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Volume 35 Issue 2
Nov.  2019
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LOU Li-hua, ZENG Jing, JIANG Hai-yan, YAN Qiao, WANG Zheng-chun. An Experimental Study of Tissue Culture of Chamelaucium uncinatum ‘Snow Flake’[J]. Journal of Sichuan Forestry Science and Technology, 2014, 35(2): 34-36,56. doi: 10.16779/j.cnki.1003-5508.2014.02.008
Citation: LOU Li-hua, ZENG Jing, JIANG Hai-yan, YAN Qiao, WANG Zheng-chun. An Experimental Study of Tissue Culture of Chamelaucium uncinatum ‘Snow Flake’[J]. Journal of Sichuan Forestry Science and Technology, 2014, 35(2): 34-36,56. doi: 10.16779/j.cnki.1003-5508.2014.02.008

An Experimental Study of Tissue Culture of Chamelaucium uncinatum ‘Snow Flake’


doi: 10.16779/j.cnki.1003-5508.2014.02.008
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  • Received Date: 2013-12-04
  • As a new generation of woody cut flowers, C. uncinatum ‘Snow Flake’ has a high ornamental and economic value. Based on the study of tissue culture of ‘Snow Flake’,the aim of this experiment was to lay the foundation for Industrial production of ‘Snow Flake’. The results showed that 7 minutes were the best time to sterilize explants by using 0.1% HgCl2. MS1 + 6-BA1.0 mg·L-1 + IBA0.2 mg·L-1 + KT0.5 mg·L-1 was the optimum primary culture medium, the best subcultuer medium was WPM1 + 6-BA 1.0 mg·L-1 + IBA 0.2 mg·L-1 + GA3 1.5 mg·L-1,multiplication coefficient was 4.2,multiplication was 3~6. The most suitable rooting medium was 1/2MS2 + IBA0.2 mg·L-1 + 0.1 mg·L-1 GGR.
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    沈阳化工大学材料科学与工程学院 沈阳 110142

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An Experimental Study of Tissue Culture of Chamelaucium uncinatum ‘Snow Flake’

doi: 10.16779/j.cnki.1003-5508.2014.02.008
  • Chongqing Academy of Forestry, Chongqing Key Laboratory of Three Gorges Area Forest Ecology Protection and Restoration, Chongqing 400036, China

Abstract: As a new generation of woody cut flowers, C. uncinatum ‘Snow Flake’ has a high ornamental and economic value. Based on the study of tissue culture of ‘Snow Flake’,the aim of this experiment was to lay the foundation for Industrial production of ‘Snow Flake’. The results showed that 7 minutes were the best time to sterilize explants by using 0.1% HgCl2. MS1 + 6-BA1.0 mg·L-1 + IBA0.2 mg·L-1 + KT0.5 mg·L-1 was the optimum primary culture medium, the best subcultuer medium was WPM1 + 6-BA 1.0 mg·L-1 + IBA 0.2 mg·L-1 + GA3 1.5 mg·L-1,multiplication coefficient was 4.2,multiplication was 3~6. The most suitable rooting medium was 1/2MS2 + IBA0.2 mg·L-1 + 0.1 mg·L-1 GGR.

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