红叶山茶(Camellia japonica)叶片色素含量与叶色参数的相关性分析

以3个红叶山茶品种‘红叶黑魔法’、‘黑魔法’和‘黑蛋石’为试验材料,分别测定叶片不同发育阶段叶绿素、类胡萝卜素、总花青苷含量及叶色参数L~*、a~*、b~*值,并通过相关性分析探讨叶色参数与叶片色素含量变化之间的关系。结果表明,首先,3个不同发育阶段叶片中叶绿素a、叶绿素b和类胡萝卜素含量呈上升趋势,不同品种同一发育阶段的色素含量相近。‘红叶黑魔法’和‘黑蛋石’叶片总花青苷含量在新叶展开10 d左右达到最大值,此后极显著下降,而‘黑魔法’叶片的花青苷含量则变化不大。其次,从色素比值来看,在新叶展开10 d时,花青苷的所占比值最大,‘红叶黑魔法’和‘黑蛋石’的花青苷比值分别达到87.88%和79.08%,极显著地高于叶绿素所占比值。到50 d时,花青苷比值下降至31.74%和23.68%,且3个品种花青苷含量相近,而叶绿素和类胡萝卜素比例则显著增加,这一结果较好地解释了这3个品种叶片的呈色变化,说明花青苷含量及其各种色素含量的比例变化是导致红叶山茶叶色变化的主要原因。最后,3个品种的a*值均与花青苷含量呈显著正相关,而与叶绿素a、叶绿素b、类胡萝卜素呈负相关,a~*值可作为描述红叶山茶品种叶色变化的代表性参数。     

龟纹瓢虫对草地贪夜蛾卵和低龄幼虫的捕食作用

为明确龟纹瓢虫Propylaea japonica对草地贪夜蛾Spodoptera frugiperda的控害潜力,在(25±1)℃、L∥D=16 h//8 h、RH (60±5)%的条件下研究了龟纹瓢虫雌、雄成虫和4龄幼虫对草地贪夜蛾卵、1龄和2龄幼虫的捕食能力。结果表明,龟纹瓢虫4龄幼虫和雌、雄成虫对草地贪夜蛾卵、1龄和2龄幼虫的捕食反应均符合HollingⅡ模型。龟纹瓢虫雌、雄成虫和4龄幼虫对草地贪夜蛾卵的日最大捕食量分别为204.6、110.9粒和124.7粒,瞬时攻击率分别为1.125、1.658和1.429,处理时间分别为0.004 9、0.009 0 d和0.008 0 d;对草地贪夜蛾1龄幼虫的日最大捕食量分别为242.4、265.5头和109.4头,瞬时攻击率分别为1.233、1.038和1.411,处理时间分别为0.004 1、0.003 8 d和0.009 1 d;对草地贪夜蛾2龄幼虫的日最大捕食量分别为41.2、40.3头和27.6头,瞬时攻击率分别为1.386、1.226和1.685,处理时间分别为0.024 3、0.024 8 d和0.036 2 d。雌、雄成虫和4龄幼虫对草地贪夜蛾卵和低龄幼虫的搜寻效应均随着猎物密度的增加而降低。龟纹瓢虫对草地贪夜蛾卵和1龄幼虫的捕食量高于2龄幼虫。结果表明龟纹瓢虫对草地贪夜蛾卵和低龄幼虫具有较好的控制作用,为利用龟纹瓢虫控制草地贪夜蛾提供了理论依据。     

添加槐花粉对白三叶青贮发酵品质的影响

采用单因子随机设计，研究添加不同比例的槐(Sophora japonica)花粉对白三叶 (Trifolium repens)青贮发酵品质的影响，以期为槐花应用于青贮饲料生产提供科学依据。分别设置白三叶单独青贮(C)、95%白三叶 + 5%槐花粉青贮(T1)、90%白三叶 + 10%槐花粉青贮(T2)、85%白三叶 + 15%槐花粉青贮(T3)、80%白三叶 + 20%槐花粉青贮(T4)共5个处理。结果表明，白三叶单独青贮品质较差，添加槐花粉提高了青贮原料的干物质、水溶性碳水化合物含量和发酵系数，降低了缓冲能值，使得青贮后的感官评分、乳酸、乳酸 ? 乙酸、干物质、水溶性碳水化合物、粗蛋白质含量显著提高(P ≤ 0.05)，pH、氨氮 ? 总氮、乙酸、丁酸含量显著降低(P ≤ 0.05)。综合考虑，80%白三叶 + 20%槐花粉青贮能获得良好的青贮品质。     

