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Description

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Females are slightly larger than males and grow up to 160mm in length. These large newts are unmistakable with any other species. There is a dark stripe through the eye. The warty skin has a black background with a green marbled pattern. The belly is black with small white spots in the nominate subspecies, while this pattern in the smaller subspecies, T. m. pygmaeus, is augmented with yellow markings and larger white spots (Griffiths 1996). During the aquatic phase, the male develops a large dorsal and caudal crest. This crest shows a vertical black and green striping pattern and is not serrated, but is undulated laterally. Females do not develop a dorsal crest but instead have a permanent bright orange vertebral stripe. The tail does develop a crest in females, but this is much lower than that of the males. Males have a bright light lateral stripe along the tail and a stronger developed cloaca. During the terrestrial stage the skin gets a velvet-like texture and becomes water-repellant, and the green pattern becomes brighter. The dorsal and caudal crests diminish greatly, although they do not disappear entirely in the males (Noellert and Noellert 1992)
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Distribution and Habitat

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T. marmoratus has its centre of origin in Western Europe. Its actual distribution is restricted to sectors within the Mediterranean and the Atlantic region in the Iberian Peninsula - except for the dry southeastern part - and in southern France, up to Paris. The distribution along the northern border, in France, is patchy and unstable, because of the presence of its relative T. cristatus in the area. Both species hybridise when reproducing in the same body of water. The mosaic-like distribution of both species in the area of sympatry in central France, could be explained by the effect of competition between the species in interbreeding populations, described as reproductive self-destruction, and effecting ecological isolation. No competition with co-occurring Triturus species seems to be affecting the distribution there. Interruptions in the map of T. marmoratus distribution in Spain can be partly explained by unsuitable climate, as is the case for the higher parts of the Pyrenees and the dry areas of southeastern Spain. In other cases, a lack of inventories might explain blank areas, namely in eastern and southeastern Spain. The two subspecies replace each other over a short distance, in mountain ranges running east-west in central Spain and Portugal, which forms the watershed between the Douro and Tagus rivers. The two subspecies' distribution ranges coincide with different bioclimatic zones. T. m. marmoratus lives in Atlantic and supra-Mediterranean climates; whereas T. m. pygmaeus occurs in meso- and thermo-Mediterranean climates.The species finds its optimum in the lower and middle regions of mountains. Its altitudinal distribution in France ranges from 20m up to 950m in the Massif Central, up to 1035m in the Pyrenees. Its altitudinal distribution is wider on the Iberian Peninsula where the species can be found from sea-level up to about 1800m in Galacia (Northwestern Spain), to 1930m in Portugal and about 2100m in the mountains of central Spain. The highest altitude recorded for the subspecies T. m. pygmaeus is lower, at 1450m (Gasc 1997). Although this species is usually associated with well-vegetated ponds and woodlands, the species also occurs in more open areas like heathens and agricultural landscapes. Where it occurs sympatrically with T. cristatus it seems to prefer smaller and more vegetated habitats, while T. cristatus occupies more open areas. In the terrestrial phase it is found under logs and rocks, as well as in man-made structures like stone walls (Noellert and Noellert 1992).
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Life History, Abundance, Activity, and Special Behaviors

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Mating takes place in the water. Males usually enter the water before the females and leave the water later. The reproductive period is dependent on the altitudinal and latitudinal distribution. In northwestern France it lasts from the beginning of March until the middle of August. In central Portugal the breeding period lasts from October until May, while in Esturia it lasts from November to June. The courtship behavior is similar to that of T. cristatus. T. marmoratus produces about twice as many eggs as T. cristatus, but, like in the latter, only half of the embryos develop beyond the tail-bud stage (Griffiths 1996). A female can produce as many as 200-380 eggs with a diameter of 2mm. Each egg is individually attached to water plants. Larval development is also dependent on the altitudinal and latitudinal distribution. In the northwestern part of the distribution, metamorphosis takes place between the beginning of August and the end of September, while in the Spanish reservation of Doñana larvae could be found between December and May. Larvae grow op to 70-90mm in total length. Sexual maturity is reached at an age of about 5 years. Longevity in the wild is up to 15 years, while in captivity a specimen lived for 25 years. During the aquatic phase the animals are mostly diurnal, while activity is nocturnal during the terrestrial phase. In the northern parts of its distribution, hibernation usually occurs under water. In the southern parts of the distribution, hibernation does not occur, but the animals spend the dry summer period on humid places on land. The diet includes various invertebrates, but can also include larvae of T. boscai or larvae of its own species. When threatened the tail is erected and swayed from side to side. This display is usually accompanied by an elevation of the rear trunk (Noellert and Noellert 1992).
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Life History, Abundance, Activity, and Special Behaviors

