Cerbera odollam

From Wikipedia, the free encyclopedia
Jump to: navigation, search
Suicide tree
Cerbera manghas - Köhler–s Medizinal-Pflanzen-175.jpg
Leaves, flowers and seeds of C. odollam From Koehler's Medicinal-Plants 1887
Scientific classification
Kingdom: Plantae
(unranked): Angiosperms
(unranked): Eudicots
(unranked): Asterids
Order: Gentianales
Family: Apocynaceae
Genus: Cerbera
Species: C. odollam
Binomial name
Cerbera odollam
Gaertn.

Cerbera odollam is a dicotyledonous angiosperm, a plant species in the Family Apocynaceae and commonly known as the suicide tree, pong-pong, and othalanga. It is a species native to India and other parts of southern Asia, growing preferentially in coastal salt swamps and in marshy areas but also grown as a hedge plant between home compounds.[not verified in body] It yields a potent poison that has been used for suicide and murder.

Common names[edit]

Cerbera odollam is known by a number of vernacular names depending on the region. These include othalanga maram in the Malayalam language used in Kerala, India; kattu arali in the adjacent state of Tamil Nadu; famentana, kisopo, samanta or tangena in Madagascar; and pong-pong, buta-buta, bintaro or nyan in Southeast Asia.[1][non-primary source needed] In Sri Lanka, it is known as "ගොන් කදුරු" ("gon kaduru") in Sinhala.[citation needed]

Description[edit]

Cerbera odollam bears a close resemblance to oleander, another highly toxic plant from the same family. Its branchlets are whorled about the trunk, and its leaves are terminally crowded, with tapering bases, acuminate apices, and entire margins. The plant as a whole yields a milky, white latex.

Its fruit, when still green, looks like a small mango, with a green fibrous shell enclosing an ovoid kernel measuring approximately 2 cm × 1.5 cm and consisting of two cross-matching white fleshy halves. On exposure to air, the white kernel turns violet, then dark grey, and ultimately brown, or black.

Growth range[edit]

C. odollam is native to India and other parts of southern Asia, growing preferentially in coastal salt swamps and in marshy areas, but also being grown as a hedge plant between home compounds.[citation needed] Specifically, it grows wild along the coast in many parts of Kerala, India.[citation needed]

Toxicity[edit]

Flowers of Cerbera odollam

The kernels of C. odollam contain cerberin, a digoxin-type cardenolide and cardiac glycoside toxin that blocks the calcium ion channels in heart muscle, causing disruption of the heart beat, most often fatally.[citation needed] The difficult in detecting cerberin in autopsies and its the ability of strong spices to mask its taste make it an agent of homicide and suicide in India: in 2004, a team led by scientist Yvan Gaillard documented more than 500 cases of fatal Cerbera poisoning between 1989 and 1999 in the southwest Indian state of Kerala alone.[1][2]

Uses[edit]

The fruits are used for manufacturing bioinsecticides and deodorants.[3][4][better source needed]

Investigations have also been made into the feasibility of using the seeds as a feedstock in the production of biodiesel.[5][non-primary source needed]

References[edit]

  1. ^ a b Gaillard Y, Krishnamoorthy A, Bevalot F., 2004, "Cerbera odollam: a 'suicide tree' and cause of death in the state of Kerala, India," J. Ethnopharmacol. 95(2-3):123-126.[non-primary source needed]
  2. ^ James Randerson, 2004, "'Suicide tree' toxin is 'perfect' murder weapon" [commentary on Gaillard, et al., 2004, op. cit.], New Scientist (online), November 26, 2004, see [1], accessed 18 June 2015.
  3. ^ P.I. Rajeev, 2007, "‘Suicide fruit’ now a rich harvest?," The Indian Express (online), February 3 2007, see [2], accessed 18 June 2015.[better source needed]
  4. ^ Sarah Kaplan, 2015, "Morning Mix: The brutal harvest of India’s ‘suicide tree’," The Washington Post (online), May 8, 2015, see [3], accessed 18 June 2015.[better source needed]
  5. ^ Jibrail Kansedo, Keat Teong Lee & Subhash Bhatia, 2009, "Cerbera odollam (sea mango) oil as a promising non-edible feedstock for biodiesel production." Fuel 88(6):1148–1150, see [4], accessed 18 June 2015.[non-primary source needed]