阿尔泰造山带花岗岩时空演变、构造环境及地壳生长意义——以中国阿尔泰为例

阿尔泰造山带横跨中、俄、哈、蒙四国边界,是中亚造山带主要组成部分,发育大量的花岗岩等侵入体。本文研究总结这些岩体的时空演变、成因类型和构造环境,并探讨其增生造山和地壳生长意义。依据锆石年龄,这些岩体可大致分为早中古生代的470～440Ma(中晚奥陶世)和425～360Ma(晚志留世—晚泥盆世)、晚古生代的355～318Ma(早石炭世)和290～270Ma(早二叠世)以及早中生代245～190Ma(中晚三叠世—早侏罗世)3个阶段5个期次,其中425～360Ma花岗岩可进一步细分为425～390Ma和380～360Ma两个峰期。早中古生代(470～360Ma)花岗岩体分布广泛,主要为钙碱性I型,多具不同程度变形,其中470～440Ma岩体变形极强(片麻岩体)。它们为同造山俯冲增生产物,形成于活动陆缘俯冲(470～440Ma)、继续俯冲弧后盆地伸展(420～390Ma)到聚合碰撞(380～360Ma)的过程中。早石炭世岩体发育于造山带南部,为不变形圆形状或不规则状,具典型碱性花岗岩特征,为晚(后)造山产物。早二叠世岩体主要发育于阿尔泰造山带南部,少量分布于造山带内部,多为圆形,不变形,少量变形岩体集中在额尔齐斯构造带内,成因类型以I、A型为特点,伴生有大量基性岩脉(体),显示为后造山底侵伸展环境。早中生代岩体为不变形圆形或不规则状,具有高分异I型和S型花岗岩特征,伴有稀有金属矿产,具有板内环境特点。花岗岩体同位素填图显示,阿尔泰中部块体岩体具有较低的εNd(t)值和老的Nd同位素模式年龄(1～1.3Ga),暗示存在古老地壳基底;由北向南εNd(t)值增高,模式年龄变年轻,显示陆壳向南生长,其中水平和垂向生长率分别为18%～28%和7%～8%。中生代时期阿尔泰造山带保留水平增生结构,没有发生大规模构造块体垂向叠覆。阿尔泰造山带经历了古陆缘构造演化,奥陶纪—志留纪陆缘俯冲,泥盆纪陆弧及陆缘边缘裂解、弧后盆地形成,晚泥盆世最终洋盆闭合及早石炭世各块体拼合的演化过程。该研究表明增生造山带中同样存在构造演化的阶段性;中亚增生造山作用不仅具有弧前增生,而且还存在陆缘裂解再拼合作用。     

A Preliminary Study on the Present Crustal Stress of Northern South China Sea

<正>The South China Sea(SCS)is the largest marginal sea in West Pacific formed by a combined effect of the Eurasian plate,Pacific plate and India-Australian plate,and is thus considered to be a unique natural laboratory to study oceanic dynamics and tectonic evolutions(Xie et al.,2006;Luan and Zhang,2009).Besides,the SCS contains enormous petroleum resources for its favorable conditions of oil-gas generation,accumulation and preservation.It is therefore imperative to intensively study the marine in-situ     

中超长钻孔灌注桩的沉降计算

针对现有的桩基沉降计算理论不仅难以完整地描述桩－土系统的复杂程度，在应用上也难以满足各方面的要求，根据中超长钻孔灌注桩的实际情况，采取一些合理的简化措施后，提出了一种实用的桩基沉降计算方法，实例分析表明，该方法可较好地预测桩的沉降量。     

Texture Segmentation Based on Image Model and Neural Network

INTRODUCTIoNImagetextureanalysisisanimportantpartofresearchin-tocomputervision.Forobjectidentificationandunderstand-ing,textureanalysisisthebasisoftheresearchwork.Ingeneral,texturecanberegardedasakindofstructurethatconsistsofmanytextureelementsorpatternswhicharemoreorlesssimilar,i.e.,primitivesthatformtexturesandspatialdependenceorinteractionbetweentheprimitives.Ex-tensiveresearchhasbeendoneintextureanalysis,andrefer-ence(Haralick,l979)hasmadeathoroughsurvey.Amongthesetextureanalysismetho…     

Adsorption of phenanthrene on Al (oxy)hydroxides formed under the influence of tannic acid

