本文發展出以瀕臨滅絕威脅之木本藥用灌木Embelia ribes Burn.(紫金牛科)葉切片之試管培養，直接器官發生快速繁殖小植株的方法。不定的幼莖直接由培養於2至4mg/L FAP和0.2至0.6 mg/L NAA 的葉片邊緣長出，幼莖芽產生的頻率在3 mg/L FAP和0.4mg/L NAA的濃度時最高(每個培殖體平均33.6±3.63的幼莖)。在相同的培養基亦可發現發根的微小幼莖，個培殖體平均再生30±1.05有限的完整小植株，存活率為96%，且活動與活體內的再生植株外型沒有差別。

　　　　　An in vitro protocol was developed for rapid multiplication of pantalets via direct organogenesis form the leaf segments of Embelia ribes Burm. (Myrsinaceae), a rare woody medicinal shrub under threat of being extinct. Adventitious shoots were organized directly form the margin of the lamina on medium supplemented with 2 to 4 mg/L 6-furfuryl amino purine (FAP) and 0.2 to 0.6 mg/L naphthalene acetic acid (NAA). The frequency of shoot bud production was the highest (mean of 33.6±3.63 shoots per explants) at the concentration of 3 mg/L FAP and 0.4 mg/L NAA. Rooting of microshoots was also noticed on the same medium in a single-phase culture. A mean of 30±1.05 root intact plantlets was recovered per explants. The rooted plantlets were well accomplished with a survival frequency of 96%. Moreover, were no phenotypic differences observed between the in vitro regenerated and in vivo plants.