Ricinus
Ricinus communis | |
---|---|
Leaves and flowers (male flowers on top) of a Castor oil plant | |
Scientific classification | |
Kingdom: | Plantae |
(unranked): | Angiosperms |
(unranked): | Eudicots |
(unranked): | Rosids |
Order: | Malpighiales |
Family: | Euphorbiaceae |
Subfamily: | Acalyphoideae |
Tribe: | Acalypheae |
Subtribe: | Ricininae[1] |
Genus: | Ricinus L. |
Species: | R. communis |
Binomial name | |
Ricinus communis L. | |
Ricinus communis, the castorbean[2] or castor-oil-plant,[3] is a species of flowering plant in the spurge family, Euphorbiaceae. It is the sole species in the monotypic genus, Ricinus, and subtribe, Ricininae. The evolution of castor and its relation to other species are currently being studied using modern genetic tools.[4] It reproduces with a mixed pollination system which favor selfing by geitonogamy but at the same time can be an out-crosser by anemophily or entomophily.[1]
Its seed is the castor bean, which, despite its name, is not a true bean. Castor is indigenous to the southeastern Mediterranean Basin, Eastern Africa, and India, but is widespread throughout tropical regions (and widely grown elsewhere as an ornamental plant).[5]
Castor seed is the source of castor oil, which has a wide variety of uses. The seeds contain between 40% and 60% oil that is rich in triglycerides, mainly ricinolein. The seed also contains ricin, a water-soluble toxin, which is also present in lower concentrations throughout the plant.
An unrelated plant species, Fatsia japonica, is similar in appearance and known as the false castor oil plant.
Description
Ricinus communis can vary greatly in its growth habit and appearance. The variability has been increased by breeders who have selected a range of cultivars for leaf and flower colours, and for oil production. It is a fast-growing, suckering perennial shrub that can reach the size of a small tree (around 12 metres or 39 feet), but it is not cold hardy.
The glossy leaves are 15–45 centimetres (5.9–17.7 in) long, long-stalked, alternate and palmate with 5–12 deep lobes with coarsely toothed segments. In some varieties they start off dark reddish purple or bronze when young, gradually changing to a dark green, sometimes with a reddish tinge, as they mature. The leaves of some other varieties are green practically from the start, whereas in yet others a pigment masks the green colour of all the chlorophyll-bearing parts, leaves, stems and young fruit, so that they remain a dramatic purple-to-reddish-brown throughout the life of the plant. Plants with the dark leaves can be found growing next to those with green leaves, so there is most likely only a single gene controlling the production of the pigment in some varieties.[6] The stems (and the spherical, spiny seed capsules) also vary in pigmentation. The fruit capsules of some varieties are more showy than the flowers.
The flowers are borne in terminal panicle-like inflorescences of green or, in some varieties, shades of red monoecious flowers without petals. The male flowers are yellowish-green with prominent creamy stamens and are carried in ovoid spikes up to 15 centimetres (5.9 in) long; the female flowers, borne at the tips of the spikes, have prominent red stigmas.[7]
The fruit is a spiny, greenish (to reddish-purple) capsule containing large, oval, shiny, bean-like, highly poisonous seeds with variable brownish mottling. Castor seeds have a warty appendage called the caruncle, which is a type of elaiosome. The caruncle promotes the dispersal of the seed by ants (myrmecochory).
Nomenclature
The name Ricinus is a Latin word for tick; the seed is so named because it has markings and a bump at the end that resemble certain ticks. The genus Ricinus De Geer, 1778 also exists in zoology, and designates insects (not ticks) which are parasites of birds - this is possible, since name of animals and plants are ruled by different nomenclature codes.
The common name "castor oil" probably comes from its use as a replacement for castoreum, a perfume base made from the dried perineal glands of the beaver (castor in Latin).[8] It has another common name, palm of Christ, or Palma Christi, that derives from castor oil's reputed ability to heal wounds and cure ailments.
Medicinal uses
Castor oil has many uses in medicine and other applications.
