北方农牧交错区土地利用（管理）方式对土壤氮素转化的影响

土壤氮素矿化是陆地生态系统氮素转化的重要组成部分。不同的土地利用（管理）方式会改变土壤氮素转化过程，影响土壤肥力的保持，进而可能造成土壤内氮素渗漏流失。为系统了解内蒙古农牧交错区土壤氮素转化的特点，本实验采用原位培养顶盖埋管法进行野外培养，每间隔一个月定期取样，于2004年7月-2006年10月在植物所恢复生态学实验站进行了两个试验，1：选择农牧交错区四种有代表性的土地类型（围封样地：FS，放牧样地：GS，弃耕地：AF，和农田：CF），比较土地利用方式之间氮素矿化的异同;2：在施肥样地通过不同施肥处理(F0: 1g N m-2, F1: 1g N m-2, F2: 2g N m-2, F3: 4g N m-2, F4: 8g N m-2, F5: 16g N m-2, F6: 32g N m-2, F7: 64g N m-2) 的土壤氮素转化动态，确定过度放牧的典型草原围封禁牧后，植被恢复过程中最适宜的施肥量。主要结论如下： 1. 与试验初期相比，整个非生长季围封样地、弃耕地和农田的铵态氮和无机氮含量逐渐降低，培养结束时铵态氮含量分别减少了67.04％，77.31％和70.54％，而放牧地的含量增加1.63％。围封样地、放牧地、弃耕地和农田的硝态氮含量分别增加了61.61%，376.43%，199.75%和133.16%。非生长季四种土地类型的土壤氮素转化速率主要受温度影响。围封样地、放牧地、弃耕地和农田非生长季矿化速率均值分别为-0.016，0.0429，-0.0051和-0.0030 μg g-1 d-1。硝化速率均值变幅为-0.43-0.17 μg g-1d-1。 2. 与没有冷冻而融化的土壤相比，冻融显著影响土壤无机氮含量的变化。只有在较低的土壤温度条件下冷冻以后，融化才会促进土壤氮素矿化。不同的冷冻时间长度下融化均会促进土壤硝化速率。土壤温度、土壤含水量变化是影响氮素转化速率的重要因子。 3. 四种土地类型的年日均矿化速率为放牧样地>农田>弃耕地>围封样地，分别为0.25，0.11，0.10，0.06μg g-1d-1，其年平均速率分别为11.65，5.50，5.00和2.46g m-2 y-1，而年日平均硝化速率分别为0.27，0.095，0.097和0.05μg g-1d-1。其中生长季日均矿化速率和日均硝化速率均为其年日均速率的两倍。因此，生长季形成的矿化氮是全年的93％，而形成的硝态氮占全年的86％。四种土地类型年均矿化氮的累积量平均为615.04 kg ha-1，而硝化作用的累积量变幅为230.44-1218.86 kg ha-1。四种土地类型的矿化速率和硝化速率的季节动态变化与气候因子的变化一致。 4. 不同施肥处理对典型草原土壤氮素转化均有显著影响。与对照相比，少量施肥（F1，F2）土壤铵态氮，硝态氮和无机氮含量分别减少20.57％，11.18％和17.18％。当施肥量大于F4（8g N m-2）时，随施肥量增加土壤铵态氮，硝态氮和无机氮含量增加18％-1191％。除F5（16g N m-2）外，与对照相比，随施肥量增加，土壤矿化速率增加了5-21倍。4 g N m-2 (F3)左右是典型草原生态系统比较合适的施肥量。 5. 氨气挥发速率的季节动态特征与气象因子的变化一致，其速率变幅为17.65 - 1228.39µg m-2 d-1，其中7月挥发量占全年的37％。与对照相比，少量施肥氨气挥发速率降低了1-2％，施肥量大于F3 (4g N m-2)，速率增加了1-4倍。实验期间总的流失量变幅为23.76-84.91mg m-2，而且通过氨气挥发流失量低于土壤全氮的3%。氨气挥发不是典型草原过量氮素流失的主要方式。 6. 氮素限制的典型草原，植被恢复过程中外源氮素添加阈值为：4 g N m-2 (F3)。与对照相比，短期施肥（3年）不会显著影响根系碳储量和土壤碳氮储量。施肥处理的土壤硝态氮和无机氮含量显著增加，说明施肥显著刺激硝化作用。典型草原60%植物根系主要分布在地下0-10cm，这里的碳储量占地下储量（0-50cm）的63%以上。随土壤深度增加，土壤全氮，全碳，无机氮储量降低。而铵态氮储量和可利用的无机氮含量随土壤深度增加，说明植物根系主要吸收利用上层可利用氮素，而且下层氮素矿化速率降低。

