Diclidurus albusnorthern ghost bat

Ge­o­graphic Range

Di­clidu­rus albus is rare but wide­spread, rang­ing from Mex­ico to east­ern Brazil. It is also found on some Caribbean Is­lands in­clud­ing Trinidad. Dur­ing the sum­mer months no sight­ings of D. albus have been made in Mex­ico, the north­ern edge of its range. This sug­gests that mem­bers of this species mi­grate south sea­son­ally, from May to Oc­to­ber. Lit­tle in­for­ma­tion is avail­able on D. albus mi­gra­tion pat­terns. (Ce­bal­los and Medellin, 1988; Jones and Hood, 1993; Ce­bal­los and Medellin, 1988; Jones and Hood, 1993; Ce­bal­los and Medellin, 1988; Eisen­berg and Red­ford, 1999; Jones and Hood, 1993)

Habi­tat

North­ern ghost bats pre­fer humid habi­tats like ri­par­ian and trop­i­cal rain­forests but have been found in hu­man-dis­turbed areas like plan­ta­tions, clear­ings, and over vil­lages. They pre­fer to roost un­der­neath the fronds of palms, in­clud­ing co­conut, cho­cho palms, and co­quito palms. These bats have also been seen in less mesic habi­tats, like de­cid­u­ous and ever­green forests. Di­clidu­rus albus mi­grates within the Neotrop­ics. They occur from sea level to 1500 m. They were ob­served at high­est el­e­va­tions in Costa Rica. (Ce­bal­los and Medellin, 1988; Eisen­berg and Red­ford, 1999; Jones and Hood, 1993; LaVal, 2004)

  • Range elevation
    0 to 1500 m
    0.00 to 4921.26 ft

Phys­i­cal De­scrip­tion

Di­clidu­rus albus is a dis­tinc­tive look­ing bat species. The com­mon name, north­ern ghost bats, refers to their soft, long, white pelage. Some­times the prox­i­mal ends of the hairs are grey in color, while the dis­tal ends are white, giv­ing the an­i­mal an ashy grey tone. The pata­gia are pink­ish and translu­cent and the tail is short, about one third the length of the uropatag­ium. The tail punc­tures the uropatag­ium, with the end pro­ject­ing dor­sally. The uropatag­ium is large with about two-thirds cov­ered in fur, and ex­tends be­yond the hind feet. North­ern ghost bats have nearly naked faces with large eyes and shorter, yel­low­ish ears. They do not have a nose leaf, and their tra­gus is promi­nent, broad, and rounded. (Ce­bal­los and Medellin, 1988; Eisen­berg and Red­ford, 1999; En­gstom and Lim, 1999; Jones and Hood, 1993; Vaughan, et al., 2000)

Di­clidu­rus albus lacks the wing sacs that other Em­bal­lonuri­dae have. In­stead, these bats have a unique gland on their uropatag­ium. This gland has two valves and is tri­an­gu­lar in shape. Its ac­tual func­tion isn’t known, but it is larger in males, and be­comes even more promi­nent dur­ing the breed­ing sea­son. North­ern ghost bats have ves­ti­gial thumbs, un­like other species in the genus. (Ce­bal­los and Medellin, 1988; En­gstom and Lim, 1999; Jones and Hood, 1993)

The skull is dis­tinc­tive. The ros­trum an­gles up­ward steeply from the brain­case. The zy­go­matic arches are com­plete and the skull has strong supra­or­bital ridges. Pre­max­il­lae do not meet and have nasal branches only. The ca­nines pro­ject for­ward and out­ward. The den­tal for­mula is I: 1/3, C: 1/1, PM: 2/2, M: 3/3 = 32. Cheek teeth are dil­amb­dodont and have cin­gula. (Ce­bal­los and Medellin, 1988; Jones and Hood, 1993; Vaughan, et al., 2000)

