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flower, the characteristic reproductive structure of angiosperms. As popularly used, the term “flower” especially applies when part or all of the reproductive structure is distinctive in colour and form.

In their range of colour, size, form, and anatomical arrangement, flowers present a seemingly endless variety of combinations. They range in size from minute blossoms to giant blooms. In some plants, such as poppy, magnolia, tulip, and petunia, each flower is relatively large and showy and is produced singly, while in other plants, such as aster, snapdragon, and lilac, the individual flowers may be very small and are borne in a distinctive cluster known as an inflorescence. Regardless of their variety, all flowers have a uniform function, the reproduction of the species through the production of seed.

Form and types

Basically, each flower consists of a floral axis upon which are borne the essential organs of reproduction (stamens and pistils) and usually accessory organs (sepals and petals); the latter may serve to both attract pollinating insects and protect the essential organs. The floral axis is a greatly modified stem; unlike vegetative stems, which bear leaves, it is usually contracted, so that the parts of the flower are crowded together on the stem tip, the receptacle. The flower parts are usually arrayed in whorls (or cycles) but may also be disposed spirally, especially if the axis is elongate. There are commonly four distinct whorls of flower parts: (1) an outer calyx consisting of sepals; within it lies (2) the corolla, consisting of petals; (3) the androecium, or group of stamens; and in the centre is (4) the gynoecium, consisting of the pistils.

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The sepals and petals together make up the perianth, or floral envelope. The sepals are usually greenish and often resemble reduced leaves, while the petals are usually colourful and showy. Sepals and petals that are indistinguishable, as in lilies and tulips, are sometimes referred to as tepals. The androecium, or male parts of the flower, comprise the stamens, each of which consists of a supporting filament and an anther, in which pollen is produced. The gynoecium, or female parts of the flower, comprises one or more pistils, each of which consists of an ovary, with an upright extension, the style, on the top of which rests the stigma, the pollen-receptive surface. The ovary encloses the ovules, or potential seeds. A pistil may be simple, made up of a single carpel, or ovule-bearing modified leaf; or compound, formed from several carpels joined together.

A flower having sepals, petals, stamens, and pistils is complete; lacking one or more of such structures, it is said to be incomplete. Stamens and pistils are not present together in all flowers. When both are present the flower is said to be perfect, or bisexual, regardless of a lack of any other part that renders it incomplete (see photograph). A flower that lacks stamens is pistillate, or female, while one that lacks pistils is said to be staminate, or male. When the same plant bears unisexual flowers of both sexes, it is said to be monoecious (e.g., tuberous begonia, hazel, oak, corn); when the male and female flowers are on different plants, the plant is dioecious (e.g., date, holly, cottonwood, willow); when there are male, female, and bisexual flowers on the same plant, the plant is termed polygamous.

A flower may be radially symmetrical (see photograph), as in roses and petunias, in which case it is termed regular or actinomorphic. A bilaterally symmetrical flower, as in orchids (see photograph) and snapdragons, is irregular or zygomorphic.

Pollination

The stamens and pistils are directly involved with the production of seed. The stamen bears microsporangia (spore cases) in which are developed numerous microspores (potential pollen grains); the pistil bears ovules, each enclosing an egg cell. When a microspore germinates, it is known as a pollen grain. When the pollen sacs in a stamen’s anther are ripe, the anther releases them and the pollen is shed. Fertilization can occur only if the pollen grains are transferred from the anther to the stigma of a pistil, a process known as pollination.

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There are two chief kinds of pollination: (1) self-pollination, the pollination of a stigma by pollen from the same flower or another flower on the same plant; and (2) cross-pollination, the transfer of pollen from the anther of a flower of one plant to the stigma of the flower of another plant of the same species. Self-pollination occurs in many species, but in the others, perhaps the majority, it is prevented by such adaptations as the structure of the flower, self-incompatibility, and the maturation of stamens and pistils of the same flower or plant at different times. Cross-pollination may be brought about by a number of agents, chiefly insects and wind. Wind-pollinated flowers (see photograph) generally can be recognized by their lack of colour, odour, or nectar, while animal-pollinated flowers (see photograph) are conspicuous by virtue of their structure, colour, or the production of scent or nectar.