Ballistic Single-Electron Quputer

We propose a new solid state implementation of a quantum computer (quputer) using ballistic single electrons as flying qubits in 1D nanowires. We use a single electron pump (SEP) to prepare the initial state and a single electron transistor (SET) to measure the final state. Single qubit gates are implemented using quantum dots as phase shifters and electron waveguide couplers as beam splitters. A Coulomb coupler acts as a 2-qubit gate, using a mutual phase modulation effect. Since the electron phase coherence length in GaAs/AlGaAs heterostructures is of the order of 30$\mu$m, several gates (tens) can be implemented before the system decoheres.

三种萝藦科植物中C21甾类成分的研究

　　本实验对三种萝藦科植物通光散(Marsdenia tenacissima)、黑水藤（Biondia insignis Tsiang）和徐长卿（Cynanchum Paniculatum）中的C21甾体化合物进行了研究。从通光散藤茎乙酸乙酯提取物的水解产物中，分离得到两类八个C21甾类甙元。经光谱鉴定，它们的结构分别为11α-O-(2-甲基)-丁酰基-12β-O-顺芷酰通光藤甙元乙（1），11α-O-乙酰基-12β-O-乙酰基通光藤甙元乙（2），11α-O-（2-甲基）-丁酰基-12β-O-乙酰基通光藤甙元乙(3), 11α-O-苯甲酰基-12β-O-乙酰基通光藤甙元乙(4)， 11α-O-顺芷酰基-12β-O-乙酰基通光藤甙元乙（5）11α-O-顺芷酰基-12β-O-顺芷酰基通光藤甙元乙（6），12β-O-乙酰基通光藤甙元甲（7）和12β-O-顺芷酰基通光藤甙元甲（8）。其中，化合物2和8为新化合物。从黑水藤乙醇提取物的水解产物中，分离得到了两个C21甾体化合物。经1D、2D NMR技术鉴定，分别为（3β，14β，15β，17β）-3, 14-二羟基-15，16-裂-孕甾-5-烯-15-醛-16-半缩醛-20-酮（1）和白前甙元C（2）。其中1为15，16-裂环的新骨架类型的C21甾体化合物，命名为黑水藤甙元甲。从采购于昆明、浙江、湖南三地药材市场的徐长卿的根及根茎中，分离得到了18个化合物（其中昆明徐长卿6个，浙江徐长卿9个，湖南徐长卿3个）。经光谱数据分析，这些化合物被鉴定为：cynapanoside-C (1), cynapanoside-A (2), 白前甙元B 3-O-β-D-磁嘛吡喃糖甙(3)，白前甙元C 3-O-β-D-葡萄吡喃糖基-(1 → 4)-α-L-2-脱氧洋地黄吡喃糖基-（1 → 4）-β-D-洋地黄吡喃糖基-（1 → 4）-β-D-夹竹吡喃糖甙（4），白前甙元C3-O-β-D-葡萄吡喃糖基-(1 → 4)-α-D-夹竹桃吡喃糖基-(1 → 4)-β-D-洋地黄吡喃糖基-(1 → 4)-β-D-夹竹桃吡喃糖甙（5），白前甙元C 3-O-β-D-葡萄吡喃糖基-（1 → 4）-β-D-葡萄吡喃糖基-（1 → 4）-α-D-夹竹桃吡喃糖基-（1 → 4）-β-D-洋地黄吡喃糖基-（1 → 4）-β-D-夹竹桃吡喃糖甙（6），cynatratoside-B (7)，cynatratoside-C (8);glaucoside A(9)，新白薇甙元B 3-O-β-L-磁嘛吡喃糖基-（1 → 4）-β-D-洋黄吡喃糖基-（1 → 4）-β-D-夹竹桃吡喃糖甙（10），白前甙元 A 3-O-α-L-磁嘛吡喃糖基-（1 → 4）-β-D-洋地黄吡喃糖基-（1 → 4）-β-D-磁嘛吡喃糖甙（11），白前甙元 B 3-O-α-L-磁糖基吡喃糖基-(1 → 4)-β-D-磁嘛吡喃糖基-(1 → 4)-β-D-磁嘛吡喃糖甙(12)，白前甙元D 3-O-α-L-磁嘛吡喃糖基（1 → 4）-β-D-洋地黄吡喃糖基-（1 → 4）-β-D-磁嘛吡喃糖甙（13），白前甙元 C 3-O-β-D-葡萄吡喃糖基-（1 → 4）-β-D-葡萄吡喃糖基-（1 → 4）-α-L-2-脱氧洋地黄吡喃糖基-（1 → 4）-β-D-磁嘛吡喃糖基-（1 → 4）-β-D-夹竹桃吡喃糖甙（14），白前甙元 C 3-O-β-D-葡萄吡喃糖基-（1 → 4）-β-D-葡萄吡喃糖基-（1 → 4）-α-L-磁嘛吡喃糖基-（1 → 4）-β-D-洋地黄吡喃糖基-（1 → 4）-β-D-夹竹桃吡喃糖甙（15），白前甙元 B 3-O-α-D-夹竹桃吡喃糖基-(1 → 4)-β-D-洋地黄吡喃糖基-（1 → 4）-β-D-磁嘛吡喃糖甙（16），白前甙元 D 3-O-α-D-夹竹桃吡喃糖基-(1 → 4)-β-D-洋地黄吡喃糖基-(1 → 4)-β-D-磁嘛吡喃糖甙(17)，白前甙元月B 3-O-α-L-磁嘛吡喃糖基-(1 → 4)-β-D-洋地黄吡喃糖基-(1 → 4)-β-D-磁嘛吡喃糖甙（18）。其中，化合物3-6，10-18为新化合物，10的甙元为一个新甙元，命名为新白薇甙无B。

