A 'flower', also known as a 'bloom' or 'blossom', is the
reproductive structure found in
flowering plants (plants of the division ''Magnoliophyta'', also called angiosperms). The flower's structure contains the plant's reproductive organs, and its function is to produce
seeds. After
fertilization, portions of the flower develop into a
fruit containing the seeds. For the higher plants, seeds are the next generation, and serve as the primary means by which individuals of a species are dispersed across the landscape. The grouping of flowers on a plant is called the
inflorescence.
In addition to serving as the reproductive organs of flowering plants, flowers have long been admired and used by humans, mainly to beautify their environment but also as a source of food.
Function
The biological function of a flower is to mediate the union of male and female
gametes in order to produce
seeds. The process begins with
pollination, is followed by
fertilization, and continues with the formation and
dispersal of the seed.
Morphology
Flowering plants are ''heterosporangiate'', producing two types of reproductive
spores.
The
pollen (male spores) and
ovules (female spores) are produced in different
organs, but the typical flower is a ''bisporangiate strobilus'' in that it contains both organs.
A flower is regarded as a modified
stem with shortened internodes and bearing, at its
nodes, structures that may be highly modified
leaves.
[1] In essence, a flower structure forms on a modified shoot or ''axis'' with an apical
meristem that does not grow continuously (growth is ''determinate''). Flowers maybe attached to the plant in a few ways, if the flower has no stem but forms in the axil of a leaf it is called sessile, when one flower is produced the stem holding the flower is called a
peduncle, if the peduncle ends with groups of flowers - each stem that holds a flower is called a
pedicel. The flowering stem forms a terminal end which is called the ''torus'' or receptacle. The parts of a flower are arranged in
whorls on the torus. The four main parts or whorls (starting from the base of the flower or lowest node and working upwards) are as follows:

Morphology of ''
Oxalis acetosella'' flower. 1 - petal, 2 - sepal, 3 - anther, 4 - stigma, 5 - ovary, 6 - ovary, 7 - ovule.
★ ''
Calyx'' – the outer whorl of ''
sepals''; typically these are green, but are petal-like in some species.
★ ''
Corolla'' – the whorl of ''
petals'', which are usually thin, soft and colored to attract insects that help the process of
pollination.
★ ''
Androecium'' (from Greek ''andros oikia'': man's house) – one or two whorls of
stamens, each a
filament topped by an
anther where
pollen is produced. Pollen contains the male
gametes.
★ ''
Gynoecium'' (from Greek ''gynaikos oikia'': woman's house) – one or more
pistils. The female reproductive organ is the
carpel: this contains an ovary with ovules (which contain female gametes). A pistil may consist of a number of carpels merged together, in which case there is only one pistil to each flower, or of a single individual carpel (the flower is then called ''apocarpous''). The sticky tip of the pistil, the
stigma, is the receptor of pollen. The supportive stalk, the style becomes the pathway for
pollen tubes to grow from pollen grains adhering to the stigma, to the ovules, carrying the reproductive material.
Although the floral structure described above is considered the "typical" structural plan, plant species show a wide variety of modifications from this plan. These modifications have significance in the evolution of flowering plants and are used extensively by botanists to establish relationships among plant species. For example, the two subclasses of flowering plants may be distinguished by the number of floral organs in each whorl:
dicotyledons typically having 4 or 5 organs (or a multiple of 4 or 5) in each whorl and
monocotyledons having three or some multiple of three. The number of carpels in a compound pistil may be only two, or otherwise not related to the above generalization for monocots and dicots.

This ''
Crateva religiosa'' flower is perfect: it has both stamens (outer ring) and a pistil (center)
In the majority of species individual flowers have both
pistils and stamens as described above. These flowers are described by botanists as being ''perfect'', ''bisexual'', or ''
hermaphrodite''. However, in some species of plants the flowers are ''imperfect'' or ''unisexual'': having only either male (stamens) or female (pistil) parts. In the latter case, if an individual plant is either male or female the species is regarded as ''
dioecious''. However, where unisexual male and female flowers appear on the same plant, the species is considered ''
monoecious''.

