Dasypodidae is the only extant family in the order Cingulata, which also contains extinct families Glyptodontidae and Pampatheriidae. Dasypodidae contains three subfamilies: Tolypeutinae, Euphractinae, and Dasypodinae. These are further divided into one, six and three genera, respectively. Armadillos are by far the most diverse group of xenarthrans, with a total of twenty-one extant species and two extinct species identified in the family Dasypodidae. These species vary in size, form, and behavior, but all possess characteristic bony armor. ("Armadillos", 1990; "Checklist of Mammal Names", 2005)
Armadillos have a strictly New World distribution, ranging from the central United States (Missouri) through Central and South America, as far south as Cape Horn (at the southern tip of South America).
Nine-banded armadillos (Dasypus novemcinctus) have the most northern distribution. Their range originally spanned from South America into Mexico but has expanded steadily northward into the Southern United States Their range currently extends throughout the Midwest, and nine-banded armadillos have recently been found as far north as Nebraska. Scientists speculate that global climate change and loss of natural predators could contribute to the northward expansion of this typically more neotropical species. ("Armadillos", 1990)
Armadillos are found in a wide array of habitats, from deserts and mountains to wetlands and sandy coastal regions. All members of Dasypodidae are terrestrial, and most are fossorial, living in burrows. They typically remain on the ground, because their plated armor and heavy bones prevent them from climbing trees (as with most members of the closely related family Pilosa) or swimming. Dasypus novemcinctus is an exception, as it is known to swim awkwardly. Some dasypodids, such as members of Tolypeutinae, are strictly terrestrial and not fossorial. ("Armadillos", 1990; Vizcaino and Milne, 2005)
Dasypodidae is currently classified under order Cingulata, which contains all prehistoric and extant armadillos, identifiable by their ossified dermis. Order Cingulata is currently included in superorder Cingulata, which also contains the hairy xenarthrans of order Pilosa (sloths and anteaters).
All xenarthrans have specialized and unique lateral articulations on their vertebrae and share a strictly New World distribution. Xenarthrans were formerly classified with pangolins (order Pholidota) and aardvarks (order Tubulidentata) in Edentata because of their reduced dentition. Edentata was reclassified when genetic data demonstrated that the order is polyphyletic. Pangolins and aardvarks strictly inhabit the Old World and lack xenarthran vertebral articulations. Edentata is occasionally used interchangeably with Cingulata but is no longer an accepted classification. ("Armadillos", 1990; McBee and Baker, 1982)
Armadillos are an ancient group; fossilized scutes are known from the late Paleocene of South America. Armadillos evolved and diversified in that continent during the Tertiary, probably entering North America when a land bridge connected the continents in the Pliocene. (Barlow, 1984)
All members of Dasypodidae have armor on their sides, back and tail, as well as the top of their head, which makes up their characteristic “shell.” This armor is composed of a series of plates of ossified scutes covered with a leathery keratinous skin. The scutes are arranged into movable bands, which usually overlap to effectively seal gaps in the armor. Areas of soft skin and sometimes hair are located between the bands. In some species, the ventral surface is covered in dense hairs. The belly is soft and unprotected by bone, although some species are able to curl into a ball. The limbs have irregular plates covering at least parts of their surfaces, and they also may be hairy. The top of the head is always covered by a shield of keratin-covered scutes, and the long rat-like tail is covered by bony rings.
The armor may be an adaptation for protection and defense against predation, but also could serve as protection against abrasive soil and biting insects (beneficial to the fossorial lifestyle). The arrangement of armor plates and bands varies widely and is used to differentiate species and families. The armor may constitute fifteen percent of the animal's entire body weight. ("Armadillos", 1990; McBee and Baker, 1982)
Dasypodids range in size from pink fairy armadillos (Chlamyphorus truncatus: 90 g, 11.4 to 15 cm) to giant armadillos (Priodontes maximus: 50 kg, 80 to 100 cm). Armadillos have a long snout, and their ears range in size from small to very large and protuberant. Sexual dimorphism is limited, but sometimes males are slightly larger. Males have no scrotum, and their testes do not descend past the pelvic girdle. Females lack a true vagina, but instead have a singular urogenital exit. Body colors are mostly gray or brown, though pink fairy armadillos have a pinkish shell and pure white, dense fur on their sides and venters.
