优质高产大花生新品种潍花6号的选育研究

潍花6号是潍坊市农科院以79266做母本，鲁花11号为父本进行有性杂交，系统选育而成。经1998—2001年山东、河北两省区试、生产试验及高产示范表明，该品种具有早熟、高产稳产、果大仁大、出仁率高、耐贮性好、口味佳等突出特点，2001年和2002年分别通过山东、河北两省农作物品种审定委员会审定，是一个适于中国北方花生产区栽培的优质高产大花生新品种。     

Identification and mapping of a novel Turnip mosaic virus resistance gene TuRBCS01 in Chinese cabbage (Brassica rapa L.)

We aimed to identify Turnip mosaic virus (TuMV) resistance genes in Chinese cabbage by analysing the TuMV resistance of 43 P₁ (resistant), 88 P₂ (susceptible), 26 F₁, 104 B₁ (F₁ × P₁), 108 B₂ (F₁ × P₂) and 509 F₂ individuals. All parents and progeny populations were mechanically inoculated with TuMV‐C4. Both F₁ and B₁ populations showed TuMV resistance. Resistant: susceptible ratios in the B₂ and F₂ populations were 1 : 1 and 3 : 1, respectively. TuMV resistance in P₁ was controlled by a dominant gene, TuRBCS01. Bulked segregation analysis was performed to identify simple sequence repeat or insertion or deletion markers linked to TuRBCS01. Data from 108 B₂ individuals with resistant or susceptible phenotypes were analysed using mapmake r/exp 3.0. Polymorphic marker sequences were blast searched on http://brassicadb.org/brad/ . TuRBCS01 was found to be linked to eight markers: SAAS_mDN192117a_159 (3.3 cM), SAAS_mDN192117b_196 (4.0 cM), SAAS_mDN192403_148 (13.0 cM), SAAS_mGT084561_233 (6.8 cM), BrID10723 (3.3 cM), mBr4041 (3.3 cM), SAAS_mBr4055_194 (2.6 cM) and mBr4068 (4.0 cM). Further, TuRBCS01 was mapped to a 1.98‐Mb region on chromosome A04 between markers BrID10723 and SAAS_mBr4055_194.     

绿肥还田对双季稻根际土壤产甲烷古菌群落结构的影响

利用PCR-DGGE技术及克隆文库构建方法研究,尿素、紫云英鲜草翻压还田、黑麦草鲜草翻压还田和不施氮肥4种处理对双季稻不同生育时期(早稻季:分蘖期,拔节期,成熟期;晚稻季:分蘖期,扬花期,成熟期)稻田根际土壤中产甲烷群落结构的影响。结果表明,双季稻不同取样时期和各处理中产甲烷古菌群落结构稳定且相似,早稻季和晚稻季的优势群落均为甲烷微菌目(Methanomicrobiales)、Rice Cluster I(RC-I)、甲烷鬃菌科(Methanosaetaceae)、甲烷杆菌属(Methanobacterium),但早稻季产甲烷古菌群落的Shannon-Weiner指数(H)和丰富度指数(R)整体低于晚稻季。紫云英和黑麦草鲜草翻压还田处理较尿素处理更为明显地提高了双季稻(一年)稻田根际土壤中产甲烷古菌群落的Shannon-Weiner指数和丰富度指数,但均暂未对产甲烷群落结构产生决定性影响。     

不同紫花苜蓿品种引种试验研究

引进了国外8个苜蓿品种,在2003年至2005年对其产量、株高、营养价值、越冬率、越夏性、抗倒伏和经济效益等方面进行了比较,结果表明这8个苜蓿品种在郑州地区均表现了良好的适应性,其中WL232和猎人河是推广的首选品种。     

不结球白菜游离小孢子培养成胚影响因素的研究

以17个不同基因型的不结球白菜为供试材料,对影响小孢子胚胎发生频率的若干因素进行了研究。结果表明:在秋冬季日光温室内,供试植株主花序第一朵花开后第7~14天取样,即初花期是最佳取样时期;不同基因型间小孢子胚胎发生能力差异很大,在接种的17个基因型中,有12个诱导出胚,诱导成功率71%;其中102号产胚量最高,达到32.78个/蕾;在已产胚材料中,产胚量最高的基因型是产胚量最低的基因型的546倍;较易抽薹型材料的产胚能力大于易抽薹型和不易抽薹型。以B5有机成分代替NLN有机成分,能够提高产胚量,尤其是对难成胚基因型的小孢子胚胎发生有较好的促进作用,甘露醇对小孢子分裂无促进作用。     

抗病优质大白菜“秋白70”的选育

优质、抗病的大白菜新品种——秋白70是利用天津青麻叶为母体，进行游离小孢子培养，并结合人工接种鉴定技术于2002年育成功。该品种长势旺，成熟期70d，株型较直立，株高48cm，开展度51cm，外叶8片，叶形长倒卵形，叶色深绿，叶面多皱，绿帮；叶球长筒形，颜色绿，叶球内叶颜色浅黄，心叶拧抱，舒心；叶球高44cm，直径14cm，单球重2.2kg左右，净菜率82.3%。品质优良，口味佳。较抗霜霉病和病毒病。平均产量10.8kg/m2。     