Some flowers have modified structures. Here the style is extended into an umbrella shape which catches pollen and aids pollination. (''
Sarracenia'')
Additional discussions on floral modifications from the basic plan are presented in the articles on each of the basic parts of the flower. In those species that have more than one flower on an axis—so-called ''composite flowers''— the collection of flowers is termed an ''
inflorescence''; this term can also refer to the specific arrangements of flowers on a stem. In this regard, care must be exercised in considering what a ‘‘flower’’ is. In botanical terminology, a single
daisy or
sunflower for example, is not a flower but a flower ''
head''—an inflorescence composed of numerous tiny flowers (sometimes called florets). Each of these flowers may be anatomically as described above. Many flowers have a symmetry, if the perianth is bisected through the central axis from any point, symmetrical halves are produced - the flower is called regular or actinomorphic e.g. rose or trillium. When flowers are bisected and produce only one line that produces symmetrical halves the flower is said to be irregular or zygomorphic. e.g. snapdragon or most orchids.
Floral formula
A ''floral formula'' is a way to represent the structure of a flower using specific letters, numbers, and symbols. Typically, a general formula will be used to represent the flower structure of a plant
family rather than a particular species. The following representations are used:
'Ca' = calyx (sepal whorl; e.g. Ca
5 = 5 sepals)
'Co' = corolla (petal whorl; e.g., Co
3(x) = petals some multiple of three )
'Z' = add if ''zygomorphic'' (e.g., CoZ
6 = zygomorphic with 6 petals)
'A' = ''androecium'' (whorl of stamens; e.g., A
∞ = many stamens)
'G' = ''gynoecium'' (carpel or carpels; e.g., G
1 = monocarpous)
''x'' - to represent a "variable number"
∞ - to represent "many"
A floral formula would appear something like this:
:'Ca
5Co
5A
10 - ∞G
1'
Several additional symbols are sometimes used (see
Key to Floral Formulas).
Pollination

Grains of pollen sticking to this bee will be transferred to the next flower it visits
Main articles: pollination
The primary purpose of a flower is
reproduction by the joining of pollen of one plant with the ovules of another (or in some cases its own ovules) in order to form seed which grows into the next generation of plants. Sexual reproduction produces genetically unique offspring, allowing for
adaptation to occur. As such, each flower has a specific design which best encourages the transfer of this pollen. Many flowers are dependent upon the wind to move pollen between flowers of the same species. Others rely on animals (especially
insects) to accomplish this feat. Even large animals such as birds, bats, and
pygmy possums can be employed. The period of time during which this process can take place (the flower is fully expanded and functional) is called ''anthesis''.
Attraction methods

Bee orchid mimics a female bee in order to attract a male bee pollinator
Many flowers in nature have evolved to attract animals to pollinate the flower, the movements of the pollinating agent contributing to the opportunity for genetic recombination within a dispersed plant population. Flowers that are insect-pollinated are called ''entomophilous'' (literally "insect-loving"). Flowers commonly have glands called ''nectaries'' on their various parts that attract these animals.
Birds and
bees are common
pollinators: both having color vision, thus opting for "colorful" flowers. Some flowers have patterns, called
nectar guides, that show pollinators where to look for nectar; they may be visible to us or only under
ultraviolet light, which is visible to bees and some other insects. Flowers also attract pollinators by
scent. Many of their scents are pleasant to our sense of smell, but not all. Some plants, such as ''
Rafflesia'', the
titan arum, and the North American
pawpaw (''Asimina triloba''), are pollinated by
flies, so they produce a scent
imitating rotting meat. Flowers pollinated by night visitors such as bats or moths are especially likely to concentrate on scent - which can attract pollinators in the dark - rather than color: most such flowers are white.
Still other flowers use mimicry to attract pollinators. Some species of orchids, for example, produce flowers resembling female bees in color, shape, and scent. Male bees move from one such flower to another in search of a mate.
Pollination mechanism
The pollination mechanism employed by a plant depends on what method of pollination is utilized.
Most flowers can be divided between two broad groups of pollination methods:
''Entomophilous'' - flowers attract and use insects, bats, birds or other animals to transfer pollen from one flower to the next. Often they are specialized in shape and have an arrangement of the stamens that ensures that pollen grains are transferred to the bodies of the pollinator when it lands in search of its attractant (such as nectar, pollen, or a mate). In pursuing this attractant from many flowers of the same species, the pollinator transfers pollen to the stigmas - arranged with equally pointed precision - of all of the flowers it visits. Many flower rely on simple proximity between flower parts to ensure pollination. Others, such as the ''
Sarracenia'' or
lady-slipper orchids, have elaborate designs to ensure pollination while preventing
self-pollination.
''Anemophilous'' - flowers use the wind to move pollen from one flower to the next, examples include the
grasses, Birch trees, Ragweed and Maples. They have no need to attract pollinators and therefore tend not to be "showy" flowers. Whereas the pollen of entomophilous flowers tends to be large-grained, sticky, and rich in
protein (another "reward" for pollinators), anemophilous flower pollen is usually small-grained, very light, and of little nutritional value to
insects, though it may still be gathered in times of dearth. Honeybees and bumblebees actively gather anemophilous corn (
maize) pollen, though it is of little value to them.
Some flowers are self pollinated and use flowers that never open or are self pollinated before the flowers open, these flowers are called clestigomous. Many Viola species and some Salvia have these types of flowers.
Flower-pollinator relationships
Many flowers have close relationships with one or a few specific pollinating organisms. Many flowers, for example, attract only one specific species of insect, and therefore rely on that insect for successful reproduction. This close relationship is often given as an example of
coevolution, as the flower and pollinator are thought to have developed together over a long period of time to match each other's needs.
This close relationship compounds the negative effects of
extinction. The extinction of either member in such a relationship would mean almost certain extinction of the other member as well. Some
endangered plant species are so because of
shrinking pollinator populations.
Fertilization and dispersal
Main articles: biological dispersal

