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Description

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Desmognathus aeneus is a small terrestrial salamander of the North American Southeast. Adults have dark bellies and a chestnut to yellow dorsal stripe flanked by darker sides. The dorsal stripe is often wavy and occasionally consists of chevrons or “herring bone” segments. Adults have 13-14 costal groves with a total length of 38-57 mm between the snout and tail tip (Petranka 1998). Like all members of the plethodontid family, D. aeneus do not have lungs and have a nasolabial groove which runs from the nares to the dorsal lip.

References

  • Beachy, C. K. (1993). ''Differences in variation in egg size for several species of salamanders (Amphibia: Caudata) that use different larval environments.'' Brimleyana, 18, 71-82.
  • Collazo, A. and Marks, S. B. (1989). ''Development and evolution in two species of plethodontid salamanders with differing life histories.'' American Zoologist, 29(4), 86A.
  • Donavan, L. A. and Folkerts, G. W. (1972). ''Food of the Seepage Salamander Desmognathus aeneus.'' Herpetologica, 28(1), 35-37.
  • Folkerts, G. W. (1968). The genus Desmognathus Baird (Amphibia: Plethodontidae) in Alabama. Ph.D. dissertation. Auburn University, Auburn, Alabama.
  • Hairston, N. G. (1980). ''Species packing in the salamander genus Desmognathus: what are the interspecific interactions involved?'' American Naturalist, 15(3), 354-366.
  • Hairston, N. G., Sr., and Wiley, R. H. (1993). ''No decline in salamander (Amphibia: Caudata) populations: a twenty-year study in the Southern Appalachians.'' Brimleyana, (18), 59-64.
  • Harrison, J. R. (1992). ''Desmognathus aeneus (Brown and Bishop). Cherokee Salamander.'' Catalogue of American Amphibians and Reptiles. Society for the Study of Amphibians and Reptiles, 534.1-534.4.
  • Jones, R. L. (1982). ''Distribution and ecology of the Seepage Salamander Desmognathus aeneus (Amphibia Plethodontidae) in Tennessee, USA.'' Brimleyana, 7, 95-100.
  • Livingston, P. G., Spencer, C. C., and Stuart, B. L. (1995). ''Caudata: Desmognathus aeneus (Seepage Salamander).'' Herpetological Review, 26(4), 207.
  • Marks, S. A. and Collazo, A. (1988). ''Post-neurula development in a plethodontid salamander Desmognathus aeneus.'' American Zoologist, 28(4), 12A.
  • Marks, S. B. (1994). ''Development of the hyobranchial apparatus in Desmognathus aeneus, a direct developing salamander.'' Journal of Morphology, 220(3), 371.
  • Marks, S. B., Shubin, N., and Wake, D. (1992). ''Limb development in the plethodontid salamander genus Desmognathus: Separating hypotheses of ancestry, function, and life history.'' American Zoologist, 32(5), 147A.
  • Marks, S. and Collazo, A. (1998). ''Direct development in Desmognathus aeneus (Caudata: Plethodontidae): a staging table.'' Copeia, 1988(3), 637-648.
  • Promislow, D. E. L. (1987). ''Courtship behavior of a plethodontid salamander Desmognathus aeneus.'' Journal of Herpetology, 21(4), 298-306.
  • Redmond, W. H., and Scott, A. F. (1996). Atlas of Amphibians in Tennessee. Miscellaneous Publication 12, The Center for Field Biology, Austin Peay State University, Clarksville, Tennessee.
  • Titus, T. A. and Larson, A. (1996). ''Molecular phylogenetics of desmognathine salamanders (Caudata: Plethodontidae): a reevaluation of evolution in ecology, life history, and morphology.'' Systematic Biology, 45(4), 451-472.
  • Verrell, P. A., and Mabry, M. (2000). ''The courtship of plethodontid salamanders: form, function and phylogeny.'' The Biology of Plethodontid Salamanders. R. C. Bruce, R. G. Jaeger, and L. D. Houck, eds., Kluwer Academic/ Plenum Press, New York, NY.
  • Wake, D. B. and Hanken, J. (1996). ''Direct development in the lungless salamanders: what are the consequences for developmental biology, evolution, and phylogenesis?'' International Journal of Developmental Biology, 40, 859-869.
  • Wake, D. B., Roth, G. and Nishikawa, K. C. (1987). ''The fate of the lateral line system in plethodontid salamanders.'' American Zoologist, 27(4), 166A.
  • Wake, D.B. (1966). ''Comparative osteology and evolution of the lungless salamanders, family Plethodontidae.'' Memoirs of the Southern California Academy of Sciences , 4, 1-111.

