Shenandoah salamander

Last updated

Shenandoah salamander
Shenandoah Salamander (33329749601).jpg
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Amphibia
Order: Urodela
Family: Plethodontidae
Subfamily: Plethodontinae
Genus: Plethodon
Species:
P. shenandoah
Binomial name
Plethodon shenandoah
Highton and Worthington, 1967
Shenandoah Salamander Plethodon shenandoah distribution map 3.png
The habitat of the Shenandoah salamander is limited to 3 talus slopes within the Shenandoah National Park in Virginia
Synonyms [4]

Plethodon richmondi shenandoahHighton and Worthington, 1967 [5]

Contents

The Shenandoah salamander (Plethodon shenandoah) is a small, terrestrial salamander found exclusively in Shenandoah National Park in Virginia. The Shenandoah salamander inhabits a very small range of land on just three mountain peaks. Due to the small habitat range, interspecies competition, and climate change, the population of the Shenandoah salamander is vulnerable to extinction. Mitigating human effects on the habitat of the species will be essential in attempting to preserve and grow the population.

Description

The adult Shenandoah salamander is slender and moderate in size, with a total length of 3.5 to 4.5 inches (7 cm - 10 cm). [6] The species has two distinct color phases: striped and unstriped. The striped color phase has a narrow stripe down the center of its back that can range in color from red to yellow, while the unstriped color phase is uniformly dark with occasional scattered brass-colored flecks. [7] In both color phases, white or yellow spots occur along the sides of the body. The Shenandoah salamander is similar in appearance to the red-backed salamander ( Plethodon cinereus ). However, the two species can be distinguished in many ways. The stripe on the Shenandoah salamander takes up one-third of its dorsal area, while the stripe on the red-backed salamander is wider and takes up approximately two-thirds of the dorsal area. In addition, the Shenandoah salamander lacks the “salt and pepper” color pattern on its underside that is characteristic of P. cinereus, and has a slightly larger and more broadly rounded head. Shenandoah salamanders are members of the family Plethondontidae, the lungless salamanders that breathe through the surface of their skin. [8] Due to the lack of lungs, successful respiration depends on the ability to maintain skin moisture, thus restricting body size and necessitating a moist environment such as forested areas. This species is chiefly nocturnal, hunting for food at night and taking cover in dark, damp locations like rock crevices and underneath logs during the day. [6]

Life history

Like most woodland salamanders, the Shenandoah salamander eats mites, flies, small beetles, springtails, and other soil invertebrates. [9] No direct observation of predation of the Shenandoah salamander has ever been reported, but potential predators residing within the habitat of the Shenandoah salamander include ring-necked snakes, short-tailed shrews, brown thrashers, and towhees. [10] The Shenandoah salamander’s life history is not well understood, though adult salamanders have a high survival rate, some even reaching 25 years of age. [6] Like many salamanders, the breeding season for the Shenandoah salamander occurs during late spring or summer. [11] Female salamanders do not breed prior to 4 years of age and lay an average clutch size of 13 eggs every other year. Clutches are laid in areas of moisture and incubate for 1–3 months. Fertilization occurs internally and the entire developmental process takes place within the egg—there is no aquatic larval stage. For the duration of the incubation period, females guard the nest and do not forage. [12]

All salamanders, including the Shenandoah salamander, have an important impact on ecosystem functions. Salamanders regulate population dynamics via predation of insects and other invertebrates, aerate the soil through burrowing behavior, and influence large-scale processes such as decomposition. [6]

Distribution

Habitat range

The Shenandoah salamander species is believed to have originated in the Appalachians of eastern North America, though the historical abundance of this species is unknown. [7] Currently, Shenandoah salamanders are exclusively found on the north-facing talus slopes of three mountains within the Shenandoah National Park in Virginia: Hawksbill, The Pinnacles, and Stony Man (see range map). Each of the three talus slopes houses an isolated salamander population residing at approximately 3,000 feet above sea level. [3] The talus slopes are typically dry, so the Shenandoah salamander is generally found within moist microhabitats scattered throughout the talus environment. Although the dry talus slopes are not optimal, the Shenandoah salamander is excluded from optimal forested areas containing deep, moist soil due to competition with the red-backed salamander. [13]

