Neotoma magisterAllegheny woodrat

Ge­o­graphic Range

Al­legheny woodrats, Neotoma mag­is­ter, live along the Ap­palachian Moun­tains of the United States. Since 1928, their dis­tri­b­u­tion has nar­rowed around this moun­tain range. Dense pop­u­la­tions of Al­legheny woodrats can be found on the Al­legheny Cum­ber­land Plateau in West Vir­ginia, Ten­nessee and Ken­tucky. (An­thony, 1928; Castle­berry and Laerm, 2008; Castle­berry, et al., 2006; Schwartz and Odum, 1957)

Habi­tat

Al­legheny woodrats are com­monly found on steep rocky cliffs, in which they make their homes, as well as rocky ledges and crevices built into ex­posed rock above. They are ge­n­ear­lly found above 640 m in el­e­va­tion, though his­tor­i­cal re­gions place them in pied­mont (hilly) re­gions of lower el­e­va­tions. Al­legheny woodrats also in­habit areas with di­verse veg­e­ta­tion. (Bal­com and Yah­ner, 1996; Castle­berry and Laerm, 2008; Castle­berry, et al., 2002a; Castle­berry, et al., 2006)

  • Range elevation
    640 (low) m
    2099.74 (low) ft

Phys­i­cal De­scrip­tion

Al­legheny woodrats have soft agouti fur that is brown­ish-gray to brown on their dor­sal side. Their un­der­side, in­clud­ing the throat and feed, is white. Their tail has a no­tice­able amount of fur, which is bi-col­ored and blends with the rest of the body. The ven­tral side of the tail is lighter in color than the dor­sal side. Ju­ve­niles have gray fur that be­comes browner as they ma­ture. Al­legheny woodrats also have long whiskers. Adult range from 203 to 444 g in mass and from 311 to 451 mm in length. The head of Al­legheny woodrats ap­pears sim­i­lar to that of a mouse and is not very pointed, due to au­di­tory bul­lae. Their eye sock­ets are "de­pressed" into the skull (Linzey, 1998). Al­legheny woodrats are also very sim­i­lar to east­ern woodrats, and the only dif­fer­ence be­tween the two is the pres­ence of the max­illo vomer­ine notch (skull struc­ture) in Al­legheny woodrats. (Castle­berry and Laerm, 2008; Castle­berry, et al., 2006; Kays and Wil­son, 2002; Linzey, 1998)

  • Sexual Dimorphism
  • sexes alike
  • Range mass
    203 to 444 g
    7.15 to 15.65 oz
  • Range length
    311 to 451 mm
    12.24 to 17.76 in

Re­pro­duc­tion

Mat­ing sys­tems of Al­legheny woodrats have not been stud­ied in the wild. A cap­tive pair, how­ever, pro­vides some in­for­ma­tion about their mat­ing be­hav­iors. Dur­ing courtship, a male and fe­male "box," like kan­ga­roos, which can be vi­o­lent. They stand on their hind legs and brace them­selves with their tail while hit­ting each other with their front paws. Al­legheny woodrats are monog­a­mous for their sin­gle mat­ing ses­sion, but it is cur­rently un­known if they main­tain this monogamy. (Poole, 1940)

Al­legheny woodrats gen­er­ally breed dur­ing the early spring to late sum­mer, from March to Oc­to­ber. Some, how­ever, breed year-round due to mild win­ters and/or an abun­dance of food within their habi­tat. Fe­male Al­legheny woodrats have 1 to 2 pups in their first lit­ter. After their first sea­son, they av­er­age 3 pups per lit­ter, though they can have more than 4. Be­cause the fe­male only has 4 nip­ples, how­ever, sur­vival of pups in lit­ters of greater than 4 in­di­vid­u­als is lim­ited. Al­legheny woodrats have 2 to 3 lit­ters a year. The ges­ta­tion pe­riod of Al­legheny woodrats is 30 to 36 days. Pups are born blind, deaf, pink, and hair­less and weigh be­tween 14 and 17 g (av­er­age 15 g). Their in­cisors are not straight but rather form a di­a­mond shape where the top two meet the bot­tom two in­cisors. How­ever, their in­cisors straighten within 21 days after birth. Wean­ing be­gins around 17 days, when off­spring may begin to eat solid foods. Wean­ing ends around 21 days of age when the eyes are fully opened. By 24 days of age, most ju­ve­niles can suf­fi­ciently sus­tain them­selves but may re­main near the nest for a few ad­di­tional weeks. Ju­ve­niles be­come in­de­pen­dent be­tween 28 and 60 days of age. Fe­male Al­legheny woodrats are be­lieved to reach sex­ual ma­tu­rity around 3 to 4 months of age, and it is un­known if males ma­ture at the same age. (Castle­berry and Laerm, 2008; Castle­berry, et al., 2006; Linzey, 1998; Man­jerovic, et al., 2009; Men­gak, 2002; Poole, 1940)

