Animal Diversity Web U of M Museum of Zoology ADW Home ADW Home ADW Home University of Michigan Help About Aninal Names Teaching Special Topics About Us




Structured Inquiry Search — preview

Home -> Kingdom Animalia -> Phylum Chordata -> Subphylum Vertebrata -> Class Mammalia -> Order Rodentia -> Suborder Hystricomorpha -> Family Ctenomyidae -> Species Ctenomys talarum

Ctenomys talarum
Talas tuco-tuco



2008/09/07 10:29:32.241 GMT-4

By Nicholas Jurich

Kingdom: Animalia
Phylum: Chordata
Subphylum: Vertebrata
Class: Mammalia
Order: Rodentia
Suborder: Hystricomorpha
Family: Ctenomyidae
Genus: Ctenomys
Species: Ctenomys talarum

Geographic Range

Ctenomys talarum is a South American rodent found only in eastern Argentina. They are also known as Talas tuco-tucos. Three subspecies are morphologically similar and are distinguished only by the specific region which each occupies: C. t. occidentalis along the eastern border of the province of La Pampa; C. t. recessus along the southern coast; and C. t. talarum along the eastern coast of the province of Buenos Aires. (Justo, De Santis, and Kin, 2003)

Biogeographic Regions:
neotropical (native ).

Habitat

Talas tuco-tucos spend most of their lives in underground burrows, which can be found in pastures with flat terrain. Burrows have a branching structure, measure 6 to 8 cm in diameter, are shorter than 25 m in length, and are at least 30 cm in depth. Compared to neighboring sympatric species C. australis, C. talarum prefers firmer, more organic soils, which tend to host a denser composition of vegetation. (Redford and Eisenberg, 1992; Schleich and Antinuchi, 2004)

These animals are found in the following types of habitat:
temperate ; terrestrial .

Terrestrial Biomes:
savanna or grassland .

Physical Description

Mass
0.09 to 0.19 kg
(0.2 to 0.42 lbs)


Length
212 to 254 mm; avg. 233.40 mm
(8.35 to 10 in; avg. 9.19 in)


Basal Metabolic Rate
1.08 to 2 cm^3 oxygen/hour

Ctenomys talarum has a cylindrical body, reduced neck, and short tail. Mean total length ranges from 212.0 to 254.0 mm, mean length of head and body is 167.5 mm, and the mean tail length is 66.7 mm. The mean skull length and mean nasal length are 37.4 mm and 11.9 mm, respectively. The average breadth of braincase for C. talarum is 14.6 mm. Males and females have mean masses of 186.0 g and 128.0 g, respectively, while the average mass for all recorded individuals is 133.0 g. Baculum is small and narrow, with a mean length and proximal and distal breadth of 6.4 mm, 1.32 mm, and 0.9 mm, respectively. (Justo, De Santis, and Kin, 2003; Redford and Eisenberg, 1992)

The short, fine hair of C. talarum is dark grey to black dorsally, blending to reddish-brown laterally and cream ventrally. Distinct white patches are found at the base of each ear, as well as in the inguinal and axillary areas. The tail is brown and dark grey. Hind feet have white, bristle-like hairs, and both front and hind feet have long, curved claws. Both eyes and ears are small. Cteonmys talarum molts during the summer and autumn seasons. Some intersexual differences exist in the five-phase molt; females molt earlier than males. (Justo, De Santis, and Kin, 2003; Redford and Eisenberg, 1992)

Ctenomys talarum is distinguished from closely related species in that it is, by measure of total length, smaller than C. azarae, C. australis, and C. mendocinus. Tail length of C. talarum is also noticeably smaller than that of C. australis and C. mendocinus. Compared to C. azarae, C. talarum has short and broad nasals. Ctenomys talarum is distinguished from C. minutus and C. torquatus by its smaller, flatter baculum. (Justo, De Santis, and Kin, 2003)

Some key physical features:
endothermic ; homoiothermic; bilateral symmetry .

Reproduction

Breeding interval
The reproductive cycle for C. talarum is bimodal, with two litters produced per year. An inactive period of 6 to 8 months separates these episodes.

