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Behavior

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Atlantic bamboo rats use vocalizations to defend resources and warn conspecifics of potential threats. Often performing vocalizations after dark, they sit on bamboo culms and thrust their head forward with each call. They remain secluded amongst the bamboo leaves, rarely exposing their position. During alarm calls, they call once and run to an area of greater cover, and continue calling for several minutes. When conspecifics hear a call, they escape to areas with greater cover and counter-call.

Communication Channels: acoustic

Perception Channels: visual ; tactile ; acoustic ; chemical

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cruz, M. 2011. "Kannabateomys amblyonyx" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Kannabateomys_amblyonyx.html
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Conservation Status

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Atlantic bamboo rats are naturally rare; a study in Rio Grande do Sul State reports a density of 4.28 individuals per km^2. However, due to their wide distribution and large population, Atlantic bamboo rats are listed as "least concern" on IUCN Red List of Threatened Species. Atlantic bamboo rats are locally threatened in Minas Gerais State, Brazil due to habitat destruction largely due to logging.

US Federal List: no special status

CITES: no special status

State of Michigan List: no special status

IUCN Red List of Threatened Species: least concern

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cruz, M. 2011. "Kannabateomys amblyonyx" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Kannabateomys_amblyonyx.html
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Benefits

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Information regarding potential negative economic impacts of Atlantic bamboo rats on humans has not been documented. However, bamboo rats and mole rats in the subamily Rhizomyinae are known to affect tapioca and sugarcane crops in Thailand.

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cruz, M. 2011. "Kannabateomys amblyonyx" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Kannabateomys_amblyonyx.html
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Benefits

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Information regarding potential economic impacts of Atlantic bamboo rats on humans has not been documented.

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cruz, M. 2011. "Kannabateomys amblyonyx" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Kannabateomys_amblyonyx.html
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Associations

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Atlantic bamboo rats are important seed dispersers of various bamboo species. In addition, the manner by which they feed on bamboo is thought to be beneficial to the overall health of bamboo stands in which they reside. They may also be an important food source for brown capuchins, and although it has not been documented, Atlantic bamboo rats are likely host to a number of endo- and ectoparasites as well.

Ecosystem Impact: disperses seeds

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cruz, M. 2011. "Kannabateomys amblyonyx" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Kannabateomys_amblyonyx.html
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Trophic Strategy

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Atlantic bamboo rats are specialized herbivores, feeding on bamboo shoots, stems, and leaves. They are arboreal browsers and feed predominately at night. They also feed on the shoots of young Phyllostachys species, but appear to avoid feeding on Bambusa tuldoides.

Plant Foods: leaves; wood, bark, or stems

Primary Diet: herbivore (Folivore )

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cruz, M. 2011. "Kannabateomys amblyonyx" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Kannabateomys_amblyonyx.html
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Distribution

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Atlantic bamboo rats, Kannabateomys amblyonyx, are native to the southeastern and southern Atlantic Forest, in Brazil, eastern Paraguay and northeastern Argentina.

Biogeographic Regions: neotropical (Native )

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cruz, M. 2011. "Kannabateomys amblyonyx" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Kannabateomys_amblyonyx.html
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Habitat

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Atlantic bamboo rats are found in moist tropical forests, particularly bamboo thickets located near water. They build arboreal nests in native giant climbing bamboo (Guadua angustifoila), as well as in introduced species of bamboo, such as several Phyllostachys spp. and Chinese bamboo (Bambusa tuldoides). Native Guadua stands are rare in southeastern and southern Brazil due to deforestation practices. However, with the introduction of Phyllostachys spp. and B. tuldoides, Atlantic bamboo rats are able to re-inhabit parts of their native range.

Habitat Regions: tropical

Terrestrial Biomes: rainforest

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cruz, M. 2011. "Kannabateomys amblyonyx" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Kannabateomys_amblyonyx.html
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Life Expectancy

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The average lifespan of Atlantic bamboo rats has not been documented.

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cruz, M. 2011. "Kannabateomys amblyonyx" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Kannabateomys_amblyonyx.html
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Morphology

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Atlantic bamboo rats are large rodents, ranging in size from 230 to 347 cm long, with a long tail of 300 to 420 cm long. They weigh between 350 to 600 g. Their dorsal pelage is olive-green to brown-orange with orange ventral pelage and white patches on their throat and chest. They have a square-like snout, gray cheeks, long whiskers and white lips. Thick fur covers the base of their tail, which tapers to a small tuft of dark-brown distal hairs. They have four long digits, an elongated and broadened third and forth digit separated by a gap, and flat nails, which allow them to have a firm grip on bamboo culms. The dental formula for members of the family Echimayidae is 1/1 0/0 1/1 3/3 for a total of 20 teeth. Atlantic bamboo rats have flat-crowned cheek teeth and differ from other Dactylomys spp. by having narrow enamel ridges present on their upper cheek teeth, as well as an absence of a constricted palate. Atlantic bamboo rats are sexually dimorphic. Although coloration is similar between sexes, males are generally larger than females. However, a monogamous population inhabiting Itapuã State Park in southern Brazil showed no sexual dimorphism.

