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The experiments were conducted to establish micropropagation method for Anthurium andreanurn, ´Hazrija´ and ´Ingrid´, for cut flower, and A. scherzerianutn ´Belinda´, for pot flower through shoot tip and callus cultures. 0.5-2.0 ㎎/L BA was most effective in inducing callus and shoot of A. andreanum ´Hazrija´ from shoot tip culture. In ´Ingrid´, 0.5-2.0 ㎎/L 2iP induced callus. Shoot and root formation was suppressed in all treatment. In ´Belinda´, only 1.0-5.0 ㎎/L kinetin and 2iP induced callus and shoot. Combined treatments of IAA, 2,4-D, and cytokinin did not induce shoot formation and callus growth compared with cytokinin test. Gorwth of callus from shoot tip culture of ´Hazrija´ was better with 2,4-D treatment while BA was effective for ´Ingrid´. Callus culture seemed to be a more effective way of micropropagation in Anthurium spp. rather than shoot tip culture.
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