has a slender, elongate body averaging 23 to 25 cm in length from head to tail. The torso is cylindrical and has about two-dozen costal grooves along each side. The tail is laterally compressed, with small fins running along the top and bottom. The head is elongate with a broad snout that is blunted at the end. Its eyes are very small and do not even breach the skin. The skin is usually creamy white, but may have a pinkish hue. When exposed to light, the skin turns dark violet to black. Darkening of the skin is reversed when it is returned to the darkness. On the ventral side of the body the skin is translucent and reveals the contours of internal organs. Directly behind the head on each side are three large, feathery, bright pink gills. This species exhibits little sexual dimorphism in appearance, but females are larger than males.
Juveniles may be distinguished from adults by the faint yellow or red blotches on their skin, and their better developed eyes. Black olms, a variant of this species previously known as Proteus anguinus parkelj, have permanently dark skin and a shorter head. (Arnold and Burton, 1978; Bulog, 1999; Sessions, 2010a; Steward, 1969)
Unlike those of most amphibians, olm larvae do not go through a distinct period of metamorphosis. Instead, the hatchling juveniles have developed directly into adults, retaining some of their larval characters such as gills and tail fins. Environmental temperature plays an important role in the development of eggs as well as juveniles. Within the range of 8° to 15°C, development time is relatively shorter (86 days) in warm temperatures and longer (182 days) in cold temperatures. (Arntzen, 2009; Bulog, 1999; Durand, 1981; Sessions, 2010a; Sessions, 2010b; Steward, 1969)
is an aseasonal breeder. During times of breeding, males become territorial and physically defend their territories. The qualities of an ideal territory are unknown. Once a mating territory is established by the male, he waits for females. Eventually a female will approach a male within his territory and courtship begins. It is unclear whether males and/or females release pheromones to communicate with each other. A male may potentially mate with multiple females, but a female mates with just one male.
The courtship process is distinctive. A female approaches a male, and he fans his tail towards her head. The male then touches the female's cloaca with his snout, and she reciprocates. The male walks in front of the female and deposits a spermatophore, which the female immediately picks up with her cloaca and stores in a special structure called a spermathecae. (Sessions, 2010a; Sessions, 2010b)
A female olm guards her eggs while they incubate (2 to 6 months). She does not provide food or protection once the eggs are hatched. Males exhibit no parental investment beyond the initial sperm. (Bulog, 1999; Sessions, 2010a)
Because olms live in such secluded environments, little is known about their lifespan or longevity in the wild. In fact, much of the information available concerning (Bulog, 1999)has been gathered from observing populations in captivity. The average age of an individual in captivity was 68.5 years, and the expected life expectancy is over 100 years.
Due to olms' secretive lifestyle, little information has been gathered in the wild regarding its general behavior. Usually a gregarious salamander occupying space under rocks or in cracks, (Bulog, 1999; Sessions, 2010a)only becomes territorial during times of breeding. Migratory behavior for this species is unknown, but it is expected to be mainly sedentary.
Because the adult (Bulog, 1999)occupies caves that are largely inaccessible to humans, the extent of an individual's range is not known.
Because it inhabits permanently dark environments, Proteus contain an ampullary electroreceptor which is used to detect electric fields. The main function of their ampullary electroreceptor is not known, but it is suspected top be used for locating prey. Behavioral studies suggest that is also able to detect and orient itself to magnetic fields.has developed non-visual sensory systems to better suit an aphotic lifestyle. Its eyes still retain some light sensitivity, but they are greatly reduced. Highly sensitive chemoreceptors allow olms to detect extremely low concentrations of organic material in the water. Olms use this ability to distinguish species of prey and their abundance. Functional ears, which may register sounds from the surrounding water as well as the ground, are complemented by olms' lateral line organ, which detects low-frequency water displacement in the nearby surrounding environment. All members of the genus
Little is known about the forms of intraspecies communication of olms. Potential mates have been observed using tactile stimulation – each mate touching its snout to the others cloaca. Before this, the male waves his tail in front of the female’s head. Because visual perception is minimal in the species, the purpose of such courtship behaviors is believed to be linked to pheromones and chemoreception. To establish and defend their territories, males are not known to use chemical clues, but rely on physical competition. The specialized sensory adaptations observed in olms have led scientists to use the species as a model for studying the effects of permanent darkness on the evolution of such traits. (Arntzen, 2009; Bulog, 1989; Bulog, 1999; Dumas, 1998; Sessions, 2010a)
Olms are insectivores, but will eat most anything that they can capture and fit into their mouths. They prey on arthropods and small invertebrates such as Oniscus asellus as well as organsims of the genera Belgrandiella and Niphargus. They also feed on a wide variety of insect larvae belonging to the orders Trichoptera, Ephemeroptera, Plecoptera, and Diptera. To locate and capture their prey, olms use a combination of chemoreceptors, electroreceptors, and mechanoreceptors. In captivity, olms have been recorded eating worms, tiny fish, and even small pieces of raw meat. (Bulog, 1999; Steward, 1969)
has no known predators.
