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Necromys lasiurus
hairy-tailed akodont
(Also: hairy-tailed bolo mouse)


By Shivani Raval

Kingdom: Animalia
Phylum: Chordata
Subphylum: Vertebrata
Class: Mammalia
Order: Rodentia
Family: Cricetidae
Genus: Necromys
Species: Necromys lasiurus

Geographic Range

Necromys lasiurus (hairy-tailed bolo mouse) is distributed throughout central South America. Their range extends from Brazil and Paraguay to Bolivia and into the northern Argentine province of Misiones. (Redford and Eisenberg, 1992; Redford and Eisenberg, 1999)

Biogeographic Regions
neotropical (Native )

Habitat

Hairy-tailed bolo mice are usually found in grassland or savanna habitats. In Brazil, they can be found in the Cerrado, the regional name giveg to the Brazilian savannas or the Caatinga in the northeastern part of Brazil. They may sometimes be found in forests, typically inhabiting the area near the edges. Occasionally hairy-tailed bolo mice are known to reside in cultivated or abandoned fields. (Cangussu, et al., 2002; Henriques and Alho, 1991; Redford and Eisenberg, 1992; Redford and Eisenberg, 1999)

Habitat Regions
tropical ; terrestrial

Terrestrial Biomes
savanna or grassland ; forest

Other Habitat Features
agricultural

Physical Description

Average mass
35 g
(1.23 oz)

Average length
178 mm
(7.01 in)

Hairy-tailed bolo mice are an olive-gray color with a lighter grayish white color on their belly, although the fur color does vary slightly according to geographic range. Aside from the lighter belly, they are uniformly colored. They have short ears, small eyes, and their hind feet are somewhat darker than their backs. They lack any distinctive facial markings. Their tail, for which they are named, is shorter than the length of their head and body and is lightly haired. On average, the head and body of the mice measures around 103 mm and the tail measures 75 mm. The average weight is 35 g. There is slight sexual dimorphism in that males sre larger than the females. (Cangussu, et al., 2002; Redford and Eisenberg, 1992; Redford and Eisenberg, 1999)

Other Physical Features
endothermic ; homoiothermic; bilateral symmetry

Sexual Dimorphism
male larger

Reproduction

Although there have been many studies on the reproduction of this species, there is little information on the mating systems of hairy-tailed bolo mice.

Breeding interval
Multiple times a year

Breeding season
January-March

Average number of offspring
3-6

Reproductive activity of hairy-tailed bolo mice increases during the rainy seasons (January to March) compared to the dry seasons (July to September). Reproductive rate probably follows rainfall because rainfall affects food availability, growth of vegetation, and the probability of fire. Although the peak in reproductive rate occurs during the rainy season, there is also high reproductive activity in the late dry season from October to November. Hairy-tailed bolo mice also produce more than one time a year and on average have 3-6 young per litter. (Cangussu, et al., 2002; Francisco, et al., 1995; Redford and Eisenberg, 1992; Redford and Eisenberg, 1999)

Key Reproductive Features
iteroparous ; seasonal breeding ; gonochoric/gonochoristic/dioecious (sexes separate); viviparous

Little is known about the parental investment provided by hairy-tailed bolo mice but in related species of mice in the family Muridae offspring are altricial and the mother provides most of the parental care. ("Animal Diversity Web", 2004)

Parental Investment
altricial ; pre-fertilization (Provisioning, Protecting: Female); pre-hatching/birth (Provisioning: Female, Protecting: Female); pre-weaning/fledging (Provisioning: Female)

Lifespan/Longevity

Although Necromys lasiurus is fairly well studied, the lifespan of this mouse is unknown.

