Allium Explained

Allium is a genus of monocotyledonous flowering plants with hundreds of species, including the cultivated onion, garlic, scallion, shallot, leek, and chives. It is one of about 57 genera of flowering plants with more than 500 species.[1] It is by far the largest genus in the Amaryllidaceae, and also in the Alliaceae in classification systems in which that family is recognized as separate.[2]

Allium species occur in temperate climates of the Northern Hemisphere, except for a few species occurring in Chile (such as A. juncifolium), Brazil (A. sellovianum), and tropical Africa (A. spathaceum). They vary in height between NaNcm (-2,147,483,648inches). The flowers form an umbel at the top of a leafless stalk. The bulbs vary in size between species, from small (around 2–3 mm in diameter) to rather large (8–10 cm). Some species (such as Welsh onion A. fistulosum and leeks (A. ampeloprasum)) develop thickened leaf-bases rather than forming bulbs as such.

Carl Linnaeus first described the genus Allium in 1753. The generic name Allium is the Latin word for garlic,[3] and the type species for the genus is Allium sativum which means "cultivated garlic".[4] The decision to include a species in the genus Allium is taxonomically difficult, and species boundaries are unclear. Estimates of the number of species are as low as 260, and as high as 979.[5] In the APG III classification system, Allium is placed in the family Amaryllidaceae, subfamily Allioideae (formerly the family Alliaceae).[6] In some of the older classification systems, Allium was placed in Liliaceae.[7] [8] [9] [10] Molecular phylogenetic studies have shown this circumscription of Liliaceae is not monophyletic.

Various Allium have been cultivated from the earliest times, and about a dozen species are economically important as crops, or garden vegetables, and an increasing number of species are important as ornamental plants.[11] Plants of the genus produce chemical compounds, mostly derived from cysteine sulfoxides, that give them a characteristic onion or garlic taste and odor. Many are used as food plants, though not all members of the genus are equally flavorful. In most cases, both bulb and leaves are edible. The characteristic Allium flavor depends on the sulfate content of the soil the plant grows in. In the rare occurrence of sulfur-free growth conditions, all Allium species completely lose their usual pungency.

Description

The genus Allium (alliums) is characterised by herbaceous geophyte perennials with true bulbs, some of which are borne on rhizomes, and an onion or garlic odor and flavor.

The bulbs are solitary or clustered and tunicate and the plants are perennialized by the bulbs reforming annually from the base of the old bulbs, or are produced on the ends of rhizomes or, in a few species, at the ends of stolons. A small number of species have tuberous roots. The bulbs' outer coats are commonly brown or grey, with a smooth texture, and are fibrous, or with cellular reticulation. The inner coats of the bulbs are membranous.

Many alliums have basal leaves that commonly wither away from the tips downward before or while the plants flower, but some species have persistent foliage. Plants produce from one to 12 leaves, most species having linear, channeled or flat leaf blades. The leaf blades are straight or variously coiled, but some species have broad leaves, including A. victorialis and A. tricoccum. The leaves are sessile, and very rarely narrowed into a petiole.

The flowers, which are produced on scapes are erect or in some species pendent, having six petal-like tepals produced in two whorls. The flowers have one style and six epipetalous stamens; the anthers and pollen can vary in color depending on the species. The ovaries are superior, and three-lobed with three locules.

The fruits are capsules that open longitudinally along the capsule wall between the partitions of the locule.[12] [13] The seeds are black, and have a rounded shape.

The terete or flattened flowering scapes are normally persistent. The inflorescences are umbels, in which the outside flowers bloom first and flowering progresses to the inside. Some species produce bulbils within the umbels, and in some species, such as Allium paradoxum, the bulbils replace some or all the flowers. The umbels are subtended by noticeable spathe bracts, which are commonly fused and normally have around three veins.

Some bulbous alliums increase by forming little bulbs or "offsets" around the old one, as well as by seed. Several species can form many bulbils in the flowerhead; in the so-called "tree onion" or Egyptian onion (A. × proliferum) the bulbils are few, but large enough to be pickled.

Many of the species of Allium have been used as food items throughout their ranges. There are several unrelated species that are somewhat similar in appearance to Alliums but are poisonous (e.g. in North America, death camas, Toxicoscordion venenosum), but none of these has the distinctive scent of onions or garlic.[14] [15]

Taxonomy

See main article: Taxonomy of Allium. With over 850 species Allium is the sole genus in the Allieae, one of four tribes of subfamily Allioideae (Amaryllidaceae). New species continue to be described and Allium is one of the largest monocotyledonous genera, but the precise taxonomy of Allium is poorly understood, with incorrect descriptions being widespread. The difficulties arise from the fact that the genus displays considerable polymorphism and has adapted to a wide variety of habitats. Furthermore, traditional classifications had been based on homoplasious characteristics (the independent evolution of similar features in species of different lineages). However, the genus has been shown to be monophyletic, containing three major clades, although some proposed subgenera are not. Some progress is being made using molecular phylogenetic methods, and the internal transcribed spacer (ITS) region, including the 5.8S rDNA and the two spacers ITS1 and ITS2, is one of the more commonly used markers in the study of the differentiation of the Allium species.

