Plethodon kiamichi

Highton, 1989

Kiamichi Slimy Salamander

G2Imperiled Found in 1 roadless area NatureServe Explorer →
G2ImperiledGlobal Rank
VulnerableIUCN
Very high - mediumThreat Impact
Identity
Unique IDELEMENT_GLOBAL.2.103518
Element CodeAAAAD12330
Record TypeSPECIES
ClassificationSpecies
Classification StatusStandard
Name CategoryVertebrate Animal
IUCNVulnerable
Endemicendemic to a single nation
KingdomAnimalia
PhylumCraniata
ClassAmphibia
OrderCaudata
FamilyPlethodontidae
GenusPlethodon
Concept Reference
Highton, R., G.C. Maha, and L.R. Maxson. 1989. Biochemical evolution in the slimy salamanders of the Plethodon glutinosus complex in the eastern United States. Illinois Biological Monographs 57:1-153.
Taxonomic Comments
Highton et al. (1989) regarded P. glutinosus (sensu lato) as a complex of multiple species, most of which can be recognized only by biochemical characteristics (allele frequencies). Taxa formerly included in P. glutinosus and recognized as distinct species by Highton et al. (1989) include: P. teyahalee, P. chattahoochee, P. chlorobryonis, P. variolatus, P. ocmulgee, P. kiamichi, P. mississippi, P. kisatchie, P. sequoyah, P. grobmani, P. cylindraceus, P. albagula, P. savannah, P. aureolus, and P. kentucki. Some salamander taxonomists question the practice of recognizing species that are distinguished only by differences in allele frequencies, particularly in the absence of direct information on reproductive isolation (Wake, in Highton et al. 1989; Frost and Hillis 1990).

Petranka (1998) regarded P. aureolus, P. kentucki, and P. teyahalee (as P. oconaluftee) as distinct species, but he regarded P. chattahoochee, P. chlorobryonis, P. variolatus, P. ocmulgee, P. kiamichi, P. mississippi, P. kisatchie, P. sequoyah, P. grobmani, P. cylindraceus, P. albagula, and P. savannah as conspecific with (and junior synonyms of) P. glutinosus. Petranka felt that the split of P. glutinosus into multiple species was premature because of the lack of detailed information on genetic interactions at contact zones between the nominal taxa.
Conservation Status
Rank MethodLegacy Rank calculation - Excel v3.1x
Review Date2017-12-15
Change Date2001-10-01
Edition Date2017-12-15
Edition AuthorsHammerson, G. (2001), Smith-Patten, B. and D. B. Shepard (2017)
Threat ImpactVery high - medium
Range Extent250-5000 square km (about 100-2000 square miles)
Number of Occurrences6 - 20
Rank Reasons
Plethodon kiamichi is a regional endemic that is currently documented as being restricted to the Kiamichi Mountains, a subrange of the Ouachita Mountains that is >1700 km sq. in extent. The species’ area of occupancy is much more limited, possibly as little as 100 km sq., given that it is found primarily on northerly facing slopes. The vast majority of the species’ range is found within Oklahoma (only about 25 km sq. of the species’ described range lies in Arkansas). The species has been documented from only one county in Arkansas (Polk) and three counties in Oklahoma (Atoka, Le Flore, and Pushmataha). The majority (approximately 75%) of the species’ limited range is not protected, is highly fragmented, and is regularly logged by clearcutting of pine plantations. The threat risk, as calculated by NatureServe’s rank/threat assessment calculator, ranges from medium to very high.
Range Extent Comments
Plethodon kiamichi is restricted to the Kiamichi Mountains, a subrange of the Ouachita Mountains that is >1700 km sq. in extent. The vast majority of the species’ range is found within Oklahoma (only about 25 km sq. of the species’ described range lies in Arkansas). The species has been documented from only one county in Arkansas (Polk) and three counties in Oklahoma (Atoka, Le Flore, and Pushmataha). Known occurrences encompass about 500 km sq.

It should be noted that preliminary results of genetic sequencing indicate that P. kiamichi may have a wider distribution than once thought (DB Shepard, pers. comm.); however, for now the species’ range should be considered as being confined to the Kiamichi Mountains, spanning from its farthest eastern reaches in Polk County, Arkansas, to its foothills in the McGee Creek Natural Scenic Area, Atoka County, Oklahoma.
Occurrences Comments
There are currently 13-15 confirmed localities if calculating using the separation distances of 1 km for unsuitable habitat and 3 km for suitable habitat.
Threat Impact Comments
The majority (approximately 75%) of the species’ limited range is not protected, is highly fragmented, and is regularly logged by clearcutting of pine plantations. Other threats include herbicide and pesticide use, being killed on roadways, and issues related to climate change. Climate change will likely be a future threat if it produces more xeric conditions and the species is unable to find sufficient refugia. More erratic temperatures, droughts, and storms would also impact this species.
Ecology & Habitat

Description

Black dorsally (on the back) with small whitish or brassy spots or flecks that also extend to sides where spotting may be heavier (Sievert & Sievert 2011). Individual variation in spotting. Dark gray or slate ventrally (on the belly) with pale spotting. Dark or strongly mottled throat.