An alcoholic extract of the leaf was shown, in lab rats, to protect the liver from damage from certain poisons.[9][10][11] Methanolic extracts of the leaves of Ricinus communis were used in antimicrobial testing against eight pathogenic bacteria in rats and showed antimicrobial properties. The extract was not toxic.[12] The pericarp of Ricinus showed central nervous system effects in mice at low doses. At high doses mice quickly died.[13] A water extract of the root bark showed analgesic activity in rats.[13] Antihistamine and anti-inflammatory properties were found in ethanolic extract of Ricinus communis root bark.[14]
Other uses
Extract of Ricinus communis exhibited acaricidal and insecticidal activities against the adult of Haemaphysalis bispinosa Neumann (Acarina: Ixodidae) and hematophagous fly Hippobosca maculata Leach (Diptera: Hippoboscidae).[15]
The Bodo tribals of Bodoland, Assam (India), use the leaves of this plant to feed and rear the larvae of muga and endi silkworms.
Castor oil is an effective motor lubricant and has been used in internal combustion engines, including those of World War I airplanes, some racing cars and some model airplanes. It has historically been popular for lubricating two-stroke engines due to high resistance to heat compared to petroleum-based oils. It does not mix well with petroleum products, particularly at low temperatures, but mixes better with the methanol based fuels used in glow model engines. In total-loss-lubrication applications, it tends to leave carbon deposits and varnish within the engine. It has been largely replaced by synthetic oils that are more stable and less toxic.
Jewelry is often made of castor beans, particularly necklaces and bracelets.[16]
Habitat, growth and horticultural uses
Although Ricinus communis is indigenous to the southeastern Mediterranean Basin, Eastern Africa, and India, today it is widespread throughout tropical regions.[5] In areas with a suitable climate, castor establishes itself easily where it can become an invasive plant and can often be found on wasteland.
It is also used extensively as a decorative plant in parks and other public areas, particularly as a "dot plant" in traditional bedding schemes. If sown early, under glass, and kept at a temperature of around 20 °C (68 °F) until planted out, the castor oil plant can reach a height of 2–3 metres (6.6–9.8 ft) in a year. In areas prone to frost it is usually shorter, and grown as if it were an annual.[5] However, it can grow well outdoors in cooler climates, at least in southern England, and the leaves do not appear to suffer frost damage in sheltered spots, where it remains evergreen. It was used in Edwardian times in the parks of Toronto, Ontario, Canada. Although not cultivated there, the plant grows wild in Southern California, notably Griffith Park in Los Angeles.[17]
Cultivars
Selections have been made by breeders for use as ornamental plants (heights refer to plants grown as annuals) and for commercial production of castor oil.[7]
Ornamental varieties:
- 'Gibsonii' has red-tinged leaves with reddish veins and pinkish-green seed pods;
- 'Carmencita Pink' is similar, with pinkish-red stems;
- 'Carmencita Bright Red' has red stems, dark purplish leaves and red seed pods;
(all the above grow to around 1.5 metres (4.9 ft) tall as annuals)[5]
- 'Impala' is compact (only 1.2 metres or 3.9 feet tall) with reddish foliage and stems, brightest on the young shoots;
- 'Red Spire' is tall (2–3 metres or 6.6–9.8 feet) with red stems and bronze foliage;
- 'Zanzibarensis' is also tall (2–3 metres or 6.6–9.8 feet), with large, mid-green leaves (50 centimetres or 20 inches long) that have white midribs.[7]
Varieties for oil production:
- 'Hale' was launched in the 1970s for the State of Texas, United States. It is short (up to 1.2 m or 3 ft 11 in) and has several racemes.
- 'Brigham' is a variety with reduced ricin content adapted for Texas, United States. It grows up to 1.8 m (5 ft 11 in) and has 10% of the ricin content of variety Hale.
- 'BRS Nordestina' was developed by Embrapa (Brazil) 1990 for hand harvest and semi-arid environments.
- 'BRS Energia" was developed by Embrapa (2004) for mechanised or hand harvest.
- 'GCH6' was developed by Sardarkrushinaga Dantiwada University (India), 2004. It is resistant to root rot and tolerant to fusarium wilt.
- 'GCH5' was developed by Sardarkrushinaga Dantiwada University (India), 1995. It is resistant to fusarium wilt.
- 'Abaro' was developed by Ethiopian Institute of Agricultural Research, EORC (Ethiopia) for hand harvest.
- 'Hiruy' was developed by Ethiopian Institute of Agricultural Research, Melkassa and Wondo Genet (Ethiopia) for hand harvest during 2010/2011.
Plant-animal interactions
Ricinus communis is the host plant of the common castor butterfly (Ariadne merione), the Eri silkmoth (Samia cynthia ricini), and the castor semi-looper moth (Achaea janata). It is also used as a food plant by the larvae of some other species of Lepidoptera, including Hypercompe hambletoni and the nutmeg (Discestra trifolii).
