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Mou Zong-min, Yan Ning, Li Shu-yun and Hu Hong

Paphiopedilum armeniacum S. C. Chen et F. Y. Liu is endemic to China and has great ornamental value. Little is known about its nutrient requirement for growth and reproduction after deflasking (transplantation of seedlings from culture vessels to pots). We studied the effects of adding nitrogen (N) (0, 105, 210, and 420 mg·L−1) on the vegetative growth and reproduction of P. armeniacum. N enrichment improved leaf area and lengthened the leaf lifespan during the vegetative stage. The effects of N application on flower size were minor. The intermediate N level of 210 mg·L−1 (MN) increased the seed capsule weight, seed germination rate, and improved the growth of seedlings that developed from seeds of MN-treated plants. N fertilizer exerted little influence on ramet emergence and ramet number per plant, but a low N concentration of 105 mg·L−1 promoted the leaf number and leaf area of ramets. Appropriate N levels for P. armeniacum in production and cultivation should be determined according to different production objectives.

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Guo-Gui Ning, Xue-Ping Shi, Hui-Rong Hu, Yan Yan and Man-Zhu Bao

A set of Petunia hybrida plants encompassing a range of ploidy levels was developed through colchicine-mediated induction of chromosome doubling. The resulting double-flower tetraploid plants were cross-hybridized with inbred single-flower diploid lines to generate F1 populations with segregation for ploidy level and flower type. The initial in vivo application of colchicine to seedling apical tips produced mixoploid plants of petunia at a high rate of efficiency. Thus, 95% of the shoot tips treated with colchicine for 48 h resulted in polyploid mutant plants, and no difference in this efficiency was observed using concentrations of colchicine between 0.2 and 2.0 mg·mL−1. Of the polyploid plants, 10% were found to be tetraploid and 85% were mixoploid (chimeric). Compared with their diploid counterparts, polyploid plants underwent reduced elongation growth during the first 2 weeks and had thicker stems and shorter internodes resulting in dwarfing of the whole plant. In extreme cases, very slow growth rates produced stunted plantlets. Polyploid plants also had larger, thicker leaves and, in some cases, the leaves that developed after 1 month of growth appeared seriously malformed. Octoploid plants were also obtained and these tended to have more extreme phenotypes. Pure tetraploid plants of double-flower petunia were isolated by the in vitro culture of explants from the initial chimeric tetraploid mutants. These were crossed with three inbred single-flower diploid lines (S1, S2, and S3) thereby generating F1 populations that showed segregation for flower type and ploidy level and included the generation of triploid plants. In the tetraploid plants, flower diameter and the number of flower petals were not changed significantly (P > 0.05) compared with the original diploid double-flower plants, but observation of the pollen grains revealed segregation for size consistent with the increased ploidy level. Analysis of the F1 progeny plants also indicated that chromosome number is not necessary but sufficient to cause the production of semidouble-flowered plants. Flower color and flower diameter were also analyzed in the F1 progeny and complex patterns of inheritance were inferred. In addition to single and double flowers, semidouble-flowered plants were also suggested to be generated by the hybridization of 2n or 3n pollen from the double-flower tetraploid plants with the single-flower diploid lines.