Geographic Range
Bolomys 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.
- Biogeographic Regions
- neotropical
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.
- Habitat Regions
- tropical
- terrestrial
- Terrestrial Biomes
- savanna or grassland
- forest
- Other Habitat Features
- agricultural
Physical Description
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.
- 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.
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.
- Key Reproductive Features
- iteroparous
- seasonal breeding
- gonochoric/gonochoristic/dioecious (sexes separate)
- sexual
- 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.
- Parental Investment
- altricial
-
pre-fertilization
- provisioning
-
protecting
- female
-
pre-hatching/birth
-
provisioning
- female
-
protecting
- female
-
provisioning
-
pre-weaning/fledging
-
provisioning
- female
-
provisioning
Lifespan/Longevity
Although Bolomys 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.
- Key Behaviors
- terricolous
- diurnal
- nocturnal
- crepuscular
- motile
- 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.
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.
- Communication Channels
- chemical
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.
- 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.
- 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.
- Negative Impacts
-
injures humans
- carries human disease
- crop pest
Conservation Status
At this time, hairy-tailed bolo mice are not threatened and they are under no special
status on IUCN Red List and CITES.
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
.
Additional Links
Contributors
Matthew Wund (editor), University of Michigan-Ann Arbor.
Shivani Raval (author), University of Michigan-Ann Arbor, Phil Myers (editor, instructor), Museum of Zoology, University of Michigan-Ann Arbor.
- Neotropical
-
living in the southern part of the New World. In other words, Central and South America.
- native range
-
the area in which the animal is naturally found, the region in which it is endemic.
- tropical
-
the region of the earth that surrounds the equator, from 23.5 degrees north to 23.5 degrees south.
- terrestrial
-
Living on the ground.
- tropical savanna and grassland
-
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.
- savanna
-
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.
- temperate grassland
-
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.
- forest
-
forest biomes are dominated by trees, otherwise forest biomes can vary widely in amount of precipitation and seasonality.
- agricultural
-
living in landscapes dominated by human agriculture.
- endothermic
-
animals that use metabolically generated heat to regulate body temperature independently of ambient temperature. Endothermy is a synapomorphy of the Mammalia, although it may have arisen in a (now extinct) synapsid ancestor; the fossil record does not distinguish these possibilities. Convergent in birds.
- bilateral symmetry
-
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.
- iteroparous
-
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).
- seasonal breeding
-
breeding is confined to a particular season
- sexual
-
reproduction that includes combining the genetic contribution of two individuals, a male and a female
- viviparous
-
reproduction in which fertilization and development take place within the female body and the developing embryo derives nourishment from the female.
- altricial
-
young are born in a relatively underdeveloped state; they are unable to feed or care for themselves or locomote independently for a period of time after birth/hatching. In birds, naked and helpless after hatching.
- diurnal
-
- active during the day, 2. lasting for one day.
- nocturnal
-
active during the night
- crepuscular
-
active at dawn and dusk
- motile
-
having the capacity to move from one place to another.
- solitary
-
lives alone
- territorial
-
defends an area within the home range, occupied by a single animals or group of animals of the same species and held through overt defense, display, or advertisement
- chemical
-
uses smells or other chemicals to communicate
- visual
-
uses sight to communicate
- tactile
-
uses touch to communicate
- acoustic
-
uses sound to communicate
- chemical
-
uses smells or other chemicals to communicate
- cryptic
-
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.
- herbivore
-
An animal that eats mainly plants or parts of plants.
- granivore
-
an animal that mainly eats seeds
References
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.
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Henriques, R., C. Alho. 1991. Microhabitat Selection by Two Rodent Species in the Cerrado of Central Brazil. Mammalia , 55(1): 49-56.
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