Dasypodids can be considered slightly heterothermic, because their regulatory systems are not advanced enough to completely prevent fluctuations in body temperature due to changes in ambient temperature. However, they do maintain a relatively constant body temperature under non-stressful conditions and thus are typically described as homoiothermic. ("Armadillos", 1990; Cetica, et al., 2005; McBee and Baker, 1982)
Most armadillos have short, thick limb bones that include expanded crests and processes for the attachment of muscles. The tibia and fibula are fused both proximally and distally. Digging habits and abilities are correlated with forelimb, but not hindlimb, morphology. Armadillo forelimbs have 3 to 5 toes, depending on the species, but their hindlimbs always have 5. The toes are armed with heavy, curved claws, which aid in digging and defense.
The postcranial skeleton of armadillos is modified for digging and to accommodate the armor. The axial skeleton is rigid and may or may not contact the carapace. The pelvis of some species is especially strongly built and enlarged. The ribs may be broadened, and parts of ribs that in most mammals are cartilage are ossified in some species of armadillos. ("Armadillos", 1990; McBee and Baker, 1982; Vizcaino and Milne, 2005)
Armadillos have a flattened skull and a flattened, long lower jaw. The zygomatic arch is complete and a jugal is present. Armadillo dentition is simple and homodont, as the teeth similar, reduced, and peg-like in adults. Adults lack canines, and most have no incisors. Dasypodids actually have 4 to 6 primordial incisors at birth, but these teeth are absorbed early in life. The premaxillae and lacrimals are small. Their dental formulae simply provide upper / lower (number of upper over number of lower teeth) due to the lack of incisors and canines and similarity between the peg-like teeth that do exist. After development is complete, cheek teeth (molars and premolars) vary from 7-8/7-8 to 18/19. Adult teeth completely lack enamel and are made up of a dentine core surrounded by cementum, which wears down very easily. Dental formula and tooth shape vary among species, and even among members of the same species, due to different wear patterns and differences in developmental patterns among individuals. ("Armadillos", 1990; McBee and Baker, 1982)
Most species of Dasypodidae are polygynous. Males and females of some species engage in courtship prior to mating. The best accounts of courtship are documented for nine-banded armadillos (Dasypus novemcinctus) and, to a lesser extent, southern three-banded armadillos (Tolypeutes matacus).
Male and female D. novemcinctus pair when the female is in estrus. Males of this species pair with 1 to 3 females in a single breeding season, while females pair with only 1 to 2 males. Mate pairings last anywhere from 1 to 4.5 months. Breeding male members of the species maintain prime living territory through aggression.
In D. novemcinctus, the male member of a mating pair forages with the female for several days prior to mating. Periodically, the male attempts to mount the female, or touches her back with his claws, causing her to lift her tail. Once she lifts her tail, the male sniffs her anal region to detect changes in anal secretions that indicate her sexual interest. When she is sexually receptive, the female lies flat on the ground as the male sniffs and licks the area near her anus. In order to mate, the female must flip onto her back so the male can mount her without her dorsal armor getting in the way. The male scratches at the female’s dorsal armor and continues to lick and scratch near the anus until the female fully turns over. Copulation lasts anywhere from 3 to 15 minutes.
Southern three-banded armadillos (T. matacus) also form mating pairs during the breeding season, though the duration of this pairing is not known. Prior to copulation, the male softly touches the female’s dorsal armor to assess her sexual receptiveness.
Six-banded armadillos (Euphractus sexcinctus) in captivity do not display mate-pairing behavior. Instead, males and females randomly meet while foraging, nuzzle, and then mate. Males and females do not closely associate before or after periods of copulation. ("Armadillos (Dasypodidae)", 2003; "Armadillos", 1990; Feldhamer, et al., 2003)
Armadillos are dioecious, iteroparous, and viviparous. The age at which males and females become sexually mature varies with species. Male and female large hairy armadillos (Chaetophractus villosus) reach sexual maturity after 9 months of age. Male Dasypus novemcinctus become sexually mature about 6 months after birth, while females become sexually mature after about 1 year. Male and female giant armadillos (Priodontes maximus) and Pichi armadillos (Zaedyus pichiy) reach sexual maturity between 9 and 12 months of age.
