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Galictis cuja
lesser grison


By Robert Melrose

Kingdom: Animalia
Phylum: Chordata
Subphylum: Vertebrata
Class: Mammalia
Order: Carnivora
Family: Mustelidae
Genus: Galictis
Species: Galictis cuja

Geographic Range

Galictis cuja is found across central and southern South America. It has been encountered from southern Peru, throughout Paraguay, and from central Chile extending south to Argentina's Chubut Province. (Redford and Eisenberg, 1992)

Biogeographic Regions
neotropical (Native )

Habitat

Range elevation
0 to 4000 m
(0.00 to 13123.36 ft)

Lesser grisons occupy a wide range of habitats, and can be found in the extremes of the arid Chaco while also inhabiting environments with extensive vegetation cover in conjuction with open water. Other habitat types include deciduous and evergreen forests, savananas and mountainous regions. Elevations above 4000 meters are not occupied. (Redford and Eisenberg, 1992)

Lesser grisons often frequent rock pilings, hollow trees, and borrows of other animals in search of food or refuge. (Mares, et al., 1989)

Habitat Regions
temperate ; tropical ; terrestrial

Terrestrial Biomes
desert or dune ; savanna or grassland ; chaparral ; forest ; scrub forest ; mountains

Physical Description

Range mass
1 to 2.5 kg
(2.20 to 5.51 lb)

Range length
280 to 508 mm
(11.02 to 20.00 in)

Like most other mustelids, G. cuja has a long body with stout legs. It is similar in apearance to its larger cousin G. vittata which inhabits northern latitudes and lower altitudes. In comparison to the genus Mustela, G. cuja is more robust and heavier bodied. (Nowak, 1999)

Galictis cuja is characterized by black coloration begining from the rostrum and extending below the ears and into the chest and underbelly. The diagnostic white "headband" sweeps across the forehead, terminating around the shoulder region. Dorsal coloration is grizzled with yellowish undertones. Color variation and patterning may vary among individuals throughout the geographic range of the species. (Redford and Eisenberg, 1992)

The head and body length of this species is reportedly between 280 and 508 mm, with the tail adding an additional 120 to 193 mm to the total length. These animals weigh between 1 and 2.5 kg. (Nowak, 1999)

Sexual dimorphism is evident among many smaller mustelid species. Larger males maximize their ability to take larger prey, thereby limiting competion with females. Polygyny is correlated with such size dimorphism. Along with large size comes increased breeding fitness and superior fighting ability in competition among other males for females. Sexual dimorphism is suggested in G. cuja, but has not been substantiated. (Nowak, 1999)

Dental Formula: 3/3,1/1,3/4,1/1=34 (Mares, et al., 1989)

Sexual Dimorphism
male larger

Reproduction

While mating habits of G. cuja are not documented, many male mustelids are polygynous. Females can be brought to ovulate only by freguent and rigorous copulation. Delayed implantation is also evident in more thatn 16 mustelid species but has not been recorded in G. cuja. (King and Macdonald, 1999)

Breeding interval
The breeding interval of these animals is not reported.

Breeding season
The breeding season of these animals in the wild is not reported.

Range number of offspring
2 to 4

Range gestation period
39 to 40 days

Gestation in G. cuja is complete after about 40 days, when 2 to 4 offspring are produced. Young are born in March, August, October and September. (Nowak, 1999)

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

The parental behavor of this species has not been reported. As in all mammals, the female provides her young with food and protection. Most mustelids are altricial, and it is likely that lesser grison are similar. The young are probably born in a burrow or den of some sort, although this has not been documented. The role of males in parental care has not been established. (Nowak, 1999)

Parental Investment
no parental involvement; altricial ; pre-fertilization (Protecting: Female); pre-hatching/birth (Provisioning: Female, Protecting: Female); pre-weaning/fledging (Provisioning: Female, Protecting: Female)

Lifespan/Longevity

Average lifespan
Status: captivity

10.2 years
[External Source: AnAge]

Greater grisons (G. vittata) have lived more than 10 years in captivity. Longevity in lesser grisons is unknown. (Nowak, 1999)

Behavior

Grisons are some of the more social of mustelid species. Although they are solitary hunters, they have been observed in groups of 2 or more. In a captive setting, grisons have been kept in groups or pairs in a single enclosure. Wild grisons have also been seen moving together in groups comprising of an adult female and young. Evidence of social hiearchy has not been substantiated. (King and Macdonald, 1999)

Galictis cuja is active during both daylight and nighttime. (Mares, et al., 1989)

Members of this genus are reported to be easily tamed if captured young. They are said to make interesting pets. (Nowak, 1999)

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

Home Range

The size of the home range of these animals has not been reported.

