dcsimg

Description

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This salamander ranges from 6.5 to 14 cm in length. Terrestrial N. viridescens ("red efts") are juveniles and thus generally smaller in size (3.5 to 8.6 cm in length); efts are orange-red to reddish-brown in color. Aquatic adults are generally green with two dorsal rows of red to orange spots; the dorsum may also be yellow-brown, olive-green, or dark brown. The venter is yellow. Breeding aquatic males have brighter and redder spots than females (Davis and Grayson 2008), as well as enlarged hind legs, swollen vents and a broadly keeled tail, and black keratinized structures on the inner thigh and toe regions (Behler and King 1996). Terrestrial adults have granular skin, in contrast to aquatic adults, which have smooth mucous skin (Walters and Greenwald 1977).Subspecies include N. v. dorsalis, N. v. louisianesis, N. v. piaropicola, and N. v. viridescens (Behler and King 1996) . However, phylogenetic analyses have identified clades that do not correspond to the current subspecies designations (Takahashi 2008).

References

  • Bommarito, T. (2009). Toxicity of Sediments Containing Coal-tar Pavement Sealants to Notophthalmus viridescens and Ambystoma maculatum, Surrogate Species for Eurycea sosorum. M. S. Thesis. Southern Illinois University at Carbondale
  • Brandon, R. A., Labanick, G. M., and Huheey, J. E. (1979). ''Learned avoidence of brown efts, Notophthalmus viridescen louisianensis (Amphibia, Urodela, Salamandridae), by chickens.'' Journal of Herpetology, 13, 171-176.
  • Brimley, C. S. (1921). ''The life history of the American Newt.'' Copeia, 1921, 31-32.
  • Brodie, E. D. (1968). ''Investigations on the skin toxin of the red-spotted newt, Notophthalmus viridescens viridescens.'' American Midland Naturalist, 80, 276-280.
  • Brodie, E. D. Jr., and Formanowicz, D. R. Jr. (1981). ''Larvae of the predaceous diving beetle Dytiscus verticalis acquire an avoidance response to skin secretions of the newt Notophthalmus viridescens.'' Herpetologica, 37, 172-176.
  • Davis, A. K., and Grayson, K. L. (2007). ''Improving natural history research with image analysis: the relationship between skin color, sex, size, and stage in adult red-spotted newts (Notophthalmus viridescens viridescens).'' Herpetological Conservation and Biology , 2, 65-70.
  • Davis, A. K., and Grayson, K. L. (2008). ''Spots of adult male red-spotted newts are redder and brighter than in females: evidence for a role in mate selection?'' Herpetological Journal, 18, 83-89.
  • DuRant, S. E., and Hopkins, W. A. (2008). ''Amphibian predation on larval mosquitoes.'' Canadian Journal of Zoology, 86, 1159-1164.
  • Duffus, A. L. J., Wozney, K., Brunetti, C. R., and Berrill, M. (2008). ''Frog virus 3-like infections in aquatic amphibian communities.'' Journal of Wildlife Diseases, 44, 109-120.
  • Forester, D. C. and Lykens, D. V. (1991). ''Age structure in a population of red-spotted newts from the Allegheny Plateau of Maryland.'' Journal of Herpetology, 25, 373-376.
  • Gage, S. H. (1891). ''Life-history of the vermilion-spotted newt (Diemyctylus viridescens Raf.).'' American Naturalist, 25, 1084-1110.
  • Gill, D. E. (1978). ''Effective population size and interdemic migration rates in a metapopulation of the red-spotted newt, Notophthalmus viridescens (Rafinesque).'' Evolutionary Ecology Research, 32, 839-849.
  • Gill, D. E. (1978). ''The metapopulation ecology of the red-spotted newt, Notophthalmus viridescens (Rafinesque).'' Ecological Monographs, 48, 145-166.
  • Grayson, K. L., and Wilbur, H. M. (2009). ''Sex- and context-dependent migration in a pond-breeding amphibian.'' Ecology, 90, 306-312.
  • Healy, W. R. (1973). ''Terrestrial activity and home range in efts of Notophthalmus viridescens.'' American Midland Naturalist, 93, 131-138.
  • Howard, R. R., and Brodie, E. D. (1971). ''Experimental study of mimicry in salamanders involving Notophthalmus viridescens viridescens and Pseudotriton ruber schencki.'' Nature, 233, 277.
  • Huheey, J. E.. and Brandon, R. A. (1974). ''Studies in warning coloration and mimicry. VI. Comments on the warning coloration of red efts and their presumed mimicry by red salamanders.'' Herpetologica, 30, 149-155.
  • Hurlbert, S. H. (1970). ''Predator responses to the vermilion-spotted newt (Notophthalmus viridescens).'' Journal of Herpetology, 4, 47-55.
  • Morgan, A. H., and Grierson, M. C. (1932). ''Winter habits and yearly food consumption of adult spotted newts, Triturus viridescens.'' Ecology, 13, 54-62.
  • Padgett-Flohr, G. E., Bommarito, T., and Sparling, D. (2007). ''Amphibian chytridiomycosis in commercially purchased research amphibians.'' Herpetological Review, 38, 390-393.
  • Park, D., Hempleman, S. C., and Propper, C. R. (2001). ''Endosulfan exposure disrupts pheromonal systems in the red-spotted newt: a mechanism for subtle effects of environmental chemicals.'' Environmental Health Perspectives, 109, 669-673.
  • Park, D., and Propper, C. R. (2002). ''Endosulfan affects pheromonal detection and glands in the male red-spotted newt, Notophthalmus viridescens.'' Bulletin of Environmental Contaminants and Toxicology, 69, 609-616.
  • Pough, F. H. (1971). ''Leech-repellent property of eastern red-spotted newts, Notophthalmus viridescens.'' Science, 174, 1144-1146.
  • Raffel, T. R., Bommarito, T., Barry, D. S., Witiak, S. M., and Shackelton, L. A. (2008). ''Widespread infection of the Eastern red-spotted newt (Notophthalmus viridescens) by a new species of Amphibiocystidium, a genus of fungus-like mesomycetozoan parasites not previously reported in North America.'' Parasitology, 135, 203-215.
  • Raffel, T. R., Michel, P. J., Sites, E. W., and Rohr, J. R. (2010). ''What drives chytrid infections in newt populations? Associations with substrate, temperature, and shade.'' EcoHealth, doi: 10.1007/s10393-010-0358-2.
  • Relyea, R. A., and Jones, D. K. (2009). ''The toxicity of Roundup Original Max® to 13 species of larval amphibians.'' Environmental Toxicology and Chemistry, 28, 2004-2008.
  • Roe, A. W., and Grayson, K. L. (2008). ''Terrestrial movements and habitat use of juvenile and emigrating adult eastern red-spotted newts, Notophthalmus viridescens.'' Journal of Herpetology, 42, 22-30.
  • Rothermel, B. B., Walls, S. C., Mitchell, J. C., Dodd, C. K. Jr., Irwin, L. K., Green, D. E., Vazquez, V. M., Petranka, J. W., and Stevenson, D. J. (2008). ''Widespread occurrence of the amphibian chytrid fungus Batrachochytrium dendrobatidis in the southeastern USA .'' Diseases of Aquatic Organisms, 82, 3-18.
  • Shure, D. J., Wilson, L. A., and Hochwender, C. (1989). ''Predation on aposematic efts of Notophthalmus viridescens.'' Journal of Herpetology, 23, 437-439.
  • Takahashi, M. (2009). Ecological Divergence of the Eastern Newt, Notophthalmus viridescens. Ph.D. dissertation. The University of Memphis, Tennessee.
  • Takahashi, M. K., and Parris, M. J. (2008). ''Life cycle polyphenism as a factor affecting ecological divergence within Notophthalmus viridescens.'' Oecologia, 158, 23-24.
  • Wakely, J. F., Fuhrman, G. J., Fuhrman, F. A., Fischer, H. G., and Mosher, H. S. (1966). ''The occurrence of tetrodotoxin (tarichatoxin) in amphibia and the distribution of the toxin in the organs of newts (Taricha).'' Toxicon, 3, 195-203.
  • Walters, P. J., and Greenwald, L. (1977). ''Physiological adaptations of aquatic newts (Notophthalmus viridescens) to a terrestrial environment.'' Physiological Zoology, 50, 88-98.
  • Webster, D. A. (1960). ''Toxicity of the spotted newt, Notophthalmus viridescens, to trout.'' Copeia, 1960, 1-2.
  • Yotsu-Yamashita, M., and Mebs, D. (2003). ''Occurrence of 11-oxotetrodotoxin in the red-spotted newt, Notophthalmus viridescens, and further studies on the levels of tetrodotoxin and its analogues in the newt's efts.'' Toxicon, 41, 893-897.