The breeding season for most species of Dasypodidae begins during the spring and summer months, between April and June. Some species in captivity are able to breed anytime throughout the year. Gestation period also varies with species. For individuals of the genus Dasypus, gestation is extended due to embryonic diapause. Embryonic diapause is a delay in embryo implantation that lasts anywhere from 4 months to 2 years depending on the species. This delay is advantageous, as it allows a female to give birth during times of seasonal and environmental prosperity, when chances of offspring survival are greater.
In most species, female armadillos produce a litter of 1 to 3 offspring, usually born between the months of February and July. However, species of the genus Dasypus undergo a process called monozygotic polyembryony, in which 1 egg produces between 2 and 12 identical embryos depending on the species. All offspring born from this process are the same sex.
Gestation period and litter size vary with species. Small hairy armadillos (Chaetophractus vellerosus) have a gestation period of about 65 days and give birth to 1 to 2 offspring. Large hairy armadillos (Chaetophractus villosus) are unique in that they are able to give birth more than once a year, producing 1 to 2 offspring in each litter. The gestation period of C. villosus is 60 to 75 days. Giant armadillos (Priodontes maximus) have a gestation period of about 4 months and produce 1 or 2 offspring per year. Southern three-banded armadillos (Tolypeutes matacus) produce 1 offspring per breeding season, though timing of gestation is unknown. Six-banded armadillos (Euphractus sexcinctus) produce 1 to 3 offspring after a gestation period of about 60 days. Pichi armadillos (Zaedyus pichiy) have a gestation period of about 60 days, after which 1 to 3 offspring are born. Data on litter size and gestation period for most other species are not yet available. ("Armadillos (Dasypodidae)", 2003; "Armadillos", 1990; Anderson and Jones Jr., 1984; Feldhamer, et al., 2003; Hayssen, et al., 1993; MacDonald, 1987; Nowak, 1999; Vaughan, et al., 2000)
Depending on the species, armadillos are precocial or altricial. Juvenile nine-banded armadillos (Dasypus novemcinctus) weigh 28.6 to 114 grams at birth, are born with their eyes open and able to walk fairly quickly. Newborns of this species possess pink leathery skin. After several days, the skin solidifies to form the dorsal armor. About 20 days after birth, D. novemcinctus move around outside of their nests, and within 2 to 3 weeks, they are able to leave the burrow for short periods of time. Weaning occurs 4 to 5 months after birth. Males of this species do not provide care to their offspring.
Southern three-banded armadillos (Tolypeutes matacus) also produce precocial young. Newborns are very similar in appearance to adults. Newborns weigh on average 113 g, possess developed claws, and have scute marks. Their eyes remain closed, and they are unable to hear for the first 3 to 4 weeks of life. On the day their are born, however, they are able roll into the protective sphere that is characteristic of the species.
Some species, such as giant armadillos (Priodontes maximus), possess a thick skin at birth but are blind and need their mother's help in order to survive. Weaning in this species occurs between 4 and 5 months after birth. Weaning times known for other species are estimated to be about 6 weeks (Zaedyus pichiy), and 7 to 8 weeks (Chaetophractus vellerosus).
A high level of female parental investment is noted among six-banded armadillos (Euphractus sexcinctus). Newborns are soft and vulnerable at birth. Mothers are extremely protective of their offspring, and if they sense a threat, they become aggressive. Mothers may pick up their young and move them to a safer burrow, if necessary. (Nowak, 1999; "Armadillos", 1990; Feldhamer, et al., 2003; Nowak, 1999)
The lifespan of armadillos varies with species. Some species live only 9 years (Zaedyus pichiy), while others can live as long as 23 years (Chaetophractus villosus). In captivity, Euphractus sextinctus has been documented to live up to 18 years, and Tolypeutes matacus up to 17.