Allergenic potential
Ricinus is extremely allergenic, and has an OPALS allergy scale rating of 10 out of 10. The plant is also a very strong trigger for asthma, and allergies to Ricinus are commonplace and severe.[18]
The castor oil plant produces abundant amounts of very light pollen, which easily become airborne and can be inhaled into the lungs, triggering allergic reactions. The sap of the plant causes skin rashes. Individuals who are allergic to the plant can also develop rashes from merely touching the leaves, flowers, or seeds. These individuals can also have cross-allergic reactions to latex sap from the related Hevea brasiliensis plant.[18]
Toxicity
The toxicity of raw castor beans is due to the presence of ricin. Although the lethal dose in adults is considered to be four to eight seeds, reports of actual poisoning are relatively rare.[19] According to the 2007 edition of Guinness World Records, this plant is the most poisonous in the world. Symptoms of overdosing on ricin, which can include nausea, diarrhea, tachycardia, hypotension and seizures persisting for up to a week. However, the poison can be extracted from castor by concentrating it with a fairly complicated process similar to that used for extracting cyanide from almonds.
If ricin is ingested, symptoms may be delayed by up to 36 hours but commonly begin within 2–4 hours. These include a burning sensation in mouth and throat, abdominal pain, purging and bloody diarrhea. Within several days there is severe dehydration, a drop in blood pressure and a decrease in urine. Unless treated, death can be expected to occur within 3–5 days, however in most cases a full recovery can be made.[20][21]
Poisoning occurs when animals, including humans, ingest broken seeds or break the seed by chewing: intact seeds may pass through the digestive tract without releasing the toxin.[20] Toxicity varies among animal species: four seeds will kill a rabbit, five a sheep, six an ox or horse, seven a pig, and eleven a dog. Ducks have shown far more resistance to the seeds: it takes an average of 80 to kill them.[22] The toxin provides the castor oil plant with some degree of natural protection from insect pests such as aphids. Ricin has been investigated for its potential use as an insecticide.[22] The castor oil plant is also the source for undecylenic acid, a natural fungicide.
Commercially available cold-pressed castor oil is not toxic to humans in normal doses, either internal or externally.[23]
Chemistry
Three terpenoids and a tocopherol-related compound have been found in the aerial parts of Ricinus communis. Compounds named (3E,7Z,11E)-19-hydroxycasba-3,7,11-trien-5-one, 6α-hydroxy-10β-methoxy-7α,8α-epoxy-5-oxocasbane-20,10-olide, 15α-hydroxylup-20(29)-en-3-one, and (2R,4aR,8aR)-3,4,4a,8a-tetrahydro-4a-hydroxy-2,6,7,8a-tetramethyl-2-(4,8, 12-trimethyltridecyl)-2H-chromene-5,8-dione were isolated from the methanol extracts of Ricinus communis by chromatographic methods.[24] Partitioned h-hexane fraction of Ricinus communis root methanol extract resulted in enrichment of two triterpenes: lupeol and urs-6-ene-3,16-dione (erandone). Crude methanolic extract, enriched n-hexane fraction and isolates at doses 100 mg/kg p.o. exhibited significant (P < 0.001) anti-inflammatory activity in carrageenan-induced hind paw oedema model.[25]
Modern commercial usage
Global castor seed production is around two million tons per year. Leading producing areas are India (with over three-quarters of the global yield), China and Mozambique, and it is widely grown as a crop in Ethiopia. There are several active breeding programmes.
Production
Top ten castor oil seed producers – 2013 | ||||
---|---|---|---|---|
Country | Production (Tonnes) | Footnote | ||
India | 1,744,000 | |||
People's Republic of China | 60,000 | * | ||
Mozambique | 60,000 | F | ||
Ethiopia | 13,000 | * | ||
Thailand | 12,000 | * | ||
Brazil | 11,953 | |||
Paraguay | 11,000 | * | ||
South Africa | 6,200 | F | ||
Pakistan | 6,000 | * | ||
Vietnam | 6,000 | * | ||
World | 1,854,775 | A | ||
No symbol = official figure, F = FAO estimate, * = Unofficial/Semi-official/mirror data, A = Aggregate (may include official, semi-official or estimates); |
Other modern uses
- Whether natural, blended, or chemically altered, castor oil still has many uses. For example, it remains of commercial importance as a non-freezing, antimicrobial, pressure-resistant lubricant for special purposes, either of latex or metals, or as a lubricating component of fuels.[26]
- Castor products are sources of various chemical feedstocks.[27]
- In Brazil, castor oil (locally known as mamona oil) is a raw material for some varieties of biodiesel.