  • Breeding interval
    Allegheny woodrats usuallly have 2 to 3 litters per year.
  • Breeding season
    Mating of Allegheny woodrats usually occurs between March and October, though in some areas breeding can occur year-round.
  • Range number of offspring
    1 to 4
  • Average number of offspring
    2.8
  • Range gestation period
    30 to 36 days
  • Range weaning age
    17 to 28 days
  • Average weaning age
    21 days
  • Range time to independence
    28 to 60 days
  • Range age at sexual or reproductive maturity (female)
    3 to 4 months

The ma­jor­ity of parental in­vest­ment of Al­legheny woodrats oc­curs be­fore birth. Fe­males make nests made of fi­brous ma­te­ri­als such as shred­ded bark of hem­lock, red cedar, bass­wood, and other trees, as well as rope, yarn, grasses, and oc­ca­sion­ally feath­ers. Nests are con­structed sim­i­lar to bird nests with coarser ma­te­ri­als on the out­side and softer ma­te­ri­als on the in­side. Prepa­ra­tion for birth con­sists of gath­er­ing food for the mother and even­tu­ally for the off­spring once weaned. Both males and fe­males gather food, though the male plays a very small role in the care of off­spring. After pups are born, the mother is the pri­mary care­taker, and she re­mains so until the pups are in­de­pen­dent. Pups are born com­pletely de­pen­dent on the mother for warmth, food, pro­tec­tion, and san­i­ta­tion. A fe­male nurses her pups until they are weaned. Ju­ve­nile learn­ing is in­di­rect; through con­sum­ing food in their mother's cache, ju­ve­niles learn what is op­ti­mal and safe to con­sume. (Poole, 1940)

  • Parental Investment
  • altricial
  • female parental care
  • pre-hatching/birth
    • provisioning
      • male
      • female
    • protecting
      • female
  • pre-weaning/fledging
    • provisioning
      • female
  • pre-independence
    • provisioning
      • female
    • protecting
      • female

Lifes­pan/Longevity

The ex­pected lifes­pan of Al­legheny woodrats in the wild is 49 to 58 months. In cap­tiv­ity, their lifes­pan is about 48 months. (Castle­berry, et al., 2006; Linzey, 1998)

  • Typical lifespan
    Status: wild
    49 to 58 months
  • Typical lifespan
    Status: captivity
    48 (high) months

Be­hav­ior

Al­legheny woodrats are noc­tur­nal and soli­tary. They are known for their habit of col­lect­ing shiny and col­or­ful ob­jects, in­clud­ing an­thro­pogenic items such as china and spoons. They also col­lect rac­coon feces, which can in­clude eggs from the par­a­site Baylisas­caris pro­cy­o­nis. This par­a­site and other mem­bers of the same genus can in­fect and kill the woodrats. When Al­legheny woodrats take some­thing for their col­lec­tion, they oc­ca­sion­ally leave some­thing be­hind, like a pine cone, peb­ble, or nut. Al­legheny woodrats also cache food items. Caches are made with sticks in­stead of the fi­brous ma­te­ri­als they use for their nests. Al­legheny woodrats are sur­pris­ingly clean crea­tures, only defe­cat­ing in one area away from the nest. Defe­ca­tion sites are usu­ally lo­cated in an area with ample air­flow on a flat rock or a rock with a con­cave in­den­ta­tion. (Castle­berry, et al., 2006; Linzey, 1998; Poole, 1940)