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T. marmoratus is protected by law in every country where it occurs. However, specimens are still collected for the pet trade and are for sale in the Netherlands and Germany for instance. T. marmoratus is an endangered species in central France and probably less so in southern France.The species is considered not in danger in Spain and Portugal. Nevertheless, loss and change of habitats are serious threats in the whole area, caused byagricultural intensification and loss and pollution of fresh water. T. m. pygmaeus is especially threatened by the growing exploitation of ground water (Gasc 1997). Populations that interbreed with T. cristatus should be monitored more carefully, because the reduced viability of the hybrids reduces the reproductive capacity of each species (Noellert and Noellert 1992).
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Lifespan, longevity, and ageing

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Maximum longevity: 25 years (captivity) Observations: Studies in Portugal have shown that in mountain populations animals tend to mature later and live longer, in some cases up to 16 years. In captivity they can live for 25 years (Smirina 1994).
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Marbled newt

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The marbled newt (Triturus marmoratus) is a mainly terrestrial newt native to western Europe. They are found in the Iberian Peninsula and France, where they typically inhabit mountainous areas.

Habitat and distribution

The marbled newt is typically found in habitats characterized by hilly and forestry terrain, away from open and exposed areas.[2] Marbled newts live in temporary habitats, such as ponds, that are subject to change depending on the climate conditions of the region. When rainfall is high and the temperature is lower, typically in the fall and winter months, adult marbled newts stay in the ponds. However, these shallow ponds are subject to drought in warmer spring and summer months, which forces the marbled newts to remain on land. Due to this constant change in the habitat conditions, marbled newts have the ability to adapt to different climatic conditions and habitat changes.[3]

The characteristics of the marbled newt's habitat have also been found to affect the maturity of both males and females. Newts found in Mediterranean regions have been found to mature earlier than those in regions of France and Portugal. Due to the harsher conditions associated with the climate in Mediterranean regions, marbled newts experience a higher rate of adult mortality; therefore, maturing earlier is advantageous.[3]

Description

Marbled newt in the Peneda-Gerês National Park, Portugal.

Marbled newts have dark brown or black bodies with irregular patterns of green. They have black bellies with off-white specks. Adult females have an orange stripe running down the back from the head to the tip of the tail. Juveniles also have this stripe, but the stripe fades on males at about 9 months.[4] Breeding males have a large wavy crest that runs from its neck down to the tip of its tail, but is a little bit shorter where the tail meets the body. The crest is striped yellowish-white with black. Adult marbled newts range from 5 inches (13 cm) to 6.5 inches (17 cm) long.[4]

Life history

Both males and females follow similar directions for pre- and post-breeding migrations. Migration occurring in the spring is also significantly different from winter. Migration also puts the newts at increased risk of predation due to exposition to a larger group of predators. Desiccation as a result of migration is also a concern.[5] Marbled newts typically migrate a short distance initially, covering a distance of about 10 meters. However, the newts have been shown to migrate up to 160 meters away from their initial habitat. Migration routes filled with trees and bushes are preferred because they allow for adequate shelter, minimizing the amount of open area that the newt could be exposed to. The newts can also migrate through open areas if underground refuges are available as coverage.[2]

Reproduction and life cycle

Life cycle

Marbled newt in water

Differences in environmental conditions are responsible for changes in bone density and formation for marbled newts living in different areas. The marbled newts, like some other amphibians, experience a phase of growth in the spring and summer. This is then followed by growth arrest in the winter. Observing the changes in growth is an important benchmark to have in marbled newts, as climate change is significantly impacting their typical environmental conditions. The breeding season for the newts begins in February and larvae hatch in late March. The metamorphosis phase is from April until the end of June, with new juveniles leaving at the end of June at the latest. During the most intense part of the summer (July-September), breeding ponds dry up. This causes a significant decrease in activity, which increases again only when rainfall began again in August.[3]

The marbled newt locates breeding ponds primarily through celestial cues. It was found that when these cues are unavailable, they do not migrate. When tested under clear and overcast sky conditions, the newts were not able to orient themselves accordingly. However, when altering the geomagnetic field of their location, the newts showed no change in orientation, which suggests that an altered geomagnetic field does not affect orientation. Other possibilities for orientation include specific odors of the pond as well as visual landmarks that can serve as cues of correct or incorrect location.[6]