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Distribution and Habitat

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The range of Desmognathus aeneus is patchy from far southwestern North Carolina through central Alabama. There is a large western Alabama population, as well as isolated populations in Georgia and South Carolina (Petranka 1998; Livingston et al. 1995). The northern extent of its range is probably marked by the Little Tennessee River in North Carolina and Tennessee (Jones 1981). They are found in leaf litter along seepage areas of streams and springs in hardwood forests, and their egg masses are often found beneath patches of moss (Jones 1981).
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Life History, Abundance, Activity, and Special Behaviors

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Desmognathus aeneus is characterized as having direct development, which does not contain a free-living larval stage. Along with a precocious adult morphology at birth, D. aeneus also lacks substantial gills or a caudal fin, and forms eyelids as an embryo (Wake 1966; Marks and Collazo 1988; Collazo and Marks 1989; Marks and Collazo 1998). These features combined indicate that D. aeneus is a true direct developing salamander. This unique life history is shared with only one other member of its genus, Desmognathus wrighti. All other members of the genus exhibit the standard biphasic amphibian lifestyle with aquatic larvae and terrestrial or semi-terrestrial adults. Unlike many direct developing frogs or bolitoglossine and plethodontine salamanders, the development of D. aeneus is associated with little developmental repatterning. The embryo develops a hyobranchial apparatus, lateral line system, and limbs that at least partially resemble the larval development of metamorphosing desmognathines (Marks 1994; Wake et al. 1987; Marks et al. 1992). The development of these features is dramatically altered in the direct developing members of the plethodontine and bolitoglossine tribes (reviewed in Wake and Hanken 1996). In their revision of the desmognathine salamander phylogeny Tom Titus and Allan Larson (1996) placed both species of direct developing Desmognathus (D. aeneus and D. wrighti) as basal to the genus (see Tree of Life web page). This positioning along with the placement of the direct developing Phaeognathus as the closest out-group suggests that direct development is the ancestral condition for the genus. This controversial finding is unique in claiming that metamorphosis has re-evolved in the evolution of desmognathine salamanders.Desmognathus aeneus young hatch between mid-June and mid-July. The clutch sizes range from 8-15 eggs. Their eggs are large with white embryos that can be seen through a transparent jelly coat and associated membranes. The adults primarily feed on arthropods with beetle larvae (Staphylinidae and Carabidae) its most common food source (Donavan and Folkerts 1972). Adult stomachs have also contained collembolas, arachnids, immature diptera, and even other D. aeneus, although cannibalism is thought to be uncommon (Jones 1981; Donavan and Folkerts1972).The reproductive behavior of Desmognathus aeneus is similar to its congeners. Like all plethodontids the desmognathine salamanders use a tail-straddling walk to transfer a spermatophore from the male to the female. This walk is the culmination of an elaborate courtship ritual that involves inputs from both the female and male salamanders (see Verrell and Mabry 2000). Unlike most other plethodontids, D. aeneus along with D. wrighti use a “prolonged biting phase,” in which the male bites the female while forcefully restraining her. This biting is used to transfer male pheromones to the female and is associated with vigorous rhythmic thrashing of the head (Promislow 1987).
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Life History, Abundance, Activity, and Special Behaviors

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Desmognathus aeneus has a Global Heritage Status of G3G4 (16Oct2001) (natureserve.org (http://www.natureserve.org)). It is described as moderately threatened and declining due to its patchy distribution and habitat preferences. Current logging practices and habitat loss have raised concern for its status in Tennessee (Redmond and Scott 1996)and Alabama (Folkerts 1968). While there is evidence that populations of this species vacillate widely in density (Hairston and Wiley 1993) it is unlikely that these populations can survive the dried habitat of clear-cut forests (Folkert 1968).
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Seepage salamander

