从动力地质作用原理探讨沙漠化成因

大规模沙漠化从岩石记录中可以追溯到中生代中期，第四纪以来南北两半球各存在一条中纬度沙漠带，中国的沙漠化是这个全球沙漠化进程的一个组成部分。沙漠化是在地质演化过程中受内、外动力地质作用联合控制的地质事件。是岩石圈与大气圈、生物圈及水圈强烈作用在地壳表层形成的一种特殊地质现象。这种现象的形成与演化是漫长的和具有周期性的，不会因为局部的条件变化而发生整体意义上的突变。人类活动是局部的，在整个地球沙漠化进程中只是起到一个加速剂的作用。沙漠化过程可分为3个阶段，即物理风化与沙源积聚阶段、风沙作用阶段和沙漠化阶段。沙漠期后沙丘沙经过固化生草、胶结成岩阶段后即形成风成砂岩。     

未熟-低熟烃源岩的有机岩石学特征

采用全岩光片镜鉴和显微荧光分析方法 ,对我国不同地区 5 0 0余块未熟 低熟烃源岩样品进行了系统的有机岩石学研究。未熟 低熟烃源岩显微组分组成具有显著的非均质性 ,不同地区显示出陆源组分与水生生源组分不同的“配比”关系 ,反映出其有机质组成的复杂性 ,并确认藻类体、孢子体、树脂体、木栓质体、壳屑体和矿物沥青基质等组分是其最常见的生烃组分。基于对镜质组反射率Ro和孢子体荧光变化等演化指标特征的分析 ,认为未熟 低熟烃源岩有机质早期热演化具有明显的阶段性 ,一般都表现为“二段式”变化 ,其变化界限大致以Ro等于 0 .5 0 %～ 0 .5 5 %为界。     

凤眼莲根系分泌物对栅藻结构及代谢的影响

研究了凤眼莲（Ｅｉｃｈｈｏｒｎｉａ ｃｒａｓｓｉｐｅｓ）根系分泌物对栅藻（Ｓｃｅｎｅｄｅｓｍｕｓ ａｒｃｕａｔｕｓ Ｌｅｍｍ）超微结构及生长代谢的影响，结果显示，凤眼莲对栅藻有明显的克生作用，藻的数量逐步减少，栅藻生长受影响后，细胞中绿体片层肿用甚至解体，线粒体嵴消失，质膜、核膜受破坏，光合放氧化速度明显下降，可溶性蛋白折含量四天后４线下降，超氧阴离子（Ｏ２－）、丙二醛（ＭＤＡ）的含量上升，知值都     

川西北哲波山微细浸染型金矿床岩浆岩特征

对川西北哲波山金矿区内出露的中 -酸性岩脉、岩株的类型、化学成分、地质特征以及微量元素、同位素、稀土元素等特征进行了研究 ,指出印支晚期和燕山早期的岩浆岩均属钙碱质岩系列 ,均起源于幔壳混源区 ,原始岩浆在成分上和演化上又存在着一定的差异性。岩浆岩为成矿提供了一定的物质基础。     

海水、大气化学演化对动物起源和进化方向的制约

动物的起源主要依赖于氨基酸等有机小分子在海水中能否进行脱水缩合反应而生成生物高分子，后者则依赖于海水pH值升高和大气CO2浓度降低的历史演化进程。有机小分子只有在海水pH值演化到近中性，即寒或纪时彼此才能发生脱水缩合反应而合成生物高分子。只有大气CO2分压降到1000Pa以下，即泥盆纪以后，陆地上才能出现稳定的土壤层和植物，动物也才能从海洋扩展到陆地。随后大气CO2浓度继续降低导致了气温下降和植物生长率的衰减，促使动物进一步演化。     

欧亚大陆东南缘大陆地壳基底研究与展望

本文从不同方面和断代论述了中国东南地区的基底杂岩时代、性质、构造环境、边界变质条件、地球物理场及其反映的构造格局、断裂体系、中生代火山活动的基底构造及类型分区。在此基础上提出了东南地区的构造划分及构造演化阶段和格局。并提出了不同类型的地体及其分类、大陆裂解、增生的新概念。     

