生根处理和扦插时间对杉木容器扦插育苗效果的影响

以通过审定的广西杉木(Cunninghamia lanceolata)良种为扦插材料,探讨不同的生根处理方法和扦插月份对扦插生根效果及成活率的影响。结果表明:使用生根剂处理的穗条,其生根率、成活率、根系数量及整齐度均极显著高于对照,ABT1和IBA处理的穗条根系萌发最快,根系萌发时间均为22 d,比对照提前13 d;ABT1处理的穗条生根率(97.8%)和平均根系数(4.2)最高,整齐度最好,其次为IBA;ABT1、IBA和NAA处理的穗条成活率分别为97.8%、97.2%和93.1%,对照成活率为81.5%;杉木扦插苗培育的最佳扦插时间为3~5月。     

天山樱桃EST-SSR引物开发及PCR反应体系优化

以新疆天山樱桃叶片为试材,从NCBI数据库中搜索天山樱桃EST序列,利用SSRHunter 1.3软件查找SSR位点,结合Primer 6.0设计引物,通过正交实验和单因素试验优化天山樱桃SSR-PCR反应体系,并用最佳体系对所开发的引物进行验证,以期为研究天山樱桃遗传多样性、构建遗传连锁图谱奠定基础。结果表明:从58对备选引物中随机挑选30对引物进行试验,有21对引物能够扩增出特异性条带,有效扩增率为70%。20μL天山樱桃SSR-PCR最佳反应体系为dNTP 0.2mmol·L~(-1)、引物0.4μmol·L~(-1)、Taq酶0.75U、模板DNA 60ng。     

微囊型甲醛捕捉剂对薄木饰面人造板甲醛释放量的影响

随着薄木饰面板在家具、装修领域中的使用量越来越大,人造板的游离甲醛释放问题也愈发引起人们关注,现有的甲醛捕捉剂一般只能在短期内发挥效果,而对人造板甲醛的长期释放控制效果并不理想。为解决人造板甲醛释放的长期性问题,以尿素为芯材、乙基纤维素为壁材制备微囊型甲醛捕捉剂,探讨不同乳化剂及芯壁比制备的微囊型甲醛捕捉剂对饰面人造板甲醛控释效果的影响。结果表明,当乳化剂为十二烷基硫酸钠、芯壁比为3∶1,乳化剂用量1%、壁材质量分数3%、搅拌速度1000 r/min时,制备出的微胶囊芯材负载效果最好,负载量达到36.24%、负载效率为8.05%。采用该微胶囊以2%的质量比与脲醛树脂胶黏剂混配进行饰面板贴面热压时,得到的薄木贴面板的甲醛释放量相比未处理饰面板降低了37.9%。经过20 d后,微胶囊对其饰面板甲醛的释放仍表现出一定的控制效果,饰面板的甲醛释放量为0.99 mg/L,仅为未处理饰面板的56.9%。说明用微囊型甲醛捕捉剂对饰面人造板进行处理不仅能够对饰面板中的甲醛进行控释,而且在长期的放置、使用过程中也能够持续发挥作用,从而达到降低室内空气中甲醛浓度的目的。     

施肥量对泰兴香荷芋生长及产量效益的影响

通过对泰兴香荷芋施肥量研究,考查了各处理主要生育期的苗情与长势、成熟期子孙芋产量及商品芋产值效益。结果显示:基施腐熟脱水猪粪15t·hm-2,苗期追施(3.1叶)脱水猪粪15t·hm-2+13-10-18高钾复合肥675kg·hm-2的处理子孙芋产量最高为23 421.90kg·hm-2,商品芋效益为88 506.60元·hm-2;基施有机肥7 500kg·hm-2+苗期追施(3.1叶)有机肥7 500kg·hm-2+13-10-18高钾复合肥450kg·hm-2+膨大肥(8.1叶)13-10-18高钾复合肥900kg·hm-2的处理产量相对较高。     

低温贮藏对猕猴桃果实成熟软化相关基因表达影响

为探究低温对果实采后成熟软化与淀粉降解的影响,以红阳猕猴桃果实为试验材料,研究在低温贮藏期间,猕猴桃果实硬度,可溶性固形物、乙烯、淀粉含量以及淀粉酶相关基因的变化。结果表明,低温贮藏能显著抑制猕猴桃果实采后成熟软化,延缓果实淀粉的降解和可溶性固形物含量的增加,维持贮藏期间果实较高的硬度。低温贮藏抑制乙烯合成关键基因AcACO1和AcACS1的表达,抑制乙烯合成。同时,低温贮藏显著抑制淀粉降解相关基因AcAMY1、AcBAM1/3、AcISA3、AcLDA1和AcDPE1的表达。在低温贮藏后期,淀粉酶相关基因AcAMY1、AcBAM1/3、AcLDA1和AcDPE1的表达与乙烯释放速率有关。综上,低温贮藏延缓猕猴桃采后成熟软化进程与淀粉降解密切相关,可能主要通过抑制乙烯合成,从而影响贮藏后期淀粉降解速率,最终延缓果实软化进程。本研究结果为猕猴桃采后低温贮藏提供了理论依据。     

