践表明,复合喷锚支护是一种有效的深基坑支护型式,它可用于土层条件差、安全性要求高、变形控制严格的基坑工程中。复合支护中锚杆为主要受力构件,竖向花管为辅助受力构件,可起到限制、减小土体变形的作用。由于竖向注浆花管的加入,花管及注浆体抗剪作用加强,使基坑的整体稳定性得以大幅度提高。探讨了复合喷锚支护整体稳定性分析方法,建议将滑动区域分为加固土和原土两部分,将锚管注浆形成的注浆体等效为一层加固土,按喷锚支护模型计算复合喷锚支护整体稳定性。     

石龟山大桥直径3～4.4m空心桩施工技术

施工φ３￣４．４ｍ空心桩，需要预制空心桩节和护筒，搭建水上平台，进而介绍了钻孔施工，桩节组拼以及压浆等工艺。与实心桩相比，空心桩显示了独特的优越性。     

玄武岩深源岩石包体及金伯利岩中的尖晶石

我国东部新生代玄武岩中深源岩石包体内的尖晶石类矿物属铬尖晶石和铁尖晶石，金伯利岩及其地幔岩包体和金刚石中的尖晶石类矿物主要为铝铬铁矿。玄武岩中橄榄岩类包体内的尖晶石比其辉石岩类包体中的尖晶石含Ｃｒ高，含Ａｌ低，这与Ｃｒ为相容元素、Ａｌ为不相容元素、玄武岩中橄榄岩类包体是上地幔部分熔融出玄武岩浆后的残留物及其上地幔岩石的捕虏体、而辉石岩类是玄武岩浆结晶的产物有关。玄武岩中深源岩石包体中的尖晶石明显地比金伯利岩中的粗晶、地幔岩石包体及金刚石中的尖晶石含Ｃｒ低，含Ａｌ高，其主要原因是前者比后者形成的压力低     

Mineral inclusions in diamonds from the Sputnik kimberlite pipe, Yakutia

The Sputnik kimberlite pipe is a small “satellite” of the larger Mir pipe in central Yakutia (Sakha), Russia. Study of 38 large diamonds (0.7-4.9 carats) showed that nine contain inclusions of the eclogitic paragenesis, while the remainder contain inclusions of the peridotitic paragenesis, or of uncertain paragenesis. The peridotitic inclusion suite comprises olivine, enstatite, Cr-diopside, chromite, Cr-pyrope garnet (both lherzolitic and harzburgitic), ilmenite, Ni-rich sulfide and a Ti-Cr-Fe-Mg-Sr-K phase of the lindsleyite-mathiasite (LIMA) series. The eclogitic inclusion suite comprises omphacite, garnet, Ni-poor sulfide, phlogopite and rutile. Peridotitic ilmenite inclusions have high Mg, Cr and Ni contents and high Nb/Zr ratios; they may be related to metasomatic ilmenites known from peridotite xenoliths in kimberlite. Eclogitic phlogopite is intergrown with omphacite, coexists with garnet, and has an unusually high TiO₂ content. Comparison with inclusions in diamonds from Mir shows general similarities, but differences in details of trace-element patterns. Large compositional variations among inclusions of one phase (olivine, garnet, chromite) within single diamonds indicate that the chemical environment of diamond crystallisation changed rapidly relative to diamond growth rates in many cases. P-T conditions of formation were calculated from multiphase inclusions and from trace element geothermobarometry of single inclusions. The geotherm at the time of diamond formation was near a 35 mW/m² conductive model; that is indistinguishable from the Paleozoic geotherm derived by studies of xenoliths and concentrate minerals from Mir. A range of Ni temperatures between garnet inclusions in single diamonds from both Mir and Sputnik suggests that many of the diamonds grew during thermal events affecting a relatively narrow depth range of the lithosphere, within the diamond stability field. The minor differences between inclusions in Mir and Sputnik may reflect lateral heterogeneity in the upper mantle.     

Abbau von Monochlornitrobenzolen durch Pseudomonas acidovorans CA50

Degradation of Monochloronitrobenzenes by Pseudomonas acidovorans CA50 Pseudomonas acidovorans strain CA50 was used for degradation experiments with monochloronitrobenzenes in aerobic batch culture. The monochloronitrobenzenes were reduced to the corresponding monochloroanilines. The reduction only occurred with an additional carbon and nitrogen source. Chlorocatechols were found to be present. 3-Chlorocatechol accumulated in the presence of 2-chloroaniline, whereas 4-chlorocatechol was an intermediate metabolite of 3- and 4-chloroaniline. Contrary to the degradation of monochloronitrobenzenes, Pseudomonas acidovorans strain CA50 used the monochloroanilines as a sole source of carbon, energy, and nitrogen for growth. The oxidation of monochloroanilines was not repressed by the additional substrates. 2-Chloronitrobenzene was degraded with the lowest rate because of the low turnover of the intermediate metabolite 2-chloroaniline. 3-Chloronitrobenzene was completely degraded also in a mixture. A complete degradation of 4-chloronitrobenzene was achieved only when it was the sole chloronitrobenzene. The results suggest that a dechlorination and mineralization of monochlornitrobenzenes is possible, but for a final proof, further investigations will be necessary.