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Distribution and Habitat

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This species is one of the most widely distributed salamanders in North America, occurring primarily from Nova Scotia to Florida, and also southwest to Ontario. It prefers ponds and lakes with dense, submerged vegetation and relatively undisturbed stretches of streams, swamps, neighboring woodlands and ditches (Behler and King 1996).
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Life History, Abundance, Activity, and Special Behaviors

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Raffel et al. (2010) found that eastern newts in 12 of 16 central Pennsylvania ponds were widely infected with the amphibian chytrid fungal pathogen Batrachochytrium dendrobatidis (Bd), although they appeared healthy and did not show any overt signs of chytridiomycosis. N. viridescens may thus act as a reservoir species for Bd (Raffel et al. 2010). In the southeastern United States, Bd-infected N. viridescens have been found in Georgia, North Carolina, and Virginia, but sampling was negative in Louisiana and Tennessee (Rothermel et al. 2008). Eight dead Bd-infected newts were found in Virginia, although these individuals were apparently not part of a mass mortality event and newt populations did not decline between 2006 and 2008 (Rothermel et al. 2008). Padgett-Flohr et al. (2007) also reported Bd infections in commercially purchased N. viridescens, but did not note where infected individuals originated. Recently a new species of mesomycetozoan parasite (Amphibiocystidium viridescens) was reported to be widespread (Pennsylvania, West Virginia, and Massachusetts) and to have caused mortality in eastern newt populations. Infection presents as subcutaneous cysts, visible as raised bumps under the skin and in the liver. This may be another recently emerged pathogen, like the chytrid fungal pathogen Bd. Peaks in infection prevalence were found to occur in winter and early spring (Raffel et al. 2008).N. viridescens may be a carrier of iridoviruses. Duffus et al. (2008) examined FV3 prevalence in pond-dwelling amphibian communities of southeastern Ontario, Canada. Of five N. viridescens individuals sampled from a single pond, one was infected with frog virus 3 (FV3) but did not show clinical signs of infection, in contrast to syntopic wood frogs.Pollutants can affect this species. Relyea and Jones (2009) found that the glyphosate-based herbicide Roundup (in the Original Max formulation, which contains the surfactant polyethoxylated tallowamine, or POEA) was moderately toxic to larval N. viridescens, similar to the toxicity for larval ambystomatid salamanders and less than the toxicity for larval anurans. In another study, adult N. viridescens exposed to sediments with low amounts of coal-tar sealant (which can originate from asphalt parking lots), as well as to UV light, showed sublethal effects including decreased righting ability and decreased swimming speed. Although these effects did not directly result in mortality, they could potentially influence survival by decreasing the ability to catch prey or evade predators (Bommarito 2009). Likewise, exposure to the insecticide endosulfan has been shown to reduce mating success in N. viridescens by inhibiting release or potency of female pheromones and by delaying male responses to female odors (Park et al. 2001; Park and Propper 2002).
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Life History, Abundance, Activity, and Special Behaviors