  • Average territory size
    2060 m^2

Home Range

Al­legheny woodrats are soli­tary an­i­mals, and they do not ag­gres­sively de­fend a ter­ri­tory. How­ever, their hom­ing mech­a­nism is strong; they have been known to re­turn to their nest when re­lo­cated up to 403 m away. Be­cause their food sources are lo­cated only in cer­tain areas and are there­fore de­pleted quickly, mem­bers of this species may travel from 180 to 6,500 sq m each day. On av­er­age, Al­legheny woodrats travel 2,060 sq m daily. (Castle­berry, et al., 2006; Linzey, 1998)

Com­mu­ni­ca­tion and Per­cep­tion

Al­legheny woodrats have ex­cep­tional senses of hear­ing, sight, touch, and smell. They have big ears which can cap­ture sounds and de­tect the di­rec­tion from which the sound came. Al­legheny woodrats have large eyes and can see well even in the dark. A sim­i­lar species, east­ern woodrats (Neotoma flori­dana), can see red lights that many other an­i­mals can­not, and it is likely that Al­legheny woodrats can as well. Al­legheny woodrats have par­tic­u­larly long whiskers for ro­dents, and the longest whisker recorded was 9 cm in length. These long whiskers are sen­si­tive to touch and allow woodrats to feel their sur­round­ings. Whiskers help with nav­i­ga­tion of caves and crevasses and to de­tect nearby move­ment, alert­ing them to pos­si­ble dan­ger. Dur­ing the breed­ing sea­son, Al­legheny woodrats use elon­gated scent glands along the sides of their stom­achs to com­mu­ni­cate their lo­ca­tion to po­ten­tial mates. These glands se­crete an oily, smelly liq­uid. Woodrats drag their bod­ies across the ground to trans­fer the scent and mark their ter­ri­tory. (Poole, 1940; Zer­vanos and Davis, 1968)

Food Habits

Al­legheny woodrats are pri­mar­ily her­bi­vores and eat a va­ri­ety plants, berries, fruits, and seeds. They have also been known to con­sume bats and in­sects on oc­ca­sion. Their diet mostly con­sists of fun­gus, and, at the peak of mush­room sea­son, fun­gus can make up more than 12% of their diet. The amount of mush­rooms eaten varies from re­gion to re­gion. Acorns are also very im­por­tant to Al­legheny woodrats, be­cause they are high in pro­tein, car­bo­hy­drates, fats, min­er­als, and vi­t­a­mins. (Castle­berry, et al., 2002b; Men­gak and Laerm, 2008; Poole, 1940)

  • Animal Foods
  • mammals
  • insects
  • Plant Foods
  • leaves
  • roots and tubers
  • wood, bark, or stems
  • seeds, grains, and nuts
  • fruit
  • flowers
  • bryophytes
  • lichens
  • Other Foods
  • fungus

Pre­da­tion

Al­legheny woodrats have many preda­tors, many of which are large and noc­tur­nal. Preda­tors in­clude great horned owls, bob­cats, striped skunks, gray foxes, east­ern spot­ted skunks, long tailed weasles as well as other snakes and owls. The fur of Al­legheny woodrats blends in with the for­est floor to help keep them hid­den from preda­tors while look­ing for food. (Linzey, 1998; Poole, 1940)

  • Anti-predator Adaptations
  • cryptic

Ecosys­tem Roles

Be­cause of their caching be­hav­iors, Al­legheny woodrats dis­perse spread seeds and spores. This species is host to many dif­fer­ent types of fleas (Or­cho­peas sex­den­ta­tus penn­syl­van­i­cus and Epite­dia cav­er­ni­cola), mites (Atri­cholae­laps glas­gowi), ticks (Ixodes woodi, Der­ma­cen­tor vari­abilis, and Ixodes au­gus­tus), round­worms (Baylisas­caris pro­cy­o­nis and Baylisas­caris proaber­rant), and bot­flies. The main threat for Al­legheny woodrats is from the species of ne­ma­tode Baylisas­caris proaber­rant, the eggs of which are found in rac­coon feces. Al­legheny woodrats col­lect rac­coon feces and be­come in­fected with this "fatal neu­ro­log­i­cal dis­ease." This par­a­site ap­pears to threaten the Al­legheny woodrat's pop­u­la­tion more-so than pre­da­tion. (Castle­berry and Laerm, 2008; Linzey, 1998; Parker, et al., 2009; Poole, 1940)

