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Anguis

Anguis is a genus of legless lizards in the family Anguidae, consisting of five extant species commonly known as slowworms or blindworms. These reptiles are characterized by their elongate, snake-like bodies lacking external limbs, smooth scales, and a maximum length of up to 50 cm in some species. Native to the Western Palearctic region, they are distributed across much of Europe and into western Asia, favoring temperate and humid habitats such as grasslands, woodlands, and gardens.^[1]^[2]^[3] The genus Anguis, established by Linnaeus in 1758, derives its name from the Latin word for "snake," reflecting its superficial resemblance to serpents despite being true lizards. The recognized species include A. fragilis (common slowworm), A. colchica (eastern slowworm), A. graeca (Greek slowworm), A. veronensis (Italian slowworm), and A. cephallonica (Peloponnese slowworm), each adapted to specific subregions within their overall range. Phylogenetic studies indicate that Anguis represents an ancient lineage within Anguidae, with divergence events dating back millions of years, contributing to their morphological uniformity and ecological specialization.^[1]^[4]^[5] Slowworms are ovoviviparous, giving birth to live young after internal development of eggs, and exhibit slow, deliberate movements that belie their name. They primarily feed on invertebrates like slugs, worms, and insects, playing a beneficial role in garden ecosystems by controlling pests. Despite their widespread occurrence, populations face threats from habitat loss and road mortality, though they are generally not considered endangered across their range. Hibernation occurs from October to February or March in burrows or under cover, aiding survival in cooler climates.^[3]^[2]^[6]

Taxonomy and Phylogeny

Etymology and History

The genus name Anguis derives from the Latin word for "snake," reflecting the legless, elongated body form of its members that mimics serpentine reptiles.^[7] Carl Linnaeus formally established the genus in the 10th edition of Systema Naturae in 1758, with Anguis fragilis—the common slow worm—as the type species.^[7] Early taxonomic treatments largely treated the genus as monospecific under A. fragilis, but accumulating morphological evidence in the late 20th century hinted at cryptic diversity, particularly in southern European populations. A major revision occurred in 2010 when Gvoždík et al. analyzed mitochondrial (ND2 and tRNAs) and nuclear (C-mos and PRLR) DNA sequences across the Western Palearctic range, uncovering deep genetic divergences within A. fragilis sensu lato and confirming it as a species complex. Their findings supported the recognition of A. cephallonica as a valid species and elevated two lineages to full species status: A. colchica (eastern Europe to Iran) and A. graeca (southern Balkans), each with distinct phylogeographic structuring linked to Pleistocene refugia. Building on this, Gvoždík et al. in 2013 examined Italian Peninsula populations using similar genetic markers (mtDNA cyt b, nDNA PRLR) alongside morphology, identifying an ancient basal lineage divergent since the Miocene.^[8] They resurrected the taxon Anguis veronensis Pollini, 1818—originally described from Verona, Italy—as a full species, distinguished by unique haplotypes, subtle cranial differences, and a distribution spanning the Italian Peninsula, southern Alps, and southeastern France.^[8] This elevation resolved prior subspecific uncertainties and highlighted the role of vicariance events, such as Alpine orogeny, in the genus's diversification.

Classification and Species

The genus Anguis is classified within the family Anguidae, subfamily Anguinae, a group of legless lizards characterized by their elongated bodies and distribution across the Northern Hemisphere.^[9] Phylogenetic analyses based on molecular data, including mitochondrial and nuclear genes, have resolved the relationships among Anguis species, revealing five distinct genetic clades that correspond to the recognized extant taxa. A key study using multilocus datasets identified these clades as deeply diverged lineages originating from an ancient radiation, with A. cephallonica as the basal species and the remaining four forming a "fragilis complex" clade supported by nuclear DNA, though mitochondrial data show some discordance suggestive of historical introgression.^[9] Five extant species are currently recognized in the genus Anguis, each distinguished primarily by genetic markers such as sequence divergences in cytochrome b and nuclear loci (e.g., >5% mitochondrial divergence between clades), alongside subtle morphological traits like mid-body scale row counts and head scalation patterns used in taxonomic diagnoses.^[10] These species are allopatric or parapatric, with contact zones exhibiting hybridization in some regions, such as between A. fragilis and A. veronensis in southeastern France.^[10] The following table summarizes the species, their common names, and primary distributions:

Scientific Name	Common Name	Primary Distribution
Anguis cephallonica Werner, 1894	Peloponnese slow worm	Peloponnese Peninsula, southern Greece
Anguis colchica Nordmann, 1840	Eastern slow worm	Eastern Europe to western Russia, northern Turkey, Caucasus, northern Iran
Anguis fragilis Linnaeus, 1758	Common slow worm	Western and central Europe, from Iberian Peninsula and British Isles to southeastern Europe and western Russia
Anguis graeca Bedriaga, 1884	Greek slow worm	Balkan Peninsula, including Greece, Albania, and North Macedonia
Anguis veronensis Pollini, 1818	Italian slow worm	Italian Peninsula and southeastern France

Taxonomic revisions remain ongoing, with recent phylogenomic studies using genome-wide markers confirming the monophyly of Anguis.^[9] Further research into hybridization and mitonuclear discordance, particularly in A. veronensis, may lead to additional refinements in species boundaries.^[10]^[9]

Fossil Record

The fossil record of the genus Anguis spans the Miocene to the present day, while the subfamily Anguinae to which it belongs has an earlier history extending back to the Eocene, approximately 48 million years ago.^[11] This temporal range provides evidence for the evolution of legless forms within Anguinae, with early fossils indicating progressive limb reduction from limbed Anguidae ancestors in Europe during the Paleogene.^[11] Osteological remains, such as vertebrae and cranial elements, from these sites reveal elongated bodies and vestigial limb structures, marking adaptations to semifossorial lifestyles.^[12] Key fossil species include Anguis rarus, the earliest recognized member of the genus, described from the Early Miocene (approximately 20 million years ago) of Germany based on a well-preserved parietal bone, the first such record for the genus, exhibiting cranial features consistent with legless morphology. Additional Miocene records of Anguis sp. come from European localities such as Anatolia and the Czech Republic, where fragmentary osteoderms and vertebrae further document the genus's distribution and morphological stasis in limb reduction.^[13] These fossils illuminate the evolutionary divergence of Anguis from limbed ancestors around 40–50 million years ago in the Eocene, coinciding with climatic shifts that facilitated the radiation of Anguidae across the Northern Hemisphere.^[11] The legless condition in Anguinae likely evolved once from a limbed common ancestor, with Anguis representing a specialized lineage adapted to forested and temperate environments of Eurasia.^[12] This record underscores the role of Anguinae in understanding parallel limb loss events within Squamata and the biogeographic expansion of anguimorph lizards during the Cenozoic.^[11]

