Malvaceae

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Malvaceae
Malva parviflora small.jpg
Least mallow, Malva parviflora
Scientific classification edit
Kingdom: Plantae
Clade: Angiosperms
Clade: Eudicots
Clade: Rosids
Order: Malvales
Family: Malvaceae
Juss.[1]
Subfamilies
Synonyms[2]
  • Bombacaceae Kunth
  • Brownlowiaceae Cheek
  • Byttneriaceae R.Br.
  • Dombeyaceae Kunth
  • Durionaceae Cheek
  • Helicteraceae J.Agardh
  • Hermanniaceae Marquis
  • Hibiscaceae J.Agardh
  • Lasiopetalaceae Rchb.
  • Melochiaceae J.Agardh
  • Pentapetaceae Bercht. & J.Presl
  • Philippodendraceae A.Juss.
  • Plagianthaceae J.Agardh
  • Sparmanniaceae J.Agardh
  • Sterculiaceae Vent.
  • Theobromataceae J.Agardh
  • Tiliaceae Juss.

Malvaceae, or the mallows, is a family of flowering plants estimated to contain 244 genera with 4225 known species.[3][4] Well-known members of economic importance include okra, cotton, cacao and durian. There are also some genera containing familiar ornamentals, such as Alcea (hollyhock), Malva (mallow) and Lavatera (tree mallow). The largest genera in terms of number of species include Hibiscus (300 species), Sterculia (250 species), Dombeya (250 species), Pavonia (200 species) and Sida (200 species).[5]

Taxonomy and nomenclature

The circumscription of the Malvaceae is controversial. The traditional Malvaceae sensu stricto comprise a very homogeneous and cladistically monophyletic group. Another major circumscription, Malvaceae sensu lato, has been more recently defined on the basis that molecular techniques have shown the commonly recognised families Bombacaceae, Tiliaceae, and Sterculiaceae, which have always been considered closely allied to Malvaceae s.s., are not monophyletic groups. Thus, the Malvaceae can be expanded to include all of these families so as to compose a monophyletic group. Adopting this circumscription, the Malvaceae incorporate a much larger number of genera.[citation needed]

Subfamilies

This article is based on the second circumscription, as presented by the Angiosperm Phylogeny Website.[4] The Malvaceae s.l. (hereafter simply "Malvaceae") comprise nine subfamilies. A tentative cladogram of the family is shown below. The diamond denotes a poorly supported branching (<80%).

Byttnerioideae: 26 genera, 650 species, pan-tropical, especially South America

Grewioideae: 25 genera, 770 species, pan-tropical

Sterculioideae: 12 genera, 430 species, pan-tropical

Tilioideae: three genera, 50 species, northern temperate regions and Central America

Dombeyoideae: about 20 genera, about 380 species, palaeo-tropical, especially Madagascar and Mascarenes

Brownlowioideae: eight genera, about 70 species, especially palaeo-tropical

Helicteroideae: eight to 12 genera, 10 to 90 species, tropical, especially Southeast Asia

Malvoideae: 78 genera, 1,670 species, temperate to tropical

Bombacoideae: 12 genera, 120 species, tropical, especially Africa and America

It is important to point out the relationships between these subfamilies are still either poorly supported or almost completely obscure. There are continuing disagreements over the correct circumscription of these subfamilies, including the preservation of the family, Bombacaceae.[6] The circumscription of the family may change dramatically as new studies are published.

If looking for information about the traditional Malvaceae s.s., we recommend referring to Malvoideae, the subfamily that approximately corresponds to that group.

Synapomorphies

The relationships between the "core Malvales" families used to be defined on the basis of shared "malvean affinities." These included the presence of malvoid teeth, stems with mucilage canals, and stratified wedge-shaped phloem.[7] These affinities were problematic because they were not always shared within the core families.[8] Later studies revealed more unambiguous synapomorphies within Malvaceae s.l.. Synapomorphies identified within Malvaceae s.l. include the presence of tile cells, trichomatous nectaries, and an inflorescence structure called a bicolor unit.[9] Tile cells consist of vertically positioned cells interspersed between and dimensionally similar to procumbent ray cells. Evidence of Malvean wood fossils have confirmed their evolutionary link in Malvaceae s.l., as well explained their diverse structures.[10] Flowers of Malvaceae s.l. exhibit nectaries consisting of densely arranged multicellular hairs resembling trichomes. In most of Malvaceae s.l., these trichomatous nectaries are located on the inner surface of the sepals, but flowers of the subfamily, Tiliodeae, also have present nectaries on the petals.[11] Malvean flowers also share a unifying structure known as a bicolor unit, named for its initial discovery in the flowers of Theobroma bicolor. The bicolor unit consists of an ordered inflorescence with determinate cymose structures. The inflorescence can branch off the main axis, creating separate orders of the flowers, with the main axis developing first. Bracts on the peduncle subtend axillary buds that become these lateral stalks. One bract within this whorl is a sterile bract. The bicolor unit is a variable structure in complexity, but the presence of fertile and sterile bracts is a salient character.[12]