Population size

Based on data from 2008/2009 there was a population estimate between 110,262 to 140,625, but current population trends and estimates cannot be established until surveys with marked animals are conducted. [14]

Major threats

Red-backed salamander

The Shenandoah salamander species is threatened by competition by the aggressive red-backed salamander, which restricts the Shenandoah salamander to dry, sub-optimal talus environments and prevents Shenandoah salamander populations from expanding into heavily forested areas. [15] Furthermore, the talus habitat of the Shenandoah salamander is in a state of disintegration due to erosion. [3] Eventually, this weathering will result in soil formation and a subsequent increase in moisture, thus making the talus environment suitable for red-backed salamander invasion and increasing the possibility of extinction of the Shenandoah salamander species [6]

Both laboratory and field experiments have provided evidence of the red-backed salamander’s aggressive, territorial behavior toward the Shenandoah salamander. [16] [17] The two species compete for large cover objects that provide cool temperatures and high moisture levels, but the territoriality of P. cinereus results in competitive exclusion of the Shenandoah salamander from moist soil environments. As a result, the Shenandoah salamander, which has a higher tolerance for dry conditions, is restricted to the talus slope environments in which the red-backed salamander cannot survive. [18]

Invasive species

Invasive insect species in the Shenandoah National Park, namely the gypsy moth (Lymantria dispar dispar) and the hemlock woolly adelgid (Adelges tsugae), also threaten the survival of the Shenandoah salamander. [6] Gypsy moth larvae feed on tree leaves, resulting in widespread defoliation and tree mortality. This loss of overstory dramatically alters the Shenandoah salamander habitat, reducing the ground moisture and potentially altering the Shenandoah salamander’s ability to catch prey. Hemlock woolly adelgids are a major cause of hemlock tree mortality within Shenandoah National Park, contributing to overstory loss and talus slope habitat dehydration. [19] In addition, hemlock mortality increases the amount of hemlock needles in the soil, which lowers the pH of the soil. Acid deposition due to acid rain and/or air pollution also contributes to soil acidification and has been well-documented in Shenandoah National Park. [19] Although the direct effects of soil acidification on the Shenandoah salamander have not been documented, studies have shown that amphibians are extremely vulnerable to this process. [20] [21] These results suggest that soil acidification within the Shenandoah salamander habitat could reduce reproduction, affect food supply, lower egg hatchability, and increase newborn salamander mortality. [6]

Chytrid fungus

Batrachochytrium salamandrivorans or salamander chytrid fungus causes the infectious disease chytridiomycosis, which is considered to be a large factor in the declining populations of amphibians globally. [22] In 2016, an interim rule by the U.S. Fish and Wildlife Service (USFWS) added all species of salamander to the list of injurious amphibians. This rule prevented the importation or transportation of any live of dead specimens, including parts, of the 20 genera of salamanders into the United States and interstate transportation between States, the District of Columbia, the Commonwealth of Puerto Rico, or any territory or possession of the United States. [23] Only with the exception of permit for zoological, educational, medical, or scientific purposes or by Federal agencies without a permit solely for their own use. [23] This interim rule was a proactive rule to protect the wildlife from the introduction, establishment, and spread of Batrachochytrium salamandrivorans. While this fungus had a lethal effect on many salamander species, it was not currently known to be found in the United States; however, the potential introduction of the fungus upon the salamander species could have an incredibly devastating effect. [23]

Anthropogenic factors

Anthropogenic factors also appear to potentially further endanger the Shenandoah salamander. In the 1994 recovery plan, it was thought that further debilitation of overstory vegetation, changes in soil chemistry, and direct impacts to the salamanders associated with acid deposition and other sources of air pollution were potential threats. While there were no effects of acid deposition and other sources of air pollution on the Shenandoah salamander, there have been numerous studies which indicate amphibians to be very vulnerable to effects of acid deposition, especially in montane areas. [6] Acidification of the habitat could affect the salamander’s food supply, could impair reproduction by affecting courtship, egg hatchability, or neonatal viability. [6] Studies showed that soil acidity decreased the abundance of the red-backed salamander, making it likely for the Shenandoah salamander to also be negatively affected. [6] Finally, there was the potential disturbance to the habitat of the Shenandoah salamander due to hiking trail maintenance, use, and backcountry camping. [6]

