Laticifers are the specialized cells or duct systems that produce latex—the milky sap found in plants like rubber trees, figs, and euphorbias. These remarkable structures come in two fundamental architectural types, each with distinct developmental origins and distributions.
These are single, extremely long cells (coenocytes) that originate early in the embryo and grow intrusively through the plant, weaving between other cells without fusing. They can stretch from root tips to leaves, branching rarely or not at all. Their walls are cellulosic, and they remain multinucleate and metabolically active throughout the plant's life. The latex accumulates in a large central vacuole.
These form complex, branching networks created by the fusion of many cells. They develop through the differentiation of parenchyma cells at their tips, followed by the dissolution of end walls between adjacent cells (anastomosis).
Cells connect via plasmodesmata (e.g., Allium - onion) or by forming true pores in the end walls (e.g., Musa - banana, Manilkara - sapodilla). Protoplasm often degenerates at maturity.
Cells fuse completely, creating a three-dimensional network throughout the plant (e.g., Hevea brasiliensis - rubber tree, Papaver - poppy, Taraxacum - dandelion). In rubber trees, the network resides mainly in the phloem and bark. Latex is harvested by tapping (incisions at ~30° angle). The rubber particles (lutoides) are suspended in the cytoplasm.
In species like Asclepias syriaca (milkweed) and Nerium oleander, laticifer tips secrete pectinase to soften the middle lamella of walls they penetrate, facilitating their intrusive growth.
The article concludes with a section on autonyms—automatically created names for infrageneric or infraspecific taxa (e.g., Euphorbia sect. Euphorbia)—which have priority over other names published at the same rank.
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