Breeding season
Although males are reproductively capable for nearly eight months of the year, the breeding season for females is much more restricted. The majority of mating episodes occur in the months of July and August.

Number of offspring
4 to 5; avg. 4.55

Gestation period
102 days (average)

Birth Mass
8 g (average)
(0.28 oz)
[External Source: AnAge]


Time to weaning
30 days (average)

Time to independence
60 days (average)

Age at sexual or reproductive maturity (female)
6 to 8 months

Age at sexual or reproductive maturity (male)
6 to 8 months

Ctenomys talarum clearly recognizes interspecific chemical signals from cues in urine, feces, and soiled wood shavings. Each sex distinguishes the scents of same and other sexes. Furthermore, C. talarum identifies the reproductive status of individuals of the opposite sex and selects mates via such chemical cues. (Zenuto and Fanjul, 2002; Zenuto, Fanjul, and Busch, 2004)

Mating behaviors of C. talarum depend a great deal on vocalizations. Only males produce the “tuc” sound, which gives rise to the common name of the family (tuco-tuco). The song consists of multiple “tuc” sounds, lasts roughly ten to twenty seconds, and serves to establish the spacing of individual males within the area. (Redford and Eisenberg, 1992)

Paternity tests using DNA analysis and analyses of testes size have shown that C. talarum is polygynous. In these studies, a single male was found to have sired offspring litters with multiple females. (Zenuto, Lacey, and Busch, 1999; Zenuto, Malizia, and Busch, 1999)

Usually, C. talarum is solitary, and only one individual inhabits each burrow. However, during the breeding season, males and females are often found together in the same burrow. (Redford and Eisenberg, 1992)

Mating systems:
polygynous .

Male Talas tuco-tucos have extended reproductive availability, covering most of winter and into summer. Females are more restricted in their breeding availability. Talas tuco-tucos have two reproductive periods, interrupted by an inactive period of 6 to 8 months. All males are reproductive in July, and the majority of pregnancies occur in August. During the breeding season, the mean prevalence of pregnancy is 0.66. (Justo, De Santis, and Kin, 2003)

Most births occur between October and December, and average litter size is between 4 and 5 offspring. The energetic costs of gestation and lactation are similar, although the gestation period is twice as long as that of lactation. When young are about 30 days old, females refuse to allow suckling. Females exhibit postpartum estrus, and it is possible that a female may be pregnant and lactating at the same time. At the point of sexual maturity, the average weights of females and males are 137.52 g and 176.62 g, respectively. Females tend to maintain a constant weight after reaching maturity. (Busch et al., 1989; Zenuto, Antinuchi, and Busch, 2002)

In captivity, the age of first reproduction is eight months, and females come into estrus two times per year. Captive C. talarum has an average gestation period of 102 days and a mean litter size of 5 offspring, with a range of between 1 and 7 individuals. (Redford and Eisenberg, 1992)

Key reproductive features:
iteroparous ; seasonal breeding ; gonochoric/gonochoristic/dioecious (sexes separate); sexual ; viviparous ; post-partum estrous.

Apart from the mating episode, male and female Ctenomys talarum do not interact. Thus, females are responsible for all aspects of caring for offspring. Male C. talarum provide no prenatal or parental care. (Zenuto, Antinuchi, and Busch, 2002)

Parental investment:
pre-fertilization (provisioning, protecting: female); pre-hatching/birth (provisioning: female, protecting: female); pre-weaning/fledging (provisioning: female, protecting: female).

Lifespan/Longevity

Average lifespan (wild)
20 to 22 months

In wild populations, the overall mortality rate of C. talarum is 0.05 per week. The probability of survival during the winter (March to October) is 0.19, while the probability of survival during the summer (October to March) is 0.38. With a lifespan of 20 to 22 months, individuals rarely live through more than two reproductive seasons. (Busch et al., 1989)

In captivity, Ctenomys talarum develops hyperglycemia and cataracts. As much as 40% of individuals in a colony show deteriorative eye change. Blood sugar levels may increase nearly 75%. (Justo, De Santis, and Kin, 2003)

