Smooth newt

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Smooth newt
Triturus vulgaris maennchen cropped.jpg
Male during land phase
Scientific classification OOjs UI icon edit-ltr.svg
Kingdom: Animalia
Phylum: Chordata
Class: Amphibia
Order: Urodela
Family: Salamandridae
Genus: Lissotriton
Species:
L. vulgaris
Binomial name
Lissotriton vulgaris
(Linnaeus, 1758)
Subspecies [2]
  • L. vulgaris ampelensis(Fuhn, 1951)
  • L. vulgaris meridionalis(Boulenger, 1882)
  • L. vulgaris vulgaris(Linnaeus, 1758)
Lissotriton vulgaris distribution.svg
Synonyms

48, [3] including:

  • Lacerta vulgarisLinnaeus, 1758
  • Salamandra exigua Laurenti, 1768
  • Triton palustrisLaurenti, 1768
  • Molge punctata Merrem, 1820
  • Triturus vulgaris Dunn, 1918

The smooth newt, European newt, northern smooth newt or common newt (Lissotriton vulgaris) is a species of newt. It is widespread in Europe and parts of Asia, and has also been introduced to Australia. Individuals are brown with a spotted underside that ranges in colour from orange to white. They reach an average length of 8–11 cm (3.1–4.3 in), with males being larger than females. The newts' skins are dry and velvety when they are living on land, but become smooth when they migrate into the water to breed. Males develop a more vivid colour pattern and a conspicuous skin seam (crest) on their back during the breeding season.

Contents

The smooth newt was originally described by Carl Linnaeus as a lizard, and was then given different genus names before being classified as a member of Lissotriton . There are currently three accepted subspecies of smooth newt. Formerly, there were also four subspecies—all with more restricted ranges that are now classified as separate species, because they have been found to be distinct genetically as well as in appearance: the Caucasian smooth newt, the Greek smooth newt, Kosswig's smooth newt and Schmidtler's smooth newt. Together with these four species and the Carpathian newt, the smooth newt forms what is known as a species complex: some of the species hybridise with each other.

For most of the year, smooth newts live on land, are mostly nocturnal, and hide during the day. They can adapt to a wide range of natural or semi-natural habitats, from forests at field edges to parks and gardens. Their diet consists mainly of invertebrates such as insects and earthworms and they are mainly preyed upon by fish, birds and snakes. Between spring and summer, they breed in ponds or similar bodies of water. Males court females with a ritualised underwater display. Females lay their eggs on water plants, and larvae hatch after 10 to 20 days. The larvae develop for around three months before metamorphosing into terrestrial juveniles, at which point they become known as efts. They reach maturity after two to three years, and the adults live for up to 14 years.

The smooth newt is abundant over much of its range and is classified as a species of least concern by the International Union for Conservation of Nature (IUCN). However, it has been negatively affected by habitat destruction and fragmentation, as well as the introduction of new species of fish. Like other European amphibians, the smooth newt has now been listed as a protected species by the Berne Convention.

Taxonomy

Swedish naturalist Carl Linnaeus described the smooth newt in 1758 as Lacerta vulgaris, placing it in the same genus as the green lizards. [4] :370 It was later re-described under several different species and genus names, including Triton , Molge , Salamandra and Lissotriton , with in total 48 species synonyms published. [3] Most recently, it was included in the genus Triturus , along with most European newts. [5] :221 This genus was found to be polyphyletic, containing several unrelated lineages, [6] [7] [8] and the small-bodied newts, including the smooth newt, were therefore split off as separate genus in 2004 by García-París and colleagues. [9] :233 They used the name Lissotriton, introduced by the English zoologist Thomas Bell in 1839 with the smooth newt as type species [10] :132 but then considered a synonym of Triturus. [3] "Lissotriton" is a combination of the Greek λισσός (lissós), meaning "smooth", and the name of Triton, an ancient Greek god of the sea, while the species epithet vulgaris means "common" in Latin. [11] :17

