Asteraceae

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Asteraceae
Temporal range: 49–0Ma
Eocene[1] - recent
Asteracea poster 3.jpg
A poster with 12 different species of Asteraceae from the Asteroideae, Cichorioideae and Carduoideae subfamilies
Scientific classification
Kingdom: Plantae
(unranked): Angiosperms
(unranked): Eudicots
(unranked): Asterids
Order: Asterales
Family: Asteraceae
Bercht. & J.Presl[2]
Type genus
Aster
L.
Subfamilies

Asteroideae Lindley
Barnadesioideae Bremer & Jansen
Carduoideae Sweet
Cichorioideae Chevallier
Corymbioideae Panero & Funk
Gochnatioideae Panero & Funk
Gymnarrhenoideae Panero & Funk
Hecastocleidoideae Panero & Funk
Mutisioideae Lindley
Pertyoideae Panero & Funk
Stifftioideae Panero
Wunderlichioideae Panero & Funk

Diversity
1,600 genera
Synonyms

Compositae Giseke
Acarnaceae Link
Ambrosiaceae Bercht. & J. Presl
Anthemidaceae Bercht. & J. Presl
Aposeridaceae Raf.
Arctotidaceae Bercht. & J. Presl
Artemisiaceae Martinov
Athanasiaceae Martinov
Calendulaceae Bercht. & J. Presl
Carduaceae Bercht. & J. Presl
Cassiniaceae Sch. Bip.
Cichoriaceae Juss.
Coreopsidaceae Link
Cynaraceae Spenn.
Echinopaceae Bercht. & J. Presl
Eupatoriaceae Bercht. & J. Presl
Helichrysaceae Link
Inulaceae Bercht. & J. Presl
Lactucaceae Drude
Mutisiaceae Burnett
Partheniaceae Link
Perdiciaceae Link
Senecionaceae Bercht. & J. Presl
Vernoniaceae Burmeist.

Source: GRIN[3]

The Asteraceae or Compositae (commonly referred to as the aster, daisy, composite,[4] or sunflower family) are an exceedingly large and widespread family of flowering plants (Angiospermae).[5][6] The group has more than 23,000 currently accepted species, spread across 1,620 genera (list) and 12 subfamilies. In terms of numbers of species, the Asteraceae are rivaled only by the Orchidaceae.[5][7] (Which of the two families is actually larger is unclear, owing to uncertainty about exactly how many species exist in each family.) The main feature of the family is the composite flower type in the form of capitula surrounded by involucral bracts. The name "Asteraceae" comes from Aster, the most prominent genus in the family, that derives from the Greek ἀστήρ, meaning star, and is connected with its inflorescence star form. As for the term "Compositae", more ancient but still valid, it obviously makes reference to the fact that the family is one of the few angiosperm ones to have composite flowers.[8] This family has a remarkable ecological and economical importance and is present from the polar regions to the tropics, colonizing all available habitats. The Asteraceae may represent as much as 10% of autochthonous flora in many regions of the world.

Most members of Asteraceae are herbaceous, but a significant number are also shrubs, vines, or trees. The family has a worldwide distribution and is most common in the arid and semiarid regions of subtropical and lower temperate latitudes.[9]

The Asteraceae are an economically important family. Some members provide products, including cooking oils, lettuce, sunflower seeds, artichokes, sweetening agents, coffee substitutes, and herbal teas. Several genera are popular with the horticultural community, including marigold, pot marigold (also known as calendula), cone flowers, various daisies, fleabane, chrysanthemums, dahlias, zinnias, and heleniums. Asteraceae are important in herbal medicine, including Grindelia, Echinacea, yarrow, and many others.[10] A number of species have come to be considered invasive, including, most notably in North America, dandelion, which was originally introduced by European settlers who used the young leaves as a salad green.[11]

Etymology[edit]

The Latin name "Asteraceae" is derived from the type genus Aster, which is a Greek term that means "star".[12] "Compositae", an older but still valid name,[13] means "composite" and refers to the characteristic inflorescence, a special type of pseudanthium found in only a few other angiosperm families. The study of this family is known as synantherology.

The vernacular name "daisy", widely applied to members of this family, is derived from its Old English name: dægesege, from dæges eage, meaning "day's eye". This is because the petals (of Bellis perennis) open at dawn and close at dusk.