Physical Characteristics

External Morphology

Members of the genus Anguis exhibit a snake-like body form characterized by an elongated trunk and the complete absence of external limbs in extant species, an adaptation facilitating a fossorial and serpentine lifestyle.^[14] This limbless condition contrasts with some fossil anguimorphs, where vestigial hindlimbs are present, highlighting the evolutionary reduction within the Anguidae family.^[15] The body is covered by smooth, cycloid dorsal scales that overlap in regular rows, providing a glossy, flexible integument suited for burrowing, while the ventral surface features multiple rows of small, smooth scales, similar to the dorsal but without enlarged scutes.^[16] These scales are underlain by osteoderms—dermal bones that form imbricating plates of woven-fibred and lamellar bone, enhancing protection without impeding movement.^[17] Sensory structures distinguish Anguis from snakes, including movable eyelids that allow blinking and external ear openings for auditory perception, features absent in ophidians.^[18] The tongue is short, wide, and notched at the tip rather than forked, with filamentous papillae facilitating chemosensory detection via the vomeronasal organ during substrate exploration.^[19] Osteologically, the skull is kinetic with flexible joints enabling cranial kinesis for prey manipulation, complemented by pleurodont teeth that bear longitudinal grooves to secure soft-bodied invertebrates during ingestion. A key defensive adaptation is caudal autotomy, where the tail detaches at specialized fracture planes in the autotomous vertebrae, located anterior to the transverse processes, allowing escape from predators.^[18] The shed tail regenerates partially, though the regrown portion lacks fracture planes and osteoderms, resulting in a less robust structure.^[20] This mechanism is widespread in the genus, underscoring its role in survival despite the energetic costs of regeneration.^[21] While descriptions primarily apply to the widespread A. fragilis, other species show minor variations in scale arrangement and body proportions.^[1]

Size, Coloration, and Sexual Dimorphism

Members of the genus Anguis are legless lizards that attain adult total lengths of up to 50 cm, with snout-vent lengths typically ranging from 12 to 20 cm and tails of comparable length.^[3]^[22] Neonates are born live at lengths of approximately 7 to 10 cm.^[23] Growth is rapid in the first year, reaching about 10 cm snout-vent length, followed by slower increments in subsequent years until maturity around 3 to 5 years of age.^[3] The base coloration across Anguis species is generally grey-brown, though variations occur; for instance, A. fragilis adults range from uniform grey-brown to coppery hues.^[3] Juveniles often exhibit pale gold or silver tones with darker lateral and ventral markings, which fade with age.^[3] Females typically display a coppery sheen, prominent dorsal stripes, and darker flanks, while males are slimmer and more uniformly colored, occasionally showing blue spots during the breeding season in some populations.^[3]^[24] Sexual dimorphism in Anguis is pronounced, with females achieving greater lengths and weights—up to 100 g—compared to slimmer males, which may exhibit brighter breeding coloration.^[25]^[26] Lifespans reach up to 30 years in the wild and 54 years in captivity.^[22]^[3] These lizards undergo annual ecdysis as adults, shedding their skin in one piece.^[18]

Distribution and Habitat

Geographic Distribution

The genus Anguis is distributed across the Western Palearctic, encompassing much of Europe from the United Kingdom and Portugal in the west to the Ural Mountains and northern Iran in the east, and from Scandinavia in the north to Greece and Anatolia in the south.^[27] This range includes species exhibiting largely allopatric distributions and minimal overlap, primarily in parapatric contact zones along major geographic features.^[27] Among the five recognized species, Anguis fragilis occupies the northwestern and central European portion of the genus range, extending from the Iberian Peninsula and the British Isles through central Europe (including France, Germany, and the Balkans) to the Baltic states and southern Scandinavia, with a total area of about 2.1 million km².^[27] Anguis colchica, the most widespread species, ranges from central Europe (Czech Republic, Poland, Slovakia) and northward to Finland eastward through Ukraine, southern Russia (to the Urals and Dagestan), the Caucasus, northern Turkey, Armenia, and northern Iran, covering roughly 3.3 million km² overall (2.9 million km² in Europe).^[27]^[28] In contrast, Anguis veronensis is restricted to southeastern France and the Italian Peninsula, spanning about 183,000 km².^[27] The Balkan endemics Anguis graeca and Anguis cephallonica have more limited ranges: A. graeca in the southern Balkans (Greece, Albania, North Macedonia, Montenegro), covering 65,000 km², while A. cephallonica is confined to the Peloponnese Peninsula and nearby Ionian Islands (Kefalonia, Ithaca, Zakynthos), with an area of 15,000 km²; these two show partial sympatry in the northern Peloponnese.^[27]^[29] Biogeographically, Anguis species belong to the Palearctic realm, with chorotypes reflecting post-glacial expansions from refugia: A. fragilis likely originated from Balkan refugia and spread northwestward, while A. colchica expanded from eastern refugia toward the west and Asia.^[27] Major barriers such as the Alps (separating A. fragilis from A. veronensis) and the Black Sea (limiting A. colchica's eastward spread within Europe) have promoted isolation and shaped these allopatric patterns.^[27] A population of A. fragilis in Ireland is considered introduced from Great Britain.^[30]