Three subspecies are accepted by Pabijan, Wielstra and colleagues: L. v. vulgaris, L. v. ampelensis and L. v. meridionalis. [2] [12] These authors, followed by Amphibian Species of the World, [3] recognise four former subspecies from southern Europe and west Asia as separate species, as they are morphologically and genetically distinct: the Greek smooth newt (L. graecus), Kosswig's smooth newt (L. kosswigi), the Caucasian smooth newt (L. lantzi) and Schmidtler's smooth newt (L. schmidtleri). The five smooth newt species and the Carpathian newt (L. montadoni), which is their sister species, have collectively been referred to as the "smooth newt species complex". [12]

To distinguish the smooth newt from its close relatives, the English name "northern smooth newt" has been suggested. [12] Other common names that have been used in the literature include: common newt, great water-newt, common water-newt, warty eft, water eft, common smooth newt, small newt, small eft, small evet, and brown eft. [3]

Evolution

Molecular phylogenetic analyses have shown that the smooth newt is distinct from its four close relatives – the Caucasian, Greek, Kosswig's, and Schmidtler's smooth newt – which were formerly considered to be subspecies (see section Taxonomy above). The relationships within this species complex remain unclear. Within the smooth newt itself, genetic groups do not entirely correspond to the currently accepted subspecies (ampelensis, meridionalis, vulgaris), which were described based on morphology. [2] It is estimated that the five smooth newt species collectively were estimated to have diverged from the Carpathian newt around four to six million years ago. [13] [14]

Genetic analyses have also demonstrated ongoing gene flow between the smooth newt and its relatives. Although the Carpathian newt is clearly different in appearance, hybridisation between the two species is frequent. [11] :26 It has been shown that smooth newt mitochondrial DNA has introgressed into and completely replaced that of the Carpathian newt populations. [15] Partial introgression has also occurred from the smooth newt to the Greek smooth newt. [2] These patterns are likely due to the range expansion and secondary contact of species after the Last Glacial Maximum, which they likely survived in refugia mainly in southern and eastern Europe. [15] [14] [16] The palmate newt (Lissotriton helveticus), although often occurring in the same habitats, almost never hybridises with the smooth newt. [11] :25 Artificial crosses with even more distant species such as the alpine (Ichthyosaura alpestris) and northern crested (Triturus cristatus) newts were successful in laboratory experiments. [11] :29

Description

Throat and belly are spotted. The spots are larger in males (pictured) than in females. Schiermonnikoog - Kleine watersalamander (Lissotriton vulgaris) cropped.jpg
Throat and belly are spotted. The spots are larger in males (pictured) than in females.
During breeding season, males develop vivid colours and a crest. Teichmolch maennchen web.jpg
During breeding season, males develop vivid colours and a crest.
The cloaca is swollen in breeding males. Schwanheim fg17.JPG
The cloaca is swollen in breeding males.
Breeding females are drab in colour and have no dorsal crest. Triturus vulgaris.jpg
Breeding females are drab in colour and have no dorsal crest.

General characteristics

Adult male smooth newts reach a head-to-tail length of around 9–11 cm (3.5–4.3 in) and are thus slightly larger than the females, which reach 8–9.5 cm (3.1–3.7 in). Adult body weight varies between 0.3–5.2 g (0.011–0.183 oz), decreasing during the breeding season. The head is longer than it is wide and has two to three longitudinal grooves on the top. The elongated snout is blunt in the male and rounded in the female. The skin is velvety and water-repellent on land but smooth during the aquatic phase. It contains mucus and toxin glands and the upper layer is shed off regularly. [11] :80–93 [5] :233–234

Outside of the breeding season, both sexes are yellow-brown, brown or olive-brown. Males have dark, round spots, while females have smaller spots of the same colour, which sometimes form two or more irregular lines along the back. Males have an orange stripe the underside of the tail and an orange to white throat and belly in males with small dark, rounded spots (these are lighter with smaller spots in females). Size and colour vary with the environment, and newts tend to be smaller in northern latitudes. [11] :80–93 [5] :233–234 Albinistic and leucistic individuals have been described. [11] :94 [17]

The smooth newt is diploid (i.e. it has two copies of each chromosome), with 24 chromosomes in total. [11] :107

