林业科学
林業科學
임업과학
SCIENTIA SILVAE SINICAE
2014年
6期
55-60
,共6页
施琼%胡峰%黄烈健%詹妮
施瓊%鬍峰%黃烈健%詹妮
시경%호봉%황렬건%첨니
马大杂种相思%有效增殖倍数%单株繁殖系数%继代次数%腋芽增殖
馬大雜種相思%有效增殖倍數%單株繁殖繫數%繼代次數%腋芽增殖
마대잡충상사%유효증식배수%단주번식계수%계대차수%액아증식
Acacia mangium × A. auriculiformis%efficient proliferation rate%propagation coefficient%subculture%axillary bud multiplication
以马大杂种相思组培苗为研究对象,通过筛选最佳的增殖培养基,调整增殖时间,探讨芽体长度、继代次数对增殖的影响,增殖培养对生根的影响,建立马大杂种相思腋芽高效组培增殖体系。结果表明:将健壮的初代培养无菌芽剪成含1个腋芽的茎段,接入最佳增殖培养基(改良 MS +6-BA1.5 mg·L -1+NAA0.1 mg·L -1+Ac0.04 g·L -1,添加蔗糖3%和琼脂7 g·L -1)中连续培养7代,7次继代的平均增殖倍数为2.52,增殖时间为35天,单株平均繁殖系数为14.99,且7次继代增殖倍数变化小、增殖芽质量好。将增殖芽的茎段(含2~3个腋芽)接入1/2MS+IBA1.0 mg·L -1+ NAA0.5 mg·L -1(添加蔗糖3%和琼脂7 g·L -1)进行生根培养,15天生根率可达96.5%,移栽后存活率为95.0%。
以馬大雜種相思組培苗為研究對象,通過篩選最佳的增殖培養基,調整增殖時間,探討芽體長度、繼代次數對增殖的影響,增殖培養對生根的影響,建立馬大雜種相思腋芽高效組培增殖體繫。結果錶明:將健壯的初代培養無菌芽剪成含1箇腋芽的莖段,接入最佳增殖培養基(改良 MS +6-BA1.5 mg·L -1+NAA0.1 mg·L -1+Ac0.04 g·L -1,添加蔗糖3%和瓊脂7 g·L -1)中連續培養7代,7次繼代的平均增殖倍數為2.52,增殖時間為35天,單株平均繁殖繫數為14.99,且7次繼代增殖倍數變化小、增殖芽質量好。將增殖芽的莖段(含2~3箇腋芽)接入1/2MS+IBA1.0 mg·L -1+ NAA0.5 mg·L -1(添加蔗糖3%和瓊脂7 g·L -1)進行生根培養,15天生根率可達96.5%,移栽後存活率為95.0%。
이마대잡충상사조배묘위연구대상,통과사선최가적증식배양기,조정증식시간,탐토아체장도、계대차수대증식적영향,증식배양대생근적영향,건립마대잡충상사액아고효조배증식체계。결과표명:장건장적초대배양무균아전성함1개액아적경단,접입최가증식배양기(개량 MS +6-BA1.5 mg·L -1+NAA0.1 mg·L -1+Ac0.04 g·L -1,첨가자당3%화경지7 g·L -1)중련속배양7대,7차계대적평균증식배수위2.52,증식시간위35천,단주평균번식계수위14.99,차7차계대증식배수변화소、증식아질량호。장증식아적경단(함2~3개액아)접입1/2MS+IBA1.0 mg·L -1+ NAA0.5 mg·L -1(첨가자당3%화경지7 g·L -1)진행생근배양,15천생근솔가체96.5%,이재후존활솔위95.0%。
To build an efficient axillary bud multiplication system of Acacia mangium × A. auriculiformis,the aseptic plantlets of A. mangium × A. auriculiformis were used to screen the optimal protocol for in vitro multiplication. The optimal multiplication medium and period,length of the sterile stems,subculture times,rooting and transplant survival rate were studied. The results showed that after being cultured 7 times on improved-MS+ 0. 5 mg·L -16-BA+0. 1 mg·L -1 NAA +0.04 g·L -1Ac(with combination of 3% sugar and 7 g·L -1 agar),which was the best multiplication medium screened from the trial test,the average proliferation times of the stem with one axillary bud were 2. 52,and the propagation coefficient of the plantlet was around 14. 99 after 35 days. Moreover,the plantlets grew well and there was no obvious variation of the multiplication ratio. The aseptic stem with 2 or 3 axillary buds was inoculated to 1/2MS +IBA1. 0 mg·L -1 +NAA0. 5 mg·L -1 ( with combination of 3% sugar and 7 g·L -1 agar) for rooting culture,the rooting rate was 96. 5% in 15 day and the transplant survival rate was 95. 0%.