High tilt angle FLC SLM for optical interconnects

The use of high tilt angle FLC SLM for optical interconnects was discussed. The transmissive SLM was designed as a 320×1 pixels glass SLM with 20 μm pitch pixels and 2 μm pixel deadspace. The SLM was fabricated using standard class 100 cleanroom facilities to make a glass on glass 1D SLM. The results show that a N×N optical switch can be built using the two-hologram architecture.

Numerical simulation of the growth of ZnO nanostructures in a tube furnace by physical vapour deposition

Zinc oxide is a versatile II-VI naturally n-type semiconductor that exhibits piezoelectric properties. By controlling the growth kinetics during a simple carbothermal reduction process a wide range of 1D nanostructures such as nanowires, nanobelts, and nanotetrapods have been synthesized. The driving force: for the nanostructure growth is the Zn vapour supersaturation and supply rate which, if known, can be used to predict and explain the type of crystal structure that results. A model which attempts to determine the Zn vapour concentration as a function of position in the growth furnace is described. A numerical simulation package, COMSOL, was used to simultaneously model the effects of fluid flow, diffusion and heat transfer in a tube furnace made specifically for ZnO nanostructure growth. Parameters such as the temperature, pressure, and flow rate are used as inputs to the model to show the effect that each one has on the Zn concentration profile. An experimental parametric study of ZnO nanostructure growth was also conducted and compared to the model predictions for the Zn concentration in the tube. © 2008 Materials Research Society.

