Plethodon jordani ranges from southwestern Virginia to extreme northeastern Georgia. Plethodon jordani has been collected from elevations of 213 to 1951 m, but populations are usually constrained to elevations above 600 m. (Petranka, 1998)
Plethodon jordani is restricted to cool, mesic forests. Jordan's salamanders are found in areas with high annual precipitation from deep mountain gorges to the ridgeline in suitable habitat. Populations occur at their lowest elevations in the southern portions of their range. Individuals are most often found on the forest floor during the night when they emerge to forage, they are sometimes found under logs and rocks during the day, although they mostly remain underground when not foraging. Jordan's salamanders are most abundant in red spruce (Picea rubens) - Fraser fir (Abies fraseri) forest but are also found on hardwood-covered ridges. The forest floor where this species is most abundant is covered with a heavy layer of moss with only a little soil over a mass of large boulders. (Petranka, 1998; Stupka and Huheey, 1967)
Plethodon jordani is a large species of Plethodon that varies in color according to locality. The dorsal color varies from slate gray to bluish black and the back usually lacks both red pigments and white spots. Depending on geographic location, the adults may be unmarked or have red cheeks (Great Smoky Mountains, Tennessee), red legs (Nantahala and Tusquitee mountains and on Cheoah Mountain, North Carolina), reddish frosting on the back (extreme northwestern South Carolina and on Fishhawk Mountain, North Carolina), or gold frosting on the back in the southernmost part of their range. Jordan's salamanders have sixteen costal grooves. Adults average 12.5 cm in total length. (Conant and Collins, 1998)
Nests of Plethodon jordani have never been found. Gravid females move underground in late spring or early summer and oviposit in deep underground recesses. Females oviposit in May and hatching usually occurs in late summer or early autumn, about 2 to 3 months after the eggs were deposited. Newborns remain underground for 10 to 12 months after hatching. Metamorphosis occurs before hatching, so individuals emerge from eggs in small adult form, there is no aquatic larval stage. Small individuals judged to be nearly 1 year old first appear on the surface in May or June. Individuals increase by an average of 12 mm (snouth-vent length) between May and October of their second year. (Adams, 2004; Stupka and Huheey, 1967)
Courtship begins when a male approaches a female and being to nudge or tap her with his snout. The male then places his mental gland on the female's nasolabial grooves and begins a "foot dance". The foot dance is described as the limbs being raised and lowered off the ground one at a time. The male then moves towards the female's head. The male turns his head under the female's chin and lifts. The male then begins to circle under the female's chin and laterally moves his tail as he circles her. If the female is responsive, she places her chin on his tail and moves forward to the base of his tail. The couple then engages in a tail-straddle walk that may last for an hour. During the walk the male may turn and slap his mental gland on the female's nasolabial region. The male eventually stops moving and begins a series of lateral rocking movements of his sacrum. The female begins with a series of head movements, opposite to the rocking movements of the male. The male then presses his vent to the substratum and releases a spermatophore. Next he flexes his tail to one side and leads the female forward. She stops when her vent is over the spermatophore, then lowers her sacrum and picks up the sperm cap. During this process the male arches the sacral region and does "push-ups" with his hind limbs. The pair usually splits up after the spermatophore is deposited even if the female is unsuccessful at picking it up.