Among nine-banded armadillos (Dasypus novemcinctus), prenatal mortality is common, and juveniles tend to have a higher mortality rate than adults. Pre- and postnatal mortality information for this and other species, however, is not well known. ("Armadillos", 1990; "Encyclopædia Britannica", 2009; Burton and Burton, 1969; Feldhamer, et al., 2003; Nowak, 1999)
Most species of Dasypodidae forage and live alone, though some have been found to socialize and forage in pairs or small groups. Most species are nocturnal or crepuscular. Six-banded armadillos (Euphractus sexcinctus) and Pichi armadillos (Zaedyus pichiy) are able to forage during the brightest hours of the day, despite high temperatures. As seasons change from summer to winter and temperatures cool, many species of Dasypodidae become more diurnal. Zaedyus pichiy and Chaetophractus nationi are the only two species of Dasypodidae known to hibernate.
Armadillos are highly fossorial, and most dasypodids sleep and nest within underground burrows. These burrows are large and deep and are usually located near food sources. While a single burrow may be used multiple times by the same animal, members of several species construct a new burrow each day. Members of other species divide their time among each of several burrows at different locations. Nine-banded armadillos (Dasypus novemcinctus) build burrows that have several passages that all lead to one space underground. In times of danger, individuals use the closest passage as an escape. Many species sleep for at least 16 hours a day.
Dasypus novemcinctus display a wide variety of interesting behaviors. They are good swimmers and can cross a body of water by several means. In one approach, they inflate their stomach and intestines, which increases their buoyancy and allows them to “float” along the surface of the water. A second method is to “doggy-paddle” through the water, using their snouts as a sort of snorkel. Alternatively, they can walk across the bottom of the body of water (at low to moderate depths) due to their high specific gravity and ability to hold their breath for long periods of time. This species has also been known to take mud baths and climb fences in captivity. ("Armadillos (Dasypodidae)", 2003; "Armadillos", 1990; Anderson and Jones Jr., 1984; Burton and Burton, 1969; Feldhamer, et al., 2007; Feldhamer, et al., 2003; MacDonald, 1987; McBee and Baker, 1982; Nowak, 1999; Reid, 1997; Sebeok, 1968; "Wild Animals of North America", 1998; Wilson and Ruff, 1999)
Dasypodids have a well-developed sense of smell and hearing. Vision, however, varies with species; some species have adequate and others have poor vision. Poor vision may be associated with the nocturnal or crepuscular behavior of most species. Armadillos tend to have acute hearing and are able to pick up and react to certain noises that signify potential danger. However, some species, such as Dasypus novemcinctus, tend to ignore even threatening sounds if they are busy foraging. All species of Dasypodidae use their acute sense of smell to find other individuals (such as potential mates), their burrows, prey, or predators. Their taste buds and sense of taste are not well developed.
Armadillos communicate mainly through sound and smell. They release secretions from glands within skin pouches, located on different areas of their bodies. These secretions are used to mark their burrows and identify other individuals, such as potential mates or offspring. During estrus, female nine-banded armadillos (D. novemcinctus) produce a secretion near the anus indicating that she is receptive to mating. Six-banded armadillos (Euphractus sexcinctus) mark their burrows by secreting a foul-smelling substance from yellow glands located on their pelvic shields.
Members of Dasypodidae are able to produce several forms of vocalizations. While foraging for food, some species produce a muffled grunting sound. Male and female nine-banded armadillos (D. novemcinctus) let out a “chucking” sound while in their mating pairs. Also within this species, mothers and their offspring softly buzz to one another. When startled, some species of Dasypodidae scream or growl. Greater fairy armadillos (Calyptophractus retusus) are able to create an unusual sound similar to that of a crying human baby. ("Armadillos (Dasypodidae)", 2003; "Armadillos", 1990; Anderson and Jones Jr., 1984; Feldhamer, et al., 2003; Nowak, 1999; Talmage and Buchanan, 1954)
Armadillos are primarily insectivorous, although diet varies greatly among species. Some species are omnivorous foragers, feeding on a variety of sources such as small animals, plant matter, insects, and arachnids. Others are strictly myrmecophagic (ant-eating), using the sticky substance on their tongues to capture large numbers of insects. Some members of Dasypodidae eat carrion, and there have been documented cases of armadillos raiding human graveyards in South America.
