Alpine newt

The alpine newt (Ichthyosaura alpestris) is a species of newt native to continental Europe and introduced to Great Britain and New Zealand. Adults measure 7–12 cm (2.8–4.7 in) and are usually dark grey to blue on the back and sides, with an orange belly and throat. Males are more conspicuously coloured than the drab females, especially during breeding season.

Alpine newt
Temporal range:
Two newts with orange bellies under water
Two males during breeding season
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Amphibia
Order: Urodela
Family: Salamandridae
Genus: Ichthyosaura
Latreille, 1801
Species:
I. alpestris
Binomial name
Ichthyosaura alpestris
(Laurenti, 1768)
Subspecies
  • I. a. alpestris
  • I. a. apuana
  • I. a. cyreni
  • I. a. veluchiensis

(debated, see text)

Synonyms

Around 80,[3] including:

  • Triton alpestris (Laurenti, 1768)
  • Triturus alpestris (Dunn, 1918)
  • Mesotriton alpestris (García-París, Montori, and Herrero, 2004)

The alpine newt occurs at high altitude as well as in the lowlands. Living mainly in forested land habitats for most of the year, the adults migrate to puddles, ponds, lakes or similar water bodies for breeding. Males court females with a ritualised display and deposit a spermatophore. After fertilisation, females usually fold their eggs into leaves of water plants. The aquatic larvae grow up to 5 cm (2.0 in) in around three months before metamorphosing into terrestrial juvenile efts, which mature into adults at around three years. In the southern range, the newts sometimes do not metamorphose but keep their gills and stay aquatic as paedomorphic adults. Larvae and adults feed mainly on diverse invertebrates and themselves fall prey to dragonfly larvae, large beetles, fish, snakes, birds or mammals.

Populations of the alpine newt started to diverge around 20 million years ago. At least four subspecies are distinguished, and some argue there are several distinct, cryptic species. Although still relatively common and classified as Least Concern on the IUCN Red List, alpine newt populations are decreasing and have locally gone extinct. The main threats are habitat destruction, pollution and the introduction of fish such as trout into breeding sites. Where it has been introduced, the alpine newt can potentially transmit diseases to native amphibians, and it is being eradicated in New Zealand.

Taxonomy

Nomenclature

The alpine newt was first described in 1768 by Austrian zoologist Laurenti, as Triton alpestris, from the Ötscher mountain in the Austrian Alps (alpestris meaning "alpine" in Latin).[4] He used that name for a female and described the male (Triton salamandroides) and the larva (Proteus tritonius) as different species.[5] Later, the alpine newt was placed in the genus Triturus along with most other European newts. When genetic evidence showed that Triturus as then defined contained several unrelated lineages,[6][7][8] García-París and colleagues in 2004 split off the alpine newt as the monotypic genus Mesotriton,[9] which had been erected as a subgenus by Bolkay in 1928.[10]

However, the name Ichthyosaura had been introduced in 1801 by Sonnini de Manoncourt and Latreille for "Proteus tritonius", the larva of the alpine newt.[11]: 310  It therefore has priority over Mesotriton and is now the valid genus name.[12][13]: 9–10  "Ichthyosaura", Greek for "fish lizard", refers to a nymph-like creature in classical mythology.[12]

Subspecies

Four subspecies (see table below) were recognised for the alpine newt by Roček and colleagues (2003),[14] followed by later authors,[15]: 214 [13]: 16–36  while some previously described subspecies were not retained. The four subspecies correspond only in part to the five major lineages identified within the species (see section Evolution below): The western populations of the nominate subspecies I. a. alpestris, together with the Cantabrian I. a. cyreni and the Apennine I. a. apuana form one group, while the eastern populations of I. a. alpestris are genetically closer to the Greek I. a. veluchiensis.[1] Differences in body shape and colour between the subspecies are not consistent.[15]: 214 [13]: 16–36 

Several authors argued that the ancient lineages of the alpine newt might represent cryptic species.[3][16] Four species were therefore distinguished by Raffaëlli in 2018,[16] but Frost considers this premature.[3]