Climate change

Climate change also directly impacts the habitat of the Shenandoah salamander. Cloud base elevation, which is influenced by climate variables, is likely to continue to shrink the suitable range of the Shenandoah salamander. [24] One study found that elevation is strongly correlated with the lower elevation range boundary for the Shenandoah salamander, despite previous assumptions that the range was limited only to competitive interactions. [24] The lower elevational range is sensitive to climate variables, so climate change in high elevation habitats will directly affect the species’ distribution. [24]

Conservation status

In December 1982, the U.S. Fish and Wildlife Service categorized the Shenandoah salamander as a “Category 2” in its Review of Vertebrate Wildlife for Listing as Endangered or Threatened Species. [25] In 1989, the Shenandoah salamander was formally classified as “Endangered” under the Endangered Species Act (ESA). [3]

The Shenandoah salamander was first listed as Endangered (E) by the IUCN in 1994, and retained its Endangered status in a 1996 assessment. [1]   In 2004, the Shenandoah salamander was listed as Vulnerable D2 (VU) by the IUCN, with the justification that it was found in only three locations. [1]

Critical habitat

In 2015, the Center for Biological Diversity presented a petition for designating a critical habitat for nine species including the Shenandoah salamander. The Center requested that the U.S. Fish and Wildlife Service designate 16,891 acres within the Shenandoah National Park as critical habitat for the Shenandoah salamander. [26] As the salamander requires very specific habitat conditions, and is restricted to the high-elevation mountains in Virginia, it is under an increasing threat from climate change, invasive species, pollution, and human activities. [26] Designating this area as a critical habitat would address potentially incompatible Park Service management and would be beneficial for the conservation of the salamander species. [26]

Current conservation efforts

Original 1994 Recovery Plan

The 1994 recovery plan explained that due to the interspecific competition, the Shenandoah salamander differs from other listed species. Because of this competition, it would not be advisable to attempt to increase population numbers, transplant individuals, or reduce naturally occurring competitors. [6] Attempts to repopulate the salamander on talus areas between or adjacent to known populations would be unfeasible, costly, and unnecessary. Instead, recovery attempts should focus on minimizing human-related impacts on the Shenandoah and red-backed salamander populations. [6]

The actions needed for the recovery of the Shenandoah salamander included determining the boundaries of occupied habitat and to determine if additional populations exist, monitoring the known salamander populations on a long-term basis, determining and minimizing the impact of human-related factors such as herbicides and air-pollutants on the salamander, investigating aspects of the salamander’s life history, ensuring compatibility of park maintenance and management activities with the salamander populations, and promoting information exchange on the salamander. This recovery plan was estimated to take 3 fiscal years with a total cost of $155,000. [6]

5-Year reviews

In both 2008 and 2012, a 5-Year Review of several species, including the Shenandoah salamander, was conducted. These reviews aimed to find whether these species were properly classified under the Endangered Species Act. In both reviews the Shenandoah salamander retained the status of “endangered". [27] [28]

Biological Opinion by the U.S. Fish and Wildlife Service

In 2012, the USFWS submitted a Biological Opinion on the National Park Service’s (NPS) management activities, which highlighted some proposed actions to protect the areas of the Shenandoah National Park. This proposed action in fire management, natural resource protection, and natural resource monitoring and research. [14] A policy that would specifically impact the Shenandoah salamander was the proposed aerial spraying of Bacillus thuringiensis as a pest management technique to reduce the impact of gypsy moths.

Supplemental Finding for the Shenandoah Salamander Recovery Plan

An additional resource to the Shenandoah salamander recovery plan was published in July, 2019. This resource explained why it remained impractical, as of 2019, to de-list the Shenandoah salamander. [29] In 1994, the sole threat to the species was competition with the red-backed salamander. In the absence of anthropogenic threats, the USFWS determined that it was not possible to establish criteria to de-list or down-list the species in the foreseeable future. [6] [29] As the species is endemic to higher elevations and the range is protected by the National Park Services, human impacts are minimized. [6] [29]

However, in the time since the 1994 recovery plan, available science has brought the original analysis into question. Since the recovery plan was established, evidence has emerged that climate change may be a primary threat to the species, potentially influencing competition. [29]