Communication and Perception

Galictis cuja utilizes a range of vocalizations which include a sharp, growling bark when threatened. It is likely that these vocalizations are also used for communication within the species. As with other mammals, tactile communiction plays an important role between mates, rival, and between mothers and their offspring. Because these animals are active during the day and are social, they probably use some visual signals, such as body posture, to communicate intentions to conspecific. Scent cues are usually important in Mustelids, which have well developed anal scent glands. (Nowak, 1999)

Communication Channels
visual ; tactile ; acoustic ; chemical

Other Communication Modes
scent marks

Perception Channels
visual ; acoustic

Food Habits

The diet of G. cuja consists of small mammals, birds, eggs, cold-blooded vertebrates, and invertebrates as well as fruit. The stomach contents of one speciemen collected in Peru contained mice and a lizard. (Nowak, 1999; Redford and Eisenberg, 1992)

Athough percieved to be a generalist, studies have shown that the consumtion of introduced European rabbits (Oryctolagus cuniculus) is high among populations of G. cuja where rabbit populations are high. (Duik-Wasser and Cassini, 1998)

We may assume that these animals are capable of hunting chincillas, as they are sometimes kept in captivity for this purpose. (Nowak, 1999)

Animal Foods
birds; mammals; amphibians; reptiles; eggs; insects; terrestrial non-insect arthropods

Plant Foods
fruit

Predation

The predators of these animals have not been reported.

Ecosystem Roles

Lesser grisons feed on a variety of small mammals and other vertebrates. They therefore have a negative impact on populations of their prey species. (Duik-Wasser and Cassini, 1998; Redford and Eisenberg, 1992)

Economic Importance for Humans: Positive

A study of functional response among lesser grisons toward high populations of exotic European rabbits in Patagonia may confirm G. cuja as effective rabbit control. Young grison are also tamed easily and have been used in the past to capture chinchillas. (Mares, et al., 1989; Nowak, 1999)

Positive Impacts
controls pest population

Economic Importance for Humans: Negative

There are no reported negative effects of this species on humans.

Conservation Status

IUCN Red List [Link]
Lower Risk - Least Concern

US Federal List [Link]
No special status

CITES [Link]
Appendix III

Lesser grisons are listed by CITES as Appendix III. They have no special conservation status with IUCN Redlist or with the US Department of Fish and Wildlife.

For More Information

Find Galictis cuja information at

Contributors

Nancy Shefferly (editor), Animal Diversity Web Staff.

Robert Melrose (author), University of Wisconsin-Stevens Point, Chris Yahnke (editor, instructor), University of Wisconsin Stevens Point.

References

Duik-Wasser, M., M. Cassini. 1998. A study on the diet of minor grisons and a preliminary analysis of their role in the control of rabbits in Patagonia. Studies on Neotropical Fauna and the Environment, 33(1): 3-6.

King, C., D. Macdonald. 1999. Weasels and Polecats. Pp. 110-115 in The Encyclopedia of Mammals. Oxford: Andromeda.

Mares, M., R. Ojeda, R. Barquez. 1989. Guide to the Mammals of Salta Province, Argentina. Norman, OK: University of Oklahoma Press.

Mella, J., J. Simonetti, L. Ebensperger. 1991. Trophic-Niche relationships among Galictis cuja, Dusicyon culpaeus, and Tyto alba in central Chile. Journal of Mammalogy, 72: 820-823.

Nowak, R. 1999. Walker's Mammals of the World, Sixth Edition. Baltimore and London: The Johns Hopkins University Press.

Redford, K., J. Eisenberg. 1992. Mammals of the Neotropics. Chicago, Illinois: University of Chicago Press.

To cite this page: Melrose, R. 2004. "Galictis cuja" (On-line), Animal Diversity Web. Accessed February 12, 2012 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Galictis_cuja.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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