黑龙江省大豆品质区划的探讨

从大豆品质入手,依据大豆化学品质与地理分布、环境条件、地理状况、土壤类型、气禾躜件与大豆商品贸易和利用的关系,把黑龙江省大豆生产区域分成三大区,即东西部高油大豆生产区(Ⅰ区),该区分成二个亚区,西部高油大豆产区(Ⅰ区-A)与东部的高油大豆产区(Ⅰ区-B);中部与东南部的高蛋白生产区(Ⅱ区),该区分成二个亚区,中部高蛋白生产区(Ⅱ区-A)与东南部高蛋白生产区(Ⅱ区-B);北部与东部沿江地区的蛋白油分平衡区,该区分成二个亚区,北部蛋白油分平衡区(Ⅲ区-A)与东部沿江地区蛋白油分平衡区(Ⅲ区-B).     

两种形态氮源条件下磷对大豆结瘤固氮的影响

用营养液培养大豆7周,研究两种氮源条件下,磷对大豆结瘤固氮的影响.在本试验的各取样时期,随营养液中磷水平的增加,生物固氮植株的根瘤数增加较多,尤其是处理后第6周,磷对根瘤形成的影响最大.磷对硝态氮处理根瘤数的影响不大,但本试验条件下,在16μmol/L磷水平,根瘤数较多.硝态氮处理根瘤数远没有生物固氮处理多,表现出氮素对大豆结瘤的抑制作用,导致根瘤固定的氮量减少.因此,硝态氮植株体内含氮量随磷水平的增加而降低,而生物固氮植株增加.生物固氮处理根中N/P与根瘤数之间存在显著的负相关关系,r=-0.5816*,硝态氮处理根中N/P与根瘤数之间不相关.     

氮磷钾底肥对大豆蛋白质含量的效应

采用正交回归旋转设计方法,建立了氮、磷、钾肥对大豆蛋白质含量的综合作用模型.依据该模型探讨氮、磷、钾肥对大豆蛋白质含量影响的规律.氮、磷、钾肥对大豆蛋白质含量的单因素效应、二因素互作效应受到其它因素水平的影响.氮肥对蛋白质含量的影响均为负效应,降低速度随着氮肥编码值增高而加快.磷肥对蛋白质含量的作用有正有负.钾肥对蛋白质含量的作用为负效应,其降低幅度随钾的增加而提高.施尿素量为1.93～4.70g/盆,施重过磷酸钙量为8.13～20.59g/盆,施硫酸钾量为1.27～3.37g/盆,采用这个比例施肥有95%的可能使蛋白质含量高于43.5%.     

大豆对SMV株系SC-11的抗性遗传及抗病基因的等位性研究

利用对我国北方大豆产区流行株系SC-11表现抗病的材料科丰1号、邳县茶豆、大白麻、齐黄22、诱变30、PI96983、Kwanggyo和感病材料南农1138-2、南农18-6配制的抗感和抗抗杂交组合,研究了对SC-11的抗性遗传以及不同材料的抗病基因间的等位性关系.结果表明,科丰1号、邳县茶豆、大白麻、PI96983、Kwanggyo、齐黄22、诱变30与感病品种杂交的F1表现抗病,F2呈3抗:1感分离比例,F2:3家系呈1抗:2分离:1感病的分离比率,证明它们对SC-11的抗性由单显性基因控制.PI96983×Kwanggyo和齐黄22×诱变30杂交后的F2群体未发现抗感分离,表明PI96983与Kwanggyo以及齐黄22与诱变30对SC-11的抗性基因是等位或紧密连锁的.大白麻与科丰1号、邳县茶豆、诱变30,科丰1号与Kwanggyo,PI96983与邳县茶豆杂交的F2呈15抗:1感的比例分离,初步表明大白麻与科丰1号、邳县茶豆、诱变30,科丰1号与Kwanggyo,PI96983与邳县茶豆所携带的抗SC-11的基因是不等位的,而且2个抗性基因独立遗传.     