- In rural areas, the abundant seeds are used by children for slingshot balls, as they have the right weight, size, and hardness.
- Because castor seeds are attractively patterned, they are popular in low-cost personal adornments, such as non-durable necklaces and bracelets.
- Castor oil has long been used on the skin to prevent dryness. Either purified or processed, it still is a component of many cosmetics.
- The high percentage of ricinoleic acid residues in castor oil and its derivatives, inhibits many microbes, whether viral, bacterial or fungal. They accordingly are useful components of many ointments and similar preparations.
- Castor oil is the major raw material for Polyglycerol polyricinoleate, a modifier that improves the flow characteristics of cocoa butter in the manufacture of chocolate bars,and thereby the costs.
- Castor oil is used in the USA to repel moles and voles for lawn care.
Historical usage
Castor seeds have been found in Egyptian tombs dating back to 4000 BC; the slow burning oil was used mostly to fuel lamps. Herodotus and other Greek travellers noted the use of castor seed oil for lighting, body ointments, and improving hair growth and texture. Cleopatra is reputed to have used it to brighten the whites of her eyes. The Ebers Papyrus is an ancient Egyptian medical treatise believed to date from 1552 BC. Translated in 1872, it describes castor oil as a laxative.[28]
The use of castor bean oil ("eranda") in India has been documented since 2000 BC in lamps and in local medicine as a laxative, purgative, and cathartic in Unani, Ayurvedic and other ethnomedical systems. Traditional Ayurvedic medicine considers castor oil the king of medicinals for curing arthritic diseases. It is regularly given to children orally, for de-worming.
Castor seed and its oil have also been used in China for centuries, mainly prescribed in local medicine for internal use or use in dressings.
Castor oil was used as an instrument of coercion by the paramilitary Blackshirts under the regime of Italian dictator Benito Mussolini. Dissidents and regime opponents were forced to ingest the oil in large amounts, triggering severe diarrhea and dehydration, which could ultimately cause death. This punishment method was originally thought of by Gabriele D'Annunzio, the Italian poet and Fascist supporter, during the First World War. (See also: Castor oil's use as a means of intimidation in Fascist Italy.)
See also
References
- 1 2 Rizzardo, RA; Milfont, MO; Silva, EM; Freitas, BM (December 2012). "Apis mellifera pollination improves agronomic productivity of anemophilous castor bean (Ricinus communis).". Anais da Academia Brasileira de Ciencias. 84 (4): 1137–45. doi:10.1590/s0001-37652012005000057. PMID 22990600.
- ↑ "Ricinus communis". Natural Resources Conservation Service PLANTS Database. USDA. Retrieved 1 February 2016.
- ↑ "BSBI List 2007". Botanical Society of Britain and Ireland. Archived from the original (xls) on 2015-02-25. Retrieved 2014-10-17.
- ↑ "Euphorbiaceae (spurge) genomics". Institute for Genome Sciences. University of Maryland Medical School. Retrieved 2009-03-09.
- 1 2 3 4 Phillips, Roger; Rix, Martyn (1999). Annuals and Biennials. London: Macmillan. p. 106. ISBN 0-333-74889-1.
- ↑ e.g. http://database.prota.org/publishedspeciesEn.htm
- 1 2 3 Christopher Brickell, ed. (1996). The Royal Horticultural Society A-Z Encyclopedia of Garden Plants. London: Dorling Kindersley. pp. 884–885. ISBN 0-7513-0303-8.
- ↑ "The Complex Case of Castor's Etymology".
- ↑ Joshi M.; Waghmare S.; Chougule P.; Kanase A. (2004). "Extract of Ricinus communis leaves mediated alterations in liver and kidney functions against single dose of CCl
4 induced liver necrosis in albino rats.". Journal of Ecophysiology and Occupational Health. 4 (3–4): 169–173. ISSN 0972-4397. - ↑ Sabina E.P., Rasool M.K., Mathew L., Parameswari (May–August 2009). "Studies on the protective effect of Ricinus communis leaves extract on carbon tetrachloride hepatotoxicity in albino rats". Pharmacologyonline. 2: 905–916. ISSN 1827-8620.
- ↑ Kalaiselvi P.; Anuradha B.; Parameswari C.S. (2003). "Protective effect of Ricinus communis leaf extract against paracetamol-induced hepatotoxicity". Biomedicine. 23 (1–2): 97–105.
