Temporal range: Early Paleocene – Present, 61.7–0Ma
|Clockwise from top, capybara, spring hare, golden-mantled ground squirrel, house mouse and beaver representing the suborders Hystricomorpha, Anomaluromorpha, Sciuromorpha, Myomorpha, and Castorimorpha|
|Combined range of all rodent species|
Rodents are mammals of the order Rodentia, characterized by a single pair of continuously-growing incisors in each of the upper and lower jaws. About forty percent of all mammal species are rodents, and they are found in vast numbers on all continents except Antarctica. They are the most diversified mammalian clade and can be found in a variety of terrestrial habitats including human-made environments. There are species that are arboreal, fossorial, and even semi-aquatic. Well known rodents include mice, rats, squirrels, prairie dogs, porcupines, beavers, guinea pigs, and hamsters, but rabbits, hares and pikas are now considered to be in a separate order, Lagomorpha.
Most rodents are small animals with robust bodies, short limbs and long tails, but there are exceptions to this. They use their sharp incisors to gnaw food, excavate burrows and defend themselves. Most eat seeds or other plant material, but some have more varied diets. They tend to be social animals and many species live in societies with complex ways of communicating with each other. Mating among rodents can vary from monogamy, to polygyny, to promiscuity. Many have litters of underdeveloped, altricial young, while others have precocial young which are relatively well developed at birth.
The earliest fossil record of rodents dates to the Paleocene on the supercontinent of Laurasia. They greatly diversified in the Eocene, as they spread across continents, sometimes even finding means to cross oceans. Rodents reached both South America and Madagascar from Africa; they were also the only terrestrial placental mammals to reach and colonize Australia.
Rodents have been put to use as food, in clothing, as pets and as laboratory animals in research. Some species are serious pests, eating and spoiling food stored by humans, and spreading diseases. Accidentally introduced species of rodents are often considered to be invasive, as they sometimes threaten the survival of native species such as island birds previously isolated from land-based predators.
- 1 Characteristics
- 2 Distribution and habitat
- 3 Behavior and life history
- 4 Classification and evolution
- 5 Interaction with humans
- 6 References
- 7 Further reading
- 8 External links
With most species weighing less than 100 g (3.5 oz), rodents are generally small animals. Some reach exceptional size, the largest being the capybara, which can weigh as much as 66 kg (146 lb). Rodents typically have squat bodies and short limbs. The fore-limbs usually have five digits, including a thumb that is sometimes vestigial, while the hind-limbs have three to five digits. The elbow gives the fore-arms great flexibility. The majority of species are plantigrade, walking on both the palms and soles of their feet, and have claw-like nails. In general, rodents are not well adapted for running but a few species, like the agouti are fleet-footed, being digitigrade and having hoof-like nails. Kangaroo mice and jerboas can hop at 48 km/h (30 mph). Semi-aquatic species like the beaver have webbed feet and squirrels have well-developed dexterity in their front paws. The majority of species have tails, which can be of many shapes and sizes. Some tails are prehensile, as in the Eurasian harvest mouse and the pelage on the tails can vary from bushy to completely bald. Some species have vestigial tails or no tails at all. In some species, the tail is capable of regeneration if a part is broken off.
Rodents generally have well-developed senses of smell, hearing and vision. Nocturnal species often have enlarged eyes and some are sensitive to ultraviolet light. Many species have long, sensitive vibrissae for touch or "whisking". Some rodents have cheek pouches which may be lined with fur. These can be turned inside out for cleaning. In many species, the tongue cannot reach past the incisors. Rodents have efficient digestive systems, absorbing nearly 80 percent of ingested energy. When eating cellulose, the food is softened in the stomach and passed to the cecum where bacteria reduce it to its carbohydrate elements. The rodent then re-ingests the food from its anus so that the nutrients can be absorbed by the gut. Rodents therefore often produce a hard and dry fecal pellet. In males, the penis contains a bone and the testes can be located either abdominally or at the groin.
Sexual dimorphism occurs in many rodent species. In some rodents, males are larger than females while in others, the reverse is true. Male-bias sexual dimorphism is typical for ground squirrels, kangaroo rats, solitary mole rats and pocket gophers and likely developed due to sexual selection and greater male-male combat. Female-bias sexual dimorphism exists among chipmunks and jumping mice. It is not understood why this pattern occurs, but in the case of yellow-pine chipmunks it may be that males selected larger females due to their greater reproductive success. In some species, like voles, sexual dimorphism can vary from population to population. In bank voles, females are typically larger than males. Male-bias sexual dimorphism occurs in alpine populations, possibly because of the lack of predators and greater competition between males.
Dentition and jaw musculature
The most defining feature of the rodents is their teeth, particularly their razor-sharp incisors which have thick layers of enamel on the front and little enamel on the back. Because the incisors do not stop growing, the animal must continue to wear them down so that they do not grow far enough to reach or even pierce the skull. As the incisors grind against each other, the softer dentine on the rear of the teeth wears away, leaving the sharp enamel edge like the blade of a chisel. Most species have up to 22 teeth (an exception being the silvery mole rat which has 28 teeth) with no canines or anterior premolars. There is a gap, or diastemata, between the incisors and the molars. This lets rodents suck in their cheeks or lips to shield their mouths and throats from wood shavings or other inedible material, and discard this from the side of the mouth.
The molars are relatively large, intricately structured and covered with convoluted ridges of enamel which are arranged transversely. They are well equipped to grind food into small particles. The jaw musculature is strong. The lower jaw is thrust forward while gnawing and is pulled backwards during chewing. Rodent groups differ in the arrangement of the jaw muscles and associated skull structures. The Sciuromorpha or squirrel-like rodents have a very simple jaw muscle that extends onto the snout in front of the eye. The Myomorpha or mouse-like rodents have jaw muscles that anchor on the side of the nose - these are the most efficient chewers amongst the rodents. The Caviomorpha or cavy-like rodents have very large cheekbones and muscles that anchor to the side of the face.
Distribution and habitat
One of the most widespread group of mammals, rodents can be found on every continent expect Antarctica. They are the only terrestrial placental mammals that have colonized Australia and New Guinea without human intervention. Humans have also allowed the animals to spread to many remote oceanic islands (e.g., the Polynesian rat). Rodents have adapted to almost every terrestrial habitat, from cold tundra (where they can live under snow) to hot deserts. Some species are arboreal, some live underground where they build complex burrow systems and others dwell on the surface. Beavers and muskrats are known for being semi-aquatic. Rodents have also thrived in human-created environments such as agricultural and urban areas.
Though some species are common pests for humans, rodents also play important ecological roles. Burrowing rodents may eat the fruiting bodies of fungi and spread spores through their feces, thereby allowing the fungi to disperse and form symbiotic relationships with the roots of plants (which usually cannot thrive without them). As such, these rodents may play a role in maintaining healthy forests.
Some rodents are considered keystone species and ecosystem engineers in their respective habitats. In the Great Plains of North America, the burrowing activities of prairie dogs play important roles in soil aeration and nutrient redistribution, raising the organic content of the soil and increasing the absorption of water. They maintain these grassland habitats, and some large herbivores like bison and pronghorn prefer to graze near prairie dog colonies due to the increased nutritional quality of forage. Prairie dogs can also lead to regional and local biodiversity loss, increased seed depredation and the establishment and spread of invasive shrubs.
In many temperate regions, beavers play an essential hydrological role. When building their dams and lodges, beavers alter the paths of streams and rivers and allow for the creation of extensive wetland habitats. One study found that engineering by beavers leads to a 33 percent increase in the number of herbaceous plant species in riparian areas. Another study found that beavers increase wild salmon populations.
Behavior and life history
Most rodents are herbivorous, feeding exclusively on plant material such as seeds, stems, leaves, flowers and roots. Some are omnivorous and others are carnivorous. The field vole is a typical herbivorous rodent and feeds on grasses, herbs, root tubers, moss and other vegetation, and gnaws on bark during the winter. It occasionally eats invertebrates such as insect larvae. The plains pocket gopher eats plant material found underground during tunneling, and also collects grasses, roots and tubers in its cheek pouches and caches them in underground larder chambers. The Texas pocket gopher avoids emerging onto the surface to feed by seizing the roots of plants with its jaws and pulling them downwards into its burrow. It also practices coprophagy, eating its own fecal pellets. The African pouched rat forages on the surface, gathering anything that might be edible into its capacious cheek pouches until its face bulges out sideways. It then returns to its burrow to sort through the material it has gathered and eats the nutritious items.
