滇中冷凉山区不同播期反季花椰菜产量效益分析

为摸索滇中高海拔冷凉山区反季节栽培花椰菜的最佳播期以集成高效栽培技术推广应用,于2017—2018年选择海拔2250 m的云南省峨山县塔甸镇大西村地块进行9个播期的2年随机区组试验。结果表明,花椰菜生育期随播期推迟而延长,而花球采收期除播期7月10日外随播期推迟而逐渐增长;花椰菜株高、外叶数、开展度、球高、球径和单球重等农艺性状有随播期延迟呈现先逐渐减小而后又逐渐增大的趋势;莲座期黑腐病和霜霉病的病情指数随着播期的延迟呈现先逐渐升高而后又逐渐下降的趋势;花椰菜小区产量随着播期的延迟呈现先逐渐下降而后又逐渐提高的趋势,播期4月20日和4月30日与其余7个播期产量之间的差异达极显著水平。综合花椰菜在冷凉山区反季节栽培的生产实际和各播期产量产值及商品性表现,推荐滇中高海拔冷凉山区反季节栽培花椰菜的最佳播期为4月20—30日。     

甘露糖修饰的壳聚糖聚乳酸-羟基乙酸共聚物纳米微球作为口蹄疫病毒核酸疫苗递送载体的特性评价

旨在对制备的甘露糖修饰的壳聚糖聚乳酸-羟基乙酸共聚物[poly （D，L-lactide-co-glycolide），PLGA]纳米微球作为口蹄疫病毒（foot-and-mouth disease virus，FMDV）核酸疫苗递送载体进行评价。采用西佛碱反应和元素分析制备具有一定取代度的甘露糖修饰的壳聚糖衍生物（mannose modified chitosan，MCS），然后，经双重乳化挥发法制备得到甘露糖修饰的壳聚糖PLGA纳米微球（MCS-PLGA-NPs）。采用纳米粒径仪检测MCS-PLGA-NPs粒径分布和表面电势（zeta）、扫描电镜考察其形态、琼脂糖凝胶电泳观察其对质粒的吸附和吸附质粒后抵抗核酸酶降解能力、CCK-8法检测MCS-PLGA-NPs的细胞毒性、激光共聚焦观察巨噬细胞对MCS-PLGA-NPs-质粒DNA复合物的摄取、荧光显微镜和Western blot验证MCS-PLGA-NPs加载质粒DNA在细胞中的表达。元素分析结果表明，成功制备了取代度为5%~10%的MCS。纳米粒径测定和扫描电镜结果表明，MCS-PLGA-NPs的zeta为正值、粒径分布均匀且形态规则呈球形。琼脂糖凝胶电泳结果显示，MCS-PLGA-NPs吸附质粒的能力随着其质量的增加而增强并且可以在一定程度上抵抗核酸酶降解质粒DNA。在细胞毒性试验中，不同浓度的MCS-PLGA-NPs与RAW264.7细胞共孵育24 h后，细胞存活率仍在85%以上。在细胞摄取试验中，用激光共聚焦显微镜可以明显观察到质粒DNA结合到纳米微球表面被RAW264.7细胞摄取。荧光显微镜和Western blot试验证明MCS-PLGA-NPs加载质粒DNA可以在细胞中进行表达。综上表明，本研究成功制备了MCS以及具有递送核酸疫苗能力的MCS-PLGA-NPs，为FMDV核酸疫苗的递送研究提供了新的方向和见解，也为该递送载体携带特定抗原靶向抗原递呈细胞表面甘露糖受体以及应用于动物免疫的研究奠定基础。     

不同水肥条件下夏玉米/冬小麦农田生态系统碳平衡研究

农田生态系统碳平衡取决于农作物固定碳量和土壤异养呼吸排放碳量。为揭示水肥用量对农田生态系统碳平衡的综合影响，设置3个灌水水平：高水、中水和低水（W1、W0.85、W0.7夏玉米季分别为90、76.5、63mm，冬小麦季分别为140、119、98mm），4个施氮水平：高氮、中氮、低氮和不施氮（N1、N0.85、N0.7、N0夏玉米季分别为300、255、210、0kg/hm2，冬小麦季分别为210、178.5、147、0kg/hm2），4个施磷水平：高磷、中磷、低磷和不施磷（P1、P0.85、P0.7和P0夏玉米季分别为90、76.5、63、0kg/hm2，冬小麦季分别为150、127.5、105、0kg/hm2）进行了田间试验。结果表明：不同水肥处理下夏玉米/冬小麦农田生态系统表现为碳汇，夏玉米季净生态系统生产力固碳量（CNEP）为6805~7233kg/hm2，冬小麦季CNEP为5842~6434kg/hm2，夏玉米CNEP高于冬小麦。在高、中、低肥水平下，增加灌水量，夏玉米/冬小麦周年净初级生产力固碳量（CNPP）提高2.48%~5.96%，土壤微生物异养呼吸碳释放量（CRm）增加2.15%~15.20%，净生态系统生产力固碳量（CNEP）增加1.16%~6.47%。在高、中、低供水水平下，增加施肥量，夏玉米/冬小麦周年CNPP增加2.95%~3.43%，土壤CRm增加5.23%~18.67%，CNEP增加0.93%~2.79%，CNEP增加比例与供水水平呈负相关。在低水条件下，氮磷肥配施处理夏玉米/冬小麦农田周年CNEP较单施氮、磷肥分别增加4.86%、7.34%，且氮磷肥交互作用显著（P<0.05），水肥供应水平相差15%时对冬小麦农田CNEP有显著的正交互作用。氮磷肥配施、水肥协调供应均有助于促进夏玉米/冬小麦农田生态系统的净碳输入，在节水节肥原则下，夏玉米和冬小麦分别在W0.85N0.85P0.85和W0.7N0.85P0.85水肥供应条件下有利于增加农田CNEP。     