Breeding characteristics

During the aquatic breeding season, males develop an uninterrupted skin crest running along their back and tail. This crest is 1–1.5 mm (0.039–0.059 in) high at mid-body, but higher along the tail. The tail also has a lower fin and a pointed end. The cloaca (the single digestive, urinary and reproductive orifice) of breeding males is swollen, round and dark-coloured. Depending on the subspecies, the hindfeet have more or less developed toe flaps. Colours are generally more vivid than during the land phase. The dark spots grow larger, and the crest often has vertical dark and bright bands. There are five to seven longitudinal stripes on the head. The lower edge of the tail is red with a silver-blue flash and black spots. Females have develop low straight tail fins, but no crest or toe flaps, and are more drably coloured. [18] :26 [5] :233–234

Subspecies differ slightly in terms of the male secondary characteristics: L. v. ampelensis has strongly developed toe flaps and a tail that tapers into a fine thread (but not a distinct filament). The body is also slightly square in cross-section. L. v. meridionalis also has toe flaps and a pointed tail, its crest is smooth-edged, and its body is square-shaped. In the nominate subspecies, L. v. vulgaris, the crest is clearly denticulated, toe flaps are only weakly developed and the body is round. [5] :234–236

Larvae

The aquatic larvae are 6.5–7 mm (0.26–0.28 in) long and yellow-brown with two longitudinal stripes at hatching. They initially have, In addition to their gills, they initially have only two balancers at the sides of their heads, short appendages for attaching to plants which are resorbed within a few days. [5] :237 As with all salamanders, the forelegs develop before the hindlegs. The colour of the larvae changes to a more cryptic, darkly marbled yellow to brown as they grow. Larvae are very slender and resemble those of the palmate newt. They develop a skin seam running from the neck to the pointed tail, which is as long as the head and trunk combined. The larvae grow to 3–4.5 cm (1.2–1.8 in), which is also the size of the efts (terrestrial juveniles) just after metamorphosis. [11] :188–192

Similar species

The smooth newt resembles the other, less widespread Lissotriton species. It can be confused especially with the closely related "smooth newt complex" species (marked with * in the table below) and the more distant palmate newt, which often occurs in the same area. [12] [11] :25 Females are particularly challenging to distinguish, as the distinguishing features are primarily observed in the males during the breeding season. [11] :19–41 [5] :225–235

Comparison of the smooth newt and related Lissotriton species [11] :19–41 [5] :225–235
SpeciesDistributionBreeding male characteristicsOther
Body shapeDorsal crestToe flaps (hind feet)Tail end
Smooth newt*
L. vulgaris
widespread from British Isles to Central Asia round to square (depending on subspecies)smooth or denticulated (depending on subspecies)weakly to well developed (depending on subspecies)pointed to elongated, no filament
Bosca's newt
L. boscai
West Iberian Peninsula slightly squarenonenoneshort filamentbelly with some dark spots, especially at sides
Carpathian newt*
L. montandoni
Carpathians squarevery low, smooth-edgedweakly developedblunt, with filamentbelly unspotted
Caucasian smooth newt*
L. lantzi
Caucasus slightly squarehigh (less than 1 mm (0.039 in) at mid-body), denticulated (almost spine-shaped)moderately developedpointed, but no filament
Greek smooth newt*
L. graecus
Southern Balkans squarelow (less than 1 mm (0.039 in) at mid-body), smooth-edgedwell developedlong filamentlower tail fin unspotted
Italian newt
L. italicus
Southern Italyslightly squarenonenonepointed, no filamentvery small, 4.5–7.5 cm (1.8–3.0 in); throat with few or no spots; golden-yellow patch behind eyes in both sexes
Kosswig's smooth newt*
L. kosswigi
Northern Anatolia squarelow (less than 1 mm (0.039 in) at mid-body) but higher at tail basestrongly developedlong filament
Palmate newt
L. helveticus
Western Europesquarelow, smooth-edgedstrongly developedlong filament (both sexes)throat unspotted
Schmidtler's smooth newt*
L. schmidtleri
Anatolia and eastern Balkansslightly squarehigh (more than 2 mm (0.079 in) at mid-body), denticulatedweakly developedelongated, no filamentvery small, 5–7 cm (2.0–2.8 in)