Diagnostic Characteristics

Length: 4.5-6.0 inches (11.4-15.2 cm, total length, as reported by Sievert & Sievert 2011; 4.8-7.5 cm SVL, as reported by Anthony 2005)

Habitat

Generally found at higher elevations on northerly facing slopes having mesic oak-hickory forest (Sievert and Sievert 2011) and sometimes ravines (Anthony 2005). The shortleaf pine-dominated southerly facing slopes and the valleys between ranges are likely dispersal barriers for the species. The lower elevation range limits are not well known. Found under or in rotting logs, stumps, leaf litter, or under rocks (G Hammerson, in litt.).

Reproduction

Development is direct, meaning that larvae develop within the egg and then emerge as a miniature adults. Eggs are laid in rotting logs, underground, or in rock crevices (G Hammerson, in litt.). Other aspects of reproduction are not well known.
Terrestrial Habitats
Forest - Hardwood
Other Nations (1)
United StatesN2
ProvinceRankNative
ArkansasS1Yes
OklahomaS2Yes
Threat Assessments
ThreatScopeSeverityTiming
4 - Transportation & service corridorsRestricted (11-30%)Negligible or <1% pop. declineHigh (continuing)
4.1 - Roads & railroadsRestricted (11-30%)Negligible or <1% pop. declineHigh (continuing)
5 - Biological resource usePervasive (71-100%)Serious - moderateHigh (continuing)
5.3 - Logging & wood harvestingPervasive (71-100%)Serious - moderateHigh (continuing)
9 - PollutionLarge (31-70%)Moderate - slightHigh (continuing)
9.3 - Agricultural & forestry effluentsLarge (31-70%)Moderate - slightHigh (continuing)
11 - Climate change & severe weatherPervasive (71-100%)Serious - moderateHigh (continuing)
11.2 - DroughtsPervasive (71-100%)Serious - moderateHigh (continuing)
11.3 - Temperature extremesPervasive (71-100%)Serious - moderateHigh (continuing)
11.4 - Storms & floodingLarge (31-70%)Moderate - slightHigh (continuing)

Roadless Areas (1)
Oklahoma (1)
AreaForestAcres
Beech CreekOuachita National Forest8,303
References (11)
  1. Anthony, C. D. 2005a. <i>Plethodon kiamichi</i> Highton, 1989, KIAMICHI SLIMY SALAMANDER. Pages 819-820 in M. Lannoo, editor. Amphibian Declines: The Conservation Status of United States Species. University of California Press, Berkeley, California, USA.
  2. Crother, B. I. (editor). 2017. Scientific and standard English names of amphibians and reptiles of North America north of Mexico, with comments regarding confidence in our understanding. 8th edition. SSAR Herpetological Circular 43:1-104. [Updates in SSAR North American Species Names Database at: https://ssarherps.org/cndb]
  3. Frost, D. R. 2017. Amphibian Species of the World: an Online Reference. Version 6.0. Electronic Database accessible at http://research.amnh.org/herpetology/amphibia/index.html. American Museum of Natural History, New York, USA.
  4. Frost, D.R. 2020. Amphibian Species of the World: an Online Reference. Version 6.0. American Museum of Natural History, New York, USA. Online: http://research.amnh.org/herpetology/amphibia/index.html
  5. Frost, D. R., and D. M. Hillis. 1990. Species in concept and practice: herpetological applications. Herpetologica 46:87-104.
  6. Highton, R., G.C. Maha, and L.R. Maxson. 1989. Biochemical evolution in the slimy salamanders of the <i>Plethodon glutinosus</I> complex in the eastern United States. Illinois Biological Monographs 57:1-153.
  7. Highton, R., R. M. Bonett, and E. L. Jockusch. 2017. Caudata - Salamanders. In Scientific and standard English names of amphibians and reptiles of North America north of Mexico, with comments regarding confidence in our understanding. Eighth edition. Society for the Study of Amphibians and Reptiles, Herpetological Circular No. 43.
  8. Petranka, J. W. 1998. Salamanders of the United States and Canada. Smithsonian Institution Press, Washington, D.C.
  9. Powell, R., R. Conant, and J. T. Collins. 2016. Peterson Field Guide to Reptiles and Amphibians of Eastern and Central North America, fourth edition. Houghton Mifflin Harcourt, Boston and New York. 512 pp.
  10. Sievert, G., and L. Sievert. 2011. A field guide to Oklahoma’s Amphibians and Reptiles. Oklahoma Department of Wildlife Conservation, Oklahoma City, Oklahoma, USA.
  11. Wake, D. B., and E. L. Jockusch. 2000. Detecting species borders using diverse data sets: examples from plethodontid salamanders in California. Pages 95-119 in Bruce, R. C., R. G. Jaeger, and L. D. Houck, editors. The biology of plethodontid salamanders. Kluwer Academic/Plenum Publishers, New York.