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DEVELOPMENTAL MORPHOLOGY OF THE FLOWER AND INHERITANCE OF AN APETALOUS MUTANT IN BRASSICA CARINATA A. BRAUN.

机译:芥菜花的发育和遗传突变的遗传形态。

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摘要

An apetalous mutant of Ethiopian mustard (Brassica carinata A. Braun) was studied to determine both its floral development and the inheritance of the trait. It has been speculated that apetally will benefit the plant by eliminating dried petals which, when they stick to the plant, are infection sites for the pathogen Sclerotinia sclerotiorum (McClean, 1958; Kruger, 1974).; Scanning electron and light microscopy of developing flower buds of petalous and apetalous types indicated that the sequence of floral development was sepals, androecium and gynoecium simultaneously, and lastly the corolla. Until corolla initiation, the development of apetalous and petalous types was similar. Petal development appeared to be in delicate balance with the internal and external environment, manifested by apetalous flowers on petalous plants and petalous flowers on apetalous plants and also by the frequent presence of rudimentary petals in apetalous types.; Reciprocal crosses of two plants of each of the apetalous and petalous parents provided F(,1) plants that were all similar to the petalous parent, indicating the absence of cytoplasmic effects and the presence of dominant gene action. Studies of F(,2), F(,3) and F(,1) and F(,2) progeny of testcrosses indicated that two major genes governed the degree of petally. The presence of variable numbers of partially petaled plants in segregating populations complicated the studies and indicated the presence of an unidentified number of modifying genes. No true-breeding partially petaled type was found, possibly because such types are heterozygous but perhaps also because such types are very sensitive to the internal and external environments.; It is assumed that the ancestral species of B. carinata, B. nigra and B. oleracea each contributed a gene that governed petally.
机译:研究了埃塞俄比亚芥菜(Brassica carinata A. Braun)的一个无性突变体,以确定其花序发育和该性状的遗传。据推测,花瓣将通过消除干燥的花瓣而有益于植物,当干燥的花瓣粘在植物上时,花瓣是病原菌核盘菌的感染部位(McClean,1958; Kruger,1974)。扫描的电子和光学显微镜观察到的花瓣和非花瓣类型的发育中的花芽表明,花的发育顺序是萼片,雄蕊和雌蕊同时发生,最后是花冠。在花冠开始之前,花瓣和花瓣类型的发育相似。花瓣的发育似乎与内部和外部环境达到了微妙的平衡,表现为花瓣植物上的花瓣花和花瓣植物上的花瓣花,以及花瓣形式的原始花瓣的频繁出现。花瓣状和花瓣状亲本中的每一种的两种植物的相互杂交提供了全部与花瓣状亲本相似的F(,1)植物,表明没有细胞质作用并且存在显性基因作用。对测试杂交的F(,2),F(,3)和F(,1)和F(,2)后代的研究表明,两个主要基因控制着花瓣的程度。在分离种群中存在数量不定的部分花瓣植物使研究复杂化,并表明存在数目不明的修饰基因。没有找到真正繁殖的部分花瓣类型,可能是因为这种类型是杂合的,但也可能是因为这种类型对内部和外部环境非常敏感。据推测,B。carinata,B。nigra和B. oleracea的祖先物种各自贡献了一个花瓣控制基因。

著录项

  • 作者

    RANA, MASOOD AMJAD.;

  • 作者单位

    University of California, Davis.;

  • 授予单位 University of California, Davis.;
  • 学科 Biology Genetics.
  • 学位 Ph.D.
  • 年度 1984
  • 页码 103 p.
  • 总页数 103
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 遗传学;
  • 关键词

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