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Classification System: APG IV

Superregnum: Eukaryota
Regnum: Plantae
Cladus: Angiosperms
Cladus: Monocots
Cladus: Commelinids
Ordo: Poales

Familia: Poaceae
Subfamilia: Panicoideae
Tribus: Andropogoneae
Subtribus: Tripsacinae
Genus: Zea
Sectiones: Z. sect. Luxuriantes – Z. sect. Zea

Species: Z. diploperennisZ. luxuriansZ. mays - Z. mexicanaZ. nicaraguensis - Z. perennis

Name

Zea L. Sp. Pl. 2: 971. (1753)

Type species: Zea mays L. sp. Pl. 971–972. (1753)

Synonyms

Heterotypic
Mays Mill., Gard. Dict. Abr. ed. 4: s.p. (1754), nom. superfl.
Mais Adans., Fam. Pl. 2: 39, 573 (1763), nom. superfl.
Mayzea Raf., Med. Fl. 2: 241 (1830).
Euchlaena Schrad., Index Seminum (GOET) 1832: 3 (1832).
Reana Brign., Ann. Sci. Nat., Bot., III, 12: 365 (1849).
Thalysia Kuntze, Revis. Gen. Pl. 2: 794 (1891), nom. superfl.
× Euchlaezea Jan.Ammal ex Bor, Grass. Burma, Ceylon, India & Pakistan: 266 (1960).

References

Linnaeus, C. 1753. Species Plantarum 2: 971.
Clayton, W.D., Vorontsova, M.S., Harman, K.T. and Williamson, H. (2006 onwards) GrassBase - The Online World Grass Flora. Zea. Published online. Accessed 24 Sept. 2013.
Govaerts, R. et al. 2013. Zea in World Checklist of Selected Plant Families. The Board of Trustees of the Royal Botanic Gardens, Kew. Published on the internet. Accessed: 2013 Sept. 21. Reference page.
Tropicos.org 2013. Zea. Missouri Botanical Garden. Published on the internet. Accessed: 2013 Sept. 21.
International Plant Names Index. 2013. Zea. Published online. Accessed: 21. Sept. 2013.
Wang, P., Lu, Y., Zheng, M., Rong, T. & Tang, Q. 2011. RAPD and internal transcribed spacer sequence analyses reveal Zea nicaraguensis as a section Luxuriantes species close to Zea luxurians. PLoS ONE 6(4): e16728. DOI: 10.1371/journal.pone.0016728 Open access Reference page.
GBIF.

Vernacular names
беларуская: Кукуруза
dansk: Majs-slægten
English: Teosinte
suomi: Maissit
Nordfriisk: Meis
français: Téosinte
magyar: Kukorica nemzettség
русский: Кукуруза

Zea is a genus of flowering plants in the grass family. The best-known species is Z. mays (variously called maize, corn, or Indian corn), one of the most important crops for human societies throughout much of the world. Several wild species are commonly known as teosintes and are native to Mesoamerica.

Etymology

Zea is derived from the Greek name (ζειά) for another cereal grain (possibly spelt).[2]
Recognized species
teosinte (top), maize-teosinte hybrid (middle), maize (bottom)

The five accepted species names in the genus are:[3][4]

Ear Plant Scientific name Common Name Distribution
Perennial Teosinte ear (Zea diploperennis) - Detail.jpg Zea diploperennis01.jpg Zea diploperennis H.H.Iltis et al. diploperennial teosinte Jalisco
Pl. I Report of the Commissioner of Agriculture (U.S.) 1887.jpg
Zea luxurians (Durieu & Asch.) R.M.Bird Maíz de Monte, Florida teosinte and Guatemalan teosinte Chiapas, Guatemala, Honduras
Maize J7.jpg Belize - panoramio (47).jpg Zea mays L. Corn, Maize southern Mexico, Guatemala; cultivated in many places
Zea nicaraguensis H.H.Iltis & B.F.Benz Nicaraguan teosinte Nicaragua
Zea perennis (Hitchc.) Reeves & Mangelsd. perennial teosinte Jalisco

Zea mays is further divided into four subspecies: Z. m. huehuetenangensis, Z. m. mexicana, Z. m. parviglumis (Balsas teosinte, the ancestor of maize), and Z. m. mays. The first three subspecies are teosintes; the last is maize, or corn,[4] the only domesticated taxon in the genus Zea.

The genus is divided into two sections: Luxuriantes, with Z. diploperennis, Z. luxurians, Z. nicaraguensis, Z. perennis; and Zea with Z. mays. The former section is typified by dark-staining knobs made up of heterochromatin that are terminal on most chromosome arms, while most subspecies of section Zea may have none to three knobs between each chromosome end and the centromere and very few terminal knobs (except Z. m. huehuetenangensis, which has many large terminal knobs).
Description
Microscopic view of Zea seed

Both annual and perennial teosinte species occur. Z. diploperennis and Z. perennis are perennial, while all other species are annual. All species are diploid (n=10) with the exception of Z. perennis, which is tetraploid (n=20). The different species and subspecies of teosinte can be readily distinguished based on morphological, cytogenetic, protein, and DNA differences and on geographic origin. The two perennials are sympatric and very similar and some consider them to be one species. What many consider to be the most puzzling teosinte is Z. m. huehuetenangensis, which combines a morphology rather like Z. m. parviglumis with many terminal chromosome knobs and an isozyme position between the two sections. Considered to be phenotypically the most distinctive, as well as the most threatened, teosinte is Zea nicaraguensis. This teosinte thrives in flooded conditions along 200 m of a coastal estuarine river in northwest Nicaragua.