Habitat Preferences and Microhabitats

Species of the genus Anguis, particularly A. fragilis in Europe, inhabit temperate biomes such as woodlands, grasslands, heathlands, hedgerows, and even urban gardens, where they avoid extreme arid conditions and high altitudes beyond occasional alpine populations.^[31] These lizards favor mid-successional habitats with a mix of open sunny areas and vegetated cover, including pine-dominated forests and chalk grasslands, but they steer clear of overly wet wetlands or barren dry sites.^[32] Their distribution spans much of Europe, aligning with these moderate climates from lowlands to edges of higher elevations.^[31] Within these biomes, Anguis species select humid microhabitats providing shelter and foraging opportunities, such as dense grass tussocks, leaf litter, compost heaps, and areas under stones or logs, where they burrow into loose soil for refuge.^[31] They prefer sites with moderate shrub and grass cover (around 40-50%) alongside scattered stones or ruins for hiding, often in intact forest understories with feather moss mats that offer both concealment and thermal stability.^[32] Juveniles and adults alike utilize these refuges without strong age-based partitioning, frequently sharing artificial or natural shelters in sun-exposed, low-vegetation zones.^[33] Seasonally, Anguis adapts by hibernating communally in burrows, root systems, or dense vegetation from late October to early March, emerging in spring to bask in sunny, south-facing spots for thermoregulation.^[31] Active primarily during the day in warmer months, they rely on diffuse canopy cover in pine stands to maintain body temperatures between 21.5-27.7°C, with peak activity on clear days.^[32] Habitat fragmentation poses challenges due to their limited dispersal—home ranges typically span hundreds of square meters—making them vulnerable in isolated patches; they thrive in connected green corridors like hedgerows that link woodlands and grasslands.^[31] Preference for older pine stands (over 80 years) further underscores their need for structurally diverse, contiguous habitats over disturbed or fragmented ones.^[34]

Biology and Behavior

Diet and Predation

Anguis species exhibit a carnivorous diet focused on soft-bodied invertebrates, including slugs, snails, earthworms, insect larvae such as caterpillars, and occasionally spiders and millipedes.^[35]^[36] In a study of a Danish population, gastropods (small snails at 44% and slugs at 12% of prey items) and earthworms (20.5%) dominated the diet, with pill millipedes (22.4%) and Lepidoptera larvae (7.3%) also common, reflecting a preference for slow-moving, nutrient-rich prey.^[36] Similarly, analysis of specimens from northeastern Italy revealed earthworms comprising 33.33% of prey items and slug-snails 35.41%, alongside smaller contributions from Diptera (12.10%) and Coleoptera larvae (9.37%).^[35] Juveniles target smaller prey like tiny snails to accommodate their size, though overall dietary composition shows no significant ontogenetic shifts.^[36] These lizards employ an opportunistic foraging strategy as ground hunters, actively patrolling habitats during early morning, twilight, or after rain when prey is surface-active, and partly utilizing fossorial habits to ambush invertebrates.^[35] Prey is captured using recurved teeth adapted for gripping soft-bodied items, then swallowed whole without venom, constriction, or extensive mastication, as evidenced by gut content analyses showing intact remains.^[37] Anguis individuals serve as prey for various predators, including birds such as owls, magpies, and other raptors, as well as mammals like foxes, badgers, domestic cats, and hedgehogs, with juveniles particularly vulnerable to smaller avian species.^[38] To counter threats, they display defensive behaviors including crypsis through immobility (feigning death), rapid burrowing or fleeing into vegetation, and caudal autotomy, where the tail is shed and continues wriggling to distract attackers.^[39] In their trophic role, Anguis contribute to ecosystem balance by controlling populations of garden and crop pests, notably slugs, with molecular studies detecting slug remains in 45% of examined individuals (30% Arion spp. and 22% Deroceras reticulatum).^[40] This predation supports natural pest management without chemical interventions.^[40]