Retaining axial-lateral orthogonality in steered ultrasound data to improve image quality in reconstructed lateral displacement data

Ultrasound elastography tracks tissue displacements under small levels of compression to obtain images of strain, a mechanical property useful in the detection and characterization of pathology. Due to the nature of ultrasound beamforming, only tissue displacements in the direction of beam propagation, referred to as 'axial', are measured to high quality, although an ability to measure other components of tissue displacement is desired to more fully characterize the mechanical behavior of tissue. Previous studies have used multiple one-dimensional (1D) angled axial displacements tracked from steered ultrasound beams to reconstruct improved quality trans-axial displacements within the scan plane ('lateral'). We show that two-dimensional (2D) displacement tracking is not possible with unmodified electronically-steered ultrasound data, and present a method of reshaping frames of steered ultrasound data to retain axial-lateral orthogonality, which permits 2D displacement tracking. Simulated and experimental ultrasound data are used to compare changes in image quality of lateral displacements reconstructed using 1D and 2D tracked steered axial and steered lateral data. Reconstructed lateral displacement image quality generally improves with the use of 2D displacement tracking at each steering angle, relative to axial tracking alone, particularly at high levels of compression. Due to the influence of tracking noise, unsteered lateral displacements exhibit greater accuracy than axial-based reconstructions at high levels of applied strain. © 2011 SPIE.

Karyotype Differentiation in Newly Discovered Members of the Drosophila obscura Species Group from Yunnan , China

观察了新近发现于我国云南的果蝇属暗果蝇种组( Drosophila obscura species group ) 种类 D1luguensis 、D1 dianensis 和D1limingi 的有丝分裂中期核型, 并将3 个种的核型与各自的近缘种类进行了比较。 D1luguensis 具2n = 12 条染色体, 包括3 对中央着丝粒(V 形) 染色体、2 对近端着丝粒(棒状) 染色体以及1 对微小(点状) 染色体。其中X 和Y染色体均为中央着丝粒染色体。D1 dianensis 和D1limingi 具2n = 10 条染 色体, 包括1 对大的V 形常染色体, 1 对小的V 形常染色体, 2 对J 形(亚中着丝粒型) 常染色体和1 对点状染 色体。其中X 染色体为J 形, Y染色体为短棒状。基于核型比较的结果以及D1sinobscura 亚组地理分布的资料, 结合种间系统发育关系研究结果, 认为D1 luguensis 可能保留了该亚组祖先种类的核型。D1sinobscura 的核型(2n = 12 : 2V , 1J , 2R , 1D) 可能由一个pre2“sinobscura2hubeiensis”谱系的一个分支通过臂间倒位演化而来, 而D1 hubeiensis 的核型(2n = 10 : 4V , 1D) 可能由该谱系的另一分支通过着丝粒融合(2 对近端着丝粒常染色 体的融合) 而形成。推测在D1 dianensis 和近缘欧洲种D1subsilvestris (2n = 12 : 3V , 2R , 1D) 间、D1limingi 和 东亚近缘种D1tsukubaensis (2n = 12 : 3V , 2R , 1D) 间的物种分化过程中, 可能有相似的染色体变异类型发生。

藤三七中一个新黄烷醇和抗HIV活性成分

利用各种色谱(硅胶和凝胶)方法,从藤三七[Boussingaultia gracilis Miers var.pseudobaselloides Bailey]的70%(体积分数)的乙醇提取物中分离得到2个黄烷醇类化合物(1,2)和4个黄酮类化合物(3～6).采用UV,IR,MS 和1D,2D NMR方法,分别鉴定出如下化合物: 7-羟基-5-甲氧基-8-甲基-6-甲酰基-3,4-黄烷二醇,命名为藤三七醇A(1);4,7-二羟基-5-甲氧基-8-甲基-6-甲酰基黄烷(2);7-O-methylunonal(3);5,7-二羟基-6,8-二甲基-2-苯基-4H-1-苯并吡喃-4-酮(4);Desmosflavone(5)和Demethoxymatteucinol(6).其中化合物1是一个新的黄烷二醇化合物,化合物2～6为首次从该植物中分离得到.抗HIV-1活性筛选结果表明: 化合物1,2,5,6对HIV-1诱导合胞体的形成具有一定的抑制作用,其半数有效浓度(EC50)分别为45.09,48.73,55.47 和 82.75 μmol/L,治疗指数(TI)分别为1.41,1.20,7.15 和》8.51.