Subspecies[14][15]: 214 [13]: 16–36 Raffaëlli (2018) classification[16]Distribution
I. a. alpestris (Laurenti, 1768)
– Alpine newt		western populationsretained as I. alpestris alpestrisNorthwestern France to northern Carpathians in Romania, southern Denmark in to Alps and France just north of the Mediterranean
eastern populationsI. reiseri (species), with subspecies reiseri, carpathica and montenegrinaBalkan peninsula north of Greece to Bulgaria and southern Carpathians in Romania
I. a. apuana (Bonaparte, 1839)
– Apennine alpine newt		I. apuana (species), with subspecies apuana and inexpectata (Calabria)Extreme southeastern France, Apennines to Lazio in central Italy, isolated populations in Calabria
I. a. cyreni (Mertens & Muller, 1940)
– Cantabrian alpine newt		retainedSpain: Cantabrian mountains and Sierra de Guadarrama (introduced)
I. a. veluchiensis (Wolterstorff, 1935)
– Greek alpine newt		I. veluchiensis (species)Greece: mainland and northern Peloponnese

Evolution

Alpine newt populations have separated since the Early Miocene, around 20 million years ago, according to a molecular clock estimate by Recuero and colleagues.[1] Known fossil remains are much more recent: they were found in the Pliocene of Slovakia[13]: 38  and the Pleistocene of Northern Italy.[17] An older, Miocene fossil from Germany, Ichthyosaura randeckensis, may be the sister species of the alpine newt.[18]

Molecular phylogenetic analyses showed that alpine newts split into a western and an eastern group. Each of these again contains two major lineages, which in part correspond to described subspecies (see section Distribution and subspecies above).[1][19] These ancient genetic differences suggest that the alpine newt may be a complex of several distinct species.[1][3][16] Higher temperatures during the Miocene or sea level oscillations may have separated early populations, leading to allopatric speciation, although admixture and introgression between lineages probably took place. Populations from Vlasina Lake in Serbia have mitochondrial DNA that is distinct from and more ancient than that of all other populations; it may have been inherited from a now extinct "ghost" population.[1] The Quaternary glaciation probably led to cycles of retreat into refugia, expansion and range shifts.[1][20]

Description
Dorsal view of a male (bright blue, left) courting a female (mottled grey, right) in a shallow pond
Dorsal view of a male (bright blue, left) courting a female (mottled grey, right) in a shallow pond
View of the orange underside of an alpine newt
Throat and belly are orange and usually unspotted.
Biofluorescence in an alpine newt

The alpine newt is medium-sized and stocky. It reaches 7–12 cm (2.8–4.7 in) length in total, females measuring roughly 1–2 cm (0.39–0.79 in) longer than males, and a body weight of 1.4–6.4 g. The tail is compressed sideways and is half as long or slightly shorter than the rest of the body. During their life in water, both sexes develop a tail fin, and males a low (up to 2.5 mm), smooth-edged crest on their back. The cloaca of males swells during breeding season. The skin is smooth during the breeding season and granular outside it, and is velvety during the animal's land phase.[15]: 213 [13]: 10–13 

The characteristic dark grey to bright blue of the back and sides is strongest during breeding season. This base colour may vary to greenish and is more drab and mottled in females. The belly and throat are orange and only occasionally have dark spots. Males have a white band with black spots and a light blue flash running along the flanks from the cheeks to the tail. During breeding season, their crest is white with regular dark spots. Juvenile efts, just after metamorphosis, resemble adult terrestrial females, but sometimes have a red or yellow line on the back. Very rarely, leucistic individuals have been observed.[15]: 213 [13]: 12–36 

While these traits apply to the widespread nominate subspecies, I. a. alpestris, the other subspecies differ slightly. I. a. apuana often has dark spots on the throat and sometimes on the belly. I. a. cyreni has a slightly rounder and larger skull than the nominate subspecies but is otherwise very similar. In I. a. veluchiensis, females have a more greenish colour, spots on the belly, sparse dark spots on the lower tail edge, and a narrower snout, but these differences between subspecies are not consistent.[15]: 214–215 [13]: 33–36 

Larvae are 7–11 mm long after hatching and grow to 3–5 cm (1.2–2.0 in) just before metamorphosis. They initially have only two small filaments (balancers), between the eyes and gills on each side of the head, which later disappear as the forelegs and then the hindlegs develop.[15]: 215 [13]: 97–104  The larvae are light brown to yellow and initially have dark longitudinal stripes, which later dissolve into a dark pigmentation that is stronger towards the tail. The tail is pointed and sometimes ends in a short filament. Alpine newt larvae are more robust and have wider heads than those of the smooth newt and palmate newt.[15]: 215 [13]: 13–14 