Teosintes strongly resemble maize in many ways, notably their tassel (male inflorescence) morphology. Teosintes are distinguished from maize most obviously by their numerous branches each bearing bunches of distinctive, small female inflorescences. These spikes mature to form a two-ranked 'ear' of five to 10 triangular or trapezoidal, black or brown disarticulating segments, each with one seed. Each seed is enclosed by a very hard fruitcase, consisting of a cupule or depression in the rachis and a tough lower glume. This protects them from the digestive processes of ruminants that forage on teosinte and aid in seed distribution through their droppings. Teosinte seed exhibits some resistance to germination, but will quickly germinate if treated with a dilute solution of hydrogen peroxide.
Origin of maize and interaction with teosintes

Teosintes are critical components of maize evolution, but opinions vary about which taxa were involved. According to the most widely held evolutionary model, the crop was derived directly from Z. m. parviglumis by selection of key mutations;[5] but in some varieties up to 20% of its genetic material came from Z. m. mexicana through introgression.[6]

All but the Nicaraguan species of teosinte may grow in or very near corn fields, providing opportunities for introgression between teosinte and maize. First, and later-generation hybrids are often found in the fields, but the rate of gene exchange is quite low. Some populations of Z. m. mexicana display Vavilovian mimicry within cultivated maize fields, having evolved a maize-like form as a result of the farmers' selective weeding pressure. In some areas of Mexico, teosintes are regarded by maize farmers as a noxious weed, while in a few areas, farmers regard it as a beneficial companion plant, and encourage its introgression into their maize.
Early dispersal of maize in the Americas

According to Matsuoka et al., the available early maize gene pool can be divided into three clusters:

An Andean group, that includes the hand-grenade-shaped ear types and some other Andean maize (35 plants);
All other South American and Mexican maize (80 plants);
U.S. maize (40 plants)

Also, some other intermediate genomes, or admixtures of these clusters occur.

According to these authors, "The maize of the Andes Mountains with its distinctive hand grenade-shaped ears was derived from the maize of lowland South America, which in turn came from maize of the lowlands of Guatemala and southern Mexico."[5]
Ecology

Zea species are used as food plants by the larvae (caterpillars) of some Lepidoptera species including (in the Americas) the fall armyworm (Spodoptera frugiperda), the corn earworm (Helicoverpa zea), and the stem borers Diatraea and Chilo; in the Old World, it is attacked by the double-striped pug, the cutworms heart and club and heart and dart, Hypercompe indecisa, the rustic shoulder-knot, the setaceous Hebrew character and turnip moths, and the European corn borer (Ostrinia nubilalis), among many others.

Virtually all populations of teosintes are either threatened or endangered: Z. diploperennis exists in an area of only a few square miles; Z. nicaraguensis survives as about 6000 plants in an area of 200 × 150 m. The Mexican and Nicaraguan governments have taken action in recent years to protect wild teosinte populations, using both in situ and ex situ conservation methods. Currently, a large amount of scientific interest exists in conferring beneficial teosinte traits, such as nitrogen fixation,[7] insect resistance, perennialism, and flood tolerance, to cultivated maize lines, although this is very difficult due to linked deleterious teosinte traits.
References

Kew World Checklist of Selected Plant Families
Gledhill, David (2008). "The Names of Plants". Cambridge University Press. ISBN 9780521866453 (hardback), ISBN 9780521685535 (paperback). pp 411
"ITIS - Report: Zea".
Wu, Chi-Chih; Diggle, Pamela K.; Friedman, William E. (2011-03-06). "Female gametophyte development and double fertilization in Balsas teosinte, Zea mays subsp. parviglumis (Poaceae)". Sexual Plant Reproduction. International Association of Sexual Plant Reproduction Research (Springer). 24 (3): 219–229. doi:10.1007/s00497-011-0164-1. ISSN 0934-0882. PMID 21380710. S2CID 8045294.
Matsuoka, Y.; Vigouroux, Y; Goodman, MM; Sanchez G, J; Buckler, E; Doebley, J (2002). "A single domestication for maize shown by multilocus microsatellite genotyping". Proceedings of the National Academy of Sciences. 99 (9): 6080–4. doi:10.1073/pnas.052125199. PMC 122905. PMID 11983901.
Hufford, Matthew (2013). "The Genomic Signature of Crop-Wild Introgression in Maize". PLOS Genetics. 9 (5): e1003477. doi:10.1371/journal.pgen.1003477. PMC 3649989. PMID 23671421.
Van Deynze, Allen; Zamora, Pablo; Delaux, Pierre-Marc; Heitmann, Cristobal; et al. (August 7, 2018). "Nitrogen fixation in a landrace of maize is supported by a mucilage-associated diazotrophic microbiota". PLOS Biology. 16 (8): e2006352. doi:10.1371/journal.pbio.2006352. PMC 6080747. PMID 30086128.

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