Armadillos have very poor eyesight and thus hunt and find food primarily with their sense of smell. Armadillos are strong diggers and use their claws to dig up a variety of otherwise unavailable food sources. Another indication of their generalist life-style is their lack of specialized teeth. (Whitman, 2006)
Two of the major threats currently facing wild armadillos are domestic dogs and humans (many armadillo species are hunted for their meat). Wild cats (pumas and jaguars), wild dogs (coyotes and bush dogs), and bears may also prey on dasypodids, although predation does not seem to have a large effect on armadillo populations.
When threatened, armadillos often retreat to the safety of a burrow. Their armor also acts as a deterrent to predators. However, there is considerable variation in response to predators among dasypodids. For example, armadillos of the genus Tolypeutes can roll completely into a ball, while nine-banded armadillos (Dasypus novemcinctus) have the ability to leap vertically into the air. If a nine-banded armadillo (D. novemcinctus) is captured by a predator, its most common response is to play dead. Some speices, such as hairy armadillos (Chaetophractus nationican), snarl to frighten predators. As a last resort, armadillos may use their powerful digging legs to claw at attackers. ("Armadillos (Dasypodidae)", 2003; Feldhamer, et al., 2003; McBee and Baker, 1982; Schaefer and Hostetler, 2008)
Although armadillos can exist in relatively high densities (dasypodids account for the highest mammalian biomass after sloths in tropical rainforests), they have relatively little impact on their respective environments. This is due in part to their low metabolism. Additionally, armadillos primarily prey upon invertebrates, which have extremely short life cycles so populations are able to recover from predation quickly. As omnivores, most species of armadillos do not heavily rely on any single prey source. As a result, dasypodids do not seem to exhibit much of an impact on prey populations. ("Armadillos (Dasypodidae)", 2003; Whitman, 2006)
Armadillos are generally terrestrial to fossorial and can thrive in a variety of habitats. They are known for their tendency to construct elaborate burrows on agricultural land. While a nuisance to farmers, these burrows provide homes for a variety of other species, including rabbits, skunks, and possums. ("Armadillos (Dasypodidae)", 2003; Whitman, 2006)
Armadillos are relatively resistant to parasites, as their shells and sparsely-haired venters limit their vulnerability to ectoparasites. Among those that do affect members of Dasypodidae are fungi, viruses, protozoans, helminths, and various arthropods. Armadillo species in South America have a noticeably wider array of arthropod parasites than their North American counterparts, although throughout the range of Dasypodidae there are only around fifty known parasites. Armadillos are known to host the bacterium Mycobacterium leprae, which causes leprosy. Transmission to humans is rare, but possible. (Diniz, et al., 1997; Feldhamer, et al., 2003)
Armadillos have long been used as a food source in a variety of cultures, and although certain species such as giant armadillos (Priodontes maximus) are being over-harvested, most populations remain stable. Armadillos help control the populations of a variety of harmful insect species, including fire ants (Solenopsis). The negative view of armadillos by the agriculture industry is slowly changing, in part due to the fact that armadillos are the only predator of fire ants in North America. Dasypodids are also used in research on reproduction, as some species are able to produce identical, same-sex offspring. In addition, armadillos are used to study organ transplants, birth defects, and diseases including leprosy, typhus, and trichinosis. ("Armadillos (Dasypodidae)", 2003; "Armadillos (Dasypodidae)", 2003; "Armadillos (Dasypodidae)", 2003)
Armadillos are generally viewed as pests, as they can cause destruction of suburban and agricultural areas through excessive digging. This view is especially prominent within the agricultural community, as holes created by burrowing species of Dasypodidae can harm both crops and livestock. Additionally, armadillos host the bacterium Mycobacterium leprae, which causes leprosy. Transmission to humans, while rare, is possible. The public view of dasypodids, is slowly becoming more positive as awareness of their economic benefits increases. ("Armadillos (Dasypodidae)", 2003; "Armadillos (Dasypodidae)", 2003)
While only two members of Dasypodidae, giant armadillos (Priodontes maximus) and pink fairy armadillos (Chlamyphorus truncatus), are listed as endangered, 12 of 20 members are currently listed as vulnerable, endangered, near threatened, or data deficient. Because many species of Dasypodidae are fossorial, they have not been thoroughly studied, so the status of many groups is not well defined. For example, hairy long-nosed armadillos (Dasypus pilosus) are recognized as a species based only on a few skins from Peru. Due to a lack of information, it is very difficult to ascertain the exact conservation status of many dasypodids. ("Animal Life Resource", 2009)