Distribution

Native range

The smooth newt has been described as "the most ubiquitous and widely distributed newt of the Old World". [5] :237 The nominate subspecies, L. v. vulgaris, is most widespread and ranges natively from Ireland (where the smooth newt is the only newt species) [11] :42 and Great Britain in the west to Siberia and northern Kazakhstan in the east. In the north it reaches central Fennoscandia, and its southern limit is central France, northern Italy, the central Balkans and the dry Eurasian steppe of Ukraine and Russia. [19] [12] [5] :234–238 [11] :42–44 The subspecies L. v. ampelensis only occurs in the Carpathians of Ukraine and the Danube delta of northern Romania, and L. v. meridionalis in the northern half of Italy, southern Switzerland, Slovenia and Croatia. [5] :234–235

In the Carpathians, the smooth newt generally prefers lower elevations than the Carpathian newt. In the Balkans, the precise contact zones with the Greek smooth newt and Schmidtler's smooth newt are not yet clear. [12] In central Italy, where the range of the smooth newt subspecies L. v. meridionalis overlaps with that of the Italian newt (L. italicus), it was found that the latter prefers a warmer and drier climate. [20]

Introduced range

The nominate subspecies, L. v. vulgaris, has been introduced to Australia, which has no native salamander species. The smooth newt was available in the Australian pet trade until 1997, when it was declared a "controlled pest animal" because of the risk of introduction. The first wild sighting was recorded near Melbourne in 2011, and larvae were later found, indicating successful reproduction. There are fears that it will have negative impacts on the native fauna, including predation on and competition with native frogs and freshwater invertebrates, as well as toxicity and disease spread. The smooth newt could spread further in south-eastern Australia, where large areas have a suitable climate. [21]

Within Europe, the subspecies L. v. meridionalis was introduced north of the Alps near Geneva, where it hybridises with the native L. v. vulgaris. [22]

Habitat and ecology

Sun-exposed, stagnant, shallow water bodies with abundant vegetation but without fish, such as this ditch, are typical breeding sites. Fosse Houssen Lissotriton vulgaris.jpg
Sun-exposed, stagnant, shallow water bodies with abundant vegetation but without fish, such as this ditch, are typical breeding sites.

The smooth newt is primarily a lowland species, though it can occasionally be found at elevations above 1,000 m (3,300 ft). [11] :78–80 This species has a wide habitat breadth, as it is able to thrive in a variety of terrestrial and aquatic environments. On land, it inhabits wooded areas (dense coniferous woods are avoided), as well as more open areas such as damp meadows, field edges, parks, and gardens. It can also tolerate human disturbance and urban environments and will hide under structures such as logs or stones or in small mammal burrows. [11] :120–134 [19] [5] :238 Smooth newts may also climb vegetation, although the exact function of this behaviour is currently unknown. [23]

Freshwater breeding sites are usually exposed to the sun, free from fish, and filled with stagnant water for at least three months of the year. They are typically close to similar bodies of water and have shallow areas with an abundance of water plants. These sites can range in size from small puddles to larger ponds or shallow parts of lakes. Water quality is less important, with pH values ranging from 4 (more acidic) to 9.6 (more alkaline) being tolerated. In Germany, smooth newts have even been found in slightly brackish water. [11] :121–129 They often share breeding sites with other amphibians, including other newts. In northern France, for example, there are ponds with five newt species: smooth, palmate, alpine, northern crested and marbled (T. marmoratus) newt – have been described. [11] :151–152

Lifecycle and behaviour

Smooth newts live on land for most of the year and are mainly nocturnal. They also usually hibernate on land, often in groups of several individuals in winter shelters, such as under logs or in burrows, but they can be active during mild weather. [24] The efts turn into mature adults at two to three years of age, and newts can live for 6–14 years in the wild. [5] :238 The newts recognise familiar territory using smell and visual cues, but they are unable to orient themselves in experiments when they were transported far away from the home range. [25]