Behavior

Territory Size
7.90 to 15.60 m^2

Talas tuco-tucos are solitary, only one individual occupies a burrow, and males and females distribute themselves uniformly over an area in high-density populations. A population density of 207 individuals per hectare has been observed in grazed pasture. Other studies have found that smaller populations have aggregated distributions, with several adult females and a single male in relatively close proximity. (Busch et al., 1989; Redford and Eisenberg, 1992)

As a mean of thermoregulation, the pelage of C. talarum varies seasonally. Both ventral and dorsal fur is significantly shorter and ventral fur is less dense during the warm season. This fur change serves to facilitate heat loss in the tunnel environment. Additionally, pregnant and lactating female C. talarum show increasingly less dense ventral fur, which allows them to more effectively conduct heat to newly-born offspring in the nest. (Cutrera and Antinuchi, 2004)

It was hypothesized that Talas tuco-tucos, like several other subterranean rodents, have the ability to spatially orient through perception of the earth’s magnetic field. Research did not support this hypothesis. (Schleich and Antinuchi, 2004)

The presence of a thick medulla on the kidneys means that Talas tuco-tucos can excrete highly concentrated urine and do not need free water for drinking. (Justo, De Santis, and Kin, 2003)

Home Range

The mean home-range size of males is 12.3 square meters, and that of females is 8.7 square meters. (Busch et al., 1989)

Communication and Perception

Although Talas tuco-tucos are fairly solitary animals, spatial organization within a population is socially important. They clearly recognize odors from urine, feces, and wood shavings from other individual members of the population. Scent recognition helps to uniformly distribute burrows within a specific area. In addition to being spatial cues, these sex distinctions are significant in mating behavior. (Justo, De Santis, and Kin, 2003)

Talas tuco-tucos also communicate with vocalizations. Only males produce the “tuc” sound, which gives rise to the common name of the family (tuco-tuco). The song consists of multiple “tuc” sounds, lasts roughly ten to twenty seconds, and serves to establish spatial organization. This means of communication is also implicated in mating behavior. (Redford and Eisenberg, 1992)

Communicates with:
acoustic ; chemical .

Other communication keywords:
scent marks .

Perception channels:
visual ; tactile ; acoustic ; chemical .

Food Habits

Talas tuco-tucos are herbivorous, feeding on roots and grasses. Unlike most subterranean rodents, Talas tuco-tucos leave their burrows to forage for vegetation above ground. Captive C. talarum preferentially consume the grass species Bromus unioloides. (Justo, De Santis, and Kin, 2003)

Primary Diet:
herbivore (folivore ).

Plant Foods:
leaves; roots and tubers.

Predation

Known predators

Talas tuco-tucos are preyed on by several species of carnivorous birds, including Athene cunicularia, Asio flammeus, and Tyto alba. Predators also include several carnivore species, such as Galictis cuja and Leopardus geoffroyi. Near urban areas, domestic cats and domestic dogs prey on Talas tuco-tucos. The primary predator-avoidance strategies include cryptic fur coloration and the ability to dig rapidly and efficiently close openings to their underground tunnels. (Justo, De Santis, and Kin, 2003; Rossin, Malizia, and Denegri, 2004; Weir, 1971)

Anti-predator adaptations::
cryptic .

Ecosystem Roles

This species is an herbivore. Its grazing activities and burrowing impact the composition of plant communities where it lives.

Ctenomys talarum is parasitized by several families of the order Nematoda, as well as several lice species, such as Eulinognathus americanus, Gyropus parvus, and Phtheropoios forficulatus. Although prevalence of parasitism does not differ between sexes of C. talarum, the intensity does vary. (Justo, De Santis, and Kin, 2003)

In populations near urban areas of the Buenos Aires Province, C. talarum is an intermediate host of the cestode parasite Taenia taeniaeformis. A prevalence of 64% in some populations indicates that C. talarum is an important host to the parasite, whose final host is domestic dogs, a common predator of C. talarum in urban areas. (Rossin, Malizia, and Denegri, 2004)

Key ways these animals impact their ecosystem:
creates habitat; soil aeration .