The agouti is one of the few animals that can break open the large capsules of the Brazil nut fruit. There are too many seeds inside to be consumed in one meal, so the agouti carries some off and caches them. This helps dispersal of the seeds as any that the agouti fails to retrieve are distant from the parent tree when they germinate. Other nut-bearing trees tend to bear a glut of fruits in the autumn. These are too numerous to be eaten in one meal and squirrels gather and store the surplus in crevices and hollow trees. In desert regions, seeds are often only available for short periods. The kangaroo rat collects all it can find and stores them in larder chambers in its burrow.
A strategy for dealing with seasonal plenty is to eat as much as possible and store the surplus nutrients as fat. Marmots do this, and may be 50 percent heavier in the autumn than in the spring. They rely on their fat reserves during their long winter hibernation. Beavers feed on the leaves, buds and inner bark of growing trees, as well as aquatic plants. They store food for winter use by felling small trees and leafy branches in the autumn and immersing them in their pond, sticking the end into the mud to anchor them. Here they can access their food supply underwater even when their pond is frozen over.
One of the few largely carnivorous rodents is the grasshopper mouse found in dry regions of North America. This mouse feeds on insects, scorpions, other small mice and only a small portion of plant material. It has a chunky body with short legs and tail, but is agile and can easily overpower prey as large as itself. Another is the Australian water rat which feeds on crustaceans, insects, small fish, frogs and mollusks. Some plant matter is also eaten, especially in the winter.
Rodents exhibit a wide range of types of social behavior ranging from the only known mammalian caste systems of some mole rats, the extensive "town" of the colonial prairie dog, through family groups to the independent, solitary life of the edible dormouse.
In the case of the dormouse, males and females live independently, only coming together briefly in the breeding season to mate. Their feeding ranges may overlap but they live in individual nests and feed separately. The female raises the young without any assistance from the male. The pocket gopher is also a solitary animal outside the breeding season, each individual digging a complex tunnel system and maintaining a territory.
Larger rodents tend to live in family units where parents and their offspring live together until the youngsters disperse. Beavers live in extended family units typically with a pair of adults, this year's kits, the previous year's offspring and sometimes older young.
Brown rats usually live in small colonies with up to six females sharing a burrow and one male defending a territory around the burrow. At high population densities, this system breaks down and males show a hierarchical system of dominance with overlapping ranges. Female offspring remain in the colony while male young disperse.
The prairie vole is monogamous and forms a lifelong pair bond. Outside the breeding season, prairie voles live in close proximity with others in small colonies. A male is not aggressive towards other males until he has mated, after which time he defends a territory, a female and a nest against other males. The pair huddle together, groom one another, and share nesting and pup-raising responsibilities.
Among the most social of rodents are the ground squirrels, which typically form colonies based on female kinship, males dispersing after weaning and becoming nomadic as adults. Co-operation in ground squirrels varies between species and typically includes making alarm calls, defending territories, sharing food, protecting nesting areas and preventing infanticide. The black-tailed prairie dog forms large towns that may cover many hectares. The burrows do not interconnect but are excavated and occupied by territorial family groups known as coteries. A coterie often consists of an adult male, three or four adult females, several non-breeding yearlings and this year's offspring. Individuals within coteries are friendly with each other, but hostile towards outsiders.
Perhaps the most extreme examples of colonial behavior in rodents are the eusocial naked mole rat and Damaraland mole rat. These are considered to be the only two eusocial mammals. The naked mole rat lives completely underground and can form colonies of up to eighty individuals. Only one female and up to three males in the colony reproduce, while the rest of the members are smaller, sterile and function as workers. Some individuals are of intermediate size. They help with the rearing of the young and can take the place of a reproductive if one dies. The Damaraland mole rat is characterized by having a single reproductively active male and female in a colony where the remaining animals are not truly sterile, but only become fertile if they establish a colony of their own.
Many rodent species, particularly those that are diurnal and social, have a wide range of alarm calls that are emitted when they perceive threats. There are both direct and indirect benefits of doing this. A potential predator may stop when it knows it has been detected, or, an alarm call can allow conspecifics or related individuals to take evasive action. Several species, for example prairie dogs, have complex anti-predator alarm call systems. These species may have different calls for different predators (e.g. aerial predators or ground-based predators) and each call contains information about the nature of the precise threat. The urgency of the threat is also conveyed by the acoustic properties of the call.
Social rodents have a wider range of vocalizations than do solitary species. Fifteen different call-types have been recognized in adult Kataba mole rats and four in juveniles. Similarly, degus, another social, burrowing rodent, exhibit a wide array of communication modalities and have an elaborate vocal repertoire comprising fifteen different categories of sound. Ultrasonic calls play a part in social communication between dormice and are used when the individuals are out of sight of each other.
Rats emit short, high frequency, ultrasonic, vocalizations during purportedly pleasurable experiences such as rough-and-tumble play, before receiving morphine, during mating, and when tickled. The vocalization, described as a distinct "chirping", has been likened to laughter, and is interpreted as an expectation of something rewarding. In clinical studies, the chirping is associated with positive emotional feelings, and social bonding occurs with the tickler, resulting in the rats becoming conditioned to seek the tickling. However, as the rats age, the tendency to chirp declines. Like most rat vocalizations, the chirping is at frequencies that are too high for humans to hear without special equipment. Bat detectors are often used by pet owners for this purpose.
Rodents use scent marking in many social contexts including for inter-species communication, the marking of trails and the establishment of territories. Their urine provides genetic information about individuals including the species, the sex and individual identity, and metabolic information on dominance, reproductive status and health. The chemicals involved are the major histocompatibility complex and several urinary proteins which are detected and interpreted by two olfactory bulbs. The odor of a predator depresses scent marking behavior. The urine of many rodents strongly reflects ultraviolet light but the amount reflected decreases with time. This may in some instances be disadvantageous; kestrels in Finland have been shown to use it and have greater hunting success when they assess whether vole trails are currently in use. Ultraviolet reflectivity is of dubious value for nocturnal rodents.
Using olfaction, rodents are able to recognize close relatives. This allows them to express nepotism (preferential behavior toward their kin) and also avoid inbreeding. This kin recognition is by olfactory cues from urine, feces and glandular secretions. The main assessment may involve the major histocompatibility complex (MHC), where the degree of relatedness of two individuals is correlated to the MHC genes they have in common. In non-kin communication where more permanent odor markers are required, as at territorial borders, then non-volatile major urinary proteins (MUPs), which function as pheromone transporters, may also be used. MUPs may also signal individual identity, with each male house mouse excreting urine containing about a dozen genetically encoded MUPs.
Vibrations can provide cues to conspecifics about specific behaviors being performed, predator warning and avoidance, herd or group maintenance, and courtship. The Middle East blind mole rat was the first mammal for which vibrational communication was documented. These fossorial rodents bang their head against the walls of their tunnels, which was initially interpreted as part of their tunnel building behavior. It was eventually realized that they generate temporally patterned vibrational signals for long-distance communication with neighboring mole rats. Footdrumming is used widely as a predator warning or defensive action. It is used primarily by fossorial or semi-fossorial rodents. The banner-tailed kangaroo rat produces several complex footdrumming patterns in a number of different contexts, one of which is when it encounters a snake. The footdrumming may alert nearby offspring but most likely conveys that the rat is too alert for a successful attack, thus preventing the snake's predatory pursuit. Several studies have indicated intentional use of ground vibrations as a means of intra-specific communication during courtship among the Cape mole rat. Footdrumming has been reported to be involved in male-male competition where the dominant male indicates its resource holding potential by drumming, thus minimizing physical contact with potential rivals.
Several different mating systems exist among rodents. Some species practice monogamy where an adult male and female form a pair bond. Monogamy can come in two forms; obligate and facultative. In obligate monogamy, both parents care for the offspring and play an important part in their survival. This occurs in California mice, oldfield mice, Malagasy giant rats and beavers. In these species, males usually mate only with their partners. In addition to increased care for young, obligate monogamy can also be beneficial to the adult male as it decreases the chances of never finding a mate or mating with an infertile female. In facultative monogamy, the males do not provide direct parental care and stay with one female because they cannot access others due to being spatially dispersed. Prairie voles appear to be an example of this form of monogamy, with males guarding and defending females within their vicinity.