Reproduction and Development

Anguis fragilis is viviparous, with embryos developing internally within the female until live birth.^[18] The gestation period typically lasts 3-4 months, varying slightly by region and environmental conditions.^[25] Females give birth to litters of 4-12 offspring, with an average of around 7 neonates per litter.^[41] Births occur primarily in late summer, between July and August in southern populations, though they may extend into September in northern areas.^[41] Mating takes place in spring, from March to May, following emergence from hibernation.^[3] Males engage in combat displays to compete for access to females, often intertwining bodies and attempting to pin rivals to the ground, with larger males typically prevailing.^[42] This intrasexual competition is facilitated by sexual dimorphism, where breeding males possess relatively larger heads compared to females, aiding in combat.^[26] Females appear to mate with dominant males based on outcomes of these size-dependent contests, though direct choice mechanisms remain less documented.^[42] Neonates are born fully formed and independent, measuring approximately 40-50 mm in snout-vent length and weighing about 0.5 g.^[41] They exhibit a distinctive golden or silver dorsal coloration with a black vertebral stripe and dark flanks, providing effective camouflage against soil and leaf litter substrates.^[22] No parental care is provided after birth, leaving juveniles vulnerable to predation by birds, snakes, and mammals, resulting in high early mortality rates.^[3] Sexual maturity is reached at 3-5 years of age, depending on growth conditions and latitude, with females often maturing slightly later than males.^[3] Females typically reproduce biennially thereafter, conserving energy for gestation in this low-energy lifestyle.^[41]

Daily and Seasonal Behaviors

Anguis fragilis exhibits predominantly diurnal activity patterns, emerging during daylight hours to bask on sunny surfaces for thermoregulation, which helps maintain optimal body temperatures ranging from 25°C to 26°C in controlled gradients.^[43]^[44] This basking behavior is particularly evident in open habitats during spring and summer, allowing the lizard to exploit solar radiation despite its semifossorial lifestyle. Nocturnal activity is rare, limited mostly to brief movements under cover. Locomotion in A. fragilis is characterized by slow, undulating lateral movements, with maximum speeds reaching approximately 0.13 m/s (0.3 mph) on smooth substrates, though typical velocities are much lower at around 0.01–0.05 m/s during routine travel.^[45] This serpentine motion relies on body undulations to propel the limbless form forward, adapting to rough terrain through slide-pushing or concertina-like contractions when necessary. The tail plays a key role in propulsion and balance, and in cases of threat, individuals may autotomize it to facilitate escape, with partial regeneration occurring over subsequent months, though the replacement is shorter and lacks original functionality.^[39] As a largely solitary species, A. fragilis shows no evidence of territorial behavior, with individuals maintaining overlapping home ranges without aggressive interactions toward conspecifics.^[46] Social contacts are minimal outside of brief encounters, but communal hibernation occurs in winter, where multiple individuals aggregate in underground burrows, crevices, or compost heaps from October to March to conserve heat.^[3] This seasonal clustering enhances survival during cold periods, with activity resuming in spring as temperatures rise, peaking from May to August.^[47] Sensory behaviors emphasize chemosensation via the Jacobson's organ, where the tongue collects environmental chemicals for analysis, aiding in predator detection and navigation in low-visibility conditions.^[48] Auditory cues are perceived through visible ear openings, allowing response to vibrations and low-frequency sounds, which complement visual and olfactory inputs for threat assessment. Primary defensive responses include fleeing into cover or hiding under vegetation, with tail autotomy reserved for direct capture attempts.^[49] Human interactions often stem from misidentification of A. fragilis as a venomous snake due to its elongate form, leading to unnecessary persecution and contributing to population declines across its range.^[50] Despite being harmless, this fear-driven killing, particularly in gardens and rural areas, underscores the need for public education to mitigate such threats.^[3]

