Sabtu, 21 Mei 2011

PENYERBUKAN - 授粉 - Pollination

PENYERBUKAN - 授粉 - Pollination

Penyerbukan - 授粉 - Pollination

Penyerbukan, atau polinasi (dari bahasa Inggris, pollination cf. pollen, "serbuk sari 花粉"), adalah jatuhnya serbuk sari pada permukaan putik (雌蕊). Pada sebagian besar bunga, peristiwa ini berarti "jatuh pada bagian kepala putik". Penyerbukan merupakan bagian penting dari proses reproduksi tumbuhan berbiji. Penyerbukan yang sukses akan diikuti segera dengan tumbuhnya buluh serbuk yang memasuki saluran putik menuju bakal biji. Di bakal biji terjadi peristiwa penting berikutnya, pembuahan.         

Name the functions
Anther 花葯:
where pollen is produced
the stalk of the stamen, which holds the anther in the right position
the part of the ovary where the ripened pollen has to fall
the long extension of the ovary that bears the stigma
the place where the ovules are formed
Seedbed / ovulum:
the body that develops into a seed when it is fertilised
part of the corolla, which attracts insects (by colour)
Sepal / calyx-leaf:
protects the flower in its bud stage
the male reproductive part of a flower, consisting of the anther and the filament
the female reproductive part of a flower, consisting of the stigma, style and carpel
Footstalk / peduncle:
the small stalk that bears the flower in the right position.

Pollination - 授粉 - Penyerbukan

Pollination is the process by which pollen is transferred in plants, thereby enabling fertilization and sexual reproduction. Pollen grains, which contain the male gametes (sperm) to where the female gamete(s) are contained within the carpel;[1] in gymnosperms the pollen is directly applied to the ovule itself. The receptive part of the carpel is called a stigma in the flowers of angiosperms. The receptive part of the gymnosperm ovule is called the micropyle. Pollination is a necessary step in the reproduction of flowering plants, resulting in the production of offspring that are genetically diverse.
The study of pollination brings together many disciplines, such as botany, horticulture, entomology, and ecology. The pollination process as an interaction between flower and vector was first addressed in the 18th century by Christian Konrad Sprengel. It is important in horticulture and agriculture, because fruiting is dependent on fertilisation, which is the end result of pollination.


 Abiotic pollination

Abiotic pollination refers to situations where pollination is mediated without the involvement of other organisms. Only 10% of flowering plants are pollinated without animal assistance.[2] The most common form of abiotic pollination, anemophily, is pollination by wind. This form of pollination is predominant in grasses, most conifers, and many deciduous trees. Hydrophily is pollination by water and occurs in aquatic plants which release their pollen directly into the surrounding water. About 80% of all plant pollination is biotic. In gymnosperms,biotic pollination never takes place. These plants always exhibit anemophily that is wind pollination. Of the 20% of abiotically pollinated species, 98% is by wind and 2% by water.

Biotic pollination

More commonly, the process of pollination requires pollinators: organisms that carry or move the pollen grains from the anther to the receptive part of the carpel or pistil. This is biotic pollination. The various flower traits (and combinations thereof) that differentially attract one type of pollinator or another are known as pollination syndromes.
There are roughly 200,000 varieties of animal pollinators in the wild, most of which are insects.[2] Entomophily, pollination by insects, often occurs on plants that have developed colored petals and a strong scent to attract insects such as, bees, wasps and occasionally ants (Hymenoptera), beetles (Coleoptera), moths and butterflies (Lepidoptera), and flies (Diptera). In zoophily, pollination is performed by vertebrates such as birds and bats, particularly, hummingbirds, sunbirds, spiderhunters, honeyeaters, and fruit bats. Plants adapted to using bats or moths as pollinators typically have white petals and a strong scent, while plants that use birds as pollinators tend to develop red petals and rarely develop a scent (few birds have a sense of smell).
Insect pollinators such as honeybees (Apis millifera),[3] bumblebees (Bombus terrestris),[4][5] and butterflies (Thymelicus flavus) [6] have been observed to engage in flower constancy, which means they are more likely to transfer pollen to other conspecific plants.[7] This can be beneficial for the pollenisers, as flower constancy prevents the loss of pollen during interspecific flights and pollinators from clogging stigmas with pollen of other flower species.[8]