In polygynous species, males will try to monopolize and mate with multiple females. As with monogamy, polygyny in rodents can come in two forms; defense and non-defense. Defense polygyny involves males controlling territories which contain resources that attract females. This occurs in ground squirrels like yellow-bellied marmots, California ground squirrels, Columbian ground squirrels and Richardson's ground squirrels. Males with territories are known as "resident" males and the females that live within the territories are known as "resident" females. In the cause of marmots, resident males do not appear to ever lose their territories and always win encounters with invading males. Some species are also known to directly defend their resident females and the ensuing fights can lead to severe wounding. In species with non-defense polygyny, males are not territorial and wander widely in search of females to monopolize. These males establish dominance hierarchies with the high ranking males having access to the most females. This occurs in Belding's ground squirrels and some tree squirrel species.
Promiscuity, in which both males and females mate with multiple partners, also occurs in rodents. In species such as the white-footed mouse, females give birth to litters with multiple paternities. Promiscuity leads to increased sperm competition and males tend to have larger testicles. In the Cape ground squirrel, the male's testes can be 20 percent of its head-body length.
Several rodent species have flexible mating systems which can vary between monogamy, polygyny and promiscuity. Females play an active role in choosing their mates. Factors that contribute to female preference may include the size, dominance and spatial ability of the male. In the eusocial naked mole rats, a single female monopolizes mating from at least three males.
In most rodent species, for example rats and mice, ovulation occurs on a regular cycle while in others, such as voles, it is induced by mating. During copulation, males of some rodent species deposit a mating plug in the female's genital opening, both to prevent sperm leakage and to protect against other males inseminating the female. Females can remove the plug and may do so either immediately or after several hours.
Birth and parenting
Rodents may be born either altricial (blind, hairless and relatively underdeveloped) or precocial (mostly furred, eyes open and fairly developed) depending on the species. The altrical state is typical for squirrels and mice; while the precocial state usually occurs in species like guinea pigs and porcupines. Females with altrical young typically build elaborate nests before they give birth and maintain them until their offspring are weaned. The female gives birth sitting or lying down and the young emerge in front of their mother. The newborns first venture out of the nest a few days after they have opened their eyes and initially keep returning regularly. As they get older and more developed, they visit the nest less often and leave permanently when weaned.
In precocial species, the mothers invest little in nest building and some do not build nests at all. The female gives birth standing and the young emerge behind her. Mothers of these species maintain contact with their highly mobile young with maternal contact calls. Though relatively independent and weaned within days, precocial young may continue to nurse and be groomed by their mothers. Rodent litter sizes also vary and females with smaller litters spend more time in the nest than those with larger litters.
Mother rodents provide both direct parental care, such as nursing, grooming, retrieving and huddling, and indirect parenting, such as food caching, nest building and protection to their offspring. In many social species, young may be cared for by individuals other then their parents, a practice known as alloparenting or cooperative breeding. This is known to occur in black-tailed prairie dogs and Belding's ground squirrels where mothers have communal nests and nurse alien young along with their own. There is some question as to whether these mothers can distinguish which young are theirs. In the Patagonian mara, young are also placed in communal warrens but mothers do not permit alien young to nurse.
Infanticide exists in numerous rodent species and may be practiced by adult conspecifics of either sex. Several reasons have been proposed for this behavior, including nutritional stress, resource competition, avoiding misdirecting parental care and, in the case of males, attempting to make the mother sexually receptive. The latter reason is well supported in primates and lions but less so in rodents. Infanticide appears to be widespread in the black-tailed prairie dogs, including infanticide from invading males and immigrant females, as well as occasional cannibalism of an individual's own offspring. To protect against infanticide from other adults, female rodents may employ avoidance or direct aggression against potential perpetrators, multiple mating, territoriality or early termination of pregnancy. Feticide can also occur among rodents; in Alpine marmots, dominant females tend to suppress the reproduction of subordinates by being antagonistic towards them while they are pregnant which causes stress and causes the young to abort.
Rodents have some cognitive abilities and can master simple tasks. They can quickly learn to avoid poisoned baits, which makes them difficult pests to deal with. Guinea pigs can learn and remember complex pathways to food. Squirrels are able to locate where they buried their food, perhaps by memory and not just by smell.
Because mice and rats are often used as scientific models to further our understanding of biology, we know a great deal about their cognitive capacities. In a series of studies, scientists discovered that rats can consider their own learning and then make decisions based on what they know, or, do not know. The researchers put the rats through a series of tests where they could get a large treat for choosing a correct answer, get no treat for selecting an incorrect answer, or get a small treat if they declined to take the test. The rats tended to decline difficult tests (preferring to get a small treat instead of possibly nothing) but would take the risk on easier tests to get a big reward. This showed that rats have some level of understanding of their own cognition and can make strategic decisions based on that knowledge. This is known as metacognition. Similar tests on birds have been inconclusive. Further studies have suggested that the rats may have been following simple operant conditioning principles, or a behavioral economic model.
Rats exhibit cognitive bias. In a 2012 study, rats were trained to respond to a tone that signals them to press a lever to receive a treat, and a tone that signals them to press a lever to avoid being shocked. When the animals mastered this, some of them were subject to tickling by the handlers who recorded the number of chirps they produced. The rats were then put to the same test again, this time with a tone they had not heard before. Tickled rats that emitted chirps were more likely to press the lever that gave them food in response to the ambiguous tone. The researchers stated that they had demonstrated "...for the first time, a link between the directly measured positive affective state and decision making under uncertainty in an animal model..".
Classification and evolution
The fossil record of rodent-like mammals begins during the Paleocene, shortly after the extinction of the non-avian dinosaurs 66 million years ago, in Laurasia, the supercontinent composed of today's North America, Europe, and Asia. Some molecular clock data suggest modern rodents (members of the order Rodentia) had appeared by the late Cretaceous, although other molecular divergence estimations are in agreement with the fossil record.
The history of the colonization of the world's continents by rodents is complex. The movements of the large Muroidea superfamily (including hamsters, gerbils, true mice and rats) may have involved up to seven colonizations of Africa, five colonizations of North America, four of Southeast Asia, two of South America and up to ten re-colonizations of Eurasia.
During the Eocene, rodents began to diversify; some fossil species, such as the giant beavers, Castoroides, and a giant dormouse, Leithia, attained great size. The largest known rodent was Josephoartigasia monesi, a giant pacarana. Beavers appear in North America in the late Eocene before spreading to Eurasia. Late in the Eocene, hystricognaths colonized Africa, most probably having originated in Asia at least 39.5 million years ago. From Africa, fossil evidence shows that some hystricognaths (caviomorphs) migrated to South America, which had been an isolated continent during the Oligocene and Miocene epochs, possibly making use of ocean currents and the Ceara and Sierra Leone Rises in the Atlantic. Caviomorphs had arrived in South America by 41 million years ago (implying a date at least as early as this for hystricognaths in Africa). By 20 million years ago Miocene fossils recognizably belonging to the current families such as Muridae appear. By the Miocene, when Africa had collided with Asia, African rodents such as the porcupine began to spread into Eurasia.