Reproduction

External videos
Nuvola apps kaboodle.svg The life cycle of the newt , British Council, 1942. Educational film on the smooth newt (10:08 min).
Well-developed larva shortly before metamorphosis TriturusVulgarisLarva.JPG
Well-developed larva shortly before metamorphosis
Two juveniles (efts) after the transition to land Smooth Newt Juveniles (Lissotriton vulgaris) (8618458053).jpg
Two juveniles (efts) after the transition to land

Migration to the breeding sites can begin as early as February, but in the northernmost parts of the range and at higher altitudes, it may not start before summer. After entering the water, it takes a few weeks for the breeding characters, especially the male's crest, to develop. [5] :238

The mating process involves an elaborate courtship display: the male swims in front of the female and sniffs her cloaca in an attempt to attract her. He then vibrates his tail against his body, sometimes violently it lashing, thereby fanning pheromones towards her. In the final phase, he moves away from her, his tail quivering. If she is still interested, she will follow him, touching his cloaca with her snout, whereupon he deposits a packet of sperm (a spermatophore). He then guides her over the spermatophore, enabling her to pick it up with her cloaca. Males often try to lead females away competitors that are displaying. [5] :238–240

Eggs are fertilised internally and the offspring of one female usually have multiple fathers. Females tend to mate preferentially with unrelated males, probably to avoid inbreeding depression. [26]

Females lay 100–500 eggs, which they usually fold into the leaves of aquatic plants. The eggs are 1.3–1.7 mm (0.051–0.067 in) in diameter (2.7–4 mm (0.11–0.16 in) with jelly capsule) and light brown to greenish or grey in colour. Depending on temperature, larvae typically hatch after 10–20 days, and metamorphose into terrestrial efts after around three months. [5] :238–240

Paedomorphism, where adults remain aquatic and retain their gills and skin seams, or only partially resorb them, occurs regularly, but only in a small proportion of individuals. This trait does not appear to be genetically determined, but is favoured by cold water, low population density and abundant aquatic prey. Wild paedomorphic individuals often metamorphosed when they were transferred into an aquarium. [11] :192–193

Diet, predators and parasites

Grass snake eating a smooth newt Ringelnatter, Natrix natrix mit Teichmolch edit.JPG
Grass snake eating a smooth newt

Smooth newts, including their larvae, are unselective carnivores that feed mainly on diverse invertebrates such as earthworms, snails, slugs, bivalves, spiders, ticks, mites, springtails or insects and insect larvae, as well as smaller plankton. [27] Cannibalism also occurs, primarily through the predation of eggs of their own species. Various predators eat smooth newts, including waterbirds, snakes and frogs, but also larger newts such as the northern crested newt. [5] :238

Various pathogens and parasites have been found to infect smooth newts, including ranaviruses, [28] a picornavirus, [29] various protozoans, [11] :164 trematodes [30] [11] :164 (of which Parastrigea robusta was found to cause the local decline of a population in Germany) [31] and at least 31 species of helminths. [32]

Threats and conservation

The smooth newt is common over much of its range. [1] [5] :237 In 2008, the IUCN, assessed its threat status as Least Concern and found no general decline in populations. [1] However, this assessment included subspecies that are now recognised as separate species (see section Taxonomy above) and it therefore needs updating. [12] Despite the overall low level of concern, the smooth newt is now listed on some national red lists, e.g. in Switzerland, the Czech Republic, and the Netherlands. [11] :196 Like all amphibians, it is also listed as protected species in the Berne Convention (Appendix III). [33] Disturbance, capture, killing and trade are prohibited in Ireland under the Wildlife Act 1976, [34] and trade in the UK under the Wildlife and Countryside Act 1981. [35]

The threats facing smooth newts are similar to those affecting other amphibians. These include the loss of breeding ponds due to destruction or the introduction of fish, as well as the fragmentation of population caused by roads. [11] :196–197 Secondary habitats can help sustain the species, e.g. former gravel pits or quarries left open. [11] :204–205 The value of artificial water bodies as habitat can be improved when nearby hiding structures like stones or wood are added on land. [36] Garden ponds are readily colonised if they are sun-exposed, have abundant water plants, no fish, and nearby hiding structures. [11] :206–218 Artificial hibernation sites ("newt hotels") were readily used in a study in Norway, especially by juveniles. [37]

