Brazilian pit vipers have a geographic range including southern Brazil, northern Argentina, and northeastern Paraguay. They are primarily found in the Brazilian Atlantic Forest, a region that has undergone many ecological changes due habitat fragmentation. This species continues to be found in Rio de Janeiro and Sao Paulo, with populations extending to Mato Grasso. It also inhabits numerous islands, up to 35 km offshore, off the coasts of Argentina and Paraguay. (Araujo and Martins, 2006; Campbell and Lamar, 2004; Grazziotin, et al., 2006; McDiarmid, et al., 1999; Oliveira and Santori, 1999)
Brazilian pit vipers prefer dense evergreen and deciduous tropical forests in the Brazilian Atlantic rainforest, up to 1000 m above sea level. They are also found in scrub, savanna, semitropical upland forests, and cultivated fields with nearby vegetative cover; even when basking, they are found under some sort of cover. They are considered semi-arboreal; adults are largely terrestrial, while juveniles are more arboreal, presumably to avoid predators. (Araujo and Martins, 2006; Campbell and Lamar, 2004; Gomes and Almeaida-Santos, 2012; Grazziotin, et al., 2006; McDiarmid, et al., 1999; Oliveira and Martins, 2002; Sazima, 1991)
Brazilian pit vipers have flat, sharply ridged heads. Their heads are tan to medium dark brown, with black patterning. On the head is a pronounced dark brown strip, outlined by a definite pale coloration, originating behind the eye and continuing posteriorly to the jaw. Overall dorsal coloration may be olive, brown, gray, tan, yellow, or maroon. Coloration is related to geographical variations in the colors of substrates, suggesting that dorsal background color is subject to selective pressures. Dark brown trapezoidal to subtriangular markings are present on both flanks, surrounded by more pale coloration. These markings can be juxtaposed or opposite each other, most frequently lacking a definite pattern. They are pale green to pale yellow ventrally, with irregular blotching of gray pigment throughout. Their eyes have a gold to greenish gold iris, complemented with somewhat darker interlaced lines and eyelids with a pointed canthus (characteristic of species within their genus). Juveniles most often have a light tip on their tails, used for caudal luring of prey. (Campbell and Lamar, 2004; Furtado, et al., 2006; Grazziotin, et al., 2006; McDiarmid, et al., 1999; Sazima, 1991)
Brazilian pit vipers are slender, with weekly-keeled head scalation comprised of 5 to 12 intersupraoculars. Supralabial scales average 8-9 in number, with the second fused to form part of the lacunal scales, a characteristic exclusive to crotaline snakes. Lacunolabials are also present on the head. Midbody is made up of 23-25 rows of body scales. Ventral scales range from 170-218 total in males and females, respectively. The number of subcaudal scales, which are predominantly paired, ranges from 51-71 scales for males and females, respectively. Average length is approximately 60 cm, but there have been individuals of up to 160 cm reported. These snakes are sexually dimorphic, with females larger than males; females also produce significantly more (220 mg vs 40 mg), and more lethal, venom than males. Venom composition varies significantly between males and females, with male venom containing more protein diversity. Female venom is more potent for hyaluronidasic and hemorrhagic activities, and is more lethal. In contrast, male venom is more potent for coagulant, phospholipasic, and myotoxic activities. These developmental characteristics may therefore demonstrate niche partitioning between genders as well, particularly in terms of diet. (Campbell and Lamar, 2004; Furtado, et al., 2006; Grazziotin, et al., 2006; McDiarmid, et al., 1999)
There are currently five congeneric species considered possibly sympatric to Brazilian pit vipers, but there are no currently recognized sub-species. All exhibit similarities, inculding fusion of the the supralabial scales anterior to the temporal scales. This species is smaller and lighter than the jaracacussa (Bothrops jararacussa), also exhibiting more intersuprascapular and ventral scales than this snake. Distinguishable differences between Brazilian pit vipers and Brazilian lanceheads (Bothrops moojeni) include size (Brazilian pit vipers being smaller) and coloration; Brazilian pit vipers have a darker, lower residing canthus with a wider postorbital stripe, and lack a sinuous marking on the nape. (Campbell and Lamar, 2004; Grazziotin, et al., 2006; McDiarmid, et al., 1999)