Although there has been substantial research done on adsorption of metals/metalloids by Al (oxy)hydroxides, little is known regarding the adsorption of polyaromatic hydrocarbons (PAHs) on Al (oxy)hydroxides, especially those formed in the presence of organic acid. This paper investigated the adsorption of phenanthrene on Al (oxy)hydroxides formed with initial tannate/Al molar ratios (MRs) 0, 0.001, 0.01, and 0.1 (referred to MR0, MR0.001, MR0.01, and MR0.1, respectively) through batch adsorption experiments and FTIR study. The results showed that Al (oxy)hydroxides were important sorbents for phenanthrene. The adsorption kinetic data were fitted well with the pseudo-second-order equation. According to a modified Freundlich model, the adsorption capacities of Al (oxy)hydroxides followed a descending order of MR0.1 > MR0 ≥ MR0.01 > MR0.001, which was inconsistent with the organic carbon content in the Al (oxy)hydroxides. Adsorption capacity correlated with the specific surface area, micropore area, and micropore diameter of Al (oxy)hydroxides, yet the relationships were not statistically significant (P > 0.05). FTIR results showed that physical interaction was essential in phenanthrene adsorption onto the Al (oxy)hydroxides, which could be explained by an entropy-driven process. Surface hydrophobicity of Al (oxy)hydroxides played a key role in phenanthrene adsorption. Additional π–π electron donor–acceptor interaction of phenanthrene (acting as electron donor) with aromatic ring of tannic acid (electron acceptor) could be also important in phenanthrene adsorption by high MR Al (oxy)hydroxides, yet it needs further study. The findings obtained in the present study are of fundamental significance in understanding the mechanism of immobilization of PAHs in low organic matter but oxide-rich soils.     

黑河下游土壤和地下水盐分特征分析

根据405个土壤样品和101个水样,分析了黑河下游土壤盐分分布规律以及与地形地貌部位、地下水水化学的关系.结果表明:额济纳三角洲地区的土壤具有质地粗、含盐量高、盐分表聚性强的特征,该地区呈现盐碱化和沙漠化严重、可利用土地资源骤减、生态环境恶化的状况.在所有剖面上盐分的分布呈现漏斗型分布,土壤中盐分随地形变化较为复杂,但与地下水化学变化相一致.地下水矿化度普遍比较高,大多数地区的矿化度在800~3000 mg·L^-1之间变化;水化学类型主要有HCO₃·SO₄-Na、Cl·SO₄-Na(Ca)、HCO₃·Cl-Na(Ca)SO₄·Cl-Na和SO₄·Cl-Na(Ca-Mg).地下水矿化度的高低与补给源的距离远近密切相关,在河岸附近的矿化度变化幅度较小;在远离河道地区,随离岸距离的增减而升降,体现了矿化度的高低主要依赖于上游补给水量变化.     

长江口及邻近海域现代沉积速率及其对长江入海泥沙去向的指示意义

对长江口及附近海域的16根重力柱样进行了210Pb沉积速率测试, 结合以往成果, 揭示了该区现代沉积速率分布格局, 对其控制因素以及其对认识长江入海泥沙去向的指示意义进行了探讨.沉积速率最高值分布在南支口外、杭州湾口群岛北部的前三角洲地区, 最高可达6.3m/a, 总体上在3cm/a以上; 次高值分布在杭州湾北部, 约1.7~3.0cm/a, 南部略低, 约0.4~1.0cm/a; 长江口水下负地形北部海域存在小片沉积速率较高的区域, 最高值达2.58cm/a; 低值主要分布在苏北辐射沙洲、过渡沉积区以及浅海陆架的大片区域, 基本保持在1cm/a以下.研究表明, 长江泥沙出口门后主要在水下三角洲地区进行了堆积, 其次有相当部分在涨潮流顶托下进入杭州湾, 进入杭州湾南部的泥沙又在落潮流作用下经杭州湾南侧向舟山海域方向输运; 长江入海物质向外海的扩散基本被控制在123°E以西, 苏北辐射沙洲、过渡沉积区以及浅海陆架的大片区域缺乏现代长江物质供应; 长江悬浮泥沙对研究区东北部陆架区影响较小, 废黄河口被侵蚀物质和黄海悬浮物质为其较高沉积速率的主要贡献者.      

胶东焦家断裂带与金矿的成生关系

文中着重阐述了控矿断裂活动与焦家金矿Ⅱ、Ⅰ、Ⅲ号矿体之间的成生关系。指出:焦家金矿Ⅱ号矿体与控矿断裂第一期活动有关,Ⅰ号矿体与第二期活动有关,Ⅲ号矿体与第三期活动有关。控矿断裂第一、二期活动显压扭性,第三期活动则显张扭性特征,Ⅰ、Ⅱ号矿体的矿化类型为破碎蚀变岩型,Ⅲ号矿体为多金属硫化物脉型。      

资阳地区震旦系古岩溶储层特征及测井评价

位于四川盆地的资阳地区在震旦系灯影组中发现了继威远震旦系气藏之后的又一大型气藏。区内７口钻井揭露的地层显示本区灯影组主要由一套震层状白云岩民,基质岩块具低孔低渗特点,有效的储集空间是由受古岩溶作用产生的溶蚀孔洞和构造作用产徨的裂缝共同构成,溶洞具有数量多,大洞多,发育集中的特点,裂缝具有成因,多期次,多产状的特点,对这套以缝洞型为玉的储层,由常规测井资料计算单一的物性参数（如孔隙度等）的方法难以其     

洮河泥沙分布及变化分析

以洮河红旗站1956~2005年水文监测资料为依据,通过对泥沙分布特征、年内年际变化规律和水沙匹配情况进行分析,得出洮河泥沙具有含量高、输沙总量大、产沙的区域性、年际的波动性、年内的不均匀性和时间的集中性六大特点。