Necturus punctatusDwarf Waterdog

Ge­o­graphic Range

Dwarf wa­ter­dogs (Nec­turus punc­ta­tus) are lo­cated in the Pied­mont re­gion of the Ap­palachian High­lands, and more com­monly in the south­ern At­lantic Coastal Plain in the east­ern United States. They are found in rivers and streams through­out east­ern Geor­gia and reach as far north as Vir­ginia. The west­ern­most bound­ary of their ge­o­graphic range ex­tends into the broad low­lands of the Tri­as­sic Basin in North Car­olina. Dwarf wa­ter­dogs are pre­sent in the Chesa­peake Bay re­gion, but only in south­east­ern Vir­ginia. (Du­ell­man and Sweet, 1999; Dunn, 1918; Hardy Jr., 1972; Martof, et al., 1980)

Habi­tat

Op­ti­mal habi­tat for dwarf wa­ter­dogs con­sists of silt-bot­tomed stream pools with leafy cover. They are also found in open sandy areas and pre­fer slow-mov­ing water over areas with high flow rates. (Jen­son, et al., 2008)

  • Aquatic Biomes
  • rivers and streams

Phys­i­cal De­scrip­tion

Dwarf wa­ter­dogs are the small­est of all water dog species. Adults range in head to tail length from 11.5 to 15.9 mm. For com­par­i­son, adult black war­rior wa­ter­dogs typ­i­cally range in size from 175 and 200 mm. Fe­males gen­er­ally have longer tails than males of the same body length, how­ever, males and fe­males of a given body length are typ­i­cally the same mass. Dwarf wa­ter­dogs are slate-gray or brown with small, scat­tered pale spots. The dor­sum tends to be dark, while the ven­ter is often pale in color. In gen­eral, wa­ter­dogs have red ex­ter­nal gills that pro­trude from both sides of the or­gan­ism’s head. (Bart, et al., 1997; Co­nant and Collins, 1998; Lan­noo, 2005; Martof, et al., 1980; Meffe and Shel­don, 1987)

  • Sexual Dimorphism
  • female larger

De­vel­op­ment

Dwarf wa­ter­dogs do not un­dergo meta­mor­pho­sis and lar­vae are con­sid­ered adults once their re­pro­duc­tive sys­tem has fully ma­tured. The lar­val stage lasts for a min­i­mum of 2 years. The small­est re­ported larva was only 28 mm long. As lar­vae, their bod­ies are uni­formly brown in color. Ju­ve­niles are often found in more shal­low water than adults and com­monly occur in bun­dles of leaves. Like lar­vae, ju­ve­niles are brown, but de­velop a bluish white color along the ven­ter. Dwarf wa­ter­dogs be­come sex­u­ally ma­ture by 5 years of age, and when fully ma­ture, they range in length from 26 to 116 mm. (Lan­noo, 2005; Will­son, et al., 1999)

Re­pro­duc­tion

There is no in­for­ma­tion avail­able re­gard­ing the mat­ing sys­tem of dwarf wa­ter­dogs.

Lit­tle is know of the re­pro­duc­tive be­hav­ior of dwarf wa­ter­dogs, how­ever, other wa­ter­dog species re­pro­duce aquat­i­cally. The larger a dwarf wa­ter­dog, the greater the num­ber of oocytes in the ovaries, which con­tain yolked and un­y­olked oocytes dur­ing mid-au­tumn. Most preg­nant fe­males carry 15 to 55 eggs. Av­er­age egg di­am­e­ter has been re­ported as 4 and 4.2 mm and may de­pend on the num­ber of eggs being car­ried. Prior to mat­ing, which oc­curs dur­ing win­ter, male testes be­come large, firm, and yel­low with dark pig­men­ta­tion. De­spite gen­der, in­di­vid­u­als reach re­pro­duc­tive ma­tu­rity by age 5 or when they be­come 65 to 70 mm in head-body length. Al­though no nests have been dis­cov­ered, it is thought that dwarf wa­ters at­tach their eggs to the un­der­side of logs and other ob­jects in the water. (Folk­erts, 1971; Lan­noo, 2005; Meffe and Shel­don, 1987)

  • Breeding season
    Dwarf waterdogs breed during winter.
  • Range number of offspring
    15 to 55
  • Average age at sexual or reproductive maturity (female)
    5 years
  • Average age at sexual or reproductive maturity (male)
    5 years

There is no in­for­ma­tion avail­able re­gard­ing parental care in dwarf wa­ter­dogs.

