宁夏地区大籽蒿精油成分分析及其抑菌性研究

为探究宁夏大籽蒿(Artemisia sieversiana Ehrhart ex Willd.)精油成分、抑菌功能及安全性,采用水蒸气蒸馏法进行精油提取,通过气相色谱-质谱连用法(GC-MS)进行成分分析,采用滤纸片法测定其对3种菌的抑菌圈直径,测定最低抑菌浓度(MIC)、最低杀菌浓度(MBC),并通过cck-8法检测大籽蒿精油对于2种皮肤细胞的毒性作用。结果表明,宁夏大籽蒿精油的主要成分为母菊薁(29.61%),樟脑(4.80%)、桉叶油醇(4.32%)、异木香酸甲酯(4.02%);精油对铜绿假单胞菌和大肠杆菌的最低抑菌浓度为0.0781 μg/mL,最低杀菌浓度为0.3125 μg/mL;金黄色葡萄球菌MIC为0.0195 μg/mL,MBC为0.078125 μg/mL;当精油浓度小于100 μg/mL时对角质细胞(HaCaT)和皮肤成纤维细胞(NHSF)均无毒性。综上,宁夏地区大籽蒿精油具有较强的抑菌活性且安全性较高,以上结果为宁夏大籽蒿精油开发提供理论依据,以期为当地脱贫致富提供科技支撑。     

不同生态区粳稻资源表型遗传多样性综合评价

为探究粳稻种质资源遗传多样性,提高粳稻育种组合选配的针对性和育种效率,通过变异系数、遗传多样性指数、聚类分析、相关分析、主成分分析、二维排序分析和逐步回归分析方法对不同生态区80份粳稻种质资源的8个表型性状的多样性水平进行了分析。结果表明：8个表型性状的变异系数为11.06%~36.97%,其中,千粒重的变异系数最小,每穗总粒数的变异系数最大;8个表型性状的遗传多样性指数为1.54~2.06,其中,单株有效穗数的遗传多样性指数最高,结实率的遗传多样性指数最低;在欧式距离9.0处,可将80份参试材料分为4类,各类表型性状差异明显;根据主成分分析和综合评价结果,80份粳稻种质资源中贵州的毕大香6号综合性状排名第1位,同时筛选到每穗实粒数、千粒重、株高、穗长和单株有效穗数性状可作为粳稻种质资源综合评价的关键指标;利用主成分二维排序分析筛选到矮秆、大穗、分蘖能力强及结实率高的4类优异种质资源,结合二维排序结果,大方晚糯是在二维排序重叠种质,可作为育种中间材料。同时基于主成分构建了粳稻种质资源的综合评价方程。     

2CZD-1型段茎式甘蔗种植机设计与试验

研制了2CZD-1型段茎式甘蔗种植机,可一次性完成甘蔗种植的开沟、施肥、自动取种、自动排种、覆土和覆膜等工序,适用于宽窄行甘蔗种植。设计了机架、取送种机构、转盘施肥机构、旋耕覆土机构、覆膜机构和液压传动系统等结构,其中取送种机构采用排冗结构实现均匀排种。利用有限元分析软件ANSYS对甘蔗种植机的机架进行模态分析,并通过田间试验获得甘蔗种植机的覆土厚度合格率、种植密度、伤芽率、漏植率及总排肥量稳定性变异系数等性能参数。模拟结果表明,当激励频率为8~80 Hz时,机架容易发生共振,且最大位移可达28.12 mm。田间试验表明,该种植机的种植密度为142325芽/hm^2,覆土厚度合格率为93.6%,伤芽率为2.8%,漏植率为4.7%,种植深度合格率为89.3%,总排肥量稳定性变异系数为5.8%,工作生产率为0.32 hm2/h,符合甘蔗种植机的设计要求,能够显著提高甘蔗种植的效率。     

不同光质对马铃薯腋芽薯结薯特性及光合性能的影响

将“延薯4号”单叶节茎段转入白光、红光、蓝光、红蓝光（4:1）下,测定了腋芽薯结薯特性、蔗糖和淀粉含量及光合性能等指标。结果表明,蓝光处理腋芽薯形成最早,单薯重和结薯率最高;在腋芽薯形成过程中,叶片蔗糖含量、干物质含量、叶绿素a（Chla）、叶绿素b（Chlb）、净光合速率（P_n）、相对电子传递速率（ETR）、光化学猝灭系数（q_P）、实际量子产量（Y_PSⅡ）显著高于其他光质处理;红光处理叶片的蒸腾速率（T_r）、胞间二氧化碳浓度（C_i）、气孔导度（G_s）显著高于其他光质处理,蓝光处理最低;相同扦插时间叶片的潜在最大光能利用率（F_v/F_m）在不同光质处理间无显著性差异。基于上述结果,蓝光为诱导马铃薯单叶节茎段腋芽薯的理想人工光源。     

DNA Barcoding:An Effective Tool for Species Identification of Lepidopteran Oak Pests

