Hubbry Logo
SheltopusikSheltopusikMain
Open search
Sheltopusik
Community hub
Sheltopusik
logo
8 pages, 0 posts
0 subscribers
Be the first to start a discussion here.
Be the first to start a discussion here.
Sheltopusik
Sheltopusik
Sheltopusik
View on Wikipedia
from Wikipedia

Sheltopusik
Scientific classification Edit this classification
Kingdom: Animalia
Phylum: Chordata
Class: Reptilia
Order: Squamata
Suborder: Anguimorpha
Family: Anguidae
Genus: Pseudopus
Species:
P. apodus
Binomial name
Pseudopus apodus
(Pallas, 1775)
Synonyms[2]
List

The sheltopusik, also spelled scheltopusik, sheltopusick, scheltopusick, sheltopusic, or scheltopusic /ˌʃɛltəˈpjuːzɪk/ (Pseudopus apodus), and also commonly known as Pallas's glass lizard,[3] the European legless lizard, or the European glass lizard, is a species of large glass lizard found from Southern Europe to Central Asia.

Taxonomy

[edit]

The sheltopusik was previously included in the genus Ophisaurus, but has since been placed in its own genus Pseudopus. It was originally described in 1775 by Peter Simon Pallas as Lacerta apoda.[4]

There are three subspecies:[5][6]

  • P. a. apodus (Pallas, 1775) – the type subspecies, ranging from Crimea through Transcaucasia, east to Central Asia as far as Kazakhstan
  • P. a. levantinus Jablonski, Ribeiro-Junior, Meiri, Maza, Mikulíček & Janzik, 2021 – restricted to the Levant, from southern Turkey south to Israel and Palestine
  • P. a. thracicus (Obst, 1978) – the westernmost subspecies, ranging from Croatia to Greece, east to western Turkey

Despite only being described in 2021, P. a. levantinus is the largest and most genetically diverse of the subspecies, indicating an older and more complex evolutionary history compared to its sister subspecies.[6]

Etymology

[edit]

Pseudopus apodus comes from Greek ψευδοποδος άποδος, literally meaning "fake-legged" or without legs.

The common name "sheltopusik" comes from Russian желтопузик (zheltopuzik), which translates most directly as "yellow-bellied".[7]

Skull anatomy

[edit]
In Greece

The skull is elongated, twice as long as it is wide and widest at the posteroventral portions of the jugals, where the cheeks proceed to narrow into the snout. The exonarial fenestra (external naris) is similarly elongated and elliptical. The orbits, which lie in a posterior portion of the anterior part of the skull, are large.[8]

The premaxillary–maxilla has an elongated opening and has rounded ends. It is positioned between the forked premaxillary process of the maxilla and the maxillary and vomeromaxillary processes of the premaxilla.[8]

Description

[edit]

The sheltopusik can reach a length of 135 cm (4.43 ft). It is tan colored, paler on the ventral surface and the head, with a ring-like/segmented appearance that makes it look like a large earthworm with a distinctive fold of skin down each side called a lateral groove. Small (2-mm) rear legs are sometimes visible near the cloaca. Though the legs are barely discernible, the sheltopusik can be quickly distinguished from a snake by its ears, eyelids, and ventral scales. This species exhibit sexual dimorphism as males are on average larger than females.[9]

Adult
Juvenile

Habitat and behaviour

[edit]
Musking

P. apodus inhabits open country, such as short grassland or sparsely wooded hills. It consumes arthropods and small mammals. Snails and slugs appear to be its favorite prey, which may explain why it is particularly active in wet weather, although it prefers a dry habitat. Breaking through the shells of snails is an especially easy task due to their teeth and jaw structure.

Defensive behaviour

[edit]
Shown here with a missing tail. Sheltopusiks can autotomize their tails.

Due to its size, the sheltopusik tends to respond to harassment by hissing, biting, and musking. It is less likely to drop off its tail than some other species that display caudal autotomy. However, these occasional displays of caudal autotomy are responsible for the name "glass lizard" (or "glass snake"). The released tail may break into pieces, leading to the myth that the lizard can shatter like glass and reassemble itself later. In reality, if the tail is lost, it grows back slowly, but is shorter and darker. The replacement tail may grow back to full length after an extended period of time.