Females may court several times and mate with two or more males in one season. Males will often attempt to mate other males and mimic the behaviors of a female. This is a form of competition in which males cause other males to waste their gametes. In a laboratory study, researchers inhibited females from smelling the male's pheromones, which greatly reduced the response of the female to the courtship ritual. In most cases the female did not respond at all to the male during courtship behavior. (Adams, 2004; Arnold and Feder, 1982)
Male Plethodon jordani mature sexually at approximately 3 years of age. An estimated 25% of females oviposit for the first time 4 years after hatching, another 25% oviposit for the first time 1 year later. The remaining 50% wait until they are 6 years old before they oviposit for the first time. After their first oviposit, females reproduce every other year for the remainder of their lives. Clutch sizes of 3 to 10 have been estimated. (Adams, 2004)
Plethodon jordani is a solitary species active during moist weather. Plethodon salamanders in general are mostly found in moist areas. Plethodon jordani tends to move to areas where moisture is the greatest within its preferred habitat. (Dunn, 1926)
In a study discussed by Petranka (1998), Plethodon salamanders were studied to determine home range and territory size. In the study the maximum distance moved for males was 120.4 meters and 60.6 meters for females. Plethodon jordani is an exceptionally philopatric species of Plethodon and home range sizes may be only a few square meters. (Petranka, 1998)
The most common form of communication for Plethodon jordani is the use of pheromones. These chemicals play a key role in courtship behaviors and the act of mating. (Martof, et al., 1980; Petranka, 1998)
Both male and female salamanders eat the same type and size of prey. On dry nights the majority of individuals will forage on vegetation, whereas, on wet nights, they will roam the forest floor in search of invertebrate prey. Food items in 204 specimens from the Great Smoky Mountains included annelids, snails, millipedes, centipedes, isopods, phalangids, pseudoscorpions, mites, spiders, and a variety of insects. Millipedes are more important during the spring and insect larvae are more important during the fall. Collembolans and annelids tend to increase in importance in higher altitudes. In a study performed by Whitaker and Rubin (1971), the 10 most important prey by volume were: ants, spiders, lepidopteran larvae, beetle larvae, collembolans, millipedes, centipedes, mites, snails, and dipteran larvae. (Conant and Collins, 1998)
Common garter snakes (Thamnophis sirtalis) are the largest threats to Plethodon salamanders. The first defense mechanism of Jordan’s salamanders is the bright red cheeks or legs possessed by some individuals. This aposematic coloration is a warning sign to predators. Snake predation upon Plethodon salamanders also elicits other behaviors, including writhing and thrashing movements that coat the predator with slimy secretions, tail autotomy (tail loss), and biting. Bennett and Licht (1974) suggested that the particular antipredator behaviors of amphibian species are correlated with the extent of anaerobiosis during a burst of activity. According to a study by Arnold and Feder (1982), predatory encounters are especially suitable for demonstration of anaerobiosis during spontaneous natural activity, if it does occur. In one trial conducted by Arnold and Feder (1982), a Jordan's salamander escaped the snake by producing thick secretions which actually glued the snake to the substrate (rendering it immobile). Predatory birds are also likely to be important predators of Jordan's salamanders, especially at higher elevations where there are fewer garter snakes. (Arnold and Feder, 1982)
Hairston et al. (1956) conducted a series of studies on interspecific relationships between P. jordani and P. oconaluftee in the southern Appalachians. In all the studies, the researchers found that the removal of P. jordani caused an increase in P. ocanaluftee. Removal of P. ocanaluftee did not affect P. jordani but did increase the proportion of juveniles in the population. Hairston et al. concluded that competition did exist between the two species but they could not conclude which resource they were competing for. (Hairston, 1956; Petranka, 1998)
There is no known benefit provided to humans from Plethodon jordani
There are no known adverse effects of Plethodon jordani on humans.
Populations of Plethodon jordani and other salamanders are often absent or greatly reduced in number on recent clear-cuts in western North Carolina. Less intensive harvesting practices that leave the basic structure of the forest intact would benefit this and other salamander species in southern Appalachian forests. (Mitchell and Reay, 1999; Petranka, 1998)
Highton (2005) noted significant decline (>40%) across the range of Plethodon. Logging roads, even those no longer in use, have been shown to negatively affect Plethodon abundance. (Highton, 2005; Rittenhouse and Semlitsch, 2006)
There are disagreements in the literature with species and subspecies distinctions. According to the latest data, color variation and geographic location are the two main factors in determining the species identification of a particular salamander. There are disagreements in the literature with species and subspecies distinctions. (Adams, 2004; Petranka, 1998; Adams, 2004; Petranka, 1998; Adams, 2004; Petranka, 1998; Adams, 2004; Petranka, 1998)
The Plethodon jordani complex was recently recognized by Highton and Peabody (2000), which contains 7 species (P. jordani, P. metcalfi, P. shermani, P. cheoah, P. amplus, P. meridianus, and P. montanus). The splitting of P. jordani appears to be gaining acceptance. (Center for North American Herpetology, 2008)
Tanya Dewey (editor), Animal Diversity Web.
