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Ocoee Salamander with red legs
Dark colored Ocoee Salamander

Description[edit]

The Ocoee salamander (Desmognathus ocoee) is a small mountain dusky salamander that exhibits a wide range of colors and patterns. Some individuals have distinct red, yellow, or orange patches on their legs and cheeks. Populations in central Tennessee, northwestern Georgia, and northeastern Alabama usually have a dark brown or black color, and faded larval spots. Compared to other Desmognathus species, Desmognathus ocoee have smaller bodies (around 7-11 cm), shorter and narrower heads, longer limbs, and no vomerine teeth in adult males[1]. Juveniles have pairs of alternating pale spots on their middorsal line. As they move on to adulthood, these spots might fuse[2].

Habitat and Distribution[edit]

Habitat[edit]

Semi-aquatic salamanders like the Ocoee salamander contribute considerably to terrestrial vertebrate biomass. Their dependence on water for reproduction and their short larval period allows them to take advantage of wetted habitats such as small streams and wet rock faces. Despite this, they are the most terrestrial of the stream-breeding Desmognathus salamanders. Under moist conditions, they will leave streambeds and move into the forest. They prefer cove forests of more than 85 years of age, with a significant amount of emergent rocks. These rocks are important for soil moisture retention, and are thus vital for the survival of D. ocoee eggs during brooding. As vertebrate predators, D. ocoee are integral to the dynamics of the food webs around their habitat. They eat invertebrates, insects, flies, ants, wasps, beetles, spiders, mites, and a whole variety of other organisms. They can often be found some distance from a water source, usually in the forest at higher elevations. Population densities on wet rock faces are around six adults per meter square. Overall, the population trends for the Ocoee salamanders in the Appalachian Mountains have not changed significantly in the last twenty years[3].

Geographic distribution, including map[edit]

The species gets its name from the flower Passiflora incarnata (Passionflower), which is the Tennessee state wildflower and the state symbol. The Cherokee in the area called this flower ocoee. The Ocoee River and the Ocoee salamander were thus named after the Cherokee word for passionflower[1].

Population structure, speciation, and phylogeny[edit]

Close relatives[edit]

The Ocoee salamander has gone through various classifications in the last century. Originally considered a single species (D. ochrophaeus), populations of Desmognathus salamanders across the Appalachians are now divided into five distinct species D. abditus, D. carolinensis, D. ochrophaeus, D. ocoee, and D. orestes. These five species don’t form a phylogenetic clade and are differently related to one another, but complete reproductive isolation is rarely observed in distantly related Desmognathus, and thus some hybridization between geographically-close lineages occurs. The “gray zone” that contains the potential arguments on species delimitation still exists, but genetic analyses provide enough evidence for the delimitation of these five species[1].

Genetic population structure[edit]

Before the advancement of genetic and molecular techniques, the classification of plethodontids was limited by geographical and morphological differences between individuals and groups. This was not a very accurate method for taxonomy because the color patterns and phenotypic variations among the family of Plethodontids was conserved and the genetic underpinnings of these morphological traits were not well known. In genetic studies in the past few decades, by the use of biochemical markers, it’s been shown that this conservatism of morphological traits in many of the salamanders of the Plethodontidae family actually sometimes masks complex patterns of genetic differentiation. These genetic studies ultimately allowed for better-defined species delimitation of Desmognathus ocoee[4].

Mating[edit]

Pheromones[edit]

Pheromonal communication is very common in salamanders, newts, and even in some frogs and toads. Pheromones are chemosensory stimuli that are used to signal information between individuals of the same species. In vertebrates, there are two types of pheromones. Releasing pheromones are usually peptides and proteins that influence behaviors (such as male-female or male-male interactions) through neural systems that detect and process pheromones. Priming pheromones modify the endocrine system or the psychological mood of the individual. Usually, these different types of pheromones exist as a mixture, so they have complex behavioral and psychological effects. Pheromones from other individuals are detected by the chemosensory receptors on the vomeronasal organ and main olfactory epithelium[5]. Chemosensory cues such as pheromones play an important role in mating because they bring males and females together in both aquatic and terrestrial environments. These cues can signal a variety of information to others in the surrounding area, including the species, sex, and the reproductive condition of the individual. Once suitable partners have been attracted, these cues can also help determine mate quality[5].

Courting[edit]

Sexually active adults use a variety of tools to court each other before copulation occurs. As is common in the plethodontids, a female is exposed to tactile, chemical, and visual stimuli presented by the male. The females will also signal attractivity through chemical cues, inhibited tendencies to flee from courting males, and a willingness to engage in tail-straddle walk, which is the phase in courtship where insemination occurs. This course of behaviors from both individuals will lead to successful copulation[6].

Copulation[edit]

Ocoee salamanders do internal fertilization. When a female is ready for mating, the male uses a spermatophore to transfer his sperm to a female. A spermatophore is a gelatinous capsule containing spermatozoa, and it is accepted into the female’s reproductive organ, the cloaca, where it is stored until fertilization. The male typically leads the female to the spermatophore for her to pick it up[5].

Number of mates[edit]

Ocoee salamanders do internal fertilization and thus postcopulatory sexual selection plays an important role in their reproduction. In adult Desmognathus ocoee, the mating period lasts from early fall to late spring. Females tend to engage in multiple matings throughout these 9 months, and store sperm in their bodies for extensive periods. This means that a clutch of female eggs can be fertilized by stored sperm from multiple competing males. Usually it’s around two to three males. Sperm competition within males is thus an important aspect of sexual selection. Sperm from the males are stored in spermatheca, an organ in the female’s reproductive tract, until June and July, during which ovulation, fertilization, and oviposition all occur rapidly. Until the fertilization event, sperm require hospitable conditions to survive in, and are stored in the spermatheca, where they remain viable[7].