After a pollen grain has reached the stigma, it germinates, and a pollen tube protrudes from it. This tube, containing two male gametes (sperms), extends into the ovary and reaches the ovule, discharging its gametes so that one fertilizes the egg cell, which becomes an embryo, and the other joins with two polar nuclei to form the endosperm. (Normally many pollen grains fall on a stigma; they all may germinate, but only one pollen tube enters any one ovule.) Following fertilization, the embryo is on its way to becoming a seed, and at this time the ovary itself enlarges to form the fruit.

Cultural significance

Flowers have been symbols of beauty in most civilizations of the world, and flower giving is still among the most popular of social amenities. As gifts, flowers serve as expressions of affection for spouses, other family members, and friends; as decorations at weddings and other ceremonies; as tokens of respect for the deceased; as cheering gifts to the bedridden; and as expressions of thanks or appreciation. Most flowers bought by the public are grown in commercial greenhouses or horticultural fields and then sold through wholesalers to retail florists. See also articles on individual flowers (e.g., carnation; lotus; petunia; rose; tulip).

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This article was most recently revised and updated by Melissa Petruzzello.
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pollination, transfer of pollen grains from the stamens (the flower parts that produce them) to the ovule-bearing organs or to the ovules (seed precursors) themselves. In gymnosperm plants such as conifers and cycads, in which the ovules are exposed, the pollen is simply caught in a drop of fluid secreted by the ovule. In flowering plants, however, the ovules are contained within a hollow organ called the pistil, and the pollen is deposited on the pistil’s receptive surface, the stigma. There the pollen germinates and gives rise to a pollen tube, which grows down through the pistil toward one of the ovules in its base. In an act of double fertilization, one of the two sperm cells within the pollen tube fuses with the egg cell of the ovule, making possible the development of an embryo, and the other cell combines with the two subsidiary sexual nuclei of the ovule, which initiates formation of a reserve food tissue, the endosperm. The growing ovule then transforms itself into a seed.

As a prerequisite for fertilization, pollination is essential to the perpetuation of the vast majority of the world’s wild plants as well as to the production of most fruit and seed crops. It also plays an important part in programs designed to improve plants by breeding. Furthermore, studies of pollination are invaluable for understanding the evolution of flowering plants and their distribution in the world today. As sedentary organisms, plants usually must enlist the services of external agents for pollen transport. In flowering plants, these are (roughly in order of diminishing importance) insects, wind, birds, mammals, and water. See also major types of pollinators.

Types: self-pollination and cross-pollination

An egg cell in an ovule of a flower may be fertilized by a sperm cell derived from a pollen grain produced by that same flower or by another flower on the same plant, in either of which two cases fertilization is said to be due to self-pollination (autogamy); or, the sperm may be derived from pollen originating on a different plant individual, in which case the process is called cross-pollination (heterogamy). Both processes are common, but cross-pollination clearly has certain evolutionary advantages for the species: the seeds formed may combine the hereditary traits of both parents, and the resulting offspring generally are more varied than would be the case after self-pollination. In a changing environment, some of the individuals resulting from cross-pollination still may be found capable of coping with their new situation, ensuring survival of the species, whereas the individuals resulting from self-pollination might all be unable to adjust. Self-pollination, or selfing, although foolproof in a stable environment, thus is an evolutionary cul-de-sac. There also is a more direct, visible difference between selfing and outbreeding (cross-pollination): in those species where both methods work, cross-pollination usually produces more, and better quality, seeds. A dramatic demonstration of this effect is found with hybrid corn (maize), a superior product that results from cross-breeding of several especially bred lines.

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