Distribution[edit]

Asteraceae have a cosmopolitan distribution, and are found everywhere except Antarctica and the extreme Arctic. They are especially numerous in tropical and subtropical regions (notably Central America, eastern Brazil, the Andes, the Mediterranean, the Levant part of the Middle East, southern Africa, central Asia, and southwestern China).[7]

Taxonomy[edit]

Compositae were first described in 1792 by the German botanist Paul Dietrich Giseke.[14] Traditionally, two subfamilies were recognised: Asteroideae (or Tubuliflorae) and Cichorioideae (or Liguliflorae). The latter has been shown to be extensively paraphyletic, and has now been divided into 11 subfamilies, but the former still stands. The phylogenetic tree presented below is based on Panero & Funk (2002).[15] The diamond denotes a very poorly supported node (<50% bootstrap support), the dot a poorly supported node (<80%).[5]



Barnadesioideae: 9 genera, 93 species. South America, mainly the Andes.




Stifftioideae: South America and Asia.



Mutisioideae: 58 genera, 750 species. South America.



Wunderlichioideae: 8 genera, 24 species, mostly in Venezuela and Guyana




Gochnatioideae: 4 or 5 genera, 90 species.




Hecastocleidoideae: Only Hecastocleis shockleyi. Southwestern United States.




Carduoideae: 83 genera, 2,500 species. Worldwide.




Pertyoideae: 5 or 6 genera, 70 species.




Gymnarrhenoideae: Only Gymnarrhena micrantha. Northern Africa.



Cichorioideae: 224 genera, 3,200 species. Worldwide.




Corymbioideae: Only the genus Corymbium, with 9 species.



Asteroideae: 1,130 genera and 16,200 species. Worldwide.














It is noteworthy that the four subfamilies Asteroideae, Cichorioideae, Carduoideae and Mutisioideae contain 99% of the species diversity of the whole family (approximately 70%, 14%, 11% and 3% respectively).

Because of the morphological complexity exhibited by this family, agreeing on generic circumscriptions has often been difficult for taxonomists. As a result, several of these genera have required multiple revisions.[16]

Characteristics[edit]

Asteraceae are mostly herbaceous plants, but some shrubs, trees and climbers do exist. Asteraceae are generally easy to distinguish from other plants, mainly because of their characteristic inflorescence and other shared characteristics.[16] However, determining genera and species is notoriously difficult (see "damned yellow composite" for example).

Roots and stems[edit]

Asteraceae generally produce taproots, but sometimes they possess fibrous root systems. Stems are generally erect, but can be prostrate to ascending. Some species have underground stems in the form of caudices or rhizomes. These can be fleshy or woody depending on the species.[9]

Leaves[edit]

The leaves and the stems very often contain secretory canals with resin or latex (particularly common among the Cichorioideae). The leaves can be alternate, opposite, or whorled. They may be simple, but are often deeply lobed or otherwise incised, often conduplicate or revolute. The margins can be entire or lobed or toothed.

Flowers[edit]

Floral heads[edit]

In many plants of the Asteraceae family, what appears to be a single flower is actually a cluster of much smaller flowers.[17] The overall appearance of the cluster, as a single flower, functions in attracting pollinators in the same way as the structure of an individual flower in some other plant families.[17] The older family name, Compositae, comes from the fact that what appears to be a single flower, is actually a composite of smaller flowers.[17] The "petals" or "sunrays" in a sunflower head are actually individual strap-shaped[18] flowers called "ray flowers", and the "sun disk" is made of smaller circular shaped individual flowers called "disc flowers".[17] The word aster means "star" in Greek, referring to the appearance of some family members, as a "star" surrounded by "rays".[17] The cluster of flowers that may appear to be a single flower, is called a head.[17] The entire head may move tracking the sun, like a "smart" solar panel, which maximizes reflectivity of the whole unit and can thereby attract more pollinators.[17]

A ray flower is a 3-tipped (3-lobed), strap-shaped, individual flower in the head of some members of the Asteraceae family.[17][18] Sometimes a ray flower has 2 tips (or 2-lobes).[17] The corolla of the ray flower may have 2 tiny teeth opposite the 3 lobed strap, or tongue, indicating evolution by fusion from an originally 5 part corolla.[17] Sometimes, the 3:2 arrangement is reversed, with 2 tips on the tongue, and 0 or 3 tiny teeth opposite the tongue.[17] A ligulate flower is a 5 tipped, strap-shaped, individual flower in the heads of other members.[17] A ligule is the strap-shaped tongue of the corolla of either a ray flower or of a ligulate flower.[18] A disk flower is a radially symmetric (i.e., with identical shaped petals arranged in circle around the center) individual flower in the head, which is ringed by ray flowers when both are present.[17][18] Sometimes ray flowers may be slightly off from radial symmetry, or weakly bilaterally symmetric, as in the case of desert pincushions Chaenactis fremontii.[17]