Pollination can be accomplished by cross-pollination or by self-pollination :
  • Cross-pollination, also called allogamy occurs when pollen is delivered to a flower from a different plant. Plants adapted to outcross or cross-pollinate often have taller stamens than carpels or use other mechanisms to better ensure the spread of pollen to other plants' flowers.
  • Self-pollination occurs when pollen from one flower pollinates the same flower or other flowers of the same individual.[9] It is thought to have evolved under conditions when pollinators were not reliable vectors for pollen transport, and is most often seen in short-lived annual species and plants that colonize new locations.[10] Self pollination may include autogamy, where pollen moves to the female part of the same flower; or geitonogamy, when pollen is transferred to another flower on the same plant. Plants adapted to self-fertilize often have similar stamen and carpel lengths. Plants that can pollinate themselves and produce viable offspring are called self-fertile. Plants that cannot fertilize themselves are called self-sterile, a condition which mandates cross pollination for the production of offspring.
  • Cleistogamy: is self-pollination that occurs before the flower opens. The pollen is released from the anther within the flower or the pollen on the anther grows a tube down the style to the ovules. It is a type of sexual breeding, in contrast to asexual systems such as apomixis. Some cleistogamous flowers never open, in contrast to chasmogamous flowers that open and are then pollinated. Cleistogamous flowers by necessity are self-compatible or self-fertile plants.[11] Many plants are self-incompatible, and these two conditions are end points on a continuum.
Pollination also requires consideration of pollenizers. The terms "pollinator" and "pollenizer" are often confused: a pollinator is the agent that moves the pollen, whether it be bees, flies, bats, moths, or birds; a pollenizer is the plant that serves as the pollen source for other plants. Some plants are self-fertile or self-compatible and can pollinate themselves (e.g., they act as their own pollenizer). Other plants have chemical or physical barriers to self-pollination.
In agriculture and horticulture pollination management, a good pollenizer is a plant that provides compatible, viable and plentiful pollen and blooms at the same time as the plant that is to be pollinated or has pollen that can be stored and used when needed to pollinate the desired flowers. Hybridization is effective pollination between flowers of different species, or between different breeding lines or populations. see also Heterosis.
Peaches are considered self-fertile because a commercial crop can be produced without cross-pollination, though cross-pollination usually gives a better crop. Apples are considered self-incompatible, because a commercial crop must be cross-pollinated. Many commercial fruit tree varieties are grafted clones, genetically identical. An orchard block of apples of one variety is genetically a single plant. Many growers now consider this a mistake. One means of correcting this mistake is to graft a limb of an appropriate pollenizer (generally a variety of crabapple) every six trees or so.

Evolution of plant/pollinator interactions

The first fossil record for abiotic pollination is from fern-like plants in the late Carboniferous period. Gymnosperms show evidence for biotic pollination as early as the Triassic period. Many fossilized pollen grains show characteristics similar to the biotically dispersed pollen today. Furthermore, the gut contents, wing structures, and mouthpart morphologies of fossilized beetles and flies suggest that they acted as early pollinators. The association between beetles and angiosperms during the early Cretaceous period led to parallel radiations of angiosperms and insects into the late Cretaceous. The evolution of nectaries in late Cretaceous flowers signals the beginning of the mutualism between hymenopterans and angiosperms.

 In agriculture

Pollination management is a branch of agriculture that seeks to protect and enhance present pollinators and often involves the culture and addition of pollinators in monoculture situations, such as commercial fruit orchards. The largest managed pollination event in the world is in Californian almond orchards, where nearly half (about one million hives) of the US honey bees are trucked to the almond orchards each spring. New York's apple crop requires about 30,000 hives; Maine's blueberry crop uses about 50,000 hives each year.
Bees are also brought to commercial plantings of cucumbers, squash, melons, strawberries, and many other crops. Honey bees are not the only managed pollinators: a few other species of bees are also raised as pollinators. The alfalfa leafcutter bee is an important pollinator for alfalfa seed in western United States and Canada. Bumblebees are increasingly raised and used extensively for greenhouse tomatoes and other crops.

The ecological and financial importance of natural pollination by insects to agricultural crops, improving their quality and quantity, becomes more and more appreciated and has given rise to new financial opportunities. The vicinity of a forest or wild grasslands with native pollinators near agricultural crops, such as apples, almonds or coffee can improve their yield by about 20%. The benefits of native pollinators may result in forest owners demanding payment for their contribution in the improved crop results - a simple example of the economic value of ecological services.
The American Institute of Biological Sciences reports that native insect pollination saves the United States agricultural economy nearly an estimated $3.1 billion annually through natural crop production;[12] pollination produces some $40 billion worth of products annually in the United States alone.[2]
Pollination of food crops has become an environmental issue, due to two trends. The trend to monoculture means that greater concentrations of pollinators are needed at bloom time than ever before, yet the area is forage poor or even deadly to bees for the rest of the season. The other trend is the decline of pollinator populations, due to pesticide misuse and overuse, new diseases and parasites of bees, clearcut logging, decline of beekeeping, suburban development, removal of hedges and other habitat from farms, and public paranoia about bees. Widespread aerial spraying for mosquitoes due to West Nile fears is causing an acceleration of the loss of pollinators.
The US solution to the pollinator shortage, so far, has been for commercial beekeepers to become pollination contractors and to migrate. Just as the combine harvesters follow the wheat harvest from Texas to Manitoba, beekeepers follow the bloom from south to north, to provide pollination for many different crops.

