土壤干旱对小麦茎秆贮藏物质积累与再转运的影响

在防雨池栽条件下,以小麦旱地品种长武134(抗旱性强)和水地品种(抗旱性弱)为试材,研究干旱对不同抗旱性小麦茎秆及其组成节间花后干物质积累、转运及其对籽粒产量贡献率的影响。结果表明,干旱降低了主茎及其各组成节间干物质的积累量、主茎穗粒重积累量及其灌浆中后期的积累速率,长武134(除其它茎)降低幅度均小于陕253;干旱条件下茎秆贮藏物质的转运并未对籽粒产量产生补偿效应,干旱降低主茎穗粒重积累量与其它茎贮藏物质转运量和转运率较低有密切关系;抗旱性强的小麦品种其它茎的转运量、转运率降低幅度均大于抗旱性弱的小麦品种,从而导致其主茎贮藏物质转运对籽粒产量的贡献率显著降低。

黄土高原旱区长期施肥条件下土壤钾素形态空间分布特征及有效性研究

在黄土高原南部旱地长期肥料定位试验的基础上研究了土壤钾素空间分布特征及其有效性。结果表明:长期施肥后土壤中特殊吸附性钾(SAK)和非特殊吸附性钾(NSAK)储量增加,但水溶性钾(WSK)和非交换性钾(NEK)则有明显的下降,单施N水溶性钾下降了48.24%,单施P下降32.32%,NP配施和NPK配施分别下降10.61%和17.93%,非交换性钾降幅为8.56%~24.91%。增施钾肥可以缓解因长期施肥作物生长所携出的钾素,增加耕层土壤中的水溶性钾、非特殊吸附性钾及特殊吸附性钾。相关分析结果表明,土壤不同形态钾素对速效钾的重要性依次为WSK>NSAK>SAK>NEK,土壤速效钾与水溶性钾、非特殊吸附性钾呈显著相关,与特殊吸附性钾和非交换性钾无显著相关性。

黄土高原六盘山生态经济圈功能区规划研究

六盘山区位于黄河中上游,是黄土高原西部天然生态屏障和水源涵养区,在中国生态环境建设中具有重要战略地位。本区土地资源丰富,生态环境洁净,旱作农业潜力大,草畜业兴旺。六盘山生态经济圈规划了4个功能区和7大特色农业基地产业,以六盘山国家自然保护区为中心,加大退耕造林种草与管护力度,到2015年基本修复六盘山区受损的森林生态系统和灌丛草原植被;以旱作农业技术体系为支撑,建立高效可持续发展的生态农业系统和绿色农牧产品基地,为经济社会发展和新农村建设提供良好的生态环境和农业基础。

六盘山森林土壤种子库与植被演替过程

以六盘山森林植被为研究对象,通过20多年的森林土壤种子库变化与植被演替过程的试验研究,分析了8种森林群落类型的不同生长年限、生长坡位、枯枝落叶层和土壤深度对土壤种子库形成过程的影响。结果表明:六盘山森林群落不同生长坡位,土壤种子库的储量坡中部>坡下部>坡上部;不同层次土壤种子库,枯枝落叶层远高于0-15 cm深土层,8种森林群落类型排序为华北落叶松林>油松林>华山松林>辽东栎林>山杨林>白桦林>灌丛>草地;土壤种子库储量高峰期,不同群落有显著差异,华山松林和油松林在林龄的30~40年,华北落叶松林在20年,辽东栎林、山杨林、白桦林在15~20年,灌丛和草地在10~20年,其森林群落生长年限与土壤种子库储量变化趋势呈拟合曲线,符合指数方程,相关性极为显著;土壤种子库物种组成丰富,草本和灌木植物远高于乔木树种,乔木树种仅有3~5种,但多数为外来入侵种,而在每一类型中出现频率最高的草地植物多为蒿类,灌木植物为柔毛绣线菊和沙棘,乔木为辽东栎树种。因此,在六盘山林区植被自然更新与合理演替的驱动种和先锋种草地植物为蒿类,灌木植物为柔毛绣线菊和沙棘,乔木为辽东栎,其次是华北落叶松、油松和华山松。