During the Pliocene, rodent fossils appeared in Australia. Although marsupials are the most prominent mammals in Australia, many rodents, all belonging to the Murinae, are among the continent's mammal species, with about 50 'old endemics' and ten true rats (Rattus), of which eight are 'new endemics' and two have been introduced by Europeans. After the Americas became joined by the Isthmus of Panama, around 3 mya, in the Piacenzian age, some rodents participated in the resulting Great American Interchange; sigmodontines surged southward and a small number of species such as the New World porcupines (Erethizontidae) headed north.
|Genus||Species||Notes||Location||Approx. max. weight||Stratigraphy||Image|
|Castoroides||giant beavers||North America||up to 100 kg (220 lb)||Pleistocene|
|Ceratogaulus||horned gophers||North America||(smallest horned mammal)||Late Miocene to Pleistocene|
|Spelaeomys||S. florensis||a large cave rat||Flores||-||Extinct by 1500|
|"Giant hutias"||a paraphyletic group of rodents resembling large guinea pigs||West Indies||up to 200 kg (440 lb)||Pleistocene|
|Leithia||a giant dormouse||Europe (Malta, Sicily)||113 kg (249 lb)||Pleistocene|
|Neochoerus||N. pinckneyi||a large capybara||North America||100 kg (220 lb)||Pleistocene|
|Josephoartigasia||J. monesi||'giant pacarana', largest known rodent||South America||1,500 kg (3,300 lb)||Pliocene to early Pleistocene|
|Phoberomys||P. pattersoni||a horse-sized rodent||North America||probably under 280 kg (620 lb); earlier estimates up to 700 kg (1,500 lb)||Miocene|
|Telicomys||a giant rodent, to 2 metres (6 ft 7 in) long||South American||perhaps 70% of size of P. pattersoni||Late Miocene to early Pleistocene|
The use of the name "Rodentia" is attributed to the English traveler and naturalist Thomas Edward Bowdich (1821). The hares, rabbits and pikas (order Lagomorpha) have continuously growing incisors and were at one time included in the order. However they have an additional pair of incisors in the upper jaw and the two orders have quite separate evolutionary histories. The phylogeny of the rodents places them in the clades Glires, Euarchontoglires and Boreoeutheria. Below is a cladogram showing the inner and outer relations of Rodentia based on an attempt (Wu et al., 2012) to align the molecular clock with paleontological data:
The order Rodentia may be divided into suborders, infraorders, superfamilies and families. There is a great deal of parallelism and convergence among rodents caused by the fact that they have tended to evolve to fill largely similar niches. This makes classification difficult as similar traits may not be due to common ancestry. Brandt (1855) was the first to propose dividing the Simplicidentata (rodents and their closest extinct relatives) into three suborders, Sciuromorpha, Hystricomorpha and Myomorpha, based on the development of certain muscles in the jaw. This system was widely accepted and is known as the "classical" arrangement. Schlosser (1884) performed a comprehensive review of rodent fossils, mainly using the cheek teeth, and found they fitted into the classical system but Tullborg (1899) proposed just two sub-orders, Sciurognathi and Hystricognathi. These were based on the degree of inflection of the lower jaw and were to be further subdivided into Sciuromorpha, Myomorpha, Hystricomorpha and Bathyergomorpha. Matthew (1910) created a phylogenetic tree of New World rodents but did not include the more problematic Old World species. Further attempts at classification continued without agreement, with some authors adopting the classical three suborder system and others Tullborg's two suborders.
While these disagreements have been going on, the rodent families themselves have remained relatively stable, it being just the higher clades that are in dispute. Nor have molecular studies fully resolved the situation though they have confirmed the monophyly of the group and that the clade has descended from a common Paleocene ancestor. Carleton and Musser (2005) in Mammal Species of the World have provisionally adopted a five suborder system, Sciuromorpha, Castorimorpha, Myomorpha, Anomaluromorpha, and Hystricomorpha. These include 33 families, 481 genera and 2277 species:
Order Rodentia (from Latin, rodere, to gnaw)
- Suborder Anomaluromorpha
- Suborder Castorimorpha
- Suborder Hystricomorpha
- Family incertae sedis Diatomyidae: Laotian rock rat
- Infraorder Ctenodactylomorphi
- Family Ctenodactylidae: gundis
- Infraorder Hystricognathi
- Parvorder Caviomorpha
- Family †Heptaxodontidae: giant hutias
- Family Abrocomidae: chinchilla rats
- Family Capromyidae: hutias
- Family Caviidae: cavies, including Guinea pigs and the capybara
- Family Chinchillidae: chinchillas, viscachas
- Family Ctenomyidae: tuco-tucos
- Family Dasyproctidae: agoutis
- Family Cuniculidae: pacas
- Family Dinomyidae: pacaranas
- Family Echimyidae: spiny rats
- Family Erethizontidae: New World porcupines
- Family Myocastoridae: nutria, coypu
- Family Octodontidae: octodonts
- Suborder Myomorpha
- Superfamily Dipodoidea
- Family Dipodidae: jerboas and jumping mice
- Superfamily Muroidea
- Family Calomyscidae: mouse-like hamsters
- Family Cricetidae: hamsters, New World rats and mice, muskrats, voles, lemmings
- Family Muridae: true mice and rats, gerbils, spiny mice, crested rat
- Family Nesomyidae: climbing mice, rock mice, white-tailed rat, Malagasy rats and mice
- Family Platacanthomyidae: spiny dormice
- Family Spalacidae: mole rats, bamboo rats, zokors
- Superfamily Dipodoidea
- Suborder Sciuromorpha
Monophyly versus polyphyly
In 1991, a paper published by Nature proposed that caviomorphs should be reclassified as a separate order (similar to Lagomorpha), based on an analysis of the amino acid sequences of guinea pig proteins. This hypothesis was refined in a 1992 paper, which asserted the possibility that caviomorphs may have diverged from myomorphs prior to later divergences of Myomorpha; this would mean caviomorphs, or possibly hystricomorphs, would be moved out of the rodent classification into a separate order. A minority scientific opinion argued that guinea pigs, degus, and other caviomorphs are not rodents, while several papers were put forward in support of rodent monophyly. Subsequent studies published since 2002, using wider taxon and gene samples, have restored a majority opinion among mammalian biologists that the order Rodentia is monophyletic, although there is not a complete consensus.
Interaction with humans
While rodents are not the most seriously threatened order of mammals, there are 168 species in 126 genera which "deserve conservation attention" in the face of limited appreciation by the public. Since 76 percent of rodent genera contain only one species, much phylogenetic diversity could be lost with a comparatively small number of extinctions. In the absence of more detailed knowledge of species at risk and accurate taxonomy, conservation must be based mainly on higher taxa (such as families rather than species) and geographical hot spots. For example, in Colombia, the brown hairy dwarf porcupine was recorded from only two mountain localities in the 1920s, while the red crested soft-furred spiny rat is known only from its type locality on the Caribbean coast, so these species are considered vulnerable. The IUCN Species Survival Commission writes "We can safely conclude that many South American rodents are seriously threatened, mainly by environmental disturbance and intensive hunting".
The "three now cosmopolitan commensal rodent pest species" (the brown rat, the black rat and the house mouse) have been dispersed in association with humans, partly on sailing ships in the Age of Exploration, and with a fourth species in the Pacific, Rattus exulans, have severely damaged island biotas around the world. For example, when the black rat reached Lord Howe Island in 1918, over 40 percent of the terrestrial bird species of the island became extinct within ten years. Similar destruction has been seen on Midway Island (1943) and Big South Cape Island (1962). Conservation projects can with careful planning completely eradicate these pest rodents from islands using an anticoagulant rodenticide such as brodifacoum. This approach has been successful on the island of Lundy in the United Kingdom where the eradication of an estimated 40,000 rats is giving populations of Manx shearwater and Atlantic puffin a chance to recover from near extinction.
Since they started wearing clothes, humans have used animal skins for this purpose, the leather being durable and the fur providing extra insulation. The native people of North America made much use of beaver pelts, tanning and sewing them together to make robes. Europeans appreciated the quality of these and the North American fur trade developed and became of prime importance to early settlers. In Europe, people wore beaver hats and trimmed their clothing with the fur. Later, the coypu took over as a cheaper source of pelts and was much farmed in America and Europe, but fashions change, new materials become available and the fur industry declined. The chinchilla has a soft and silky coat and the demand for its fur was so high that it was nearly wiped out in the wild before farming took over as the main source of pelts.
At least 89 species of rodent, mostly Hystricomorpha such as guinea pigs, agoutis and capybaras, are eaten by humans; in 1985, there were at least 42 different societies in which people eat rats. Guinea pigs were first raised for food around 2500 B.C. and by 1500 B.C. had become the main source of meat for the Inca Empire. Romans raised dormice in special pots called "gliraria" and in large outdoor enclosures where they were fed walnuts, chestnuts, and acorns for fattening. They were also caught from the wild in autumn when they were fattest, and either roasted and dipped into honey or baked while stuffed with a mixture of pork, pine nuts, and other flavorings. Among indigenous Amazonians, when large mammals are scarce, pacas and common agoutis can account for 39 percent of the annual game take by weight, but in forested areas where larger mammal species are abundant, these rodents comprised only about 3 percent of the take.
