Английская Википедия:Bothrops atrox

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Bothrops atrox — also known as the common lancehead, fer-de-lance, barba amarilla[1] and mapepire balsain — is a highly venomous pit viper species found in the tropical lowlands of northern South America east of the Andes, as well as the Caribbean island of Trinidad.[2] No subspecies are currently recognized.[3]

Taxonomy

The common lancehead was one of the many reptile and amphibian species described by Carl Linnaeus in the landmark 1758 10th edition of his Systema Naturae, where it was given the binomial name Coluber atrox.[4] The taxonomy of this species is controversial; it may include B. leucurus and B. moojeni, and some of its populations are sometimes said to be separate species. B. asper was formerly included in this species, but most authorities now consider it distinct.

Names

Common names include lancehead, fer-de-lance, barba amarilla, and mapepire balsain, among others.[1]

The Spanish common name barba amarilla (yellow beard), an allusion to the pale yellow chin color, is also used in English. In Venezuela, it is called mapanare. In Colombia, it is known as mapaná (Llanos of Vichada) and talla equis. In Guyana and Suriname, it is called labaria[5] or labarria.[6] In Peru, it is called aroani (Yagua), cascabel (juveniles), ihdóni (Bora), jergón, jergona, jergón de la selva, macánchi (Alto Marañón), machacú, marashar and nashipkit (Aguaruna names). The name jergón[1] is an allusion to the x-like markings of the color pattern. In Ecuador and Panama, these x-like markings have led to the snake simply being referred to as equis (the Spanish name of the letter 'x'). In Trinidad it is known as mapepire balsain.[7] In Bolivia it is called Yoperojobobo. In Brazil the common names are Jararaca[8] or Jararaca-do-norte. The name fer-de-lance comes from French, meaning, "head of a lance", "spearhead", or literally "lance iron".[9][10]

Description

A terrestrial species, adults usually grow to a total length 75–125 cm (about 30-50 inches) and are moderately heavy-bodied. Reports of the maximum size are not clear, as this species is often confused with B. asper. Soini (1974) mentioned of a series of 80 specimens collected in northeastern Peru, the largest was a female of Шаблон:Convert. The largest specimen measured by Campbell and Lamar (2004) was a female with a total length of Шаблон:Convert.[1]

The scalation includes 23-29 (usually 23-25) rows of dorsal scales at midbody, 169-214 and 177-214 ventral scales in males and females, respectively, 52-86 (usually 75 or fewer) subcaudal scales in males, which are usually divided, and 47-72 subcaudals in females. On the head, the rostral scale is about as high, or slightly higher, than it is wide. There are three to 11 (usually five to 9) keeled intersupraocular scales, seven to 13 (usually eight to 11) sublabial scales and six to 9 (usually seven) supralabial scales, the second of which is fused with the prelacunal to form a lacunolabial.[1]

Файл:Bothrops atrox - Arima.jpg
Bothrops atrox in Arima, Trinidad and Tobago.

The color pattern is highly variable, including a ground color that may be olive, brown, tan, gray, yellow, or (rarely) rusty. The body markings are highly variable, as is the degree of contrast: in some specimens the pattern is very well defined, while in others it may be virtually absent. In general, however, the body pattern consists of a series of dorsolateral blotches, rectangular or trapezoidal in shape, which extend from the first scale row to the middle of the back. These blotches may oppose or alternate across the midline, often fusing to form bands. They also have pale borders, which in some cases may be prominent, and may be invaded from below by tan or gray pigment, occasionally dividing them into pairs of ventrolateral spots. The belly may be white, cream or yellowish gray, with an increasing amount of gray to black mottling posteriorly that may fade again under the tail. The head usually does not have any markings other than a moderately wide postocular stripe that runs from behind the eye back to the angle of the mouth. The iris is gold or bronze, with varying amounts of black reticulation, while the tongue is black.[1]

Distribution and habitat

This species is found in the tropical lowlands of South America east of the Andes, including southeastern Colombia, southern and eastern Venezuela, the island of Trinidad (although there is some confusion regarding the taxonomical systematics of this population), Guyana,[11] Suriname, French Guiana, eastern Ecuador, eastern Peru, Panama, northern Bolivia and the northern half of Brazil.[2] The type locality is listed as "Asia", which is obviously a mistake. Schmidt and Walker (1943:295) proposed this be corrected to "Surinam".[2]

Despite the vast destruction of rain forests, it is among the most numerous and common of pit vipers and is not endangered. In Trinidad, it prefers wet forests from sea level to 940 m.[12] Along with Bothrops caribbaeus and B. lanceolatus, it is one of three Bothrops species found in the West Indies.

Behavior

Although generally terrestrial, it is also an excellent swimmer and even climbs trees when necessary to reach prey. Generally nocturnal, it may forage at any time of the day, though, if necessary. These snakes are also easily agitated.