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The seepage salamander (Desmognathus aeneus) is a small, terrestrial species of salamander in the family Plethodontidae. It is endemic to the United States. They are found in small areas of Tennessee, North Carolina, Georgia, and Alabama.[3] Its natural habitats are temperate forests, intermittent rivers, and freshwater springs. It gets its name from the seepages around which it lives. It is very similar in its appearance and life history to the pygmy salamander (Desmognathus wrighti). These two species differ greatly from the other Desmognathus species. They are the smallest salamanders in the genus, measuring only 3–5 cm (1–2 in) in length. They are also the only two terrestrial, direct-developing Desmognathus species. However, the two species are not often seen to coexist, differing in distribution by elevation; although there are exceptions. The seepage salamander is currently listed as Near Threatened, with its numbers declining in most of states in which it is found. It is threatened by habitat loss, with logging having a major effect.

Description

The seepage salamander is a very small and slender salamander, ranging from 4.4–5.7 cm (1.75–2.25 in). The adults possess vomerine teeth.[2] The tail is terete and rounded. The seepage salamander has a pale dorsal stripe, with a wide, wavy to almost straight shape, and ranging in color from yellow or tan to reddish brown.[4] The stripe is sometimes flecked with a darker pigment. A mid-dorsal, dark line is also seen and is continuous with a Y-shaped mark on the head. There is a dark brown band on the sides, fading towards the belly. The underbelly is pale and is mottled with brown and white, but it may also be plain, with no other coloration.[4]

The seepage salamander is easily confused with the Pygmy Salamander (Desmognathus wrighti). These two species overlap in a small area of southern North Carolina. D. wrighti and D. aeneus are the smallest species in the genus Desmognathus and are the only terrestrial direct-developers, lacking a free-swimming larval stage.[5] They both have vomerine teeth, and similar tail length to total body length ratios; however, they have different patterns and coloration.[2] Seepage salamanders have a smoother top of the head. The mental glands are also shaped differently in the males. The pygmy salamander has a large, U-shaped mental gland while the seepage salamander's is small and kidney shaped.

General description and taxonomy

The seepage salamander is part of the genus Desmognathus and the family Plethodontidae. Like all other plethodontids, the seepage salamander is lungless and respires through its skin and the lining of its mouth.[4] They also have a naso-labial groove and a relatively immoveable lower jaw which allows them to force their way under objects. As with all species in Desmognathus, they have a pale line running diagonally from the eye to the angle of the jaw. This line may be hard to see in older, darker adults. Their hind legs are larger and stouter than the forelegs. Their body is short and stout and they are good jumpers, often used as an escape.

According to the phylogenetic tree, the seepage salamander branched deep within the tree of the Desmognathus species. D. aeneus is a sister group to all species of Desmognathus except D. wrighti, which is an outgroup.[6] D. aeneus and D. wrighti have distinct character differences from the rest of the Desmognathus species. They are the smallest species, direct-developers, and the most terrestrial, with all other species being semi-aquatic or aquatic. Since these two species branch the earliest, evolution has moved toward larger body size, lengthened larval periods, and more aquatic habitats within Desmognathus.[7]

Geographic distribution

Seepage salamanders get their name from the seepages where they are often found. However, they are also found near streams and under leaf litter, leaf mold, and rotten logs.[8] They are a terrestrial species.