Reproduction

[edit]

About 10 weeks after mating, the female P. apodus lays about eight eggs, which she hides under bark or a stone, and often guards them. The young hatch after 45 to 55 days. They are typically about 15 cm (5.9 in) long and usually start to eat after four days.

In captivity

[edit]
With an ocellated lizard at the Artis Royal Zoo

Sheltopusiks are frequently available in the exotic pet trade, though rarely captive-bred. They do not typically tolerate a large amount of handling, but they adapt to captivity well, feeding on crickets, meal worms, small mice, eggs, snails, or pieces of meat. They are even known to accept these meals from a keeper's tweezers, or even from their hands once they become used to captivity. However, sheltopusiks do get excited around food and have surprisingly powerful jaws. They make hardy captives, capable of living up to 50 years.

Relationship with humans

[edit]

Remains of the Levant subspecies (P. a. levantinus) are known from Natufian sites in Israel, suggesting that it was eaten by the local population at the time.[6][10]

[edit]

References

[edit]

Further reading

[edit]
[edit]
Revisions and contributorsEdit on WikipediaRead on Wikipedia

Sheltopusik

View on Grokipedia
from Grokipedia
The sheltopusik (Pseudopus apodus), also known as the European glass lizard, is a large, in the Anguidae, characterized by its elongated, smooth-scaled body that can reach total s of up to 135 cm, with a comprising about 150% of the snout-vent length. Native to southeastern Europe, the , Asia Minor, the , and , it is the only extant member of the genus Pseudopus and inhabits dry, open environments such as arid grasslands, rocky hillsides, sparsely wooded valleys, Mediterranean macchia, pastures, and areas near human settlements. Distinguished from snakes by its visible openings, movable eyelids, lateral grooves along the body, and tiny vestigial hind limbs (about 2 mm long), the sheltopusik has a tan to brown coloration in adults—paler on the underside—and juveniles are typically grey-greenish with darker stripes. Its is notably fragile, capable of autotomizing (breaking off) as a defense mechanism, earning it the "glass lizard" moniker. This diurnal and crepuscular is a burrowing generalist predator, actively after or in cooler conditions, with low mobility typically limited to short distances (up to 5 m recorded). Its diet consists primarily of arthropods (such as and gastropods including snails and slugs), supplemented by small mammals, birds, eggs, and occasionally vertebrates, reflecting its opportunistic feeding habits in fragmented habitats. Sheltopusiks exhibit in some populations, with males engaging in combat during the breeding season, and females lay clutches of about 8 eggs after a 10-week , with incubation lasting 45–55 days; hatchlings measure around 15 cm and begin feeding within 4 days. With a lifespan of 20–30 years in captivity and potentially up to 50 years, these demonstrate morphological plasticity across their range, adapting to varied ecological pressures from arid to olive groves. Globally assessed as Least Concern by the IUCN (as of 2009) due to its wide distribution and adaptable nature, the sheltopusik faces threats from habitat loss and degradation due to and , as well as collection for the pet trade. In some regions, such as , it is regionally assessed as Vulnerable. As one of Europe's largest , it plays a key role in controlling populations and serves as an indicator species for dry habitat health.