Brazilian pit vipers are ovovivoparous; neonates are venomous upon birth and hunt on their own. At birth, females measure 23.5-26.5 cm SVL (snout to vent length), while males measure 24.0-27.9 cm SVL; females weigh 7.0-8.5 g, while males weigh 6.0-9.0 g. Both sexes grow at similar rates until reaching approximately one year of age, at which point females grow significantly faster; within three years, females are significantly larger and heavier than males. Venom of juveniles has a greater anticoagulant effect than that of adults. As young develop, the differences in venom composition and complexity discussed above become more pronounced. (Almeida-Santos and Salomão, 2002; Campbell and Lamar, 2004; Furtado, et al., 2006; Martins, et al., 2002; Polachowski and Werneburg, 2013)
Males have been observed to mate with more than one female. Generally, male-male fighting occurs in viperids, activated by the presence of sex steroids such as androgens and estrogens, prior to copulation. Male-male fighting, as well as any other establishment of dominance, may be less likely in this species than other viperids, however, as females are significantly larger than males. (Campbell and Lamar, 2004; Furtado, et al., 2006; Martins, et al., 2002; McDiarmid, et al., 1999; Oliveira and Martins, 2002)
Courtship and mating occur between April and May. Females have been found with uterine muscular twisting from April through September, indicating that they store sperm in order to delay fertilization. Females demonstrate secondary vitellogenesis and this, along with ovulation and fertilization, occurs in the spring (October through December or January). Parturition time ranges between February and April, as evidenced by a greater presence of juveniles during these months. Long-term sperm storage ensures that development and birth occur during more suitable resource conditions; birth is correlated with high food availability and seasonal rainy periods. Male testes reach their largest size in the summer, although they possess mobile spermatozoa year round (contained within the ductus deferens). It is believed that individuals of both sexes reach sexual maturity by two years of age. On average, 10-14 offspring are produced per season. Females may only reproduce biennially, depending in part on their own nutritional status, as they must have sufficient nutritional resources to produce egg yolk. (Almeida-Santos and Salomão, 2002; Campbell and Lamar, 2004; Furtado, et al., 2006; Martins, et al., 2002; McDiarmid, et al., 1999; Sazima, 1991)
There is little information currently available on the life expectancy for this species. They are known to live for at least 6.5 years in captivity, but similar species have significantly longer lifespans, indicating that this may be the case for wild Brazilian pit vipers as well. ("AnAge entry for Bothrops jararaca", 2012; Campbell and Lamar, 2004)
Brazilian pit vipers are encountered most frequently in a coiled, hunting state at night. During the day, they are often found in foliage, in sites at higher elevations. There is a significant reduction in activity during the colder months of the year and peak activity is usually observed during warmer/rainier months, concurrent with breeding. Young spend much more time in trees or other off-ground cover, to avoid predators, while adults are predominantly terrestrial. (Campbell and Lamar, 2004; Martins, et al., 2002; Troncone and Silveira, 2001)
There is no current information available on any average home range of Brazilian pit vipers. (Campbell and Lamar, 2004)
Brazilian pit vipers assess their environments by interpreting tactile, infrared, chemical, and visual stimuli. They have highly acute olfactory organs and can sense sexual chemical cues. They also possess the defining feature of pit vipers: infrared sensory pits located on both sides of the head, between the eyes and nostrils. These pits are externally comparable to nostrils, but house organs that detect a range of infrared wavelengths. They also house heat-detecting nerves and are highly vascularized. This enables the snakes to use this sensory information not only for prey detection, but also for thermoregulation. The location of the pits on either side of their heads allow these snakes to sense small deviations in infrared wavelengths, informing them of a potential prey item's location, as well as the distance of prey while hunting at night. Another common feature of pit vipers is refined binocular vision for depth perception, aided by vertical slits in their pupils. (Campbell and Lamar, 2004; Martins, et al., 2002; McDiarmid, et al., 1999; Newman, et al., 1980)