Distribution

The alpine newt is native to continental Europe. It is relatively common over a large, more or less continuous range from northwestern France to the Carpathians in Romania, and from southern Denmark in the north to the Alps and France just north of the Mediterranean in the south, but absent from the Pannonian basin. Isolated areas of distribution in Spain, Italy and Greece correspond to distinct subspecies (see section Taxonomy: Subspecies above).[15]: 214–215 [13]: 39–46 [1][16] Alpine newts have been deliberately introduced to parts of continental Europe, including within the boundaries of cities such as Bremen and Berlin.[13]: 39–46  Other introductions have occurred to Great Britain,[21] mainly England but also Scotland,[22] and Coromandel Peninsula in New Zealand.[23]

The alpine newt can occur at high elevation and has been found up to 2,370 m (7,780 ft) above sea level in the Alps. It also occurs in the lowlands down to sea level. Towards the south of its range, most populations are found above 1,000 m (3,300 ft).[13]: 51–59 

Habitats
Shady pond surrounded by forest and
Shady ponds surrounded by forest (here in the Vosges, France) are typical breeding sites for alpine newts.
Young alpine newt sitting in rotting wood
Juvenile eft hibernating in dead wood

Forests, including both deciduous and coniferous forests (pure spruce plantations are avoided), are the main land habitat. Less common are forest edges, brownfield land, or gardens. Populations can be found above tree line in the high mountains, where they prefer south-exposed slopes. The newts use logs, stones, leaf litter, burrows, construction waste or similar structures as hiding places.[15]: 216 [13]: 54–59 

Aquatic breeding sites close to adequate land habitat are critical. While small, cool water bodies in forested areas are preferred, alpine newts tolerate a wide range of permanent or non-permanent, natural or human-made water bodies. These can range from shallow puddles over small ponds to larger, fish-free lakes or reservoirs and quiet parts of streams. Damming by beavers creates suitable breeding sites. Overall, the alpine newt is tolerant regarding chemical parameters such as pH, water hardness and eutrophication. Other European newts such as the crested, smooth, palmate or Carpathian newt often use the same breeding sites, but are less common at higher elevation.[15]: 216 [13]: 47–54 

Lifecycle and behaviour

Alpine newts are usually semiaquatic, spending most of the year (9–10 months) on land and only returning to the water for breeding. The efts are probably terrestrial until they reach sexual maturity.[13]: 54  At lower altitudes this occurs in males after around three years, and in females after four to five years. Lowland alpine newts can reach the age of ten. At higher altitudes, maturity is reached only after 9–11 years, and the newts can live for up to 30 years.[15]: 215 

Terrestrial phase
Newt curling up its tail
Defensive position, with tail curled up

On land, alpine newts are mainly nocturnal, hiding for most of the day and moving and feeding during the night or in the twilight. Hibernation also usually takes place in terrestrial hiding places. They have been observed to climb up to 2 metres (6.6 ft) on vertical walls of basement ducts, where they hibernated, on wet nights. [13]: 105–107  Migration to breeding sites occurs on sufficiently warm (above 5 °C) and humid nights and may be delayed or interrupted for several weeks in unfavourable conditions. The newts can also leave the water in case of a sudden cold snap.[13]: 89–90 

Alpine newts tend to stay close to their breeding sites and only a small proportion, mainly juvenile efts, disperse to new habitats. A dispersal distance of 4 km (2.5 mi) has been observed, but such large distances are uncommon. Over short distances, the newts use mainly their sense of smell for navigation, while over long distances, orientation by the night sky, and potentially through magnetoreception are more important.[13]: 122–128 

Aquatic phase and breeding

The aquatic phase starts at snowmelt, from February in the lowlands to June at higher altitudes, while egg laying follows a few months later and can continue until August.[15]: 216 [13]: 87–90  Some southern populations in Greece and Italy appear to stay aquatic most of the year and hibernate underwater.[13]: 104–105  In the Apennine subspecies, I. a. apuana, two rounds of breeding and egg-laying in autumn and spring have been observed .[13]: 96 

