延迟收获对长江中游春玉米农艺性状及机收质量的影响

为探明长江中游玉米籽粒机械直收适宜品种与配套农艺措施，2018—2019年选用不同玉米品种，测定不同机收时间下玉米关键农艺性状、产量及机收质量指标。结果表明，收获时间对春玉米机收产量与机收质量均有显著影响。延迟1周收获后籽粒容重显著增加，机收产量显著提高，2年平均提高9.72%；而延迟2周收获则有降低机收产量的趋势。2年收获时杂质率总体≤3%，而机收籽粒破碎率与损失率均>5%，是该区域春玉米籽粒机收面临的主要问题。籽粒厚度、籽粒含水率和百粒重是影响机收籽粒破碎率的关键性状，三者与机收籽粒破碎率均呈显著的倒二次曲线关系；玉米的倒伏率、穗位高和重心高度是影响机收损失率的关键性状，倒伏率与机收损失率呈显著正相关，而穗位高和重心高度与机收损失率均呈显著的二次曲线关系。延迟收获能显著降低籽粒含水量，从而降低籽粒破碎率，但继续延迟收获有增加倒伏的风险。综上，长江中游春玉米成熟后适时延迟7~10 d收获，可有效降低籽粒含水量与机收籽粒破碎率，提高玉米籽粒机收产量。     

采种大白菜地膜复盖的研究

为了提高大白菜(B. campestris ssp pekinensis.)种子的产量和质量,我们进行了两年地膜覆盖研究。结果表明:无论直播小株、育苗小株、老株那种采种方式,凡使用地膜覆盖的均比不覆盖的产量增加30％左右,质量也明显的提高;聚乙烯、聚氯乙烯都是良好的地而覆盖材料,在大白菜种子生产中可以取得相近似的效果。     

地膜覆盖对棉枯萎病发生的影响

地膜覆盖显著降低了棉花枯萎病的发病率与病情指数，极显著地提高了棉花的产量。     

烤烟适宜施氮量试验初报

试验结果表明,烤烟施氮量以90.0~112.5kg/hm2为佳,在此条件下,烤烟的产量和产值最高。     

棉花膜下滴灌计算机辅助设计系统的研制开发

介绍了棉花膜下滴灌计算机辅助设计系统的结构、系统设计思想、程序设计模型以及具体实现时的有关算法。运用现代软件编程和系统集成技术,开发出先进、实用、可靠和界面友好的应用软件,并在新疆兵团推广应用,并提出了进一步研究的方向。     

更新林相图的计算机辅助方法

常规编制与更新林相图的方法要求昂贵的光学机械纠正仪器、较高的操作技术和成本。文章提出一种利用计算机辅助纠正航空象片更新林相图的方法,可以降低成本,提高成图效率。为了实现这种方法,首先根据航空摄影理论分析,推导出适合编程的航空纠正数字化线性模型和算法。该模型要求在底图和航片上有四对控制点坐标,求算纠正参数。采用数字化仪测定这些坐标,求解参数,然后根据该线性模型对航片上编图要素的数字化坐标进行非共面变换,进而更新林相图。为完成这一过程需要四个程序模块和处理流程。使用这种方法更新林相图既能保证精度要求,又具有操作简单的优点。     

催干剂对氨基环氧树脂阴极电泳漆的影响

以氨基环氧树脂为基体树脂，Co^2 ,Pb^2 盐为催干剂合成了阴极电泳漆，并对膜性能进行考察，结果表明，所合成的阴极电泳涂料在PH值为6－7、电泳时间2min的条件下。加入不同的催干剂，在不同的烘干温度下，得到性能不同的漆膜。经过膝膜综合性能试验，结果表明，加入钴和铅复合催化剂，在160℃左右烘干20min，可得到完全固化，硬度较高、耐潮、耐盐、耐酸碱性较好的漆膜。     

甜菜不同种植方式的研究

通过试验明确了覆膜移栽纸筒苗栽培方法具有覆盖地膜和育苗移栽双重效应，促进甜菜早发棵，早封垄。提早进入叶丛快速生长期和块根糖分积累期；改善了甜菜光合性能，增加了光合势、净光合率和光合产物经济系数，比不覆膜移栽纸筒苗的增产31％，产糖量增加27．12％，投入产出比大幅度增加。     

Biochemical properties of the pathogenesis-related proteins from tobacco

This review describes the discovery and identification of the pathogenesis-related proteins (PRs) from tobacco. In crude leaf extracts the PRs are distinguished from the proteins in uninfected plants by their solubility at pH 3, resistance to a range of proteases, and mobility in polyacrylamide gels upon electrophoresis (PAGE) in non-denaturing conditions. PAGE has been used as a qualitative and semi-quantitative assay for PRs, and their migration in gels made from different acrylamide concentrations has been used to identify charge and size isomers and electrophoretically identical PRs in different tobacco cultivars. The subunit composition and molecular weight (mol. wt) of the four PRs identified first in Xanthi-nc were determined by SDS-PAGE; staining the gels has shown that these same four proteins in Samsun NN did not contain carbohydrate, lipid or nucleic acid, nor were they isozymic forms of twenty five enzymes known to increase in activity following infection with TMV. Evidence suggests that most of the PRs in Xanthi-nc and Samsun NN are extracellular.The purification of several PRs from Xanthi-nc, Samsun NN and other tobaccos is described, as well as their mol. wt, subunit and amino acid composition. PRs 1a, b and c consist of a single polypeptide and have similar mol. wt and amino acid compositions. Antisera prepared against purified Xanthi-nc b₁ protein have been used to determine serological relationships between PRs and form the basis of a very sensitive quantitative assay using ELISA. The regulation of synthesis of some PRs has been shown to involve translational control.     

Some coat protein constituents from strawberry latent ringspot virus expressed in transgenic tobacco protect plants against systematic invasion following root inoculation by nematode vectors

The coding sequences in RNA2 for the coat proteins (CP) of strawberry latent ringspot virus (SLRSV) were modified and amplified using polymerase chain amplification reactions (PCR) to facilitate their expression inAgrobacterium tumefaciens-transformedNicotiana tabacum Xanthi-nc. The coding sequences for the smaller capsid protein (S, 29kDa) and that for the theoretical precursor of L and S (P, 73kDa) had ATG initiation codon sequences added at the 5-proximal Ser/Gly (S/G) cleavage site in the unmodified sequence. The sequence coding for the larger of the two proteins of mature SLRSV capsids (L, 44kDa) had an ATG codon added at its 5 S/G site and a TAG stop codon sequence added at the 3-proximal S/G site. The P, L and S proteins were expressedin planta to a maximum concentration of 0.01 % of total extractable proteins but did not assemble into virus-like particles. When challenged by mechanical inoculation with virus particles or viral RNA, and compared with control plants, tobacco plants (primary transgenic clones or S1 and S2, kanamycin-resistant seedlings) expressing the virus capsid subunits separately, or their precursor, decreased the accumulation of SLRSV particles in inoculated leaves and fewer plants became invaded systemically. In experiments in which the roots of seedlings were exposed to SLRSV-carrying vector nematodes (Xiphinema diversicaudatum), SLRSV was detected in the roots of non-transformed control tobacco plants (6/20) and in transgenic tobacco expressing the L protein (7/40), but not in any of 25 tobacco plants expressing the S protein or in 35 expressing the P protein. This is the second example of CP-mediated resistance to virus inoculation by nematode vectors.