Lifes­pan/Longevity

Only lim­ited in­for­ma­tion on the lifes­pan of dwarf wa­ter­dogs ex­ists. A sin­gle spec­i­men cap­tured in the wild and taken to the Cincin­nati Zoo lived for 5 years and 8 months. Be­cause they reach sex­ual ma­tu­rity at 5 years of age, dwarf wa­ter­dogs likely live for more than 10 years. How­ever, no in­for­ma­tion ex­ists to con­firm this. (Folk­erts, 1971; Lan­noo, 2005)

Be­hav­ior

Lit­tle in­for­ma­tion is avail­able con­cern­ing the gen­eral be­hav­ior of dwarf wa­ter­dogs. Nu­mer­ous dwarf wa­ter­dogs are com­monly found in­hab­it­ing a sin­gle area, sug­gest­ing these an­i­mals are not ter­ri­to­r­ial. They do not hi­ber­nate, re­main­ing ac­tive even dur­ing the win­ter­time. In order to min­i­mize the ef­fects of cold dur­ing win­ter, dwarf wa­ter­dogs often heap to­gether in leaf lit­ter. (Lan­noo, 2005)

Home Range

The av­er­age home range size of dwarf wa­ter­dogs is cur­rently un­known. Black war­rior wa­ter­dogs in the Grand River of north­east­ern Ohio have an av­er­age home range of 136.1 square me­ters dur­ing the sum­mer. How­ever, this is the largest of wa­ter­dog species and thus, it likely has a larger home range than do dwarf wa­ter­dogs. (Lan­noo, 2005)

Com­mu­ni­ca­tion and Per­cep­tion

There is no in­for­ma­tion avail­able con­cern­ing com­mu­ni­ca­tion and per­cep­tion in dwarf wa­ter­dogs. (Folk­erts, 1971; Lan­noo, 2005)

Food Habits

Dwarf wa­ter­dogs are preda­tory and com­monly con­sume gas­tropods, pele­cy­pods, oligochaetes, arach­nids, isopods, clado­cer­ans, os­tra­cods, cope­pods, am­phipods, chilopods, and a va­ri­ety of in­sects. In ad­di­tion, adults often com­sume an­nelids, cray­fish , and even other sala­man­ders, sug­gest­ing they may be can­ni­bal­is­tic. Young have been known to eat an­nelids, am­phi­pod, mil­li­pedes, and in­sects and their lar­vae. Ev­i­dence sug­gests that males re­duce, or even dis­con­tinue feed­ing ac­tiv­ity dur­ing the breed­ing sea­son, though lar­vae are thought to feed through­out the en­tire year. (Braswell and Ash­ton Jr., 1985; Folk­erts, 1971; Meffe and Shel­don, 1987)

  • Animal Foods
  • amphibians
  • fish
  • insects
  • terrestrial non-insect arthropods
  • terrestrial worms

Pre­da­tion

Al­though no ev­i­dence ex­ists sug­gest­ing preda­tors spe­cific to this species, dwarf wa­ter­dogs likely fall prey to preda­ceous or­gan­isms in­hab­it­ing the same areas. Po­ten­tial preda­tors in­clude aquatic in­sects and snakes, cray­fish, and large sala­man­ders. Al­though no ev­i­dence ex­ists re­gard­ing anti-preda­tory be­hav­ior in dwarf wa­ter­dogs, they likely hide from po­ten­tial threats in the soft sub­strate. Their col­oration cam­ou­flages them from po­ten­tial preda­tors and likely helps re­duce risk of pre­da­tion. (Lan­noo, 2005)

  • Anti-predator Adaptations
  • cryptic

Ecosys­tem Roles

Dwarf wa­ter­dogs prey upon the aquatic lar­vae of nu­mer­ous arthro­pods, which may help con­trol in­sect pests through­out its ge­o­graphic range. Al­though par­a­sites spe­cific to this species are not known, the gills and skin of con­gener­ics have proven to be prime habi­tat for a num­ber of dif­fer­ent endo and ec­topar­a­sites, such as trema­todes. Pro­teochep­halids in­habit the in­testines of cer­tain wa­ter­dog species. (Lan­noo, 2005; Tobey, 1985)

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

Recre­ational fish­er­men com­monly use wa­ter­dogs as bait for large­mouth bass and cat­fish. (Lan­noo, 2005)

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

There are no known ad­verse ef­fects of dwarf wa­ter­dogs on hu­mans.

Con­ser­va­tion Sta­tus

Al­though dwarf wa­ter­dogs are clas­si­fied as a species of least con­cern on the IUCN's Red List of Threat­ened Species, cur­rent pop­u­la­tion trends are un­known and thus, po­ten­tial threats to their per­sis­tence are dif­fi­cult to pre­dict. Dwarf wa­ter­dogs occur in sev­eral pro­tected areas through­out their ge­o­graphic range. (Lan­noo, 2005; Tobey, 1985)

Con­trib­u­tors

Lind­sey Hughes (au­thor), Rad­ford Uni­ver­sity, Gre­gory Za­gursky (ed­i­tor), Rad­ford Uni­ver­sity, John Berini (ed­i­tor), An­i­mal Di­ver­sity Web Staff.

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

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

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.

ectothermic

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

freshwater

mainly lives in water that is not salty.

heterothermic

having a body temperature that fluctuates with that of the immediate environment; having no mechanism or a poorly developed mechanism for regulating internal body temperature.

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).

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.

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.

