不同浓度NaCl对薄荷微繁的影响。

Vikash Chandra, S. Kumari, Narendra P. Roy, K. Subhash, A. K. Sharan
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摘要

对野生型薄荷进行了体外耐盐性测定。以薄荷微繁继代培养茎为材料,测定其茎长、多芽、根长、根数和出苗情况。在MS培养基中添加不同浓度的NaCl (0.1 mg/ml、0.2 mg/ml、0.3 mg/ml和0.4 mg/ml)进行不同处理。在不同时间段(7天、14天、21天、28天)记录数据。研究表明,低浓度NaCl处理(0.1 mg/ml和0.2 mg/ml)有利于增加茎长,高浓度NaCl处理(0.3mg/ml和0.4 mg/ml)有利于减少茎长。出芽数在每次处理中都有所增加。当NaCl浓度为0.4mg/ml时,其数量受到抑制。除0.4 mg/ml完全抑制根系出苗外,NaCl浓度似乎有利于根系出苗。当NaCl浓度为0.3 mg/ml时,这个数字似乎最大。除0.4 mg/ml(完全抑制生长)外,其余浓度的NaCl均抑制根长。每一种浓度的NaCl都有利于繁殖植株的出芽。0.3 mg/ml的浓度能最快地促使叶片出芽。在0.3 mg/ml和0.4 mg/ml浓度下,即使在21 d后也能观察到叶片的出芽。上述发现对今后的微繁研究具有一定的指导意义。描述了每个发现的细节。
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Effect of different concentrations of NaCl on micropropagation of Mentha sp.
Wild type species of Mentha was assayed in vitro for salinity (NaCl) tolerance. Micro propagated subcultured stem of Mentha was used to assay shoot length, multi shooting, root length, root number, and the emergence of leaves. Different concentration of NaCl (0.1 mg/ml, 0.2 mg/ml, 0.3 mg/ml and 0.4 mg/ml) supplemented in MS media was used for different treatments. Data was recorded after various periods (7 days, 14 days, 21 days, and 28 days) of time. The study reveal that shoot length increases favourably at low concentration of NaCl (0.1 mg/ml and 0.2 mg/ml) but at higher concentration (0.3mg/ml and 0.4 mg/ml) there is a reduction in length. Number of emerged shoots increases during every treatment.  The number, however, gets inhibited at 0.4mg/ml of NaCl. NaCl's concentration (except 0.4 mg/ml, which completely inhibits emergence) seems to favor the emergence of roots. The number seems to be the greatest at 0.3 mg/ml of NaCl. Every concentration of NaCl except for 0.4 mg/ml (which completely inhibits the growth) inhibits the root length.  Every concentration of NaCl has been found to favour the emergence of leaf in the propagated plantlet. A concentration of 0.3 mg/ml has been found to initiate the emergence of leaves the fastest. The emergence of leaves could also be noticed at 0.3 mg/ml and 0.4 mg/ml even after 21 days of incubation. The finding mentioned above can be useful in future research on micropropagation. The details of each finding is described.
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