Adsorption and correlation with their thermodynamic properties of triazine herbicides on soils

IntroductionAdsorptionofherbicidesonsoilfromwaterisanimportantfactoraffectingtheirfate,biologicalactivity,andpersistenceinsoil watersystem .Itisoftenaffectedbyseveralpropertiesofsoil.Betterunderstandingofadsorptionanditsaffectingfactorswillmakeitpossibletoadjusttheherbicidedosageaccordingtosoilproperties,thusreducingtheenvironmentalpollutionofherbicidesintheenvironment.Fig .1　StructuresofthreetriazineherbicidesAmongthepost emergentherbicides,triazineherbicidesaremostcommonlyusedworldwideonco…     

Starch, Poly(lactic acid), and Poly(vinyl alcohol) Blends

Research on biodegradable materials has been stimulated due to concern regarding the persistence of plastic wastes. Blending starch with poly(lactic acid) (PLA) is one of the most promising efforts because starch is an abundant and cheap biopolymer and PLA is biodegradable with good mechanical properties. Poly(vinyl alcohol) (PVOH) contains unhydrolytic residual groups of poly(vinyl acetate) and also has good compatibility with starch. It was added to a starch and PLA blend (50:50, w/w) to enhance compatibility and improve mechanical properties. PVOH (M_W 6,000) at 10%, 20%, 30%, 40%, 50% (by weight) based on the total weight of starch and PLA, and 30% PVOH at various molecular weights (M_W 6,000, 25,000, 78,000, and 125,000 dalton) were added to starch/PLA blends. PVOH interacted with starch. At proportions greater than 30%, PVOH form a continuous phase with starch. Tensile strength of the starch/PLA blends increased as PVOH concentration increased up to 40% and decreased as PVOH molecular weight increased. The increasing molecular weight of PVOH slightly affected water absorption, but increasing PVOH concentration to 40% or 50% increased water absorption. Effects of moisture content on the starch/PLA/PVOH blend also were explored. The blend containing gelatinized starch had higher tensile strength. However, gelatinized starch also resulted in increased water absorption.     

双室火灾烟气特性的实验研究

本文在１／２缩尺建筑模型中，取双室－走廊结构，以标准木垛为火源，对建筑火灾的初始阶段进行了实验模拟。着重研究了火灾初期的烟气特性及其变化，包括烟气温度及烟气中ＣＯ＿２气体和炭颗粒浓度。本文目的在于在探索和发展中等尺寸火灾实验模拟手段和方法的同时，定性地确定火源功率对烟气特性的影响，并积累一定的实验数据，为建筑火灾的分析和模化提供实验基础和依据。     

Mechanical Properties with the Functional Group of Additives for Starch/PVA Blend Film

This paper deals with the mechanical properties and degree of swelling (DS) of starch/PVA blend film with the functional groups i.e., hydroxyl and carboxyl group, of additives. Starch/PVA blend films were prepared by using the mixing process. Glycerol (GL) with 3 hydroxyl group, sorbitol (SO) with 6 hydroxyl group, succinic acid (SA) with 2 carboxyl group, malic acid (MA) with 1 hydroxyl and 2 carboxyl group, tartaric acid (TA) with 2 hydroxyl and 2 carboxyl group and citric acid (CA) with 1 hydroxyl and 3 carboxyl group were used as additives. The results of measured tensile strength (TS) and elongation (%E) verified that both hydroxyl and carboxyl group as a functional groups increased the flexibility and strength of the film. Values of DS for GL-added and SA-added films were low. However, DS values of the films added MA, TA or CA with both hydroxyl and carboxyl group were comparatively high. When the film was dried at low temperature, the properties of the films were evidently improved. The reason is probably because the hydrogen bonding was activated at low temperature.