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Objective: To develop a protocol for breaking of seed dormancy and increasing the seed germination rate of Bunium persicum.
Methods:The seeds were treated with 3.1, 6.3, 12.5, 25, 50 and 100 μmol/L of benzyl aminopurine, gibberellic acid (GA3), thidiazuron (TDZ) and forchlorfenuron. Then, seeds were transferred to two different temperature conditions including room temperature (25 °C) and chilling temperature (2-5 °C).
Results: The treatment of moist seeds with chilling temperature (2-5 °C) broke seed dormancy and showed maximum germination, which was 54.7%after 60 d treatment. Also, the treatment of dry seeds with chilling temperature broke seed dormancy with 9.3%germination rate after 120 d. Treatment of seeds with different level of plant growth regulators showed that under moist-room condition, there was evidence of higher and lower seed germination rate:GA3 (100 μmol/L) with 46.7%and TDZ (50 μmol/L) with 6.67%respectively. In addition, the results showed that under moist-chilling condition, TDZ (6.3 μmol/L) with 53.3%seed germination rate had higher influence on breaking seed dormancy. Treatment of seeds with combination of TDZ and GA3 under moist-chilling condition revealed higher rate of breaking of seed dormancy when 6.3 μmol/L TDZ was combined with 100 μmol/L GA3, showing 93.7%germination rate.
Conclusions:The effect of plant growth regulators coupled with chilling temperature on breaking of seed dormancy could provide a large number of seedlings while the long juvenile time which is the next restricting factor of plantation still remained. Thus, the subsequent growth of seedlings to provide a large number of corms is necessary for successful plantation.
Methods:The seeds were treated with 3.1, 6.3, 12.5, 25, 50 and 100 μmol/L of benzyl aminopurine, gibberellic acid (GA3), thidiazuron (TDZ) and forchlorfenuron. Then, seeds were transferred to two different temperature conditions including room temperature (25 °C) and chilling temperature (2-5 °C).
Results: The treatment of moist seeds with chilling temperature (2-5 °C) broke seed dormancy and showed maximum germination, which was 54.7%after 60 d treatment. Also, the treatment of dry seeds with chilling temperature broke seed dormancy with 9.3%germination rate after 120 d. Treatment of seeds with different level of plant growth regulators showed that under moist-room condition, there was evidence of higher and lower seed germination rate:GA3 (100 μmol/L) with 46.7%and TDZ (50 μmol/L) with 6.67%respectively. In addition, the results showed that under moist-chilling condition, TDZ (6.3 μmol/L) with 53.3%seed germination rate had higher influence on breaking seed dormancy. Treatment of seeds with combination of TDZ and GA3 under moist-chilling condition revealed higher rate of breaking of seed dormancy when 6.3 μmol/L TDZ was combined with 100 μmol/L GA3, showing 93.7%germination rate.
Conclusions:The effect of plant growth regulators coupled with chilling temperature on breaking of seed dormancy could provide a large number of seedlings while the long juvenile time which is the next restricting factor of plantation still remained. Thus, the subsequent growth of seedlings to provide a large number of corms is necessary for successful plantation.