Future conservation efforts

As of 2020, there have been no listing changes to the conservation status of the Shenandoah salamander. However, there are several studies set to begin in 2020 by the NPS and United States Geological Survey which will focus on why the Shenandoah salamander is exhibiting greater declines than most amphibian species, and biologists plan to develop a management plan at the conclusion of those studies. [29] The future 5-Year Review (set for 2022) can assess the practicality of amending the recovery plan to include de-listing criteria and updating the plan to include additional threats. [29]

Related Research Articles

<span class="mw-page-title-main">Red-backed salamander</span> Species of amphibian

The red-backed salamander is a small, hardy woodland salamander species in the family Plethodontidae. It is also known as the redback salamander, eastern red-backed salamander, or the northern red-backed salamander to distinguish it from the southern red-backed salamander. The species inhabits wooded slopes in eastern North America, west to Missouri, south to North Carolina, and north from southern Quebec and the Maritime provinces in Canada to Minnesota. It is one of 56 species in the genus Plethodon. Red-backed salamanders are notable for their color polymorphism and primarily display two color morph varieties, which differ in physiology and anti-predator behavior.

<span class="mw-page-title-main">Northern Idaho ground squirrel</span> Species of rodent

The northern Idaho ground squirrel is a species of the largest genus of ground squirrels. This species and the Southern Idaho ground squirrel were previously considered conspecific, together called the Idaho ground squirrel.

<span class="mw-page-title-main">California tiger salamander</span> Species of amphibian

The California tiger salamander is a vulnerable amphibian native to California. It is a mole salamander. Previously considered to be a subspecies of the tiger salamander, the California tiger salamander was recently designated a separate species again. The California tiger salamander distinct population segment (DPS) in Sonoma County and the Santa Barbara County DPS are listed as federally endangered, while the Central California DPS is listed as federally threatened. The Sonoma County, south San Joaquin, and the Santa Barbara County DPS have diverged from the rest of the California tiger salamander populations for over one million years, since the Pleistocene and they may warrant status as separate species.

<span class="mw-page-title-main">Jefferson salamander</span> Species of amphibian

The Jefferson salamander is a mole salamander native to the northeastern United States, southern and central Ontario, and southwestern Quebec. It was named after Jefferson College in Pennsylvania.

<span class="mw-page-title-main">Wyoming toad</span> Species of amphibian

The Wyoming toad, also known commonly as Baxter's toad, is a species of toad in the family Bufonidae. The Wyoming toad is an extremely rare amphibian that exists only in captivity and within Mortenson Lake National Wildlife Refuge in Wyoming in the United States. The Wyoming toad was listed as an endangered species in 1984, and listed as extinct in the wild since 1991. As with black-footed ferrets at the Tom Thorne and Beth Williams Wildlife Research Center at Sybille in Wheatland, Wyoming, the effort to save the Wyoming toad has been a cooperative effort among state and federal agencies and private landowners. The Wyoming toad was common from the 1950s through the early 1970s, but its distribution was limited to the Laramie Basin in Albany County. The population crashed around 1975 and was extremely low by 1980. The Wyoming toad was federally listed as endangered in January 1984. To prevent extinction, a captive-breeding program began in 1989 at the Thorne Williams Unit that produced enough offspring in its first few years to supply seven zoos, and in 1998 the Saratoga National Fish Hatchery received captive-breeding stock. Nearly 46,000 offspring were produced at the Thorne Williams Unit from 1995 until 2006, when the remaining captive stock was moved to the Red Buttes Environmental Biology Laboratory south of Laramie, and then released back into the wild. Before the sharp declines occurred, this toad had been originally classified as Bufo hemiophrys baxteri, a subspecies of the Canadian toad, by Kenneth Raymond Porter in 1968.

<i>Cupressus abramsiana</i> Species of conifer

The Santa Cruz cypress is a species of North American tree within the Cypress family. The species is endemic to the Santa Cruz Mountains within the Santa Cruz and San Mateo counties of west-central California. The U.S. Fish and Wildlife Service listed the species on the Endangered Species Act in 1987 due to increasing threats from habitat loss and disruption of natural forest fire regimes. In 2016, the conservation status of the Santa Cruz cypress changed to Threatened. The cited reasoning was a decrease in threats against their habitat.

