延安试区人工刺槐林地的土壤干层分析

8 0年代以来 ,以林草地地力衰退为特征的人工林草地土壤退化日趋严重 ,其中以土壤水分严重亏缺为特征的土壤干化现象愈益引起了人们的重视。土壤干化的直接后果是形成土壤干层 ,导致土壤退化 ,植物生长速率减缓 ,群落衰败以至大片死亡 ,严重地威胁到我国北方地区特别是黄土高原地区生态环境的建设。因此 ,研究和解决土壤干层问题已成为黄土高原植被建设的迫切任务。根据延安试区的土壤水分和植被生长状况调查资料 ,初步分析了不同条件下刺槐人工林地的水分状况。结果表明 :试区刺槐人工林地普遍形成了土壤干层 ,且已相当严重 ;坡向对土壤干层有明显影响 ,阳坡形成的干层较阴坡严重 ;坡度愈大 ,土壤干化愈剧烈 ;林龄对干层严重程度影响不明显。同时 ,研究指出了解决土壤干层问题的意义。

温度、pH及干旱胁迫对沙地樟子松外生菌根菌生长影响

通过对采集于沙地樟子松人工林内的3种外生菌根真菌(牛肝菌Boletussp.、乳菇Lactariussp.、高环柄菇Macrolepiota procera)进行纯培养,在不同温度、pH值和PEG模拟干旱胁迫条件下,观测了外生菌根菌的生长发育状况。结果表明,3种外生菌根菌生物量在不同pH范围(3~7)内存在着显著差异(P<0.05);在低于5℃和高于37℃时,3种外生菌根菌均不能生长,其最适生长温度分别为:牛肝菌,25℃高环柄菇,25~28℃,乳菇,25~30℃;在低浓度PEG胁迫处理条件下(10%,-0.20MPa),3种外生菌根菌的生长均有所增加,当PEG胁迫达到30%(-1.53 MPa)时,3种外生菌根菌的生长均受到抑制。与上述结果比较,沙地樟子松人工林地土壤的实际pH值在外生菌根菌的最适生长范围内;林地最高气温值远远超过3种外生菌根菌的最适生长值的时间在每年的生长季都会出现;在极端干旱年份(如1996年),林地土壤的实际含水量在生长季节(5~9月)远远低于抑制外生菌根菌生长的土壤含水量,可能影响到外生菌根菌的生存。因此,可以推断,沙地樟子松人工林地的外生菌根菌的生长与发育,在干旱胁迫及高温作用下受到很大程度的影响,如果仅从微生物角度分析,外生菌根菌在干旱和高温条件下不能生长或已经死亡是导致沙地樟子松人工林衰退的一个原因。

中国的褐褶菌属(担子菌门,非褶菌目)的研究(英文)

对中国褐褶菌属Gloeophyllum的种类进行了研究,并记录了此属中10个种。其中喜干褐褶菌Gloeophyllumprotractum是中国的新记录种,发现于黑龙江和四川省的针叶树倒木上。根据中国的材料详细描述了此种,并列出褐褶菌属的检索表。

实物界面下的虚拟装配

基于增强现实技术,将实物用户界面应用到虚拟装配系统中,在单摄像头的条件下,将虚拟零件模型加载至实物标记上,用户通过操作实物标记来控制虚拟模型,完成装配过程。相比于传统的虚拟装配交互方式,增强了用户操作的切实感。根据装配任务需求设计了4类实物标记。提出了3种交互技术,包括接近性原理,匹配约束信息提示与判定,以及视点控制等,并且结合碰撞检测来实现精确而又自然的虚拟装配。该系统可以帮助设计人员方便地对产品设计进行分析和改进,降低用户的学习难度。

湘西多金属矿区汞铅污染土壤的环境质量

以湘西典型多金属矿区为现场,研究了矿区土壤中汞、铅等重金属污染状况及成因.结果表明,湘西矿区是汞、铅污染严重的区域,与中国土壤元素背景值相比,汞矿区土壤中汞、铅含量分别增加1315倍和3.1倍,铅锌矿区土壤中汞、铅含量分别增加14.8倍和16.1倍.运用Muller地积指数进行风险评价,证实湘西矿区是汞、铅等重金属的复合污染区,汞矿区汞污染以极重污染为主,铅污染以中度和轻污染为主;铅锌矿区铅污染以中度和中-重污染为主,汞污染以中-重污染为主.矿区土壤中的重金属污染物来源和分布受原生地球化学条件的控制,而人为采矿活动对矿区土壤中汞、铅的污染格局产生重要影响.

Relationship between charge transfer energies of Yb3+ and Sm3+ and crystal environmental factor

Relationship between charge transfer energies E-CT of Yb3+ and Sm3+ and environmental factors h(e) in various crystals was investigated using a dielectric chemical bond method. Both results show that they have an exponential relation E-CT = A+B exp(-kh(e)), but the exponential factors are different, which indicates that the interaction between the rare earth ions and environment is connected with the kind of rare earth ion. This result provides a method of determining charge transfer energies of Yb3+ and Sm3+ from a crystal structure.

