[Microscopic identification of dai medicine alpiniae kwangsiensis rhizoma and its confused species].

OBJECTIVE: To observe microscopic characteristics of rhizome of Alpinia kwangsiensis, Alpinia platychilus, Alpinia blepharocalyx, and to provide basis for their identification. METHODS: Microscopic identification of root transverse section by paraffin tissue section and free-hand section and powder were carried out to distinguish them. RESULTS: The microscopic identification can be made by cell structure of epidermis and endodermis, the existence of nonglandular hair, the lignification degree of vascular bundle fiber, the number and existence style of vascular bundle fiber, the number and size of tube, and so on. The powder identification can be made mainly according to the existence of nonglandular hair and spiral vessel, the shape of starch grain, and so on. CONCLUSION: The microscopic characteristics of rhizome can provide basis for the identification of three Alpinia species.

[Pharmacognostical studies on the rhizome, root and leaf of Alpinia jianganfeng T.L. Wu].

Morphological and histological characters of the rhizome, root and leaf of Alpinia jianganfeng T.L. Wu used as the origin of a traditional Chinese medicine, were described and illustrated with line drawing. These studies provide referential information for the identification and quality control.

[Pharmacognostical studies on the rhizome and root of Alpinia nigra].

Morphological and histological characters of the rhizome and root of Alpinia nigra (Gaertn.) Burtt, used as the origin of a traditional Chinese medicine, were described and illustrated with line drawing. These studies provide referential information for the identification and quality control.

Subcellular localization of calcium during Alpinia mutica Roxb. (Zingiberaceae) style movement.

The subcellular localization of calcium in Alpinia mutica Roxb. during style movement was studied in two morphs. In the styles, Ca-antimonate precipitates (ppts) were principally located in apoplasts, with some minimal accumulation in the nucleus. At different movement, stages of movement, the ppts in the abaxial and adaxial sides changed, and no lateral gradient of ppts in the apoplast was established. The increase or decrease of ppts in the apoplast was not accompanied with equivalent changes in the cytoplasm. These results indicate that calcium could not affect the curvature by inhibiting cell elongation but may play a role in style movement by acting as a secondary messenger. EGTA-treatment affected style movement, providing further evidence supporting a role for calcium as a secondary messenger.