Geographic Range
Tympanoctomys barrerae
is endemic to west-central and southern Argentina, between 29° south and 43° south
(Ojeda, 2010). It is known from 8 localities in the provinces of San Juan, Mendoza,
Neuquén, La Pampa, and Chubut of Argentina (Diaz and Ojeda, 2000; Odeja, 2010).
- Biogeographic Regions
- neotropical
Habitat
Tympanoctomys barrerae
inhabits the Monte and Patagonia deserts, where it burrows in arid, lowland, sand
dune vegetation belts along the periphery of saline lakes (Torres et al., 2003; Ojeda,
2010). The salt content of in these lakes is very high, resulting in a local abundance
of halophytic vegetation. High burrow activity has been noted in vegetation belts
surrounding these lakes where salt content is much higher (Mares et al., 1997). It
is important to note that
T. barrerae
occurs in low population densities throughout these habitats (Ojeda, 2010).
- Habitat Regions
- terrestrial
- Terrestrial Biomes
- desert or dune
Physical Description
Tympanoctomys barrerae
has a relatively large head. Cranial width is greater than the cranial length due
to highly developed auditory bullae, which extend posteriorly beyond the braincase.
Its ears are short with terminal pale hair tufts. Dorsal pelage is buffy-yellow and
ventral pelage is white. Its hind feet are relatively short and are covered in long
white hair. Its long, bicolored tail makes up 49 to 54% of its total length and is
covered with long hair that becomes dark to reddish brown near the tip (Diaz and Ojeda,
2000; Grzimek, 2004). It can be distinguished from similar species, such as
Octomys mimax
, by its short hind feet, long tail, and shorter skull.
Tympanoctomys barrerae
has well-developed tympanic bones, short and rounded nasals, and a short maxillary
tooth row (Diaz and Ojeda, 2000). It ranges in mass from 51.8 to 104 g and males tend
to be larger than females. Finally,
T. barrerae
has a basal metabolic rate ranging from 0.9 to 1.25 cm^3 oxygen/hour.
- Other Physical Features
- endothermic
- bilateral symmetry
- Sexual Dimorphism
- male larger
Reproduction
The mating system for
Tympanoctomys barrerae
has not been determined.
Little information is available on reproduction in
Tympanoctomys barrerae
. On average, captive females have four litters per year (Diaz and Ojeda, 2000). Captive-born
pups weigh about 4 g at birth and 8 g at five days old. They open their eyes at 6
days old and they can eat solid food at 10 days old (Diaz and Ojeda, 2000; Grzimek,
2004). Pups are not completely weaned by the time they begin eating solid food (Diaz
and Ojeda, 2000).
- Key Reproductive Features
- iteroparous
- gonochoric/gonochoristic/dioecious (sexes separate)
- sexual
- viviparous
Little information exists regarding parental investment in red vizcacha rats. However,
young are born in a precocial state and use saltbush and orache leaves (Genus:
Atriplex
) during foraging, which is thought to be learned from their mothers (Diaz and Ojeda,
2000). Although weaning age in wild red viscacha rats is unknown, captive-born pups
nurse until they are at least 10 days old.
- Parental Investment
- precocial
- female parental care
-
pre-hatching/birth
-
provisioning
- female
-
protecting
- female
-
provisioning
-
pre-weaning/fledging
-
provisioning
- female
-
provisioning
Lifespan/Longevity
Little information exists regarding lifespan or longevity in red vizcacha rats.
Behavior
Red vizcacha rats are nocturnal rodents that live in complex burrow systems consisting
of several entrance holes (Mares et al., 1997, Diaz and Ojeda, 2000). Research suggests
that numerous entrances allow burrows to receive direct sunlight during winter and
indirect sunlight throughout summer (Torres et al., 2003). Generally, entrances are
located at the base of shrubs (Mares et al., 1997). Burrows also contain up to three
levels of food chambers and tunnels (Diaz and Ojeda, 2000). The largest burrow recorded
consisted of 33.7 m of tunnel. Along with their feces, the branches and leaves of
saltbush (Genus:
Atriplex
) and seepweed (Genus:
Suaeda
) plants were found scattered throughout the tunnel system (Mares et al., 1997). Burrows
are on average 13.59 m long, 8.71 m wide, and 1.25 m deep (Diaz and Ojeda, 2000).
