摘要
以有髯鸢尾1A(印度首领×白与蓝)继代5次组培苗为试验材料,以MS+2. 0 mg/L 6-BA+0. 5 mg/L IBA为基本培养基,分别添加不同质量浓度的多效唑(PP_(333))、比久(B9)、矮壮素(CCC)、脱落酸(ABA)、甘露醇、山梨醇,采用单因素试验设计,研究不同药剂及其质量浓度对组培苗离体保存的影响,并应用隶属函数法对各药剂浓度的保存效果进行综合评价。结果表明,6种药剂对有髯鸢尾1A组培苗的生长有较强的抑制作用。同一药剂不同浓度间指标的差异不同,分别添加PP_(333)、B9、甘露醇、山梨醇时,不同质量浓度处理的组培苗存活率均为100%;分别添加CCC、ABA时,不同质量浓度的组培苗存活率差异明显。当PP_(333)为8. 0 mg/L及16. 0 mg/L、CCC为20. 0 mg/L及40. 0 mg/L、甘露醇为30. 0 g/L及40. 0 g/L、山梨醇为30. 0 g/L时,株丛黄叶率均为0;当CCC为5. 0 mg/L时,株丛增殖倍数最高,为5. 8倍;当PP_(333)为1. 0 mg/L时,株高最大,为10. 5 cm。综合考虑,PP_(333)、B9、CCC、ABA和甘露醇、山梨醇的最适质量浓度分别为8. 0、15. 0、40. 0、4. 0 mg/L和40. 0、30. 0 g/L。隶属函数法综合评价结果表明,有髯鸢尾1A组培苗种质离体保存的最佳处理为甘露醇40. 0 g/L,培养至120 d时,其株丛存活率为100%,无黄叶现象,增殖倍数为2. 9,株高为2. 6 cm。
Bearded Iris 1A( reciprocal cross offspring of Iris germanica Indian Chief and Iris germanica Baiyulan) were used as experimental materials. Using single factor design method,the effects of PP_(333),B9,CCC,ABA,mannitol and sorbitol on preservation in vitro were studied. The results showed that,the growth of tissue culture seedlings was greatly inhibited by 6 growth regulators. The difference of indicators between different concentrations was different. When PP_(333),B9,mannitol and sorbitol were added respectively,the survival rates of tissue culture seedlings reached 100%,When CCC and ABA were added respectively,the survival rates of tissue culture seedlings were obviously different. When the concentration of PP_(333) was 8. 0 mg/L and 16. 0 mg/L,CCC was 20. 0 mg/L and 40. 0 mg/L,mannitol was 30. 0 g/L and40. 0 g/L,sorbitol was 30. 0 g/L,the rate of yellow leaves was 0. When the concentration of CCC was5. 0 mg/L,the multiplication multiple was the highest(5. 8 times);When the concentration of PP_(333)was1. 0 mg/L,the plant height was the highest(10. 5 cm). Comprehensive consideration showed that the optimum treatment of PP_(333),B9,CCC,ABA,mannitol and sorbitol were 8. 0 mg/L,15. 0 mg/L,40. 0 mg/L,4. 0 mg/L,40. 0 g/L and 30. 0 g/L,respectively. The comprehensive evaluation results of membership function method showed that the optimum treatment of 1A was mannitol with the concentration of40. 0 g/L. When cultured to 120 d,the survival rate was 100%,and there was no yellow leaf,the multiplication rate was 2. 9,and the plant height was 2. 6 cm.
引文
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