A typical anther contains four microsporangia. The microsporangia form sacs or pockets (locules) in the anther. The two separate locules on each side of an anther may fuse into a single locule. Each microsporangium is lined with a nutritive tissue layer called the tapetum and initially contains diploid pollen mother cells. These undergo meiosis to form haploid spores. The spores may remain attached to each other in a tetrad or separate after meiosis. Each microspore then divides mitotically to form an immature microgametophyte called a pollen grain.
The pollen is eventually released by the opening (dehiscence) of the anther, generally by means of longitudinal slits, but sometimes by pores, as in the heath family (Ericaceae), or by valves, as in the barberry family (Berberidaceae). In some plants, notably members of the Orchidaceae and the Asclepiadoideae, the pollen remains in masses called pollinia, usually specialised in ways adapted to being carried by particular pollinating agents such as birds or large insects. More commonly, mature pollen grains separate and are dispensed in ways suitable for wind or water transport, or for dusting onto pollinating insects, whether large or small.
When ready, the pollen is carried by some external agent (wind, water or some member of the animal kingdom) to the receptive surface of the carpel of the same or another flower. This process is known as pollination. After successful pollination, the pollen grain (immature microgametophyte) completes its development by growing a pollen tube and undergoing mitosis to produce two male gametes (sperm).
The stamens in a flower are collectively called theandroecium. The androecium forms a whorl surrounding the gynoecium (carpels) and inside the perianth (the petals and sepals together) if there is one.
Stamens can be free or fused in various ways. A column formed from the fusion of multiple filaments is known as anandrophore.
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