Another form of locating breeding ponds for marbled newts are acoustic cues. It has been found that marbled newts sometimes use the calls of another frog, B. calamita, to locate their breeding ponds. While the ears of newts are not as complex as those of humans, they have inner ears capable of processing sound. Sound can be used to aid in finding breeding ponds, but celestial cues remain essential for successful location of breeding ponds.[7]

Female marbled newt with male in background in Girona, Spain[8]

Sexual selection

Males have shown a preference for larger female newts. This is because larger females show increased efficiency in oviposition in comparison to smaller female newts. Such increased efficiency allows for a decrease in parental investment and energy cost associated with oviposition.[9]

Marbled newts experience a female-biased sexual dimorphism with regards to size. Females are not only significantly larger than males, but also experience a longer life span. This combined with reaching sexual maturity at a younger age in comparison to males are causes for increased female fecundity. Larger females are thought to produce larger offspring, who in turn have more reproductive success.[10] Males have a discernible crest selected for by females. The height of the crest offers an indication of good fitness and physical condition, making mates with a higher crest more desirable by females.[10]

During courtship with females, males perform ‘tail-lashing’ in order to spread their pheromones. This also draws attention to the males and accentuates their long tailfin, another trait also selected for by female choice. Males are able to spread these pheromones because they are equipped with a set of glands that females do not have. This trait directly affects male reproductive success as it is used solely in attracting a mate and offers no other benefits.[10]

Oviposition

Since males do not need to be present for egg deposition, females have full control of oviposition, choosing both location and time. Females prefer to lay their eggs in a different location each time in an attempt to decrease mortality. Each egg is deposited and carefully folded by its hind legs within an aquatic leaf that had been carefully chosen by the female. The female smells and inspects the chosen leaf prior to wrapping it around the egg.[9]

Failures in egg laying can occur. These typically follow or come before the successful deposition of an egg. In some cases, the leaf chosen is too small for deposition or is already occupied by another egg. The eggs are folded within leaves as a way to provide parental care. The time taken to choose and carefully wrap each egg within a leaf is a form of parental investment from the mother as a way to protect the egg. The process of oviposition also interrupts breathing; therefore, the time taken for this process is very important. There are cases in which female marbled newts are forced to halt oviposition in order to take a breath at the surface. It has been found that larger females experience more success in oviposition because they are able to endure longer periods of time without taking a breath relative to smaller females. By the same reasoning, larger females also experience fewer failed attempts at oviposition than their smaller counterparts, allowing them to be more efficient at reproduction.[9]

Conservation

The marbled newt is listed as near-threatened on the French national red list of species.[11] Conservation planning should take into consideration buffer zones surrounding ponds and the ecological requirements associated with them while the marbled newts are migrating. These wetlands in the buffer zone are important in order to allow the newts to successfully complete their biological cycles. It is important to ensure that there are adequate, good-quality, shelters for marbled newts to use during migration in order to reduce the predation and desiccation risk associated with migration.[5]

Changes in the marbled newt habitat have occurred over the last few years. With the loss of many forest areas, their typical ranges are being diminished along with their population. This loss of habitat is allowing the range and population of another newt, T. cristatus, to expand. This newt species prefers open and flat areas.[2] The largest cause of habitat loss is climate change, with land use cover being the secondary cause. Climate change directly affects the water cycle and temperature—two very important environmental factors for amphibian species. These changes have the ability to directly affect the migration range and general territory of the marbled newts. The range of the newts has been reduced over the past few years and is expected to experience further restrictions over the course of the 21st century. While large-scale experiments have been done to assess the general risk of climate change and direct human impact on the habitat of marbled newts, more local and smaller-scale studies must be performed to determine the full range of effects on these newts.[11]

Hybridization

Adolescent male marbled newt (Triturus marmoratus). [12]

T. cristaus and T. marmoratus (marbled newts) overlap in some areas in France where their habitat preferences overlap; this allows them to hybridize.[13] T. cristaus has been known to occupy increasingly larger areas due to climate change fragmenting the habitat of the marbled newt. Despite the loss of habitat, the marbled newt has experienced more reproductive success. Females have a longer life-span and thus more years to reproduce. The eggs of both T. cristaus and T. marmoratus suffer the same mortality rates. The hybrids of these two species have even more fecundity than the marbled newts, but their eggs and embryos are less likely to survive.[13]