- ↑ Oyewole O.I.; Owoseni A.A.; Faboro E.O. (2010). "Studies on medicinal and toxicological properties of Cajanus cajan, Ricinus communis and Thymus vulgaris leaf extracts". Journal of Medicinal Plant Research. 4 (19): 2004–8. doi:10.5897/JMPR10.363. ISSN 1996-0875.
- 1 2 Williamson E. M. (ed) "Major Herbs of Ayurveda", Churchill Livingstone 2002
- ↑ Lomash V, Parihar SK, Jain NK, Katiyar AK (2010). "Effect of Solanum nigrum and Ricinus communis extracts on histamine and carrageenan-induced inflammation in the chicken skin". Cell. Mol. Biol. (Noisy-le-grand). 56 (Suppl): OL1239–51. PMID 20158977.
- ↑ Zahir AA, Rahuman AA, Bagavan A, et al. (August 2010). "Evaluation of botanical extracts against Haemaphysalis bispinosa Neumann and Hippobosca maculata Leach". Parasitol. Res. 107 (3): 585–92. doi:10.1007/s00436-010-1898-7. PMID 20467752.
- ↑ http://www.nbcnews.com/id/31130769/ns/health-pet_health/t/growing-danger-toxic-plants-pose-pet-threat/#.VEOiHxaNrIU
- ↑ Toronto Star, 9 June 1906, p. 17
- 1 2 Ogren, Thomas (2015). The Allergy-Fighting Garden. Berkeley, CA: Ten Speed Press. pp. 184–185. ISBN 978-1-60774-491-7.
- ↑ Wedin GP, Neal JS, Everson GW, Krenzelok EP (May 1986). "Castor bean poisoning". Am J Emerg Med. 4 (3): 259–61. doi:10.1016/0735-6757(86)90080-X. PMID 3964368.
- 1 2 Soto-Blanco B, Sinhorini IL, Gorniak SL, Schumaher-Henrique B (June 2002). "Ricinus communis cake poisoning in a dog". Vet Hum Toxicol. 44 (3): 155–6. PMID 12046967.
- ↑ Ricinus communis (Castor bean)—Cornell University 2008. "Archived copy". Archived from the original on 8 May 1998. Retrieved 8 May 1998. Check date values in:
|access-date=
(help) - 1 2 Union County College: Biology: Plant of the Week: Castor Bean Plant
- ↑ Irwin R (March 1982). "NTP technical report on the toxicity studies of Castor Oil (CAS No. 8001-79-4) In F344/N Rats And B6C3F1 Mice (Dosed Feed Studies)". Toxic Rep Ser. 12: 1–B5. PMID 12209174.
- ↑ Tan Q.-G.; Cai X.-H.; Dua Z.-Z.; Luo X.-D. (2009). "Three terpenoids and a tocopherol-related compound from Ricinus communis". Helvetica Chimica Acta. 92 (12): 2762–8. doi:10.1002/hlca.200900105.
- ↑ Srivastava, Pooja; Jyotshna; Gupta, Namita; Kumar Maurya, Anil; Shanker, Karuna (2013). "New anti-inflammatory triterpene from the root of Ricinus communis". Natural Product Research. doi:10.1080/14786419.2013.861834.
- ↑ R. M. Mortier; S. T. Orszulik (6 December 2012). Chemistry and Technology of Lubricants. Springer. pp. 226–. ISBN 978-1-4615-3272-9.
- ↑ Castor Oil World
- ↑ Tunaru S, Althoff TF, Nusing RM, Diener M, Offermanns S. Castor Oil Induces Laxation and Uterus Contraction via Ricinoleic Acid Activating Prostaglandin EP3 Receptors. Proceedings of the National Academy of Sciences of the United States of America 2012; 109(23)9179-9184.
Further reading
- Everitt, J.H.; Lonard, R.L.; Little, C.R. (2007). Weeds in South Texas and Northern Mexico. Lubbock: Texas Tech University Press. ISBN 0-89672-614-2.
External links
Wikimedia Commons has media related to Ricinus communis. |
- A Bean Called Castor Can Cut Carbon & Fuel the Future
- Ricinus communis L. — at Purdue University.
- Castor beans — at Purdue University.
- Ricinus communis (castor bean) at Cornell University
- Ricinus communis in Wildflowers of Israel;
- Castor oil plant Flowers in Israel