Each burrow may also have up to 14 satellite mounds within 3 m of the main burrow,
which serve as alternate feeding sites or shelter. Only one individual resides in
each burrow (Mares et al., 1997).
Home Range
Little information is available on red vizcacha rats' mean territory size.
Communication and Perception
Little information is available on communication and perception in red vizcacha rats. However, based on their enlarged auditory bullae, they likely rely heavily on auditory signals.
Food Habits
Red vizcacha rats are strictly herbivorous and are specialized for consuming halophytic
plants. Plant species found in feces as well as in mound tunnels and food chambers
include
Allenrolfea vaginata
,
Suaeda divaricata
,
Atriplex lampa
,
Alternanthera nodifera
,
Atriplex argentina
, and
Heterostachys ritteriana
(Diaz and Ojeda, 2000). In addition, dietary analysis suggests that they also feed
on plants from the
Verbenaceae
,
Nyctaginaceae
,
Solanaceae
,
Fabaceae
, and
Graminaceae
plant families. However,
Atriplex lampa
accounts for about 76% of their diet (Mares et al., 1997).
Bristle brushes are an important structure that are unique to Tympanoctomys barrerae . Located posteriorly to the upper incisors, bristle brushes resemble a second set of the upper incisors. Bristle brushes, paired with lower incisors, strip the salt-filled surface from the leaves of halophytic plants prior to ingestion, which greatly reduces electrolyte consumption (Mares et al., 1997; Diaz and Ojeda, 2000). Similar to other desert rodents, Tympanoctomys barrerae uses its elongated renal papilla and relative medullary thickness to concentrate its urine, which allows it to excrete excess salt (Diaz and Ojeda, 2000). Bristle brushes and renal adaptations make T. barrerae highly adapted for the consumption of halophytic plants.
- Plant Foods
- leaves
- wood, bark, or stems
- Foraging Behavior
- stores or caches food
Predation
Red vizcacha rat skulls been reported in barn owl (
Tyto alba
) pellets. Although little information is available concerning the depredation of
red vizcacha rats, other potential predators may include snakes (
Bothrops newiedii
,
Bothrops ammodytoides
), owls (
Bubo virginianus
, Genus:
Athenecunicularia
), mustelids (
Lyncodon patagonieus
,
Galictis cuja
), pampas cats (
Lynchailurus pajeros
), and pampas foxes (
Lycalopex gymnocercus
; Diaz and Ojeda, 2000).
Ecosystem Roles
Tympanoctomys barrerae
greatly modify the ecosystem they occur in. Burrows provide ideal microhabitats for
desert shrubs, which are more abundant on active burrows than between them (Mares
et al., 1997).
Atriplex
species are especially prominent on burrow structures, providing
T. barrerae
with shelter and a convenient, primary food source (Mares, Braun and Channell, 1997).
Burrows also provide habitat for other animals, including some species of arachnids
(e.g., spiders and scorpions) and other species of rodent (Genus: Eligmodontia).
Tympanoctomys barrerae
is also host to a number of different parasites including fleas (
Siphonaptera
) and chigger fleas (
Hectopsylla
).
- Ecosystem Impact
- creates habitat
- soil aeration
- fleas ( Siphonaptera )
- chigger fleas ( Hectopsylla )
- sigmodontine mice ( Eligmodontia spp.)
- spiders and scorpions ( Arachnida )
Economic Importance for Humans: Positive
There are no known positive effects of
Tympanoctomys barrerae
on humans.
Economic Importance for Humans: Negative
There are no known adverse effects of
Tympanoctomys barrerae
on humans.
Conservation Status
Tympanoctomys barrerae
may be a keystone species for xeric halophytic shrublands surrounding salt basins
(Mares et al., 1997). Due to its patchy and restricted distribution, habitat and dietary
specialization, low colonization rates, and low population densities, its populations
are vulnerable to decline and should be considered in biodiversity assessments (Diaz
and Ojeda, 2000). Fossil remains imply that the present distribution of
T. barrerae
was at one point more continuous and widespread (Gallardo et al., 2006). The IUCN
Red List of Threatened Species lists
T. barrerae
as "near threatened" and suggests that the expansion of petroleum industry throughout
South America is a threat to its persistence.
