Strinati's Cave Salamander

''Speleomantes strinatii'', the French cave salamander, North-west Italian cave salamander, or Strinati's cave salamander is a small (10-12.5 cm long) species of salamander found in northwest Italy and southeast France. It is very similar in appearance to the Italian cave salamander (''Speleomantes italicus''), but has a paler belly.

Description

''S. strinatii'' is a completely terrestrial plethodontid, meaning that they are a fully land-based species. ''S. strinatii'' is one of seven species of plethodontid salamanders found in southern Europe.Lanza, B., Pastorelli, C., Laghi, P. and Cimmaruta, R. 2005. A review of systematics, taxonomy, genetics, biogeography, and natural history of the genus Speleomantes Dubois, 1984 (Amphibia Caudata Plethodontidae). Atti Mus. Civ. Stor. Nat. Trieste, Suppl. 52: 5-`35.

''S. strinatii'' can vary widely in size. ''S. strinatii'' is highly sexually dimorphic. Male ''S. strinatii'' average about 96 millimeters in length, and can grow to up to 116 millimeters long. Females average about 100 millimeters and have been observed at a maximum length of 123 millimeters. ''S. strinatii'' have an oval-shaped head, a rounded snout, and a slight overbite that is more pronounced in males. ''S. strinatii's'' hind limbs are slightly longer than their front limbs. The salamanders' hind feet have five digits each, and their front feet only have four digits. The ''S. strinatii'' also have highly variable coloration and patterns.

''S. strinatii'' are commonly brown and black in color. However, some of these salamanders have different patterns on their skin, such as spots, blotches, or striped reticular patterns in red, yellow, gray, green, or metallic sheen.Boehme, W., Grossenbacher, K., and Thiesmeier, B. (1999). Handbuch der Reptilien und Amphibien Europas, band 4/I:Schwanzlurche (Urodela). Aula-Verlag, Wiesbaden.

Habitat and distribution

''S. strinatii'' are found in the Southeast region of France as well as in Northwest Italy. This species ranges from Alpes de Haute Provence to Northwest Tuscany, through the Maritime Alps, Ligurian Alps, and Ligurian Apennines. ''S. strinatii'' are commonly found at 0 to 2290 meters above sea level. However, in the Maritime Alps, ''S. strinatii'' have been observed at a higher elevation of 2432 meters.Gasc, J. P. (2004). Atlas of Amphibians and reptiles in Europe. Societas Europaea Herpetologica.

''S. strinatii'' are not obligate cave dwellers. For example, during times of extreme heat, ''S. strinatii'' retreat to underground environments that are cooler and more comfortable.Ficetola, Gentile Francesco & Pennati, Roberta & Manenti, Raoul. (2013). Spatial segregation among age classes in cave salamanders: Habitat selection or social interactions?. Population Ecology. 55. 217-226. 10.1007/s10144-012-0350-5.

''S. strinatii'' can be active throughout the year. They prefer humid environments, such as the caves for which they are named. The salamander is found in caves, crevices, and other cavities from late spring to summer.Bologna MA, Salvidio S (2006) Speleomantes strinatii (Aellen, 1958). In: Sindaco R, Doria G, Razzetti E, Bernini F (eds) Atlas of Italian amphibians and reptiles. Polistampa, Firenze, pp 258–261

Conservation

''S. strinatii'' was most recently assessed for The IUCN Red List of Threatened Species in 2021. This list declared ''S. strinatii'' an endangered species, because the population size was declining. There are many known contributing factors. Known threats to ''S. strinatii'' include residential and commercial development, climate change and severe weather, biological resource use, and invasive species. There is a localized loss of habitat due to logging, tourist developments, and urbanization. Climate change is likely to be a major threat to ''S. strinatii'' due to the narrow climatic preferences of this species.

Behavior

Territoriality

When in cave environments, ''S. strinatii'' movement is extremely limited and easily detected. ''S. strinatii'' have displayed spatial age-class segregation, with juveniles living closer to the cave entrances and older salamanders living deeper in the caves. It has been theorized that this segregation occurs because the juveniles are attempting to avoid cannibalistic behaviors that have been observed in older salamanders.Salvidio S, Pastorino MV (2002) Spatial segregation in the European plethodontid Speleomantes strinatii in relation to age and sex. Amphibia-Reptilia 23:505–510 Adult salamanders have been seen traveling 3 to 49 meters from their caves, while juveniles do not stray as far from their homes, only seen exploring between 1 and 12 meters from their cave habitats. ''S. strinatii'' can move about 10 meters per day when moving along the forest floor in favorable conditions.

There have been no observed sex-based differences in the homing capacities of ''S. strinatii''.Salvidio, Sebastiano. (2013). Homing behavior in Speleomantes strinatii (Amphibia Plethodontidae): A preliminary displacement experiment. North-Western Journal of Zoology. 9. 429-432.

Diet

''S. strinatii'' appear to be opportunistic hunters with a wide range of invertebrate prey.Thiesmeier, B., Grossenbacher, K., &; Franzen, M. (2004). Handbuch der Reptilien und Amphibien Europas. Aula. These salamanders tend to eat more in autumn.

Reproduction and life cycle

Fertilization

There is little to no research on the reproduction of ''S. strinatii'' in the wild. However, it is known that sperm transfer takes place through cloacal contact. ''S. strinatii'' have an observable mating season, with most pregnant females being found in the fall.Salvidio, S. (1993). ''Life history of the European plethodontid salamander Speleomantes ambrosii (Amphibia, Caudata).'' Herpetological Journal, 3, 55-59. Observations of ''S. strinatii'' in captivity see the salamanders hiding their eggs around loose rocks and leaf litter. Their eggs are ivory white and are about 5 to 6 millimeters in diameter. After 8 months, the eggs will double in size.