<span class="mw-page-title-main">Northern slimy salamander</span> Species of amphibian

The northern slimy salamander is a species of terrestrial plethodontid salamander found throughout much of the eastern two-thirds of the United States.

<span class="mw-page-title-main">Red Hills salamander</span> Species of amphibian

The Red Hills salamander is a fairly large, terrestrial salamander growing to about 255 millimetres (10.0 in). Its body color is gray to brownish without markings, and its limbs are relatively short. It is the official state amphibian of Alabama, the state it is endemic to. It is the only species in the genus Phaeognathus.

<span class="mw-page-title-main">Van Dyke's salamander</span> Species of amphibian

Van Dyke's salamander is a small woodland salamander in the family Plethodontidae, the lungless salamanders. These animals breathe through their skin and are largely terrestrial. Compared to other salamanders in Plethodon it is relatively stocky with long legs. Usually associated with streams, seepages, and rock outcrops, it is endemic to Washington where it is found in a limited number of small, isolated populations.

<span class="mw-page-title-main">Cheat Mountain salamander</span> Species of amphibian

The Cheat Mountain salamander is a species of small woodland salamander in the family Plethodontidae. The species is found only on Cheat Mountain, and a few nearby mountains, in the eastern highlands of West Virginia. It and the West Virginia spring salamander are the only vertebrate species with geographic ranges restricted to that state.

<i>Desmognathus fuscus</i> Species of amphibian

Desmognathus fuscus is a species of amphibian in the family Plethodontidae. The species is commonly called the dusky salamander or northern dusky salamander to distinguish it from populations in the southern United States which form several distinct species, the southern dusky salamanders. The northern dusky salamander is the most widespread representative of its genus in Canada. It can be found in eastern North America from extreme eastern Canada in New Brunswick south to South Carolina. The size of the species' total population is unknown, but is assumed to easily exceed 100,000. The species' habitat differs somewhat geographically; dusky salamanders in the northern part of the range prefer rocky woodland streams, seepages, and springs, while those in the south favor floodplains, sloughs, and muddy places along upland streams. They are most common where water is running or trickling. They hide under various objects, such as leaves or rocks, either in or near water. Alternatively, they may enter burrows for protection. The dusky salamander lays its eggs close to water under moss or rocks, in logs, or in stream-bank cavities. The larval stage which follows is normally aquatic.

<span class="mw-page-title-main">Scott Bar salamander</span> Species of amphibian

The Scott Bar salamander is a species of salamander in the family Plethodontidae, endemic to the United States, where it is restricted to a very small range in the Scott River drainage in Siskiyou County, California, at altitudes between 700 and 1,300 metres above sea level. Described in 2005, it is one of the most recently described species in the large genus Plethodon.

<span class="mw-page-title-main">Caddo Mountain salamander</span> Species of amphibian

The Caddo Mountain salamander is a species of salamander in the family Plethodontidae endemic to Arkansas in the south-central United States, and only known from the Caddo Mountains, a part of the Ouachita Mountains.

<span class="mw-page-title-main">Peaks of Otter salamander</span> Species of amphibian

The Peaks of Otter salamander is a species of salamanders in the family Plethodontidae. It is endemic to the Peaks of Otter area in the Blue Ridge Mountains of Virginia. It is a montane salamander found at elevations above 442 m (1,450 ft), but more commonly above 760 m (2,490 ft). It can be locally common, but its distribution is small and patchy. This makes it vulnerable to local threats such as timber harvesting, recreational development, defoliation by gypsy moths, and spraying to control the latter.

The Jemez Mountains salamander is a species of salamander in the family Plethodontidae endemic to New Mexico in the United States. Its natural habitat is temperate forests. It is threatened by habitat loss, is in rapid decline, and was placed on the IUCN Red List in 2013.

<span class="mw-page-title-main">Cow Knob salamander</span> Species of amphibian

Plethodon punctatus, commonly known as the Cow Knob salamander or white-spotted salamander, is a species of salamander in the family Plethodontidae. It is endemic to high mountain forests on the border of Virginia and West Virginia in the United States. Nearly all occurrences are on Shenandoah Mountain, Nathaniel Mountain and Great North Mountain in George Washington National Forest. Cow Knob salamanders are a member of the P. wehrlei species complex, which includes many other Appalachian salamanders historically referred to Plethodon wehrlei.