To mark and track individuals and monitor populations, researchers have often amputated phalanges of fingers and toes but these grow back quickly. A safer and less harmful approach is to record the unique patterns on the underside of the animals' bellies through photography. [11] :223–224 Researchers have also developed genetic methods based on microsatellite distribution to assess patterns of genetic diversity. [38]

Captivity

Smooth newts can be kept in captivity, but they must come from a legal source in accordance with the relevant legislation due to their protected status (see above). They require both a land and water phase, and hibernate for two to three months at 5–10 °C (41–50 °F). [11] :210–215 Juveniles remain terrestrial and will only return to water at maturity. In captivity, individuals have been known to live to ages of 4–8, and exceptionally up to 20 years. [5] :240

References

  1. 1 2 3 Arntzen, J.W.; Kuzmin, S.; Beebee, T.; et al. (2009). "Lissotriton vulgaris". IUCN Red List of Threatened Species . 2009: e.T59481A11932252. doi: 10.2305/IUCN.UK.2009.RLTS.T59481A11932252.en . Retrieved 1 November 2020.
  2. 1 2 3 4 Pabijan, M.; Zieliński, P.; Dudek, K.; Stuglik, M.; Babik, W. (2017). "Isolation and gene flow in a speciation continuum in newts". Molecular Phylogenetics and Evolution. 116: 1–12. Bibcode:2017MolPE.116....1P. doi:10.1016/j.ympev.2017.08.003. PMID   28797693.
  3. 1 2 3 4 5 Frost, D.R. (2020). "Lissotriton vulgaris (Linnaeus, 1758)" . 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 12 August 2020. Retrieved 18 April 2020.
  4. Linnaeus, C. (1767). Systema Naturae per Regna Tria Naturae, Secundum Classes, Ordines, Genera, Species, cum Characteribus, Differentiis, Synonymis, Locis (in Latin). Vol. 1 (part 1) (10 ed.). Stockholm, Sweden: L. Salvii. doi:10.5962/bhl.title.37256. Archived from the original on 23 September 2020. Retrieved 20 December 2020.
  5. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 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.
  6. Titus, T.A.; Larson, A. (1995). "A molecular phylogenetic perspective on the evolutionary radiation of the salamander family Salamandridae". Systematic Biology. 44 (2): 125–151. doi:10.1093/sysbio/44.2.125.
  7. Weisrock, D.W.; Papenfuss, T.J.; Macey, J.R.; et al. (2006). "A molecular assessment of phylogenetic relationships and lineage accumulation rates within the family Salamandridae (Amphibia, Caudata)". Molecular Phylogenetics and Evolution. 41 (2): 368–383. Bibcode:2006MolPE..41..368W. doi:10.1016/j.ympev.2006.05.008. PMID   16815049.
  8. Steinfartz, S.; Vicario, S.; Arntzen, J.W.; Caccone, A. (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. Bibcode:2007JEZB..308..139S. doi: 10.1002/jez.b.21119 . 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. Bell, T. (1839). A History of British Reptiles. London: John van Voorst. doi:10.5962/bhl.title.5498.
  11. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 Große, W-R. (2011). Der Teichmolch[The smooth newt]. Die neue Brehm-Bücherei (in German). Vol. 117. Magdeburg, Germany: VerlagsKG Wolf. ISBN   978-3-89432-476-6.
  12. 1 2 3 4 5 6 7 Wielstra, B.; Canestrelli, D.; Cvijanović, M.; et al. (2018). "The distributions of the six species constituting the smooth newt species complex (Lissotriton vulgaris sensu lato and L. montandoni) – an addition to the New Atlas of Amphibians and Reptiles of Europe" (PDF). Amphibia-Reptilia. 39 (2): 252–259. doi: 10.1163/15685381-17000128 . Archived (PDF) from the original on 28 April 2019. Retrieved 19 April 2020.