云南砚山浴仙湖省级重要湿地资源现状及保护修复措施

云南浴仙湖省级重要湿地是云南第四批认定的省级重要湿地,湿地资源具有较高保护价值.由于连年干旱,周边村庄环绕,导致该湿地生态系统出现退化.采取有力措施,保护修复浴仙湖湿地生态功能,迫在眉睫.通过对浴仙湖湿地资源现状进行调查,分析其存在的威胁,进而提出浴仙湖湿地资源保护及修复措施.     

过氧化氢(H2O2)介导的光合诱导系统信号

研究光照玉米幼苗顶部叶片产生的系统信号对底部叶片光合诱导过程的影响,探讨玉米叶片对光斑高效利用可能机制.以玉米(Zea mays L.)幼苗为试验材料,光照其顶部叶片,其余叶片处于遮蔽状态,利用Li-6400便携式光合仪测定玉米幼苗底部叶片光合诱导过程.通过预先光照玉米幼苗顶部叶片,底部叶片光合诱导过程从最低值到达最高值所需时间显著缩短,中间叶片光合诱导过程T50和T90分别下降,底部叶片光合诱导过程T50和T90分别下降29％和37％.玉米叶片全部遮荫条件下,底部叶片喷施过氧化氢(H2O2)促进光合诱导过程.三氯乙酸(TCA)和二苯基碘化钾(DPI)处理玉米顶部叶片基部,即使顶部叶片受到预光照,也无法改变底部叶片光合诱导过程.预先光照玉米顶部叶片,产生系统信号,信号物质为H2O2,通过韧皮部转运,可调节其他叶片光合诱导过程,有利于玉米底部叶片对动态光能利用和碳积累.该系统信号对玉米冠层底部叶片高效利用光斑发挥重要作用.     

Screening and Verification of Low Nitrogen Tolerant and Nitrogen Sensitive Cotton Germplasm

[Objective] The aim of this study is to evaluate nitrogen efficient cotton germplasms and improve nitrogen use efficiency. [Method] Eighty cotton germplasms were selected and evaluated in the hydroponic experiment under low (0.25 mmol·L^－1) and high (5 mmol·L^－1) nitrogen concentration. Different traits for screening were identified and nitrogen use efficiency types were classified. Field experiments were also performed for comparison and confirmation of the identified germplasms. [Result] The results showed that there were significant differences in the total plant dry matter, shoot nitrogen accumulation and nitrogen absorption efficiency in cotton germplasms at the two nitrogen levels. Based on coefficient of variation, principal component analysis and correlation, six traits including total plant dry matter, shoot dry matter, root dry matter, total nitrogen accumulation, shoot nitrogen accumulation and nitrogen absorption efficiency were used as screening indicators. According to the Heatmap clustering analysis and the nitrogen efficiency comprehensive index, two germplasms (Lu05R59 and CCRI 69) were identified as low nitrogen tolerant and nitrogen efficient, and two germplasms (Coker 201 and Xinluzhong 30) as low nitrogen sensitive and nitrogen inefficient. The results of field experiment were consistent with the results of the hydroponic culture at the seedling stage. [Conclusion] It was finally determined that Lu05R59 and CCRI 69 were the low nitrogen tolerant and nitrogen efficient germplasms, and Coker 201 and Xinluzhong 30 were low nitrogen sensitive and nitrogen inefficient germplasms. The results of these studies provide the possibility for screening and rapid identification of nitrogen use efficiency in cotton at the seedling stage, and provide the ideal materials and theoretical basis for further study of cotton nitrogen efficient.     