Brazilian pit vipers are generalist feeders that demonstrate an ontogenetic diet shift from ectothermic prey (up to 75% anurans, as well as arthropods) as juveniles to endothermic prey (small mammals, approximately 80% rodents) as adults. They are ambush predators, and are equipped with intricate camouflage and very toxic venom. Juveniles often employ caudal luring to attract prey, coiling up and moving the tip of the tail, which is light in color, across their bodies. The tip of the tail looks very similar to an insect larva, which serves to lure in prey. These snakes tend to feed infrequently, likely due to their sedentary habits and occurrence in moderate climates. When they do feed, two different strike strategies have been observed. One strategy tends to be used with prey that an individual is less familiar with: a snake envenomates its prey and then retracts its head, allowing their venom to take effect and later retrieving and swallowing its prey. With prey that they are habituated to, their strategy for attack is to bite and hold prey in their mouths, without retracting their fangs, while the venom takes effect. (Campbell and Lamar, 2004; Martins, et al., 2002; Sazima, 1991; Troncone and Silveira, 2001)
Brazilian pit vipers are prey to many larger animals, likely including mammals, snakes, and birds. In particular, white eared oppossums (Didelphis albiventris) have been observed to systematically attack and kill these snakes with a lethal bite to their neck or head. In order to avoid predation, Brazilian pit vipers have developed base colorations similar to local substrate. Additionally, a number of defensive behaviors have been observed for this species, including striking (the most common defensive maneuver), tail vibration (warning of an imminent strike), head/neck elevation, and body thrashing. They may also use cryptic and escape behaviors (such as head hiding and body compression). These snakes may vary their defensive behaviors based on predator type. (Araujo and Martins, 2006; Campbell and Lamar, 2004; Oliveira and Santori, 1999)
In addition to their roles as predator and prey, Brazilian pit vipers may serve as hosts to a variety of endoparasites. Even heavily infested individuals do not appear to be severely affected, with only minor lesions apparent. (Campbell and Lamar, 2004; Grazziotin, et al., 2006; Grego and Gardiner, 2004; Martins, et al., 2002; Oliveira and Martins, 2002)
This species was the focus of pioneering work on the use of venom in drug development and discovery. Researchers found the venom of Brazilian pit vipers to contain a peptide that caused a severe drop in blood pressure in mice; it was used in the development of the first angiotensin converting enzyme inhibitors, for treatment of people with hypertension and congestive heart failure. The venom also possesses haemocoagulase enzyme, which is used as an antihemorrhagic drug. These snakes may also help to keep populations of agricultural pests, such as rodents, in check. (Campbell and Lamar, 2004; Martins, et al., 2002; McDiarmid, et al., 1999)
Bothrops species account for the most human deaths in the New World, and Brazilian pit vipers pose a significant risk to humans. Encounter rates are high because the species is abundant within its geographical range and its preferred habitats include agricultural fields. The toxins present in their venom cause swelling at the envenomation site, necrosis, blistering, hemorrhagic blebs, systemic bleeding into the skin, gums, and nose, and subconjunctival hemorrhage. Collectively, these effects can lead to death due to shock, renal failure, and intrancranial hemorrhage, compounded by severe hypotension. (Brown, 1973; Campbell and Lamar, 2004; Warrell, 2004; Zelanis, et al., 2010)
Adam Murphy (author), Indiana University-Purdue University Fort Wayne, Mark Jordan (editor), Indiana University-Purdue University Fort Wayne, Jeremy Wright (editor), University of Michigan-Ann Arbor.
living in the southern part of the New World. In other words, Central and South America.
uses sound to communicate
living in landscapes dominated by human agriculture.
Referring to an animal that lives in trees; tree-climbing.
having body symmetry such that the animal can be divided in one plane into two mirror-image halves. Animals with bilateral symmetry have dorsal and ventral sides, as well as anterior and posterior ends. Synapomorphy of the Bilateria.
an animal that mainly eats meat
uses smells or other chemicals to communicate
having markings, coloration, shapes, or other features that cause an animal to be camouflaged in its natural environment; being difficult to see or otherwise detect.
a substantial delay (longer than the minimum time required for sperm to travel to the egg) takes place between copulation and fertilization, used to describe female sperm storage.
a substance used for the diagnosis, cure, mitigation, treatment, or prevention of disease
animals which must use heat acquired from the environment and behavioral adaptations to regulate body temperature
union of egg and spermatozoan
forest biomes are dominated by trees, otherwise forest biomes can vary widely in amount of precipitation and seasonality.