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

Ref­er­ences

Bart, H., M. Bai­ley, Jr., R. Ash­ton, P. Moler. 1997. Tax­o­nomic and Nomen­clat­ural Sta­tus of the Upper Black War­rior River Wa­ter­dog. Jour­nal of Her­petol­ogy, 31 (2): 192-201. Ac­cessed Jan­u­ary 29, 2011 at http://​www.​jstor.​org/​stable/​1565387.

Braswell, A., R. Ash­ton Jr.. 1985. Dis­tri­b­u­tion, ecol­ogy, and feed­ing habits of Nec­turus lewisi. Brim­leyana, 10: 13-35.

Co­nant, R., J. Collins. 1998. Field Guide to Rep­tiles and Am­phib­ians. New York, New York: Houghton Mif­flin Har­court.

Du­ell­man, W., S. Sweet. 1999. Dis­tri­b­u­tion pat­terns of am­phib­ians in the Nearc­tic re­gion of North Amer­ica. Bal­ti­more, Mary­land: John Hop­kins Uni­ver­sity Press.

Dunn, E. 1918. The Col­lec­tion of Am­phibia Cau­data of the Mu­seum of Com­par­a­tive Zo­ol­ogy. Bul­letin of the Mu­seum of Com­par­a­tive Zo­ol­ogy at Har­vard Col­lege, 62: 443-472.

Folk­erts, G. 1971. Notes on South Car­olina Sala­man­ders. Jour­nal of the El­isha Mitchell Sci­en­tific So­ci­ety, 87: 206-208.

Gunter, G., W. Brode. 1964. Nec­turus in the State of Mis­sis­sippi with Notes on Ad­ja­cent Areas. Her­peto­log­ica, 20 (2): 114-126. Ac­cessed Feb­ru­ary 01, 2011 at http://​www.​jstor.​org/​stable/​pdfplus/​3890579.​pdf.

Hardy Jr., J. 1972. Am­phib­ians of the Chesa­peake Bay Re­gion. Chesa­peake Sci­ence, 13: S123-S128.

In­di­viglio, F. 2010. Newts and sala­man­ders: every­thing about se­lec­tion, care, nu­tri­tion, dis­eases, breed­ing, and be­hav­ior. Haup­pauge, New York: Bar­ron's Ed­u­ca­tional Se­ries.

Jen­son, J., C. Camp, W. Gib­bons. 2008. Am­phib­ians and Rep­tiles of Geor­gia. Athens, Geor­gia: The Uni­ver­sity of Geor­gia Press.

Lan­noo, M. 2005. Am­phib­ian de­clines: the con­ser­va­tion sta­tus of United States species. Berke­ley, Cal­i­for­nia: Uni­ver­sity of Cal­i­for­nia Press.

Martof, B., W. Palmer, J. Bai­ley, J. Har­ri­son III. 1980. Am­phib­ians and Rep­tiles of the Car­oli­nas and Vir­ginia. Chapel Hill, North Car­olina: The Uni­ver­sity of North Car­olina Press.

Meffe, G., A. Shel­don. 1987. Habi­tat Use by Dwarf Wa­ter­dogs (Nec­turus punc­ta­tus) in South Car­olina Streams, with Life His­tory Notes. Her­peto­log­ica, 43 (4): 490-496. Ac­cessed Jan­u­ary 28, 2011 at http://​www.​jstor.​org/​stable/​3892150.

Neill, W. 1948. Hi­ber­na­tion of Am­phib­ians and Rep­tiles in Rich­mon County, Geor­gia. Her­peto­log­ica, 4 (3): 107-114. Ac­cessed Feb­ru­ary 01, 2011 at http://​www.​jstor.​org/​stable/​pdfplus/​27669570.​pdf?​acceptTC=true.

Palmer, W., A. Braswell. 1995. Retiles of North Car­olina. Chapel Hill, North Car­olina: Chapel Hill Uni­ver­sity of North Car­olina Press.

Scott, D., B. Metts, W. Gib­bons. 2003. Sea­sonal Wet­lands and Golf Courses. Golf Course Man­age­ment, 2003: 85-89. Ac­cessed Feb­ru­ary 01, 2011 at http://​archive.​lib.​msu.​edu/​tic/​gcman/​article/​2003nov85.​pdf.

Sher­man, C. 1943. A Hand­book of Sala­man­ders. The Sala­man­ders of the United States, of Canada, and of Lower Cal­i­for­nia.. Ithaca, New York: Com­stock Pub­lish­ing Com­pany.

Tobey, F. 1985. Vir­ginia's Am­phib­ians and Rep­tiles: A Dis­tri­b­u­tional Sur­vey. Pur­cel­lville, VA: Mr. Print.

Vitt, L., J. Cald­well. 2009. Her­petol­ogy. Mary­land Heights, Mis­souri: Aca­d­e­mic Press.

Will­son, J., Y. Ko­rnilev, W. An­der­son, G. Con­nette, E. Eskew. 1999. "Dwarf Wa­ter­dog Nec­turus Punc­ta­tus" (On-line). Herps of North Car­olina. Ac­cessed April 28, 2011 at http://​www.​herpsofnc.​org/​herps_​of_​nc/​salamanders/​Necpun/​Nec_​pun.​html.