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Volume 37 Issue 5
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LIU Hai-ying, WAN Xue-qin, LIU Jun-li, YANG Xiao-rong. A study of Culture in Vitro and Propagation of Superior Clones of Cunninghamia lanceolata[J]. Journal of Sichuan Forestry Science and Technology, 2016, 37(5): 1-6. doi: 10.16779/j.cnki.1003-5508.2016.05.001
Citation: LIU Hai-ying, WAN Xue-qin, LIU Jun-li, YANG Xiao-rong. A study of Culture in Vitro and Propagation of Superior Clones of Cunninghamia lanceolata[J]. Journal of Sichuan Forestry Science and Technology, 2016, 37(5): 1-6. doi: 10.16779/j.cnki.1003-5508.2016.05.001

A study of Culture in Vitro and Propagation of Superior Clones of Cunninghamia lanceolata


doi: 10.16779/j.cnki.1003-5508.2016.05.001
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  • Received Date: 2016-06-12
  • Culture in Vitro and propagation were carried out by using basal sprouts of superior clones 3-3 Cunninghamia lanceolata as explants. The result showed that the optimal cutting trunk height was 30 cm in March and the average number of bud was 47.2; Best explants disinfection solution was to immerse 15s in 70% alcohol and use sterile water to wash twice and then to soak 6 min in 0.1% mercuric chloride and wash 6 times with sterile water; MS culture medium was the optimal basic culture in primary culture; Subculture medium was MS+BA(0.5 mg·L-1~0.7 mg·L-1)+IBA(0 mg·L-1~0.2 mg·L-1); Inducing-root medium was 1/2MS~1/4MS+0.5 mg·L-1~1.0 mg·L-1IBA+0.1 mg·L-1NAA; The most suitable soil matrix proportion of transplanting was peat soil:yellow subsoil:vermiculite=4:2:1.
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A study of Culture in Vitro and Propagation of Superior Clones of Cunninghamia lanceolata

doi: 10.16779/j.cnki.1003-5508.2016.05.001
  • Department of Forestry, Sichuan Aguicultural University, Ya'an 625014, China;Sichuan Acadamy of Forestry, Chengdu 610081, China

Abstract: Culture in Vitro and propagation were carried out by using basal sprouts of superior clones 3-3 Cunninghamia lanceolata as explants. The result showed that the optimal cutting trunk height was 30 cm in March and the average number of bud was 47.2; Best explants disinfection solution was to immerse 15s in 70% alcohol and use sterile water to wash twice and then to soak 6 min in 0.1% mercuric chloride and wash 6 times with sterile water; MS culture medium was the optimal basic culture in primary culture; Subculture medium was MS+BA(0.5 mg·L-1~0.7 mg·L-1)+IBA(0 mg·L-1~0.2 mg·L-1); Inducing-root medium was 1/2MS~1/4MS+0.5 mg·L-1~1.0 mg·L-1IBA+0.1 mg·L-1NAA; The most suitable soil matrix proportion of transplanting was peat soil:yellow subsoil:vermiculite=4:2:1.

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