Other Comments
Tympanoctomys barrerae
is the first known tetraploid mammal (2n=102). Larger cell dimensions are expected
in polyploid species, and spermatozoa, liver cells, lymphocytes, and female reproductive
cells are larger in
T. barrerae
than in most other rodent species (Diaz and Ojeda, 2000; Gallardo et al. 2002; Gallardo
et al., 2006).
Additional Links
Contributors
Jaclyn Ramsey (author), University of Wisconsin-Stevens Point, Stefanie Stainton (editor), University of Wisconsin-Stevens Point, Christopher Yahnke (editor), University of Wisconsin-Stevens Point, John Berini (editor), Animal Diversity Web Staff.
- 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.
- terrestrial
-
Living on the ground.
- desert or dunes
-
in deserts low (less than 30 cm per year) and unpredictable rainfall results in landscapes dominated by plants and animals adapted to aridity. Vegetation is typically sparse, though spectacular blooms may occur following rain. Deserts can be cold or warm and daily temperates typically fluctuate. In dune areas vegetation is also sparse and conditions are dry. This is because sand does not hold water well so little is available to plants. In dunes near seas and oceans this is compounded by the influence of salt in the air and soil. Salt limits the ability of plants to take up water through their roots.
- 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).
- 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.
- young precocial
-
young are relatively well-developed when born
- female parental care
-
parental care is carried out by females
- fossorial
-
Referring to a burrowing life-style or behavior, specialized for digging or burrowing.
- nocturnal
-
active during the night
- motile
-
having the capacity to move from one place to another.
- solitary
-
lives alone
- visual
-
uses sight to communicate
- tactile
-
uses touch to communicate
- acoustic
-
uses sound to communicate
- chemical
-
uses smells or other chemicals to communicate
- stores or caches food
-
places a food item in a special place to be eaten later. Also called "hoarding"
- soil aeration
-
digs and breaks up soil so air and water can get in
- herbivore
-
An animal that eats mainly plants or parts of plants.
- folivore
-
an animal that mainly eats leaves.
- 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.
References
Bozinovic, F., L. Contreras. 1990. Basal Rate of Metabolism and Temperature Regulation of Two Desert Herbivorous Octodontid Rodents: Octomys mimax and Tympanoctomys barrerae. Oecologia , Vol. 84, No. 4: 567-570.
Diaz, G., R. Ojeda. 2000. Tympanoctomys barrerae. Mammalian Species , No. 646: 1-4.
Gallardo, M., R. Ojeda, C. Gonzalez, C. Rios. 2006. "The Octodontidae Revisited" (On-line). Accessed August 01, 2010 at http://lem.dm.cl/publicaciones/pdf/2006/OctoRevisitedFinal%202006.pdf .
Gallardo, M., F. Mondaca, R. Ojeda, N. Kohler, O. Garrido. 2002. Morphological Diversity in the Sperms of Caviomorph Rodents. Mastozoologia Neotropical , Vol. 9, No. 2: 159-170.
Grzimek, B. 2004. Tympanoctomys barrerae. Pp. 438 in Grzimek's Animal Life Encyclopedia - Mammals , Vol. Vol. 16, Second Edition. Farmington Hills, MI: Gale.
Mares, M., J. Braun, R. Channell. 1997. Ecological Observations on the Octodontid Rodent, Tympanoctomys barrerae, in Argentina. The Southwestern Naturalist , Vol. 42, No. 4: 488-493.
Mares, M., R. Ojeda, C. Borghi, S. Giannoni, G. Diaz, J. Braun. 1997. How Desert Rodents Overcome Halophytic Plant Defenses. BioScience , Vol. 47, No. 10: 699-704.
Ojeda, A. 2010. Phylogeography and genetic variation in the South American rodent Tympanoctomys barrerae (Rodentia: Octodontidae). Journal of Mammalogy , Vol. 91, No. 2: 302-313.
Torres, R., C. Borghi, S. Giannoni, A. Pattini. 2003. Portal Orientation and Architecture of Burrows in Tympanoctomys barrerae (Rodentia, Octodontidae). Journal of Mammalogy , Vol. 84, No. 2: 541-546.