(as keyword in perception channel section) This animal has a special ability to detect heat from other organisms in its environment.
offspring are produced in more than one group (litters, clutches, etc.) and across multiple seasons (or other periods hospitable to reproduction). Iteroparous animals must, by definition, survive over multiple seasons (or periodic condition changes).
the area in which the animal is naturally found, the region in which it is endemic.
active during the night
reproduction in which eggs develop within the maternal body without additional nourishment from the parent and hatch within the parent or immediately after laying.
Referring to a mating system in which a female mates with several males during one breeding season (compare polygynous).
rainforests, both temperate and tropical, are dominated by trees often forming a closed canopy with little light reaching the ground. Epiphytes and climbing plants are also abundant. Precipitation is typically not limiting, but may be somewhat seasonal.
scrub forests develop in areas that experience dry seasons.
breeding is confined to a particular season
remains in the same area
reproduction that includes combining the genetic contribution of two individuals, a male and a female
mature spermatozoa are stored by females following copulation. Male sperm storage also occurs, as sperm are retained in the male epididymes (in mammals) for a period that can, in some cases, extend over several weeks or more, but here we use the term to refer only to sperm storage by females.
uses touch to communicate
Living on the ground.
the region of the earth that surrounds the equator, from 23.5 degrees north to 23.5 degrees south.
A terrestrial biome. Savannas are grasslands with scattered individual trees that do not form a closed canopy. Extensive savannas are found in parts of subtropical and tropical Africa and South America, and in Australia.
A grassland with scattered trees or scattered clumps of trees, a type of community intermediate between grassland and forest. See also Tropical savanna and grassland biome.
A terrestrial biome found in temperate latitudes (>23.5° N or S latitude). Vegetation is made up mostly of grasses, the height and species diversity of which depend largely on the amount of moisture available. Fire and grazing are important in the long-term maintenance of grasslands.
an animal which has an organ capable of injecting a poisonous substance into a wound (for example, scorpions, jellyfish, and rattlesnakes).
movements of a hard surface that are produced by animals as signals to others
uses sight to communicate
young are relatively well-developed when born
2012. "AnAge entry for Bothrops jararaca" (On-line). AnAge: The Animal Ageing and Longevity Database. Accessed July 11, 2013 at http://genomics.senescence.info/species/entry.php?species=Bothrops_jararaca.
Almeida-Santos, S., M. Salomão. 2002. Biology of the Vipers. Eagle Mountain, Utah: Eagle Mountain Publishing.
Araujo, M., M. Martins. 2006. Defensive behaviour in pit vipers of the genus Bothrops (Serpentes, Viperidae). The Herpetological Journal, 16/3: 297-303. Accessed July 10, 2013 at http://eco.ib.usp.br/labvert/Araujo%26Martins.pdf.
Brown, J. 1973. Toxicology and Pharmacology of Venoms from Poisonous Snakes. Springfield, Illinois: Charles C. Thomas.
Campbell, J., W. Lamar. 2004. The Venomous Reptiles of the Western Hemisphere. Ithaca & London: Comstock Publishing Associates.
Furtado, M., S. Travaglia-Cardoso, M. Rocha. 2006. Sexual dimorphism in venom of Bothrops jararaca. Toxicon, 48/4: 401-410. Accessed July 10, 2013 at http://www.ecoevo.com.br/publicacoes/alunos/silvia_cardoso/toxiconsexualdimorphismbjararaca_2006.pdf.
Gomes, C., S. Almeaida-Santos. 2012. Microhabitat use by species of the genera Bothrops and Crotalis. Journal of Venomous Animals and Toxins Including Tropical Diseases, 18/4: 393-398. Accessed July 10, 2013 at http://www.scielo.br/scielo.php?pid=S1678-91992012000400007&script=sci_arttext.
