Eurycea lucifugaCave Salamander

Ge­o­graphic Range

Cave sala­man­ders (Eu­rycea lu­cifuga) are found through­out the east­ern United States. Their range stretches from north­east­ern Ok­la­homa to west­ern Vir­ginia. Pop­u­la­tions of cave sala­man­ders are more con­cen­trated in the Ap­palachian Moun­tain range, reach­ing from Al­abama to north­ern Vir­ginia. An­other dense area in­cludes a span ex­tend­ing through south­ern In­di­ana, Ken­tucky and mid­dle to east­ern Ten­nessee. The west­ern­most part of their range cov­ers mid to south­ern Mis­souri, north­east­ern Ok­la­homa and north­ern Arkansas. (Brig­gler and Prather, 2006; Camp, et al., 2014; Lanoo, 2005; Pe­tranka, 2010)

Habi­tat

Cave sala­man­ders are troglophiles, mean­ing they can live en­tirely in caves and de­pend on cave-like con­di­tions to com­plete their life cy­cles. Cave sala­man­ders are mainly found in moist, dark places such as caves, or under rocks and logs. They have been re­ported in rock crevices along river­sides. In south­ern Illi­nois adults also in­habit rocky bor­ders of cy­press swamp areas. Much of their pop­u­la­tion, though, live in twi­light zones of caves that are con­fined to lime­stone re­gions. (Camp, et al., 2014; Lanoo, 2005; Pe­tranka, 2010)

  • Aquatic Biomes
  • rivers and streams
  • Other Habitat Features
  • caves

Phys­i­cal De­scrip­tion

Cave sala­man­ders are among the largest of their genus. Dur­ing adult­hood their dor­sal pig­men­ta­tion ranges from bright red­dish-or­ange to a bland yel­low. Their ven­tral col­or­ing is a light yel­low and does not con­tain spots. Younger adults are typ­i­cally more dull in color.

The max­i­mum recorded length of an adult is 181 mm. Cave sala­man­ders have broad, flat­tened heads. Their large eyes mea­sure roughly the same size as their snout length. Snout lengths for fe­males mea­sure to 62 mm on av­er­age while males have snouts that mea­sure 60 mm on av­er­age. Both sexes have pre­hen­sile tails that con­sti­tute 52 to 68% of their total length. Cave sala­man­ders have four slen­der legs, two long fore­limbs, and two short hind limbs. Their front legs have four toes and their back legs have five toes that are webbed.

Sexes are dis­tin­guished by a num­ber of phys­i­cal fea­tures. Vents on ma­ture males have large mar­gins con­toured with papil­lae. Ma­ture males are also dis­tin­guish­able by their longer tail com­pared to those of fe­males. Male men­tal glands are also more rounded in com­par­i­son to fe­males. (Hutchi­son, 1966; Lanoo, 2005; Pe­tranka, 2010)

  • Sexual Dimorphism
  • sexes shaped differently
  • Range length
    125 to 181 mm
    4.92 to 7.13 in

De­vel­op­ment

Cave sala­man­ders go through meta­mor­pho­sis, al­though pop­u­la­tions of this species may ma­ture at dif­fer­ent ages. Meta­mor­pho­sis can occur as early as 6 months and as late as 18 months of age. Young lar­vae are ac­tive day and night. They switch to a more noc­tur­nal lifestyle as they ma­ture.

Their eggs have been mea­sured up to 5 mm in di­am­e­ter with white yolk that is 2.4 to 3 mm in di­am­e­ter. Their eggs have two trans­par­ent outer en­velopes. The out­er­most of these 2 en­velopes is made up of a pe­riph­eral gel, while the inner en­ve­lope is filled with fluid. Lar­vae mea­sure up to 10 mm in length when newly hatched. Hatch­lings start off at a mere 9 to 12 mm, but can reach up to 58 mm as they ap­proach adult­hood. Young lar­vae have a broad tail fin. These tail fins start at their hind legs and ex­tend to the tips of their tails. Their skin lacks pig­men­ta­tion, but con­tains gray spot­ting. These spots darken as they ma­ture. As cave sala­man­ders grow, their bod­ies be­come brighter or darker in color. They begin col­or­less and later turn a dull yel­low to a bright red­dish-or­ange. (Bishop, 1943; Hutchi­son, 1966; Lanoo, 2005; Pe­tranka, 2010)