Guinea pigs are used in the cuisine of Cuzco, Peru in dishes such as cuy al horno, baked guinea pig. In addition, the traditional Andean stove, known as a qoncha or a fogón, is made from mud and clay reinforced with straw and hair from animals such as guinea pigs. In Peru, there are at any time 20 million domestic guinea pigs, which annually produce 64 million edible carcasses. This animal is an excellent food source since the flesh is 19% protein. In the United States, mostly squirrels, but also muskrat, porcupine, and ground hog are eaten by humans. The Navajo people ate prairie dog baked in mud while the Paiute ate gophers, squirrels, and rats.
Rodents make convenient pets where space is limited, and the different types exhibit differing qualities as pets. Animals kept for this purpose include guinea pigs, mice, rats, hamsters, gerbils, chinchillas, degus and chipmunks. Most are normally kept in cages of suitable sizes and have varied requirements for space and social interaction. If handled from a young age, they are usually docile and do not bite. Rats also need plenty of space and can become very tame, can learn tricks and seem to enjoy human companionship. Mice are short-lived but take up very little space. Hamsters are solitary but tend to be nocturnal. They have interesting behaviors but unless handled regularly they may be defensive. Gerbils are not usually aggressive, rarely bite and are sociable animals that enjoy the company of humans and their own kind.
Rodents are used widely as model organisms in animal testing. The house mouse is the most commonly used laboratory rodent, and in 1979 it was estimated that fifty million were used annually worldwide. They are favored because of their small size, fertility, short gestation period and ease of handling and because they are susceptible to many of the conditions and infections that afflict humans. They are used in research into genetics, developmental biology, cell biology, oncology and immunology. Guinea pigs were popular laboratory animals until the late 20th century; about 2.5 million guinea pigs were used annually in the United States for research in the 1960s, but that total decreased to about 375,000 by the mid-1990s. In 2007, they constituted about 2% of all laboratory animals. Guinea pigs played a major role in the establishment of germ theory in the late 19th century, through the experiments of Louis Pasteur, Émile Roux, and Robert Koch. They have been launched into orbital space flight several times—first by the USSR on the Sputnik 9 biosatellite of March 9, 1961 with a successful recovery. The naked mole rat is the only known mammal that is poikilothermic and also does not produce the neurotransmitter substance P; it is used in studies on thermoregulation and pain.
Rodents have a sensitive olfactory sense which has been used by humans to detect odors or chemicals of interest. The Gambian pouched rat is able to detect tuberculosis bacilli with a sensitivity of up to 86.6%, and specificity (detecting the absence of the bacilli) of over 93%; the same species has been trained to detect land mines. Rats have been studied for possible use in hazardous situations such as in disaster zones, as they can be trained to respond to commands which may be given remotely, even in brightly lit areas, which rats usually avoid.
As pests and disease vectors
Some rodent species are agricultural pests, eating large quantities of food stored by humans. For example, in 2003, the amount of rice lost to mice and rats in Asia was estimated to be enough to feed 200 million people.
Rodents are also vectors of disease. The black rat, with the fleas that it carries, plays a primary role in spreading the bacterium Yersinia pestis responsible for bubonic plague, and also carries the organisms responsible for typhus, Weil's disease, toxoplasmosis and trichinosis.
Because rodents are a nuisance and endanger public health, human societies often attempt to control them. Traditionally this involved poisoning and trapping, methods which were not always safe or effective. More recently, integrated pest management attempts to improve control with a combination of surveys to determine the size and distribution of the pest population, the establishment of tolerance limits (levels of pest activity at which to intervene), interventions, and evaluation of effectiveness based on repeated surveys. Interventions may include education, making and applying laws and regulations, modifying the habitat, changing farming practices, biological control using pathogens or predators, as well as poisoning and trapping. The use of pathogens such as Salmonella has the drawback that they can infect man and domestic animals, and after a while, rodents often become resistant. The use of predators including ferrets, mongooses and monitor lizards has been found unsatisfactory. Domestic and feral cats are able to control rodents effectively provided the rodent population is not too large.
- Single, G.; Dickman, C. R.; MacDonald, D. W. (2001). "Rodents". In MacDonald, D. W. The Encyclopedia of Mammals (2nd ed.). Oxford University Press. pp. 578–587. ISBN 978-0-7607-1969-5.
- Nowak, R. M. (1999). Walker's Mammals of the World. Johns Hopkins University Press. p. 1244. ISBN 0-8018-5789-9.
- Schulte-Hostedde, A. I. (2008). "Chapter 10: Sexual Size Dimorphism in Rodents". In Wolff, Jerry O.; Sherman, Paul W. Rodent Societies: An Ecological and Evolutionary Perspective. University of Chicago Press. pp. 117–119. ISBN 978-0-226-90538-9.
- Waggoner, Ben (15 August 2000). "Introduction to the Rodentia". University of California Museum of Paleontology. Retrieved 4 July 2014.
- "Rodents". pet.justanswer.co.uk. Retrieved 14 July 2014.
- Pérez, F.; Castillo-Guevara, C.; Galindo-Flores, G.; Cuautle, M.; Estrada-Torres, A (2012). "Effect of gut passage by two highland rodents on spore activity and mycorrhiza formation of two species of ectomycorrhizal fungi (Laccaria trichodermophora and Suillus tomentosus)". Botany 90 (11): 1084–1092. doi:10.1139/b2012-086.
- Martínez-Estevez, L.; Balvanera, P.; Pacheco, J.; Ceballos, G. (2013). "Prairie dog decline reduces the supply of ecosystem services and leads to desertification of semiarid grasslands". PLoS ONE 8 (10): e75229. doi:10.1371/journal.pone.0075229.
- Krueger, K. (1986). "Feeding relationships among bison, pronghorn, and prairie dogs: an experimental analysis". Ecology 67 (3): 760–770. doi:10.2307/1937699.
- Burchsted, D.; Daniels, M.; Thorson, R.; Vokoun, J. (2010). "The river discontinuum: applying beaver modifications to baseline conditions for restoration of forested headwaters". BioScience 60 (11): 908. doi:10.1525/bio.2010.60.11.7.
- Wright, J. P.; Jones, C. G.; Flecker, A. S. (2002). "An ecosystem engineer, the beaver, increases species richness at the landscape scale". Oecologia 132 (1): 96–101. doi:10.1007/s00442-002-0929-1.
- Kemp, P. S.; Worthington, T. A.; Langford, T. E. l.; Tree, A. R. J.; Gaywood, M. J. (2012). "Qualitative and quantitative effects of reintroduced beavers on stream fish". Fish and Fisheries 13 (2): 158. doi:10.1111/j.1467-2979.2011.00421.x.
- Hansson, Lennart (1971). "Habitat, food and population dynamics of the field vole Microtus agrestis (L.) in south Sweden". Viltrevy 8: 268–278. ISSN 0505-611X.
- Connior, M. B. (2011). "Geomys bursarius (Rodentia: Geomyidae)". Mammalian Species 43 (1): 104–117. doi:10.1644/879.1.
- "Texan pocket gopher". The Mammals of Texas: Rodents. NSRL: Museum of Texas Tech University. Retrieved 4 July 2014.
- Attenborough, David (2002). The Life of Mammals. BBC Books. pp. 61–86. ISBN 978-0-563-53423-5.
- Müller-Schwarze, Dietland; Sun, Lixing (2003). The Beaver: Natural History of a Wetlands Engineer. Cornell University Press. pp. 67–75. ISBN 978-0-8014-4098-4.
- "Northern grasshopper mouse". The Mammals of Texas: Rodents. NSRL: Museum of Texas Tech University. Retrieved 4 July 2014.
- "Hydromys chrysogaster: Water rat". Water for a healthy country. CSIRO. 30 June 2004. Retrieved 4 July 2014.
- Stefoff, Rebecca (2008). The Rodent Order. Marshall Cavendish. pp. 71–73. ISBN 978-0-7614-3073-5.
- Baker, Bruce W.; Hill, Edward P. (2003). "Chapter 15: Beaver". In Feldhamer, George A.; Thompson, Bruce C.; Chapman, Joseph A. Wild Mammals of North America: Biology, Management, and Conservation. JHU Press. pp. 288–310. ISBN 978-0-8018-7416-1.
- Hanson, Anne (25 October 2006). "Wild Norway rat behavior". Rat behavior and biology. Retrieved 1 July 2014.