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N. viridescens has a complex life cycle, with four distinct stages: egg, aquatic larva, red eft (terrestrial juvenile), and adult (Petranka 1998). The breeding season lasts from late winter to early spring (Behler and King 1996). A single batch of 200-400 eggs is typically laid by the females on submerged vegetation, with an incubation period of 3-8 weeks (Behler and King 1996). On hatching, a larva measures about 8 mm in size (Behler and King 1996). Larvae may develop along one of three possible pathways: metamorphosis via a terrestrial juvenile (eft) stage to an aquatic lunged adult; metamorphosis directly to an aquatic lunged adult; or paedomorphosis (maturation directly to an aquatic gilled adult with no metamorphosis) (Takahashi 2008; Takahashi and Parris 2008). Generally, following metamorphosis from the aquatic larval stage, juveniles disperse away from their home ponds and spend three to seven years as terrestrial red efts (Forester and Lykens 1991). Efts return to aquatic habitats to reproduce when they become sexually mature, and undergo a second transformation to a more aquatic adult form during breeding season. Aquatic adults become green in coloration, have smoother, mucous skin and develop large tail fins, particularly pronounced in breeding males (Gage 1891; Gill 1978a). The change from terrestrial phenotype to aquatic phenotype may take days to weeks (Grayson and Wilbur 2009). After breeding season is over, adults may remain aquatic or may return to terrestrial habitat; if they disperse terrestrially, the skin texture and color changes and the tail fin reduces in size (Brimley 1921; Walters and Greenwald 1977; Davis and Grayson 2007). Terrestrial newts can migrate across both open and forested habitat (Healy 1973); the use of fluorescent tracking powder showed that efts meandered more while adult newts were found to make more linear trails away from the pond (Roe and Grayson 2008). After periods of rain, concentrations of efts in forest regions may be high (Behler and King 1996). Terrestrial efts and adults make use of a variety of surface or near-surface microhabitats, mostly under forest debris such as leaves, logs, and branches; they are never found in subterranean habitat or mammal burrows (Roe and Grayson 2008). Emergence from refuges and continued movement depend on having a moist surface environment (Roe and Grayson 2008). Distance traveled by efts or adults depended on the humidity and precipitation levels of the previous day (Roe and Grayson 2008). Some postbreeding newts were found to travel over 50 m in 24 hours (Roe and Grayson 2008). When out and active, individuals tracked by using fluorescent powder were often found to have climbed up ferns and logs, probably to forage (Roe and Grayson 2008).The adult diet includes worms, insects, small crustaceans, amphibian eggs and larvae (Behler and King 1996). Feeding occurs year-round (Morgan and Grierson 1932). Adults were found to be capable of consuming an average of 316 mosquito larvae per day (DuRant and Hopkins 2008).Cutaneous secretions of toxic substances (tetrodotoxin and its analogues 6-epiTTX and 11-oxoTTX) serve as a defense mechanism from potential predators (Webster 1960; Brodie 1968; Hurlburt 1970; Pough 1971; Brandon et al. 1979; Brodie and Formanowicz 1981; Shure et al. 1989). Although the bright coloration of juveniles (red efts) is presumed to be aposematic, one study supported that conclusion by finding that efts were more toxic than non-aposematic adults (Wakely et al. 1966), but a different study found that efts and non-aposematic adults were equally toxic (Yotsu-Yamashita and Mebs 2003). It is thought that the nontoxic plethodontid salamander Pseudotriton ruber, which is bright red, may be mimicking the coloration of efts (Howard and Brodie 1971; Huheey and Brandon 1974).
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Lifespan, longevity, and ageing

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Maximum longevity: 25 years (captivity) Observations: As in other similar species, these newts feature extensive regeneration capabilities (McGann et al. 2001). They can live up to 15 years in the wild (http://amphibiaweb.org/). One specimen kept as a pet was still alive when over 25 years of age (website feedback), which is a plausible anecdote. A female reportedly lived for 15 years in captivity (http://www.pwrc.usgs.gov/neparc/). In some populations, sexual maturity can be reached in 1 year, but it usually takes at least 3 years. Some data suggests males may reach sexual maturity slightly sooner than females (http://amphibiaweb.org/).
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Morphology

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The aquatic larvae have laterally compressed tails, olive colored skin, and feathery gills. The hatchlings range in length from 7 to 9mm and have fairly smooth skin with little toxicity. Although the length of the larval period and the size at metamorphosis varies, they usually transform into a terrestrial "eft" stage after 2 to 5 months. The eft is reddish-orange in color with two rows of black-bordered red spots. It has well-developed lungs, limbs, and eyelids. The eft's skin is dry and somewhat rough and its color is a sign of its toxicity to predators. The eft has a long-slender body with a laterally flattened tail and ranges in length from 3.4 to 4.5 cm. The eft usually transforms into the mature, breeding stage after 2 to 3 years on land. The adult newt varies in color depending on its age and sex, ranging from yellowish-brown to greenish-brown dorsally and have black-bordered red spots. Its ventral color is yellow and black spots speckle the belly. The newt is slightly moist (just enough to keep its skin from drying out), with rough-scaleless skin and indistinct coastal grooves. Its size ranges in length from 7 to 12.4 cm and it has small eyes with a horizontal pupil. During the breeding season, males can be easily identified by their enlarged hind legs, with black-horny structures on the inner surfaces of their thighs and toe tips (used for gripping females during mating), swollen vents, and broadly keeled (high-wavy crest) tails.

Range length: 7 to 12.4 cm.

Other Physical Features: ectothermic ; heterothermic ; bilateral symmetry ; poisonous

Sexual Dimorphism: ornamentation

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Riemland, S. 2000. "Notophthalmus viridescens" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Notophthalmus_viridescens.html
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Shannon Riemland, Michigan State University
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Untitled

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N. viridescens appears to be involved in a Mullerian mimicry complex, with several other salamander species possibly mimicking the red eft, with its toxic skin secretions.

This newt is capable of locating its home pond through true navigation using its olfaction and light-dependent magnetic compass.

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Riemland, S. 2000. "Notophthalmus viridescens" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Notophthalmus_viridescens.html
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Shannon Riemland, Michigan State University
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Behavior

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Carnivorous throughout their lives, eastern newts use both chemical and visual cues to locate food. Adults seem to rely more on visual cues when feeding. They don't have a specialized diet, but temperature and water clarity, as well as prey density, can effect the feeding process.

Communication Channels: visual ; tactile ; chemical

Perception Channels: visual ; tactile ; chemical

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Riemland, S. 2000. "Notophthalmus viridescens" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Notophthalmus_viridescens.html
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Shannon Riemland, Michigan State University
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Associations

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Predators of N. viridescens include birds, mammals, fish, and other amphibians, however many of them are deterred by the newt's toxic skin secretions.