Names

The English common name 'mallow' (also applied to other members of Malvaceae) comes from Latin malva (also the source for the English word "mauve"). Malva itself was ultimately derived from the word for the plant in ancient Mediterranean languages.[13] Cognates of the word include Ancient Greek μαλάχη (malákhē) or μολόχη (molókhē), Modern Greek μολόχα (molóha), modern Arabic: ملوخية‎ (mulukhiyah) and modern Hebrew: מלוחיה‎ (molokhia).[13][14]

Description

Alcea rosea is a common garden flower in Malvaceae

Most species are herbs or shrubs, but some are trees and lianas.

Leaves and stems

Stellate hairs on the underside of a dried leaf of Malva alcea

Leaves are generally alternate, often palmately lobed or compound and palmately veined. The margin may be entire, but when dentate, a vein ends at the tip of each tooth (malvoid teeth). Stipules are present. The stems contain mucous canals and often also mucous cavities. Hairs are common, and are most typically stellate.[citation needed]. Stems of Bombacoideae are often covered in thick prickles.[15]

Flowers

The flowers are commonly borne in definite or indefinite axillary inflorescences, which are often reduced to a single flower, but may also be cauliflorous, oppositifolious, or terminal. They often bear supernumerary bracts in the structure of a bicolor unit.[12] They can be unisexual or bisexual, and are generally actinomorphic, often associated with conspicuous bracts, forming an epicalyx. They generally have five valvate sepals, most frequently basally connate, with five imbricate petals. The stamens are five to numerous, and connate at least at their bases, but often forming a tube around the pistils. The pistils are composed of two to many connate carpels. The ovary is superior, with axial placentation, with capitate or lobed stigma. The flowers have nectaries made of many tightly packed glandular hairs, usually positioned on the sepals.[11]

Fruits

Durian fruits

The fruits are most often loculicidal capsules, schizocarps or nuts.

Pollination

Self-pollination is often avoided by means of protandry. Most species are entomophilous (pollinated by insects). Bees from the Emphorini tribe of the Apidae (including Ptilothrix, Diadasia, and Melitoma) are known to specialize on the plants.

Importance

A number of species are pests in agriculture, including Abutilon theophrasti and Modiola caroliniana, and others that are garden escapes. Cotton (four species of Gossypium), kenaf (Hibiscus cannabinus), cacao (Theobroma cacao), kola nut (Cola spp.), and okra (Abelmoschus esculentus) are important agricultural crops. The fruit and leaves of baobabs are edible, as is the fruit of the durian. A number of species, including Hibiscus syriacus, Hibiscus rosa-sinensis and Alcea rosea are garden plants.

