Pollination is part of sexual reproduction in plants. It describes how the pollen grains get to the female parts of a plant. Pollen grains, which contain the male gametes, need to get to where the female gamete(s) are.
What happens is basically the same as sexual reproduction in animals. Each pollen grain is haploid: it has half of the DNA (genetic information) that is needed to make a new plant. During fertilization this combines with the DNA that is in the egg of the female part and a zygote is formed. In seed plants a seed is started.
Ways of pollinating[change | change source]
In flowering plants, pollen has to get from one flower to another. There are two main ways that this can happen: by non-living things like wind or water, or by living things such as insects or birds.
- Maize and the wind
Maize (called corn in some parts of the world) is pollinated by wind. The male anthers let go of their pollen and it blows over to a nearby female flower on another corn plant. Most of the flowers are either male or female on a corn plant (monoecious), rather than both sexes in one flower (hermaphrodite).
Maize flowers have evolved (changed over time) to use wind for pollination. They do not need pretty petals. The pollen is light so it can blow around, and the ends of the female parts (stigma) are fluffy to catch all the tiny pollen grains.
- Tomatoes and bees
With tomato plants, bees move the pollen from the male parts of one flower (anthers), to the female parts of another flower (stigma). The bee moves between flowers as it collects the nectar that the flowers make. The bees take the nectar and some pollen back to their hive, and the tomato plants get to reproduce (make new tomato plants).
Because the tomato flowers have evolved to attract bees, they have spread-out petals and are white to human eyes (bees, like most insects, can see into the ultraviolet range as well as our visual range of wavelengths). The pollen is often stuck together in clumps called pollinia, which in turn get stuck to the bee. Bees are extremely hairy, and carry tiny electric charges which attract the pollen onto their bodies. Honey bees have special pollen baskets, usually on their rear legs; they groom the pollen off their bodies into these pockets.
Much of the pollen gets taken back to the nest or hive, where it is used as a source of protein, most needed by the larvae. Some gets rubbed off on the next flower, where the female stigma is sticky. A pollen tube grows down to permit the male gamete to fertilize an egg and make a seed.
What happens after pollination[change | change source]
What happens after pollination is fertilisation. In plants it is a double fertilisation in which two sperm cells fertilize cells in the plant ovary. One of these is a normal fertilisation, which produces the embryo. The other is a unique kind of fertilisation which produces the seed endosperm.
The process begins when a pollen grain sticks to the stigma of the pistil (female reproductive structure). Then it germinates, and grows a long pollen tube. While this pollen tube is growing, a haploid cell travels down the tube behind the tube nucleus. This cell divides by mitosis into two haploid sperm cells.
As the pollen tube grows, it makes its way from the stigma, down the style and into the ovary. Here the pollen tube reaches the ovule and releases its contents (which include the sperm cells). One sperm makes its way to fertilize the egg cell, producing a diploid (2n) zygote. The second sperm cell fuses with two cell nuclei, producing a triploid (3n) cell.
As the zygote develops into an embryo, the triploid cell develops into the endosperm, which serves as the embryo's food supply. The ovary now will develop into a fruit and the ovule will develop into a seed.
Distribution of pollinating methods[change | change source]
Gymnosperms[change | change source]
There is evidence that some gymnosperms were insect-pollinated in the Triassic period, but pollination by animals is not the main method in this group. Most are wind-pollinated. Some gymnosperms and their insect pollinators are co-evolved for pollination. The best-known examples are members of the order Cycadales and their associated species of beetle.
Families of flowering plants[change | change source]
Really widespread and specialised animal pollination came with the Angiosperms (flowering plants). Different families of flowering plants usually specialise in a particular pollination method. Sometimes a few genera shift from one method to another.p53
- Ranunculaceae: pollinated by insects. Only one genus is pollinated by wind.
- Compositae (Asteraceae): this, the largest family, is almost entirely pollinated by insects. Two groups of genera have changed to wind pollination.
- Cyperaceae: almost entirely wind-pollinated. One genus is insect-pollinated.
- Moraceae: this, the mulberry family, is the best example of a widespread change from wind to insect pollination. All its related families (Ulmaceae, Cannabaceae, Urticaceae) are wind pollinated.
- Gramineae (Poaceae): the grasses have extreme adaptations for wind pollination. Only two genera have changed to insect pollination.
Pollination syndrome[change | change source]
Wind pollination[change | change source]
Wind pollinated flowers are usually small and inconspicuous (not showy). They do not have a scent or produce nectar. The anthers may produce a large number of pollen grains, while the stamens are generally long and stick up out of the flower. Their stigmas may be large and feathery to catch the pollen grains. Insects may visit them to collect pollen; there are some examples of flowers which are both wind and insect pollinated.