Allium includes a number of taxonomic groupings previously considered separate genera (Caloscordum Herb., Milula Prain and Nectaroscordum Lindl.) Allium spicatum had been treated by many authors as Milula spicata, the only species in the monospecific genus Milula. In 2000, it was shown to be embedded in Allium.

History

When Linnaeus formerly described the genus Allium in his Species Plantarum (1753), there were thirty species with this name. He placed Allium in a grouping he referred to as Hexandria monogynia (i.e. six stamens and one pistil) containing 51 genera in all.

Subdivision

Linnaeus originally grouped his 30 species into three alliances, e.g. Foliis caulinis planis. Since then, many attempts have been made to divide the growing number of recognised species into infrageneric subgroupings, initially as sections, and then as subgenera further divided into sections. For a brief history, see Li et al. (2010) The modern era of phylogenetic analysis dates to 1996. In 2006 Friesen, Fritsch, and Blattner described a new classification with 15 subgenera, 56 sections, and about 780 species based on the nuclear ribosomal gene internal transcribed spacers. Some of the subgenera correspond to the once separate genera (Caloscordum, Milula, Nectaroscordum) included in the Gilliesieae. The terminology has varied with some authors subdividing subgenera into Sections and others Alliances. The term Alliance has also been used for subgroupings within species, e.g. Allium nigrum, and for subsections.

Subsequent molecular phylogenetic studies have shown the 2006 classification is a considerable improvement over previous classifications, but some of its subgenera and sections are probably not monophyletic. Meanwhile, the number of new species continued to increase, reaching 800 by 2009, and the pace of discovery has not decreased. Detailed studies have focused on a number of subgenera, including Amerallium. Amerallium is strongly supported as monophyletic. Subgenus Melanocrommyum has also been the subject of considerable study (see below), while work on subgenus Allium has focussed on section Allium, including Allium ampeloprasum, although sampling was not sufficient to test the monophyly of the section.

The major evolutionary lineages or lines correspond to the three major clades. Line one (the oldest) with three subgenera is predominantly bulbous, the second, with five subgenera and the third with seven subgenera contain both bulbous and rhizomatous taxa.

Evolutionary lines and subgenera

See also: List of Allium species. The three evolutionary lineages and 15 subgenera here represent the classification schemes of Friesen et al. (2006) and Li (2010), and subsequent additional species and revisions.

Evolutionary lines and subgenera (number of sections/number of species)

First evolutionary line

Although this lineage consists of three subgenera, nearly all the species are attributed to subgenus Amerallium, the third largest subgenus of Allium. The lineage is considered to represent the most ancient line within Allium, and to be the only lineage that is purely bulbous, the other two having both bulbous and rhizomatous taxa. Within the lineage Amerallium is a sister group to the other two subgenera (Microscordum+Nectaroscordum).

Second evolutionary line

Nearly all the species in this lineage of five subgenera are accounted for by subgenus Melanocrommyum, which is most closely associated with subgenera Vvedenskya and Porphyroprason, phylogenetically. These three genera are late-branching whereas the remaining two subgenera, Caloscordum and Anguinum, are early branching.

Third evolutionary line

The third evolutionary line contains the greatest number of sections (seven), and also the largest subgenus of the genus Allium: subgenus Allium, which includes the type species of the genus, Allium sativum. This subgenus also contains the majority of the species in its lineage. Within the lineage, the phylogeny is complex. Two small subgenera, Butomissa and Cyathophora form a sister clade to the remaining five subgenera, with Butomissa as the first branching group. Amongst the remaining five subgenera, Rhizirideum forms a medium-sized subgenus that is the sister to the other four, larger, subgenera. This line may not be monophyletic.

Proposed infrageneric groups

Names from[16]

Etymology

Some sources refer to Greek ἀλέω (aleo, to avoid) due to the odor of garlic.

Distribution and habitat

The majority of Allium species are native to the Northern Hemisphere, being spread throughout the holarctic region, from dry subtropics to the boreal zone, predominantly in Asia. Of the latter, 138 species occur in China, about a sixth of all Allium species, representing five subgenera. A few species are native to Africa and Central and South America.[12] A single known exception, Allium dregeanum occurs in the Southern Hemisphere (South Africa). There are two centres of diversity, a major one from the Mediterranean Basin to Central Asia and Pakistan, while a minor one is found in western North America. The genus is especially diverse in the eastern Mediterranean.