Re­pro­duc­tion

Males pur­sue fe­male sala­man­ders to ini­ti­ate courtship. Male cave sala­man­ders court fe­males first by push­ing and rub­bing the snout of the fe­male. Males then press their cheeks against fe­males and move for­ward. Fe­males use their cheeks to main­tain con­tact with the backs of males. Males press their pelvic area against the fe­males once they have their tails po­si­tioned un­der­neath fe­males. Once this is ini­ti­ated, they both en­gage in a tail-strad­dle walk. Dur­ing this courtship, chem­i­cal com­mu­ni­ca­tion takes place. Pheromones are known to stim­u­late the vomeronasal or­gans of cave sala­man­ders. Pheromones also pass neural in­for­ma­tion to the hy­po­thal­a­mus. This is a part of the brain re­spon­si­ble for the con­trol of sex­ual re­cep­tiv­ity. Not enough re­search has been done to know the exact mat­ing sys­tems of cave sala­man­ders. All that is known is that one male courts one fe­male at a time. (Houck and Ver­rell, 1993; Pe­tranka, 2010)

Fe­males typ­i­cally lay their eggs deep in caves. They lay 49 to 87 eggs, ei­ther singly or clus­tered, at one time. Lit­tle knowl­edge is known about the re­pro­duc­tion of cave sala­man­ders be­cause of their pref­er­ence for cave habi­tats. Eggs are mostly laid in springs un­der­ground, streams found in caves, or lime­stone pools away from cave open­ings. The num­ber of days until hatch­ing de­pends tem­per­a­ture. The colder the tem­per­a­tures, the longer it takes for the eggs to hatch. (Pe­tranka, 2010; Ringia and Lips, 2007)

  • Breeding season
    Cave salamanders breed from October to January.
  • Range number of offspring
    49 to 87
  • Range time to hatching
    10 to 20 days

No parental in­vest­ment, be­yond egg-lay­ing, has been re­ported for cave sala­man­ders. (Lanoo, 2005)

  • Parental Investment
  • no parental involvement

Lifes­pan/Longevity

Cave sala­man­ders can in cap­tiv­ity for up to 9.1 years. Their lifes­pan in the wild is un­known. (Lanoo, 2005; Slavens and Slavens, 1999)

  • Range lifespan
    Status: captivity
    9.1 (high) years
  • Average lifespan
    Status: captivity
    9.1 years
    AnAge

Be­hav­ior

Cave sala­man­ders in­habit the twi­light zones of caves along with long-tailed sala­man­ders (Eu­rycea long­i­cauda). This may cause in­ter­spe­cific com­pe­ti­tion due to their sim­i­lar diets. Cave sala­man­ders, along with sev­eral other am­phib­ians, have a unique abil­ity to use the earth's mag­netic field for nav­i­ga­tion. They use this sense as a com­pass to mi­grate to dif­fer­ent lo­cales within caves.

Cave sala­man­ders de­pend on cave-like con­di­tions to com­plete stages of their life cy­cles, such as meta­mor­pho­sis. These sala­man­ders mi­grate in the sum­mer to what is known as their sum­mer habi­tat and home range. They tend to be more ac­tive at the sur­face of the water dur­ing sum­mer months. (Hofrichter, 2000; Lanoo, 2005)

Home Range

Ac­tive ranges for cave sala­man­ders changes ac­cord­ing to the sea­son. How­ever, no areas have been re­ported for home range. These sala­man­ders do not de­fend ter­ri­to­ries. (Lanoo, 2005)

Com­mu­ni­ca­tion and Per­cep­tion

Male cave sala­man­ders court fe­males first by push­ing and rub­bing the snouts of fe­males. It is as­sumed that mat­ing sea­son oc­curs dur­ing sum­mer and early fall. Cave sala­man­ders com­mu­ni­cate using pheromones. Men­tal glands on their heads as­sist with trans­fer­ring pheromones, and Ja­cob­son's or­gans help them de­tect chem­i­cal sig­nals. Cave sala­man­ders also use the earth's mag­netic field to nav­i­gate in dark caves. (Houck and Ver­rell, 1993; Lanoo, 2005; Pe­tranka, 2010)