Known Predators:

  • birds (Aves)
  • carnivorous mammals (Mammalia)
  • fish (Actinopterygii)
  • amphibians (Amphibia)

Anti-predator Adaptations: aposematic ; cryptic

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Riemland, S. 2000. "Notophthalmus viridescens" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Notophthalmus_viridescens.html
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Shannon Riemland, Michigan State University
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Conservation Status

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There is no special status listed for Notophthalmus viridescens. Newts have declined in the face of habitat degradation by humans, but remain locally common in parts of their range. Adult newts will readily colonize man-made bodies of water, even in the presence of predatory fish, as their toxic skin secretions may reduce fish predation. Researchers do believe, however, that eastern newts may be suffering at higher than normal rates from diseases caused by viruses, bacteria, and fungi, due to a variety of environmental problems including pollution. Acid precipitation and deforestation may be other cause of depleted populations.

US Federal List: no special status

CITES: no special status

State of Michigan List: no special status

IUCN Red List of Threatened Species: least concern

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Riemland, S. 2000. "Notophthalmus viridescens" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Notophthalmus_viridescens.html
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Shannon Riemland, Michigan State University
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James Harding, Michigan State University
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George Hammond, Animal Diversity Web
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Life Expectancy

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Eastern newts have a lifespan of up to 12 to 15 years. However, mortality is high in eggs and larvae.

Range lifespan
Status: captivity:
15 (high) years.

Average lifespan
Status: captivity:
15.0 years.

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Riemland, S. 2000. "Notophthalmus viridescens" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Notophthalmus_viridescens.html
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Shannon Riemland, Michigan State University
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James Harding, Michigan State University
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George Hammond, Animal Diversity Web
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Habitat

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Notophthalmus viridescens inhabits both deciduous and coniferous forests. Immature larvae and the adult newts live in small bodies of freshwater (ponds, small lakes, ditches, and marshes) usually with mud bottoms. Adults can survive on land if their aquatic habitat becomes unsuitable; adults may move onto land during dry periods when the water is low or to rid themselves of ectoparasites. The juvenile "eft" stage lives in lakeshore and woodland habitats and is often seen in forest litter on rainy nights.

Habitat Regions: temperate ; terrestrial ; freshwater

Terrestrial Biomes: forest

Aquatic Biomes: lakes and ponds

Wetlands: marsh

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Riemland, S. 2000. "Notophthalmus viridescens" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Notophthalmus_viridescens.html
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Shannon Riemland, Michigan State University
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James Harding, Michigan State University
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Distribution

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The eastern newt, Notophthalmus viridescens, is one of only a few species in the Family Salamandridae native to North America. This newt ranges throughout most of eastern North America, from the Canadian Maritime Provinces west to the Great Lakes and south to Texas, Alabama, Georgia, and Florida (Dunn and Hagen 1999; Petranka 1998; Richmond 1997). There are four recognized subspecies: the red-spotted newt (N. v. viridescens) of the eastern and northeastern U.S. and Canada, the central newt (N. v. louisianensis) of the central states and the deep south, the broken-striped newt (N. v. dorsalis) of the Carolina coastal plains, and the peninsula newt (N. v. piaropicola) of peninsular Florida.

Biogeographic Regions: nearctic (Native )

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Riemland, S. 2000. "Notophthalmus viridescens" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Notophthalmus_viridescens.html
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Shannon Riemland, Michigan State University
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James Harding, Michigan State University
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George Hammond, Animal Diversity Web
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Trophic Strategy

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The aquatic larvae eat small invertebrates including water fleas, snails, and beetle larvae; the terrestrial efts eat small invertebrates, mainly those found in humus and leaf litter, including snails, spring tails, and soil mites; the adult newts eat mainly midge larva and other aquatic immature stages of insects. Adults don't have a specialized diet, eating any small invertebrate that they can find.

Animal Foods: insects; terrestrial non-insect arthropods; mollusks; terrestrial worms; aquatic crustaceans; zooplankton

Primary Diet: carnivore (Insectivore , Eats non-insect arthropods)

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Riemland, S. 2000. "Notophthalmus viridescens" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Notophthalmus_viridescens.html
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Shannon Riemland, Michigan State University
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James Harding, Michigan State University
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George Hammond, Animal Diversity Web
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Associations

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Eastern newts are important predators of small invertebrates in the freshwater ecosystems of eastern North America.

Leeches appear to be a major source of adult mortality. Adults will generally flee the water and begin biting or scratching themselves in an attempt to rid their bodies of these ectoparasites, however they're not always successful.

Commensal/Parasitic Species:

  • leeches (Hirudinea)
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Riemland, S. 2000. "Notophthalmus viridescens" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Notophthalmus_viridescens.html
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Shannon Riemland, Michigan State University
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James Harding, Michigan State University
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George Hammond, Animal Diversity Web
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Benefits

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The eastern newt may benefit humans by helping to control the populations of aquatic insects, including mosquitoes. They are aesthetically interesting and may play an important ecological role in freshwater and woodland habitats. Eastern Newts are sometimes kept as aquarium or terrarium pets and have even been commercially collected for the pet trade. Effects of this trade on exploited populations is not well documented.

Positive Impacts: pet trade

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Riemland, S. 2000. "Notophthalmus viridescens" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Notophthalmus_viridescens.html
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Shannon Riemland, Michigan State University
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James Harding, Michigan State University
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George Hammond, Animal Diversity Web
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Benefits

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This species does not have any significant negative economic importance.

Negative Impacts: injures humans (poisonous )

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Riemland, S. 2000. "Notophthalmus viridescens" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Notophthalmus_viridescens.html
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Shannon Riemland, Michigan State University
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Life Cycle

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The incubation of the eggs is somewhat dependent on temperature, but generally lasts from 3 to 8 weeks. In early fall, 3 to 4 months later, the aquatic larvae lose their gills, acquire sac-like lungs (heart transforms from two chambered heart to three, capable of supporting lungs), and emerge onto land as an eft. Two to 3 years later, the eft develops a powerful, flattened tail and returns to the water to breed, as an adult, and remains there the rest of its life, if water is permanent. (Lacking permanent water, adult newts will estivate and overwinter on land and enter vernal ponds in spring to breed.) Some eastern newt populations skip the eft stage and immediately transform into breeding adults. There are some coastal populations of eastern newts that become reproductively mature while retaining a gilled "larval" form (i.e., are neotenic). In other populations, newts enter the eft stage but never undergo a complete second metamorphosis, and enter the water only to breed. Both of these latter two cases may be in response to harsher than average environmental conditions.