At the base of the head, and surrounding the flowers before opening, is a bundle of sepal-like bracts or scales called phyllaries, which together form the involucre that protects the individual flowers in the head before opening.[17] The individual heads have the smaller individual flowers arranged on a round or dome-like structure called the receptacle.[17] The flowers mature first at the outside, moving toward the center, with the youngest in the middle.[17]

The individual flowers in a head have 5 fused petals (rarely 4), but instead of sepals, have threadlike, hairy, or bristly structures called pappus, which surround the fruit and can stick to animal fur or be lifted by wind, aiding in seed dispersal.[17] The whitish fluffy head of a dandelion commonly blown on by children, is made of the pappus, with tiny seeds attached at the ends, whereby the pappus provides a parachute like structure to help the seed be carried away in the wind.[17]

A radiate head has disc flowers surrounded by ray flowers.[17] A ligulate head has all ligulate flowers.[17] When a sunflower family flower head has only disk flowers that are sterile, male, or have both male and female parts, it is a discoid head.[17] Disciform heads have only disc flowers, but may have two kinds (male flowers and female flowers) in one head, or may have different heads of two kinds (all male, or all female).[17] Pistillate heads have all female flowers. Staminate heads have all male flowers.[17]

Sometimes, but rarely, the head contains only a single flower, or has a single flowered pistillate (female) head, and a multi-flowered male staminate (male) head.[17]

Floral structures[edit]

Flower diagram of Carduus (Carduoideae) shows (outermost to innermost): subtending bract and stem axis; fused calyx; fused corolla; stamens fused to corolla; gynoecium with two carpels and one locule
A typical Asteraceae flower head (here Bidens torta) showing the individual flowers
Ray floret (as in Cichorioideae, and the outer florets in Asteroideae)
Disc floret (as in Asteroideae)

The most evident characteristic of Asteraceae is perhaps their inflorescence: a specialised capitulum, technically called a calathid or calathidium, but generally referred to as flower head or, alternatively, simply capitulum.[19] The capitulum is a contracted raceme composed of numerous individual sessile flowers, called the florets, all sharing the same receptacle.

The capitulum of Asteraceae has evolved many characteristics that make it look superficially like a single flower. This type of flower-like inflorescence is fairly widespread amongst angiosperms, and has been given the name of pseudanthia.

A set of bracts forms an involucre surrounding the base of the capitulum. These are called "phyllaries", or "involucral bracts". They may simulate the sepals of the pseudanthium. These are mostly herbaceous but can also be brightly coloured (e.g. Helichrysum) or have a scarious (dry and membranous) texture. The phyllaries can be free or fused, and arranged in one to many rows, overlapping like the tiles of a roof (imbricate) or not (this variation is important in identification of tribes and genera).

Each floret may itself be subtended by a bract, called a "palea" or "receptacular bract". These bracts as a group are often called "chaff". The presence or absence of these bracts, their distribution on the receptacle, and their size and shape are all important diagnostic characteristics for genera and tribes.

The florets have five petals fused at the base to form a corolla tube and they may be either actinomorphic or zygomorphic. Disc florets are usually actinomorphic, with five petal lips on the rim of the corolla tube. The petal lips may be either very short, or long, in which case they form deeply lobed petals. The latter is the only kind of floret in the Carduoideae, while the first kind is more widespread. Ray florets are always highly zygomorphic and are characterised by the presence of a ligule, a strap-shaped structure on the edge of the corolla tube consisting of fused petals. In the Asteroideae and other minor subfamilies these are usually borne only on florets at the circumference of the capitulum and have a 3+2 scheme – above the fused corolla tube, three very long fused petals form the ligule, with the other two petals being inconspicuously small. The Cichorioidea has only ray florets, with a 5+0 scheme – all five petals form the ligule. A 4+1 scheme is found in the Barnadesioideae. The tip of the ligule is often divided into teeth, each one representing a petal. Some marginal florets may have no petals at all (filiform floret).

The calyx of the florets may be absent, but when present is always modified into a pappus of two or more teeth, scales or bristles and this is often involved in the dispersion of the seeds. As with the bracts, the nature of the pappus is an important diagnostic feature.

There are usually five stamens. The filaments are fused to the corolla, while the anthers are generally connate (syngenesious anthers), thus forming a sort of tube around the style (theca). They commonly have basal and/or apical appendages. Pollen is released inside the tube and is collected around the growing style, and then, as the style elongates, is pushed out of the tube (nüdelspritze).