Taxonomy

Classification

The sheltopusik, scientifically named Pseudopus apodus (Pallas, 1775), derives its binomial from Greek roots: "pseudos" meaning false and "pous" (genitive podos) meaning foot, combined with "a-" (without) and "podos," alluding to its legless yet lizard-like form. This belongs to the order , suborder Diploglossa, family Anguidae (known as glass lizards for their fragile tails), subfamily , and genus Pseudopus, which is monotypic in contemporary , with P. apodus as its only extant member. Three subspecies are currently recognized: the nominal P. a. apodus (Pallas, 1775), distributed widely from the Crimea through the Caucasus and Transcaucasia to Central Asia; P. a. thracius (Obst, 1978), confined to the Balkans and western to northern Anatolia; and P. a. levantinus (Jablonski, Meiri et al., 2021), an endemic form described from the Levant region encompassing southern Turkey, Syria, Lebanon, Israel, and possibly Jordan, representing the smallest geographic range (approximately 30,000 km²) but the largest body size (snout-vent length up to 610 mm, total length up to 1,367 mm) and highest genetic diversity among the subspecies. The levantinus subspecies exhibits distinct morphological traits, such as 10 preanal scales and a proportionally longer, wider head, alongside genetic markers including 3.5–3.6% mitochondrial DNA divergence from the other subspecies and elevated microsatellite polymorphism (100% loci polymorphic, expected heterozygosity 0.639 ± 0.092). Phylogenetically, Pseudopus represents an ancient lineage within Anguidae, with the three subspecies aligning to distinct evolutionary clades; P. a. levantinus shows the deepest divergence, estimated at 8–3 million years ago during the to , suggesting diversification and ancient origins potentially traceable to several million years in the . relatives include the extinct Pseudopus pannonicus (Kretzoi, 1969), a giant form from reaching up to 2 meters in length, known from late to deposits and regarded as the largest anguine lizard ever documented. Historically, P. apodus was classified under the Ophisaurus (e.g., as Ophisaurus apodus), but Pseudopus was resurrected as a distinct by Klembara (1979) based on morphological . Although Macey et al. (1999) proposed inclusion in Ophisaurus for , subsequent genetic and morphological studies, including post-2018 multilocus , have supported the separation of Pseudopus and its monotypic status based on deep divergence from other Anguidae.

Etymology

The "sheltopusik" derives from the Russian term želtopuzik (желтопузик), literally meaning "yellow belly" or "yellow paunch," in reference to the lizard's pale underside. Alternative spellings include "scheltopusik," which reflects its adoption into German and English herpetological . The scientific name Pseudopus apodus breaks down into Greek roots: the Pseudopus combines pseudes (ψευδής, "false") and pous (πούς, "foot"), while the epithet apodus merges a- (ἀ-, "without") and pous ("foot"), collectively emphasizing the animal's legless, snake-like form despite vestigial hind limb remnants. This species was first formally described in 1775 by the German naturalist under the binomial Lacerta apoda in his work on Russian fauna. In other languages, it is known as the European glass lizard, a name originating from its tail's tendency to fracture easily through , resembling shattering glass.

Anatomy

External morphology

The sheltopusik (Pseudopus apodus) is a large, characterized by its elongated, snake-like body, which can reach a maximum total length of 135 cm in adults. Males may attain slightly larger maximum sizes than females in some populations. The tail length is typically about 1.5 times the snout-vent length (SVL), comprising approximately 60% of the total length, though proportions vary across populations (0.6–1.7 times SVL). This robust build, combined with a cylindrical form, allows for efficient burrowing and movement through vegetation. The dorsal surface is typically tan to yellowish-brown or gray-olive, often with scattered darker spots, while the ventral side is paler yellow or whitish, providing subtle in arid or grassy habitats. The skin is covered in smooth to slightly arranged in longitudinal rows, with prominent lateral grooves that create a ring-like, segmented appearance reminiscent of a worm or snake. There are typically 111–129 ventral scales along the body, forming a continuous shield-like underbelly. Sexual differences in coloration may occur, with females sometimes exhibiting reddish-brown tones and white speckling dorsally. Distinguishing the sheltopusik from snakes are several key external features, including vestigial hind limbs visible as small, flap-like rudiments measuring about 2 mm in length near the . It also has movable eyelids and distinct external ear openings, both absent in snakes. For chemosensation, the sheltopusik employs a long, notched tongue—unlike the deeply of —which it flicks to gather environmental cues. The tail is particularly fragile and adapted for defense, featuring fracture planes that facilitate , where it can break off easily when grasped by predators. Following , the tail regenerates slowly and imperfectly, resulting in a shorter, darker replacement that lacks the original's full functionality and brittleness. This regenerative capacity, while vital for survival, underscores the evolutionary trade-offs in the ' limbless morphology.

