UV-B辐射增强对长白山五种藓类植物生长的影响

对生长在中国长白山的5种藓类植物——垂枝藓、拟垂枝藓、塔藓、星塔藓和高山金发藓分别以辐射强度为0.2(自然光照,对照)、3.0(紫外线中等辐射强度)和6.0kJ.m-2.d-1(高剂量辐射强度)的UV-B照射40d后,测定其株高、生物量及叶绿素含量.结果表明:中等和高强度的UV-B辐射使拟垂枝藓和塔藓的株高、生物量和叶绿素含量分别下降了32.3%、62.4%、81.3%和21.4%、59.4%、62.8%,其相对生长速率均为负值;高剂量UV-B辐射处理下垂枝藓的生物量稍有上升,而高山金发藓地下部分的生物量增加1倍,但叶绿素含量变化不明显.高山金发藓和垂枝藓抵抗UV-B辐射的能力较强,拟垂枝藓和塔藓对UV-B辐射较敏感.

UV-B增强对番茄的伤害及H_2O_2的防护作用

UVB辐射使番茄叶片的叶绿素a,叶绿素b及总叶绿素含量先升高后降低,同样使叶片的抗氧化酶过氧化氢酶(CAT)和过氧化物酶(POD)活性先升高随后降低,而使超氧化物歧化酶(SOD)活性升高,膜脂过氧化产物MDA的含量增加;中等剂量(5mmol·l-1)的H2O2预处理能提高叶绿素b的含量,明显提高抗氧化酶的活性,并延缓CAT活性的降低,抑制膜质过氧化产物MDA的产生.中等浓度H2O2预处理能提高番茄对UVB增强的抗性.

红酵母YR-1对偶氮染料酸性红B的脱色研究

从活性污泥中分离得到1株对偶氮染料酸性红B具有明显脱色效果的酵母菌株YR-1,鉴定为红酵母Rhodotorulasp。YR-1对酸性红B脱色机制属于降解脱色,能在30h内使质量浓度50mg·L-1的酸性红B溶液脱色率达到99%以上。研究了各种因素对酸性红B脱色效果的影响,最佳脱色条件为:初始pH为5.0、接种质量分数5%、温度30℃;最佳碳源是葡萄糖,其次是蔗糖;最佳氮源是酵母膏或蛋白胨。在替换分批脱色试验和连续补料脱色试验中,脱色率一直保持在75%以上,显示YR-1在上述脱色体系中均具有良好适应性。

金黄色葡萄球菌肠毒素B基因的克隆和在大肠杆菌中高效表达

利用PCR方法从金黄色葡萄球菌TSTw基因组DNA中扩增出约 70 0bp的DNA片段 ,将之克隆到pGEM 7Zf(+)载体上并转化大肠杆菌DH5α菌株。重组质粒的测序结果表明克隆到了seb基因 ,它含有 717bp(不包括N端81bp的信号肽编码区 ) ,其核苷酸序列与文献报道完全一致。将其连接于表达载体 7ZTS上 ,转化到大肠杆菌JM10 9(DE3)内。表达的SEB占总蛋白 33.5 %。

基于遥感-过程耦合模型的1988～2004年青海三江源区净初级生产力模拟

三江源区不仅是地处青藏高原的全球气候变化的敏感区,也是我国甚至亚洲最重要河流的上游关键源区。作为提供物质基础的植被净初级生产力(Netprimaryproduction,NPP),是评价生态系统状况的重要指标。该文应用已在碳通量观测塔验证,扩展到区域水平的遥感-过程耦合模型GLOPEM-CEVSA,以空间插值的气象数据和1km分辨率的AVHRR遥感反演的FPAR数据为模型主要输入,模拟并分析了1988～2004年该区NPP时空格局及其控制机制。结果表明,该区植被平均NPP为143.17gC·m–2·a–1,呈自东南向西北逐渐降低的空间格局,其中,以森林NPP最高(267.90gC·m–2·a–1),其次为农田(222.94gC·m–2·a–1)、草地(160.90gC·m–2·a–1)和湿地(161.36gC·m–2·a–1),荒漠最低(36.13gC·m–2·a–1)。其年际变化趋势在空间上呈现出明显的差异,西部地区NPP表现为增加趋势,每10a增加7.8～28.8gC·m–2;而中、东部表现为降低趋势,每10a降低13.1～42.8gC·m–2。根据显著性检验,NPP呈增加趋势(趋势斜率b>0),显著性水平高于99%和95%的区域占研究区总面积的13.43%和20.34%,主要分布在西部地区;NPP呈降低趋势(趋势斜率b<0),显著性水平高于99%和95%的区域占研究区面积的0.75%和3.77%,主要分布在中、东部地区,尤以该区长江和黄河等沿线区分布更为集中,变化显著性也更高。三江源NPP的年际变化趋势的气候驱动力分析表明,整个区域水平上该地区植被生产力受气候变化的主导,西部地区暖湿化趋势,造成了该地区生产力较为明显的、大范围的增加趋势;但东、中部地区则主要受人类活动的影响,特别是长江、黄河等河流沿线,是人类居住活动密集的地区,造成这些地区放牧压力较大、草地退化严重,而该地区暖干化趋势加剧了这一过程。

Biodegradable Interpolyelectrolyte Complexes Based on Methoxy Poly(ethylene glycol)-b-poly(alpha,L-glutamic acid) and Chitosan

We synthesized methoxy poly(ethylene glycol)-b-poly(alpha,L-glutamic acid) (mPEGGA) diblock copolymer by ring-opening polymerization of N-carboxy anhydride of gamma-benzyl-L-glutamate (NCA) using amino-terminated methoxy polyethylene glycol (mPEG) as macroinitiator. Polyelectrolyte complexation between mPEGGA as neutral-block-polyanion and chitosan (CS) as polycation has been scrutinized in aqueous solution as well as in the solid state.