The pistil consists of two connate carpels. The style has two lobes. Stigmatic tissue may be located in the interior surface or form two lateral lines. The ovary is inferior and has only one ovule, with basal placentation.

Fruits and seeds[edit]

The fruit of the Asteraceae is achene-like, and is called a cypsela (plural cypselae). Although there are two fused carpels, there is only one locule, and only one seed per fruit is formed. It may sometimes be winged or spiny because the pappus, which is derived from calyx tissue often remains on the fruit (for example in dandelion). In some species, however, the pappus falls off (for example in Helianthus). Cypsela morphology is often used to help determine plant relationships at the genus and species level.[20] The mature seeds usually have little endosperm or none.[16]

Metabolites[edit]

Asteraceae generally store energy in the form of inulin. They produce iso/chlorogenic acid, sesquiterpene lactones, pentacyclic triterpene alcohols, various alkaloids, acetylenes (cyclic, aromatic, with vinyl end groups), tannins. They have terpenoid essential oils which never contain iridoids.[5]

Evolution[edit]

Diversification of Asteraceae appears to have taken place roughly 42-36 million years ago, the stem group perhaps being up to 49 million years old.[5]

It is still unknown whether the precise cause of their great success was the development of the highly specialised capitulum, their ability to store energy as fructans (mainly inulin), which is an advantage in relatively dry zones, or some combination of these and possibly other factors.[5]

Ecology[edit]

Seeds are dispersed by the wind in Carlina
Epizoochory in Bidens tripartita

Asteraceae are especially common in open and dry environments.[16]

Many members of the Asteraceae are pollinated by insects, which explains their value in attracting beneficial insects, but anemophyly is also present (e.g. Ambrosia, Artemisia). There are many apomictic species in the family.

Seeds are ordinarily dispersed intact with the fruiting body, the cypsela. Wind dispersal is common (anemochory) assisted by a hairy pappus. Another common variation is epizoochory, in which the dispersal unit, a single cypsela (e.g. Bidens) or entire capitulum (e.g. Arctium) provided with hooks, spines or some equivalent structure, sticks to the fur or plumage of an animal (or even to clothes, like in the photo) just to fall off later far from its mother plant.

Uses[edit]

Commercially important plants in the Asteraceae include the food crops Lactuca sativa (lettuce), Cichorium (chicory), Cynara scolymus (globe artichoke), Helianthus annuus (sunflower), Smallanthus sonchifolius (yacón), Carthamus tinctorius (safflower) and Helianthus tuberosus (Jerusalem artichoke).

Many members of the family are grown as ornamental plants for their flowers, and some are important ornamental crops for the cut flower industry. Some examples are Chrysanthemum, Gerbera, Calendula, Dendranthema, Argyranthemum, Dahlia, Tagetes, Zinnia, and many others.

Other commercially important species include Compositae used as herbs and in herbal teas and other beverages. Chamomile, which comes from two different species, the annual Matricaria recutita (or German chamomile) and the perennial Chamaemelum nobile (also called Roman chamomile). Calendula (also called the pot marigold) is grown commercially for herbal teas and the potpourri industry. Echinacea (Echinacea purpurea) is used as a medicinal tea. Winter tarragon (also called Mexican mint marigold), or Tagetes lucida, is commonly grown and used as a tarragon substitute in climates where tarragon will not survive. Finally, the wormwood genus Artemisia includes absinthe (A. absinthium) and tarragon (A. dracunculus).

Compositae have also been used for industrial purposes. Common in all commercial poultry feed, marigold (Tagetes patula) is grown primarily in Mexico and Central American nations. Marigold oil, extracted from Tagetes minuta, is used in the cola and cigarette industries.

Plants in Asteraceae are medically important in areas that don't have access to Western medicine. They are also commonly featured in medical and phytochemical journals because the sesquiterpene lactone compounds contained within them are an important cause of allergic contact dermatitis. Allergy to these compounds is the leading cause of allergic contact dermatitis in florists in the US.[21] Pollen from ragweed Ambrosia is among the main causes of so-called hay fever in the United States.[22]

Many members of Asteraceae are copious nectar producers and are useful for evaluating pollinator populations during their bloom. Centaurea (knapweed), Helianthus annuus (domestic sunflower), and some species of Solidago (goldenrod) are major "honey plants" for beekeepers. Solidago produces relatively high protein pollen, which helps honey bees over winter.[citation needed]

Some members of the Asteraceae are economically important as weeds. Notable in the United States are the ragwort, Senecio jacobaea, groundsel Senecio vulgaris, and Taraxacum (dandelion).