References

  1. ^ Jan Willem Arntzen, Robert Jehle, Jaime Bosch, Claude Miaud, Miguel Tejedo, Miguel Lizana, Iñigo Martínez-Solano, Alfredo Salvador, Mario García-París, Ernesto Recuero Gil, Paulo Sá-Sousa, Rafael Marquez (2009). Triturus marmoratus. In: IUCN 2012. IUCN Red List of Threatened Species. Version 2012.2.
  2. ^ a b c Jehle, R.; Arntzen, J. W. (July 2000). "Post‐breeding migrations of newts ( Triturus cristatus and T. marmoratus ) with contrasting ecological requirements". Journal of Zoology. 251 (3): 297–306. doi:10.1111/j.1469-7998.2000.tb01080.x. ISSN 0952-8369.
  3. ^ a b c Jakob, Christiane; Seitz, Alfred; Miaud, Claude; Crivelli, Alain (2002). "Growth cycle of the marbled newt (Triturus marmoratus) in the Mediterranean region assessed by skeletochronology". Amphibia-Reptilia. 23 (4): 407–418. doi:10.1163/15685380260462329. ISSN 0173-5373.
  4. ^ a b Triturus (Rafinesque, 1815), Mesotriton (Bolkay, 1927), Ommatotriton (Gray, 1850), and Lissotriton (Bell, 1839). livingunderworld.org
  5. ^ a b Marty, P.; AngÉlibert, S.; Giani, N.; Joly, P. (May 2005). "Directionality of pre- and post-breeding migrations of a marbled newt population(Triturus marmoratus): implications for buffer zone management". Aquatic Conservation: Marine and Freshwater Ecosystems. 15 (3): 215–225. doi:10.1002/aqc.672. ISSN 1052-7613.
  6. ^ Diego-Rasilla, Javier; Luengo, Rosa (2002-09-01). "Celestial orientation in the marbled newt ( Triturus marmoratus )". Journal of Ethology. 20 (2): 137–141. doi:10.1007/s10164-002-0066-7. ISSN 0289-0771. S2CID 8565821.
  7. ^ Diego-Rasilla, F. Javier; Luengo, Rosa M. (2004-04-01). "Heterospecific call recognition and phonotaxis in the orientation behavior of the marbled newt, Triturus marmoratus". Behavioral Ecology and Sociobiology. 55 (6): 556–560. doi:10.1007/s00265-003-0740-y. ISSN 0340-5443. S2CID 22875124.
  8. ^ "Marbled Newts". Britannica ImageQuest. 2016-05-25. Retrieved 2022-11-30.
  9. ^ a b c Diaz-Paniagua, Carmen (June 1989). "Oviposition Behavior of Triturus marmoratus pygmaeus". Journal of Herpetology. 23 (2): 159–163. doi:10.2307/1564022. JSTOR 1564022.
  10. ^ a b c Zuiderwijk, Annie; Sparreboom, Max (1986). "Territorial Behaviour in Crested Newt Triturus Cristatus and Marbled Newt T. Marmoratus (Amphibia, Urodela)". Bijdragen tot de Dierkunde. 56 (2): 205–213. doi:10.1163/26660644-05602002. ISSN 0067-8546.
  11. ^ a b Préau, Clémentine; Bertrand, Romain; Sellier, Yann; Grandjean, Frédéric; Isselin‐Nondedeu, Francis (April 2022). "Climate change would prevail over land use change in shaping the future distribution of Triturus marmoratus in France". Animal Conservation. 25 (2): 221–232. doi:10.1111/acv.12733. ISSN 1367-9430. S2CID 238169190.
  12. ^ "Triturus marmoratus". Britannica ImageQuest. 2016-05-25. Retrieved 2022-11-30.
  13. ^ a b Arntzen, J. W.; Hedlund, Linda (December 1990). "Fecundity of the newts Triturus cristatus, T. marmoratus and their natural hybrids in relation to species coexistence". Ecography. 13 (4): 325–332. doi:10.1111/j.1600-0587.1990.tb00625.x. ISSN 0906-7590.

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Marbled newt: Brief Summary

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The marbled newt (Triturus marmoratus) is a mainly terrestrial newt native to western Europe. They are found in the Iberian Peninsula and France, where they typically inhabit mountainous areas.

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