Ecology

Species grow in various conditions from dry, well-drained mineral-based soils to moist, organic soils; most grow in sunny locations, but a number also grow in forests (e.g., A. ursinum),[7] or even in swamps or water.

Various Allium species are used as food plants by the larvae of the leek moth and onion fly[7] as well as other Lepidoptera including cabbage moth, common swift moth (recorded on garlic), garden dart moth, large yellow underwing moth, nutmeg moth, setaceous Hebrew character moth, turnip moth and Schinia rosea, a moth that feeds exclusively on Allium species.

Genetics

The genus Allium has very large variation between species in their genome size that is not accompanied by changes in ploidy level.[17] This remarkable variation was noted in the discussion of the evolution of junk DNA and resulted in the Onion Test, a "reality check for anyone who thinks they have come up with a universal function for junk DNA".[18] Genome sizes vary between 7.5 Gb in A. schoenoprasum and 30.9 Gb in A. ursinum, both of which are diploid.

Telomere

The unusual telomeric sequence of 'Allium cepa' was discovered and cytologically validated to be CTCGGTTATGGG [19] A bioinformatics method for detecting this unique telomere sequence was demonstrated using SERF de novo Genome Analysis[20]

Cultivation

Many Allium species have been harvested through human history, but only about a dozen are still economically important today as crops or garden vegetables.[7] [21]

Ornamental

Many Allium species and hybrids are cultivated as ornamentals.[22] These include A. cristophii and A. giganteum, which are used as border plants for their ornamental flowers, and their "architectural" qualities.[11] [23] Several hybrids have been bred, or selected, with rich purple flowers. A. hollandicum 'Purple Sensation' is one of the most popular and has been given an Award of Garden Merit (H4).[24] These ornamental onions produce spherical umbels on single stalks in spring and summer, in a wide variety of sizes and colours, ranging from white (Allium 'Mont Blanc'), blue (A. caeruleum), to yellow (A. flavum) and purple (A. giganteum). By contrast, other species (such as invasive A. triquetrum and A. ursinum) can become troublesome garden weeds.[23] [25]

The following cultivars, of uncertain or mixed parentage, have gained the Royal Horticultural Society's Award of Garden Merit:

Toxicity

Dogs and cats are very susceptible to poisoning after the consumption of certain species.[7] [33] Even cattle have suffered onion toxicosis.[34] Vegetables of the Allium genus can cause digestive disorders for human beings.[35]

Uses

The genus includes many economically important species. These include onions (A. cepa), French shallots (A. oschaninii), leeks (A. ampeloprasum), garlic (A. sativum), and herbs such as scallions (various Allium species) and chives (A. schoenoprasum). Some have been used as traditional medicines.

This genus also includes species that are abundantly gathered from the wild such as wild garlic (Allium ursinum) in Europe and ramps (Allium tricoccum) in North America.