Behavior

There is not much information about the behavior of hairy-tailed bolo mice. What is known is that they are terrestrial, sometimes active during the day, and they dig and live in burrows. They build nests from grass, leaves, and other such debris. They live in burrows underground with multiple openings and tunnels. (Magnusson, et al., 1995; Redford and Eisenberg, 1992; Redford and Eisenberg, 1999)

Key Behaviors
terricolous; diurnal ; nocturnal ; crepuscular ; solitary ; territorial

Home Range

Home ranges differ between males and females: female home ranges being approximately 35% the area of male home ranges. The average home range size for males is from 4138-21880 m^2 while for females the range is from 1317-5480 m^2. Female home ranges tend to be exclusive while males tend to overlap with females' ranges. The most likely reason for this difference as well as the difference in range sizes between sexes is that females can maximize their reproductive potential by defending their food source while males can benefit by coming into contact with as many females as possible. (Magnusson, et al., 1995)

Communication and Perception

There is little known about the communication among hairy-tailed bolo mice. There is also little information about the perception channels used by these mice but they probably rely heavily on their sense of touch and smell as opposed to vision. (Redford and Eisenberg, 1992)

Communication Channels
chemical

Perception Channels
visual ; acoustic

Food Habits

Hairy-tailed bolo mice are primarily granivores, with 82% of their diet consisting of seeds. Such a large dependence on seeds can be a problem, especially when fires at the end of the dry season affect the vegetation and seed sources. This may be part of why there are such a large fluctuations in population size related to seed production. As a result of the fires, the mice show an increased dependence on invertebrates or insects during the following rainy season. (Feliciano, et al., 2002; Francisco, et al., 1995; Magnusson, et al., 1995; Redford and Eisenberg, 1992)

Primary Diet
herbivore (Granivore )

Animal Foods
insects; terrestrial non-insect arthropods

Plant Foods
seeds, grains, and nuts

Predation

While there is little written about the predators of hairy-tailed bolo mice, there is no doubt that predation on these animals is strong, as in other small rodents.

Anti-predator Adaptations
cryptic

Ecosystem Roles

Hairy-tailed bolo mice play an important role in the ecosystem as seed dispersers. They are also a food source for their predators. (Francisco, et al., 1995; Redford and Eisenberg, 1992)

Ecosystem Impact
disperses seeds

Economic Importance for Humans: Positive

Little is known about the economic importance of hairy-tailed bolo mice for humans.

Economic Importance for Humans: Negative

Like most mice, hairy-tailed bolo mice are known to carry diseases and parasites. They may also damage some crops if they are living in cultivated fields. (Redford and Eisenberg, 1992)

Negative Impacts
injures humans (carries human disease); crop pest

Conservation Status

IUCN Red List of Threatened Species [Link]
Least Concern
More Information

US Federal List [Link]
No special status

CITES [Link]
No special status

At this time, hairy-tailed bolo mice are not threatened and they are under no special status on IUCN Red List and CITES. ("2003 IUCN Red List of Threatened Species", 2003; "Convention on International Trade in Endagered Species of Wild Fauna and Flora", 2004)

Other Comments

Hairy-tailed bolo mice have also be known as Bolomys lasiurus, Akodon lasiurus, A. arviculoides, A. lenguarum, Necromys lasiurus, Cabreramys lasiurus, and Zygodontomys lasiurus. (Redford and Eisenberg, 1992; Redford and Eisenberg, 1999)

For More Information

Find Necromys lasiurus information at

Contributors

Matthew Wund (editor), University of Michigan.

Shivani Raval (author), University of Michigan, Phil Myers (editor, instructor), Museum of Zoology, University of Michigan.

References

2003. "2003 IUCN Red List of Threatened Species" (On-line). Accessed April 01, 2004 at http://www.redlist.org.

2004. "Animal Diversity Web" (On-line). Accessed April 01, 2004 at http://animaldiversity.ummz.umich.edu.

2004. "Convention on International Trade in Endagered Species of Wild Fauna and Flora" (On-line). Accessed April 01, 2004 at http://www.cites.org/eng/resources/species.html.

Alho, C., L. Pereira. 1985. Population ecology of a cerrado rodent community in Central Brazil. Revista Brasileira de Biologia, 45(4): 597-608.