Females that experience courtship that ends with successful insemination do not become inseminated when they encounter sexually active males for about four nights after the first insemination. This is caused by a temporary inhibition of female sexual responsiveness, which happens during the initial insemination. Upon the female taking in the spermatophore into her reproductive tract, the sperm mass remains externally visible in the female’s cloaca for around 38 hours. This extended stay of the sperm mass likely results in tactical and chemical stimulation, which inhibits the female’s sexual responsiveness and her willingness to perform behavioral patterns necessary for successful courtship and sperm transfer. Ultimately, this seems to be a mechanism developed in males to compete with other males for egg fertilization[6].

Parental Care[edit]

Oviposition[edit]

When the time comes, ovulation and fertilization occur. As a final step, oviposition occurs from June to September on land, after which the female tends her clutch of 9-32 eggs for 6-8 weeks. Clutch sizes can vary from female to female, and is closely related to the body size of the female. During oviposition, females tend to deposit their eggs in cavities under rocks, moss, decaying logs, leaf litter, springs, and behind vegetation or in other crevices. It is important to pick a spot with just enough moisture to avoid the desiccation and loss of eggs[7].

Egg guarding[edit]

After oviposition, maternal care for the clutch lasts for about 3 months, and ends after the eggs hatch into larvae. Maternal care during brooding includes defense against predators, removal of dead eggs, reduction of egg desiccation and fungal infections, and helping the hatchlings with cracking open their shells. If left unguarded, the eggs are in danger of being eaten by surrounding salamanders. Males do not provide resources to either the female or the offspring[7].

Oophagy seems to be a normal behavior in brooding females, but is usually suppressed. In the case of limited foraging availability, disturbed or starved females may choose to eat their own eggs. This may also be done if the egg is dead-- the female will eat the dead egg in order to remove it from the clutch before it infects other eggs around it. Fungal infections from dead eggs (if not removed in time) will usually lead to the embryos in viable eggs being smothered and killed[8].

Larvae are smaller than in other subspecies, reaching around 8-10 mm at hatching. Upon hatching, D. ocoee larvae have short and silvery external gills, and they often have distinctive larval spots that other species don’t have. The tails of the larvae are keeled and they narrow to a knife edge along the dorsal surface. Once out of the egg, the larvae quickly disperse to a nearby water source. During their development, they are found in shallow waters or in thin films of water, they feed on small aquatic invertebrates. In captivity, they can also eat worms. Usually, the larvae metamorphose into their adult form in the following few weeks, the time depending on the availability of food, other resources in the environment, and the temperature[9].

References[edit]

  1. ^ a b c Pyron, R. Alexander, and David A. Beamer. “Systematics of the Ocoee Salamander (Plethodontidae: Desmognathus Ocoee), with Description of Two New Species from the Southern Blue Ridge Mountains.” Zootaxa, vol. 5190, no. 2, 2022, pp. 207–240., https://doi.org/10.11646/zootaxa.5190.2.3.
  2. ^ Valentine, Barry D. “Variation and Distribution of Desmognathus Ocoee Nicholls (Amphibia: Plethodontidae).” Copeia, vol. 1961, no. 3, 1961, p. 315., https://doi.org/10.2307/1439806. Accessed 13 Oct. 2022.
  3. ^ Connette, Grant M., et al. “The Distribution of Stream-Breeding Salamander, Desmognathus Ocoee, in Terrestrial Habitat Suggests the Ecological Importance of Low-Order Streams.” Copeia, vol. 104, no. 1, 2016, pp. 149–56. JSTOR, http://www.jstor.org/stable/44972610. Accessed 13 Oct. 2022.
  4. ^ Tilley, Stephen G., and Meredith J. Mahoney. “Patterns of Genetic Differentiation in Salamanders of the Desmognathus Ochrophaeus Complex (Amphibia: Plethodontidae).” Herpetological Monographs, vol. 10, 1996, pp. 1–42. JSTOR, https://doi.org/10.2307/1466979. Accessed 13 Oct. 2022.
  5. ^ a b c Woodley, Sarah K. “Pheromonal Communication in Amphibians.” Journal of Comparative Physiology A, vol. 196, no. 10, 2010, pp. 713–727., https://doi.org/10.1007/s00359-010-0540-6.
  6. ^ a b Verrell, Paul A. “Insemination Temporarily Inhibits Sexual Responsiveness in Female Salamanders (Desmognathus Ochrophaeus).” Behaviour, vol. 119, no. 1/2, 1991, pp. 51–64. JSTOR, http://www.jstor.org/stable/4534975. Accessed 13 Oct. 2022.
  7. ^ a b c Adams, Erika M., et al. “Multiple Paternity in a Natural Population of a Salamander with Long-Term Sperm Storage.” Molecular Ecology, vol. 14, no. 6, 2005, pp. 1803–1810., https://doi.org/10.1111/j.1365-294x.2005.02539.x.
  8. ^ Tilley, Stephen G. “Aspects of Parental Care and Embryonic Development in Desmognathus Ochrophaeus.” Copeia, vol. 1972, no. 3, 1972, pp. 532–40. JSTOR, https://doi.org/10.2307/1442927. Accessed 13 Oct. 2022.
  9. ^ Tilley, Stephen G., et al. “Systematics of Dusky Salamanders, Desmognathus (Caudata: Plethodontidae), in the Mountain and Piedmont Regions of Virginia and North Carolina, USA.” Zoological Journal of the Linnean Society, vol. 152, no. 1, 2008, pp. 115–130., https://doi.org/10.1111/j.1096-3642.2007.00336.x.