  • Ecosystem Impact
  • disperses seeds
Com­men­sal/Par­a­sitic Species

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

Al­legheny woodrats are not known to have any pos­i­tive im­pact on hu­mans. (Whitaker Jr. and Hamil­ton Jr., 1998)

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

In cap­tiv­ity, Al­legheny woodrats eat a va­ri­ety of food that is found on farms or in gar­dens such as ap­ples, cab­bage, car­rots, cel­ery, grapes, toma­toes, corn, wheat, wild rice stalks, and white pota­toes. They may con­sume these items on agri­cul­tural land lo­cated in their habi­tat. Be­cause the pop­u­la­tion of Al­legheny woodrats is small com­pared to other pests, there is no con­sid­er­able eco­nomic cost to hu­mans, even with po­ten­tial dam­age of crops. (Poole, 1940)

Con­ser­va­tion Sta­tus

Al­legheny woodrats are listed as "vul­ner­a­ble" on the IUCN Red List. How­ever, risk varies by state. In Ken­tucky pop­u­la­tions are sta­ble, but in Al­abama, Vir­ginia, and other states this species is threat­ened or vul­ner­a­ble. In North Car­olina, this species is now en­dan­gered. The ex­tinc­tion of Amer­i­can chest­nut and de­cline in oak trees may have con­tributed to the de­crease in the Al­legheny woodrat pop­u­la­tions. Habi­tat de­struc­tion has also con­tributed to de­cline in pop­u­la­tions in some areas. (Castle­berry and Laerm, 2008; Castle­berry, et al., 2006)

Con­trib­u­tors

Lind­sey Stanesa (au­thor), Rad­ford Uni­ver­sity, Karen Pow­ers (ed­i­tor), Rad­ford Uni­ver­sity, Gail Mc­Cormick (ed­i­tor), An­i­mal Di­ver­sity Web Staff, Cather­ine Kent (ed­i­tor), Spe­cial Pro­jects.

Glossary

Nearctic

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.

World Map

acoustic

uses sound to communicate

altricial

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.

bilateral symmetry

having body symmetry such that the animal can be divided in one plane into two mirror-image halves. Animals with bilateral symmetry have dorsal and ventral sides, as well as anterior and posterior ends. Synapomorphy of the Bilateria.

chemical

uses smells or other chemicals to communicate

cryptic

having markings, coloration, shapes, or other features that cause an animal to be camouflaged in its natural environment; being difficult to see or otherwise detect.

endothermic

animals that use metabolically generated heat to regulate body temperature independently of ambient temperature. Endothermy is a synapomorphy of the Mammalia, although it may have arisen in a (now extinct) synapsid ancestor; the fossil record does not distinguish these possibilities. Convergent in birds.

female parental care

parental care is carried out by females

folivore

an animal that mainly eats leaves.

forest

forest biomes are dominated by trees, otherwise forest biomes can vary widely in amount of precipitation and seasonality.

frugivore

an animal that mainly eats fruit

granivore

an animal that mainly eats seeds

herbivore

An animal that eats mainly plants or parts of plants.

monogamous

Having one mate at a time.

motile

having the capacity to move from one place to another.

mountains

This terrestrial biome includes summits of high mountains, either without vegetation or covered by low, tundra-like vegetation.

mycophage

an animal that mainly eats fungus

native range

the area in which the animal is naturally found, the region in which it is endemic.

nocturnal

active during the night

scent marks

communicates by producing scents from special gland(s) and placing them on a surface whether others can smell or taste them

seasonal breeding

breeding is confined to a particular season

sedentary

remains in the same area

sexual

reproduction that includes combining the genetic contribution of two individuals, a male and a female

solitary

lives alone

stores or caches food

places a food item in a special place to be eaten later. Also called "hoarding"

tactile

uses touch to communicate

temperate

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).

terrestrial

Living on the ground.

vibrations

movements of a hard surface that are produced by animals as signals to others

visual

uses sight to communicate

viviparous

reproduction in which fertilization and development take place within the female body and the developing embryo derives nourishment from the female.

year-round breeding

breeding takes place throughout the year

Ref­er­ences

An­thony, H. 1928. Field Book of North Amer­i­can Mam­mals. New York: The Knicker­bocker Press.