沂蒙山区金银花光合效率对土壤水分的响应

为探索抗旱灌木光合作用效率对土壤水分的响应特征与阈值效应，以沂蒙山区优势灌木金银花为材料布设盆栽模拟试验，通过人工灌水与植物自然耗水的方法进行控水处理，在不同水分梯度下测定分析了金银花的光合作用参数，并对土壤水分有效性进行了分级。结果表明:1）金银花叶片净光合速率（P_n）和水分利用效率（WUE）对土壤相对含水量（RSWC）具有明显的阈值响应规律，当RSWC分别为79.59%和47.43%时，金银花P_n、WUE达到最大值。当RSWC=29.71%时，制约光合效率的主要因子由气孔限制转为非气孔限制。2）确定了金银花光合作用的5个特征水分阈值:P_n水分补偿点、P_n水分均值点、P_n水分饱和点、WUE水分均值点和WUE水分高效点。同时，将金银花的土壤水分有效性划分了5个等级:高产高效水、高产中效水、中产高效水、低产低效水和无产无效水。3）田间水分管理时，为维持金银花较高的光合作用水平，应维持的土壤水分范围为:42.38%≤RSWC≤96.05%，避免土壤水分低于29.71%。研究结果可为沂蒙山区干旱逆境下金银花的风险诊断和田间水分管理提供科学依据。     

黄金槐的嫁接繁育及园林应用

我们采用上年秋季栽植砧木国槐，提前生根，第二年春季采用插皮接，对接穗进行蜡封，存放0-5℃的冷库内推迟发芽，延长嫁接时间，具有省时、省工、管理方便、成活率高等特点，而且砧木国槐可选择树干稍弯的等外苗，经过取直处理，节约了成本，值得推广。简要介绍了黄金槐在园林上的应用。     

江西一季籼粳杂交稻稻曲病防治药剂及次数研究

选择合适的防治药剂和防治次数是减轻稻曲病危害的关键。本研究以籼粳杂交稻甬优12为材料,比较了6种药剂和3种喷施次数对稻曲病的防控效果和产量性状差异。结果表明,在6种药剂中,阿米妙收处理的病穗率防效和病指防效最好,分别达到91.53%和96.63%,但与其他药剂无显著性差异。在防治次数上,爱苗和拿敌稳均为防治3次的处理病指防效最好,分别为81.73%和80.15%,显著高于防治次数3次以下的处理。阿米妙收处理的产量最高,达11 719.52 kg/hm~2,显著高于其他处理。     

药用植物金银花Dof基因家族的筛选及表达分析

Dof(DNA-binding one zinc finger)蛋白是一类植物所特有的转录因子,N-末端具有高度保守的C₂-C₂单锌指结构域,C-末端的转录调控区的氨基酸具有高度多样性,其在植物光合、细胞周期及逆境响应等过程中发挥着重要的作用。本研究基于金银花测序数据,利用生物信息学的方法筛选了候选的LjDof基因,并对其理化性质、亚细胞定位、同源序列比对、保守基序、系统进化发育和表达模式进行了深入分析。结果表明,金银花Dof转录因子家族包含11个基因,编码的氨基酸的个数为157~492,理论等电点为5.45~9.48,均为不稳定亲水性蛋白。亚细胞定位显示,LjDof基因都在细胞核中有定位,个别在其他部位也有定位。同源比对和Motif分析发现,11个LjDof基因都含有完整的C₂-C₂单锌指结构。系统进化发育分析表明,金银花Dof蛋白分为五个亚类。实时荧光定量PCR及表达模式分析表明,LjDof基因在金银花低温胁迫不同时间下有着不同的表达规律。本研究结果为进一步研究金银花Dof基因在逆境胁迫下的功能提供了理论基础。     