云南西北部四县林地的分布和受威胁程度评价以及该地区鸡形目鸟类的保护状况分析

横断山区拥有独特的生物区系和丰富的生物多样性，成为研究生物和地学许 多重大理论问题的关键性区域。然而该地区复杂的高山峡谷地形不利于大范围实 地考察工作的开展，而传统的调查方法也较难直接地获取野生动物及其生境的一 些量化数据，如某种或某类生物元素的分布、变化情况以及保护状况等，因此长 期以来对于该地区保护网络的规划和管理效果一直缺乏系统地评价，保护工作的 进一步开展依然面临很多难题。近年来地理信息系统（Geographic Information System, GIS）和遥感技术（Remote Sensing, RS）已经广泛应用于野生动物及其 生境保护的各个方面，为横断山区的保护工作拓展了新的研究思路和方法借鉴。 本研究以位于云南西北部横断山区的四个县（德钦、维西、丽江、香格里拉） 作为核心研究地区，以野生动物的主要栖息地——林地为对象，借助RS 和GIS 手段研究该地区内林地的分布、变化以及受威胁程度；并针对鸡形目鸟类的保护 状况进行了分析，为该地区林地和鸡形目鸟类的保护及评价提供科学的方法指导 和建议。具体如下： （1）林地分布以及针叶林的进一步细分。在地面真实数据的辅助下，通过 对Landsat TM/TM+影像的预处理、分类、分类后处理等过程，将研究地区中的 林地与非林地进行划分；针对暖温性针叶林和寒温性针叶林这两种较难区分的类 别，采用导引聚类（guided clustering）的分类方法，进一步对针叶林进行细分。 精度评估的结果显示，林地与非林地的划分总体精度为94.3%，而针叶林细分为 暖温性针叶林和寒温性针叶林的总体精度为74.8%。该方法可以较为准确地划分 该地区不同的生境类型，为野生动物及其生境的保护奠定基础。（2）林地的受威胁程度评价。通过分析研究地区中的林地在40 多年时间跨 度里（1958-2001 年）的变化情况和保护现状，从而评价其受威胁程度，结果反 映出每个县的林地面积都有不同程度的减少，丽江和香格里拉这两个县的林地受 威胁程度相对较高。进一步对丽江和香格里拉两县在不同海拔带的林地分布和变 化情况进行分析，结果表明，丽江的林地主要分布于2000-3500 米的海拔范围内 （占该县全部林地面积的89.7%），而在香格里拉则主要分布于2500 米以上（占 该县全部林地面积的95.2%）；在这两个林地分布较为集中的区域内，都是低海 拔地区林地面积减少程度较高，意味着在开展保护工作时应重点关注这两个县的 低海拔林地。本研究方法可供整个横断山区乃至其他高山峡谷地区借鉴，为保护 网络的完善提供快速的量化参考。 （3）鸡形目鸟类的保护状况分析。借助RS 和GIS 手段描绘研究地区中当 前林地（2001 年左右）以及早期林地（1958 年前后）的分布，针对那些主要以 林地为生境的鸡形目鸟类，在相应限制因子（例如海拔数据）的辅助下对它们当 前和过去的潜在生境进行预测，从而分析它们的保护现状和生境的变化情况。结 果表明研究地区中现有的保护区对这些鸟类的保护尚不完善，并且在过去40 多 年的时间跨度里它们的潜在生境都有不同程度的退化。建议将来的保护工作优先 考虑那些在当前未被充分保护的物种以及潜在生境退化程度相对较高的物种。针 对这些物种，提出在将来的进一步保护工作中的一些建议，为整个横断山区鸡形 目鸟类乃至其他野生动物类群的保护提供参考。

35-PERCENT EFFICIENT NONCONCENTRATING NOVEL SILICON SOLAR-CELL

An energy conversion efficiency of 35% was obtained at 1-sun, air mass 1.5 for a novel silicon cell having an area of 2.3 X 2.3 mm2 . cell. The critical feature of the cell structure is the inclusion of local defect layers near a p-n junction. The local defect layers were proven to hold the key to achieving the exceptionally high efficiency of the novel cell fabricated via noncomplex processing.