Novel proton exchange membranes based on water resistant sulfonated poly[bis(benzimidazobenzisoquinolinones)]

Novel water resistant sulfonated poly[bis(benzimidazobenzisoquinolinones)] (SPBIBIs) were synthesized from 6,6'-disulfonic-4,4'-binaphthy]-1,1',8,8'-tetracarboxylic dianhydride (SBTDA) and various aromatic ether tetraamines. The resulting polymers with IEC in the range of 2.17-2.87 mequiv g(-1) have a combination of desired properties such as high solubility in common organic solvents, film-forming ability, and excellent thermal and mechanical properties. Flexible and tough membranes, obtained by casting from m-cresol solution, had tensile strength, elongation at break, and tensile modulus values in the range of 87.6-98.4 MPa, 35.8-52.8%, and 0.94-1.07 GPa. SPBIBI membranes with a high degree of sulfonation displayed high proton conductivity and a good resistance to water swelling as well. SPBIBI-b with IEC of 2.80 mequiv g(-1) displayed the conductivity of 1.74 x 10(-1) S cm(-1) at 100 degrees C, which was comparable to that of Nafion (R) 117 (1.78 x 10(-1) S cm(-1), at 100 degrees C).

镁锂合金表面耐蚀微弧氧化膜的研究

利用微弧氧化技术在镁锂合金的表面成功制备了微弧氧化膜。利用SEM、XRD、XPS、动电位极化和电化学交流阻抗谱对微弧氧化膜结构、相组成以及耐蚀性能进行了研究。SEM观测结果表明,氧化膜层的结构是由疏松层和致密层组成的双层结构,微弧氧化膜表面存在大量直径约2～7μm的微孔。XRD和XPS分析表明,微弧氧化膜的主要相组成为方镁石氧化镁和无定形磷酸盐化合物。动电位极化曲线以及电化学交流阻抗谱分析表明,微弧氧化处理后镁锂合金的耐蚀性能得到显著提高。

Investigations on the adsorption behavior of Neutral Red on mercaptoethane sulfonate protected gold nanoparticles

A detailed investigation on the adsorption behavior of Neutral Red (NR) molecules on mercaptoethane sulfonate-monolayer protected gold clusters (MES-MPCs) has been conducted by the spectroscopic method. It is found that cationic NR molecules are adsorbed on the negatively charged MPCs surfaces via electrostatic attractive forces. The absorption study shows that the optical properties of NR molecules are significantly influenced upon the adsorption. Based on the electrostatic adsorption nature and the excellent stability of MES-MPCs against the electrolytes, this association can be released by the addition of electrolyte salts, which can be monitored by both absorption and fluorescence spectroscopy. In addition, dication Ca2+ is found to be more effective in the release of NR than univalent Na+. Moreover, the MES-MPCs exert energy transfer quenching of NR fluorescence by both static and dynamic quenching. However, static quenching seems to be the dominating quenching mechanism. Furthermore, this energy transfer quenching exhibits strong dependence of Au core size, and 5.0 nm MPCs show stronger ability in quenching the NR fluorescence than that of 2.7 nm MPCs.

The microstructure and mechanical properties of Mg-8Zn-8Al-4RE magnesium alloy

The Mg-8Zn-8Al-4RE (RE = mischmetal, mass%) magnesium alloy was prepared by using casting method. The microstructure and mechanical properties of as-cast alloy, solid solution alloy and aged alloy samples have been investigated. Optical microscopy, X-ray diffractometery and scanning electron microscope attached energy spectrometer were used to characterize the microstructure and phase composition for the alloy. Net shaped tau-Mg-32(Al,Zn)(49) phase was obtained at the grain boundary, and needle-like or blocky Al11RE3 phase disperses in grain boundary and alpha-Mg matrix. The tau-Mg-32(Al,Zn)(49) phase disappeared during solution treatment and a new phase of Al(2)CeZn2 formed during subsequent age treatment. The mechanical properties were performed by universal testing machine at room temperature, 150 degrees C and 200 degrees C, separately. The ultimate tensile strength of as-cast alloy is lower compared to an age treatment alloy at 200 degrees C for 12h. The strengths decreased with enhancing test temperature, but elongation has not been effect by age treatment.

Mesoporous acid solid as a carrier for metallocene catalyst in ethylene polymerization and a catalyst in catalytic degradation of polyethylene

The possibility of mesoporous acid solid as a carrier for metallocene catalyst in ethylene polymerization and catalyst for polyethylene (PE) catalytic degradation was investigated. Here, HMCM- 41 and AIMCM-41, and mesoporous silicoaluminophosphate molecular sieves (SAPO1 and SAPO2) were synthesized and used as acid solid. Much more gases were produced during catalytic degradation in PE/acid solid mixtures via in situ polymerization than those via physical mixing. The particle size distribution results exhibited that the particle size of SAPO1 in the PE/SAPO1 mixture via in situ polymerization was about 1/14 times of that of the original SAPO1 or SAPO1-supported metallocene catalyst. This work shows a novel technology for chemical recycling of polyolefin.