Seepage salamanders are distributed in southeast Tennessee, southwest North Carolina, northern Georgia, and central to northern Alabama. They are found in Monroe and Polk counties in Tennessee; Fannin, Pickens, Towns, and Union counties in Georgia; Oconee County in South Carolina; and Cherokee, Clay, Graham, Macon, and Swain counties in North Carolina. In Alabama, they can be found in Calhoun, Clay, Cleburne, and Tallapoosa counties.[9] They also might be found in Cherokee, Chilton, Etowah, Hale, and Tuscaloosa counties in Alabama, but may be extirpated from these locales.[9]

Populations have a disjunct distribution and are highly localized.[8] There is an isolated colony in western Alabama, and one in northeastern Georgia. Populations are found at elevations ranging from 210–1,370 m (700–4,500 ft). However, in the colony in northeastern Georgia they can be found as low as 30 m (100 ft).[4]

Ecology

The seepage salamander does not experience much competition from other species of salamanders due to its habitat. Because it is a terrestrial salamander, it is not disturbed by the semi-aquatic and aquatic salamanders.[10] Almost all other Desmognathus species are found at closer distances to streams. The lack of competition also may be due to the fact that it is very secretive. It is seldom seen on the surface, which may be an anti-predatory response.

The only species of Desmognathus which would be found in the same habitat as the seepage salamander and create competitive pressure is the pygmy salamander (D. wrighti). However, the ranges of the two species rarely overlap. The pygmy salamander is found at higher elevations, while the seepage salamander is found at lower ones. The pygmy salamander is found on the border of North Carolina and Tennessee. The distribution range of the seepage salamander begins just below the pygmy salamander's range. However, there have been cases where the two species are found together. It has been observed that they coexist in Monroe County, Tennessee and it is possible that they coexist in Blount County, Tennessee.[11] Further studies are needed to determine their interactions and would aid in conservation efforts.[11]

Life history and behavior

Seepage salamanders are rarely seen on the surface even at night, despite being nocturnal.[10] The food sources consists mainly of arthropods, especially insect larvae and springtails.[12] Mites, spiders, earthworms, crustaceans, nematodes, myriapods, and snails have also been found to be eaten by seepage salamanders.

Life history

The seepage salamander is terrestrial and develop directly into juveniles, skipping the aquatic, larval stage. The length of time between fertilization and hatching is 68–75 days.[13] When eggs hatch, the juveniles clearly resemble the adults.

Oviposition occurs in April and May, with all eggs ready for deposition by the female being laid.[8] The eggs hatch in the late spring and summer. There have been some discrepancies about how long it takes for the eggs to hatch. Both males and females reach sexual maturation after two years. Harrison (1967) found that eggs hatched in 43–45 days, but Marks and Collazo found 68–75 days.[8][13] This may be due to different incubation temperatures, but the difference has not been fully explored.

Courtship

There is little diversity within Plethodontidae in regards to mating. The mating process consists of courting behavior, the tail straddling walk, sperm deposition in the form of a spermatophore, and insemination. However, the seepage salamander differs in its courtship behavior.

As with all other plethodontids, pheromones are secreted by males and are used during the courtship process. Most species use a pulling or snapping behavior. However, only D. aeneus and D. wrighti use biting as a delivery mechanism.[14] These two species physically and directly restrain the females and bite them. The bites can last up to several hours. Then they release pheromones into the bite wounds.[14] Other plethodontids do not directly restrain the females when excreting pheromones.

Conservation

The seepage salamander is classified as Near Threatened by the IUCN because their range is not greater than 20,000 km2 and its habitat and population size is decreasing.[1] The isolation of the different population also increases susceptibility to declines. Seepage salamanders are on the verge of becoming classified as Vulnerable.

The species is in decline in Alabama and North Carolina, but is stable in South Carolina.[1] It is listed as in need of management in Tennessee.

Logging is a main source of decline within the species, particularly in Alabama.[15] Around half of the populations known in 1976 are now extinct.[16] Other forestry practices, like clear cutting also threaten seepage salamanders.