- Winslow, James T.; Hastings, Nick; Carter, C. Sue; Harbaugh, Carroll R.; Insel, Thomas R. (1993). "A role for central vasopressin in pair bonding in monogamous prairie voles". Letters to Nature 365: 545–548. doi:10.1038/365545a0.
- Yensen, Eric; Sherman, Paul W. (2003). "Chapter 10: Ground Squirrels". In Feldhamer, George A.; Thompson, Bruce C.; Chapman, Joseph A. Wild Mammals of North America: Biology, Management, and Conservation. JHU Press. pp. 211–225. ISBN 978-0-8018-7416-1.
- Hoogland, John L. (1995). The Black-Tailed Prairie Dog: Social Life of a Burrowing Mammal. University of Chicago Press. p. 1. ISBN 978-0-226-35118-6.
- Jarvis, Jennifer (1981). "Eusociality in a mammal: Cooperative breeding in naked mole-rat colonies". Science 212 (4494): 571–573. doi:10.1126/science.7209555. JSTOR 1686202.
- Shelley, Erin L.; Blumstein, Daniel T. (2005). "The evolution of vocal alarm communication in rodents". Behavioral Ecology 16 (1): 169–177. doi:10.1093/beheco/arh148.
- Slobodchikoff, C. N.; Paseka, Andrea; Verdolin, Jennifer L (2009). "Prairie dog alarm calls encode labels about predator colors". Animal Cognition 12 (3): 435–439. doi:10.1007/s10071-008-0203-y.
- Zimmermann, Elke; Leliveld, Lisette; Schehka, Lisette (2013). "8: Toward the evolutionary roots of affective prosody in human acoustic communication: A comparative approach to mammalian voices". In Altenmüller, Eckart; Schmidt, Sabine; Zimmermann, Elke. The Evolution of Emotional Communication: From Sounds in Nonhuman Mammals to Speech and Music in Man. Oxford University Press. pp. 123–124. ISBN 978-0-19-164489-4.
- Vanden Hole, Charlotte; Van Daele, Paul A. A. G.; Desmet, Niels; Devos, Paul; Adriaens, Dominique (2014). "Does sociality imply a complex vocal communication system? A case study for Fukomys micklemi (Bathyergidae, Rodentia)". Bioacoustics 23 (2): 143–160. doi:10.1080/09524622.2013.841085.
- Long, C. V. (2007). "Vocalisations of the degu (Octodon degus), a social caviomorph rodent". Bioacoustics 16. pp. 223–244. doi:10.1080/09524622.2007.9753579. ISSN 0952-4622.
- Ancillotto, Leonardo; Sozio, Giulia; Mortelliti, Alessio; Russo, Danilo (2014). "Ultrasonic communication in Gliridae (Rodentia): the hazel dormouse (Muscardinus avellanarius) as a case study". Bioacoustics 23 (2): 129–141. doi:10.1080/09524622.2013.838146.
- Panksepp, Jaak; Burgdorf, Jeff (2003). ""Laughing" rats and the evolutionary antecedents of human joy?" (PDF). Physiology & Behavior 79 (3): 533–547. doi:10.1016/S0031-9384(03)00159-8. PMID 12954448.
- Arakawa, Hiroyuki; Blanchard, D. Caroline; Arakawa, Keiko; Dunlap, Christopher; Blanchard, Robert J. (2008). "Scent marking behavior as an odorant communication in mice". Neuroscience and Biobehavioral Reviews 32 (7): 1236–1248. doi:10.1016/j.neubiorev.2008.05.012.
- Pickrell, John (8 July 2003). "Urine Vision? How Rodents Communicate With UV Light". National Geographic News. Retrieved 8 July 2014.
- Holmes, Warren G.; Mateo, Jill M. (2008). "Chapter 19: Kin Recognition in Rodents: Issues and Evidence". In Wolff, Jerry O.; Sherman, Paul W. Rodent Societies: An Ecological and Evolutionary Perspective. University of Chicago Press. pp. 216–230. ISBN 978-0-226-90538-9.
- Randall, J. A. (2001). "Evolution and function of drumming as communication in mammals". American Zoologist 41: 1143–1156. doi:10.1093/icb/41.5.1143.
- "Vibrational communication in mammals". Map of Life: Convergent evolution online. University of Cambridge. 4 August 2010. Retrieved 5 July 2014.
- Randall, Jan A.; Matocq, Marjorie D. (1997). "Why do kangaroo rats (Dipodomys spectabilis) footdrum at snakes?". Behavioral Ecology 8: 404–413. doi:10.1093/beheco/8.4.404.
- Narins, P. M.; Reichman, O. J.; Jarvis, J. U. M.; Lewis, E. R. (1992). "Seismic signal transmission between burrows of the Cape mole-rat Georychus capensis". Journal of Comparative Physiology [A] 170: 13–22. doi:10.1007/BF00190397.
- Waterman, Jane (2008). "Chapter 3: Male Mating Strategies in Rodents". In Wolff, Jerry O.; Sherman, Paul W. Rodent Societies: An Ecological and Evolutionary Perspective. University of Chicago Press. pp. 28–39. ISBN 978-0-226-90538-9.
- Soloman, Nancy G.; Keane, Brain (2008). "Chapter 4: Reproductive Strategies in Female Rodents". In Wolff, Jerry O.; Sherman, Paul W. Rodent Societies: An Ecological and Evolutionary Perspective. University of Chicago Press. pp. 42–52. ISBN 978-0-226-90538-9.
- McGuire, Betty; Bernis, William E. (2008). "Chapter 20: Parental Care". In Wolff, Jerry O.; Sherman, Paul W. Rodent Societies: An Ecological and Evolutionary Perspective. University of Chicago Press. pp. 231–235. ISBN 978-0-226-90538-9.
- Holmes, Warren G.; Mateo, Jill M. (2008). "Chapter 19: Kin Recognition in Rodents: Issues and Evidence". In Wolff, Jerry O.; Sherman, Paul W. Rodent Societies: An Ecological and Evolutionary Perspective. University of Chicago Press. pp. 226–227. ISBN 978-0-226-90538-9.
- Ebensperger, Luis A.; Blumsperger, Daniel T. (2008). "Chapter 23: Nonparental Infanticide". In Wolff, Jerry O.; Sherman, Paul W. Rodent Societies: An Ecological and Evolutionary Perspective. University of Chicago Press. pp. 274–278. ISBN 978-0-226-90538-9.
- Hoogland, J. L. (1985). "Infanticide in prairie dogs: Lactating females kill offspring of close kin". Science 230 (4729): 1037–1040. doi:10.1126/science.230.4729.1037. PMID 17814930.
- Hackländera, Klaus; Möstlb, Erich; Arnold, Walter (2003). "Reproductive suppression in female Alpine marmots, Marmota marmota". Animal Behaviour 65 (6): 1133–1140. doi:10.1006/anbe.2003.2159.
- Charters, Jessie Blount Allen (1904). "The associative processes of the guinea pig: A study of the psychical development of an animal with a nervous system well medullated at birth". Journal of Comparative Neurology and Psychology (University of Chicago Press) XIV (4): 300–337.
- Jacobs, Lucia F.; Liman, Emily R. (1991). "Grey squirrels remember the locations of buried nuts". Animal Behaviour 41: 103–110. doi:10.1016/s0003-3472(05)80506-8.
- Carlyle, Kim (March 8, 2007). "Rats capable of reflecting on mental processes". Retrieved August 13, 2014.
- Foote, Allison L.; Crystal, J. D. (2007). "Metacognition in the Rat". Current Biology 17 (6): 551–555. doi:10.1016/j.cub.2007.01.061. PMC 1861845. PMID 17346969.
- Smith, J. David; Beran, M. J.; Couchman, J. J.; Coutinho, M. V. C. (2008). "The Comparative Study of Metacognition: Sharper Paradigms, Safer Inferences". Psychonomic Bulletin & Review 15 (4): 679–691. doi:10.3758/PBR.15.4.679.
- Jozefowiez, J.; Staddon, J. E. R.; Cerutti, D. T. (2009). "Metacognition in animals: how do we know that they know?". Comparative Cognition & Behavior Reviews 4: 29–39. doi:10.3819/ccbr.2009.40003.
- Rygula, Rafal; Pluta, Helena; Popok, Piotr (2012). "Laughing rats are optimistic". PLoS ONE 7 (12). doi:10.1371/journal.pone.0051959. PMC 3530570.