In this picture you can clearly see the stamens of the flower
Some flowers with both stamens and a pistil are capable of self-fertilization, which does increase the chance of producing seeds but limits genetic variation. The extreme case of self-fertilization occurs in flowers that always self-fertilize, such as many
dandelions. Conversely, many species of plants have ways of preventing self-fertilization. Unisexual male and female flowers on the same plant may not appear or mature at the same time, or pollen from the same plant may be incapable of fertilizing its ovules. The latter flower types, which have chemical barriers to their own pollen, are referred to as self-sterile or self-incompatible (see also:
Plant sexuality).
Evolution
While land plants have existed for about 425 million years, the first ones
reproduced by a simple adaptation of their aquatic counterparts:
spores. In the sea, plants -- and some animals -- can simply scatter out little living copies of themselves to float away and grow elsewhere. This is how early plants, such as the modern fern, are thought to have reproduced. But plants soon began protecting these copies to deal with drying out and other abuse which is even more likely on land than in the sea. The protection became the
seed...but not, yet, flowers. Early seed-bearing plants include the
ginkgo,
conifers (like pines), and
fir trees. The earliest fossil of a flowering plant, ''
Archaefructus liaoningensis'', is dated about 125 million years old.
[2]
Several groups of extinct gymnosperms, particularly
seed ferns, have been proposed as the ancestors of flowering plants but there is no continuous fossil evidence showing exactly how flowers evolved. The apparently sudden appearance of relatively modern flowers in the fossil record posed such a problem for the theory of evolution that it was called an "abominable mystery" by
Charles Darwin. Recently discovered angiosperm fossils such as ''Archaefructus'', along with further discoveries of fossil gymnosperms, suggest how angiosperm characteristics may have been acquired in a series of steps.
Recent
DNA analysis (
molecular systematics)
[3][4] show that
''Amborella trichopoda'', found on the Pacific island of
New Caledonia, is the
sister group to the rest of the flowering plants, and morphological studies
[5] suggest that it has features which may have been characteristic of the earliest flowering plants.