大豆资源对斜纹夜蛾的抗性鉴定

利用网室采集的57份大豆资源的叶片,室内喂养刚孵化的斜纹夜蛾幼虫,以幼虫重为指标,鉴定大豆资源对斜纹夜蛾的抗性.综合2001年和2002年的鉴定结果,品种间、年份间、品种与年份互作差异均达极显著水平.根据标准品种分级法对抗性鉴定结果进行划分,从供试的大豆资源中筛选出4个高抗和3个高感的标准品种,可以用于抗性的分级及抗虫新基因的发掘.     

河南栽培大豆的RAPD品种鉴定和聚类分析

用CTAB法提取了10个大豆品种总DNA,使用RAPD技术对其进行了品种鉴定和聚类分析。从73条随机引物中筛选出12条扩增出较稳定DNA条带的引物扩增这些品种总DNA,共扩增出67条带,大小0．2-5 kb,每种引物扩增出4-9条带;多态性条带共51条,多态性比例为76．12％。利用SPSS11．0软件所做的统计分析和聚类分析结果表明,10个品种间的相似系数在0．528-0．776之间,平均相似系数为0．641 6;可聚成3类:豫豆24号、周豆11号、周豆 12号、豫豆11号、周豆13号、豫豆6号,可聚为A类;中作98-3和豫豆15号可聚为B类;豫豆26号和豫豆22号聚为 C类。同一类品种间体现了一定的相关性。     

Rapid screening of genetically modified ingredients in soybean and cotton processing by-product and waste using direct qPCR

To develop a simple and fast method for screening genetically modified ingredients from processing by-product and waste, direct quantitative PCR (qPCR) kit-Taqman which omitting multi genomic DNA preparing steps was developed in this study. A total of 18 oil crop processing by-products and wastes including 10 soybean and 8 cotton materials were collected from food processing factories. Compared with 2 commercial direct qPCR kits, conditions of DNA releasing procedure and PCR amplification were optimized. Element screening was performed at the initial step of genetically modified (GM) ingredient testing procedure via direct qPCR. GM event identification was carried out in positive samples by initial screening. Totally 5 screening elements (P–35S, T-NOS, Cp4-epsps, bar and pat) for soybean materials and 6 screening elements (P–35S, T-NOS, NPTII, Cry1Ac, bar and pat) for cotton samples were detected. In GM event identification, MON531 and MON1445 were found in cotton materials. Results were further confirmed by real-time PCR with DNA extraction and purification. The direct qPCR system proposed by this research was convenient for rapid screening and identification of GM ingredients in oil crop primary by-product and waste.     

Management of yellow dwarf disease in Europe in a post‐neonicotinoid agriculture

Barley/cereal yellow dwarf viruses (YDVs) cause yellow dwarf disease (YDD), which is a continuous risk to cereals production worldwide. These viruses cause leaf yellowing and stunting, resulting in yield reductions of up to 80%. YDVs have been a consistent but low‐level problem in European cereal cultivation for the last three decades, mostly due to the availability of several effective insecticides (largely pyrethroids and more recently neonicotinoids) against aphid vectors. However, this has changed recently, with many insecticides being lost, culminating in a recent European Union (EU) regulation prohibiting outdoor use of the neonicotinoid‐insecticide compounds. This change is coupled with the growing challenge of insecticide‐resistant aphids, the lack of genetic resources against YDVs, and a knowledge deficit around the parameters responsible for the emergence and spread of YDD. This means that economic sustainability of cereal cultivation in several European countries including France and United Kingdom is now again threatened by this aphid‐vectored viral disease. In this review, we summarize the current knowledge on the YDV pathosystem, describe management options against YDD, analyse the impacts of the neonicotinoid ban in Europe, and consider future strategies to control YDV. © 2020 Society of Chemical Industry