See also

References

  1. ^ Angiosperm Phylogeny Group (2009). "An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG III" (PDF). Botanical Journal of the Linnean Society. 161 (2): 105–121. doi:10.1111/j.1095-8339.2009.00996.x. Retrieved 2013-07-06.
  2. ^ "Family: Malvaceae". Germplasm Resources Information Network (GRIN) [Online Database]. United States Department of Agriculture Agricultural Research Service, Beltsville, Maryland. 17 January 2017. Retrieved 7 June 2017.
  3. ^ Christenhusz, M. J. M.; Byng, J. W. (2016). "The number of known plants species in the world and its annual increase". Phytotaxa. Magnolia Press. 261 (3): 201–217. doi:10.11646/phytotaxa.261.3.1.
  4. ^ a b "Angiosperm Phylogeny Website". Retrieved 15 July 2014.
  5. ^ Judd, W. S., C. S. Campbell, E. A. Kellogg, P. F. Stevens and M. J. Donoghue (2008). Plant Systematics: A Phylogenetic Approach (third ed.). ISBN 0878934073.
  6. ^ Refaat, J (2012). "Bombacaceae: A phytochemical review". Pharmaceutical Biology. 51: 100–130. doi:10.3109/13880209.2012.698286.
  7. ^ Kubitzki, K (2003). The Families and Genera of Vascular Plants. Berlin: Springer-Verlag.
  8. ^ Thorne, R (1992). "Classification and geography of the flowering plants". Bot. Rev. 58 (3): 225–348. doi:10.1007/bf02858611.
  9. ^ Bayer, C. (1999). "Support for an expanded family concept of Malvaceae within a recircumscribed order Malvales: a combined analysis of plastid atpB and rbcL DNA sequences". Botanical Journal of the Linnean Society. 129 (4): 267–303. doi:10.1111/j.1095-8339.1999.tb00505.x.
  10. ^ Manchester, Steven (1978). "Tile cells and their occurrence in Malvalean fossil woods". IA WA Bulletin: 23–28 – via ResearchGate.
  11. ^ a b Erbar, C (2014). "Nectar secretion and nectaries in basal angiosperms, magnoliids and non-core eudicots and a comparison with core eudicots". Plant Div. Evol. 131 (2): 63–143. doi:10.1127/1869-6155/2014/0131-0075.
  12. ^ a b Bayer, C (1999). "The bicolor unit — homology and transformation of an inflorescence structure unique to core Malvales". Plant Systematics and Evolution. 214: 187–198. doi:10.1007/bf00985738.
  13. ^ a b Douglas Harper. "mallow". Online Etymology Dictionary. Retrieved February 3, 2012.
  14. ^ Khalid. "Molokheya: an Egyptian National Dish". THe Baheyeldin Dynasty. Retrieved September 10, 2011.
  15. ^ Heywood, V (2007). Flowering Plant Families of the World. Richmond Hill, Ontario, Canada: Firefly Books.
  • Baum, D. A., W. S. Alverson, and R. Nyffeler (1998). "A durian by any other name: taxonomy and nomenclature of the core Malvales". Harvard Papers in Botany. 3: 315–330.
  • Baum, D. A.; Dewitt Smith, S.; Yen, A.; Alverson, W. S.; Nyffeler, R.; Whitlock, B. A.; Oldham, R. L. (2004). "Phylogenetic relationships of Malvatheca (Bombacoideae and Malvoideae; Malvaceae sensu lato) as inferred from plastid DNA sequences". American Journal of Botany. 91 (11): 1863–1871. doi:10.3732/ajb.91.11.1863. PMID 21652333.
  • Bayer, C. (1999). "Support for an expanded family concept of Malvaceae within a recircumscribed order Malvales: a combined analysis of plastidatpB andrbcL DNA sequences". Botanical Journal of the Linnean Society. 129 (4): 267–303. doi:10.1006/bojl.1998.0226.
  • Bayer, C. and K. Kubitzki 2003. Malvaceae, pp. 225–311. In K. Kubitzki (ed.), The Families and Genera of Vascular Plants, vol. 5, Malvales, Capparales and non-betalain Caryophyllales.
  • Edlin, H. L. (1935). "A Critical Revision of Certain Taxonomic Groups of the Malvales Part Ii1". New Phytologist. 34 (2): 122–143. doi:10.1111/j.1469-8137.1935.tb06834.x.
  • Judd, W. S.; Manchester, S. R. (1997). "Circumscription of Malvaceae (Malvales) as Determined by a Preliminary Cladistic Analysis of Morphological, Anatomical, Palynological, and Chemical Characters". Brittonia. 49 (3): 384–405. doi:10.2307/2807839. JSTOR 2807839.
  • Maas, P. J. M. and L. Y. Th. Westra. 2005. Neotropical Plant Families (3rd edition).
  • Perveen, A.; Grafström, E.; El-Ghazaly†, G. (2004). "World Pollen and Spore Flora 23. Malvaceae Adams. P.p. Subfamilies: Grewioideae, Tilioideae, Brownlowioideae". Grana. 43 (3): 129. doi:10.1080/00173130410000730. ISSN 0017-3134.
  • Tate, J. A., J. F. Aguilar, S. J. Wagstaff, J. C. La Duke, T. A. Bodo Slotta and B. B. Simpson (2005). "Phylogenetic relationships within the tribe Malveae (Malvaceae, subfamily Malvoideae) as inferred from ITS sequence data". American Journal of Botany. 92 (4): 584–602. doi:10.3732/ajb.92.4.584. PMID 21652437. (abstract online here).
  • Alverson, William S.; Whitlock, Barbara A.; Nyffeler, Reto; Bayer, Clemens; Baum, David A. (1999). "Phylogeny of the core Malvales: evidence from ndhF sequence data". American Journal of Botany. 86 (10): 1474–1486. doi:10.2307/2656928. JSTOR 2656928.

External links

  • Malvaceae.info: Malvaceae Gallery
  • Topwalks.net: Malvaceae
  • Tree of Life.org: Core Malvales
  • HEAR.org — Malvaceae: plants of Hawaiiimage gallery.
  • GREIF Flora: Malvaceae of Mongolia
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