Andrea Helton (author), Radford University, Karen Francl (editor, instructor), Radford University.
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.
having coloration that serves a protective function for the animal, usually used to refer to animals with colors that warn predators of their toxicity. For example: animals with bright red or yellow coloration are often toxic or distasteful.
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.
an animal that mainly eats meat
uses smells or other chemicals to communicate
animals which must use heat acquired from the environment and behavioral adaptations to regulate body temperature
union of egg and spermatozoan
an animal that mainly eats leaves.
forest biomes are dominated by trees, otherwise forest biomes can vary widely in amount of precipitation and seasonality.
An animal that eats mainly plants or parts of plants.
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.
An animal that eats mainly insects or spiders.
fertilization takes place within the female's body
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).
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.
eats mollusks, members of Phylum Mollusca
having the capacity to move from one place to another.
This terrestrial biome includes summits of high mountains, either without vegetation or covered by low, tundra-like vegetation.
the area in which the animal is naturally found, the region in which it is endemic.
active during the night
reproduction in which eggs are released by the female; development of offspring occurs outside the mother's body.
chemicals released into air or water that are detected by and responded to by other animals of the same species
an animal which has a substance capable of killing, injuring, or impairing other animals through its chemical action (for example, the skin of poison dart frogs).
the kind of polygamy in which a female pairs with several males, each of which also pairs with several different females.
communicates by producing scents from special gland(s) and placing them on a surface whether others can smell or taste them
breeding is confined to a particular season
remains in the same area
reproduction that includes combining the genetic contribution of two individuals, a male and a female
uses touch to communicate
that region of the Earth between 23.5 degrees North and 60 degrees North (between the Tropic of Cancer and the Arctic Circle) and between 23.5 degrees South and 60 degrees South (between the Tropic of Capricorn and the Antarctic Circle).
Living on the ground.
uses sight to communicate
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Center for North American Herpetology, 2008. "The Center for North American Herpetology web portal" (On-line). Accessed January 21, 2008 at http://www.cnah.org/index.asp.
Conant, R., J. Collins. 1998. A field guide to reptiles & amphibians : eastern and central North America. Boston: Houghton Mifflin.
Dunn, E. 1926. The Salamanders of the Family Plethodontidae. Northampton, Mass.: Smith College.
Goin, C., O. Goin. 1962. Introduction to Herpetology. USA: W.H. Freeman and Company.
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Highton, R. 2005. Declines of eastern North American Woodland Salamanders (Plethodon). Pp. 34-46 in M Lanoo, ed. Amphibian Declines. Berkeley, California: University of California Press.
Houck, L., A. Bell, N. Reagan-Wallin, R. Feldhoff. 1998. Effects of Experimental Delivery of Male Courtshop Pheromones on the Timing of Courtship in a Terrestrial Salamander, Plethodon jordani. Copeia, 1: "214-219.
Martof, B., W. Palmer, J. Bailey, J. Harrison. 1980. Amphibians and Reptiles of the Carolina and Virginia. North Carolina: The University of North Carolina Press.
Mitchell, J., K. Reay. 1999. Atlas of Amphibians and Reptiles in Virginia. Richmond: Virginia Department of Game and Inland Fisheries.
Petranka, J. 1998. Salamanders of the United States and Canada. Washington: Smithsonian Institution Press.
Rittenhouse, T., R. Semlitsch. 2006. Grasslands as movement barriers for a forest-associated salamander: migration behavior of adult and juvenile salamanders at a distinct habitat edge. Biological Conservation, 131: 14-22.
Stupka, A., J. Huheey. 1967. Amphibians and Reptiles of the Great Smoky Mountains Nation Park. Knoxville, TN: University of Tennessee Press.