Breeding behaviour occurs mainly in the morning and at dawn. Males perform a courtship display. The male first places himself in front of the female remains static for a while, then fans his tail to stimulate the female and wave pheromones towards her. After leaning in and touching her snout, he creeps away, followed by the female. When she touches the base of his tail with her snout, he releases a sperm packet (spermatophore) and blocks the female's path so she picks it up with her cloaca. Several rounds of spermatophore deposition may follow. Males frequently interfere with displays of rivals.[15]: 215  Experiments suggest that it is mainly male pheromones that trigger mating behaviour in females, while colour and other visual cues are less relevant.[24] In a breeding season, a male can produce more than 48 spermatophores, and offspring from one female usually have several fathers.[13]: 83–86 

Young larva inside jelly capsule
Egg with larva just before hatching
Side view of larva with fore- and hindlegs
Larva with fore- and hindlegs developed

Females wrap their eggs in leaves of water plants for protection, preferring leaves closer to the surface where temperatures are higher. Where no plants are available, they may also use leaf litter, dead wood or stones for egg deposition.[13]: 94–104  They can lay 70–390 eggs in a season, which are light grey-brown and 1.5–1.7 mm in diameter (2.5–3 mm including the jelly capsule). Incubation time is longer under cold conditions, but larvae typically hatch after two to four weeks.[15]: 216  The larvae are benthic, staying in general close to the bottom of the water body.[13]: 98  Metamorphosis occurs after around three months, again depending on temperature, but some larvae overwinter and metamorphose only in the next year.[15]: 216 

Paedomorphy
Pale-coloured adult newt with gills
Paedomorphic adult of subspecies I. a. apuana

Paedomorphy, where adults do not metamorphose and instead retain their gills and stay aquatic, is more common in the alpine newt than in other European newts. It is almost exclusively found in the southern part of the range (but not in the Cantabrian subspecies, I. a. cyreni). Paedomorphic adults are paler in colour than metamorphic ones. Only part of a population is usually paedomorphic, and metamorphosis can follow if the pool dries out. Paedomorphic and metamorphic newts sometimes prefer different prey, but they do interbreed. Overall, paedomorphy appears to be a facultative strategy under particular conditions that are not fully understood.[13]: 60–65 

Diet, predators and parasites

Alpine newts are diet generalists, taking mainly different invertebrates as prey. Larvae and adults living in the water eat for example plankton, molluscs,[25] larvae of insects such as chironomids, crustaceans such as water fleas,[25] ostracods, or amphipods, and terrestrial insects falling on the surface. Amphibian eggs and larvae, including of their own species, are also eaten. Prey on land includes insects, worms, spiders and woodlice.[13]: 68–72 

Predators of adult alpine newts are snakes such as the grass snake, fish such as trout, birds such as herons or ducks, and mammals such as hedgehogs, martens or shrews. Under water, large diving beetles (Dytiscus) can prey on newts, while small efts on land may be predated by ground beetles (Carabus). For eggs and larvae, diving beetles, fish, dragonfly larvae, and other newts are the main enemies.[13]: 73–77 Predator pressure can affect the phenotype of developing alpine newts.[26] In an experiment, alpine newt larvae raised in the presence of caged dragonfly larvae took longer to emerge from the larval stage, growing slower and emerging later in the season than newt larvae that did not experience predator presence. They also exhibited traits such as darker coloration, larger body size, a proportionally larger head and tail, and more wary behavior than their predator-free counterparts.[26]

Threatened adult newts often take on a defensive position, where they expose the warning colour of their belly by bending backwards or raising their tail and secrete a milky substance.[13]: 74–75  Only trace amounts of the poison tetrodotoxin, abundant in the North American Pacific newts (Taricha), have been found in the alpine newt.[27] They also sometimes produce sounds, whose function is unknown.[13]: 74–75  When adult newts are in the presence of a predator, they tend to flee a majority of the time.[28] However, the decision of whether or not to flee can depend on the newt's sex and temperature. In an experiment, female newts fled more often and at a greater speed over a greater range of temperatures than males, who tended to flee at a slower speed and remained immobile while secreting tetrodotoxin when the temperature was outside of the normal range.[28]