Botelho, J., P. Linardi. 1996. Interrelationships between ectoparasites and rodents in wild and urban environments at Belo Horizonte, Minas Gerais State, Brazil. Revista Brasileira de Entomologia, 40(3-4): 425-430.

Cangussu, S., F. Vieira, R. Rossoni. 2002. Sexual Dimorphism and Seasonal Variation in Submandibular Glad Histology of Bolomys lasiurus (Rodentia, Muridae). Journal of Morphology, 254: 320-327.

De Oliveira, J., R. Strauss, S. Dos Reis. 1998. Assessing relative age and age structure in natural populations of Bolomys lasiurus (Rodentia: Sigmodontinae) in northeastern Brazil. Journal of Mammalogy, 79(4): 1170-1183.

Dietz, J. 1983. The Natural History of Some Small Mammals in Central Brazil. Journal of Mammalogy, Volume 64 Number 3: 521-523.

Feliciano, B., F. Fernandez, D. De Freitas, M. Figueiredo. 2002. Population dynamics of small rodents in a grassland between fragments of Atlantic Forest in southeaster Brazil. Mammalian Biology, 67(5): 304-314.

Francisco, A., W. Magnusson, T. Sanaiotti. 1995. Variation in growth and reproduction of Bolomys lasiurus (Rodentia: Muridae) in an Amazonian savanna. Journal of Tropical Ecology, 11: 419-428.

Henriques, R., C. Alho. 1991. Microhabitat Selection by Two Rodent Species in the Cerrado of Central Brazil. Mammalia, 55(1): 49-56.

Macedo, R., M. Mares. 1987. Geographic variation in the South American cricetine rodent Bolomys lasiurus. Journal of Mammalogy, 68(3): 578-594.

Magnusson, W., A. Francisco, T. Sanaiotti. 1995. Home-range size and territoriality in Bolomys lasiurus (Rodentia: Muridae) in an Amazonian savanna. Journal of Tropical Ecology, 11: 179-188.

Parreira, G., F. Cardoso. 1993. Seasonal variation of the spermatogenic activity in Bolomys lasiurus (Lund, 1841) (Rodentia, Cricetidae), from southeaster Brazil. Mammalia, 57(1): 27-34.

Redford, K., J. Eisenberg. 1999. Mammals of the Neotropics: The Central Neotropics, Volume 3. Chicago: The University of Chicago Press.

Redford, K., J. Eisenberg. 1992. Mammals of the Neotropics: The Southern Cone, Volume 2. Chicago: The University of Chicago Press.

Scheibler, D., J. Menegheti, A. Christoff. 2001. Predation of Elanus leucurus (Aves, Accipitridae) on Mus musculus (Mammalia, Muridae) and its temporal variation in agroecosystem of the Venancio Aires country, Rio Grande do Sul state, Brazil. Boletin de la Sociedad de Biologia de Concepcion, 72: 125-130.

Talamoni, S., M. Dias. 1999. Population and community ecology of small mammals in southeastern Brazil. Mammalia, 63(2): 167-181.

Vieira, E. 1999. Small mammal communities and fire in the Brazilian Cerrado. Journal of Zoology, 249(1): 75-81.

Vieira, E., L. Baumgarten. 1995. Daily activity patterns of small mammals in a cerrado area from central Brazil. Journal of Tropical Ecology, 11(2): 255-262.

Vieira, M. 2003. Seasonal niche dynamics in coexisting rodents of the Brazilian cerrado. Studies on Neotropical Fauna & Environment, 38(1): 7-15..

To cite this page: Raval, S. 2004. "Necromys lasiurus" (On-line), Animal Diversity Web. Accessed June 01, 2012 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Necromys_lasiurus.html

Disclaimer: The Animal Diversity Web is an educational resource written largely by and for college students. ADW doesn't cover all species in the world, nor does it include all the latest scientific information about organisms we describe. Though we edit our accounts for accuracy, we cannot guarantee all information in those accounts. While ADW staff and contributors provide references to books and websites that we believe are reputable, we cannot necessarily endorse the contents of references beyond our control.

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