Cranial anatomy

The of the Sheltopusik (Pseudopus apodus) is notably elongated, measuring approximately twice as long as it is wide, and reaches its maximum width at the level of the posteroventral portions of the jugal bones before tapering to a narrow, slightly rounded . This overall shape supports its legless, serpentiform body plan, with large, rounded orbits positioned in the posterior portion of the anterior half of the to enhance during and . The external narial is anteroposteriorly elongated and elliptical, an adaptation that enlarges the olfactory region for detecting prey scents in its subterranean and surface environments. A defining feature of the cranial is its reduced , which is pleurodont and consists primarily of conical teeth suited for crushing. The supports up to nine conical teeth, while the bears up to 14, with the anterior six to seven being conical and the posterior ones transitioning to rod-like forms; additional small conical teeth appear on the (up to five), (up to 10), and pterygoid (up to 12 in a lateral row). These robust, blunt teeth facilitate the of hard-shelled prey, such as gastropods that comprise approximately 8.3% of the diet in studied populations. The structure further aids predation, featuring a robust with a prominent nasal process and high lateral wall of the nasal capsule, complemented by a nearly vertical quadrate in adults that enables a wide gape for engulfing larger items. Serpentiform adaptations are prominent in the cranial morphology, including an elongated rostrum that aids burrowing and a reduced temporal region with a narrow . In adults, the postorbital and parietal bones contact directly, excluding the postfrontal from the supratemporal , which streamlines the for streamlined locomotion and reduces vulnerability during soil penetration. Compared to other anguines like fragilis and ventralis, P. apodus exhibits autapomorphic traits, such as a parallel-sided nasal on the , a convex frontal margin that reaches and ornaments the orbital border, and the retention of a parietal arch, distinguishing its derived cranial form for legless existence.

Distribution and ecology

Geographic distribution

The Sheltopusik (Pseudopus apodus) has a native range spanning southeastern to southwestern and . In , it occurs in the , including (mainland and islands such as Limnos, , , , , and ), coastal , , , , , and , as well as the Crimean Peninsula and southern . The distribution extends eastward through and the region, encompassing Georgia, , , and in . Further into Asia, the species inhabits the , including , , , , Palestine (West Bank), , and , and reaches in , , , western , southern , and . Several are recognized based on regional variations, with P. a. levantinus restricted to the , occurring in southern , western , northern and central , and . Other subspecies, such as P. a. apodus (the nominotypical form) and P. a. thracicus, align with broader portions of the range, including the coast and Transcaucasia. Fossil records reveal a historically broader distribution during the Pleistocene, with the extinct Pseudopus pannonicus—the largest known anguid lizard—documented across , including sites in , , , and , indicating a more extensive European presence before post-glacial recolonization shaped the modern range.

Habitat preferences

The sheltopusik inhabits dry, open landscapes, favoring environments such as short grasslands, rocky hillsides, sparsely wooded areas, orchards, and meadows. These habitats provide suitable conditions for its ground-dwelling lifestyle, often in proximity to human settlements where vegetation is unmanaged or lightly disturbed. It typically avoids dense forests and wetlands, selecting instead semi-arid to arid regions that support sparse to moderate vegetation cover, including shrubs and grasses. In these preferred settings, the sheltopusik exploits microhabitats like burrows excavated in loose or under rocks, stones, and , as well as crevices and abandoned structures for . Despite its affinity for drier overall environments, it shows activity in areas with elevated levels, such as those near water sources or in denser shrubby during warmer months. Its distribution spans elevations from up to approximately 2,000 meters, allowing adaptation to varied topographic features within open terrains. As a semi-fossorial , the sheltopusik plays an ecological role in turnover and through its burrowing behavior, which helps maintain habitat structure in grasslands and rocky slopes. This ground-oriented lifestyle enhances its integration into these ecosystems, where it coexists with other reptiles and contributes to nutrient cycling via subterranean activities.

Diet and foraging

The sheltopusik exhibits an omnivorous diet, though it is predominantly carnivorous, with a strong preference for that provide essential calcium, such as gastropods including snails and slugs. Arthropods form the bulk of its prey, particularly like beetles (Coleoptera, comprising up to 76.4% of contents in some populations), orthopterans, hemipterans, and spiders, alongside isopods and other small . Gastropods account for approximately 8.3% of the diet in studied Anatolian populations, valued for their calcium-rich shells that support skeletal health in this legless species. Occasionally, it consumes small vertebrates such as , , nestling birds, and eggs, as well as minor amounts of plant matter, reflecting opportunistic feeding based on local availability. Foraging occurs primarily during diurnal to crepuscular periods, with the sheltopusik employing its to detect chemical cues from prey, a chemosensory strategy common in anguine that aids in tracking scents over substrates. It uses and active pursuit tactics in open grasslands or under , relying on its robust body to or navigate terrain while . The crushes hard-shelled prey like snails with its strong jaws and conical teeth, which are adapted for durophagy. Juveniles target smaller such as soft-bodied and tiny gastropods to accommodate their size limitations, gradually shifting to larger items as they mature. Feeding activity intensifies during wet weather, when gastropods emerge, prompting heightened post-rainfall to capitalize on this preferred . In contrast, intake diminishes during winter , a period of in cooler regions where the lizard retreats underground, conserving energy until spring emergence. These patterns align with seasonal prey abundance and environmental conditions across its range.