- Kay, Emily H.; Hoekstra, Hopi E. (2008). "Rodents". Current Biology 18 (10): R406–R40=10. doi:10.1016/j.cub.2008.03.019.
- Douzery, E. J. P.; Delsuc, F.; Stanhope, M. J.; Huchon, D. (2003). "Local molecular clocks in three nuclear genes: divergence times for rodents and other mammals and incompatibility among fossil calibrations". Journal of Molecular Evolution 57: S201–13. doi:10.1007/s00239-003-0028-x. PMID 15008417.
- Horner, D. S.; Lefkimmiatis, K.; Reyes, A.; Gissi, C.; Saccone, C.; Pesole, G. (2007). "Phylogenetic analyses of complete mitochondrial genome sequences suggest a basal divergence of the enigmatic rodent Anomalurus". BMC Evolutionary Biology 7: 16. doi:10.1186/1471-2148-7-16. PMC 1802082. PMID 17288612.
- Schenk, John J.; Rowe, Kevin C.; Steppan, Scott J. (2013). "Ecological opportunity and incumbency in the diversification of repeated continental colonizations by muroid rodents". Systematic Biology 62 (6): 837–864. doi:10.1093/sysbio/syt050.
- Rinderknecht, Andrés; Blanco, R. Ernesto (2008). "The largest fossil rodent". Proceedings of the Royal Society B 275 (1637): 923–928. doi:10.1098/rspb.2007.1645. PMC 2599941. PMID 18198140.
- Samuels, Joshua X.; Zancanella, John (2011). An early hemphillian occurrence of Castor (Castoridae) from the Rattlesnake Formation of Oregon 85 (5). pp. 930–935. doi:10.1666/11-016.1.
- Marivaux, Laurent; Essid, El Mabrouk; Marzougui, Wissem; Ammar, Hayet Khayati; Adnet, Sylvain; Marandat, Bernard; Merzeraud, Gilles; Tabuce, Rodolphe; Vianey-Liaud, Monique. "A new and primitive species of Protophiomys (Rodentia, Hystricognathi) from the late middle Eocene of Djebel el Kébar, Central Tunisia". Palaeovertebrata 38 (1): 1–17.
- Gheerbrant, Emmanuel; Rage, Jean-Claude (2006). "Paleobiogeography of Africa: How distinct from Gondwana and Laurasia?". Palaeogeography, Palaeoclimatology, Palaeoecology 241: 224–246. doi:10.1016/j.palaeo.2006.03.016.
- Vekua, A.; Bendukidze, O.; Bukhsianidze, M.; Vanishvili, N.; Augusti, J.; Martinez-Navarro, B.; Rook, L. (2010). "Porcupine in the Late Neogene and Quaternary of Georgia". Bulletin of the Georgian National Academy Of Sciences 4 (3): 140–149.
- Breed, Bill; Ford, Fred (2007). Native Mice and Rats. CSIRO Publishing. pp. 3, 5, and passim. ISBN 978-0-643-09166-5.
- Baskin, Jon A.; Thomas, Ronny G. "South Texas and the Great American Interchange". Gulf Coast Association of Geological Societies Transactions 57: 37–45.
- Marshall, L. G.; Butler, R. F.; Drake, R. E.; Curtis, G. H.; Tedford, R. H. (1979). "Calibration of the Great American Interchange". Science 204 (4390): 272–279. doi:10.1126/science.204.4390.272. PMID 17800342.
- Harington, C. R. (March 1996). "Giant beaver". Yukon Beringia Interpretive Centre. Retrieved 3 July 2014.
- Hopkins, Samantha S. B. (2005). "The evolution of fossoriality and the adaptive role of horns in the Mylagaulidae (Mammalia: Rodentia)". Proceedings of the Royal Society B 272 (1573): 1705–1713. doi:10.1098/rspb.2005.3171.
- Hooijer, D. A. (1957). "Three new giant prehistoric rats from Flores Lesser Sunda Islands". Zoologische Mededelingen (Rijksmuseum van Natuurlijke Historie, Leiden) 35 (21): 299–316.
- Biknevicius, A. R.; McFarlane, Donald A.; MacPhee, R. D. E. (1993). "Body size in Amblyrhiza inundata (Rodentia: Caviomorpha), an extinct megafaunal rodent from the Anguilla Bank, West Indies: estimates and implications". American Museum Novitates (3079): 1–26.
- Petronio, C. (1970). "I roditori Pleistocenici della Grotta di Spinagallo (Siracusa)". Geol. Rom. IX: 149–194. (in Italian)
- Kurtén, Björn; Anderson, Elaine (1980). Pleistocene Mammals of North America. Columbia University Press. p. 274. ISBN 0-231-03733-3.
- Rinderknecht, Andrés; Blanco, R. Ernesto (2008). "The largest fossil rodent". Proceedings of the Royal Society B 275 (1637): 923–928. doi:10.1098/rspb.2007.1645. PMC 2599941. PMID 18198140.
- Millien, Virginie; Bovy, Helene (2010). "When teeth and bones disagree: Body mass estimation of a giant extinct rodent". Journal of Mammalogy 91 (1): 11–18. doi:10.1644/08-mamm-a-347r1.1.
- Sánchez-Villagra, M. R.; Aguilera, O.; Horovitz, I. (2003). "The anatomy of the world's largest rodent". Science 301 (5640): 1708–10. doi:10.1126/science.1089332. PMID 14500978.
- Steppan, Scott J. (18 April 2006). "Rodentia". Tree of Life Web Project. Retrieved 14 July 2014.
- Smith, Andrew T. "Lagomorph". Encyclopædia Britannica. Encyclopædia Britannica. Retrieved 11 August 2014.
- Wu, Shaoyuan; Wu, Wenyu; Zhang, Fuchun; Ye, Jie; Ni, Xijun; Sun, Jimin; Edwards, Scott V.; Meng, Jin; Organ, Chris L. (2012). "Molecular and paleontological evidence for a post-Cretaceous origin of rodents". PLOSone. doi:10.1371/journal.pone.0046445.
- Wood, Albert E. (1958). "Are there rodent suborders?". Systematic Biology 7 (4): 169–173. doi:10.2307/2411716.
- Wood, Albert E. (1955). "A Revised Classification of the Rodents". Journal of Mammalogy 36 (2): 165–187. doi:10.2307/1375874. JSTOR 1375874.
- Carleton, M. D.; Musser, G. G. (2005). "Order Rodentia". In Wilson, Don E.; Reeder, DeeAnn M. Mammal Species of the World: A Taxonomic and Geographic Reference, Volume 12. JHU Press. pp. 745–752. ISBN 978-0-8018-8221-0.
- Graur, D.; Hide, W.; Li, W. (1991). "Is the guinea-pig a rodent?". Nature 351 (6328): 649–652. doi:10.1038/351649a0. PMID 2052090.
- Li, W.; Hide, W.; Zharkikh, A.; Ma, D.; Graur, D. (1992). "The molecular taxonomy and evolution of the guinea pig.". Journal of Heredity 83 (3): 174–81. PMID 1624762.
- D'Erchia, A.; Gissi, C.; Pesole, G.; Saccone, C.; Arnason, U. (1996). "The guinea-pig is not a rodent.". Nature 381 (6583): 597–600. doi:10.1038/381597a0. PMID 8637593.
- Reyes, A.; Pesole, G.; Saccone, C. (2000). "Long-branch attraction phenomenon and the impact of among-site rate variation on rodent phylogeny.". Gene 259 (1–2): 177–87. doi:10.1016/S0378-1119(00)00438-8. PMID 11163975.
- Cao, Y.; Adachi, J.; Yano, T.; Hasegawa, M. (1994). "Phylogenetic place of guinea pigs: No support of the rodent-polyphyly hypothesis from maximum-likelihood analyses of multiple protein sequences.". Molecular Biology and Evolution 11 (4): 593–604. PMID 8078399.
- Kuma, K.; Miyata, T. (1994). "Mammalian phylogeny inferred from multiple protein data.". Japanese Journal of Genetics 69 (5): 555–66. doi:10.1266/jjg.69.555. PMID 7999372.
- Robinson-Rechavi, M.; Ponger, L.; Mouchiroud, D. (2000). "Nuclear gene LCAT supports rodent monophyly.". Molecular Biology and Evolution 17 (9): 1410–1412. doi:10.1093/oxfordjournals.molbev.a026424. PMID 10960041.