Range mass: 350 to 600 g.

Range length: 230 to 347 cm.

Other Physical Features: endothermic ; homoiothermic; bilateral symmetry

Sexual Dimorphism: male larger

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cruz, M. 2011. "Kannabateomys amblyonyx" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Kannabateomys_amblyonyx.html
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Associations

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Brown capuchins are thought to be potential predators of Atlantic bamboo rats. They have been observed foraging among bamboo stands and are known to eat rodents. When capuchins forage in thickets inhabited by Atlantic bamboo rats, rats quickly find shelter amongst the bases of bamboo clumps. After capuchins leave, rat carcasses with the head and thorax missing are often found at the base of bamboo stands. However, actual capture and feeding by brown capuchins on Atlantic bamboo rats has not been documented.

Known Predators:

  • brown capuchin (Cebus apella)

Anti-predator Adaptations: cryptic

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cruz, M. 2011. "Kannabateomys amblyonyx" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Kannabateomys_amblyonyx.html
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Reproduction

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Direct confirmation of polygny in Atlantic bamboo rats has not been documented in the wild nor have any genetic analyses on allelic contribution from either parent been conducted in order to determine polygyny or polyandry. However, physical characteristics and social patterns associated with polygyny have been reported in Atlantic bamboo rats. For example, males are larger than females and have larger home ranges, which may overlap the home ranges of several females. Stallings et al. (1994) found that when numerous bamboo patches were located close together, males were able to obtain access to multiple females, suggesting polygyny. However, in areas with low population densities, females are restricted to small, widely-spaced home ranges, which decreases the probability of males to acquire more than one mate. Under these situations, Atlantic bamboo rats are observed to be monogamous, living in mating pairs, with no co-occurrences of same-sex adults in the same bamboo patch.

Mating System: monogamous ; polygynous

Very little is known on the general behavior of the Atlantic bamboo rat during reproduction. They breed year round, yielding between 1 and 3 young per liter, with an average of 1.7 young per litter. Olmos et al (1993) found a deceased 600 g female with two near-term fetuses, both weighing approximately 20% of the mother’s weight. This suggests that neonate Atlantic bamboo rats require large demands of food and energy from their mother.

Range number of offspring: 1 to 3.

Average number of offspring: 1.7.

Key Reproductive Features: iteroparous ; gonochoric/gonochoristic/dioecious (sexes separate); sexual ; viviparous

In Itapuã State Park, Brazil, monogamous mated males showed direct parental behavior similar to that of females, including grooming, huddling, and food provisioning. Furthermore, both males and females performed indirect parental behavior, such as alarm calls and nest building. In the event of a death or disappearance to one of the parents, the surviving parent (male or female) remains with the young, indicating prolonged parental care. In patchy arboreal habitats, biparental care is advantageous for Atlantic bamboo rats, as it reduces the risks of young falling from trees and depredation when moving amongst exposed branches.

Parental Investment: male parental care ; female parental care ; pre-hatching/birth (Provisioning: Female, Protecting: Female); pre-weaning/fledging (Provisioning: Male, Female, Protecting: Male, Female); pre-independence (Provisioning: Male, Female, Protecting: Male, Female)

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Atlantic bamboo rat

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The Atlantic bamboo rat (Kannabateomys amblyonyx), or southern bamboo rat, is a spiny rat species found in humid tropical forests in Argentina, Brazil and Paraguay. It is the only member of the genus Kannabateomys.[2]

Description

The Atlantic bamboo rat can reach a head-and-body length of 25 cm (9.8 in) with a tail of 32 cm (12.6 in). Its weight is about 475 g (1 lb). The pelage is the typical agouti brown-to-grey colour of many rodents, grading to chestnut on the flanks. The chin and underparts are white tinged with reddish brown. The first 6 cm (2.4 in) of the tail are well-haired but the rest is sparsely haired. There is a distinct tuft of hairs at the tip. When fully grown, this bamboo rat with its long tail is unlikely to be mistaken for any other species.[3]