Bal­com, B., R. Yah­ner. 1996. Mi­cro­hab­i­tat and Land­scape Char­ac­ter­is­ticts As­sosi­ated with the Threat­ened Al­legheny Woodrat. Con­ser­va­tion Bi­ol­ogy, 10/2: 515-525.

Castle­berry, S., W. Ford, N. Castle­berry, P. Wood. 2002. Sum­mer Mi­cro­hab­i­tat Se­lec­tion by For­ag­ing Al­legheny Woodrats (Neotoma mag­is­ter) in a Man­aged For­est. Amer­i­can Mid­land Nat­u­ral­ist, 147/1: 93-101.

Castle­berry, S., J. Laerm. 2008. Al­legheny Woodrat Neotoma mag­is­ter. Jour­nal of Mam­mal­ogy, 89/4: 306-309.

Castle­berry, S., M. Men­gak, N. Castle­berry, W. Ford, P. Wood. 2002. Al­legheny Woodrat (Neotoma mag­is­ter) Food Habits in the Cen­tral Ap­pala­tions. Amer­i­can Mid­land Nat­u­ral­ist, 147/1: 80-92.

Castle­berry, S., M. Men­gak, W. Ford. 2006. Neotoma mag­is­ter. Mam­malian Species, 789: 1-5.

Hamil­ton, W. 1943. Mam­mals of East­ern United States. New York: Com­stock Pub­lish­ing Com­pany.

Kays, R., D. Wil­son. 2002. Mam­mals of North Amer­ica. New Jer­sey: Prince­ton Uni­ver­sity Press.

Kin­law, A. 1995. Spi­lo­gale puto­rius. Mam­malian Species, 511: 1-7.

Linzey, D. 1998. The Mam­mals of Vir­ginia. Blacks­burg, Vir­ginia: The Mc­don­ald and Wood­ward Pub­lish­ing Com­pany.

Man­jerovic, M., P. Wood, J. Ed­wards. 2009. Mast and Weather In­flunces on Pop­u­la­tion Trends of a Species of Con­cern: the Al­legheny Woodrat. The Amer­i­can Mid­land Nat­u­ral­ist: An In­ter­na­tional Jour­nal of Ecol­ogy, Evo­lu­tion and En­vi­ron­ment, 162/1: 52-61.

Men­gak, M. 2002. Re­pro­duc­tion, Ju­vinile Growth and Re­cap­ture Rates of Al­legheny Woodrats (Neotoma mag­is­ter) in Vir­ginia. Amer­i­can Mid­land Nat­u­ral­ist, 148/1: 155-162.

Men­gak, M., J. Laerm. 2008. East­ern Woodrat Neotoma flori­dana. Jour­nal of Mam­mal­ogy, 89/4: 301-305.

Parker, W., R. Ger­hardt, L. Muller, N. Cald­well, S. Castle­berry, W. Ford. 2009. Ex­ter­nal Par­a­sites of Neotoma mag­is­ter Baird (Al­legheny Woodrat) in the Cum­ber­land Moun­tains and Plateau, Ten­nessee. South­east­ern Nat­u­ral­ist, 8/1: 167-174.

Poole, E. 1940. A Life His­tory Sketch of the Al­legheny Woodrat. Jour­nal of Mam­mal­ogy, 21/3: 249-270.

Schwartz, A., E. Odum. 1957. The Woodrats of East­ern United States. Jour­nal of Mam­mal­ogy, 38/2: 197-206.

Sheffield, S., H. Thomas. 1997. Mustela fre­nata. Mam­malian Species, 570: 1-9.

Whitaker Jr., J., W. Hamil­ton Jr.. 1998. Mamm­les of the East­ern United States. Ithaca, New York: Com­stock Pub­li­hing As­so­ci­ates.

Zer­vanos, S., D. Davis. 1968. Per­cep­tion of Red Light by Woodrats (Neotoma flori­dana). Jour­nal of Mam­mal­ogy, 49/4: 759.