The influence of variant PE-b-PEO segments on physical properties of LLDPE graft copolymers

A method was adopted to fix a series of polymers of PE-b-PEO with different PEO/PE segments on the chains of LLDPE. Maleic anhydride (MA) reacting with hydroxyl group of PE-b-PEO (mPE-b-PEO) was used as the intermediate. The structures of intermediates and graft copolymers were approved by H-1 NMR and FTIR. XPS analysis revealed a great amount of oxygen on the surface of grafted copolymers although the end group of PEO was fixed on the LLDPE chains through MA. Thermal properties of the graft copolymers as determined by differential scanning calorimetry (DSC) showed that PE segments in the grafted monomers could promote the heterogeneous nucleation of the polymer, increase T., and crystal growth rate.

Guest inducing p-sulfonatocalix[4] arene into three-dimensional capsule architecture and a mixed A-B double layer framework

The reactions of sodium p-sulfonatocalix[4]arene (Na5L) and terbium/europium(III) chloride in the presence of pyrazine-N,N'-dioxide (PNNO) in aqueous solutions gave the crystalline complexes 1 and 2. Both structures contain molecular capsules of p-sulfonatocalix[4] arene with PNNO as guest molecules in the cavity of the calix[4]arenes. The molecular capsules are connected through sodium and terbium (or europium) centers forming a three-dimensional framework.

Crystallization and morphology of poly(ethylene oxide-b-lactide) crystalline-crystalline diblock copolymers

The crystallization behaviors and morphology of asymmetric crystalline-crystalline diblock copolymers poly(ethylene oxide-lactide) (PEO-b-PLLA) were investigated using differential scanning calorimetry (DSC), wide angle X-ray diffraction (WAXD), and microscopic techniques (polarized optical microscopy (POM) and atomic force microscopy (AFM)). Both blocks of PEO5-b-PLLA(16) can be crystallized, which was confirmed by WAXD, while PEO block in PEO5-b-PLLA(30) is difficult to crystallize because of the confinement induced by the high glass transition temperature and crystallization of PLLA block with the microphase separation of the block copolymer.

Molecular weight dependence of phase Behavior of PEO/P(EO-b-DMS) blends: Application of Sanchez-Lacombe lattice fluid theory

Molecular weight dependence of phase separation behavior of the Poly (ethylene oxide) (PEO)/Poly(ethylene oxide-block-dimethylsiloxane) (P(EO-b-DMS)) blends was investigated by both experimental and theoretical methods. The cloud point curves of PEO/P(EO-b-DMS) blends were obtained by turbidity method. Based on Sanchez-Lacombe lattice fluid theory (SLLFT), the adjustable parameter, epsilon*(12)/k (quantifying the interaction energy between different components), was evaluated by fitting the experimental data in phase diagrams. To calculate the spinodals, binodals, and the volume changes of mixing for these blends, three modified combining rules of the scaling parameters for the block copolymer were introduced.

The phase behavior of comblike block copolymer A(m+1)B(m)/homopolymer A mixtures

The phase behaviors of comblike block copolymer A(m+1)B(m)/homopolymer A mixtures are studied by using the random phase approximation method and real-space self-consistent field theory. From the spinodals of macrophase separation and microphase separation, we can find that the number of graft and the length of the homopolymer A have great effects on the phase behavior of the blend. For a given composition of comblike block copolymer, increasing the number of graft does not change the macrophase separation spinodal curve but decreases the microphase separation region. The addition of a small quantity of long-chain homopolymer A increases the microphase separation of comblike block copolymer/homopolymer A mixture.

Hybridization of poly(4-vinyl pyridine)-b-polystyrene-b-poly(4-vinyl pyridine) aggregates in dioxane/water solution

Self-assembly of binary blends of two triblock copolymers of poly(4-vinyl pyridine)-b-polystyrene-b-poly(4-vinyl pyridine), i.e., P4VP(43)-b-PS260-b-P4VP(43) (P1) and P4VP(43)-b-PS366-b-P4VP(43) (P2), in dioxane/water solution was studied. These two triblock copolymers individually tend to form vesicles (P2) and cylindrical micelles (P1) in dilute solution. It was found that copolymer components in the blend, sample preparation method, and annealing time had significant effect on hybridization aggregate morphology. By increasing P1 content in the copolymer blends, fraction of looped and stretched cylinders increased, while fraction of bilayers decreased. Nearly no bilayer was observed when P1 content was above 85 wt%.

利用MALDI-TOF质谱技术研究MPEG-b-PCL两嵌段共聚物的嵌段长度及嵌段分布

利用基质辅助激光解吸电离飞行时间质谱(MALDI-TOFMS)结合源后分解(PSD)技术对甲氧基封端的聚乙二醇-b-聚己内酯(MPEG-b-PCL)两嵌段共聚物进行了结构分析.根据得到的MALDI-TOFMS谱图和PSD碎片信息清晰地确定了嵌段共聚物的嵌段长度和嵌段分布.结果表明,采用MALDI-TOFMS结合PSD技术研究这类嵌段共聚物链结构非常有效.这为更好地认识和应用这类嵌段共聚物提供了重要的依据,同时也建立了分析这类嵌段共聚物的方法.