North­ern ghost bats are at the larger end of the size range for Em­bal­lonuri­dae, with total lengths rang­ing from 86.0 mm to 103.0 mm. Tail lengths vary be­tween 18.0 mm and 22.0 mm. Di­clidu­rus albus dif­fers from its con­geners in that the length of its fore­arm is be­tween 60 mm and 70 mm, while other species of this genus have fore­arms less than 60 mm or above 70 mm, or are dis­tin­guished by brown­ish pelage. Adult D. albus weigh be­tween 17 and 24 g. They are sex­u­ally di­mor­phic; fe­males tend to be larger in size and length, but this varies re­gion­ally. For ex­am­ple, in Mex­ico, both sexes were very sim­i­lar in all mea­sure­ments. The av­er­age fe­male length was 88.0 mm, with the av­er­age male length being 89.0 mm. In Guatemala, how­ever, fe­males were about 10 mm longer than the males, with an av­er­age length of 102.0 mm com­pared to 92.5 mm for males. Sam­ple sizes are rel­a­tively small, how­ever, and more re­search is needed to ver­ify the pres­ence of sex­ual di­mor­phism in D. albus. (Ce­bal­los and Medellin, 1988; En­gstom and Lim, 1999; Her­nan­dez, et al., 1985; Jones and Hood, 1993; Vaughan, et al., 2000)

  • Sexual Dimorphism
  • female larger
  • Range mass
    17.0 to 24.0 g
    0.60 to 0.85 oz
  • Average mass
    20.0 g
    0.70 oz
  • Range length
    86.0 to 103.0 mm
    3.39 to 4.06 in
  • Range wingspan
    63.0 to 69.2 mm
    2.48 to 2.72 in

Re­pro­duc­tion

There is lit­tle in­for­ma­tion on the mat­ing sys­tem of D. albus. North­ern ghost bats are soli­tary ex­cept dur­ing the breed­ing sea­son. Dur­ing this time, small groups of bats can been seen roost­ing very close to­gether. There is usu­ally a max­i­mum of four in­di­vid­u­als, and the group con­sists of one male and mul­ti­ple fe­males. The tri­an­gu­lar gland pre­sent on the uropatag­ium of D. albus grows in size dur­ing the breed­ing sea­son, and may be used by males to at­tract fe­males. (Ce­bal­los and Medellin, 1988; Jones and Hood, 1993)

Breed­ing oc­curs dur­ing the months of Jan­u­ary and Feb­ru­ary. Preg­nant fe­males have been found be­tween the months of Jan­u­ary and June. Sin­gle young are usu­ally born in May or June. The breed­ing sea­son oc­curs only once a year, so D. albus is mon­estrus. The tim­ing of wean­ing and the age at sex­ual ma­tu­rity are un­known. Di­clidu­rus albus is a rare an­i­mal to see, so its re­pro­duc­tive be­hav­iors have yet to be stud­ied in depth. (Ce­bal­los and Medellin, 1988; Her­nan­dez, et al., 1985; Jones and Hood, 1993)

  • Breeding interval
    Northern ghost bats breed once per year.
  • Breeding season
    Diclidurus albus breeds during January and February.
  • Range number of offspring
    1 to 1

Like most other bats, fe­males care for their young by nurs­ing and pro­tect­ing them. Young bats ma­ture quickly and be­come in­de­pen­dent within a few months of their birth. (Ce­bal­los and Medellin, 1988)

  • Parental Investment
  • pre-fertilization
    • provisioning
    • protecting
      • female
  • pre-hatching/birth
    • provisioning
      • female
    • protecting
      • female
  • pre-weaning/fledging
    • provisioning
      • female
    • protecting
      • female

Lifes­pan/Longevity

North­ern ghost bat lifes­pans have not been stud­ied.

Be­hav­ior

North­ern ghost bats are soli­tary. They do not form colonies and are found in small groups only dur­ing the breed­ing sea­son. North­ern ghost bats are noc­tur­nal and roost under palms dur­ing the day. They tend to fly high and in rea­son­ably straight lines. Most stud­ies of D. albus have fo­cused on phys­i­cal prop­er­ties in­stead of be­hav­ioral char­ac­ter­is­tics, so the be­hav­ior of this species is not well known. (Ce­bal­los and Medellin, 1988; Eisen­berg and Red­ford, 1999; En­gstom and Lim, 1999; Jones and Hood, 1993)

Home Range

The home range size for D. albus is un­known.

