Lachesis muta: Difference between revisions

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Adults grow to an average of 2 to 2.5 m, although 3 m is not too unusual. The largest recorded specimen was almost 3.65 m long, making this the largest of all [[Viperidae|pit viper]]s and the longest venomous snake in the [[western hemisphere]].<ref name="Meh87">Mehrtens JM. 1987. Living Snakes of the World in Color. New York: Sterling Publishers. 480 pp. ISBN 0-8069-6460-X.</ref>
Adults grow to an average of 2 to 2.5 m, although 3 m is not too unusual. The largest recorded specimen was almost 3.65 m long, making this the largest of all [[Viperidae|pit viper]]s and the longest venomous snake in the [[western hemisphere]].<ref name="Meh87">Mehrtens JM. 1987. Living Snakes of the World in Color. New York: Sterling Publishers. 480 pp. ISBN 0-8069-6460-X.</ref>


The head is broad and very distinct from the narrow neck. The snout is broadly rounded. There is no [[Canthus (snake)|canthus]]. A pair of small [[internasals]] is present, separated by small scales. The [[supraoculars]] are narrow. Other parts of the crown are covered with very small scales. Laterally, the second [[supralabial]] forms the anterior border of the loreal pit, while the third is very large. The eye is separated from the supralabials by 4-5 rows of small scales.<ref name="USN91">U.S. Navy. 1991. Poisonous Snakes of the World. US Govt. New York: Dover Publications Inc. 203 pp. ISBN 0-486-26629-X.</ref>
The head is broad and very distinct from the narrow neck. The snout is broadly rounded. There is no [[Canthus (snake)|canthus]]. A pair of small [[Internasal scales|internasals]] is present, separated by small scales. The [[supraoculars]] are narrow. Other parts of the crown are covered with very small scales. Laterally, the second [[supralabial]] forms the anterior border of the loreal pit, while the third is very large. The eye is separated from the supralabials by 4-5 rows of small scales.<ref name="USN91">U.S. Navy. 1991. Poisonous Snakes of the World. US Govt. New York: Dover Publications Inc. 203 pp. ISBN 0-486-26629-X.</ref>


The body is cylindrical, tapered and moderately stout. Midbody there are 31-37 nonoblique rows of [[dorsal scales]] which are heavily keeled with bulbous tubercles and feebly imbricate. There are 200-230 [[ventral scales]]. The tail is short with 32-50 mainly paired [[subcaudals]], followed by 13-17 rows of small spines and a terminal spine.<ref name="USN91"/>
The body is cylindrical, tapered and moderately stout. Midbody there are 31-37 nonoblique rows of [[dorsal scales]] which are heavily keeled with bulbous tubercles and feebly imbricate. There are 200-230 [[ventral scales]]. The tail is short with 32-50 mainly paired [[subcaudals]], followed by 13-17 rows of small spines and a terminal spine.<ref name="USN91"/>

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Lachesis muta
Lachesis muta muta.jpg
Scientific classification
Kingdom: Animalia
Phylum: Chordata
Subphylum: Vertebrata
Class: Reptilia
Order: Squamata
Suborder: Serpentes
Family: Viperidae
Subfamily: Crotalinae
Genus: Lachesis
Species: Lachesis muta
Binomial name
Lachesis muta
(Linnaeus, 1766)
Synonyms
  • [Crotalus] mutus - Linnaeus, 1766
  • [Coluber] crotalinus - Gmelin, 1788
  • Scytale catenatus - Latreille In Sonnini & Latreille, 1801
  • Scytale ammodytes - Latreille In Sonnini & Latreille, 1801
  • Coluber Alecto - Shaw, 1802
  • Lachesis mutus - Daudin, 1803
  • Lachesis ater - Daudin, 1803
  • Trigonocephalus ammodytes - Oppel, 1811
  • [Cophias] crotalinus - Merrem, 1820
  • Trigonoceph[alus]. crotalinus - Schinz, 1822
  • Lachesis muta - Schinz, 1822
  • Lachesis atra - Schinz, 1822
  • Scytale catenata - Schinz, 1822
  • Bothrops Surucucu - Wagler, 1824
  • C[rasedocephalus]. crotalinus - Gray, 1825
  • Lachesis mutus - Duméril, Bibron & Duméril, 1854
  • Lachesis mutus - Boulenger, 1896
  • Lachesis muta - Boettger, 1898
  • Lachesis muta muta - Taylor, 1951[1]

Common names: South American bushmaster, more.


Lachesis muta is a venomous pit viper species found in South America. Two subspecies are currently recognized, including the typical form described here.[2]

Description

Adults grow to an average of 2 to 2.5 m, although 3 m is not too unusual. The largest recorded specimen was almost 3.65 m long, making this the largest of all pit vipers and the longest venomous snake in the western hemisphere.[3]

The head is broad and very distinct from the narrow neck. The snout is broadly rounded. There is no canthus. A pair of small internasals is present, separated by small scales. The supraoculars are narrow. Other parts of the crown are covered with very small scales. Laterally, the second supralabial forms the anterior border of the loreal pit, while the third is very large. The eye is separated from the supralabials by 4-5 rows of small scales.[4]

The body is cylindrical, tapered and moderately stout. Midbody there are 31-37 nonoblique rows of dorsal scales which are heavily keeled with bulbous tubercles and feebly imbricate. There are 200-230 ventral scales. The tail is short with 32-50 mainly paired subcaudals, followed by 13-17 rows of small spines and a terminal spine.[4]