  13. Zieliński, P.; Nadachowska-Brzyska, K.; Dudek, K.; Babik, W. (2016). "Divergence history of the Carpathian and smooth newts modelled in space and time". Molecular Ecology. 25 (16): 3912–3928. Bibcode:2016MolEc..25.3912Z. doi:10.1111/mec.13724. PMID   27288862. S2CID   206183624.
  14. 1 2 Pabijan, M.; Zieliński, P.; Dudek, K.; et al. (2015). "The dissection of a Pleistocene refugium: phylogeography of the smooth newt, Lissotriton vulgaris, in the Balkans". Journal of Biogeography. 42 (4): 671–683. Bibcode:2015JBiog..42..671P. doi:10.1111/jbi.12449. S2CID   86108465.
  15. 1 2 Babik, W.; Branicki, W.; Crnobrnja-Isailovic, J.; et al. (2005). "Phylogeography of two European newt species – discordance between mtDNA and morphology". Molecular Ecology. 14 (8): 2475–2491. Bibcode:2005MolEc..14.2475B. doi:10.1111/j.1365-294X.2005.02605.x. PMID   15969729. S2CID   7484766.
  16. Skorinov, Dmitriy V.; Litvinchuk, Spartak N. (2016). "Tracing glacial refugia of the smooth newt (Lissotriton vulgaris) based on species distribution modelling". Vestnik of Saint Petersburg University. Biology. 3 (3): 136–143. doi: 10.21638/11701/spbu03.2016.323 .
  17. Modesti, Andrea; Aguzzi, Stefano; Manenti, Raoul (2011). "A case of complete albinism in Lissotriton vulgaris meridionalis" (PDF). Herpetology Notes. 4: 395–396. Archived (PDF) from the original on 23 July 2021. Retrieved 13 December 2020.
  18. Beebee, T & Griffiths, R. (2000) The New Naturalist: Amphibians and reptiles – a natural history of the British herpetofauna; Harper Collins Publishers, London.
  19. 1 2 Kuzmin, S. (1999). "AmphibiaWeb – Lissotriton vulgaris". Archived from the original on 19 April 2019. Retrieved 26 April 2020.
  20. Iannella, Mattia; Cerasoli, Francesco; Biondi, Maurizio (2017). "Unraveling climate influences on the distribution of the parapatric newts Lissotriton vulgaris meridionalis and L. italicus". Frontiers in Zoology. 14 (1): 55. doi: 10.1186/s12983-017-0239-4 . PMC   5727953 . PMID   29255477.
  21. Tingley, R.; Weeks, A.R.; Smart, A.S.; et al. (2014). "European newts establish in Australia, marking the arrival of a new amphibian order" (PDF). Biological Invasions. 17 (1): 31–37. doi:10.1007/s10530-014-0716-z. hdl: 11343/216887 . S2CID   18950725. Archived (PDF) from the original on 23 July 2021. Retrieved 10 May 2020.
  22. Dubey, Sylvain; Lavanchy, Guillaume; Thiébaud, Jacques; Dufresnes, Christophe (2019). "Herps without borders: a new newt case and a review of transalpine alien introductions in western Europe". Amphibia-Reptilia. 40 (1): 13–27. doi:10.1163/15685381-20181028. S2CID   92084541.
  23. Lynn, Vanessa J.; Allain, Steven J. R. (2022). "Observations on the climbing behaviour of the smooth newt Lissotriton vulgaris and great crested newt Triturus cristatus in south-east England". Herpetological Bulletin. 160 (160): 25–26. doi: 10.33256/hb160.2526 . S2CID   249300071.
  24. Kaczmarek, J. M.; Piasecka, M.; Kaczmarski, M. (2018). "Winter activity of the smooth newt Lissotriton vulgaris in Central Europe". The Herpetological Bulletin. 144: 21–22. Archived from the original on 22 October 2021. Retrieved 13 December 2020.
  25. Sinsch, U.; Kirst, C. (2015). "Homeward orientation of displaced newts (Triturus cristatus, Lissotriton vulgaris) is restricted to the range of routine movements". Ethology Ecology & Evolution. 28 (3): 312–328. doi:10.1080/03949370.2015.1059893. S2CID   83929007.