Com­mu­ni­ca­tion and Per­cep­tion

North­ern ghost bats use echolo­ca­tion to find prey and to nav­i­gate their way through the night­time for­est. They emit a call at 22 kHz while hunt­ing. No in­for­ma­tion is avail­able about com­mu­ni­ca­tion be­tween in­di­vid­ual bats, al­though chem­i­cal com­mu­ni­ca­tion is likely, in­clud­ing the use of gland se­cre­tions by males. (Zor­pette, 1999)

Food Habits

Like all mem­bers of the fam­ily Em­bal­lonuri­dae, north­ern ghost bats are in­sec­tiv­o­rous. Stom­ach con­tents have a high pro­por­tion of moths. (Ce­bal­los and Medellin, 1988; Eisen­berg and Red­ford, 1999; En­gstom and Lim, 1999; Jones and Hood, 1993)

  • Animal Foods
  • insects

Pre­da­tion

North­ern ghost bats are noc­tur­nal and soli­tary, which helps to pro­tect them from many preda­tors. Pre­da­tion on north­ern ghost bats has not been recorded.

Ecosys­tem Roles

North­ern ghost bat in­di­vid­u­als eat around 1,000 in­sects a night. This could af­fect in­sect pop­u­la­tions. These bats are rare, so their ef­fect on the ecosys­tem are prob­a­bly slight and can only be a hy­poth­e­sized based on the ef­fects of other bats in the area. Also, bat guano is very im­por­tant to plants, pro­vid­ing ex­cel­lent fer­til­izer. (Zor­pette, 1999)

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

North­ern ghost bats may be im­por­tant in help­ing keep agri­cul­tural pest pop­u­la­tions in check, but their rar­ity sug­gests that they might not con­tribute much to in­sect con­trol. Also, be­cause this bat is at­trac­tively col­ored and rare, may help draw eco­tourists to an area. With knowl­edge­able guides, night­time bat tours can at­tract tourists. (Lim and En­gstrom, 2005; Zor­pette, 1999)

  • Positive Impacts
  • ecotourism
  • produces fertilizer
  • controls pest population

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

Like most wild mam­mals, north­ern ghost bats can trans­mit ra­bies to hu­mans and other an­i­mals. How­ever, ra­bies trans­mis­sion to hu­mans is rare. (Jones and Hood, 1993)

Con­ser­va­tion Sta­tus

IUCN lists D. albus as being at lower risk and least con­cern. Al­though north­ern ghost bats are rare through­out their range, they are wide­spread. (Chi­roptera Spe­cial­ist Group 1996, 2004)

Other Com­ments

Two sub­species are some­times rec­og­nized, D. a. albus and D. a. virgo. Pre­vi­ously, Di­clidu­rus scu­ta­tus was con­sid­ered a syn­onym of D. albus, but is now con­sid­ered a sep­a­rate species, about which very lit­tle is known. Con­tro­versy abounds over who de­serves the credit for nam­ing D. albus. Oken may have been re­spon­si­ble, but credit is usu­ally given to Wied (1820). No fos­sils are known for the en­tire genus Di­clidu­rus. Other com­mon names in­clude murciélagos blan­cos (Span­ish), and gespen­st­flie­der­maus (Ger­man). The generic name, Di­clidu­rus arises from the gland on the tail. The Latin word di­clid means two-valved, and urus means tail. Albus in Latin means white, and re­lates to the white fur of these bats. (Ce­bal­los and Medellin, 1988; Jones and Hood, 1993)

Con­trib­u­tors

Tanya Dewey (ed­i­tor), An­i­mal Di­ver­sity Web.

Ash­ley Potchynok (au­thor), Uni­ver­sity of Michi­gan-Ann Arbor, Phil Myers (ed­i­tor, in­struc­tor), Mu­seum of Zo­ol­ogy, Uni­ver­sity of Michi­gan-Ann Arbor.

Glossary

Neotropical

living in the southern part of the New World. In other words, Central and South America.