Commensal or parasitic species (or larger taxonomic groups) that use this species as a host

Economic Importance for Humans: Negative

The mounds and burrows of C. talarum bare and erode soils in some agricultural areas. (Justo, De Santis, and Kin, 2003)

Ways that these animals might be a problem for humans:
crop pest.

Economic Importance for Humans: Positive

There are no known positive effects of Ctenomys talarum on humans.

Conservation Status

IUCN Red List: [link]:
Lower Risk - Least Concern.

US Federal List: [link]:
No special status.

CITES: [link]:
No special status.

There are no known conservation efforts for Ctenomys talarum.

Contributors

Tanya Dewey (editor), Animal Diversity Web, University of Michigan Museum of Zoology.

Nicholas Jurich (author), University of Michigan. Phil Myers (editor, instructor), Museum of Zoology, University of Michigan.

References

Busch, C., A. Malizia, O. Scaglia, O. Reig. 1989. Spatial Distribution and Attributes of a Population of Ctenomys talarum (Rodentia: Octodontidae). Journal of Mammalogy, 70 (1): 204-208.

Cutrera, A., C. Antinuchi. 2004. Fur changes in the subterranean rodent Ctenomys talarum: possible thermal compensatory mechanism. Revista Chilena de Historia Natural, 77 (2): 235-242.

Justo, E., L. De Santis, M. Kin. 2003. Ctenomys talarum. Mammalian Species, No. 730: pp. 1-5. Accessed February 01, 2006 at http://www.science.smith.edu/departments/Biology/VHAYSSEN/msi/default.html.

Lacey, E., S. Braude, J. Wieczorek. 1997. Burrow Sharing by Colonial Tuco-Tucos (Ctenomys sociabilis). Journal of Mammalogy, 78 (2): 556-562.

Redford, K., J. Eisenberg. 1992. Mammals of the Neotropics, Volume 2, The Southern Cone: Chile, Argentina, Uruguay, Paraguay. Chicago and London: The University of Chicago Press.

Rossin, A., A. Malizia, G. Denegri. 2004. The role of the subterranean rodent Ctenomys talarum (Rodentia: Octodontidae) in the life cycle of Taenia taeniaeformis (Cestoda: Taeniidae) in urban environments. Veterinary Parasitology, 122 (1): 27-33.

Schleich, C., C. Antinuchi. 2004. Testing Magnetic Orientation in a Solitary Subterranean Rodent Ctenomys talarum (Rodentia: Octodontidae). Ethology, 110: 485-495.

Weir, B. 1971. A Trapping Technique for Tuco-Tucos, Ctenomys talarum. Journal of Mammalogy, 52 (4): 836-839.

Zenuto, R., M. Fanjul. 2002. Olfactory Discrimination of Individual Scents in the Subterranean Rodent Ctenomys talarum (Tuco-Tuco). Ethology, 108: 629-641.

Zenuto, R., C. Antinuchi, C. Busch. 2002. Bioenergetics of Reproduction and Pup Development in a Subterranean Rodent (Ctenomys talarum). Physiological and Biochemical Zoology, 75 (5): 469-478.

Zenuto, R., M. Fanjul, C. Busch. 2004. Use of Chemical Communication by the Subterranean Rodent Ctenomys talarum (Tuco-Tuco) During the Breeding Season. Journal of Chemical Ecology, 30 (11): 2111-2126.

Zenuto, R., E. Lacey, C. Busch. 1999. DNA Fingerprinting Reveals Polygyny in the Subterranean Rodent Ctenomys talarum. Molecular Ecology, 8: 1529-1532.

Zenuto, R., A. Malizia, C. Busch. 1999. Sexual Size Dimorphism, Testes Size and Mating System in Two Populations of Ctenomys talarum (Rodentia: Octodontidae). Journal of Natural History, 33: 305-314.

2008/09/07 10:29:34.922 GMT-4

To cite this page: Jurich, N. and P. Myers. 2006. "Ctenomys talarum" (On-line), Animal Diversity Web. Accessed October 13, 2008 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Ctenomys_talarum.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.

Other formats: OWL

Home  ¦  About Us  ¦  Special Topics  ¦  Teaching  ¦  About Animal Names  ¦  Help

Structured Inquiry Search — preview