The stamen (plural stamina or stamens, from Latin stamen meaning "thread of the warp") is the pollen-producing reproductive organ of a flower. Stamens typically consist of a stalk called the filament (from Latin filum, meaning "thread"), and an anther (from Ancient Greek anthera, feminine of antheros "flowery," from anthos "flower"), which contains microsporangia. Anthers are most commonly two-lobed and are attached to the filament either at the base or in the middle portion. The sterile tissue between the lobes is called the connective.
The stamens in a flower are collectively called the androecium (from Greek andros oikia: man's house). The androecium forms a great variety of different patterns, some rather complex. It surrounds the gynoecium (carpels) and is inside the perianth (the petals and sepals together) if there is one. (The one exception is a few members of the family Triuridaceae, particularly Lacandonia schismatica, in which the gynoecium surrounds the androecium.)
Variation in morphology
Stamens can be free or fused to one another in many different ways, including fusion of some but not all stamens. The filaments may be fused and the anthers free, or the filaments free and the anthers fused. Rather than including two locules, one of the locules may fail to develop, or alternatively the two locules may merge late in development to give a single locule. Extreme cases of stamen fusion occur in some species of Cyclanthera (of family Cucurbitaceae) and in section Cyclanthera of genus Phyllanthus (family Euphorbiaceae) where the stamens form a ring around the gynoecium, with a single locule.
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 when the anther forms openings (dehisces). These may consist of longitudinal slits, pores, as in the heath family (Ericaceae), or by valves, as in the barberry family (Berberidaceae). In some plants, notably members of Orchidaceae and Asclepiadoideae, the pollen remains in masses called pollinia, which are adapted to attach to particular pollinating agents such as birds or insects. More commonly, mature pollen grains separate and are dispensed by wind or water, pollinating insects, birds or other pollination vectors.
Pollen of angiosperms must be transported to the stigma, the receptive surface of the carpel, of a compatible flower, for successful pollination to occur. After arriving, the pollen grain (an immature microgametophyte) typically completes its development. It may grow a pollen tube and undergoing mitosis to produce two sperm nuclei.
Sexual reproduction in plants
In the typical flower (that is, in the majority of flowering plant species) each flower has both carpels and stamens. In some species, however, the flowers are unisexual with only carpels or stamens. (monoecious = both types of flowers found on the same plant; dioecious = the two types of flower found only on different plants). A flower with only stamens is called androecious. A flower with only carpels is called gynoecious.
A flower having only functional stamens and lacking functional carpels is called a staminate flower, or (inaccurately) male. A plant with only functional carpels is called pistillate, or (inaccurately) female.
An abortive or rudimentary stamen is called a staminodium or staminode, such as in Scrophularia nodosa.
- A column formed from the fusion of multiple filaments is known as an androphore.
The anther can be attached to the filament's connective in two ways:
- basifixed: attached at its base to the filament
- pseudobasifixed: a somewhat misnomer configuration where connective tissue extends in a tube around the filament
- dorsifixed: attached at its center to the filament, usually versatile (able to move)
Stamens can be connate (fused or joined in the same whorl):
- extrorse: anther dehiscence directed away from the centre of the flower. Cf. introrse, directed inwards, and latrorse towards the side. 
- monadelphous: fused into a single, compound structure
- diadelphous: joined partially into two androecial structures
- pentadelphous: joined partially into five androecial structures
- synandrous: only the anthers are connate (such as in the Asteraceae)
Stamens can also be adnate (fused or joined from more than one whorl):
- epipetalous: adnate to the corolla
- epiphyllous: adnate to undifferentiated tepals (as in many Liliaceae)
They can be different lengths:
- didymous: two equal pairs
- didynamous: occurring in two unequal pairs of different length
- tetradynamous: occurring as a set of six filaments with four long and two shorter ones
- exserted: extending beyond the corolla
- included: not extending beyond the corolla
They may be arranged in one of two different patterns:
- spiral; or
- whorled: one or more discrete whorls (series)
They may be arranged, with respect to the petals:
- diplostemonous: in two whorls, the outer alternating with the petals, while the inner is opposite the petals.
- obdiplostemonous: in two whorls, the outer opposite the petals
|Wikimedia Commons has media related to Stamens.|
Insects collecting nectar unintentionally transfer pollen to other flowers, causing pollination
Flower of the spider tree (Crateva religiosa) with its numerous conspicuous stamens
Flowers of wheat at anthesis showing stamens.
Stamens of a daylily (Hemerocallis), thickly covered in pollen
Flowers of the "silk tree" (Albizia julibrissin) have many long thread-like stamens
Hylocereus undatus showing the style and stigma, and stamens
These Solanum anthers release pollen through a pore at their tip
Blue and red waterlily stamens deploying in the morning sun (Nymphaea caerulea)
- Sattler, R. 1973. Organogenesis of Flowers. A Photographic Text-Atlas. University of Toronto Press. ISBN 0-8020-1864-5.
- Sattler, R. 1988. A dynamic multidimensional approach to floral morphology. In: Leins, P., Tucker, S. C. and Endress, P. (eds) Aspects of Floral Development. J. Cramer, Berlin, pp. 1-6. ISBN 3-443-50011-0
- Greyson, R. I. 1994. The Development of Flowers. Oxford University Press. ISBN 0-19-506688-X.
- Leins, P. and Erbar, C. 2010. Flower and Fruit. Schweizerbart Science Publishers, Stuttgart. ISBN 978-3-510-65261-7.
- Goebel, K.E.v. (1905/1969). Organography of plants, especially of the Archegoniatae and Spermaphyta. Part 2 Special organography. New York: Hofner publishing company. pages 553–555
- Rendle, A.B. (1925). The Classification of Flowering Plants. Cambridge University Press. ISBN 9780521060578.
- Encyclopædia Britannica.com
- Encyclopædia Britannica.com
- Hickey, M.; King, C. (1997). Common Families of Flowering Plants. Cambridge University Press. ISBN 9780521576093.
- William G. D'Arcy, Richard C. Keating (eds.) The Anther: Form, Function, and Phylogeny. Cambridge University Press, 1996 ISBN 0521480639, 9780521480635
- This article incorporates text from a publication now in the public domain: Chisholm, Hugh, ed. (1911). Encyclopædia Britannica (11th ed.). Cambridge University Press.
- Simpson, Michael G. (2011). "Androecium". Plant Systematics. Academic Press. p. 371. ISBN 978-0-08-051404-8. Retrieved 6 February 2014.