World Map

acoustic

uses sound to communicate

agricultural

living in landscapes dominated by human agriculture.

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.

carnivore

an animal that mainly eats meat

causes disease in humans

an animal which directly causes disease in humans. For example, diseases caused by infection of filarial nematodes (elephantiasis and river blindness).

causes or carries domestic animal disease

either directly causes, or indirectly transmits, a disease to a domestic animal

chemical

uses smells or other chemicals to communicate

echolocation

The process by which an animal locates itself with respect to other animals and objects by emitting sound waves and sensing the pattern of the reflected sound waves.

ecotourism

humans benefit economically by promoting tourism that focuses on the appreciation of natural areas or animals. Ecotourism implies that there are existing programs that profit from the appreciation of natural areas or animals.

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.

forest

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

insectivore

An animal that eats mainly insects or spiders.

iteroparous

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).

migratory

makes seasonal movements between breeding and wintering grounds

motile

having the capacity to move from one place to another.

native range

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

nocturnal

active during the night

polygynous

having more than one female as a mate at one time

rainforest

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.

riparian

Referring to something living or located adjacent to a waterbody (usually, but not always, a river or stream).

seasonal breeding

breeding is confined to a particular season

sexual

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

solitary

lives alone

tactile

uses touch to communicate

terrestrial

Living on the ground.

tropical

the region of the earth that surrounds the equator, from 23.5 degrees north to 23.5 degrees south.

ultrasound

uses sound above the range of human hearing for either navigation or communication or both

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.

Ref­er­ences

Ce­bal­los, G., R. Medellin. 1988. Di­clidu­rus albus. Mam­malian Species, 316: 1-4.

Chi­roptera Spe­cial­ist Group 1996, 2004. "Di­clidu­rus albus" (On-line). The IUCN Red List of Threat­ened Species. Ac­cessed March 21, 2006 at http://​www.​iucnredlist.​org/​search/​details.​php?​species=6561.

Eisen­berg, J., K. Red­ford. 1999. Mam­mals of the Neotrop­ics: The Cen­tral Neotrop­ics: Ecuador, Peru, Bo­livia, Brazil. Chicago: Uni­ver­sity of Chicago Press.

En­gstom, M., B. Lim. 1999. "North­ern Ghost Bat" (On-line). Iwokrama. Ac­cessed March 21, 2006 at http://​www.​iwokrama.​org/​mammals/​guides/​bats0.​html#​dial.

Her­nan­dez, C., C. Tapia, A. Gar­duno, E. Corona, M. Hi­dalgo. 1985. Notes on Dis­tri­b­u­tion and Re­pro­duc­tion of Bats from Coastal Re­gions of Mi­choa­can, Mex­ico. Jour­nal of Mam­mal­ogy, 66/3: 549-553. Ac­cessed March 21, 2006 at http://​www.​jstor.​org/​view/​00222372/​ap050268/​05a00170/​0.

Jones, J., C. Hood. 1993. Syn­op­sis of South Amer­i­can Bats of the Fam­ily Em­bal­lonuri­dae. Oc­ca­sional Pa­pers The Mu­seum Texas Tech Uni­ver­sity, 155: 1-32. Ac­cessed March 21, 2006 at http://​www.​loyno.​edu/​~chood/joneshood1993.​pdf.

LaVal, R. 2004. Im­pact of Global Warm­ing and Lo­cally Chang­ing Cli­mate on Trop­i­cal Cloud For­est Bats. Jour­nal of Mam­mal­ogy, 85/2: 237-244.

Lim, B., M. En­gstrom. 2005. Mam­mals of Iwokrama For­est. Pro­ceed­ings of the Acad­emy of Nat­ural Sci­ences of Philadel­phia, 154: 71-108.

Vaughan, T., J. Ryan, N. Czaplewski. 2000. Mam­mal­ogy Fourth Edi­tion. Aus­tralia: Brooks/Cole.

Zor­pette, G. 1999. Chas­ing the Ghost Bat. Sci­en­tific Amer­i­can, 280/6: 82-89.