Parasites include parasitic worms, leeches, the ciliate Balantidium elongatum, and potentially toadflies.[13]: 77  A ranavirus transmitted to alpine newts from midwife toads in Spain caused bleeding and necrosis.[13]: 142  The chytridiomycosis-causing fungus Batrachochytrium dendrobatidis has been found in wild populations,[29] and the emerging B. salamandrivorans was lethal for alpine newts in laboratory experiments.[30]

Captivity

Several subspecies of the alpine newt have been bred in captivity, including a population from Prokoško Lake in Bosnia that is now probably extinct in the wild. Efts often return to the water after only one year. Captive individuals have reached an age of 15–20 years.[31][15]: 217 

Threats and conservation

Because of its overall large range and populations that are not severely fragmented, the alpine newt was classified as Least Concern on the IUCN Red List in 2009. The population trend, however, is "Decreasing", and the different geographic lineages, which may represent evolutionary significant units, have not been evaluated separately.[2] Several populations in the Balkans, some of which have been described as subspecies of their own, are highly threatened or have even gone extinct.[16][13]: 133–134 

Threats are similar to those affecting other newts and include mainly destruction and pollution of aquatic habitats. Beavers, previously widespread in Europe, were probably important in maintaining breeding sites. Introduction of fish, especially salmonids such as trout, and potentially crayfish is a significant threat that can eradicate populations from a breeding site. In the Montenegrin karst region, populations have declined as ponds created for cattle and human use were abandoned over the last decades. Lack of adequate, undisturbed land habitat (see section Habitats above) and dispersal corridors around and between breeding sites, is another problem.[15]: 216 [13]: 130–144 

Effects as introduced species

Introduced alpine newts may pose a threat to native amphibians if they carry disease. A particular concern is chytridiomycosis, which was found in at least one introduced population in the United Kingdom.[2] In New Zealand, the risk of spreading chytridiomycosis to endemic frogs[23] has led to the introduced subspecies I. a. apuana being declared an "unwanted organism", and eradication being recommended. It has proven challenging to detect and remove the newts, but over 2000 individuals have been eradicated until 2015.[32]