Photoluminescence and activation on SI-GaAs by Si+ implantation and following rapid thermal annealing

Photoluminescence (PL) and electrical characteristics of SI-GaAs, Si+-implanted and following rapid thermal annealing (RTA), were investigated, The PL spectra of Si-GA-C-As, Ga-i-Si-As, and V-As-Si-As were obtained. This paper concentrates on the PL peak at 1.36 eV which was proven as an emission of the Si-Ga-V-Ga combination by Si+ + P+ dual implantation. The results indicate that the peak at 1.36 eV appears when the ratio of As:Ga increased during the processing. Also high activation was obtained for the sample under the same conditions. More discussion on the mechanism of Si+ implanted SI-GaAs has been made based on the Morrow model [J. Appl. Phys, 64 (1988) 1889].

Optimization of Global Signal Networks for Island-Style FPGAs

We present a staggered buffer connection method that provides flexibility for buffer insertion while designing global signal networks using the tile-based FPGA design methodology. An exhaustive algorithm is used to analyze the trade-off between area and speed of the global signal networks for this staggered buffer insertion scheme, and the criterion for determining the design parameters is presented. The comparative analytic result shows that the methods in this paper are proven to be more efficient for FPGAs with a large array size.

Multimode Interference Couplers with Different Background Refractive Index *

A novel structure of MMI coupler with different background refractive index has been designed. With stronger optical confinement in multimode waveguides, more guided modes are excited to improve imaging quality. Two-dimensional finite difference beam propagation method (2-D FDBPM) was used to simulate this new structure and had proven that its imaging quality, in terms of power uniformity and excess loss, is much better than conventional structure. This structure can be applied in SOI rib waveguides by deep etching method.

Study on tapered crossed subwavelength gratings by Fourier modal method

Fourier modal method incorporating staircase approximation is used to study tapered crossed subwavelength gratings in this paper. Three intuitive formulations of eigenvalue functions originating from the prototype are presented, and their convergences are compared through numerical calculation. One of them is found to be suitable in modeling the diffraction efficiency of the circular tapered crossed subwavelength gratings without high absorption, and staircase approximation is further proven valid for non-highly-absorption tapered gratings. This approach is used to simulate the "moth-eye" antireflection surface on silicon, and the numerical result agrees well with the experimental one.

Reduction-Based Model Updating of a Scaled Offshore Platform Structure

This paper attempts to develop a reduction-based model updating technique for jacket offshore platform structure. A reduced model is used instead of the direct finite-element model of the real structure in order to circumvent such difficulties as huge degrees of freedom and incomplete experimental data that are usually civil engineers' trouble during the model updating. The whole process consists of three steps: reduction of FE model, the first model updating to minimize the reduction error, and the second model updating to minimize the modeling error of the reduced model and the real structure. According to the performance of jacket platforms, a local-rigidity assumption is employed to obtain the reduced model. The technique is applied in a downscale model of a four-legged offshore platform where its effectiveness is well proven. Furthermore, a comparison between the real structure and its numerical models in the following model validation shows that the updated models have good approximation to the real structure. Besides, some difficulties in the field of model updating are also discussed.