The main threats facing Dasypodidae are exploitation for food and habitat loss. As land is converted for agriculture, potential habitat for both giant armadillos (Priodontes maximus) and pink fairy armadillos (Chlamyphorus truncatus) is reduced. In addition, Priodontes maximus is still hunted for meat in some areas even though it is protected in Brazil, Colombia, Peru, and Suriname. Conservation efforts are planned to breed P. maximus in captivity to help protect the species. ("Armadillos (Dasypodidae)", 2003; "Animal Life Resource", 2009)
Armadillos are quick and hard to catch, but when caught and cooked, they are considered a delicacy in many parts of Latin America. Hunting is listed as the main cause for the IUCN "Vulnerable" classification of giant armadillos (Priodontes maximus). (Cuellar, et al., 2008)
Armadillos are the only mammals other than humans that can contract and carry leprosy. It is unclear why armadillos, which are so distantly related to humans, are the only other mammals to carry the disease. Because of this unique feature, dasypodids have been used as models for biomedical research with leprosy. Despite relatively high rates of carrying the disease in certain areas (especially the southern United States), health risk to humans has been deemed low by many studies, as transmission between armadillos and humans is difficult. (Storrs, et al., 1974)
Teeth are of little use to most members of Dasypodidae. They mostly eat insects, which require minimal chewing. Giant armadillos (Priodontes maximus), whose scientific name ironically means "biggest saw-teeth" in Greek, primarily eat ants and termites and cannot use their teeth for mastication because they are too weak. ("Armadillos", 1990)
Anthony Capizzo (author), University of Michigan-Ann Arbor, Erika Moses (author), University of Michigan-Ann Arbor, Ethan Shirley (author), University of Michigan-Ann Arbor, Phil Myers (author), University of Michigan-Ann Arbor, Gail McCormick (editor), Animal Diversity Web Staff.
living in the Nearctic biogeographic province, the northern part of the New World. This includes Greenland, the Canadian Arctic islands, and all of the North American as far south as the highlands of central Mexico.
living in the southern part of the New World. In other words, Central and South America.
uses sound to communicate
living in landscapes dominated by human agriculture.
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.
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.
an animal that mainly eats meat
Found in coastal areas between 30 and 40 degrees latitude, in areas with a Mediterranean climate. Vegetation is dominated by stands of dense, spiny shrubs with tough (hard or waxy) evergreen leaves. May be maintained by periodic fire. In South America it includes the scrub ecotone between forest and paramo.
uses smells or other chemicals to communicate
the nearshore aquatic habitats near a coast, or shoreline.
active at dawn and dusk
in mammals, a condition in which a fertilized egg reaches the uterus but delays its implantation in the uterine lining, sometimes for several months.
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.
At about the time a female gives birth (e.g. in most kangaroo species), she also becomes receptive and mates. Embryos produced at this mating develop only as far as a hollow ball of cells (the blastocyst) and then become quiescent, entering a state of suspended animation or embryonic diapause. The hormonal signal (prolactin) which blocks further development of the blastocyst is produced in response to the sucking stimulus from the young in the pouch. When sucking decreases as the young begins to eat other food and to leave the pouch, or if the young is lost from the pouch, the quiescent blastocyst resumes development, the embryo is born, and the cycle begins again. (Macdonald 1984)
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.
parental care is carried out by females
union of egg and spermatozoan
an animal that mainly eats leaves.
A substance that provides both nutrients and energy to a living thing.
forest biomes are dominated by trees, otherwise forest biomes can vary widely in amount of precipitation and seasonality.
Referring to a burrowing life-style or behavior, specialized for digging or burrowing.
an animal that mainly eats fruit
An animal that eats mainly plants or parts of plants.
having a body temperature that fluctuates with that of the immediate environment; having no mechanism or a poorly developed mechanism for regulating internal body temperature.
the state that some animals enter during winter in which normal physiological processes are significantly reduced, thus lowering the animal's energy requirements. The act or condition of passing winter in a torpid or resting state, typically involving the abandonment of homoiothermy in mammals.