Development - Life Cycle: neotenic/paedomorphic; metamorphosis

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Riemland, S. 2000. "Notophthalmus viridescens" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Notophthalmus_viridescens.html
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Reproduction

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The breeding season begins in late winter and lasts until early spring; at this time, the female is heavy with eggs and actively seeking a male. The courtship involves a unique form of amplexus. Females are attracted by the male's spots and he lures them to him by making fanning motions with his tail and wiggling, causing an enticing odor (a pheromone) to be released. The male positions himself above and forward of the female, gripping her sides just behind her forelegs with his hindlimbs and rubbing her snout with the side of his head. Males will deposit a sperm packet on the bottom of the pond and the female will proceed to pick it up with her cloaca, later using the sperm to fertilize her eggs. Males are often in competition with each other, but rival males who try to break up a pair already involved in amplexus are rarely successful. Sometimes the rival male may drop his sperm packet anyway and the female may pick up the packet when courtship with the other male is over. Male to male courtship is also common. Males tend to eat the sperm packets that are dropped in this case.

Mating System: polygynandrous (promiscuous)

Oviposition can take several weeks, because the female will only lay a few, widely scattered eggs, each day. It's still uncertain whether or not females will lay all of their eggs in a breeding season, however they do lay between 200 and 400 single, jelly-covered eggs on submerged vegetation, each season. As soon as the process is finished, the female newt swims away leaving her eggs to survive on their own. Both males and females reach sexual maturity around the age of 3.

Breeding interval: Eastern newts breed once per year.

Breeding season: The breeding season varies with latitude, beginning in late winter and lasting until early spring.

Range number of offspring: 200 to 400.

Range time to hatching: 3 to 8 weeks.

Average age at sexual or reproductive maturity (female): 3 years.

Average age at sexual or reproductive maturity (male): 3 years.

Key Reproductive Features: iteroparous ; seasonal breeding ; gonochoric/gonochoristic/dioecious (sexes separate); sexual ; fertilization (Internal ); oviparous

Average age at sexual or reproductive maturity (male)
Sex: male:
2000 days.

Average age at sexual or reproductive maturity (female)
Sex: female:
2000 days.

Females do not provide parental care after they deposit their eggs. Males do not invest in young past sperm production and mating.

Parental Investment: no parental involvement; pre-fertilization (Provisioning, Protecting: Female); pre-hatching/birth (Provisioning: Female)

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Riemland, S. 2000. "Notophthalmus viridescens" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Notophthalmus_viridescens.html
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Description of Notophthalmus viridescens

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One of only a few species of Salamandridae that are native to North America. Larvae and adults live in small bodies of water in deciduous and coniferous forests. The larvae have laterally compressed tails, olive colored skin, and feathery gills. The larvae develop into terrestrial ‘eft’s that are up to 4.5 cms long and are reddish-orange with two rows of black-bordered red spots. The eft matures into a breeding adult after 2 or 3 years. The adult is dorsally yellowish- to greenish-brown with black-bordered red spots. Final size up to 12.4 cm. Hind legs enlarge during the breeding season as part of adaptations to amplexus. They produce up to 400 offspring, with a gestation period of up to 2 months. Carnivorous, larvae eat small invertebrates including water fleas, snails, and beetle larvae; efts eat small invertebrates, mainly those found in humus and leaf litter, including snails, spring tails, and soil mites; the adults eat mainly midge larva and other aquatic immature stages of insects. They will live up to 15 years. Predators include birds, mammals, fish, and other amphibians, however many of them are deterred by the newt's toxic skin secretions. Leech parasites also contribute to losses from the population.  Bibliography: Petranka, J. 1998. Salamanders of the United States and Canada. Washington, D.C., USA: Smithsonian Institution Press.  
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Eastern newt

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The eastern newt (Notophthalmus viridescens) is a common newt of eastern North America. It frequents small lakes, ponds, and streams or nearby wet forests. The eastern newt produces tetrodotoxin, which makes the species unpalatable to predatory fish and crayfish.[2] It has a lifespan of 12 to 15 years in the wild, and it may grow to 5 in (13 cm) in length. These animals are common aquarium pets, being either collected from the wild or sold commercially. The striking bright orange juvenile stage, which is land-dwelling, is known as a red eft. Some sources blend the general name of the species and that of the red-spotted newt subspecies into the eastern red-spotted newt (although there is no "western" one).[3][4]

Subspecies

The eastern newt includes these four subspecies:[5]

  • Red-spotted newt (Notophthalmus viridescens viridescens)
  • Broken-striped newt (Notophthalmus viridescens dorsalis)
  • Central newt (Notophthalmus viridescens louisianensis) - Central newts measure from 2.5 in (6.4 cm) to 4 in (10 cm) in length. They are brown or green, with fine black dots all over the body. There may be a row of red spots on each side of the body. The belly is yellow or orange and is noticeably lighter than the rest of the body. The skin of newts is not as slippery as the skin of salamanders and may appear to be rough and dry for parts of their lives.
  • Peninsula newt (Notophthalmus viridescens piaropicola)

Life stages

Eastern newts have a lifespan of about 8–10 years in the wild, but some individuals have been known to live up to 15 years.[6] Eastern newts have three stages of life: (1) the aquatic larva or tadpole, (2) the red eft or terrestrial juvenile stage, and (3) the aquatic adult.

Larva

The larva possesses gills and does not leave the pond environment where it was hatched. Larvae are brown-green, and shed their gills when they transform into the red eft. The larval Eastern Newt is the most heavily preyed upon stage. They are commonly predated on by fish, aquatic insects, and other adult newts (Brossman 2014).