高寒湿地自然保护区多核心动态分区研究——以四川若尔盖湿地国家级自然保护区为例

中国拥有92466 Km2的各类高原湿地，具有湿地退化、过度放牧等相似特征，保护与利用矛盾突出。高寒湿地保护区尽管在制度上以核心区、缓冲区来约束当地的放牧等外来干扰行为，但在实际管理中却不能起到应有的作用。 本研究以四川若尔盖湿地国家级自然保护区为例，应用3S技术，建立保护区多功能动态分区工作流模型，通过不同植被类型的识别和空间特征分析、不同动物类群在上述植被生境中的时空分布特征分析、保护区主要干扰因素的时空分布特征分析，突出对保护区主要保护对象（湿地生态系统）的保护，对保护区进行管理分区，依据野生动物利用特征和植被生长特征对核心区进行年周期动态利用，缓解保护与发展的矛盾，促进保护区的优化管理。 应用归一化植被指数（NDVI）与植被盖度的相关性，将归一化植被指数（NDVI）转化为植被盖度指数（MDVI），结合保护区牧场划分和时空利用特征专家经验，结果表明，MDVI值在1-139之间主要代表着水体、裸地、沙地等；MDVI140-256为草地和高山灌丛；MDVI210是当地夏牧场和秋冬牧场的划分区间值。 合理的区划需要资金、技术和政策的支持，为保证保护区多核心动态分区的实施，本研究提出了生态工程、牧业发展方式转变、湿地特色产业发展、湿地政策、社区参与和科技支撑等六大保障措施。 In China, 92466 Km2 highland or frigid wetlands are (were) facing major management problems, such as wetland degradation and overgazing. Conflict between conservation and utilization on those wetlands can be found anywhere today. Although many nature reserves have been setup for protection of frigid wetland, and core and buffer zone has been declared to forbid any kinds of disturbance, local farmers still use these areas for grazing. As an example by Sichuan Roige Wetlands National Nature Reserve(SRWNRR), we set up a 3S flow model to analyze the character of year-round distribution patters of vegetation, wildlife, and grazing. Combined and overlapped these characters together, we select multi-core zone and buffer zone, then define a dynamic management period in different zone to optimize protection wetland in the reserve. Normalized Difference Vegetation Index（NDVI）is highly related with coverage of vegetation. When convert NDVI to MDVI (coverage index, 1-256), index 139 and 210 can be as inflexion to distinguish among water/sand/bared land, summer pasture, and autumn / winter pasture. We use these to select different layers and analyze grazing pattern. To be more realistic, we put forward some strategies to support our multi-core and dynamic management of wetland in Roige, including ecological restoration engineering, changing of stock raising industry, changing of wetland policy, community based management and technology renovation supports.