Grazziotin, F., M. Monzel, S. Echeverrigaray, S. Bonatto. 2006. Phylogeography of the Bothrops jararaca complex (Serpentes: Viperidae): past fragmentation and island colonization in the Brazilian Atlantic Forest. Molecular Ecology, 15/13: 3969-3982. Accessed July 10, 2013 at http://onlinelibrary.wiley.com.proxy.lib.umich.edu/doi/10.1111/j.1365-294X.2006.03057.x/full.
Grego, K., C. Gardiner. 2004. Comparative pathology of parasitic infections in free-ranging and captive pit vipers (Bothrops jararaca). Veterinary Record, 154/18: 559-562. Accessed July 10, 2013 at http://veterinaryrecord.bmj.com.proxy.lib.umich.edu/content/154/18/559.full.pdf+html.
Martins, M., O. Marques, I. Sazima. 2002. Biology of the Vipers. Eagle Mountain, Utah: Eagle Mountain Publishing.
Martins, M., M. Araujo, R. Sawaya, R. Nunes. 2006. Diversity and evolution of macrohabitat use, body size and morphology in a monophyletic group of Neotropical pitvipers (Bothrops). Journal of Zoology, 254/4: 529-538. Accessed July 10, 2013 at http://www.rc.unesp.br/ib/ecologia/marcio/files/Martins_etal_2001_JZool.pdf.
McDiarmid, R., J. Campbell, T. Touré. 1999. Snake Species of the World: A Taxonomic and Geographic Reference, Volume 1. Lawrence, KS: Herpetologists' League.
Newman, E., E. Gruberd, P. Hatline. 1980. The infrared trigemino-tectal pathway in the rattlesnake and in the python. The Journal of Comparative Neurology, 191: 464-477. Accessed July 10, 2013 at http://www2.neuroscience.umn.edu/eanwebsite/PDF%20EAN%20pubs/J%20Comp%20Neurol%20191%20465%201980.pdf.
Oliveira, M., M. Martins. 2002. When and where to find a pitviper: activity patterns and habitat use of the lancehead, Bothrops atrox, in central Amazonia, Brazil. Herpetological Natural History, 8/2: 101-110. Accessed July 10, 2013 at http://eco.ib.usp.br/labvert/atrox-activity.pdf.
Oliveira, M., R. Santori. 1999. Predatory behavior of the opossum Didelphis albiventris on the pitviper Bothrops jararaca. Studies on Neotropical Fauna and Environment, 34/2: 72-75. Accessed July 10, 2013 at http://www.tandfonline.com.proxy.lib.umich.edu/doi/pdf/10.1076/snfe.18.104.22.1685.
Polachowski, K., I. Werneburg. 2013. Late embryos and bony skull development in Bothropoides jararaca (Serpentes, Viperidae). Zoology, 116/1: 36-63. Accessed July 10, 2013 at http://www.sciencedirect.com/science/article/pii/S0944200612000931.
Troncone, L., P. Silveira. 2001. Predatory behavior of the snake Bothrops jararaca and its adaptation to captivity. Zoo Biology, 20/5: 399-406. Accessed July 10, 2013 at http://onlinelibrary.wiley.com.proxy.lib.umich.edu/store/10.1002/zoo.1038/asset/1038_ftp.pdf?v=1&t=hiywhi6t&s=87b1188b17f455d3fef64334acba1567983faf1d.
Warrell, D. 2004. Snakebites in Central and South America: Epidemiology, Clinical Features, and Clinical Management. Ithaca and London: Comstock Publishing Associates.
Zelanis, A., A. Tashima, M. Rocha, M. Furtado, A. Camargo, P. Ho, S. Serrano. 2010. Analysis of the ontogenetic variation in the venom proteome/peptidome of Bothrops jararaca reveals different strategies to deal with prey. Journal of Proteome Research, 9/5: 2278-2291. Accessed July 10, 2013 at http://www.incttox.com.br/wp-content/uploads/2010/05/14_ZELANI.pdf.