References
  1. Recuero, E.; Buckley, D.; García-París, M.; et al. (2014). "Evolutionary history of Ichthyosaura alpestris (Caudata, Salamandridae) inferred from the combined analysis of nuclear and mitochondrial markers" (PDF). Molecular Phylogenetics and Evolution. 81: 207–220. doi:10.1016/j.ympev.2014.09.014. ISSN 1055-7903. PMID 25263421.
  2. Arntzen, J.W.; Denoël, M.; Kuzmin, S.; et al. (2009). "Ichthyosaura alpestris (Alpine Newt)". IUCN Red List of Threatened Species. 2009: e.T59472A11946568. doi:10.2305/IUCN.UK.2009.RLTS.T59472A11946568.en. Retrieved 28 March 2020.
  3. Frost, D.R. (2020). "Ichthyosaura alpestris (Laurenti, 1768)". Amphibian Species of the World: An Online Reference. Version 6.1. New York, USA: American Museum of Natural History. doi:10.5531/db.vz.0001. Archived from the original on 21 March 2020. Retrieved 21 March 2020.
  4. Laurenti, J.N. (1768). Specimen Medicum, Exhibens Synopsin Reptilium Emendatum cum Experimentis Circa Venena et Antidota Reptilium Austriacorum (in Latin). Vienna, Austria: Joan. Thom. nob. de Trattnern. doi:10.5962/bhl.title.5108.
  5. Schmidtler, J.F. (2007). "Die Wurzeln einer bayrischen Herpetofaunistik im 18. und beginnenden 19. Jahrhundert" (PDF). Zeitschrift für Feldherpetologie (in German). 14: 93–119. Archived from the original (PDF) on 25 February 2019.
  6. Titus, T.A.; Larson, A. (1995). "A molecular phylogenetic perspective on the evolutionary radiation of the salamander family Salamandridae" (PDF). Systematic Biology. 44 (2): 125–151. doi:10.1093/sysbio/44.2.125. ISSN 1063-5157.
  7. Weisrock, D.W.; Papenfuss, T.J.; Macey, J.R.; Litvinchuk, S.N.; Polymeni, R.; Ugurtas, I.H.; Zhao, E.; Jowkar, H.; Larson, A. (2006). "A molecular assessment of phylogenetic relationships and lineage accumulation rates within the family Salamandridae (Amphibia, Caudata)" (PDF). Molecular Phylogenetics and Evolution. 41 (2): 368–383. doi:10.1016/j.ympev.2006.05.008. ISSN 1055-7903. PMID 16815049.
  8. Steinfartz, S.; Vicario, S.; Arntzen, J.W.; Caccone, Adalgisa (2007). "A Bayesian approach on molecules and behavior: reconsidering phylogenetic and evolutionary patterns of the Salamandridae with emphasis on Triturus newts". Journal of Experimental Zoology Part B: Molecular and Developmental Evolution. 308B (2): 139–162. doi:10.1002/jez.b.21119. ISSN 1552-5007. PMID 16969762.
  9. García-París, M.; Montori, A.; Herrero, P. (2004). Amphibia: Lissamphibia. Fauna Iberica. Vol. 24. Madrid: Museo Nacional de Ciencias Naturales, Consejo Superior de Investigaciones Científicas. ISBN 84-00-08292-3.
  10. Bolkay, J. (1928). "Die Schädel der Salamandrinen, mit besonderer Rücksicht auf ihre systematische Bedeutung". Zeitschrift für Anatomie und Entwicklungsgeschichte (in German). 86 (3–4): 259–319. doi:10.1007/BF02117989. ISSN 0340-2061. S2CID 10108367.
  11. Sonnini, C.S.; Latreille, P.A. (1802). Histoire naturelle des reptiles : avec figures dessinées d'apres nature (in French). Vol. 4. Paris: Imprimerie de Crapelet. doi:10.5962/bhl.title.4688.
  12. Schmidtler, J.F. (2009). "Ichthyosaura, der neue Gattungsname für den Bergmolch – ein Lehrbeispiel in Sachen Nomenklatur" (PDF). Zeitschrift für Feldherpetologie (in German). 16: 245–250. (with English abstract)
  13. Thiesmeier, B.; Schulte, U. (2010). Der Bergmolch: im Flachland wie im Hochgebirge zu Hause [The alpine newt: at home in the lowlands and the high mountains]. Beihefte der Zeitschrift für Feldherpetologie (in German). Vol. 13. Bielefeld, Germany: Laurenti-Verlag. ISBN 978-3-933066-42-8.
  14. Roček, Z.; Joly, P.; Grossenbacher, K. (2003). "Triturus alpestris (Laurenti, 1768) – Bergmolch". In Grossenbacher, K.; Thiesmeier, B. (eds.). Handbuch der Reptilien und Amphibien Europas [Handbook of the amphibians and reptiles of Europe] (in German). Vol. 4/IIA, Schwanzlurche (Urodela) IIA. Salamandridae II: Triturus 1. Wiesbaden, Germany: Aula. pp. 607–656. ISBN 978-3-89104-005-8.
  15. Sparreboom, M. (2014). Salamanders of the Old World: The Salamanders of Europe, Asia and Northern Africa. Zeist, The Netherlands: KNNV Publishing. doi:10.1163/9789004285620. ISBN 978-90-04-28562-0.
  16. Raffaëlli, J.R. (2018). "Proposal for a new taxonomic arrangement of Ichthyosaura alpestris (Laurenti, 1768) (Urodela, Salamandridae), an iconic species with a complex phylogenetic structure" (PDF). Alytes. 36: 178–193. Archived from the original (PDF) on 21 March 2020.
