Bothrops atrox

Bothrops atrox
Bothrops-atrox.jpg
Conservation status
Not evaluated (IUCN 3.1)
Scientific classification
Kingdom: Animalia
Phylum: Chordata
Subphylum: Vertebrata
Class: Reptilia
Order: Squamata
Suborder: Serpentes
Family: Viperidae
Subfamily: Crotalinae
Genus: Bothrops
Species: B. atrox
Binomial name
Bothrops atrox
(Linnaeus, 1758)
Synonyms
  • Coluber atrox - Linnaeus, 1754
  • [Coluber] atrox - Linnaeus, 1758
  • [Coluber] ambiguus - Gmelin, 1788
  • Vipera Weigeli - Daudin, 1803
  • Cophias holocericeus - Wied-Neuwied, 1821
  • Trigonoceph[alus]. atrox - Schinz, 1822
  • Vipera atrox Weigelii - Schinz, 1822
  • Trigonoceph[alus]. holocericeus - Schinz, 1822
  • Bothrops Furia - Wagler, 1824
  • Bothrops tessellatus - Wagler, 1824
  • Craspedocephalus atrox - Fitzinger, 1826
  • Craspedocephalus Weigelii - Fitzinger, 1826
  • [Bothrops] atrox - Wagler, 1830
  • [Bothrops] ambiguus - Wagler, 1830
  • T[rigonocephalus]. atrox - Schlegel, 1837
  • Trigonocephalus Colombiensis - Hallowell, 1845
  • Bothrops affinis - Gray, 1849
  • Bothrops atrox var. tessellatus - Jan & Sordelli, 1875
  • Lachesis atrox - Boulenger, 1896
  • Botrhops atrox - Recinos, 1913
  • B[othrops]. Neuvoiedii Venezuelenzi - Briceño Rossi, 1934
  • Trimeresurus atrox - Schmidt & Walker, 1943
  • Bothrops atrox atrox - Hoge, 1952
  • Bothrops colombiensis - Hoge, 1966
  • Bothrops atrox colombiensis - Gubensk, Turk & Drujan, 1978
  • Bothrops isabelae - Sander Montilla, 1979
  • Bothrops lanceolatus aidae - Sandner Montilla, 1981
  • B[othrops]. atrox aidae - Vanzolini, 1986
  • Bothrops lanceolatus nacaritae - Sandner Montilla, 1990[1]
Common names: common lancehead, fer-de-lance, barba amarilla.[2]

Bothrops atrox is a venomous pitviper species found in tropical lowlands of northern South America east of the Andes.[1] No subspecies are currently recognized.[3] This species is very dangerous and is the cause of more human fatalities than any other American reptile.

Contents

Description

B. atrox

A terrestrial species, adults usually grow to total length 75-125 cm 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 that of a series of 80 specimens collected in northeastern Peru, the largest was a female of 138.8 cm. The largest specimen measured by Campbell and Lamar (2004) was a female with a total length of 162 cm.[2]

The scalation includes 23-29 (usually 23-25) rows of dorsal scales at midbody, 169-214/177-214 ventral scales in males/females, 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 3-11 (usually 5-9) keeled intersupraocular scales, 7-13 (usually 8-11) sublabial scales and 6-9 (usually 7) supralabial scales, the second of which is fused with the prelacunal to form a lacunolabial.[2]

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 that are rectangular or trapezoidal in shape and 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 amount of black reticulation, while the tongue is black.[2]

Common names

Common lancehead, fer-de-lance, barba amarilla.[2]

The Spanish common name barba amarilla (yellow beard), an allusion to the pale yellow chin color, is also used in English. In Guyana it is called labaria[4] or labarria.[5] 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). In Venezuela it is called mapanaré. In Colombia it is known as mapaná (Llanos of Vichada) and taya equis.[2] The latter is an allusion to the x-like markings of the color pattern. In Ecuador these x-like markings have led to the snake simply being referred to as equis (the Spanish pronunciation of the letter 'x').

Geographic range

Found in the tropical lowlands of South America east of the Andes, including southeastern Colombia, southern and eastern Venezuela, Guyana, Suriname, French Guiana, eastern Ecuador, eastern Peru, northern Bolivia and the northern half of Brazil.[1] The type locality is listed as "Asia", which is obviously a mistake. Schmidt and Walker (1943:295) proposed that this be corrected to "Surinam."[1]

Habitat

Despite the vast destruction of rain forests, it is amongst the most numerous of pit vipers and is not endangered. In Trinidad it prefers wet lowland forests.[6]

Behavior

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

Feeding

The main diet includes most small mammals and birds, but also frogs and lizards. Larger prey is struck and released, after which it is tracked down via its scent trail.

Reproduction

Breeds year-round. After mating, females with developing embryos travel in and out of sunlight to keep them at a constant temperature. In equatorial regions, the gestation period is approximately 3-4 months, with an average of 60 young per litter. At birth the young are about 30 cm in 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 striking with high speed.

They are much feared because the venom is particularly toxic and fast-acting. The fatality rate used to be high, but nowadays treatment is usually possible if the victim receives medical attention soon enough.[7] Venom yield averages 124 mg, although it may be as much as 342 mg. The fatal dose in humans is just 62 mg.

The enzyme, Reptilase, derived from this snake's venom is used in modern medical laboratories to measure fibrinogen levels and to measure 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.

Taxonomy

The taxonomy of this species is controversial; it may include the B. leucurus and the 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.

See also

References

  1. 1.0 1.1 1.2 1.3 McDiarmid RW, Campbell JA, Touré T. 1999. Snake Species of the World: A Taxonomic and Geographic Reference, vol. 1. Herpetologists' League. 511 pp. ISBN 1-893777-00-6 (series). ISBN 1-893777-01-4 (volume).
  2. 2.0 2.1 2.2 2.3 2.4 2.5 Campbell JA, Lamar WW. 2004. The Venomous Reptiles of the Western Hemisphere. Comstock Publishing Associates, Ithaca and London. 870 pp. 1500 plates. ISBN 0-8014-4141-2.
  3. Bothrops atrox (TSN 634854). Integrated Taxonomic Information System. Retrieved on 6 November 2006.
  4. "Environmental Impact Assessment- Buddy's International Hotel" (pdf). Cemco, Inc. (2006). Retrieved on 2006-11-10.
  5. "Venomous Snakes of Guyana". Iwokrama International Centre for Rain Forest Conservation and Development. Retrieved on 2006-11-10. Includes a photograph.
  6. Herklots GAC. 1961. The Birds of Trinidad and Tobago. Collins, London, p. 10.
  7. Stidworthy J. 1974. Snakes of the World. Grosset & Dunlap Inc. 160 pp. ISBN 0-448-11856-4.

Further reading

  • 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 - Volume 61, Number 1, pp. 3-16.
  • Mehrtens JM. 1987. Living Snakes of the World in Color. New York: Sterling Publishers. 480 pp. ISBN 0-8069-6460-X.
  • O'Shea M. 2005. Venomous Snakes of the World. ISBN 0-691-12436-1.

External links