Food Habits

The diet of cave sala­man­ders con­sists of small in­ver­te­brates. This in­cludes spi­ders and other small in­sects. Lar­vae eat snails, spi­ders, bee­tles, and flies. Adults have a more var­ied diet, hunt­ing prey such as earth­worms, ticks, mites, and many other small arthro­pods. (Pe­tranka, 2010)

  • Animal Foods
  • terrestrial non-insect arthropods

Pre­da­tion

Cave sala­man­ders may coil their body and wave their tail above their head. This be­hav­ior in­tim­i­dates po­ten­tial preda­tors. They also have glands through­out their body that pro­duce nox­ious se­cre­tions. There are no recorded preda­tors of cave sala­man­ders. (Lanoo, 2005; Pe­tranka, 2010)

Ecosys­tem Roles

Cave sala­man­ders com­monly carry gas­troin­testi­nal par­a­sites. A study showed that 1 or more ne­ma­todes were found in 77% of the sala­man­ders tested. The types of par­a­sites found in their gas­troin­testi­nal tracts de­pends on the ge­o­graphic lo­ca­tion in which they live. Par­a­sites that were found in­clude trema­todes (Brachy­coelium sala­man­drae) and ne­ma­todes (Cap­il­laria in­equalis, Os­wal­docruzia pip­i­ens, The­landros mag­navul­varis, and Tri­choskr­jabinia).

Cave sala­man­ders may have in­ter­spe­cific com­pe­ti­tion with other species of sala­man­der. Often times, cave sala­man­ders will share the twi­light zones of caves with other species. (Cas­tle, et al., 2011)

Com­men­sal/Par­a­sitic Species
  • Ne­ma­tode Tri­choskr­jabinia sp.
  • Trema­todes Brachy­coelium sala­man­drae
  • Ne­ma­tode Cap­il­laria in­equalis
  • Ne­ma­tode Os­wal­docruzia pip­i­ens
  • Ne­ma­tode The­landros mag­navul­varis

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

There are no known pos­i­tive eco­nomic im­pacts of cave sala­man­ders for hu­mans.

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

There are no known neg­a­tive eco­nomic im­pacts of cave sala­man­ders for hu­mans.

Con­ser­va­tion Sta­tus

Cave sala­man­ders are a species of least con­cern on the IUCN Red List. They are not listed on any other fed­eral or in­ter­na­tional list. How­ever, cave sala­man­ders are listed as state-en­dan­gered in Kansas, Mis­sis­sippi, and Ohio. They are also re­ported as rare in West Vir­ginia. No known con­ser­va­tion ac­tions are cur­rently pub­lished for this species. (IUCN SSC Am­phib­ian Spe­cial­ist Group, 2014; Lanoo, 2005)

Con­trib­u­tors

Sarah Par­nell (au­thor), Rad­ford Uni­ver­sity - Fall 2015, Cari Mc­gre­gor (ed­i­tor), Rad­ford Uni­ver­sity, Zeb Pike (ed­i­tor), Rad­ford Uni­ver­sity, Karen Pow­ers (ed­i­tor), Rad­ford Uni­ver­sity, April Tin­gle (ed­i­tor), Rad­ford Uni­ver­sity, Jacob Vaught (ed­i­tor), Rad­ford Uni­ver­sity, Galen Bur­rell (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

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

ectothermic

animals which must use heat acquired from the environment and behavioral adaptations to regulate body temperature

forest

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

freshwater

mainly lives in water that is not salty.

magnetic

(as perception channel keyword). This animal has a special ability to detect the Earth's magnetic fields.

metamorphosis

A large change in the shape or structure of an animal that happens as the animal grows. In insects, "incomplete metamorphosis" is when young animals are similar to adults and change gradually into the adult form, and "complete metamorphosis" is when there is a profound change between larval and adult forms. Butterflies have complete metamorphosis, grasshoppers have incomplete metamorphosis.

