Species Description: Kuchta SR 2007 Contact zones and species limits: hybridization between lineages of the California Newt, Taricha torosa, in the southern Sierra Nevada. Herpetologica 63:332-350.
© 2012 William Flaxington (1 of 20)
During the breeding season, males have a smooth skin, an enlarged and laterally flattened tail to swim better, a lighter body color, enlarged cloacal glands, enlarged mental glands, and tiny cornified papillae on the toe tips and hindlimb bases (to aid in grasping females during amplexus) (Petranka 1998).
Hatchlings are light yellow dorsally with two irregular dark, narrow bands on the back (Twitty 1942). Taricha sierrae has dark spots or blotches along the sides of its body, which are more prominent in older larvae. Hatchlings reach 13-14 mm TL (Riemer 1958).
Distribution and Habitat
Country distribution from AmphibiaWeb's database: United States
U.S. state distribution from AmphibiaWeb's database: California
Taricha sierrae is one of two species of newts present in the Sierra Nevada of California, the other being Taricha granulosa, the Northern Rough-skinned newt. The Sierra newt ranges along the western slopes of the Sierra Nevada with drainage from Sacramento to San Joaquin Rivers, Tulare Lake (Jennings 1996).
Adult T. sierrae inhabit a variety of usually terrestrial habitats, becoming aquatic when breeding. They mostly inhabit foothills dominated by conifers, especially gray pine-blue oak and ponderosa pine communities (Petranka 1998). During the summer, the Sierra newt prefers moist habitats under woody debris or in animal burrows. Adults generally breed in relatively swift-flowing streams, but will sometimes use still water, including farm ponds, lakes, or ditches (Petranka 1998).
Life History, Abundance, Activity, and Special Behaviors
Adults typically require 6-8 weeks to reach breeding sites and both sexes breed every other year. Males arrive at breeding sites before females and stay longer after breeding (Twitty 1942). There are more males than females at breeding sites and males must compete for a mate. When courting, the male amplexes the female and, after about an hour of intermittent periods of head rubbing and tail fluttering, the male dismounts and deposits a spermatophore. The female picks up the spermatophore with her cloaca. Quickly after mating, females attach spherical masses of 11-22 eggs to the sides and bottoms of stones in fairly fast-flowing stream water. Taricha sierrae tend not to oviposit in cryptic sites, since exposed egg masses could be washed from rocks in the faster-flowing water. Total clutch size is not known. The mean egg diameter is 2.8 mm, while the jelly layers surrounding the eggs swell within hours to form a firm mass measuring 15-25 mm in diameter (Petranka 1998). Incubation may last from 14-52 days, depending on local water temperatures, population, and other factors (Storer 1925; Mosher et al. 1964; Petranka 1998). After a larval period of a few months, transformation occurs in late summer or early autumn (Riemer 1958). Larvae usually transform at 55-62 mm TL beginning in late August (Petranka 1998).
Sierra and California newts (T. sierrae and T. torosa) have a diet consisting mostly of worms, snails, eggs, larvae, insects, sowbugs, slugs, and other invertebrates, but may opportunistically take other prey, such as larval newts. A hatchling bird was even found in the stomach of one adult T. torosa. Adults feed when in breeding streams and T. torosa often cannibalize their own eggs and larvae. T. torosa females cannibalize eggs more often than males, sometimes as soon as the eggs protrude from another female's vent (Petranka 1998).
After transformation, juveniles leave the water for surrounding habitats, and the juvenile stage likely lasts 5-8 years. Adults spend the dry summer months in moist, subsurface habitats, and emerge with the onset of autumn rains. Adults are more active on the ground surface than juveniles. Adults may make clicking sounds when they encounter other newts, sometimes accompanied by rising high on the legs and wagging the tail. Another defensive pose, known as the "unken" reflex, is to assume a swaybacked position with the tail tip held straight out, exposing the bright ventral surface (in contrast to the defensive posture of T. granulosa, where the tail tip is curled). This posture can be induced by tapping newts on their bodies. Sierra newts will sometimes squeak when picked up (Petranka 1998). However, their main defense against predators is the potent neurotoxin, tetrodotoxin, present in the Sierra newt's skin, ova, and ovaries (Buchwald et al. 1964).
Trends and Threats
Buchwald, H. D., Durham, L., Fischer, H. G., Harada, R., Mosher, H. S., Kao, C. Y., and Fuhrman, F. A. (1964). ''Identity of tarichatoxin and tetrodotoxin.'' Science, 143, 474-475.
Jennings, W.B. (1996). ''Status of amphibians.'' Sierra Nevada Ecosystem Project, Final Report to Congress. Center for Water and Wildland Resources, University of California (Davis), Davis, California, 921-944.
Kuchta, S. R. (2007). ''Contact zones and species limits: hybridization between lineages of the California Newt, Taricha torosa, in the southern Sierra Nevada.'' Herpetologica, 63, 332-350.
Liss, W. J., and Larson, G. L. (1991). ''Ecological effects of stocked trout on North Cascades naturally fishless lakes.'' Park Science, 11, 22-23.
Mosher, H. S., Fuhrman, F. A., Buchwald, H. D., and Fischer, H. G. (1964). ''Tarichatoxin-tetrodotoxin: a potent neurotoxin.'' Science, 144, 1100-1110.
Petranka, J.W. (1998). Salamanders of the United States and Canada. Smithsonian Institution Press, Washington D.C.
Riemer, W. J. (1958). ''Variation and systematic relationships within the salamander genus Taricha.'' University of California Publications in Zoology, 56, 301-390.
Stebbins, R.C. (1951). Amphibians of Western North America. University of California Press, Berkeley.
Storer, T. I. (1925). "A synopsis of the amphibia of California." University of California Publications in Zoology, 27, 1-342.
Twitty, V. C. (1942). ''The species of Californian Triturus.'' Copeia, 1942, 65-76.
Written by Amy Ru Chen (amychen AT fas.harvard.edu), Harvard
First submitted 2008-05-13
Edited by Amy Ru Chen (2008-08-08)
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