Behavior

Activity patterns

The Sheltopusik (Pseudopus apodus) is primarily diurnal, with activity typically occurring between 0800 and 1900 hours to facilitate basking and under sunny conditions. In early spring (March–April), peak activity aligns with morning to early afternoon hours (0900–1400), allowing individuals to elevate body temperatures effectively. During summer (June), the species shifts to a bimodal pattern, showing heightened activity in the late morning (1000–1330) and evening (1730–1945), reflecting crepuscular tendencies to avoid midday heat. In regions with extreme summer temperatures (–), activity diminishes markedly, with remaining sheltered in burrows, indicative of estivation rather than nocturnal foraging. Seasonally, the Sheltopusik experiences a peak in activity during early spring upon emergence from winter hibernation, which generally spans October to March in temperate parts of its range, where individuals retreat to burrows to endure cold conditions. Activity remains elevated through late spring (April–May) before declining in summer due to thermal constraints, with overall observations higher in spring than in . This pattern supports and resource utilization during optimal environmental windows. The maintains a solitary outside of brief interactions, inhabiting low-density populations with individuals often observed alone or in isolated microhabitats. Territorial behaviors are minimal, though males may engage in ritualized involving wrestling and biting during the spring period to compete for access to females, without evidence of strict territory defense. Such encounters underscore intra-sexual competition rather than ongoing social grouping.

Defensive mechanisms

The sheltopusik employs several primary defensive strategies when threatened by predators, primarily relying on and chemical deterrence rather than . It produces a loud hissing sound to warn off potential threats, accompanied by the release of a foul-smelling from cloacal glands that can deter attackers through its noxious . Although capable of delivering a painful bite with its strong jaws, the sheltopusik is non-venomous and rarely resorts to biting, preferring evasion when possible. A key is caudal , where the can detach readily along specialized fracture planes in the vertebrae, allowing the sheltopusik to escape while the wriggling segment distracts the predator. This mechanism is used less frequently than in other glass lizards due to the sheltopusik's relatively shorter , which provides less effective value. Following , the regenerates over several months, but the regrown appendage is typically shorter—often only half the original length—and darker in coloration compared to the original. In addition to these tactics, the sheltopusik utilizes evasive behaviors to avoid confrontation, such as rapidly burrowing into loose or seeking cover under rocks and debris.

Reproduction and life history

Reproductive biology

The Sheltopusik (Pseudopus apodus) is oviparous, with individuals reaching at 2–3 years of age. occurs in spring, typically from mid-April to mid-May following emergence. During , males bite the female, often on the or flank, to position for cloacal alignment and copulation. Following a gestation period of approximately 10 weeks, females lay a single clutch of 6–13 eggs in June or July. Clutch sizes average around 8–10 eggs, though variation occurs across populations; for example, Crimean females produced clutches of 8 or 13 eggs in documented cases. The eggs are elongated, measuring 3.1–3.9 cm in length and 1.7–2.2 cm in diameter, with a thin, leathery white shell; females bury them in moist soil or beneath rocks or bark in a simple nest cavity. Reproduction is not strictly annual, with evidence suggesting a biennial cycle in some populations, where only about 25% of females ovulate each year. Females exhibit limited post-oviposition, coiling around and guarding the clutch for the first 35 days of incubation to regulate and , but abandon the nest thereafter with no further involvement.