世纪之交我国棉花品种改良的科技发展

近年来我国棉花生产急剧滑坡，起因是自然灾害，但缺乏突破性品种，或者说品种的遗传基础过于狭窄是内在的根本原因。我国棉花生产用种以自育品种为主的世代不会逆转。今后我国棉花品种改良的科技要点是：加强原始材料的收集和育种新亲本的创造；促进高新技术与常规育种的结合；常规育种技术亟待创新，重点是加强理论指导，方案要贴近生产实际；恢复诸如诱变及其与复合杂交相结合等方法研究；优质纤维将是遗传改良的重点性状。此外，品种立法也势在必行。     

大白菜抗根肿病基因位点CRa和CRb的分子标记鉴定

利用大白菜抗根肿病基因CRa和CRb分子标记(SC2930和KBr H129J18R)引物组,对78份大白菜材料进行抗根肿病分子标记鉴定。结果表明,在这78份材料中,有34份材料含有SC2930-T(CRa抗病标记)标记,其中杂合抗病位点材料17份,纯合抗病位点材料17份。有37份材料含有KBr H129J18R抗病标记,其中纯合抗病位点材料15份,杂合抗病位点材料22份。有20份材料不含有CRa和CRb所对应的抗病标记,23份材料含有2个抗病标记。该研究初步明确了78份参试大白菜材料所含抗根肿病基因CRa和CRb类型,为大白菜抗根肿病育种提供材料选择依据。     

Incidence and molecular markers of 2n pollen in Populus tomentosa Carr.

Microscopic examination, amplified fragment length polymorphism (AFLP) and SCAR (sequence-characterized amplified region) molecular markers were employed to determine the incidence of 2n pollen (unreduced pollen) in Chinese white poplar (Populus tomentosa Carr.) and to identify related molecular markers. The presence of a parallel and tripolar spindle at metaphase II and the absence of cytokinesis at telophase II were found to be determining factors in 2n pollen formation. A group of 298 clones that originated from their indigenous areas were investigated for the production of 2n pollen based on pollen size differences, both within a clone and between n and 2n pollen. Pollen grains were collected from 224 of the clones, six of which were subsequently determined to produce only normal pollen; the remainder produced 2n pollen at different frequencies (0.6–21.9%). The frequency at which 2n pollen was produced was significantly and highly significantly different among and within indigenous populations, respectively. Clones produced by the six normal and twenty-two 2n pollen clones were selected for AFLP analysis. Following an initial screening with 55 primer combinations, the E50-M38 (CAT/ACT) primer was identified: it generated a PCR fragment (246 bp) from the normal clones, but not from the 2n pollen producers. In addition, the E31-M50 (AAA/CAT)-amplified DNA fragment (204 bp) was present in 2n pollen producers, and absent in normal clones. These two discriminating AFLP markers were developed into easily detectable SCAR (sequence characterized amplified region) markers which can be used in combination with previously developed AFLP markers to distinguish between normal and 2n pollen clones.     

大白菜细胞质雄性不育的分子鉴定及序列分析

为了获得3种大白菜细胞质雄性不育系Ogu CMS,Pol CMS,CMS96和保持系间的多态性以及定位大白菜CMS96不育系所属的不育类型,利用设计的atp6,orf222单一和混合引物PCR扩增3组11份同核异质大白菜细胞质雄性不育系和保持系mtDNA。结果表明,atp6引物在大白菜Ogu CMS不育系扩增的200 bp片段为其特异带;orf222引物仅在大白菜Pol CMS和CMS96不育系有扩增产物,但二者有3点完全不同:大白菜Pol CMS不育系扩增产物为675bp,CMS96不育系扩增产物为669 bp,二者相差6个核苷酸,后者定名为大白菜CMS96-orf222。大白菜CMS96-orf222与甘蓝型油菜Nap CMS的nad5c基因和Nap-orf222基因同源性均为99%,E值为0.0;大白菜Pol CMS的675 bp序列具有ORF224开放阅读框,没有保守结构域,而大白菜CMS96的669 bp序列具有ORF222开放阅读框和保守结构域YMF19。另外,atp6和orf222混合引物多重PCR扩增产物存在明显多态性:800 bp为大白菜保持系的差异带型;2 300 bp和1 500 bp为大白菜Pol CMS不育系特异带型;200 bp为大白菜Ogu CMS不育系特异带型;690 bp为大白菜CMS96不育系特异带型。该方法仅用一次PCR反应快速地将3种大白菜细胞质雄性不育系和保持系一次性全部区分开,为大白菜分子育种和常规育种更好地相结合提供了简单、快速、准确和重复性好的方法和手段。