Conservation and Threats

Legal Protections

Anguis species receive protection under international agreements and national legislation across much of their European range, aimed at preventing exploitation and ensuring habitat safeguards. The common slow worm, Anguis fragilis, is listed in Annex III of the Bern Convention on the Conservation of European Wildlife and Natural Habitats, which obliges signatory states to maintain viable populations through regulated exploitation and habitat protection measures.^[51] This framework is implemented nationally within the European Union, though A. fragilis is not specifically enumerated in the EU Habitats Directive annexes.^[51] National protections vary but generally prohibit intentional harm, capture, or trade. In the United Kingdom, A. fragilis is fully protected under Schedule 5 of the Wildlife and Countryside Act 1981, making it illegal to deliberately kill, injure, possess, or sell the species without a license.^[52] In Poland, A. fragilis holds partial protection status, restricting exploitation but allowing limited activities under permit, while the recently distinguished A. colchica awaits formal inclusion in protective lists.^[53] Protections are more limited in Germany, where A. fragilis is designated as a particularly protected species under Section 44 of the Federal Nature Conservation Act, banning killing or disturbance but permitting certain relocations for development with approval.^[54] Similar protections apply in various other European countries under national biodiversity laws aligned with the Bern Convention. The International Union for Conservation of Nature (IUCN) assesses all Anguis species as Least Concern globally as of 2024, reflecting stable populations without immediate extinction risks, though regional declines warrant ongoing monitoring; for instance, A. fragilis, A. colchica, A. graeca, A. veronensis, and A. cephallonica are rated Least Concern, with A. cephallonica upassessed from Near Threatened to Least Concern in 2024.^[7]^[55]^[56]^[57] Enforcement emphasizes preventing pet trade and habitat disruption, with bans on wild collection for personal use in protected countries like the UK and Germany. Development projects impacting suitable habitats often require mitigation, such as translocation to receptor sites or habitat creation, to comply with national laws and avoid penalties.^[52]^[54]

Population Status and Threats

The genus Anguis encompasses several species of legless lizards distributed across Europe and parts of Asia, with A. fragilis being the most widespread and classified as Least Concern at the European level by the IUCN, indicating stable core populations despite local declines.^[58] However, population estimates remain challenging due to the cryptic nature of these semifossorial reptiles, with average densities of around 120 individuals per hectare in optimal habitats such as grasslands in southern Europe, though fragmented areas show reduced numbers from habitat loss.^[47] For eastern species like A. colchica, data gaps persist, but overall populations are considered stable, with no comprehensive continent-wide estimates available beyond localized studies.^[59] Major threats to Anguis species include habitat destruction and fragmentation from urbanization and agricultural intensification, which eliminate refuges like tussocky grasslands and compost heaps essential for foraging and hibernation.^[31] Road mortality exacerbates declines, as slow-moving individuals crossing paved areas face high vehicle collision risks, particularly during dispersal or migration periods.^[60] Persecution arises from frequent misidentification as venomous snakes, leading to intentional killing despite their harmless nature.^[61] Climate change poses additional risks by altering hibernation cues through fluctuating temperatures and extreme weather, potentially disrupting activity patterns and prey availability.^[62] Conservation actions focus on habitat restoration, such as maintaining diverse vegetation structures with sunny basking sites and overwintering burrows, which has stabilized populations in managed reserves across the UK and Europe.^[31] Translocation programs serve as mitigation for development projects, relocating individuals to suitable receptor sites with demonstrated short-term survival success.^[63] Education campaigns aim to dispel myths about misidentification, reducing persecution, while ongoing research addresses taxonomic uncertainties following the 2013 recognition of multiple cryptic species within the genus.^[4] The future outlook remains cautious, with Anguis species vulnerable to escalating land-use intensification; however, warming climates may enable poleward range shifts, though this could strain fragmented habitats.^[64]