Etymology

The genus name Kannabateomys derives from the three ancient greek words κάννα (kánna), meaning "reed, cane", βατέω (batéō), meaning "to mount", and μῦς (mûs), meaning "mouse, rat".[4][5][6]

The species name amblyonyx derives from the two ancient greek words ἀμβλύς (amblús), meaning "blunt, not sharp", and ὄνυξ (ónux), meaning "claw, fingernail".[4][5]

Distribution and habitat

This species is native to South America, where its range includes southeastern Brazil, eastern Paraguay and northeastern Argentina. Typical habitat is moist forests near water with dense understorey of bamboos. It is particularly associated with the giant bamboo Guadua angustifolia, which forms thickets.[7]

Ecology

The Atlantic bamboo rat is nocturnal and is highly arboreal, scrambling around in trees and bamboos, especially near water. The home range is about 1,000 m2 (1,200 sq yd). When alarmed it issues loud squeals.[3] It probably feeds on grasses, leaves, shoots, fruits and tubers.[8]

Phylogeny

Kannabateomys is a member of the Echimyini clade of arboreal Echimyidae rodents. Its closest relatives are Dactylomys and Olallamys. These South American bamboo rats share unique features and are grouped under the informal clade name of "Dactylomyines".[9] The dactylomyines are the sister genera to Diplomys and Santamartamys. All these taxa are closely related to the genera Echimys, Phyllomys, Makalata, Pattonomys, and Toromys. In turn, these genera share phylogenetic affinities with the clade containing Lonchothrix and Mesomys, and with Isothrix.[10]

Genus-level cladogram of the Echimyini.

Echimys

Phyllomys

Makalata

Pattonomys

Toromys
(Giant tree-rat)

"Dactylomyines"

Dactylomys

Olallamys

Kannabateomys
(Atlantic bamboo rat)

Diplomys

Santamartamys
(Red-crested tree-rat)

"Eumysopines"

Lonchothrix
(Tuft-tailed spiny tree-rat)

Mesomys

Isothrix

The cladogram has been reconstructed from mitochondrial and nuclear DNA characters.[11][12][13][14][15][16][17][18][10]

Status

K. amblyonyx is not a common species. In the state of Rio Grande do Sul in Brazil, for example, it has been recorded as having a density of just over four individuals per square kilometre. As a nocturnal animal it is seldom seen, but it has an extensive range and is presumed to have a large total population. In some places, such as in the state of Minas Gerais in Brazil, it is threatened locally by forest clearance, but other specific threats have not been identified and the International Union for Conservation of Nature has rated its conservation status as "least concern".[1]