Red eft

The red eft (juvenile) stage is a bright orangish-red, with darker red spots outlined in black. An eastern newt can have as many as 21 of these spots. The pattern of these spots differs among the subspecies. An eastern newt's time to get from larva to eft is about three months. During this stage, the eft may travel far, acting as a dispersal stage from one pond to another, ensuring outcrossing in the population. The striking coloration of this stage is an example of aposematism — or "warning coloration" — which is a type of antipredator adaptation in which a "warning signal" is associated with the unprofitability of a prey item (i.e., the saturation of the eft's tissues with tetrodotoxin) to potential predators.[7] Their tetrodotoxin is a neurotoxin which is also the strongest emetic that is known.[8]

Adult

After two or three years, the eft finds a pond and transforms into the aquatic adult. The adult's skin is a dull olive green dorsally, with a dull yellow belly, but retains the eft's characteristic black-rimmed red spots. It develops a larger, blade-like tail and characteristically slimy skin.

It is common for the peninsula newt (N. v. piaropicola) to be neotenic, with a larva transforming directly into a sexually mature aquatic adult, never losing its external gills. The red eft stage is in these cases skipped.

Habitat

Eastern newts are at home in both coniferous and deciduous forests. They need a moist environment with either a temporary or permanent body of water, and thrive best in a muddy environment. Eastern newts have a preference for certain types of habitats, with males preferring more open, aquatic habitats and females preferring more forested, terrestrial habitats. This preference may be related to the different roles that males and females play in the reproductive process, with males typically being more active in courtship and females spending more time on land preparing to lay eggs.

They may travel far from their original location during the eft stage. Red efts may often be seen in a forest after a rainstorm. Adults prefer a muddy aquatic habitat, but will move to land during a dry spell. Eastern newts have some amount of toxins in their skin, which is brightly colored to act as a warning. Even then, only 2% of larvae make it to the eft stage. Some larvae have been found in the pitchers of the carnivorous plant Sarracenia purpurea.[9]

Diet

Eastern newts are carnivorous, feeding on a variety of prey every two to three days. As larvae, they feed on small aquatic invertebrates, and as adults, they eat insects, worms, snails, and other small invertebrates. Eastern newts eat a variety of prey, such as insects, springtails, soil mites,[10] small mollusks and crustaceans, young amphibians, worms, and frog eggs. They also eat a lot of snails, beetles, ants, and mosquito larvae, with an annual ingestion of about 35,000 kcal.[11][12] Their dietary habits prove to be beneficial to humans because they help to control insect populations and maintain balance to their habitats. Eastern newts are a vital part of many ecosystems, serving as both predators and prey.

Behavior

Eastern newts have a number of natural predators, including fish, snakes, birds, and larger salamanders. They have several defenses against these predators, including their bright coloring, which serves as a warning signal, and their ability to secrete toxins from their skin as a defense mechanism.

Adaptability

Eastern newts are highly sensitive to changes in their environment and are able to detect and respond to changes in water quality and temperature. This sensitivity allows them to thrive in a variety of habitats, but it also makes them vulnerable to environmental changes and pollution.[13] In fact, eastern newts are considered a sensitive species, meaning that they are often used as indicators of ecosystem health. When populations of eastern newts decline, it can be a sign of environmental stress or degradation.

Hibernation

Eastern newts are ectothermic, relying on external sources of heat to regulate their body temperature. They are most active during the warmer months of the year, but they can also be found in more temperate climates where they may be active year-round. During the winter months, some eastern newts will often burrow underground or seek shelter in logs or other debris to avoid the cold.[14] However, studies have shown that some do not engage in hibernation, depending on the location of the species.[15]

Homing

Eastern newts home using magnetic orientation. Their magnetoreception system seems to be a hybrid of polarity-based inclination and a sun-dependent compass. Shoreward-bound eastern newts will orient themselves quite differently under light with wavelengths around 400 nm than light with wavelengths around 600 nm, while homing newts will orient themselves the same way under both short and long wavelengths.[3] Ferromagnetic material, probably biogenic magnetite, is likely present in the eastern newt's body.[4]

A study determined that the home range size for Eastern newts is primarily affected by food availability, substrate humidity, but not affected by dispersal ability, competition, shelter availability, or predator avoidance.[16] Distance travelled depended on humidity and precipitation. The mean distance traveled overnight was about 15 m, with longest trails ranging over 70 m.[17]

Reproduction

Eastern newts breed once per year, when breeding starts in late fall until early spring. They are known to be polygynandrous, with females and males mating with multiple partners. Males have preference towards larger females, while no evidence for female preference during mating was found.[18] The breeding migration often happens more with rainfall.[19] The male's spots attract females, luring them to him with fanning motions of his tail, causing a pheromone to be released.[20] Once the female has chosen a mate, the male will deposit a spermatophore, a package of sperm, onto the ground, which the female will then pick up and fertilize her eggs with. The female will lay her eggs in the water, attaching them to submerged vegetation or other objects. 200~400 eggs are laid in a single batch, with incubation period of 3~8 weeks.[21] For the normal and healthy development of gonads, fat-bodies are needed in proximity of the developing organs to ensure proper reproduction ability.[22]

Social interactions

The behavior of eastern newts is also influenced by their social interactions with other members of their species. Eastern newts exhibit social hierarchy, with dominant individuals exhibiting aggressive behaviors towards subordinates. This social hierarchy is thought to be related to the distribution of resources, with dominant individuals having access to more food and better mating opportunities. One such behavior is territoriality, where individuals will defend a specific area or resource from other members of their species. This behavior is commonly seen in males during the breeding season, when they will defend a territory in order to attract females and ensure access to mating opportunities.

Survival advantages

Secretion of toxins through the skin protects the newt from predators, and should therefore not be handled with bare hands. The red colors of the adult newt also act as a warning sign for predators.[23] Its ventral surface has poison glands, which makes predators reluctant to eat it.[24] However, one study observed a Belted Kingfisher (Megaceryle alcyon) beat an eastern newt on a nest box 15 times before eating it.[25] This special toxin is known as tetrodotoxin. Several studies have found that newt larvae increase the production of this toxin while in the presence of predators (dragonflies). Tetrodotoxin is known to cause muscle paralysis, skin irritation, and even death in predators, although some species mantis species have shown a resilience to this toxin.[26] The Eastern newt also has a greater tail depth and is capable of swimming quickly away from aquatic predators.