The genera Chrysanthemum, Pulicaria, Tagetes, and Tanacetum contain species with useful insecticidal properties.[citation needed]

Parthenium argentatum (guayule) is a source of hypoallergenic latex.

Genera[edit]

See also[edit]

References[edit]

  1. ^ Scott, L.; Cadman, A; McMillan, I (2006). "Early history of Cainozoic Asteraceae along the Southern African west coast". Review of Palaeobotany and Palynology 142: 47. doi:10.1016/j.revpalbo.2006.07.010. 
  2. ^ Angiosperm Phylogeny Group (2009), "An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG III", Botanical Journal of the Linnean Society 161 (2): 105–121, doi:10.1111/j.1095-8339.2009.00996.x, retrieved 10 December 2010 
  3. ^ Germplasm Resources Information Network (GRIN). "Family: Asteraceae Bercht. & J. Presl, nom. cons.". Taxonomy for Plants. USDA, ARS, National Genetic Resources Program, National Germplasm Resources Laboratory, Beltsville, Maryland. Retrieved 12 June 2008. 
  4. ^ Great Basin Wildflowers, Laird R. Blackwell, 2006, p. 275
  5. ^ a b c d e f Stevens, P. F. (2001 onwards) Angiosperm Phylogeny Website. Version 13, updated: 04/19/2014 19:57:49
  6. ^ Jeffrey, C. 2007. Compositae: Introduction with key to tribes. Pages 61-87 in Families and Genera of Vascular Plants, vol. VIII, Flowering Plants, Eudicots, Asterales (J. W. Kadereit and C. Jeffrey, eds.). Springer-Verlag, Berlin
  7. ^ a b Panero, J.L., Crozier, B.S. Tree of Life - Asteraceae
  8. ^ International Code of Botanical Nomenclature. In point 18/5 states: "The following names, used traditionally, are considered valid: Compositae (Asteraceae...).
  9. ^ a b Barkely, T.M., Brouillet, L., Strother, J.L. (2006) Flora of North America - Asteraceae" http://www.efloras.org/florataxon.aspx?flora_id=1&taxon_id=10074
  10. ^ Dr. Duke's Phytochemical and Ethnobotanical Databases
  11. ^ "dandelion Taraxacum officinale". Invasive Plant Atlas of the United States. Retrieved 10 September 2012. 
  12. ^ Merriam-Webster Dictionary. Aster. http://www.merriam-webster.com/dictionary/aster
  13. ^ International Code of Botanical Nomenclature - Article 18.5 http://ibot.sav.sk/icbn/main.htm
  14. ^ Solbrig, O.T. (1963) Subfamilial Nomenclature of Compositae. Taxon 12: 229-235 JSTOR 1216917
  15. ^ Panero, J.L., Funk, V.A. (2002) Toward a phylogenetic subfamilial classification for the Compositae (Asteraceae). Proc. Biol. Soc. Wash. 115: 909-922.
  16. ^ a b c d Judd, W.S., Campbell, C.S., Kellogg, E.A., Stevens, P.F. (2007) Plant Systematics: A Phylogenetic Approach. Sinauer Associates, Sunderland.
  17. ^ a b c d e f g h i j k l m n o p q r s t u v w x y Sia Morhardt, Emil Morhardt, California Desert Flowers, University of California Press, pp. 29-32
  18. ^ a b c d Pam MacKay, Mojave Desert Wildflowers, illustration p. 35
  19. ^ Usher, G. (1966) A dictionary of botany, including terms used in bio-chemistry, soil science, and statistics. LCCN 66 0 25447
  20. ^ McKenzie, R.J., Samuel, J., Muller, E.M., Skinner, A.K.W., Barker, N.P. (2005). "Morphology Of Cypselae In Subtribe Arctotidinae (Compositae–Arctotideae) And Its Taxonomic Implications". Annals of the Missouri Botanical Garden 92 (4): 569–594. 
  21. ^ Odom, R.B., James, W.D., Berger, T.G. (2000). Andrews' Diseases of the Skin: Clinical Dermatology. W.B. Saunders Company. pp. 1135 pages. ISBN 0-7216-5832-6. 
  22. ^ Asthma and Allergy Foundation of America. Ragweed Allergy. http://www.aafa.org/display.cfm?id=9&sub=19&cont=267

External links[edit]