[Objective] The paper was to improve the efficiency and accuracy of early forecast of Lepidopteran oak-infesting pests.[Method] DNA barcoding technique was established for quick species identification using mitochondrial cytochrome C oxidase subunit Ⅰ(COⅠ) as the standard gene.This barcoding technique was used to amplify and sequence genomic DNA samples from eggs and pupae of 11 species of Lepidopteran pests collected from oak.[Result] The DNA barcoding standard genes of 594-708 bp were determined from eggs and pupae of Lepidopteran insects.There were differences of 0-2 bases in DNA barcode sequences between conspecific eggs and pupae,with the sequence identity of 99.7%-100%.The average content of A,T,G and C of DNA barcode sequences from Lepidopteran insects were 30.7%,38.5%,14.9% and 15.9%,respectively.The obtained DNA barcode sequences had 91.4%-100% identity and 0-8.6% difference degree with GenBank-deposited DNA barcode sequences from organisms of the genetically-closest relationship.Among them,DNA barcode sequences from egg and pupa samples of 10 Lepidopteran insects(No.1-20) had 99%-100% identity and 0-1.0% difference degree with homologous sequences in GenBank database,while the remaining samples(No.21-22) had high difference degree(8.6%) with homologous sequences.[Conclusion] The established DNA barcoding technique is an effeetive tool for species identification of Lepidopteran pests using genomic DNA from eggs and pupae of Lepidopteran insects.     

真菌菌丝-木屑复合材料的物理力学性能——以灵芝菌、木耳菌为例

以木屑为基质、真菌菌丝为粘结物质,采用无胶胶合方法制备菌丝-木屑生物质复合材料;参照GB/T17657—2013《人造板及饰面人造板理化性能试验方法》,测试菌丝-木屑生物质复合材料的抗拉强度、静曲强度、内结合强度;采用扫描电子显微镜(SEM)、傅里叶变换红外光谱(FTIR),分析菌丝-木屑生物质复合材料的微观结构、主要化学成分及材料成型机理。结果表明:制备的菌丝-木屑生物质复合材料,是一种新型可降解木质复合材料;灵芝菌丝-木屑材料、木耳菌丝-木屑材料的密度,分别在为0.64~0.70、0.68~0.78 g/cm~3之间;FTIR分析显示,两种菌丝对纤维素、半纤维素、木质素均有一定的降解,灵芝菌丝对木质素的降解程度略大于木耳菌丝;SEM观察显示,以三维网状结构存在于木屑表面及孔隙中,将散碎的木屑有效的粘结成为整体;力学性能测试显示,菌丝的生长情况对材料的力学强度有一定的影响,但是菌丝-木屑生物质复合材料力学性能仅为中密度纤维板的1/4。     

Parameterization of canopy resistance for modeling the energy partitioning of a paddy rice field

Paddy and Water Environment - Models for predicting hourly canopy resistance (r c) and latent heat flux (LET) based on the Penman–Monteith (PM) and bulk transfer methods are presented. The...     

SSCP Marker Development and Analysis of Candidate Restorer Gene Rf1 for Cotton Cytoplasmic Male Sterility

[Objective] Locating the cotton cytoplasmic male sterility (CMS) restorer gene Rf₁ is important for investigating restorer gene mechanisms and improving restorer lines. In our previous study, a gene cluster, with nine Pentatricopeptide repeat(PPR) genes and nine other genes, was found within the 160-kb Rf₁ target region in Scaffold 333. The objective here was to improve the density of Rf1-linked markers in the target region and determine the expression profiles of candidate genes. [Method] Using the sequences of the 18 genes, we designed 155 single-strand conformation polymorphism (SSCP) primers covering all of the gene sequences to identify the polymorphic SSCP markers between the fertile and sterile pools. Additionally, real-time polymerase chain reaction(PCR) was performed to analyze the expression profiles of eight candidate genes in the four developmental stages of buds of sterile, maintainer and restoring lines, respectively. [Result] In total, 15 polymorphic primers were identified. A genotype analysis of the F₂ population was conducted using the 15 primers and 3 other polymorphic simple sequence repeats (SSR) markers. The markers were distributed in a 4.8 cM range. In addition, owing to the influence of sterile cytoplasm or restorer genes, most of the genes showed different expression patterns in the four developmental stages of the three lines' buds. [Conclusion] SSCP markers tightly linked to Rf₁ were identified and the expression profiles of candidate genes were determined. This study provides a basis for the further fine mapping of restorer genes and for candidate gene screening.     

Dynamics of Cotton Rhizosphere Bacterial Community Structure in Cotton Continuous Cropping Field Soil

[Objective] The aim of this study is to understand the dynamics of cotton rhizosphere bacterial community structure in cotton continuous cropping field soil. [Method] 16S rDNA genes were sequenced by high-throughput sequencing technology to determine the community structure of cotton rhizosphere bacteria in different developmental stages using an upland cotton cultivar (Gossypium hirsutum cv. TM-1). [Result] Four dominant phyla were found in the cotton rhizosphere bacterial community including Proteobacteria, Acidobacteria, Planctomycetes, and Bacteroidetes. The four dominant phyla and Firmicutes were largely influenced by cotton root. The relative abundances of Acidobacteria, Planctomycetes, Bacteroidetes were promoted, and Proteobacteria and Firmicutes were inhibited, by cotton root. There were significant differences in community structure, but not species richness or α-diversity among different developmental stages of the cotton rhizosphere bacterial community; the differences between the flowering stage and the budding stage were greater than the differences between the budding stage and the seedling stage. The diversity of the rhizosphere bacterial community in cotton continuous cropping field soil was significantly higher than that of the bulk soil; the β-diversity values of both the rhizosphere and bulk soil bacterial communities were highest in the flowering stage. [Conclusion] The structure and dynamics of the cotton rhizosphere bacterial community in cotton continuous cropping field soil was defined by high-throughput sequencing. The effect of cotton on the rhizosphere bacterial community structure was most significant in the flowering stage.