An animal that eats mainly insects or spiders.
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).
having the capacity to move from one place to another.
This terrestrial biome includes summits of high mountains, either without vegetation or covered by low, tundra-like vegetation.
the area in which the animal is naturally found, the region in which it is endemic.
active during the night
an animal that mainly eats all kinds of things, including plants and animals
having more than one female as a mate at one time
rainforests, both temperate and tropical, are dominated by trees often forming a closed canopy with little light reaching the ground. Epiphytes and climbing plants are also abundant. Precipitation is typically not limiting, but may be somewhat seasonal.
Referring to something living or located adjacent to a waterbody (usually, but not always, a river or stream).
an animal that mainly eats dead animals
communicates by producing scents from special gland(s) and placing them on a surface whether others can smell or taste them
scrub forests develop in areas that experience dry seasons.
breeding is confined to a particular season
remains in the same area
reproduction that includes combining the genetic contribution of two individuals, a male and a female
living in residential areas on the outskirts of large cities or towns.
a wetland area that may be permanently or intermittently covered in water, often dominated by woody vegetation.
uses touch to communicate
that region of the Earth between 23.5 degrees North and 60 degrees North (between the Tropic of Cancer and the Arctic Circle) and between 23.5 degrees South and 60 degrees South (between the Tropic of Capricorn and the Antarctic Circle).
Living on the ground.
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
the region of the earth that surrounds the equator, from 23.5 degrees north to 23.5 degrees south.
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.
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.
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.
uses sight to communicate
reproduction in which fertilization and development take place within the female body and the developing embryo derives nourishment from the female.
breeding takes place throughout the year
young are relatively well-developed when born
The Book Division National Geographic Society. 1998. Wild Animals of North America. Washington, D.C.: The National Geographic Society.
Net Industries. 2009. "Animal Life Resource" (On-line). Armadillos: Dasypodidae: Conservation Status. Accessed February 15, 2009 at http://animals.jrank.org/.
2003. Armadillos (Dasypodidae). Pp. 181-186 in M Hutchins, D Kleiman, V Geist, M McDade, eds. Grzimek's Animal Life Encyclopedia, Vol. 12-16, 2nd Edition. Farmington Hills, Michigan: Thomson Gale.
1990. Armadillos. Pp. 612-627 in S Parker, ed. Grzimek's Encyclopedia of Mammals, Vol. 2, 1st Edition. New York: McGraw-Hill Publishing Company.
2005. Checklist of Mammal Names. Pp. 8-9 in D Wilson, D Reeder, eds. Mammal Species of the World: A Taxonomic and Geographic Reference (3rd ed), Vol. 2, 142. United States: Johns Hopkins University Press. Accessed January 01, 2013 at http://www.vertebrates.si.edu/msw/mswcfapp/msw/index.cfm.
2009. "Encyclopædia Britannica" (On-line). Armadillo. Accessed January 01, 2013 at http://www.britannica.com/EBchecked/topic/35045/armadillo.
Anderson, S., J. Jones Jr.. 1984. Orders and Families of Recent Mammals of the World. New York: Wiley-Interscience; John Wiley & Sons.
Barlow, J. 1984. Xenarthrans and pholidotes. Pp. 219-239 in S Anderson, J Jones, Jr., eds. Orders and Families of Recent Mammals of the World. New York: John Wiley and Sons.
Burton, M., R. Burton. 1969. Armadillo. Pp. 85-87 in International Wildlife Encyclopedia, Vol. 1, 3rd Edition. New York: Marshall Cavendish Corporation. Accessed February 12, 2009 at http://books.google.com/books?id=FuExHhF9IvIC&pg=PA86&dq=Dasypodidae+lifespan#PPP1,M1.
Cetica, P., H. Aldana Marcos, M. Merani. 2005. Morphology of female genital tracts in Dasypodidae (Xenarthra,. Zoomorphology, 124: 57-65. Accessed February 17, 2009 at http://link.springer.com/article/10.1007%2Fs00435-005-0111-5.
Cuellar, E., D. Merritt, G. Porini. 2008. "Priodontes maximus" (On-line). IUCN Red List. Accessed February 15, 2009 at http://www.iucnredlist.org/details/18144.