Growth and development

The eggs of the sheltopusik (Pseudopus apodus) typically incubate for 45–60 days, depending on temperature, which ranges from 26–28°C in natural and captive settings. Hatchlings emerge measuring 11–15 cm in total length and are fully independent from birth, as the female abandons the clutch immediately after hatching. They begin feeding within one week, primarily on small such as roaches, crickets, and snails, similar to the adult diet. In the juvenile phase, sheltopusiks grow rapidly, attaining and near-adult size (up to 1.4 m in total length) within 2–3 years. At this stage, they remain highly vulnerable to predation due to their smaller body size compared to adults. Coloration also changes with age: hatchlings exhibit a beige-gray body with transverse brown spots and wavy lines for , which fades into a more uniform tan as individuals mature. Sheltopusiks have a lifespan of 20–30 years in the wild, extending up to 50 years or more in under optimal conditions.

Conservation and human relations

Conservation status

The sheltopusik (Pseudopus apodus) is classified as Least Concern on the , with the global assessment last updated in 2021 and remaining stable as of 2025. This status reflects its extensive distribution across , the , and , coupled with its adaptability to a variety of modified habitats, which collectively lower its extinction risk. Regionally, it is also assessed as Least Concern within and the , though some national evaluations, such as in , classify it as Threatened due to localized pressures. Population estimates indicate that the sheltopusik is locally abundant in many parts of its range, with densities varying by habitat; for instance, surveys in western Anatolia's Gediz Delta recorded 52 individuals across study sites using capture-recapture methods. However, comprehensive global population data remain limited, particularly in where monitoring gaps persist due to remote terrains and underreporting. No evidence suggests a widespread decline, and its numbers are considered stable overall, supported by its tolerance for human-altered landscapes. The 2025 European Red List assessment of reptiles reinforces the stable status but highlights the need for improved monitoring in to address data deficiencies. Primary threats to the sheltopusik include habitat loss and fragmentation from agricultural expansion and urbanization, which degrade its preferred dry, open environments. Collection for the international pet trade poses a notable risk in Central Asian populations, particularly in Uzbekistan, where illegal harvesting has been documented. Road mortality is another concern, as individuals crossing paved areas during dispersal or foraging face high collision rates, exacerbated by expanding infrastructure. Additionally, minor persecution occurs when the species is mistakenly identified and killed as a venomous snake, though this is not a dominant threat. Conservation measures for the sheltopusik are limited but include legal protections in select countries under Annex V of the EU , which regulates exploitation and taking from the wild to ensure . No large-scale international programs exist, but habitat safeguards through broader initiatives, such as those under the EU Birds and Habitats Directives, indirectly benefit the . Local awareness campaigns to distinguish it from snakes could further reduce human-induced mortality.

In captivity

Sheltopusiks can be kept successfully in captivity with appropriate husbandry, though they are considered intermediate-level pets due to their size and specific needs. The minimum enclosure size for a single adult is 6 feet long by 2 feet wide by 2 feet high (72" x 24" x 24"), providing ample space for movement and burrowing; larger setups are recommended for optimal welfare. Enclosures should be terrestrial and longer than tall, with secure lids to prevent escapes, as these are strong climbers despite lacking limbs. Substrate must allow burrowing and mimic natural soil conditions, consisting of a 6-12 inch deep layer of a mix like , play sand, and coconut fiber to retain moisture without becoming soggy. A proper thermal gradient is essential, with a basking area of 90-95°F (32-35°C) on the warm end and 75-82°F (24-28°C) on the cool end, dropping to 60-72°F (16-22°C) at night; this can be achieved using flood bulbs or heat emitters. UVB lighting is required to support synthesis and overall health, with a 10-12% UVB tube (such as Arcadia T5 HO 12% or Zoo Med ReptiSun 10.0) spanning half the enclosure length, positioned 12-18 inches above the basking site to achieve a UVI of 3.0-4.0. should be maintained at 40-60% during the day and 60-80% at night, achieved through occasional misting and a moist hide, while a shallow dish is provided for soaking. In captivity, sheltopusiks are fed a varied carnivorous diet approximating 60% and 40% vertebrates or , including live items like , dubia roaches, grasshoppers, captive-bred snails, earthworms, and occasional pinky mice or . should be gut-loaded and dusted with calcium (with D3) and supplements 2-3 times weekly to prevent ; adults are typically fed every other day or 2-3 times per week, with juveniles more frequently, in amounts they consume within 5-8 minutes. Breeding in is rare but achievable, often requiring a brumation period to mimic the natural cycle, with temperatures lowered to 46-50°F (8-10°C) from October to March. occurs post-brumation, typically in spring, followed by egg-laying in summer; females deposit 6-10 soft-shelled eggs in a moist , which require incubation at 77-86°F (25-30°C) with 90-99% for 60 days to achieve high hatch success. Most sheltopusiks in the pet trade are wild-caught, leading to challenges with acclimation and potential parasites, though captive-bred specimens are increasingly available from zoos and dedicated breeders. With proper care, they can live up to 50 years in captivity, far exceeding wild lifespans. Legal restrictions on import and trade exist in some regions due to collection pressures, requiring permits for ownership in certain jurisdictions.