migratory

makes seasonal movements between breeding and wintering grounds

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.

native range

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

nocturnal

active during the night

oviparous

reproduction in which eggs are released by the female; development of offspring occurs outside the mother's body.

pheromones

chemicals released into air or water that are detected by and responded to by other animals of the same species

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

social

associates with others of its species; forms social groups.

tactile

uses touch to communicate

terrestrial

Living on the ground.

visual

uses sight to communicate

Ref­er­ences

Bishop, S. 1943. Hand­book of Sala­man­ders. Ithaca, New York: Com­stock Pub­lish­ers Assoc. & Cor­nell Uni­ver­sity Press.

Brig­gler, J., J. Prather. 2006. Sea­sonal use and se­lec­tion of caves by Plethon­tid sala­man­ders in karst areas of Arkansas. Amer­i­can Mid­land Nat­u­ral­ist, 155/1: 136-148.

Camp, C., J. Wooten, J. Jensen, D. Bartek. 2014. Role of tem­per­a­ture in de­ter­min­ing rel­a­tive abun­dance in cave twi­light zones by two species of lun­g­less sala­man­der (fam­ily Pletho­d­on­ti­dae). Cana­dian Jour­nal Of Zo­ol­ogy, 92/2: 119-127.

Cas­tle, M., D. Strohlein, B. Chris­tensen. 2011. Helminth Par­a­sites of the Cave Sala­man­der, Eu­rycea lu­cifuga, from west­ern Ken­tucky. Pro­ceed­ings of the Helmintho­log­i­cal So­ci­ety of Wash­ing­ton, 54/2: 269-270.

Green, D., L. Weir, G. Casper, M. Lan­noo. 2013. North Amer­i­can Am­phib­ians Dis­tri­b­u­tion & Di­ver­sity. Berke­ley and Los An­ge­las, Cal­i­for­nia: Uni­ver­sity of Cal­i­for­nia Press.

Hair­ston, N. 1987. Com­mu­nity Ecol­ogy and Sala­man­der Guilds. New York, New York: Cam­bridge Uni­ver­sity Press.

Hofrichter, R. 2000. Am­phib­ians: The World of Frogs, Toads, Sala­man­ders and Newts. Buf­falo, New York: Fire­fly Books.

Houck, L., P. Ver­rell. 1993. Stud­ies of Courtship Be­hav­ior in Pletho­d­on­tid Sala­man­ders: A Re­view. Her­peto­log­ica, 49/2: 175-184.

Hutchi­son, V. 1966. Cate­l­ogue of Amer­i­can Am­phib­ians and Rep­tiles. Clifton Heights, PA: Amer­i­can So­ci­ety of Am­phib­ians of Ichthy­ol­o­gists and Her­po­tol­o­gists.

IUCN SSC Am­phib­ian Spe­cial­ist Group, 2014. "The IUCN Red List of Threat­ened Species" (On-line). Eu­rycea lu­cifuga. Ac­cessed No­vem­ber 06, 2015 at http://​www.​iucnredlist.​org/​details/​59269/​0.

Lanoo, M. 2005. Am­phib­ian De­clines: The Con­ser­va­tion Sta­tus of United States Species. Los An­ge­las, Cal­i­for­nia: Uni­ver­sity of Cal­i­for­nia Press.

Pe­tranka, J. 2010. Sala­man­ders of the United States and Canada. Wash­ing­ton DC: Smith­son­ian In­sti­tu­tion.

Ringia, A., K. Lips. 2007. Ovip­po­si­tion, Early De­vel­op­ment and Growth of the Cave Sala­mader, Eu­rycea lu­cifuga: Sur­face. Her­peto­log­ica, 63/3: 258-268.

Slavens, F., K. Slavens. 1999. "Rep­tiles and Am­phib­ians in Cap­tiv­ity- Breed­ing, Longevity, and In­ven­tory" (On-line). Ac­cessed No­vem­ber 20, 2015 at http://​www.​pondturtle.​com/​welcome.​html#​INDEX.