Sources

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Notes and References

  1. Frodin . David G. . 2004 . History and concepts of big plant genera . Taxon . 53 . 3 . 753–776 . 10.2307/4135449 . 4135449.
  2. Knud Rahn. 1998. "Alliaceae" pages 70-78. In: Klaus Kubitzki (editor). The Families and Genera of Vascular Plants volume III. Springer-Verlag: Berlin;Heidelberg, Germany.
  3. Gledhill, David (2008). "The Names of Plants". Cambridge University Press. (hardback), (paperback). pp 43
  4. Allium In: Index Nominum Genericorum. In: Regnum Vegetabile (see below).
  5. https://web.archive.org/web/20210616150912/http://www.theplantlist.org/tpl/search?q=Allium The Plant List, for genus Allium
  6. Chase . M.W. . Reveal . J.L. . Fay . M.F. . amp . 2009 . A subfamilial classification for the expanded asparagalean families Amaryllidaceae, Asparagaceae and Xanthorrhoeaceae . Botanical Journal of the Linnean Society . 161 . 2 . 132–136 . 10.1111/j.1095-8339.2009.00999.x . free.
  7. Book: Eric Block . Garlic and Other Alliums: The Lore and the Science . Royal Society of Chemistry . 2010 . 978-0-85404-190-9.
  8. James L. Brewster, "Onions and Other Alliums" (Wallingford: CABI Publishing, 2008)
  9. Haim D. Rabinowitch, Leslie Currah, "Allium Crop Sciences: Recent Advances" (Wallingford: CABI Publishing, 2002)
  10. Penny Woodward, "Garlic and Friends: The History, Growth and Use of Edible Alliums" (South Melbourne: Hyland House, 1996)
  11. Book: Dilys Davies . Alliums: The Ornamental Onions . Timber Press . 1992 . 978-0-88192-241-7 .
  12. Web site: Allium in Flora of China @ . Efloras.org . 2012-12-11.
  13. Web site: Allium in Flora of North America @ . Efloras.org . 2012-12-11.
  14. Peterson, R.P. 1982. A Field Guide to Edible Wild Plants: Eastern and central North America. Houghton Mifflin, Boston.
  15. Gibbons, E. 1962. Stalking the wild asparagus. David McKay, New York.
  16. Web site: Tropicos .
  17. Ricroch. A.. Yockteng. R.. Brown. S C. Nadot. S. 14787301. 2005. Evolution of genome size across some cultivated Allium species. Genome. en. 48. 3. 511–520. 10.1139/g05-017. 0831-2796. 16121247.
  18. Freeling. Michael. Xu. Jie. Woodhouse. Margaret. Lisch. Damon. 2015. A Solution to the C-Value Paradox and the Function of Junk DNA: The Genome Balance Hypothesis. Molecular Plant. en. 8. 6. 899–910. 10.1016/j.molp.2015.02.009. 25743198. free.
  19. Allium telomeres unmasked . The Plant Journal . Petr Fajkus et el, The Plant Journal . December 2015. 85 . 3 . 337–347 . 10.1111/tpj.13115 . Fajkus . Petr . Peška . Vratislav . Sitová . Zdeňka . Fulnečková . Jana . Dvořáčková . Martina . Gogela . Roman . Sýkorová . Eva . Hapala . Jan . Fajkus . Jiří . 26716914 .
  20. Web site: Allium cepa Telomere . SERF de novo Genome Analysis, BioSerf . July 2018.
  21. Book: Simon & Schuster's Guide to Herbs and Spices . Stanley Schuler . 978-0-671-73489-3 . Simonetti, Gualtiero . 1990 . Simon & Schuster, Inc .
  22. [Anthony Huxley]
  23. Brickell, Christopher (Editor-in-chief), The Royal Horticultural Society A–Z Encyclopedia of Garden Plants, p. 95, Dorling Kindersley, London, 1996,
  24. RHS Plant Finder 2009–2010, p. 68, Dorling Kindersley, London, 2009,
  25. Lloyd, Christopher & Rice, Graham, (1991). Garden Flowers From Seed, p. 45, Viking,
  26. Web site: RHS Plantfinder - Allium 'Ambassador'. Royal Horticultural Society . 2016 . 5 January 2018.
  27. Web site: RHS Plantfinder - Allium 'Beau Regard'. Royal Horticultural Society . 1995 . 5 January 2018.
  28. Web site: RHS Plantfinder - Allium 'Gladiator'. Royal Horticultural Society . 1995 . 5 January 2018.
  29. Web site: RHS Plantfinder - Allium 'Globemaster'. Royal Horticultural Society . 1995 . 5 January 2018.
  30. Web site: Allium rosenorum 'Michael H. Hoog' . RHS . 27 February 2020.
  31. Web site: RHS Plantfinder - Allium 'Round 'n' Purple'. Royal Horticultural Society . 2016 . 5 January 2018.
  32. Web site: Allium 'Universe'. RHS . 27 February 2020.
  33. R.B. . Cope . Toxicology Brief: Allium species poisoning in dogs and cats . Veterinary Medicine . August 2005 . 100 . 8 . 562–566 . Edwardsville, Kansas. 1939-1919 . 8750-7943 . Peer-reviewed..
  34. Helen A. . Rae . Onion toxicosis in a herd of beef cows . . January 1999 . 40 . 1 . 55–57 . 9919370 . 1539652 . While humans appear to be relatively resistant to onion toxicity, there is some concern about the susceptibility of certain ethnic groups that have a genetic deficiency of G6PD. / Onion toxicity depends on factors other than variation in species susceptibility. Onions contain varying amounts of disulfide and SMCO toxins, depending on the species of onion, time of year, and growing conditions. Storing onions in large piles also provides a suitable environment for contamination of the crop with other toxins, such as mycotoxins, which could contribute to the disease process..
  35. Book: Singh, Zoomi . Potential Side Effects of Chives . Chives: Nutritional Value, Health Benefits and Potential Side Effects of Chives . October 12, 2022 . Singapore. HealthifyMe . https://www.healthifyme.com/blog/chives-benefits/#Potential_Side_Effects_of_Chives . March 17, 2023.

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