The Shenandoah Mountain salamander is a species of salamander in the family Plethodontidae native to the eastern United States. It should not be confused with the Shenandoah salamander, which inhabits Shenandoah National Park, east of Shenandoah Mountain.

<span class="mw-page-title-main">Weller's salamander</span> Species of amphibian

Weller's salamander is a species of salamander in the family Plethodontidae. This species in endemic to the southeastern mountain range of the United States. It is mainly found in North Carolina near Grandfather Mountain. The salamanders have a unique metallic spotting which distinguishes them from other Plethodon species and other salamanders in the area. They mainly inhabit cool forests with rocky areas.

<span class="mw-page-title-main">Amphibians and reptiles of Mount Rainier National Park</span>

There are 14 species of amphibians and 5 species of reptiles known to occur in Mount Rainier National Park.

References

  1. 1 2 3 Amphibian Specialist Group (2023). "Plethodon shenandoah". IUCN Red List of Threatened Species . 2023: e.T17629A1437677. Retrieved 11 December 2023.
  2. "Shenandoah salamander (Plethodon shenandoah)". Environmental Conservation Online System. U.S. Fish & Wildlife Service. Retrieved 6 May 2023.
  3. 1 2 3 4 U. S. Fish and Wildlife Service (1989). Endangered and Threatened Wildlife and Plants; Determination of Threatened Status for the Cheat Mountain Salamander and Endangered Status for the Shenandoah Salamander. Federal Register, 54(159), 34464–34468. 54 FR 34464
  4. Frost, Darrel R. (2017). "Plethodon shenandoah Highton and Worthington, 1967". Amphibian Species of the World: an Online Reference. Version 6.0. American Museum of Natural History. Retrieved 26 September 2017.
  5. Highton, Richard; Worthington, Richard D. (1967). "A new salamander of the genus Plethodon from Virginia". Copeia. 1967 (3): 617–626. doi:10.2307/1442241. JSTOR   1442241.
  6. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 U.S. Fish and Wildlife Service. 1994. Shenandoah salamander (Plethodori shenandoah) Recovery Plan. Hadley, Massachusetts. 36 pp.
  7. 1 2 Highton, Richard; Worthington, Richard D. (1967-09-01). "A New Salamander of the Genus Plethodon from Virginia". Copeia. 1967 (3): 617. doi:10.2307/1442241. JSTOR   1442241.
  8. Zug, George R. (2001). Herpetology : an introductory biology of amphibians and reptiles. Vitt, Laurie J., Caldwell, Janalee P. (2nd ed.). San Diego, Calif.: Academic Press. ISBN   0-12-782622-X. OCLC   47145828.
  9. T. K. Pauley 1980. The ecological status of the Cheat Mountain Salamander. United States Department of Agriculture. Forest Service, Elkins, WV. Report 7798. 160. Pp.
  10. Jaeger, Robert G. (July 1971). "Competitive Exclusion as a Factor Influencing the Distributions of Two Species of Terrestrial Salamanders". Ecology. 52 (4): 632–637. doi:10.2307/1934151. JSTOR   1934151. PMID   28973807.
  11. Hairston, Nelson G.; Nishikawa, Kiisa C.; Stenhouse, Sarah L. (1987-07-01). "The evolution of competing species of terrestrial salamanders: niche partitioning or interference?". Evolutionary Ecology. 1 (3): 247–262. doi:10.1007/BF02067555. ISSN   1573-8477. S2CID   24808561.
  12. Brooks, Maurice (1948-12-31). "Notes on the Cheat Mountain Salamander". Copeia. 1948 (4): 239–244. doi:10.2307/1438709. JSTOR   1438709.
  13. Jaeger, Robert G. (September 1970). "Potential Extinction Through Competition Between Two Species of Terrestrial Salamanders". Evolution. 24 (3): 632–642. doi:10.2307/2406842. JSTOR   2406842. PMID   28562985.