Relationship with humans

Archaeological evidence indicates that the Sheltopusik (Pseudopus apodus) has interacted with humans since prehistoric times, with remains of the subspecies P. a. levantinus recovered from Natufian sites in the dating to approximately 12,000 BCE. These findings, including numerous osteoderms and vertebrae, include some with burning marks suggesting possible but limited consumption by early humans as part of late Epipaleolithic activities. In historical and folk contexts, the Sheltopusik is frequently mistaken for a due to its legless body and serpentine movement, leading to deliberate killings by rural communities who view it as dangerous. This misidentification persists across its range, from southeastern to Central Asia, contributing to localized population declines despite the lizard's harmless nature. Culturally, the Sheltopusik lacks significant symbolic or mythological importance in traditional narratives, unlike certain snakes or other in regional . However, it has become popular in , valued for its distinctive appearance, longevity in captivity, and relative ease of care, making it a sought-after among reptile enthusiasts. Economically, the international pet trade drives limited wild collection of the Sheltopusik, primarily from parts of its range in and , though demand is met increasingly through captive-bred specimens to minimize pressure on wild populations.

References

  1. https://animalia.bio/sheltopusik
  2. https://cincinnatizoo.org/animals-archive/sheltopusik/
  3. https://pmc.ncbi.nlm.nih.gov/articles/PMC7109015/
  4. https://www.iucnredlist.org/species/157263/5064890
  5. https://reptile-database.reptarium.cz/species?genus=Pseudopus&species=apodus
  6. https://www.gbif.org/species/2468350
  7. https://doi.org/10.3897/vz.71.e60800
  8. https://fr.pensoft.net/article/100059/
  9. https://anatomypubs.onlinelibrary.wiley.com/doi/10.1002/ar.25525
  10. https://www.monaconatureencyclopedia.com/pseudopus-apodus/?lang=en
  11. https://www.cyberlizard.org.uk/pseudopus_apoda.htm
  12. https://vertebrate-zoology.arphahub.com/article/60800/
  13. https://www.beardsleyzoo.org/legless-lizard.html
  14. https://www.researchgate.net/publication/327573930_Sexual_dimorphism_in_Pseudopus_apodus_Reptilia_Sauria_Anguidae_from_the_Steppe_Crimea
  15. https://reptile-database.reptarium.cz/species?genus=pseudopus&species=apodus
  16. https://www.sciencedirect.com/org/science/article/pii/S2535073022000018
  17. https://www.guinnessworldrecords.com/world-records/382006-longest-legless-lizard
  18. https://animals.howstuffworks.com/reptiles/glass-snake.htm
  19. https://www.danieljablonski.com/a/soubory/Jablonski_2018_Male-male_combat_Pseudopus_apodus_RJH.pdf
  20. https://anatomypubs.onlinelibrary.wiley.com/doi/10.1002/ar.23532
  21. https://www.researchgate.net/publication/275961881_Data_on_the_Food_Composition_of_European_Glass_Lizard_Pseudopus_apodus_Pallas_1775_Squamata_Anguidae_from_Canakkale_Western_Anatolia_Turkey
  22. https://www.researchgate.net/publication/368918620_The_easternmost_record_of_the_largest_anguine_lizard_that_has_ever_lived_-_Pseudopus_pannonicus_Squamata_Anguidae_new_fossils_from_the_late_Neogene_of_Eastern_Europe
  23. https://www.researchgate.net/publication/312626881_Habitat_use_and_activity_of_European_glass_lizard_Pseudopus_apodus_Pallas_1775in_southeastern_Bulgaria