Feeding

The main diet includes mostly small mammals (such as rodents and opossums) and birds, but also frogs, lizards, smaller snakes, fish, centipedes, and tarantulas.[13][14][15] Larger prey is struck and released, after which it is tracked down via its scent trail.

Reproduction

Bothrops atrox can give live birth to up to 80 offspring at once. Adults breed year-round. After mating, females with developing embryos travel in and out of sunlight to keep themselves and the embryos at a constant temperature. In equatorial regions, the gestation period is about three to four months, with an average of 60 young per litter. At birth, the young are about Шаблон:Convert in total length, more brightly colored than adults, and have yellow or beige tails.

Venom

These snakes are known to search for rodents in coffee and banana plantations. Workers there are often bitten by the snakes, which can lie camouflaged for hours, nearly undetectable, and strike with high speed.

Their venom is hemorrhagic, damaging the vascular endothelium and consuming coagulation factors in a mechanism known as “venom-induced consumption coagulopathy”.[16] As a result, clotting assays such as prothrombin time and aPTT will be highly disturbed. Spontaneous recovery from coagulopathy is seen 14 to 30 hours after bite according to a study performed in French Guiana. A Mexican polyvalent antivenom was tested but had no effect on it.[17] Bothrops atrox venom can result in several systemic and local symptoms, such as severe bleeding, kidney failure, abnormal clotting, blisters and necrosis.[18] The bite can also result in hemorrhage in the central nervous system, which leads to sequelae and even death. In a case reported in the Brazilian Amazon, symptoms such as pain and ecchymoses, headaches, nausea, vomiting, diarrhea, hypertension and blood incoagulability were reported, the patient died of stroke, even after administration of the antivenom.[19] The Common lancehead has an LD50 of 1.1 to 4.9 mg/kg, the venom of juveniles is more inflammatory, lethal, hemorrhagic and kills more quickly than that of adults, people bitten by neonates are more likely to develop coagulopathy.[20]

Venom yield averages Шаблон:Convert, although it may be as much as Шаблон:Convert.Шаблон:Citation needed The enzyme reptilase (batroxobin), derived from this snake's venom, is used in modern medical laboratories to measure fibrinogen levels and blood coagulation capability. The test is considered to be a replacement for thrombin time, and is used when heparin is present in the sample. The enzyme is unaffected by heparin.[21]

References

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Further reading

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  • Hays WST, Conant Sheila. 2007. Biology and Impacts of Pacific Island Invasive Species. 1. A Worldwide Review of Effects of the Small Indian Mongoose, Herpestes javanicus (Carnivora: Herpestidae). Pacific Science 61 (1): 3–16.
  • Linnaeus, C. 1758. Systema naturæ per regna tria naturæ, secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis. Tomus I. Tenth Edition. Holmiæ. Stockholm. 824 pp. (Coluber atrox, p. 222.)
  • Mehrtens JM. 1987. Living Snakes of the World in Color. New York: Sterling Publishers. 480 pp. Шаблон:ISBN.
  • O'Shea M. 2005. Venomous Snakes of the World. Princeton, New Jersey: Princeton University Press. 160 pp. Шаблон:ISBN.

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External links

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Шаблон:Bothrops

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  1. 1,0 1,1 1,2 1,3 1,4 1,5 Campbell JA, Lamar WW. 2004. The Venomous Reptiles of the Western Hemisphere. Comstock Publishing Associates, Ithaca and London. 870 pp. 1500 plates. Шаблон:ISBN
  2. 2,0 2,1 2,2 Ошибка цитирования Неверный тег <ref>; для сносок McD99 не указан текст
  3. Шаблон:ITIS
  4. Шаблон:Cite book
  5. Шаблон:Cite web
  6. Шаблон:Cite web Includes a photograph.
  7. Cote ce Cote la: Trinidad & Tobago Dictionary, p. 75. John Mendes. (1986) Arima, Trinidad.
  8. Шаблон:Cite web
  9. “fer-de-lance, n., Etymology”. Oxford English Dictionary, Oxford University Press, July 2023, <https://doi.org/10.1093/OED/1762061176>
  10. Шаблон:Cite web
  11. Шаблон:Cite journal
  12. Herklots GAC. 1961. The Birds of Trinidad and Tobago. Collins, London, p. 10.
  13. Шаблон:Cite web
  14. Шаблон:Cite web
  15. Шаблон:Cite web
  16. Larreche S, Mion G, Goyffon M. [Haemostasis disorders caused by snake venoms]. Ann Fr Anesth Reanim. 2008;27(4):302–309. Apr
  17. Heckmann X, Lambert V, Mion G, Ehrhardt A, Marty C, Perotti F, et al. Failure of a Mexican antivenom on recovery from snakebite-related coagulopathy in French Guiana. Clinical Toxicology. 2020 Jul 1;0(0):1–7. https://doi.org/10.1080/15563650.2020.1786108
  18. Шаблон:Cite web
  19. Шаблон:Cite journal
  20. Шаблон:Cite web
  21. Шаблон:Cite journal