  17. Villa, A.; Blain, H.-A.; Delfino, Massimo (2018). "The Early Pleistocene herpetofauna of Rivoli Veronese (Northern Italy) as evidence for humid and forested glacial phases in the Gelasian of Southern Alps" (DOCX). Palaeogeography, Palaeoclimatology, Palaeoecology. 490: 393–403. Bibcode:2018PPP...490..393V. doi:10.1016/j.palaeo.2017.11.016. hdl:2318/1652046. ISSN 0031-0182.
  18. Schoch, R.R.; Rasser, M.W. (2013). "A new salamandrid from the Miocene Randeck Maar, Germany" (PDF). Journal of Vertebrate Paleontology. 33: 58–66. doi:10.1080/02724634.2012.716113. S2CID 73644476. Archived from the original (PDF) on 8 August 2013.
  19. Sotiropoulos, K.; Eleftherakos, K.; Džukić, G.; et al. (2007). "Phylogeny and biogeography of the alpine newt Mesotriton alpestris (Salamandridae, Caudata), inferred from mtDNA sequences" (PDF). Molecular Phylogenetics and Evolution. 45 (1): 211–226. doi:10.1016/j.ympev.2007.03.012. ISSN 1055-7903. PMID 17467298.
  20. Chiocchio, A.; Bisconti, R.; Zampiglia, M.; Nascetti, G.; Canestrelli, D. (2017). "Quaternary history, population genetic structure and diversity of the cold-adapted Alpine newt Ichthyosaura alpestris in peninsular Italy". Scientific Reports. 7 (1): 2955. Bibcode:2017NatSR...7.2955C. doi:10.1038/s41598-017-03116-x. ISSN 2045-2322. PMC 5462806. PMID 28592856.
  21. Allain, Steven J. R; Lynn, Vanessa J. (Winter 2021). "Distribution of the alpine newt Ichthyosaura alpestris in Great Britain updated using social media". Herpetological Bulletin (158): 28–31. doi:10.33256/hb158.2831. S2CID 245602443.
  22. Bond, I. (2020). "Alpine Newt". Natural History Society of Northumbria. Archived from the original on 22 September 2019. Retrieved 5 April 2020.
  23. Bell, B.D. (2016). "A review of potential alpine newt (Ichthyosaura alpestris) impacts on native frogs in New Zealand". Journal of the Royal Society of New Zealand. 46 (3–4): 214–231. doi:10.1080/03036758.2016.1216455. ISSN 0303-6758. S2CID 88602702.
  24. Wicker-Thomas, C.; Treer, D.; Van Bocxlaer, I.; et al. (2013). "Love is blind: indiscriminate female mating responses to male courtship pheromones in newts (Salamandridae)". PLOS ONE. 8 (2): e56538. Bibcode:2013PLoSO...856538T. doi:10.1371/journal.pone.0056538. ISSN 1932-6203. PMC 3574087. PMID 23457580.
  25. "AmphibiaWeb - Ichthyosaura alpestris".
  26. Buskirk, Josh Van; Schmidt, Benedikt R. (November 2000). "Predator-Induced Phenotypic Plasticity in Larval Newts: Trade-Offs, Selection, and Variation in Nature". Ecology. 81 (11): 3009. doi:10.2307/177397. JSTOR 177397.
  27. Wakely, J.F.; Fuhrman, G.J.; Fuhrman, F.A.; Fischer, H.G.; 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 (3): 195–203. doi:10.1016/0041-0101(66)90021-3. ISSN 0041-0101. PMID 5938783.
  28. Polčák, Daniel; Gvoždík, Lumír (March 2014). "Should I stay or should I go? The influence of temperature and sex on predator-induced responses in newts". Animal Behaviour. 89: 79–84. doi:10.1016/j.anbehav.2013.12.024. S2CID 53146240.
  29. Zampiglia, M.; Canestrelli, D.; Chiocchio, A.; Nascetti, G. (2013). "Geographic distribution of the chytrid pathogen Batrachochytrium dendrobatidis among mountain amphibians along the Italian peninsula" (PDF). Diseases of Aquatic Organisms. 107 (1): 61–68. doi:10.3354/dao02655. ISSN 0177-5103. PMID 24270024.
  30. Martel, A.; Blooi, M.; Adriaensen, C.; et al. (2014). "Recent introduction of a chytrid fungus endangers Western Palearctic salamanders". Science. 346 (6209): 630–631. Bibcode:2014Sci...346..630M. doi:10.1126/science.1258268. PMC 5769814. PMID 25359973.
  31. Rafaëlli, J. (2014). "AmphibiaWeb – Ichthyosaura alpestris, Rafaëlli Account". Archived from the original on 15 April 2019. Retrieved 12 April 2019.
  32. van Winkel, D.; Ainley, E.; Brine, O.; et al. (2015). "A new invasive amphibian: informing survey and eradication techniques for exotic alpine newts (Ichthyosaura alpestris) in New Zealand". Recent developments in New Zealand herpetofauna research (PDF). New Zealand Department of Conservation. p. 23. ISBN 978-0-478-15053-7. Retrieved 5 December 2020.
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