小麦胚乳蛋白组分和Glu-B3位点基因核心编码区差异与小麦品质关系的研究

小麦加工品质改良已成为我国小麦育种的主要目标之一。特别是我国加入WTO以后，对小麦产品的质量提出了更高的要求，小麦品质改良的任务将更加艰巨和重要，小麦胚乳蛋白是影响小麦加工品质性状的重要因素。因此，深入了解小麦胚乳蛋白对加工品质性状的影响及其分子基础，为品质改良提供理论依据和科学指导，对加速我国小麦品质育种和优质小麦生产具有重要意义。本研究选用在麦谷蛋白5个基因位点(Glu-A1、Glu-B1、Glu-D1、Glu-B3和Glu-D3)上均含不同等位基因的小麦品种99G45和京771及Pm97034和京771杂交F9代共164个麦谷蛋白纯合系，及228个中国推广普通小麦品种和高代育成品系为试材，研究了麦谷蛋白Glu-1和Glu-3位点基因等位变异对籽粒蛋白、湿面筋含量、Zeleny沉降值和SDS沉降值间的关系；本研究还利用小麦A、B和D基因组中低分子量麦谷蛋白亚基（LMW-GS）基因特异引物，通过PCR方法克隆了1个Glu-A3位点和3个Glu-B3位点LMW-GS基因片段，在此基础上分析了不同等位基因对品质造成差异的分子基础；另外，本研究对中国近年推广的部分品种和育成的高代品系资源的多样性进行了分析。现将主要研究结果简述如下： 1. 对来自三个麦区的148份材料的醇溶蛋白组成进行了分析，结果表明，各麦区醇溶蛋白模式具有较大差异。在ω区,A7、B、E、F、G、J、P、Q、S和U仅存在于西南秋播麦区；A3、M、N、R、W和X仅存在于黄淮特种麦区；K仅存在于北方冬麦区；A6是北方冬麦区出现频率最高的带型模式，而西南秋播麦区中D出现的频率最高。ω-区的E、H和M几种模式是以前国内外未曾报道的。且初步确定，这些模式对品质性状具有正效应。至于γ区,A、B、D、E和F在各区均有出现，其中B和E在各区出现的频率都很高，在26.1-39.6％之间。相反，H 仅出现在黄淮特种麦区，J仅限于西南秋播麦区。对于β-区醇溶蛋白，B型模式在所有区中都相当高，而模式A仅存在于第三区.对于α-区，模式A在Ⅲ区而模式D在Ⅱ区出现的频率很高。1BL.1RS易位系在中国小麦品种中出现频率高达41.2％，在I, II和Ⅲ麦区的出现频率分别为 45.5、43.5和35.2%。各生态区模式的差异可能是品种适应不同生态条件和人为选择的结果，但这有待进一步证明。由于醇溶蛋白位点（Gli-1）与LMW-GS位点（Glu-3）紧密连锁，本结果可为下面确定普通小麦LMW-GS等位基因变异所用。 2. 利用Gli-1与Glu-3的紧密连锁，以228个小麦品种/系为材料，首次对中国小麦品种麦谷蛋白亚基的6个位点进行综合分析，研究小麦籽粒蛋白与品质性状间的关系，结果表明6个高分子量（HMW）和低分子量（LMW）麦谷蛋白位点对蛋白质含量的效应大小为，Glu-D1>Glu-B3>Glu-A1=Glu-B1> Glu-A3=Glu-D3；对GMP含量的效应大小为, Glu-A3>Glu-B3>Glu-D1> Glu-B1>Glu-A1>Glu-D3；对湿面筋含量的效应大小为, Glu-B1>Glu-B3= Glu-D3>Glu-A3>Glu-A1>Glu-D1；对Zeleny沉降值的效应大小为, Glu-A1> Glu-B3>Glu-D3>Glu-D1>Glu-B1>Glu-A3；对SDS沉降值的效应大小为, Glu-B3>Glu-A1=Glu-D1=Glu-A3>Glu-D3>Glu-B1。对蛋白含量而言，各位点的最佳组合方式为1、17+18、5+10、Glu-A3e、Glu-B3g、Glu-D3b；对湿面筋含量而言，各位点的最佳组合方式为1、6+8、5+10、Glu-A3d、Glu-B3c、Glu-D3b；对Zeleny沉降值而言，各位点的最佳组合方式为N、17+18、5+10、Glu-A3d、Glu-B3d、Glu-D3b；对SDS沉降值而言，各位点的最佳组合方式为1、7+8、2.2+12、Glu-A3b、Glu-B3g、Glu-D3b。另外，分析了稀有亚基对5+12与2.2+12与品质性状的关系，认为5+12对品质有负效应，2.2+12对品质有正效应。在品质育种时，应对优异组合或优异亚基加以利用。 3. 首次利用重组自交系（RILs）为材料，研究麦谷蛋白亚基表达量与品质性状的关系，通过对重组自交系中各HMW-GS表达量的分析，认为，就单个亚基的表达量而言，7亚基最高；其次为2亚基、5亚基、12亚基和10亚基；亚基9和1的表达量最小；N亚基不表达。对成对出现的亚基对而言，x型和y型亚基的总表达量2+12>5+10>7+9>17+18。就单个亚基与品质性状的关系而言，仅有10亚基的表达量与蛋白含量的相关性达5%的显著水平，2亚基的表达量与湿面筋含量呈负相关，显著水平也达5%，其余单个亚基对品质性状均无显著影响；就x型/y型亚基的比例来看，2/12和5/10对湿面筋含量都有显著的负效应；对某一位点等位基因控制的亚基表达总量来看，2+12对SDS沉降值有显著负效应。另外，本研究得出：2＋12的亚基对的负效应主要体现在2亚基上，且在同一位点上，x型亚基的表达量大于y型。所以推导稀有亚基组合2+10很可能也是劣质亚基。 4. 以 Glu-A1、Glu-B1、Glu-D1、Glu-B3和Glu-D3作为5个因素对99G45/京771和Pm97034/京771杂交后代的蛋白质含量和SDS沉降值进行多因素方差分析。结果表明，Glu-A1和Glu-D3对蛋白含量的加性效应达5％显著水平；Glu-D1 * Glu-D3对蛋白质含量的互作效应也达5%显著水平；其余位点的加性和互作效应对蛋白质含量的影响均不显著。对SDS 沉降值而言，Glu-D1的加性效应最大,贡献率为4.2 % ,达1 %显著水平,其次是Glu-B1位点,贡献率为3.3% ,达5%显著水平。其余位点对SDS 沉降值的加性和互作效应均未达5%显著水平。总体而言, 各位点对蛋白含量的效应大小为Glu-D3 > Glu-A1 > Glu-D1>Glu-B1>Glu-B3；对SDS沉降值的效应大小为Glu-D1>Glu-B1> Glu-D3>Glu-A1> Glu-B3。Glu-D1和Glu-D3位点上等位基因变异对蛋白含量有显著或极显著影响，含Glu-D1d和Glu-D3 GD、Glu-D3 JD基因的株系分别比含Glu-D1a和Glu-D3 PD基因的株系有较高的蛋白含量；在该遗传背景下，麦谷蛋白各基因位点对蛋白含量的效应大小依次排列为：Glu-A1位点1>N；Glu-B1位点7+9>17+18>14+15；Glu-D1位点5+10>2+12；Glu-B3位点GB>JB>PB；Glu-D3位点GB>JB>PB。对SDS沉降值的效应大小依次排列为：Glu-A1位点1>N；Glu-B1位点7+9=17+18>14+15；Glu-D1位点5+10>2+12；Glu-B3位点GB>JB>PB；Glu-D3位点GB>JB>PB。所以，对蛋白含量和SDS沉降值均较好的组合为1，7+9，5+10，GB，GD。 5. 因为GB和PB对品质的效应有显著差异，选取LMW-GS位点特异扩增引物对京771、99G45和Pm97034的Glu-B3位点进行扩增，结果得到三个不一样的扩增片段（Genebank号为DQ539657－DQ539659），得到的基因片段与Genebank中已报道的同类序列高度同源。