  24. https://journals.tubitak.gov.tr/zoology/vol41/iss2/10/
  25. https://www.uni-sofia.bg/index.php/bul/content/download/140636/1029569/version/2/file/39_IVAN_TELENCHEV.pdf
  26. https://www.researchgate.net/publication/275956995_Data_on_the_Food_Composition_of_European_Glass_Lizard_Pseudopus_apodus_Pallas_1775_Squamata_Anguidae_from_Canakkale_Western_Anatolia_Turkey
  27. https://pmc.ncbi.nlm.nih.gov/articles/PMC12119748/
  28. https://reptilesmagazine.com/six-legless-lizards/
  29. https://apjmt.mums.ac.ir/article_13828.html
  30. https://iers.org.ua/en/european-legless-lizard-pseudopus-apodus/
  31. https://www.lacerta.de/AF/Bibliografie/BIB_16939.pdf
  32. https://buffalozoo.org/animal/european-glass-lizard-sheltopusik/
  33. https://potterparkzoo.org/wp-content/uploads/2017/06/Sheltopusik.pdf
  34. https://www.researchgate.net/publication/276293868_A_PRELIMINARY_STUDY_ON_THE_HABITAT_SELECTION_OF_EUROPEAN_GLASS_LIZARD_PSEUDOPUS_APODUS_IN_SOUTHEAST_BULGARIA
  35. https://www.researchgate.net/publication/267630493_A_state_of_the_knowledgt_about_reproductive_biology_of_Giant_legless_lizard_REPTILIA_SAURIA_ANGUIDAE_in_the_Crimea
  36. https://www.researchgate.net/publication/361662593_CAPTIVE_BREEDING_AND_CONSERVATION_AN_EXPERIENCE_OF_CAPTIVE_INCUBATION_OF_THE_CLUTCH_OF_THE_EUROPEAN_GLASS_LIZARD_REPTILIA_SAURIA_ANGUIDAE_WITH_NOTES_ON_ITS_REPRODUCTIVE_BIOLOGY
  37. https://www.researchgate.net/publication/263094275_A_record_of_natural_nest_of_Pseudopus_apodus
  38. https://www.researchgate.net/publication/357706345_Artificial_incubation_and_mold_treatment_of_European_Glass_Lizard_Pseudopus_apodus_eggs_in_a_home-made_incubator
  39. http://e-ecodb.bas.bg/rdb/en/vol2/Psapodus.html
  40. https://genomics.senescence.info/species/entry.php?species=Pseudopus_apodus
  41. https://www.iucnredlist.org/species/157263/745759
  42. https://portals.iucn.org/library/sites/library/files/documents/RL-4-004.pdf
  43. https://eunis.eea.europa.eu/species/750
  44. https://iucn.org/news/eastern-europe-and-central-asia/201912/first-red-list-threatened-species-published-north-macedonia
  45. https://www.tandfonline.com/doi/full/10.1080/14888386.2025.2569897
  46. https://www.biolib.cz/en/taxon/id59566/
  47. https://nc.iucnredlist.org/redlist/content/attachment_files/ERL_Pulse_Reptiles_2025.pdf
  48. https://www.adb.org/sites/default/files/project-documents/55135/55135-001-iee-en_2.pdf
  49. https://www.forest-trends.org/wp-content/uploads/imported/20council-directive-1992-natural-habitats-annex-v-pdf.pdf
  50. https://reptilesupply.com/blogs/care-sheets/how-to-care-for-your-sheltopusik
  51. https://reptifiles.com/sheltopusik-care-sheet/
  52. https://dubiaroaches.com/blogs/lizard-care/sheltopusik-care-sheet
  53. https://reptilesmagazine.com/two-european-glass-lizards-hatch-at-smithsonians-national-zoo/
  54. https://digimorph.org/specimens/Ophisaurus_apodus/
  55. https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0247283
  56. https://www.researchgate.net/publication/350640113_Morphological_and_genetic_differentiation_in_the_anguid_lizard_Pseudopus_apodus_supports_the_existence_of_an_endemic_subspecies_in_the_Levant
  57. https://www.traffic.org/publications/reports/an-assessment-of-wildlife-trade-in-central-asia/
Add your contribution
Related Hubs
User Avatar
No comments yet.