Various flower colors and shapes
The general assumption is that the function of flowers, from the start, was to involve other animals in the reproduction process. Pollen can be scattered without bright colors and obvious shapes, which would therefore be a liability, using the plant's resources, unless they provide some other benefit. One proposed reason for the sudden, fully developed appearance of flowers is that they evolved in an isolated setting like an island, or chain of islands, where the plants bearing them were able to develop a highly specialized relationship with some specific animal (a wasp, for example), the way many island species develop today. This symbiotic relationship, with a hypothetical wasp bearing pollen from one plant to another much the way
fig wasps do today, could have eventually resulted in both the plant(s) and their partners developing a high degree of specialization.
Island genetics is believed to be a common source of speciation, especially when it comes to radical adaptations which seem to have required inferior transitional forms. Note that the wasp example is not incidental; bees, apparently evolved specifically for symbiotic plant relationships, are descended from wasps.
Likewise, most
fruit used in plant reproduction comes from the enlargement of parts of the flower. This fruit is frequently a tool which depends upon animals wishing to eat it, and thus scattering the seeds it contains.
While many such
symbiotic relationships remain too fragile to survive competition with mainland animals and spread, flowers proved to be an unusually effective means of production, spreading (whatever their actual origin) to become the dominant form of land plant life.
While there is only hard proof of such flowers existing about 130 million years ago, there is some circumstantial evidence that they did exist up to 250 million years ago. A chemical used by plants to defend their flowers,
oleanane, has been detected in fossil plants that old, including
gigantopterids
[6], which evolved at that time and bear many of the traits of modern, flowering plants, though they are not known to be flowering plants themselves, because only their stems and prickles have been found preserved in detail; one of the earliest examples of
petrification.
The similarity in
leaf and
stem structure can be very important, because flowers are genetically just an adaptation of normal leaf and stem components on plants, a combination of genes normally responsible for forming new shoots.
[7] The most primitive flowers are thought to have had a variable number of flower parts, often separate from (but in contact with) each other. The flowers would have tended to grow in a spiral pattern, to be
bisexual (in plants, this means both male and female parts on the same flower), and to be dominated by the
ovary (female part). As flowers grew more advanced, some variations developed parts fused together, with a much more specific number and design, and with either specific sexes per flower or plant, or at least "ovary inferior".
Flower evolution continues to the present day; modern flowers have been so profoundly influenced by humans that many of them cannot be pollinated in nature. Many modern, domesticated flowers used to be simple weeds, which only sprouted when the ground was disturbed. Some of them tended to grow with human crops, and the prettiest did not get plucked because of their beauty, developing a dependence upon and special adaptation to human affection.
[8]
Development
The molecular control of floral organ identity determination is fairly well understood. In a simple model, three gene activities interact in a combinatorial manner to determine the developmental identities of the organ primordia within the floral
meristem. These gene functions are called A, B and C-gene functions. In the first floral whorl only A-genes are expressed, leading to the formation of sepals. In the second whorl both A- and B-genes are expressed, leading to the formation of petals. In the third whorl, B and C genes interact to form stamens and in the center of the flower C-genes alone give rise to carpels. The model is based upon studies of
homeotic mutants in ''Arabidopsis thaliana'' and snapdragon, ''
Antirrhinum majus''. For example, when there is a loss of B-gene function, mutant flowers are produced with sepals in the first whorl as usual, but also in the second whorl instead of the normal petal formation. In the third whorl the lack of B function but presence of C-function mimics the fourth whorl, leading to the formation of carpels also in the third whorl. See also
The ABC Model of Flower Development.
Most genes central in this model belong to the
MADS-box genes and are
transcription factors that regulate the expression of the genes specific for each floral organ.
Flowering transition
The
transition to flowering is one of the major phase changes that a plant makes during its life cycle. The transition must take place at a time that will ensure maximal
reproductive success. To meet these needs a plant is able to interpret important endogenous and environmental cues such as changes in
plant hormones levels and seasonable
temperature and
photoperiodchanges. Many perennial and most biennial plants require
vernalization to flower. The molecular interpretation of these signals through genes such as CONSTANS and FLC ensures that flowering occurs at a time that is favorable for
fertilization and the formation of
seeds.
[9] Flower formation is initiated at the ends of stems, and involves a number of different physiological and morphological changes. The first step is the transformation of the vegetative stem primordia into floral primordia. This occurs as biochemical changes take place to change cellular differentiation of leaf,
bud and stem tissues into tissue that will grow into the reproductive organs. Growth of the central part of the stem tip stops or flattens out and the sides develop protuberances in a whorled or spiral fashion around the outside of the stem end. These protuberances develop into the sepals, petals, stamens, and carpels. Once this process begins, in most plants, it cannot be reversed and the stems develop flowers, even if the initial start of the flower formation event was dependent of some environmental cue. Once the process begins, even if that cue is removed the stem will continue to develop a flower.
Uses by humans
In everyday life

Flowers are beloved for their various fragrances
In modern times, people have sought ways to cultivate, buy, wear, or just be around flowers and blooming plants, partly because of their agreeable
smell. Around the world, people use flowers for a wide range of events and functions that, cumulatively, encompass one's lifetime:
★ For new births or
Christenings
★ As a corsage or boutonniere to be worn at social functions or for holidays
★ For wedding flowers for the bridal party, and decorations for the hall
★ As brightening decorations within the home
★ As a gift of remembrance for bon voyage parties, welcome home parties, and "thinking of you" gifts
★ For
funeral flowers and expressions of
sympathy for the grieving
People therefore grow flowers around their homes, dedicate entire parts of their living space to
flower gardens, pick wildflowers, or buy flowers from
florists who depend on an entire network of commercial growers and shippers to support their trade.
Symbolism