通过克隆片段组成的分析，发现对Pm97034的序列较京771和99G45段少一个7氨基酸的重复单元，这可能是它较另外两个片段对面筋强度影响小的主要原因；另外，在99G45的序列中，124位处出现L（亮氨酸）代替P（脯氨酸），158位处出现了T（苏氨酸）代换M(蛋氨酸)，这可能是99G45Glu-B3位点序列对SDS沉降值的效应显著优于Pm97034的原因。 6．通过对RILs各位点同普通小麦品种（系）各位点与品质关系的比较，发现对SDS沉降值的效应，各位点在不同研究材料中是不同的，普通小麦中：Glu-B3>Glu-A1=Glu-D1=Glu-A3>Glu-D3>Glu-B1，RILs中：Glu-D1>Glu-B1> Glu-D3>Glu-A1> Glu-B3。利用重组自交系材料（完全排除了1BL/1RS易位干扰）所得到的结果与Gupta and MacRitchie (1994)所得结论一致。进一步证实了1BL/1RS易位对小麦品质的重要影响。对蛋白含量而言，普通小麦品种（系）中，Glu-D1>Glu-B3>Glu-A1=Glu-B1> Glu-A3=Glu-D3，RILs中，Glu-D3 > Glu-A1 > Glu-D1>Glu-B1>Glu-B3，和对SDS沉降值的效应一样，推断在非1BL/1RS易位的情况下，各位点对其效应应为Glu-D3 > Glu-A1 > Glu-D1>Glu-B1>Glu-B3。 对同一位点的等位基因而言，普通小麦和重组自交系中Glu-A1和Glu-D1上的等位基因对品质性状的贡献是一致的，但Glu-B1上的等位基因对SDS沉降值的贡献发生了变化，普通小麦中17+18>7+9，RILs中7+9>17+18，这可能也是1BL/1RS造成的。 Baking quality improved is one of the main object of wheat bread in China. The overall objective of the present studies was to increase the understanding about protein quality in wheat, i.e. to make it possible to improve the production of wheat with desired quality for different end-uses. With the analysis of gluten protein in RILs, 99G45/Jing 771 and Pm97034/Jing, and 228 wheat cultivars or lines in China, the correlations between glutenin compositions and protein content, glutenin macropolymer(GMP), wet gluten content, Zeleny sedimentation value and SDS sedimentation value contentand breadmaking quality were studied. Also a rapid and efficient detection method of geneticpolymorphism at Glu-B3 loci in wheat was established using polymerase chain reaction(PCR).The results obtained were as follows: 1. Cultivated Chinese wheat germplasm has been a valuable genetic resource in international plant breeding. Patterns of gliadin among cultivated Chinese accessions are unknown, despite the proven value and potential novelty. The objective of this work was to analyse the diversity within improved Chinese wheat germplasm. The electrophoretic banding patterns of gliadin in common wheat cultivars and advanced lines were determined by acid-polyacrylamide gel electrophoresis. For 148 leading commercial cultivars and promising advanced lines used in our study, 48 patterns were identified, 29 corresponding to ω-gliadin, 9 to γ-gliadin, 5 to β-gliadin and 5 to α-gliadin. The most frequent patterns were A6 in ω; B in γ; B in β and A in the region of α. 116 band types appeared in the148 samples: 94 accessions had unique gliadin types, and 22 gliadin types while not unique were found in 54 accessions. The gliadin patterns of Chinese wheat cultivars and lines greatly differed from the patterns of wheat lines from other countries. Three patterns, E, J, H, M, N and O in the ω-zone had not previously been reported. Three wheat zones，the Northern Winter Wheat Region, the Yellow and Huai Valley River valleys Winter Wheat Region and the Southwestern Winter Wheat Region，in China showed different frequencies in their gliadin patterns. This information can be used to monitor genetic diversity with Chinese wheat germplasm. 2. To analyse the relationship between the loci and characteristics quality, we utilized the 228 cultivars/lines. The results showed that : For protein content, Glu-D1 >Glu-B3>Glu-A1=Glu-B1>Glu-A3=Glu-D3. For GMP content, Glu-A3>Glu-B3 >Glu-D1>Glu-B1>Glu-A1>Glu-D3. For wet gluten content, Glu-B1>Glu-B3= Glu-D3>Glu-A3>Glu-A1>Glu-D1. For Zeleny sedimentation value, Glu-A1>Glu-B3> Glu-D3>Glu-D1>Glu-B1>Glu-A3, For SDS sedimentation value, Glu-B3>Glu-A1= Glu-D1= lu-A3>Glu-D3>Glu-B1。