黔育1号菊苣与紫花苜蓿、鸭茅间作栽培效果研究

依据贵州省松桃县的气候特点和牧草种植需要,用黔育1号菊苣与北林202紫花苜蓿、黔草4号鸭茅分别进行间作试验,从产量、营养品质、生产效益等方面对间作复合群体与3种牧草单播进行比较分析,探讨黔育1号菊苣与不同牧草间作种植模式的增产效益。结果表明,在贵州松桃地区,黔育1号菊苣+北林202紫花苜蓿间作,年均鲜草产量可达87.27 t/hm²,比紫花苜蓿单播产量增加36.17%,生产效益提高20.77%,粗蛋白含量达26.83%。该研究结果可为松桃县种草养畜产业的发展提供技术支撑。     

不同厂家阿胶及动物皮胶中四种阴离子含量的测定

通过离子交换色谱法,建立不同厂家阿胶及动物皮胶中Cl~-、SO_4~(2-)、NO_3~-、PO_4~(3-)4种阴离子的测定方法。结果表明,4种阴离子分离效果良好,Cl~-、SO_4~(2-)、NO_3~-、PO_4~(3-)分别在0.000 922～0.023 1、0.001 09～0.027 3、0.000 167～0.004 18、0.000 314～0.007 86 mg/mL浓度范围内线性关系良好,平均加样回收率在98.7%～101.0%。该测定方法结果准确、灵敏、可靠,重现性较好,可用于阿胶及动物皮胶中4种阴离子含量的测定。     

礼仪教学对提升高职学生人文素养的策略研究

高等学校作为人文素质教育的主要阵地和培养主体，对提升学生的人文素养发挥着重要的作用，然而在高等职业教育实际礼仪教学中，仍存在着对学生人文素养的培育缺乏重视等现象。教育工作者在实际教学中应重视礼仪课程的建设、改革和丰富礼仪教学的方法和手段、提升师资队伍建设、塑造校园人文环境，加强和提高学生的人文素养。     

Infections Investigation of ALV and REV in Guangxi Local Poultry Breeds and Sequence Analysis of gp85 Gene of ALV Isolates

In order to investigate the infection status of avian leukosis virus (ALV) and avian reticuloendotheliosis virus (REV) in the major local breeds of Qinzhou,Guangxi,totally 953 samples of egg white,cloaca swab and serum of Ma duck,Shitou goose,Tiejiao-Ma chicken,turkey and pigeon were collected from the representing flocks and detected by the commercial ELISA kits.ALV was isolated for the ALV p27 positive samples by culturing on DF-1 cells,and gp85 gene was sequenced.The results showed that the detections of ALV were negative in the samples except those of Tiejiao-Ma chicken,while REV antibody was found positive in Ma duck,Tiejiao-Ma chicken and turkey.The nucleotide sequences of gp85 gene of two isolates shared 94.5% identity with each other,and shared 86.9% to 94.9% with reference strains.The amino acid sequences of gp85 gene of two isolates shared 91.5% identity with each other,and shared 84.0% to 91.6% with reference strains.There were many variable sites in the hyper variable region hr1 and hr2,and the vr2 and vr3 variable regions were relatively conservative.Phylogenetic tree analysis showed that the two isolates shared the highest homology with SCAU11-XG strain.     

Cloning and Sequence Analysis of Buffalo Keap1 Gene and Investigation of Its Expression Pattern in Different Tissues

In this study,the CDS sequence of buffalo Keap1 gene was cloned and analyzed,then its expression pattern in different tissues was also investigated.A pair of primers of buffalo Keap1 gene was designed based on the nucleotide sequence of Bos taurus Keap1 gene from GenBank,and then the buffalo Keap1 gene was amplified.Using the bioinformation techniques,the gene sequence and the protein structure were analyzed.The expression level of Keap1 gene in different tissues were detected with Real-time quantitative PCR.The results showed that the length of buffalo Keap1 gene coding sequence was 1 875 bp and encoded 624 amino acids.The multiple sequence alignment results showed that buffalo Keap1 gene shared 99%,96%,92% and 90% of similar nucleotide sequence with that of Bos taurus,Ovis aries,Sus scrofa and Homo sapiens,respectively.And the phyogenetic tree also showed the conservatism between several different species.The second structure of buffalo Keap1 protein was predicted as 24 alpha regions,40 beta regions,38 turn regions and 27 coil regions.In addition,the results of Real-time quantitative PCR showed that Keap1 mRNA exists in all seven tissues,but the most abundant expression was in heart and the minimal expression was in liver and spleen.The results provided an foundation for further study of Keap1-Nrf2-ARE signal pathway,for enhancing the ability of antioxidant of buffalo embryo in vitro culture.