Chemical Constituents from Fruit Hulls of Garcinia mangostana ( Cuttiferae

从山竺(Garcinia mangostana)果壳中分离得到6个化合物,通过MS,1D 1NMR以及与文献对照鉴定它们为4个(口山)酮类化合物:α-mangostin(1),β-mangostin(2),γ-mangostin(3),5,9-dihydroxy-8-methoxy-2,2-dimethyl-7-(3-methylbut-2-enyl)-2H,6H-pyrano-[3,2-b]-xanthen-6-one(4),以及表儿茶素(epicatechin,5)和一个双苄类化合物egonol(6).其中化合物5和化合物6为首次从该植物中分离得到.对化合物1～5进行抗HIV-1 RT活性筛选结果表明,化合物2和化合物5在浓度200 μg/ml的条件下,其对HIV-1 RT抑制率分别为41.97%和47.72%;同一实验结果显示化合物1,3和4没有抑制HIV-1 RT作用.

Indole and carbazole alkaloids from Glycosmis montana with weak anti-HIV and cytotoxic activities

A diprenylated indole, (E)-3-(3-hydroxymethyl-2-butenyl)-7-(3-methyl-2-butenyl)-1H-indole (1), and six known carbazole alkaloids were isolated from the twigs and leaves of Glycosmis montana Pierre (Rutaceae). Their structures were determined on the basis of analysis of spectral evidence including 1D and 2D NMR and MS. The alkaloids (1-3) exhibited weak to moderate take in vitro inhibitory activity against HIV replication in C8166 cells, and they (as well as carbalexine A and B) had cytotoxic activity against the human leukaemia cell line CCRF-CEM. (c) 2005 Elsevier Ltd. All rights reserved.

Przewalskin A: A new C-23 terpenoid with a 6/6/7 carbon ring skeleton from Salvia przewalskii maxim

Przewalskin A (1), a novel C-23 terpenoid with a 6/6/7 carbon ring skeleton, was isolated from Salvia przewalskii. Its structure was determined by comprehensive 1D NMR, 2D NMR, and MS spectroscopic analysis and subsequently confirmed by a single-crystal X

Sphenalactones A-D, a new class of highly oxygenated trinortriterpenoids from Schisandra sphenanthera

Four novel highly oxygenated trinortriterpenoids, sphenalactones A-D (1-4), were isolated from the leaves and stems of Schisandra sphenanthera and their structures were elucidated by extensive analysis of 1D and 2D NMR data. Compounds 1-4 featured a C-27

Nortriterpenoids and lignans from Schisandra sphenanthera

Nortriterpenoids, sphenadilactone C (1) and sphenasin A (2), together with four known lignans (3-6), were isolated from the leaves and stems of Schisandra sphenanthera. Their structures were elucidated by extensive analysis of 1D and 2D NMR spectroscopic

Dibenzocyclooctadiene Lignans from Schisandra wilsoniana and Their Anti-HIV-1 Activities

Twelve new dibenzocyclooctadiene lignans, marlignans A-L (1-12), together with 16 known compounds, were isolated from the leaves and stems of Schisandra wilsoniana. The structures of 1-12 were elucidated by spectroscopic methods including 1D- and 2D-NMR techniques. Compounds 1-12 were evaluated for their anti-HIV activities, of which compounds 3, 6, 8, and 12 showed modest activities with therapeutic index values of 13.2, 15.6, 17.6, and 16.4, respectively.

Chemical Constituents from the Leaves and Stems of Schisandra lancifolia

A new nortriterpenoid, 20-hydroxymicrandilactone D (1) and a novel lignan glycoside, lancilignanside A (2) were isolated from leaves and stems of Schisandra lancifolia, together with three known nortriterpenoids (3-5) and nine known phenolics (6-14). The structures of new compounds 1 and 2 were determined by detailed analysis of their 1D and 2D NMR spectra, and chemical evidences. In addition, compounds 1-2, 6-7, and 9-11 showed anti-human immunodeficiency virus (HIV)-1 activities with 50% effective concentration (EC50) in the range of 3.0-99.0 mu g/ml. Compound 12 was not bioactive in this assay with EC50 more than 200 mu g/ml.