Diniz, L., E. Costa, P. Oliveira. 1997. "NCBI Pubmed" (On-line). Clinical disorders in Armadillos (Dasypodidae, Edentata) in capitivity. Accessed February 16, 2009 at http://www.ncbi.nlm.nih.gov/pubmed/9467299?dopt=Abstract.
Feldhamer, G., L. Drickamer, S. Vessey, J. Merritt, C. Krajewski. 2007. Mammalogy: Adaptation, Diversity, Ecology. United States: The Johns Hopkins University Press.
Feldhamer, G., B. Thompson, J. Chapman. 2003. Wild Animals of North America: Biology, Management & Conservation. Baltimore, Maryland: Johns Hopkins Press.
Hayssen, V., A. Teinhoven, A. Teinhoven, S. Asdell. 1993. Asdell's Patterns of Mammalian Reproduction: A Compendium of Species-specific Data. United States: Cornell University Press. Accessed February 17, 2009 at http://books.google.com/books?id=yQzSe71g2AcC&printsec=frontcover#PPP9,M1.
MacDonald, D. 1987. Armadillos. Pp. 780-783 in The Encyclopedia of Mammals, 2 Edition. New York: Facts on File Publications.
McBee, K., R. Baker. 1982. Dasypus novemcinctus. Mammalian Species, 162: 1-9. Accessed February 27, 2009 at http://www.science.smith.edu/msi/pdf/i0076-3519-162-01-0001.pdf.
Nowak, R. 1999. Pp. 158-168 in Walker's Mammals of the World, Vol. 1, 6th Edition. Baltimore, Maryland and London: The Johns Hopkins University Press.
Paradiso, J. 1975. Walker's Mammals of the World, Third Edition. Baltimore: Johns Hopkins University Press.
Reid, F. 1997. A Field Guide to the Mammals of Central America and Southeast Mexico. New York: Oxford University Press. Accessed February 13, 2009 at http://books.google.com/books?id=TXQe9P5Z_7UC&pg=PA59&dp=Dasypodidae+lifespan#PPP1,M1.
Savage, R., M. Long. 1986. Mammal Evolution, an Illustrated Guide. New York: Facts of File Publications.
Schaefer, J., M. Hostetler. 2008. "University of Florida IFAS Extension" (On-line). The Nine-banded Armadillo (Dasypus Novemcinctus). Accessed February 16, 2009 at http://edis.ifas.ufl.edu/UW082.
Sebeok, T. 1968. Animal Communication. Bloomington, London: Indiana University Press.
Storrs, E., G. Walsh, H. Burchfield, C. Binford. 1974. Leprosy in the Armadillo: New Model for Biomedical Research. Science, 183, no. 4127: 851-852. Accessed February 15, 2009 at http://www.sciencemag.org/cgi/content/abstract/183/4127/851.
Talmage, R., G. Buchanan. 1954. The Armadillo: A Review of Its Natural History, Ecology, Anatomy and Reproductive Physiology. Pp. 1-12 in The Rice Institute Pamphlet, Vol. 41, 1st Edition. Houston, Texas: The Rice Institute.
Vaughan, T. 1986. Mammalogy. Third Edition. Fort Worth: Saunders College Publishing.
Vaughan, T., J. Ryan, N. Czaplewski. 2000. Mammalogy, Fourth Edition. United States: Thomson Learning.
Vizcaino, S., N. Milne. 2005. Structure and function in armadillo limbs (Mammalia:. Journal of Zoology, 257, 1: 117-127. Accessed February 17, 2009 at http://onlinelibrary.wiley.com/doi/10.1017/S0952836902000717/abstract.
Whitman, A. 2006. "Tree of Life Web Project" (On-line). The Armadillo's Story. Accessed February 15, 2009 at http://tolweb.org/treehouses/?treehouse_id=4288.
Wilson, D., D. Reeder. 1993. Mammal Species of the World, A Taxonomic and Geographic Reference. Washington: Smithsonian Institution Press.
Wilson, D., S. Ruff. 1999. The Smithsonian Book of North American Mammals. Washington and London: Smithsonian Institution Press in association with the American Society of Mammologists.