- Lin, Y-H.; McLenachan, P. A.; Gore, A. R.; Phillips, M. J.; Ota, R.; Hendy, M. D.; Penny, D. (2002). "Four new mitochondrial genomes and the increased stability of evolutionary trees of mammals from improved taxon sampling". Molecular Biology and Evolution 19 (12): 2060–2070. doi:10.1093/oxfordjournals.molbev.a004031. PMID 12446798.
- Hindwood, K.A. (1940). "Birds of Lord Howe Island". Emu 40: 1–86. doi:10.1071/mu940001.
- Amori, G.; Gippoliti, S. (2003). "A higher-taxon approach to rodent conservation priorities for the 21st century". Animal Biodiversity Conservation 26 (2): 1–18.
- "Rodent Conservation Assessment". WAZA. Retrieved 27 June 2014.
- Gudynas, Eduardo (1989). Lidicker, William Zander, ed. Rodents: A World Survey of Species of Conservation Concern: Based on the Proceedings of a Workshop of the IUCN/SSC Rodent Specialist Group, Held at the Fourth International Theriological Congress, August 17, 1985, Edmonton, Alberta, Canada. IUCN. p. 23.
- Buckle, A. P.; Fenn, M. G. P. (1992). "Rodent Control in the Conservation of Endangered Species". Proceedings of the 15th Vertebrate Pest Conference (Hyatt Newporter, Newport Beach, California): Paper 12. 3–5 March 1992
- "Lundy puffins back from the brink". BBC Devon. 22 February 2008. Retrieved 30 June 2014.
- Mitchell, Heather (27 May 2014). "Puffins a-plenty? New hope for Lundy and other UK seabird islands". RSPB. Retrieved 30 June 2014.
- "Introduction to the Rodentia". University of California Museum of Paleontology. Retrieved 21 June 2014.
- Innis, Harold A. (1999). The Fur Trade in Canada: An Introduction to Canadian Economic History. University of Toronto Press. pp. 9–12. ISBN 978-0-8020-8196-4.
- "Excessive trade: Clothes and trimming". Granby Zoo. Retrieved 9 August 2014.
- Fiedler, Lynwood A. (1990). "Rodents as a Food Source". Proceedings of the Fourteenth Vertebrate Pest Conference 1990. University of California, Davis.
- Knowlton, David (13 July 2011). "Guinea Pig, Pet or Festive Meal". Cuzco Eats. Retrieved 5 July 2014.
- Morveli, Walter Coraza; Knowlton, David (5 March 2012). "Traditional Mud Stoves and Ovens Make the Best Food". Cuzco Eats. Retrieved 6 July 2014.
- "Guinea pigs". RSPCA. 2014. Retrieved 21 June 2014.
- "Pet Rodents". RSPCA. 2014. Retrieved 21 June 2014.
- Broekel, Ray (1983). Gerbil Pets and Other Small Rodents. Childrens Press. pp. 5–20. ISBN 978-0-516-01679-5.
- Wolff, Jerry O.; Sherman, Paul W. (2008). Rodent Societies: An Ecological and Evolutionary Perspective. University of Chicago Press. pp. 3–8. ISBN 978-0-226-90538-9.
- Morse, Herbert C. (1981). "The Laboratory Mouse: A Historical Assessment". In Foster, Henry. The Mouse in Biomedical Research: History, Genetics, and Wild Mice. Elsevier. pp. xi, 1. ISBN 978-0-323-15606-6.
- Gad, Shayne C. (2007). Animal Models in Toxicology (2nd ed.). Taylor & Francis. pp. 334–402. ISBN 0-8247-5407-7.
- Harkness, John E.; Wagner, Joseph E. (1995). The Biology and Medicine of Rabbits and Rodents. Williams & Wilkins. pp. 30–39. ISBN 0-683-03919-9.
- Guerrini, Anita (2003). Experimenting with Humans and Animals. Johns Hopkins. pp. 98–104. ISBN 0-8018-7196-4.
- Gray, Tara (1998). "A Brief History of Animals in Space". National Aeronautics and Space Administration. Retrieved 5 March 2007.
- Sherwin, C. M., (2010). The Husbandry and Welfare of Non-traditional Laboratory Rodents. In "UFAW Handbook on the Care and Management of Laboratory Animals", Hubrecht, R. and Kirkwood, J. (Eds). Wiley-Blackwell. Chapter 25, pp. 359–369
- Wines, Michael (19 May 2004). "Gambian rodents risk death for bananas". The Age (The Age Company). Retrieved 21 June 2014.
- Bakalar, Nicholas (3 January 2011). "Detecting Tuberculosis: No Microscopes, Just Rats". New York Times.
- Mhelela, Hassan (13 September 2012). "Giant rats trained to detect land mines and tuberculosis in Africa". BBC. Retrieved 27 June 2014.
- Harder, Ben (1 May 2002). "Scientists "Drive" rats by remote control". National Geographic. Retrieved 9 November 2013.
- Solon, O. (September 9, 2013). "Man's mission to build remote control systems for dogs, roaches and sharks". Wired. Retrieved December 9, 2013.
- Xu, S.; Talwar, S. K.; Hawley, E. S.; Li, L.; Chapin, J. K. (2004). "A multi-channel telemetry system for brain microstimulation in freely roaming animals". Journal of Neuroscience Methods 133 (1–2): 57–63. doi:10.1016/j.jneumeth.2003.09.012.
- Meerburg, B. G.; Singleton, G. R; Leirs, H. (2009). "The Year of the Rat ends: time to fight hunger!". Pest Management Science 65 (4): 351–2. doi:10.1002/ps.1718. PMID 19206089.
- Stenseth, Nils Chr; Leirs, Herwig; Skonhoft, Anders; Davis, Stephen A.; Pech, Roger P.; Andreassen, Harry P.; Singleton, Grant R.; Lima, Mauricio; Machang'u, Robert S.; Makundi, Rhodes H.; Zhang, Zhibin; Brown, Peter R.; Shi, Dazhao; Wan, Xinrong (2003). "Mice, rats, and people: The bio-economics of agricultural rodent pests". Frontiers in Ecology and the Environment 1 (77): 367–375. doi:10.2307/3868189. JSTOR 3868189.
- Meerburg, B. G.; Singleton, G. R.; Kijlstra, A. (2009). "Rodent-borne diseases and their risks for public health". Critical Reviews in Microbiology 35 (3): 221–70. doi:10.1080/10408410902989837. PMID 19548807.
- McCormick, M. (2003). "Rats, communications, and plague: Toward an ecological history". Journal of Interdisciplinary History 34 (1): 1–25. doi:10.1162/002219503322645439.
- Meerburg, B. G.; Singleton, G. R.; Kijlstra, A. (2009). "Rodent-borne diseases and their risks for public health". Critical Reviews in Microbiology 35 (3): 221–70. doi:10.1080/10408410902989837. PMID 19548807.
- Centers for Disease Control and Prevention (2006). Integrated pest management: conducting urban rodent surveys. Atlanta: US Department of Health and Human Services.
- Wodzicki, K. (1973). "Prospects for biological control of rodent populations". Bulletin of the World Health Organization 48 (4): 461–467. PMC 2481104.
- Carleton, M. D.; Musser, G. G. "Order Rodentia", pages 745–752 in Wilson & Reeder (2005).
- McKenna, Malcolm C.; Bell, Susan K. (1997). Classification of Mammals Above the Species Level. Columbia University Press. ISBN 0-231-11013-8.
- Wilson, D. E.; Reeder, D. M., ed. (2005). Mammal Species of the World: A Taxonomic and Geographic Reference. Johns Hopkins University Press. ISBN 978-0-8018-8221-0.
|Wikimedia Commons has media related to Rodentia.|
|Wikispecies has information related to: Rodentia|
- Zoology, osteology, comparative anatomy
- UCMP Berkeley: Introduction to the Rodentia
- ArchéoZooThèque : Rodent osteology (photos)
- ArchéoZooThèque : Rodent skeleton drawings
- African rodentia
- Rodent photos
- Rodent Species Fact Sheets from the National Pest Management Association on Deer Mice, Norway Rats, and other rodent species
- Rodent Pests chapter in EPA and University of Florida/IFAS manual