雪山草鸡感染传染性法氏囊病病毒新型变异株的鉴定

传染性法氏囊病病毒(infectious bursal disease virus,IBDV)新型变异株正在我国广泛蔓延,给商品肉鸡群和蛋鸡群带来了新的威胁。本研究对一个疑似发生非典型传染性法氏囊病的地方品种雪山草鸡群进行了RT-PCR检测,并对分离的3株毒株进行了基因测序及序列分析。结果显示,引起该鸡群发病的病原是IBDV新型变异株,属于A2dB1基因型;这3个毒株的VP2高变区编码蛋白上含有IBDV变异株的特征性氨基酸,也具有IBDV新型变异株的独特氨基酸。结果提示,我国地方品种鸡群中也有IBDV新型变异株的流行,现有的部分商品化IBDV疫苗已不能有效预防IBDV新型变异株的流行。     

神经介素B及其受体NMBR参与抗A型流感病毒H1N1亚型感染的信号通路

NMB/NMBR通过调节A型流感病毒（IAV/H1N1/PR8）感染诱导的细胞因子表达而参与抗IAV的先天性免疫反应。为探究其发挥抗IAV/H1N1感染的信号通路，本文用PR8和WSN毒株分别感染MLE-12细胞和小鼠，用NF-κB抑制剂BAY11-7028单独或联合NMB处理MLE-12细胞，小鼠后腿肌内注射NMB和NMBRA，采用RT-PCR和qRT-PCR分析NMB、NMBR、IL-6、IFN-α和NP基因表达变化，采用Western blot分析NMB、NMBR、P65/p-P65、IκBα和NP蛋白表达的变化。结果显示，BAY11-7028可促使PR8和WSN感染的MLE-12细胞中NMB、NMBR、IL-6和IFN-α基因表达水平均下降和NP基因表达水平上升，并降低NMB、NMBR和p-P65蛋白表达水平和提升IκBα和NP蛋白表达水平。然而，NMB联合BAY 11-7028诱导PR8或WSN感染后的细胞中IL-6和NP表达出现极显著下降和IFN-α显著上升。此外，NMB抑制PR8和WSN感染的小鼠肺组织内p-P65和NP蛋白表达水平和促进IκBα蛋白表达水平；NMBRA联合NMB抵消NMB对PR8或WSN感染后的这些蛋白表达水平的调节作用。综上表明，NMB/NMBR通过调节PR8和WSN感染的MLE-12细胞和小鼠体内的NF-κB信号通路上P65蛋白磷酸化和IκBα的表达，进而影响下游细胞因子IL-6和IFN-α基因的表达，从而发挥抗IAV/H1N1感染的先天性免疫应答反应。     

瞬时转速波动在轴向柱塞泵故障诊断中的应用

针对轴向柱塞泵配流盘磨损的故障诊断所使用的信号大多存在非平稳、非线性特性的缺点,提出利用轴向柱塞泵的瞬时转速波动信号进行故障诊断.利用瞬时转速波动信号良好的抗噪性能与经过阶比分析后可以转化为角度域内的平稳信号的特点,以克服传统监测信号的不足.通过动力学分析对轴向柱塞泵瞬时转速波动的成因进行了溯源.结果表明,对于具有Z个柱塞的轴向柱塞泵,活塞的惯性力和配流副处的库仑摩擦力会产生Z倍于转频的转矩波动,从而在轴向柱塞泵主轴上产生Z阶转速波动.柱塞高压腔的压力的变化会产生2Z倍于转频的转矩波动,从而在轴向柱塞泵主轴上产生2Z阶转速波动.在变负载条件下对理论分析结果进行了试验验证,结果表明对于9柱塞的轴向柱塞泵,其9阶瞬时转速波动分量幅值的变化可以很好地反映出配流盘磨损状况的变化.随着配流盘磨损程度增加,9阶瞬时转速波动的最大幅值从1.229增大至2.023 r/min;9阶瞬时转速波动分量幅值随着配流盘磨损加剧而增大.     

Effects of DHRS3 in C2C12 Myoblast Differentiation and Mouse Skeletal Muscle Injury

Myoblast differentiation is an essential process during skeletal muscle development. C2 C12 myoblast is a commonly used experimental model to study muscle cell differentiation in vitro. Dehydrogenase/reductase(SDR family) member 3(DHRS3) is a highly conserved member in short-chain alcohol dehydrogenase/reductase superfamily and has been shown to be involved in the metabolism of retinol. Previous experimental results showed that the expression of DHRS3 increased significantly during the differentiation of myoblasts differentiation. However, the effect of DHRS3 on mouse muscle cell differentiation was unclear. The objective of current study was to determine if DHRS3 affected muscle cell differentiation, and if DHRS3 was involved in muscle regeneration. Protein expression was determined by western blot and immunofluorescence analysis. The activation and inhibition of DHRS3 increased and decreased C2 C12 myoblast differentiation respectively, which indicated that DHRS3 could affect C2 C12 myoblast differentiation. DHRS3 expression was significantly changed during muscle regeneration, with the regeneration of muscle injury, the expression of DHRS3 tended to increase first and then decrease. It suggested that DHRS3 might be involved in muscle regeneration. In summary, this study confirmed the involvement of DHRS3 in C2 C12 myoblast differentiation and mouse skeletal muscle regeneration and provided a theoretical basis for further elucidating the molecular mechanism of muscle development.