Lifespan

After hatching, the young are about 22 to 24 millimeters in length. Male ''S. strinatii'' reach sexual maturity at the age of three years, while females become sexually mature at 4 years of age.Salvidio S (1998) Estimating abundance and biomass of a Speleomantesstrinatii (Caudata: Plethodontidae) population by temporary removal sampling. Amphib–Reptil 19:113–124 Direct observation of this species in captivity provides data that they may live about six years; however, the recapture of one individual provides evidence that their lifespan may be much longer, in this case, more than 17 years.

Parental care

Post hatching parental care is known to occur in amphibians such as frogs and caecilians. However, there has not been much reported on such care in salamanders. There is little to no information regarding ''S. strinatii'' nest sites and egg clutches in the wild; however, in captivity, females have been observed to produce between six and fourteen relatively large eggs.Salvidio, S., A. Lattes, M. Tavano, F. Melodia, And M. V. Pastorino. 1994. Ecology of a Speleomantes ambrosii population inhabiting an artificial tunnel. Amphibia-Reptilia 15:35–45.Durand, J.-P. 1970. Fortplanzung und Entwicklung von Hydromantes, dem Ho ̈hlenmolch. Aqua Terra 7:42–48.

Egg Guarding

Females were observed guarding their eggs for up to ten months. During brooding, the females were seen to coil around their eggs, defending them against approaching conspecifics. Occasionally, attending females would eat their own eggs. This cannibalistic behavior is theorized to be a way of disposing of eggs that are not developing.

In a study conducted by Oneto et al. in 2007, female ''S. strinatii'' were observed using video footage for twenty-four hours a day. In this study, the researchers had one brooding female and one non-brooding female living in a terrarium that scientists created in an attempt to imitate their natural habitat. In this study, females were observed to lay eggs in small depressions on the ground. During the first week after laying their eggs, the female was in constant contact with her eggs, often seen rotating the eggs with her hind limbs. Ten days after laying her eggs, the mother began leaving her nesting site for short periods of time spanning from 3 to 46 minutes. After five days, the non-brooding female began intruding into the nesting site. After 10 days, the brooding female was seen repelling the other female from her nesting site. The brooding female was also seen aggressively defending her eggs from rats. During the brooding period, the female remained in contact with her eggs for 98% of the time. By the time the eggs began hatching, only two of the nine eggs that the female laid remained. The first egg hatched 45 weeks after being laid. The second egg hatched five days later. Due to the five-day gap between hatching, the offspring had different-sized bodies. The first hatchling was larger than the second hatchling. For the first week after hatching, the female remained motionless inside the nesting site for about 97% of the time, but this decreased by 20% by the sixth week. The hatchlings were observed to be in skin-to-skin contact with their mother often, and the mother was seen transporting her hatchlings on her back multiple times. During the sixth week, the hatchlings began leaving the nesting site alone for the first time. Forty-two days after hatching, the three animals were seen to leave the terrarium permanently.

Microbial Threats

Like other Hydromantes, ''S. strinatii'' produces a deterring secretion from dorsal skin glands as a form of protection. The bright-colored patterns on their backs can be considered aposematic. This secretion may be protective against different microbial infections. ''Batrachochytrium salamandrivorans'' and ''Batrachochytrium dendrobatidis'' are two similar single-celled fungal pathogens that have had detrimental effects on amphibian populations worldwide, including ''S. strinatii''. ''Batrachochytrium dendrobatidis'' has been known to cause disease in frogs, salamanders, and caecilians, while ''Batrachochytrium salamandrivorans'' has only been reported to infect Urodelans (newts and salamanders).Martel, A., Spitzen-van der Sluijs, A., Blooi, M., Bert, M., Ducatelle, R., Fisher, M.C., Woeltjes, A., Bosman, W., Chiers, K., Bossuyt, F. and Pasmans, F. 2013. Batrachochytrium salamandrivorans sp. nov. causes lethal chytridiomycosis in amphibians. Proceedings of the National Academy of Sciences of the United States of America Early Edition: doi: 10.1073/pnas.1307356110.''Batrachochytrium salamandrivorans'' and ''Batrachochytrium dendrobatidis'' both cause the infectious disease of chytridiomycosis. Symptoms of this fatal condition include disruptions of the amphibian's salt-water balance, destruction of the amphibian's skin, and eventual heart failure. The fungal pathogens are believed to have originated in Asia and are thought to likely have been introduced to Europe through the pet trade of salamanders. ''Batrachochytrium salamandrivorans'' has been detected in the wild in the Netherlands, Belgium, Germany, and Spain and have been shown to be highly pathogenic to most urodelan taxa. While there are currently no records of ''Batrachochytrium salamandrivorans'' in France or Italy, it is probable that it will spread through these areas in the near future, as the closest recorded outbreak is only 509 kilometers away. IUCN SSC Amphibian Specialist Group (IUCN SSC). (2021, November 18). The IUCN Red List of Threatened Species. IUCN Red List of Threatened Species. Retrieved November 14, 2022, from https://www.iucnredlist.org/species/59405/89709164 There are some current hypotheses that ''S. strinatiis skin secretions may act as protection against this fungus. The secretions have been shown to kill the fungus within 24 hours. Because of this microbial protection, researchers do not believe that Bd will have the same detrimental effect on S. strinatii populations as it had for other salamanders and amphibians.

References

{{Taxonbar, from=Q628954

strinatii
Amphibians described in 1958