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Pollen Germination and Storage of Melastoma Linn

Thursday, August 6, 2015
Napoleon Expo Hall (Sheraton Hotel New Orleans)
Donghui Peng , Fujian Agriculture and Forestry University, Fuzhou, China
Mingtao Jiang , Fujian Agriculture and Forestry University, Fuzhou, China
Shasha Wu , College of Landscape Architecture, Fujian Agriculture and Forestry University, Fuzhou, China
Junwen Zhai , Fujian Agriculture and Forestry University, Fuzhou, China
Siren Lan , Fujian Agriculture and Forestry University, Fuzhou, China
Mengmeng Gu , Texas A&M AgriLife Reseach & Extension, College Station, TX
There are nearly 100 species of Melastoma Linn. (Melastomaceae) in the world, among which 9 species and a variety are native in China. Pollen viability and suitable storage conditions for pollens of M. affine, M. candidum and M. sanguineum were investigated. Pollen viability was measured using medium culture and three staining techniques, I2-KI, 2,3,5-triphenyltetrazolium chloride (TTC), and benzidine-H2O2. In culture medium study, an orthogonal test with four factors was conducted, sucrose (5, 10, and 20 g·L-1), boric acid (50, 100, and 200 mg·L-1), calcium chloride (50, 100, and 200 mg·L-1), and temperature (20, 25, and 30℃). Pollen tube germination of pollens from both long and short stamens was examined under microscope 2 h after being placed on medium. In vitro pollen germination of M. affine and M. candidum at 25 ℃ and 30 ℃ was higher than these at 20 ℃. The best culture medium for the pollen germination of M. affine, M. sanguineum, and M. candidum are 20 g·L-1 sucrose + 200 mg·L-1 H3BO3 + 100 mg·L-1 CaCl2+30 ℃, 20 g·L-1 sucrose + 50 mg·L-1 H3BO3 + 100 mg·L-1CaCl2+20 ℃, and 10 g·L-1 sucrose + 100 mg·L-1 H3BO3 + 50 mg·L-1 CaCl2+30 ℃, respectively. For three pollens staining studies, I2-KI could not separate the viable and non-viable pollens; pollen viability determined by TTC and benzidine-H2O2 was similar to pollen germination method. For pollen storage study, pollens were enclosed in silica gel and preserved at room temperature, 4 ℃, -23 ℃, or -80 ℃, and pollen viability measured on 1, 5, 10, 15, 30, 60, 90, 120 days after storage. The results indicated that the lower preserved temperature, the higher pollen viability. -80℃ was the best pollen storage temperature, and after 120 days, the pollen viability of the three species still remained high.