  26. Jehle, R.; Sztatecsny, M.; Wolf, J.B.W; et al. (2007). "Genetic dissimilarity predicts paternity in the smooth newt (Lissotriton vulgaris)". Biology Letters. 3 (5): 526–528. doi:10.1098/rsbl.2007.0311. PMC   2391198 . PMID   17638673.
  27. "AmphibiaWeb – Lissotriton vulgaris".
  28. Saucedo, Bernardo; Garner, Trenton W. J.; Kruithof, Natasja; et al. (2019). "Common midwife toad ranaviruses replicate first in the oral cavity of smooth newts (Lissotriton vulgaris) and show distinct strain-associated pathogenicity". Scientific Reports. 9 (1): 4453. Bibcode:2019NatSR...9.4453S. doi:10.1038/s41598-019-41214-0. PMC   6418247 . PMID   30872735.
  29. Pankovics, Péter; Boros, Ákos; Tóth, Zoltán; et al. (2016). "Genetic characterization of a second novel picornavirus from an amphibian host, smooth newt (Lissotriton vulgaris)". Archives of Virology. 162 (4): 1043–1050. doi:10.1007/s00705-016-3198-8. PMID   28005212. S2CID   531673.
  30. Caffara, M.; Bruni, G.; Paoletti, C.; Gustinelli, A.; Fioravanti, M.L. (2013). "Metacercariae of Clinostomum complanatum (Trematoda: Digenea) in European newts Triturus carnifex and Lissotriton vulgaris (Caudata: Salamandridae)". Journal of Helminthology. 88 (3): 278–285. doi:10.1017/S0022149X13000151. PMID   23506789. S2CID   27758178.
  31. Sinsch, Ulrich; Kaschek, Jacqueline; Wiebe, Jessica. "Heavy metacercariae infestation (Parastrigea robusta) promotes the decline of a smooth newt population (Lissotriton vulgaris)". Salamandra. 45 (3): 210–221. Archived from the original on 22 October 2021. Retrieved 13 December 2020.
  32. Sinsch, U.; Heneberg, P.; Těšínský, M.; Balczun, C.; Scheid, P. (2018). "Helminth endoparasites of the smooth newt Lissotriton vulgaris: linking morphological identification and molecular data". Journal of Helminthology. 93 (3): 332–341. doi:10.1017/S0022149X18000184. PMID   29502544. S2CID   3709643.
  33. "Convention on the Conservation of European Wildlife and Natural Habitats". Bern: Council of Europe. 1979. Archived from the original on 15 July 2015. Retrieved 1 November 2020.
  34. Nelson, B.; Cummins, S.; Fay, L.; et al. (2019). "Checklists of protected and rare species in Ireland" (PDF). Irish Wildlife Manuals. 116. National Parks and Wildlife Service, Department of Culture, Heritage and the Gaeltacht. Archived (PDF) from the original on 25 September 2020. Retrieved 1 November 2020.
  35. Wildlife and Countryside Act 1981 (9). United Kingdom. 1981. "Wildlife and Countryside Act 1981 (Archived copy)". Archived from the original on 12 February 2019. Retrieved 22 October 2021.
  36. Mulkeen, C.J.; Gibson-Brabazon, S.; Carlin, C.; et al. (2017). "Habitat suitability assessment of constructed wetlands for the smooth newt (Lissotriton vulgaris [Linnaeus, 1758]): A comparison with natural wetlands". Ecological Engineering. 106: 532–540. Bibcode:2017EcEng.106..532M. doi:10.1016/j.ecoleng.2017.06.005. hdl: 10379/6626 . S2CID   103494922.
  37. Dervo, Børre; Museth, Jon; Skurdal, Jostein (2018). "Assessing the use of artificial hibernacula by the great crested newt (Triturus cristatus) and smooth newt (Lissotriton vulgaris) in cold climate in southeast Norway". Diversity. 10 (3): 56. Bibcode:2018Diver..10...56D. doi: 10.3390/d10030056 . hdl: 11250/2558570 .
  38. Buono, Vincenzo; Galliani, Giorgia; Mancini, Emiliano; et al. (2018). "An improved microsatellite panel to assess genetic variability of the Italian smooth newt (Lissotriton vulgaris meridionalis)". Journal of Genetics. 97 (2): 569–573. doi:10.1007/s12041-018-0934-8. hdl: 11573/1278542 . PMID   29932078. S2CID   46977273.