For protein content, the best combination of 6 loci is (1,17+18,5+10,Glu-A3e, Glu-B3g,Glu-D3b). For wet gluten content, the best combination of 6 loci is (1,6+8,5+10,Glu-A3d,Glu-B3c,Glu-D3b). For Zeleny sedimentation value, the best combination of 6 loci is (N,17+18,5+10,Glu-A3d, Glu-B3d, Glu-D3b). For SDS sedimentation value, the best combination of 6 loci is(7+8,2.2+12,Glu-A3b, Glu-B3g,Glu-D3b)。Additional, we analysed the relationship between the subunits 5+12 and 2.2+12, think that 5+12 was negative for quality, 2.2+12 is postive for quality. It should be effective utilized. 3. It’s the first time to utilize RILs to study the relationship between subunits expression quantity and characteristics quality. The results showed that: For single subunit, the expression quantity of 7 is the highest. Then the 2, 5, 12 and 10. The expression of subunit 9 and 1 is the lowest. Subunit N is not expressed. For subunits, the expression quantity of x type and y type are 2+12>5+10>7+9>17+18. The significant relation of 5% only showed between the expression quantity of subunit 10 and protein content. The relationship between expression quantity of others and characteristic quality was not significant. For x type/ytype, 2/12 and 5/10 is negative relation insignificant level. For the subunit(s) in a loci, Only 2+12 effect SDS sedimentation value negative in significant level. 4. With RILs 99G45/Jing 771 and Pm97034/Jing 771, we found that: The effective of Glu-A1, Glu-D3 and Glu-D1 * Glu-D3 for protein content is significant at 5% level. The effect of other loci for protein wre not significant. For SDS sedimentation value, the effect of Glu-D1is the highest, which contribution is 4.2 % .Then the Glu-B1, contribution is 3.3%. The effect of other loci for SDS sedimentationvalue were not significant. In total, for protein content: Glu-D3 > Glu-A1 > Glu-D1>Glu-B1>Glu-B3; for SDS sedimentationvalue: Glu-D1>Glu-B1> Glu-D3>Glu-A1>Glu-B3. The effect of alleles in Glu-D1 and Glu-D3 loci are significant at 1% or 5%. In Glu-A1, 1>N; Glu-B1, 7+9>17+18>14+15; Glu-D, 5+10>2+12; Glu-B3, GB>JB>PB; Glu-D3, GB>JB>PB. For SDS sedimentation, Glu-A1, 1>N; Glu-B1, 7+9=17+18>14+15; Glu-D1, 5+10>2+12; Glu-B3, GB>JB>PB; Glu-D3, GB>JB>PB. The best combinations for SDS sedimentation value is 1，7+9，5+10，GB，GD. 5. Because of the difference of GB and PB for SDS sedimentation value, we selected the specific primer for LMW-GS loci to amplified the Glu-B3 of Jing771, 99G45and Pm97034. We got 3 amplify fragment (Gene Bank accession number are DQ539657－DQ539659）. We found that the fragment of Pm97034 were deleted a repetitive 7 amino acid domain, which is perhaps the reason effect the gluten strength. Furthermore, in the position 124 of sequence 99G45, L has been replaced with P. Position 158, T replaced M, which may be the reason why the Glu-B3 locus of 99G45 is prefer to Pm97034 when refer to SDS sedimentation value. 6. Comparing the results of RILs and common wheat, we found that perhaps just the1BL/1RS made the difference of loci in different accession.