Limb regeneration

Eastern newts are able to regenerate their limbs that were lost to an injury. Forelimb regeneration has been considered to be close to the forelimb development; genes that play a role in forelimb regeneration are known to also be expressed in its developmental stages.[27] In addition. they are capable of regenerating their spinal cord, heart, and other organs. This ability is thought to be related to their high levels of stem cells, which allow them to repair and regenerate damaged tissues.[28]

Conservation concerns

Although eastern newts are widespread throughout North America, they, like many other species of amphibians, are increasingly threatened by several factors including habitat fragmentation, climate change, invasive species, over-exploitation, and emergent infectious diseases.[29] The biodiversity of amphibians across the United States is considered to be threatened due to the loss of wetlands and furthermore, their connectivity;[30][31] since the 1780s, more than 53% of wetlands in the United States have been lost.[32] For example, a study found the toxicity of coal-tar pavement on eastern newts sublethal, decreasing their righting ability and swimming speed.[33] Wild eastern newts are known hosts of Batrachochytrium dendrobatidis and Ranavirus, as well as the mesomycetozoan Amphibiocystidium ranae[34]. They are also highly susceptible to the newly emergent chytrid fungus Batrachochytrium salamandrivorans.[35]

Gallery

References

Citations

  1. ^ IUCN SSC Amphibian Specialist Group (2015). "Notophthalmus viridescens". IUCN Red List of Threatened Species. 2015: e.T59453A78906143. doi:10.2305/IUCN.UK.2015-4.RLTS.T59453A78906143.en. Retrieved 19 November 2021.
  2. ^ Marion, Zachary H; Hay, Mark E (2011). "Chemical Defense of the Eastern Newt (Notophthalmus viridescens): Variation in Efficiency against Different Consumers and in Different Habitats". PLOS ONE. 6 (12): e27581. Bibcode:2011PLoSO...627581M. doi:10.1371/journal.pone.0027581. PMC 3229496. PMID 22164212.
  3. ^ a b Phillips, J; Borland, S (1994). "Use of a Specialized Magnetoreception System for Homing by the Eastern Red-Spotted Newt Notophthalmus Viridescens". The Journal of Experimental Biology. 188 (1): 275–91. doi:10.1242/jeb.188.1.275. PMID 9317797.
  4. ^ a b Brassart, J; Kirschvink, J. L; Phillips, J. B; Borland, S. C (1999). "Ferromagnetic material in the eastern red-spotted newt notophthalmus viridescens". The Journal of Experimental Biology. 202 Pt 22 (22): 3155–60. doi:10.1242/jeb.202.22.3155. PMID 10539964.
  5. ^ Behler, John L.; King, F. Wayne (1979). The Audubon Society Field Guide to North American Reptiles and Amphibians (Chanticleer Press ed.). New York: Knopf. p. 276. ISBN 978-0-394-50824-5. Retrieved 4 September 2012.
  6. ^ Petranka, James W. (1998). Salamanders of the United States and Canada. Washington DC: Smithsonian Institution Press. ISBN 1-56098-828-2.
  7. ^ Santos, J. C; Coloma, L. A; Cannatella, D. C (2003). "Multiple, recurring origins of aposematism and diet specialization in poison frogs". Proceedings of the National Academy of Sciences. 100 (22): 12792–7. doi:10.1073/pnas.2133521100. JSTOR 3148039. PMC 240697. PMID 14555763.
  8. ^ Brandon, Ronald A.; Labanick, George M.; Huheey, James E. (1979). "Relative Palatability, Defensive Behavior, and Mimetic Relationships of Red Salamanders (Pseudotriton ruber), Mud Salamanders (Pseudotriton montanus), and Red Efts (Notophthalmus viridescens)". Herpetologica. 35 (4): 289–303. ISSN 0018-0831.
  9. ^ Butler, Jessica L; Atwater, Daniel Z; Ellison, Aaron M (2005). "Red-spotted Newts: An Unusual Nutrient Source for Northern Pitcher Plants". Northeastern Naturalist. 12 (1): 1–10. doi:10.1656/1092-6194(2005)012[0001:rnauns]2.0.co;2. JSTOR 3858498. S2CID 46605572.
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  11. ^ Burton, Thomas M. (1977-03-16). "Population Estimates, Feeding Habits and Nutrient and Energy Relationships of Notophthalmus v. viridescens, in Mirror Lake, New Hampshire". Copeia. 1977 (1): 139–143. doi:10.2307/1443516. JSTOR 1443516.
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  13. ^ Bommarito, Thomas; Sparling, Donald W.; Halbrook, Richard S. (2010). "Toxicity of coal-tar pavement sealants and ultraviolet radiation to Ambystoma Maculatum". Ecotoxicology. 19 (6): 1147–1156. doi:10.1007/s10646-010-0498-8. ISSN 0963-9292. PMID 20440554. S2CID 21923980.
  14. ^ Brown, Patricia Stocking; Brown, Stephen C.; Bisceglio, Isabelle T.; Lemke, Sheila M. (1983). "Breeding condition, temperature, and the regulation of salt and water by pituitary hormones in the red-spotted newt, Notophthalmus viridescens". General and Comparative Endocrinology. 51 (2): 292–302. doi:10.1016/0016-6480(83)90084-9. PMID 6311666.
  15. ^ Sever, David M. (2006). "The "False Breeding Season" of the Eastern Newt, Notophthalmus viridescens". Bull. Chicago Herp. Soc. 41 (8): 149–153.
  16. ^ Healy, William R. (1975). "Terrestrial Activity and Home Range in Efts of Notophthalmus viridescens". American Midland Naturalist. 93 (1): 131–138. doi:10.2307/2424111. JSTOR 2424111.