Most populations of seepage salamanders do not occur within protected areas. Therefore, to decrease vulnerability of populations to certain forestry practices, buffers should be set up in susceptible areas around seepages and streams.[1]

References

  1. ^ a b c d Geoffrey Hammerson, Julian Harrison (2004). "Desmognathus aeneus". IUCN Red List of Threatened Species. 2004: e.T59243A11905725. doi:10.2305/IUCN.UK.2004.RLTS.T59243A11905725.en. Retrieved 16 November 2021.
  2. ^ a b c Brown, W. C., and S. C. Bishop. 1947. A new species of Desmognathus from North Carolina. Copeia 1947: 163-166.
  3. ^ Frost, Darrel R. (2014). "Desmognathus aeneus Brown and Bishop, 1947". Amphibian Species of the World: an Online Reference. Version 6.0. American Museum of Natural History. Retrieved 1 March 2015.
  4. ^ a b c d Conant, R. and Collins, J. 1998. Peterson Field Guides: Reptiles and Amphibians (Eastern/Central North America). Houghton Mifflin Company, New York.
  5. ^ Hining, K.J., Bruce, R.C. 2005. Population Structure and Life History Attributes of Syntopic Populations of the Salamanders Desmognathus aeneus and Desmognathus wrighti (Amphibia: Plethodontidae) Southeastern Naturalist 4: 679-688.
  6. ^ Kozak, K.H., Bonett, A.L., Harmon, L.J., 2005. Phylogenetic Analysis of Ecomorphological Divergence, Community Structure, and Diversification Rates in Dusky Salamanders (Plethodontidae: Desmognathus). Evolution 59:2000-2016.
  7. ^ Titus, T. A. and Larson, A. 1996. Molecular phylogenetics of desmognathine salamanders (Caudata: Plethodontidae): a reevaluation of evolution in ecology, life history, and morphology. Systematic Biology, 45(4), 451-472.
  8. ^ a b c d Harrison, J. (1967). "Observations on the life history, ecology and distribution of Desmognathus aeneus aeneus Brown and Bishop". American Midland Naturalist. 77 (2): 356–370. doi:10.2307/2423347. JSTOR 2423347.
  9. ^ a b NatureServe. 2010. NatureServe Explorer: An online encyclopedia of life [web application]. Version 7.1. NatureServe, Arlington, Virginia. Available http://www.natureserve.org/explorer. (Accessed: April 25, 2011 )
  10. ^ a b Hairston, N.G. Sr. 1986. Species packing in Desmognathus salamanders: experimental demonstration of predation and competition. Am. Nat. 127:266-291
  11. ^ a b Reynolds, R.G., Niemiller, M.L., and Pasachnik. 2011. Occurrence of pygmy salamanders (Desmognathus wrighti) in Monroe County, Tennessee. Journal of the Tennessee Academy of Science 86(2):53–55
  12. ^ Donovan, L.A. and G.W. Folkerts. 1972. Foods of the seepage salamander, Desmognathus aeneus Brown and Bishop. Herpetologica 28:35–37.
  13. ^ a b Marks, S.B., Collazo, A. 1998. Direct Development in Desmognathus aeneus (Caudata: Plethodontidae): A Staging Table. Copeia 3: 637-648.
  14. ^ a b Promislow, D. E. L. 1987. Courtship behavior of a plethodontid salamander, Desmognathus aeneus. J. Herpetol. 21:298-306.
  15. ^ Folkerts, G.W. 1968. The genus Desmognathus Baird (Amphibia: Plethodontidae) in Alabama. Ph.D. dissertation. Auburn University, Auburn, Alabama.
  16. ^ Harrison, J. 2011. Desmognathus aeneus: Seepage Salamander. AmphibiaWeb. Berkeley, California. http://amphibiaweb.org/>
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Seepage salamander: Brief Summary

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The seepage salamander (Desmognathus aeneus) is a small, terrestrial species of salamander in the family Plethodontidae. It is endemic to the United States. They are found in small areas of Tennessee, North Carolina, Georgia, and Alabama. Its natural habitats are temperate forests, intermittent rivers, and freshwater springs. It gets its name from the seepages around which it lives. It is very similar in its appearance and life history to the pygmy salamander (Desmognathus wrighti). These two species differ greatly from the other Desmognathus species. They are the smallest salamanders in the genus, measuring only 3–5 cm (1–2 in) in length. They are also the only two terrestrial, direct-developing Desmognathus species. However, the two species are not often seen to coexist, differing in distribution by elevation; although there are exceptions. The seepage salamander is currently listed as Near Threatened, with its numbers declining in most of states in which it is found. It is threatened by habitat loss, with logging having a major effect.

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