Lilies are often used to denote life or resurrection
Many flowers have important
symbolic meanings in Western culture. The practice of assigning meanings to flowers is known as
floriography. Some of the more common examples include:
★ Red
roses are given as a symbol of love, beauty, and passion.
★
Poppies are a symbol of consolation in time of death. In the
UK,
Australia and
Canada, red poppies are worn to commemorate soldiers who have died in times of war.
★
Irises/
Lily are used in burials as a symbol referring to "resurrection/life". It is also associated with stars (sun) and its petals blooming/shining.
★
Daisies are a symbol of innocence.
Flowers within art are also representative of the female genitalia, as seen in the works of artists such as
Georgia O'Keefe,
Imogen Cunningham,
Veronica Ruiz de Velasco, and
Judy Chicago, and in fact in Asian and western classical art.
Edible flowers
Flowers provide less food than other major plants parts (
seeds,
fruits,
roots,
stems and
leaves) but they provide several important foods and
spices. Flower vegetables include
broccoli,
cauliflower and
artichoke. The most expensive spice,
saffron, consists of dried stigmas of a
crocus. Other flower spices are
cloves and
capers.
Hops flowers are used to flavor
beer.
Marigold flowers are fed to
chickens to give their egg yolks a golden yellow color, which consumers find more desirable.
Dandelion flowers are often made into wine. Bee
Pollen, pollen collected from bees, is considered a health food by some people.
Honey consists of bee-processed flower nectar and is often named for the type of flower, e.g.
orange blossom honey,
clover honey and
tupelo honey.
Hundreds of fresh flowers are edible but few are widely marketed as food. They are often used to add color and flavor to salads.
Squash flowers are dipped in breadcrumbs and fried. Edible flowers include
nasturtium,
chrysanthemum,
carnation,
cattail,
honeysuckle,
chicory,
cornflower,
Canna, and
sunflower. Some edible flowers are sometimes candied such as
daisy and
rose (you may also come across a candied
pansy).
Floristry
''Under Construction''
''Main and related articles at'':
Floristry,
Flower garden,
Gardening, and
List of flowers
Flowers can also be made into tea. Dried flowers such as chrysanthemum, rose, jasmine, camomile are infused into tea both for their fragrance and medical properties. Sometimes, they are also mixed with tea leaves for the added fragrance.
In the arts
The great variety of delicate and beautiful flowers has inspired the works of numerous poets, especially from the 18th-19th century
Romantic era. Famous examples include
William Wordsworth's ''
I Wandered Lonely as a Cloud'' and
William Blake's ''Ah! Sun-Flower''.
Because of their varied and colorful appearance, flowers have long been a favorite subject of visual artists as well. Some of the most celebrated paintings from well-known painters are of flowers, such as
Van Gogh's
sunflowers series or
Monet's water lilies.
Flowers are also dried, freeze dried and pressed in order to create permanent, three-dimensional pieces of
flower art.
Mythology
The Roman goddess of flowers, gardens, and the season of Spring is
Flora. The Greek goddess of spring, flowers and nature is
Chloris.
In
Hindu mythology, flowers have a significant status.
Vishnu, one of the three major gods in the
Hindu system, is often depicted standing straight on a
lotus flower.
[10] Apart from the association with
Vishnu, the Hindu tradition also considers the lotus to have spiritual significance.
[11] For example, it figures in the Hindu stories of creation.
[12]
See also
★
Plants
★
Plant sexuality
★
Garden
★
★
Sowing
References
1. Eames, A. J. (1961) Morphology of the Angiosperms McGraw-Hill Book Co., New York.
2. Flowers Modern & Ancient
3. First Flower
4. Amborella not a "basal angiosperm"? Not so fast
5. South Pacific plant may be missing link in evolution of flowering plants
6. Oily Fossils Provide Clues To The Evolution Of Flowers
7. Age-Old Question On Evolution Of Flowers Answered
8. Human Affection Altered Evolution of Flowers
9. Ausin et al (2005), Environmental regulation of flowering. Int J Dev Biol. 2005;49(5-6):689-705
10. Vishnu
11. Hinduism Today: God's Favorite Flower
12. The Lotus
★ Eames, A. J. (1961) ''Morphology of the Angiosperms'' McGraw-Hill Book Co., New York.
★ Esau, Katherine (1965) ''Plant Anatomy'' (2nd ed.) John Wiley & Sons, New York.
External links
★
Native Plant Information Network