As a predator of multiple different organisms, (Bulog, 1999)has a direct impact on the sizes of insect, arthropod, and other invertebrate populations within local subterranean freshwaters.
There are no known adverse effects ofon humans.
Jordan Meaton (author), University of Michigan-Ann Arbor, Phil Myers (editor), University of Michigan-Ann Arbor, Rachelle Sterling (editor), Special Projects.
living in the northern part of the Old World. In otherwords, Europe and Asia and northern Africa.
uses sound to communicate
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
humans benefit economically by promoting tourism that focuses on the appreciation of natural areas or animals. Ecotourism implies that there are existing programs that profit from the appreciation of natural areas or animals.
animals which must use heat acquired from the environment and behavioral adaptations to regulate body temperature
uses electric signals to communicate
parental care is carried out by females
union of egg and spermatozoan
mainly lives in water that is not salty.
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
referring to animal species that have been transported to and established populations in regions outside of their natural range, usually through human action.
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).
(as perception channel keyword). This animal has a special ability to detect the Earth's magnetic fields.
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.
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.
specialized for swimming
the area in which the animal is naturally found, the region in which it is endemic.
reproduction in which eggs are released by the female; development of offspring occurs outside the mother's body.
the business of buying and selling animals for people to keep in their homes as pets.
chemicals released into air or water that are detected by and responded to by other animals of the same species
having more than one female as a mate at one time
remains in the same area
reproduction that includes combining the genetic contribution of two individuals, a male and a female
associates with others of its species; forms social groups.
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).
defends an area within the home range, occupied by a single animals or group of animals of the same species and held through overt defense, display, or advertisement
movements of a hard surface that are produced by animals as signals to others
Arnold, E., J. Burton. 1978. A Field Guide to the Reptiles and Amphibians of Britain and Europe. London: Harper Collins Publishers.
Arntzen, J. 2009. "IUCN Red List of Threatened Species" (On-line). Accessed February 21, 2010 at http://www.iucnredlist.org/apps/redlist/details/18377/0.
Bulog, B. 1989. Differentiation of the inner ear sensory epithelia of Proteus anguinus (Urodela, Amphibia). Journal of Morphology, 202: 225-238.
Bulog, B. 1999. "Amphibiaweb" (On-line). Accessed February 21, 2010 at http://amphibiaweb.org/cgi-bin/amphib_query?query_src=aw_search_index&where-genus=Proteus&where-species=anguinus&rel-genus=equals&rel-species=equals.
Dumas, P. 1998. The olfaction in Proteus anguinus. Behavioural Processes, 43: 107-113.
Durand, J. 1981. Influence of temperature on the development of Proteus anguinus (Caudata: Proteidae) and relation with its habitat in the subterranean world. Journal of Thermal Biology, 6/1: 53-57.
Felice, V. 2008. Mechanisms of pigmentation loss in subterranean fishes. Neotropical Ichthyology, 6/4: 657-662. Accessed February 14, 2010 at http://csaweb109v.csa.com/ids70/view_record.php?id=2&recnum=3&log=from_res&SID=a0fnmakcebl7v5at13d51v0lv1&mark_id=search%3A2%3A0%2C0%2C10.
Gasc, J. 1997. Atlas of Amphibians and Reptiles in Europe. Paris: Societas Europaea Herpetologica.
Halliday, T., K. Adler. 2002. The New Encyclopedia of Reptiles and Amphibians. Oxford: Oxford University Press.
Hawes, R. 1945. On the eyes and reactions to light of Proteus anguinus. Quarterly Journal of Microbiological Sciences, 86/2: 1-51.
Issartel, J. 2009. High anoxia tolerance in the subterranean salamander Proteus anguinus without oxidative stress nor activation of antioxidant defenses during reoxygenation. ournal of Comparative Physiology B Biochemical Systemic and Environmental Physiology, 179/4: 543-551. Accessed February 14, 2010 at http://csaweb109v.csa.com/ids70/view_record.php?id=2&recnum=0&log=from_res&SID=a0fnmakcebl7v5at13d51v0lv1&mark_id=search%3A2%3A0%2C0%2C10.
Schegal, P., B. Bulog. 1997. Population-specific behavioral electrosensitivity of the European blind cave salamander, Proteus anguinus. Journal of Physiology, 91: 75-79.
Sessions, S. 2010. "Grzimek's Animal Life - Proteus" (On-line). Accessed February 14, 2010 at http://animals.galegroup.com.proxy.lib.umich.edu/web/grzimeks/animals/Proteidae.
Sessions, S. 2010. "Grzimek's Animal Life" (On-line). Accessed February 14, 2010 at http://animals.galegroup.com.proxy.lib.umich.edu/web/grzimeks/animals/Proteus_anguinus?searchTerms=Proteus+anguinus.
Sket, B. 2003. Distribution of Proteus (Amphibia: Urodela: Proteidae) and its possible explanation. Journal of Biogeography, 24/3: 263-280. Accessed February 21, 2010 at http://www3.interscience.wiley.com/journal/119154743/abstract?CRETRY=1&SRETRY=0.
Steward, J. 1969. The Tailed Amphibians of Europe. Great Britain: David & Charles: Newton Abbot.