  14. 1 2 U. S. Fish and Wildlife Service (2012). Programmatic Biological Opinion for Shenandoah National Park Ongoing Management Activities.
  15. Jaeger, Robert G. (1974-07-15). "Interference or Exploitation? A Second Look at Competition between Salamanders". Journal of Herpetology. 8 (3): 191–194. doi:10.2307/1563163. JSTOR   1563163.
  16. Thurow, Gordon (1976-10-25). "Aggression and Competition in Eastern Plethodon (Amphibia, Urodela, Plethodontidae)". Journal of Herpetology. 10 (4): 277–291. doi:10.2307/1563064. JSTOR   1563064.
  17. Gergits, William F.; Jaeger, Robert G. (March 1990). "Site Attachment by the Red-Backed Salamander, Plethodon cinereus". Journal of Herpetology. 24 (1): 91. doi:10.2307/1564297. JSTOR   1564297.
  18. Jaeger, Robert G. (1972). "Food as a Limited Resource in Competition between Two Species of Terrestrial Salamanders". Ecology. 53 (3): 535–546. doi:10.2307/1934249. ISSN   1939-9170. JSTOR   1934249.
  19. 1 2 Castelle, A. J.; Galloway, J. N. (1990). "Carbon Dioxide Dynamics in Acid Forest Soils in Shenandoah National Park, Virginia". Soil Science Society of America Journal. 54 (1): 252–257. Bibcode:1990SSASJ..54..252C. doi:10.2136/sssaj1990.03615995005400010040x. ISSN   1435-0661.
  20. Corn, P. S., Stolzenburg, W., & Bury, R. B. (1989). Acid precipitation studies in Colorado and Wyoming: interim report of surveys of montane amphibians and water chemistry. Washington, DC: U.S. Dept. of the Interior, Fish and Wildlife Service, Research and Development.
  21. Harte, John; Hoffman, Erika (1989). "Possible Effects of Acidic Deposition on a Rocky Mountain Population of the Tiger Salamander Ambystoma tigrtinum". Conservation Biology. 3 (2): 149–158. doi:10.1111/j.1523-1739.1989.tb00067.x. ISSN   1523-1739.
  22. Martel, An, et al. “Batrachochytrium Salamandrivorans Sp. Nov. Causes Lethal Chytridiomycosis in Amphibians.” Proceedings of the National Academy of Sciences of the United States of America, vol. 110, no. 38, 2013, pp. 15325–15329. JSTOR, www.jstor.org/stable/42713321. Accessed 2 Apr. 2020.
  23. 1 2 3 Injurious Wildlife Species; Listing Salamanders Due to Risk of Salamander Chytrid Fungus. (2016, January 13). Retrieved from https://www.federalregister.gov/d/2016-00452
  24. 1 2 3 Grant, Evan H. Campbell, et al. “Evidence That Climate Sets the Lower Elevation Range Limit in a High‐Elevation Endemic Salamander.” Ecology and Evolution, vol. 8, no. 15, 2018, pp. 7553–7562., doi : 10.1002/ece3.4198
  25. U. S. Fish and Wildlife Service (1982). Endangered and Threatened Wildlife and Plants; Review of Vertebrate Wildlife for Listing as Endangered or Threatened Species. Federal Register, 47(251), 58454-60.
  26. 1 2 3 Center for Biological Diversity (2015). Petition to the U.S. Department of Interior and the U.S. Fish and Wildlife Service for Rulemakings Designating Critical Habitat for Nine Northeast Species. https://www.biologicaldiversity.org/campaigns/freshwater_mussels/pdfs/CBD_Critical_Habitat_petition_for_9_northeast_species.pdf
  27. U. S. Fish and Wildlife Service (2008). Endangered and Threatened Wildlife and Plants; Initiation of 5-Year Reviews of 10 Listed Species. Federal Register, 73(15), 3991-93.
  28. U. S. Fish and Wildlife Service (2012). Endangered and Threatened Wildlife and Plants; Initiation of a 5-Year Review of Nine Northeastern Species. Federal Register, 77(44), 13251-53.
  29. 1 2 3 4 5 6 U. S. Fish and Wildlife Service Chesapeake Bay Field Office (2019). Supplemental Finding for Shenandoah Salamander (Plethodon shenandoah) Recovery Plan.