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鸢尾属植物种子休眠原因及提高萌发率方法综述 被引量:22

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摘要 鸢尾属植物种子普遍具有休眠特性。其休眠原因主要有三个方面:种皮的机械阻碍;种子中存在抑制物;种子需要后熟。针对其休眠特性,提高其萌发率方法有:去除珠孔端种皮;淋洗;低温层积;化学物质处理;电离辐射等。
作者 郭瑛 高亦珂
出处 《种子》 CSCD 北大核心 2006年第2期42-45,共4页 Seed
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参考文献15

  • 1Randolph,L.F.,and L.G.Cox.Factors influencing the germination of iris seed And the relation of inhibiting substances to embryo dormancy.Proc.Amer.Soc.Hort.Sci,1943,43:284-300.
  • 2伍碧华,颜济,周永红,左文霞.种皮对扁竹兰鸢尾(Iris confusa)及其杂种种子萌发的抑制作用[J].四川农业大学学报,1998,16(3):337-340. 被引量:27
  • 3A.Blumenthal,H.R.Lerner,Ella Werker.Germination preventing mechanisms in Iris seeds.Annals of Botany,1986,58(4):551-561.
  • 4Joseph Arditti and Thomas R.Pary.Dormancy factors in iris(Iridaceae)seeds Amer.J.Bot.,1969,56(3):254-259.
  • 5Seed germination of Alaska iris,Iris setosa ssp.interior.Hort-Science,1987,22(5):898-899.
  • 6Lee Eunju,Koh JeaChul.Improvement of seed germination in native Iris sanguinea Donn ex Horn.Korean Journal of Horticultural Science & Technology.Korean Society for Horticultural Science,Suwon,Korea Republic,2002,20(4):345-351.
  • 7Stratification and priming may improve seed germination of purple coneflower,Blue-flag iris and evening primrose.International Society for Horticultural Science (ISHS),2004,629:391-395.
  • 8Seed germination characteristics of Iris virginica.American Midland Naturalist,1990,124(2):209-213.
  • 9邢少辰,林秀峰.分离基因的有效手段-mRNA差异显示技术[J].吉林农业科学,2004,29(2):9-12. 被引量:12
  • 10Ishmuratova,M.M.,Rakhimova,A.F.The use of in vitro culture for the propagation of Iris L.hybrids.Rastitel'nye Resursy,1999,35(4):74-78.

二级参考文献24

  • 1Cmarik J L, Min H, Hegamyer G, et al. Differentially expressed protein Pdcd4 inhibits tumor promoter-induced neoplastic transformation. Proc. Natl. Acad. Sci. USA. 1999, 96: 14037-14042.
  • 2Matz M and Lukyanov S A. Different strategies of differential display: areas of application. Nucleic Acids Res., 1998, 26(24): 5537-5543.
  • 3Soklov B P, Prockop D J. A rapid and simply PCR-based method for isolation of cDNAs from differential expressed genes, Nucleic Acids Res, 1994, 22 (9): 4009-4015.
  • 4Callard D, Lescure B and Mazzolini L. 1994, A method for the elimination of false positives generated by the mRNA differential display technique, Biotechniques, 16: 1096-1103.
  • 5Bachem C W B, van der Hoeven R S, de Bruijn SM, et al. 1996, Visualization of differential gene expression using a novel method of RNA fingerprinting based on AFLP: analysis of gene expression during potato tuber development, plant J., 9, 745-753.
  • 6Lievens S, Goormachtig S and Holsters M. A critical evaluation of differential display as a tool to identify genes involved in legume nodulation: looking bach and looking forward. Nucleic Acids Res., 2001, 29(17): 3459-3468.
  • 7Park J M, Park C J, Lee S B, Ham B K, et al. Overexpression of the Tobacco Tsi 1 Gene Encoding an EREBP/AP2-Type Transcription Factor Enhances Resistance against Pathogen Attack and Osmotic Stress in Tobacco, The Plant Cell,2001, 13, 1035-1046.
  • 8Liang P, Pardee A B, et al. Differential display of eucaryotic messenger RNA by means of the polymerase chain reaction.Science, 1992, 257: 967-971.
  • 9Miele G, MacRae L, McBride D, et al. Elimination of false positives generated through PCR re-amplification of differential display cDNA. Biotechniques, 1998, 25(1): 138-144.
  • 10Jurecic R, Nachtman R G, Colicos S M, et al. Identification and cloning of differentially expressed genes by long-distance differential display. Anal. Bicchem. 1998, 259(2): 235-244.

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