References

  1. ^ a b Catzeflis, F.; Patton J.; Percequillo, A.; Weksler, M. (2016). "Kannabateomys amblyonyx". IUCN Red List of Threatened Species. 2016: e.T10957A22205666. doi:10.2305/IUCN.UK.2016-2.RLTS.T10957A22205666.en. Retrieved 11 November 2021.
  2. ^ Woods, C.A.; Kilpatrick, C.W. (2005). "Genus Kannabateomys". In Wilson, D.E.; Reeder, D.M (eds.). Mammal Species of the World: A Taxonomic and Geographic Reference (3rd ed.). Johns Hopkins University Press. p. 1576. ISBN 978-0-8018-8221-0. OCLC 62265494.
  3. ^ a b Eisenberg, John F.; Redford, Kent H. (2000). Mammals of the Neotropics, Volume 3: Ecuador, Bolivia, Brazil. University of Chicago Press. p. 481. ISBN 978-0-226-19542-1.
  4. ^ a b Bailly, Anatole (1981-01-01). Abrégé du dictionnaire grec français. Paris: Hachette. ISBN 978-2010035289. OCLC 461974285.
  5. ^ a b Bailly, Anatole. "Greek-french dictionary online". www.tabularium.be. Retrieved December 7, 2017.
  6. ^ Palmer, T. S. (1904). Details - Index generum mammalium: a list of the genera and families of mammals. - Biodiversity Heritage Library. Washington, Govt. Print. Off. p. 356. doi:10.5962/bhl.title.39809.
  7. ^ Londoño, X. 2000. Guadua. In E. J. Judziewicz, R. J. Soreng, G. Davidse, P. M. Peterson, T. S. Filgueiras & F. O. Zuloaga (eds.) Catalogue of New World Grasses (Poaceae): I. Subfamilies Anomochlooideae, Bambusoideae, Ehrhartoideae, and Pharoideae, Contributions from the United States National Herbarium 39: 58–62. Smithsonian Institution, Washington
  8. ^ Lord, Rexford D. (2007). Mammals of South America. JHU Press. p. 64. ISBN 978-0-8018-8494-8.
  9. ^ Fabre, Pierre-Henri; Patton, James L.; Leite, Yuri L. R. (2016). "Family Echimyidae (hutias, South American spiny-rats and coypu)". In Wilson, Don E.; Lacher, Thomas E. Jr; Mittermeier, Russell A. (eds.). Handbook of the Mammals of the World. Vol 6. Lagomorphs and Rodents I. Barcelona: Lynx Edicions. pp. 552–641. ISBN 978-84-941892-3-4.
  10. ^ a b Fabre, Pierre-Henri; Upham, Nathan S.; Emmons, Louise H.; Justy, Fabienne; Leite, Yuri L. R.; Loss, Ana Carolina; Orlando, Ludovic; Tilak, Marie-Ka; Patterson, Bruce D.; Douzery, Emmanuel J. P. (2017-03-01). "Mitogenomic Phylogeny, Diversification, and Biogeography of South American Spiny Rats". Molecular Biology and Evolution. 34 (3): 613–633. doi:10.1093/molbev/msw261. ISSN 0737-4038. PMID 28025278.
  11. ^ Lara, Márcia C.; Patton, James L.; da Silva, Maria Nazareth F. (1996). "The Simultaneous Diversification of South American Echimyid Rodents (Hystricognathi) Based on Complete Cytochrome b Sequences". Molecular Phylogenetics and Evolution. 5 (2): 403–413. doi:10.1006/mpev.1996.0035. PMID 8728398.
  12. ^ Leite, Yuri L. R.; Patton, James L. (2002). "Evolution of South American spiny rats (Rodentia, Echimyidae): the star-phylogeny hypothesis revisited". Molecular Phylogenetics and Evolution. 25 (3): 455–464. doi:10.1016/s1055-7903(02)00279-8. PMID 12450750.
  13. ^ Galewski, Thomas; Mauffrey, Jean-François; Leite, Yuri L. R.; Patton, James L.; Douzery, Emmanuel J. P. (2005). "Ecomorphological diversification among South American spiny rats (Rodentia; Echimyidae): a phylogenetic and chronological approach". Molecular Phylogenetics and Evolution. 34 (3): 601–615. doi:10.1016/j.ympev.2004.11.015. PMID 15683932.
  14. ^ Upham, Nathan S.; Patterson, Bruce D. (2012). "Diversification and biogeography of the Neotropical caviomorph lineage Octodontoidea (Rodentia: Hystricognathi)". Molecular Phylogenetics and Evolution. 63 (2): 417–429. doi:10.1016/j.ympev.2012.01.020. PMID 22327013.
  15. ^ Fabre, Pierre-Henri; Galewski, Thomas; Tilak, Marie-ka; Douzery, Emmanuel J. P. (2013-03-01). "Diversification of South American spiny rats (Echimyidae): a multigene phylogenetic approach". Zoologica Scripta. 42 (2): 117–134. doi:10.1111/j.1463-6409.2012.00572.x. ISSN 1463-6409. S2CID 83639441.
  16. ^ Loss, Ana; Moura, Raquel T.; Leite, Yuri L. R. (2014). "Unexpected phylogenetic relationships of the painted tree rat Callistomys pictus (Rodentia: Echimyidae)" (PDF). Natureza on Line. 12: 132–136.
  17. ^ Fabre, Pierre-Henri; Vilstrup, Julia T.; Raghavan, Maanasa; Der Sarkissian, Clio; Willerslev, Eske; Douzery, Emmanuel J. P.; Orlando, Ludovic (2014-07-01). "Rodents of the Caribbean: origin and diversification of hutias unravelled by next-generation museomics". Biology Letters. 10 (7): 20140266. doi:10.1098/rsbl.2014.0266. ISSN 1744-9561. PMC 4126619. PMID 25115033.
  18. ^ Upham, Nathan S.; Patterson, Bruce D. (2015). "Evolution of Caviomorph rodents: a complete phylogeny and timetree for living genera". In Vassallo, Aldo Ivan; Antenucci, Daniel (eds.). Biology of caviomorph rodents: diversity and evolution. Buenos Aires: SAREM Series A, Mammalogical Research — Sociedad Argentina para el Estudio de los Mamíferos. pp. 63–120.
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Atlantic bamboo rat: Brief Summary

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The Atlantic bamboo rat (Kannabateomys amblyonyx), or southern bamboo rat, is a spiny rat species found in humid tropical forests in Argentina, Brazil and Paraguay. It is the only member of the genus Kannabateomys.

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