The color pattern consists of a yellowish, reddish or grey-brown ground color, overlaid with a series of dark brown or black dorsal blotches that form lateral inverted triangles of the same color. The lateral pattern may be precisely or indistinctly defined, normally pale at the center.[3]

Common names

South American bushmaster. Known as the mapepire zanana or mapepire grande (pronounced ma-pa(y)-PEE za-Na-na or ma-pa(Y)-PEE GRAN-dey) in Trinidad and Tobago.[5][6]

Etymology

Lachesis is one of the three Fates in Greek mythology and was supposed to assign to man his term of life -- something this species is certainly capable of doing. The species is similar in appearance to rattlesnakes and vibrates its tail vigorously when alarmed, but has no rattle and was therefore called mutus (later muta), which is Latin for dumb or mute. However, when in the undergrowth, the tail actually makes quite a loud rustling noise.[7]

Geographic range

Found in South America in the equatorial forests east of the Andes: Colombia, eastern Ecuador, Peru, northern Bolivia, eastern and southern Venezuela, Guyana, Surinam, French Guiana and much of northern Brazil. The type locality is "Surinami" (Surinam).[1]

The species is also found on the Island of Trinidad.[6]

Habitat

Occurs in primary and secondary forests; adjacent fields and cleared areas.[3] In Trinidad it tends to prefer hilly and mountainous regions.[8]

Venom

Some reports suggest that this species produces a large amount of venom that is weak compared to some other vipers.[9] Others, however, suggest that such conclusions may not be accurate. These animals are badly affected by stress and often do not last long in captivity. This makes it difficult to obtain "good, healthy" venom for study purposes. For example, Bolaños (1972) observed that venom yield from his specimens fell from 233 mg to 64 mg while they remained in his care. As the stress of being milked regularly has this effect on venom yield, it is reasoned that it may also affect venom toxicity. This may explain the disparity described by Hardy and Haad (1998) of the low laboratory toxicity versus the high mortality rate of bite victims.[10]

Brown (1973) gives the following LD50 values for mice: 1.5 mg/kg IV, 1.6–6.2 mg/kg IP, 6.0 mg/kg SC. He also mentions a venom yield of 200-411 mg.[11]

Subspecies

Subspecies[2] Authority[2] Common name Geographic range[1]
L. m. muta (Linnaeus, 1766) South American bushmaster Colombia, eastern Ecuador, Peru, northern Bolivia, eastern and southern Venezuela, Guyana, Surinam, French Guiana and much of northern Brazil
L. m. rhombeata (Wied-Neuwied, 1824) Atlantic forest bushmaster Coastal forests of southeastern Brazil (from southern Rio Grande do Norte to Rio de Janeiro).

See also

Cited references

  1. 1.0 1.1 1.2 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 Lachesis muta (TSN 209556). Integrated Taxonomic Information System. Accessed on 25 October 2006.
  3. 3.0 3.1 3.2 Mehrtens JM. 1987. Living Snakes of the World in Color. New York: Sterling Publishers. 480 pp. ISBN 0-8069-6460-X.
  4. 4.0 4.1 U.S. Navy. 1991. Poisonous Snakes of the World. US Govt. New York: Dover Publications Inc. 203 pp. ISBN 0-486-26629-X.
  5. Mendes, John. 1986. Cote ce Cote la: Trinidad & Tobago Dictionary, Arima, Trinidad, p. 95.
  6. 6.0 6.1 List of Snakes of Trinidad and Tobago at Republic of Trinidad and Tobago Biodiversity Clearing House. Accessed 25 October 2006.
  7. Gotch AF. 1986. Reptiles -- Their Latin Names Explained. Poole, UK: Blandford Press. 176 pp. ISBN 0-7137-1704-1.
  8. Herklots GAC. 1961. The Birds of Trinidad and Tobago. Collins, London, p. 10.
  9. Lachesis muta, The Silent Fate at South American Pictures. Accessed 26 October 2006.
  10. Ripa, D. 2001. Bushmasters and the Heat Strike at VenomousReptiles.org. Accessed 26 October 2006.
  11. Brown JH. 1973. Toxicology and Pharmacology of Venoms from Poisonous Snakes. Springfield, Illinois: Charles C. Thomas. 184 pp. LCCCN 73-229. ISBN 0-398-02808-7.

Other references

  • Bolaños R. 1972. Toxicity of Costa Rican snake venoms for the white mouse. Amer. Jour. Trop. Med. Hyg. 21:360-363.
  • Hardy DL Sr, Haad JJS. 1998. A review of venom toxinology and epidemiology of envenoming of the bushmaster (Lachesis) with report of a fatal bite. Bull. Chicago Herp. Soc. 33(6):113-123.
  • O'Shea M. 2005. Venomous Snakes of the World. Princeton University Press. 160 pp. ISBN 0-691-12436-1.
  • Zamudio KR, Greene HW. 1997. Phylogeography of the bushmaster (Lachesis muta: Viperidae): implications for neotropical biogeography, systematics and conservation. Biological Journal of the Linnean Society, 62:421-442. PDF at Cornell University, Department of Ecology and Evolutionary Biology. Accessed 26 October 2006.

External links