利用CRISPR/Cas9系统编辑日本结缕草ZjSGR基因技术研究

日本结缕草(Zoysia japonica)是一种常见的具有众多优良性状的暖季型草种,秋冬季节在我国北方地区会较早出现叶片脱绿现象,在一定程度上限制了日本结缕草在北方的大面积使用。ZjSGR是从结缕草中分离出来的一种衰老诱导基因,负调控叶片滞绿性状。本研究利用CRISPR/Cas9系统,通过基因枪介导的遗传转化方法实现对日本结缕草ZjSGR基因的编辑,经测序验证获得1株单碱基缺失突变植株。突变植株叶片深绿,在正常生长温度(28~30℃)条件下,和对照相比,叶绿素含量更高(P<0.05)。本研究为进一步阐述ZjSGR基因在日本结缕草滞绿性状调控中的作用机理提供了基础研究材料,也为培育日本结缕草滞绿品种育种工作奠定了基础。     

A Sulfated Polysaccharide from Saccharina japonica Suppresses LPS-Induced Inflammation Both in a Macrophage Cell Model via Blocking MAPK/NF-κB Signal Pathways In Vitro and a Zebrafish Model of Embryos and Larvae In Vivo

Inflammation is a complicated host-protective response to stimuli and toxic conditions, and is considered as a double-edged sword. A sulfated Saccharina japonica polysaccharide (LJPS) with a sulfate content of 9.07% showed significant inhibitory effects against lipopolysaccharide (LPS)-induced inflammation in RAW 264.7 macrophage cells and zebrafish. Its chemical and structural properties were investigated via HPLC, GC, FTIR, and NMR spectroscopy. In vitro experiments demonstrated that LJPS significantly inhibited the generation of nitric oxide (NO) and prostaglandin E₂ (PGE₂) via the downregulation of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) expression and suppressed pro-inflammatory cytokines tumor necrosis factor (TNF)-α and interleukin (IL)-1β production via the nuclear factor-kappa B (NF-κB) and mitogen-activated protein kinase (MAPK) signal pathways in LPS-induced RAW 264.7 cells. Moreover, LJPS showed strong protective effects against LPS-induced inflammatory responses in zebrafish, increasing the survival rate, reducing the heart rate and yolk sac edema size, and inhibiting cell death and the production of intracellular reactive oxygen species (ROS) and NO. Its convenience for large-scale production and significant anti-inflammatory activity indicated the potential application of LJPS in functional foods, cosmetics, and pharmaceutical industries.     

Protective immune responses of recombinant outer membrane proteins OmpF and OmpK of Aeromonas hydrophila in European eel (Anguilla anguilla)

Outer membrane proteins (Omps) of Gram‐negative bacteria have been proven to be efficient subunit vaccines against bacteriosis. In this study, OmpF and OmpK of Aeromonas hydrophila were expressed, and their immune protective effects in European eel (Anguilla anguilla) were evaluated. The genomic DNA of A. hydrophila 322A was used as a template, and two kinds of prokaryotic expression plasmids, pET‐32a‐OmpF and pET‐32a‐OmpK, were constructed. Recombinant OmpF protein (r‐OmpF) and r‐OmpK were purified and were proven to have antigenicity by Western‐blot analysis. r‐OmpF and r‐OmpK were used as immunogens to immunize European eel by intraperitoneal injection. The mRNA expression of 6 immune‐related genes (IgM, IL‐10, IRF3, IRF7, LysG4 and HexB) in the liver tissues of eels at 1 hr, 3 hr, 6 hr, 12 hr, 24 hr, 72 hr and 10 days postimmunization was analysed by real‐time PCR. At 30 dpi, the serum antibody response was measured by ELISA. Fish were attacked at 15 dpi by live 322A to assess the protective immunity of r‐OmpF and r‐OmpK. All the six tested genes responded to r‐OmpF or r‐OmpK vaccination at varying degrees. The serum antibody titre of r‐OmpF‐ and r‐OmpK‐immunized groups was 1:1,600 and 1:3,200 respectively. In addition, r‐OmpF gave 35.5% of the relative immune protection rate to European eels, while r‐OmpK gave 70.0%. By analysing the protective immunity and the regulatory role in the immune‐related gene expression of the two recombinant proteins that were studied, it was found that r‐OmpK was a potential vaccine candidate against A. hydrophila.