Animal pollination[change | change source]
- Beetle pollination
Beetle-pollinated flowers are usually large, greenish or off-white in color and heavily scented. Scents may be spicy, fruity, or similar to decaying organic material. Most beetle-pollinated flowers are flattened or dish shaped, with pollen easy to get at. They may have traps to keep the beetle longer. The plant's ovaries are usually well protected from the biting mouthparts of the beetles. Beetles are important pollinators in some parts of the world, such as dry areas of southern Africa and southern California, and the montane grasslands of KwaZulu-Natal in South Africa.
- Fly pollination
On the other hand, male fruit flies are attracted to some wild orchids which do not produce nectar. Instead, they produce a precursor of the fly's sex pheromone. Flies which normally visit dead animals or dung are attracted to flowers that mimic these smelly items. They get no reward and would quickly leave, but the plant may have traps to slow them down. These plants have a strong, unpleasant odor, and are brown or orange in colour.
Their sheer numbers and the presence of some flies throughout the year make them important pollinators for many plants. Flies tend to be important pollinators in high-altitudes and high-latitudes where they are numerous, and other insect groups may be lacking.
- Bee pollination
Bee-pollinated flowers tend to be yellow or blue, often with ultraviolet nectar guides and scent. Nectar and/or pollen are offered as rewards in varying amounts. The sugar in the nectar tends to be mostly sucrose. There are different types of bees which differ in size, tongue length and behaviour (some solitary, some colonial). Some plants can only be pollinated by bees because their anthers release pollen internally, and it must be shaken out by buzzing ("sonication"). Bumblebees are the only animals that do this.
- Wasp pollination
- Lepidoptera pollination
Butterfly-pollinated flowers tend to be large and showy, pink or lavender in colour, often have a landing area, and are usually scented. Since butterflies do not digest pollen (with one exception), more nectar is offered than pollen. The flowers have simple nectar guides with the nectaries usually hidden in narrow tubes or spurs, reached by the long tongue of the butterflies.
Among the more important moth pollinators are the hawk moths (Sphingidae). Their behaviour is similar to hummingbirds: they hover in front of flowers with rapid wingbeats. Most are nocturnal or twilight feeders. So moth-pollinated flowers tend to be white, night-opening, large and showy with tubular corollas and a strong, sweet scent produced in the evening, night or early morning. A lot of nectar is produced to fuel the high metabolic rates needed to power their flight.
Other moths fly slowly and settle on the flower. They do not need as much nectar as the fast-flying hawk moths, and the flowers tend to be small (though they may be aggregated in heads).
- Bird pollination
Hummingbirds are the most familiar nectar-feeding birds for North Americans, there are analogous species in other parts of the world. Flowers attractive to hummingbirds, which hover in front of the flower, tend to be large red or orange tubes with a lot of dilute nectar produced during the day. Since birds do not have a strong response to scent, they tend to be odourless. Perching birds need a substantial landing platform, so sunbirds, honeyeaters, and the like are less associated with tubular flowers.
- Bat pollination
Bat-pollinated flowers tend to be large and showy, white or light coloured, open at night and have strong odours. They are often large and bell-shaped. Bats drink the nectar, and these plants typically offer nectar for long periods. Sight, smell, and echo-location are used to initially find the flowers, and excellent spatial memory is used to visit them repeatedly. In fact, bats can identify nectar-producing flowers using echolocation. Bat-pollinated plants have bigger pollen than their relatives.
Honey guides[change | change source]
Honey guides, nectar guides or floral guides are markings on flowers which tell insects where to go for nectar (many insects can see in the ultraviolet range). Most of these guides are invisible to humans unless seen in ultraviolet light. The benefit to the plant is that the guides increase the supply of pollinators at a relatively low cost.
History[change | change source]
A full understanding of pollination is quite recent.
In 1672 Nehemiah Grew had some idea that pollen was the means of fertilisation in higher plants. Using a microscope, he was the first to describe pollen in detail. This led to the discovery that all pollen grains in a species were alike. The study of pollen grains is called micropaleontology. The discovery of sex in plants did not occur until in 1694, when Rudolf Camerarius put his discovery into a letter.
In 1793 Christian Sprengel (1750–1816) published a work on the pollination of flowers by insects which made all the main points. Unfortunately, "his work was so far outside the standard thinking and interests of the period that it was almost completely ignored".
Two lines of work solved the main issues. One was done by studies of how the pollen cells worked to fertilise the ovum, and the other was to recognise the coevolution of the animal pollinators and the flowering plants. Both these lines of work became essentially 'modern' in the middle of the nineteenth century.
References[change | change source]
|Wikimedia Commons has media related to: Pollination|
- There are plants which are self-pollinated; and some which have no longer use sexual reproduction.
- US Forest Department, Pollinator Factsheet
- Stebbins, G. Ledyard 1974. Flowering plants: evolution above the species level. Harvard University Press. ISBN 0-674-30685-6
- P.J. Gullan and P.S. Cranston 2005. The Insects: an outline of entomology. Blackwell, Oxford, 282. ISBN 1-4051-1113-5.
