Establishment of Mass Production in Tetragonia Tetragonides, Poster Board #076

Thursday, August 2, 2012
Grand Ballroom
Beunggu Son , Pusan National University, Department of Horticultural Bioscience, Miryang, South Korea
Jumsoon Kang , Pusan National University, Department of Horticultural Bioscience, Miryang, South Korea
Youngwhan Choi , Pusan National University, Department of Horticultural Bioscience, Miryang, South Korea
Yongjae Lee , Pusan National University, Department of Horticultural Bioscience, Miryang, South Korea
Jeongmin Suh , Pusan National University, Department of Bioenvironmental Energe, Miryang, South Korea
Younghoon Park , Pusan National University, Department of Horticultural Bioscience, Miryang, South Korea
Tetragonia tetragonides is a medicinal plant native to ocean sand soil of southern provinces and has significant effects on the prevention and curing of gastroentric disorders. Despite of its popularity, supply of the plant has never met the level of demand because of the absence of an adequate culturing method. The present study was conducted for classifying the plants with geographically different characteristics, studying growth habits, developing a new culturing method, colleting germplams, and establishing a large scale propagation system of selected superior individual plants. The study was also aimed at revealing optimum conditions for seed treatment, fertilization, and efficient culturing system and thereby, for utilizing the plant as a new income source for rural communities. Germination rate was high for seeds matured for 40 days after fertilization, but deceased to 50% for seeds matured only for 20 or 30 days. Seed dormancy lasted 6 months and seed storage at humid 5 °C facilitated germination. Mechanical obstruct of seed germination was due to seed coat and removal of seed coat enhanced the germination rate. Optimum temperature for seed storage was 5 °C, and high germination rate was maintained for 350 days. However, for stratification condition or at room temperature, germination was significantly reduced as storage time increased. Optimum treatment of plant growth regulators was soaking in GA3 250 mg/L for 1 hr. The priming treatment with 50 mM Ca(NO3)2 at 20 °C for two days improved the seed germination with 10% compared to non-treated control. The treatment of 20% NaOCl for 3 hr. improved the seed germination rate up to 10% and 1 day ahead.