  17. ^ Roe, Andrew W.; Grayson, Kristine L. (2008). "Terrestrial Movements and Habitat Use of Juvenile and Emigrating Adult Eastern Red-Spotted Newts, Notophthalmus Viridescens". Journal of Herpetology. 42 (1): 22–30. doi:10.1670/07-040.1. ISSN 0022-1511. S2CID 86178641.
  18. ^ Takahashi, Mizuki K.; Takahashi, Yukiko Y.; Parris, Matthew J. (2010). "On the role of sexual selection in ecological divergence: a test of body-size assortative mating in the eastern newt Notophthalmus viridescens: SEXUAL SELECTION AND ECOLOGICAL DIVERGENCE". Biological Journal of the Linnean Society. 101 (4): 884–897. doi:10.1111/j.1095-8312.2010.01562.x. S2CID 86726095.
  19. ^ Hurlbert, Stuart H. (1969). "The Breeding Migrations and Interhabitat Wandering of the Vermilion‐Spotted Newt Notophthalmus viridescens (Rafinesque)". Ecological Monographs. 39 (4): 465–488. doi:10.2307/1942356. ISSN 0012-9615. JSTOR 1942356.
  20. ^ Rieml, Shannon. "Notophthalmus viridescens (Eastern Newt)". Animal Diversity Web. Retrieved 2022-12-21.
  21. ^ Behler, John L. (1985). The Audubon Society field guide to North American reptiles and amphibians. F. Wayne King, National Audubon Society. New York: Alfred A. Knopf. ISBN 0-394-50824-6. OCLC 4983582.
  22. ^ Rose, Francis L. (1967). "Seasonal Changes in Lipid Levels of the Salamander Amphiuma means". Copeia. 1967 (3): 662–666. doi:10.2307/1442246. ISSN 0045-8511.
  23. ^ "Eastern (Red-Spotted) Newt - Watchable Wildlife - NYS Dept. Of Environmental Conservation".
  24. ^ Hurlbert, Stuart H. “Predator Responses to the Vermilion-Spotted Newt (Notophthalmus Viridescens).” Journal of Herpetology, vol. 4, no. 1/2, 1970, pp. 47–55, https://doi.org/10.2307/1562702. Accessed 27 Apr. 2022.
  25. ^ REESE, DAVID H. (April 1977). "Ribosomal RNA Synthesis in the Eastern North-American Newt, Notophthalmus viridescens". Differentiation. 7 (1–3): 99–106. doi:10.1111/j.1432-0436.1977.tb01502.x. ISSN 0301-4681.
  26. ^ Mebs, D., Yotsu-Yamashita, M. & Arakawa, O. The praying mantis (Mantodea) as predator of the poisonous red-spotted newt Notophthalmus viridescens (Amphibia: Urodela: Salamandridae). Chemoecology 26, 121–126 (2016). https://doi.org/10.1007/s00049-016-0211-3
  27. ^ Vlaskalin, T., Wong, C.J. & Tsilfidis, C. Growth and apoptosis during larval forelimb development and adult forelimb regeneration in the newt (Notophthalmus viridescens). Dev Genes Evol 214, 423–431 (2004). https://doi.org/10.1007/s00427-004-0417-1
  28. ^ Simon, Hans-Georg; Odelberg, Shannon (2015), Maintaining Eastern Newts (Notophthalmus viridescens) for Regeneration Research, Methods in Molecular Biology, vol. 1290, New York, NY: Springer New York, pp. 17–25, doi:10.1007/978-1-4939-2495-0_2, ISBN 978-1-4939-2494-3, PMID 25740474, retrieved 2022-12-21
  29. ^ Collins, James P; Storfer, Andrew (2003). "Global amphibian declines: Sorting the hypotheses". Diversity and Distributions. 9 (2): 89–98. doi:10.1046/j.1472-4642.2003.00012.x. JSTOR 3246802.
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  31. ^ Gallant AL et al 2007. Global Rates of Habitat Loss and Implications for Amphibian Conservation, BioOne Complete. https://doi.org/10.1643/0045-8511(2007)7[967:GROHLA]2.0.CO;2. Accessed 27 April 2022
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  33. ^ Bommarito, Thomas (2009-01-01). "TOXICITY OF SEDIMENTS CONTAINING COAL-TAR PAVEMENT SEALANTS TO NOTOPHTHALMUS VIRIDESCENS AND AMBYSTOMA MACULATUM, SURROGATE SPECIES FOR EURYCEA SOSORUM". Theses.
  34. ^ Raffel, T. R.; Bommarito, T.; Barry, D. S.; Witiak, S. M.; Shackelton, L. A. (February 2008). "Widespread infection of the Eastern red-spotted newt (Notophthalmus viridescens) by a new species of Amphibiocystidium, a genus of fungus-like mesomycetozoan parasites not previously reported in North America". Parasitology. 135 (2): 203–215. doi:10.1017/S0031182007003708. ISSN 1469-8161.
  35. ^ Martel, A; Blooi, M; Adriaensen, C; Van Rooij, P; Beukema, W; Fisher, M. C; Farrer, R. A; Schmidt, B. R; Tobler, U; Goka, K; Lips, K. R; Muletz, C; Zamudio, K. R; Bosch, J; Lotters, S; Wombwell, E; Garner, T. W. J; Cunningham, A. A; Spitzen-Van Der Sluijs, A; Salvidio, S; Ducatelle, R; Nishikawa, K; Nguyen, T. T; Kolby, J. E; Van Bocxlaer, I; Bossuyt, F; Pasmans, F (2014). "Recent introduction of a chytrid fungus endangers Western Palearctic salamanders". Science. 346 (6209): 630–1. Bibcode:2014Sci...346..630M. doi:10.1126/science.1258268. PMC 5769814. PMID 25359973.

Further reading

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Eastern newt: Brief Summary

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The eastern newt (Notophthalmus viridescens) is a common newt of eastern North America. It frequents small lakes, ponds, and streams or nearby wet forests. The eastern newt produces tetrodotoxin, which makes the species unpalatable to predatory fish and crayfish. It has a lifespan of 12 to 15 years in the wild, and it may grow to 5 in (13 cm) in length. These animals are common aquarium pets, being either collected from the wild or sold commercially. The striking bright orange juvenile stage, which is land-dwelling, is known as a red eft. Some sources blend the general name of the species and that of the red-spotted newt subspecies into the eastern red-spotted newt (although there is no "western" one).

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