Experimental study on the electric-sweep scanner and ion beam emittance of electron cyclotron resonance ion source

With a latest developed electric-sweep scanner system, we have done a lot of experiments for studying this scanner system and ion beam emittance of electron cyclotron resonance (ECR) ion source. The electric-sweep scanner system was installed on the beam line of Lanzhou electron resonance ion source No. 3 experimental platform of Institute of Modem Physics. The repetition experiments have proven that the system is a relatively dependable and reliable emittance scanner, and its experiment error is about 10%. We have studied the influences of the major parameters of ECR ion source on the extracted ion beam emittance. The typical results of the experiments and the conclusions are presented in this article.

Synthesis of carbon nanotube bundles with mesoporous structure by a self-assembly solvothermal route

A kind of carbon nanotube bundle has been synthesized by a simple one-step solvothermal reaction between Na and hexachlorobenzene (HCB) using NiCl2 as catalyst precursor. Before the reaction, NiCl2 was initially dispersed ultrasonically in cyclohexane then prereduced by Na at 230degreesC to produce small Ni particles in reduced state. The tubes thus-produced have a uniform outer diameter of about 20 nm, an inner diameter of 4 nm, and are highly ordered assembled as bundles which have a 2D hexagonal arrangement as proven by SAXS and TEM experiments.