Environmental impacts

Loss of pollinators, also known as Pollinator decline (of which colony collapse disorder is perhaps the most well known) has been noticed in recent years.[13] Observed losses would have significant economic impacts. Possible explanations for pollinator decline include habitat destruction, pesticide, parasitism/diseases, and others.

See also


  1. ^
  2. ^ a b c US Forest Department: Pollinator Factsheet
  3. ^ Hill, P.S.M., P.H. Wells, and H. Wells. 1997. Spontaneous flower constancy and learning in honey bees as a function of colour. Animal Behavior, 54: 615-627.
  4. ^ Stout, J.C., J.A. Allen, and D. Goulson. 1998. The influence of relative plant density and floral morphological complexity on the behaviour of bumblebees. Oecologia, 117: 543-550.
  5. ^ Chittka, L., A. Gumbert, and J. Kunze. 1997. Foraging dynamics of bumble bees: correlates of movement within and between plant species. Behavioral Ecology, 8(3): 239-249.
  6. ^ Goulson, D., J. Ollerton and C. Sluman. 1997. Foraging strategies in the small skipper butterfly, Thymelicus flavus: when to switch? Animal Behavior, 53: 1009-1016.
  7. ^ Harder, L. D., N.M. Williams, C.Y. Jordan, and W.A. Nelson. "The effects of Floral design and display on pollinator economics and pollen dispersal". 297-317. Editors, L. Chittka and J.D. Thomson. Cognitive Ecology of Pollination: Animal Behavior and Floral Evolution. 2001. Cambridge University Press
  8. ^ Chittka, L., J.D. Thomson, and N.M. Waser. 1999. Flower constancy, insect psychology, and plant evolution. Naturwissenschaften, 86: 361-177.
  9. ^ Cronk, J. K.; Fennessy, M. Siobhan (2001). Wetland plants: biology and ecology. Boca Raton, Fla.: Lewis Publishers. p. 166. ISBN 1-56670-372-7.
  10. ^ Glover, Beverly J. (2007). Understanding flowers and flowering: an integrated approach. Oxford University Press. p. 127. ISBN 0198565968
  11. ^ Culley, Theresa M.; Klooster, Matthew R. (JAN-07). "The cleistogamous breeding system: a review of its frequency, evolution, and ecology in angiosperms". The Botanical Review
  12. ^ BioScience, April 2006, Vol. 56 No. 4, pp. 315-317
  13. ^ "What is the male, pollen-producing part of a plant called?". CNN. 2000-05-05. Retrieved 2010-05-22.
  • Crepet WL, Friis EM, Nixon KC. 1991. Fossil evidence for the evolution of biotic pollination [and discussion]. Philosophical Transactions: Biological Sciences 333(1267) 187-195.
  • Dafni, Amots; Kevan, Peter G.; and Husband, Brian C. (2005). Practical Pollination Biology. Enviroquest, Ltd. ISBN 978-0-9680123-0-7.
  • Labandeira CC, Kvacek J, & Mostovski MB. 2007. Pollination drops, pollen and insect pollination of Mesozoic gymnosperms. Taxon 56(3) 663-695.
  • Sihag, R.C. 1997.Pollination Biology: Basic and Applied Principles. Rajendra Scientific Publishers,Hisar, 210p.

External links

授粉 - Penyerbukan - Pollination

授粉 (Shòufěn) 指的是裸子植物顯花植物把雄性配子,即花粉,從花葯傳到雌蕊的柱頭,使雌性配子受精的過程。80%的種子植物靠生物 (例如蜜蜂蝴蝶果蝠)傳播花粉,其餘則靠 (例如)、等媒界傳播花粉。











种子植物特有的结构,相当于一个小孢子和由它发育的前期雄配子体。 在被子植物成熟花粉粒中包含2个或3个细胞,即一个营养细胞和一个生殖细胞或由其分裂产生的两个精子。在两个细胞的花粉粒中,两个精子是在传粉后在花粉管中由生殖细胞分裂形成的。在裸子植物的成熟花粉粒中包含的细胞数目变化较大,从1~5个或更多个细胞,其中有1~2个原叶细胞,是雄配子体中残留的几个营养细胞,形成后往往随即退化,在被子植物的雄配子体中已完全消失。







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