- Jones, GD and SD Jones 2001. The uses of pollen and its implication for Entomology. Neotropical Entomology 30 (3): 314–349. doi:10.1590/S1519-566X2001000300001
- Ollerton J. et al 2003. The pollination ecology of an assemblage of grassland asclepiads in South Africa. Annals of Botany 92: 807-834
- Kastinger C, and A Weber (2001). "Bee-flies (Bombylius spp., Bombyliidae, Diptera) and the pollination of flowers". Flora 196 (1): 3–25.
- Tan, KH and R Nishida (2000). "Mutual reproductive benefits between a wild orchid, Bulbophyllum patens, and Bactrocera fruit flies via a floral synomone.". Journal of Chemical Ecology 26 (2): 533–546. doi:10.1023/A:1005477926244.
- Tan, KH, LT Tan and R Nishida (2006). "Floral phenylpropanoid cocktail and architecture of Bulbophyllum vinaceum orchid in attracting fruit flies for pollination.". Journal of Chemical Ecology 32 (11): 2429–2441. doi:10.1007/s10886-006-9154-4. PMID 17082990.
- Jones, GD and SD Jones (2001). "The uses of pollen and its implication for Entomology". Neotropical Entomology 30 (3): 314–349. doi:10.1590/S1519-566X2001000300001.
- Larson BMH, PG Kevan, and DW Inouye (2001). "Flies and flowers: taxonomic diversity of anthophiles and pollinators". Canadian Entomologist 133 (4): 439–465. doi:10.4039/Ent133439-4.
- Fenster C.B. et al (2004). "Pollination syndromes and floral specialization". Annual Review of Ecology and Systematics 35 (1): 375–403. doi:10.1146/annurev.ecolsys.34.011802.132347.
- Sühs, R.B. et al 2009. Pollen vector wasps (Hymenoptera, Vespidae) of Schinus terebinthifolius Raddi (Anacardiaceae), Santa Cruz do Sul, RS, Brazil. Brazilian Journal of Biosciences 7, 2, 138-143. 
- Oliveira PE, PE Gibbs, and AA Barbosa (2004). "Moth pollination of woody species in the Cerrados of Central Brazil: a case of so much owed to so few?". Plant Systematics and Evolution 245 (1-2): 41–54. doi:10.1007/s00606-003-0120-0.
- Lotz, CN and JE Schondube (2006). "Sugar preferences in nectar- and fruit-eating birds: behavioral patterns and physiological causes". Biotropica 38 (1): 3–15.
- Von Helversen D, MW Holderied, and O Von Helversen (2003). "Echoes of bat-pollinated bell-shaped flowers: conspicuous for nectar-feeding bats?" (abstract page). Journal of Experimental Biology 206 (6): 1025–1034. doi:10.1242/jeb.00203. PMID 12582145. http://jeb.biologists.org/cgi/content/abstract/206/6/1025.
- Pettersson S, F Ervik, and JT Knudsen (2004). "Floral scent of bat-pollinated species: West Africa vs. the New World". Biological Journal of the Linnean Society 82 (2): 161–168. doi:10.1111/j.1095-8312.2004.00317.x. http://www.blackwell-synergy.com/links/doi/10.1111%2Fj.1095-8312.2004.00317.x.
- Stroo, A. (2000). "Pollen morphological evolution in bat pollinated plants". Plant Systematics and Evolution 222 (1-4): 225–242. doi:10.1007/BF00984104.
- Grew, Nehemiah 1672. Anatomy of plants. London.
- Manten, A.A. (1967). "Lennart von post and the foundation of modern palynology". Review of Palaeobotany and Palynology 1 (1-4): 11–22. doi:10.1016/0034-6667(67)90105-4.
- Evaluation in Sachs, Julius 1890. History of Botany (1530–1860) Oxford University Press, 359–444.
- Sprenglel C.K. 1793. Das neu entdeckte Geheimniss der Natur in Bau und Befructung der Blumen. Berlin.
- Mayr, Ernst 1982. The growth of biological thought: diversity, evolution and thought. Harvard University Press, 659.
- Sachs, Julius von 1890. History of botany 1530–1860. transl. H.E.F. Garnsey; revised by I.B. Balfour. Oxford University Press, 415.
- Hughes A. 1959. A history of cytology. London & New York: Abelard-Schuman, 59–60
- Darwin Charles 1859. The origin of species. Murray, London, 98.
- Darwin Charles 1862. On the various contrivances by which British and foreign orchids are fertilised by insects. Murray, London
- Darwin, Charles 1876. The effects of cross and self fertilisation in the vegetable kingdom. London: Murray.
- Darwin, Charles 1877. The different forms of flowers on plants of the same species. London: Murray.
- Knuth, Paul et al 1906. Handbook of flower pollination, based upon Hermann Müller's work 'The fertilisation of flowers by insects'. Oxford University Press.