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Predation on slugs was high, with 45% of slow worms (N = 400) found to have eaten them (22% D. reticulatum and 30% Arion). Predation on bothD. reticulatum and ...
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(PDF) Reproductive ecology of the slow worm (Anguis fragilis) in the ...
Aug 7, 2025 · The relationship between several variables related to offspring and their mothers showed a positive relation between size and mass of the litter ...
[41]
sexual combats, matings, and reproductive phenology in an alpine ...
Jan 11, 2016 · The most spectacular characteristic of this mating system is the occurrence of sexual combat between males for access to females. Male body size ...
[42]
Feeding state and selected body temperatures in the slow-worm ...
Aug 6, 2025 · Feeding state and selected body temperatures in the slow-worm (Anguis fragilis). January 2008; Herpetological Journal 18(1):59-62. Authors:.
[43]
Ecology of an alpine population of the Slow Worm, Anguis fragilis ...
Aug 9, 2025 · An alpine population of the live-bearing anguid Anguis fragilis LINNAEUS, 1758 was studied in this respect. ... habitat, a thick forest habitat, ...
[44]
Slow Worm - Anguis fragilis - A-Z Animals
Slow worms, also known as the deaf adder, go by the scientific name Anguis fragilis. They belong to the kingdom Animalia and Phylum Chordata. The class is ...Missing: taxonomy | Show results with:taxonomy
[45]
[PDF] A COMPARISON OF SOCIAL BEHAVIOUR OF TWO LIZARD SPECIES
Based on the results, it is assumed that the species is not territorial. In Bulgaria, the behavioural response of A. fragilis and A. colchica to their ...
[46]
Phenological, ecological, and demographic data of the slow worm ...
Aug 29, 2024 · The study area encompasses 2.9 hectares in Tarragona Province, Spain, at an altitude of 990 m. Sixteen sampling stations were established to ...
[47]
Chemosensory predator recognition induces defensive behavior in ...
Chemosensory predator recognition induces defensive behavior in the slow-worm (Anguis fragilis). Canadian Science Publishing. Canadian Journal of Zoology.Missing: sources | Show results with:sources
[48]
Slowworm | Legless, Burrowing, Nocturnal | Britannica
Oct 17, 2025 · External limbs and girdles are absent, and only a remnant of the pelvic girdle persists internally. Its elongated body form, combined with an ...
[49]
Slow-worm - Sidmouth Nature
May 15, 2024 · Slow-worms play a crucial role in controlling pest populations. Their diet mainly consists of soft-bodied invertebrates such as slugs, snails, ...
[50]
Slow worm - Anguis fragilis - Linnaeus, 1758 - EUNIS
Threat status Europe, Least Concern (IUCN). Protected by, 1 international agreement. Natura 2000 sites, 1 are designated for this species ...
[51]
Slow-worm | Amphibian and Reptile Conservation
Jul 30, 2016 · Slow-worm. Anguis fragilis. Where to find them. Distribution map of ... Juveniles have black bellies and gold or silver dorsal sides ...Missing: coloration | Show results with:coloration
[52]
Anguis - Wikipedia
The genus contains five extant living species, including the common slow worm (A. fragilis), the eastern slow worm (A. colchica), the Greek slow worm (A. graeca) ...Anguis colchica · Anguis veronensis · Common slow worm
[53]
the proposal of monitoring of slow-worm anguis fragilis l. and ...
Nov 20, 2021 · Due to the recent isolation of the Eastern slow-worm, it is still not legally protected in Poland, unlike the partially protected slow-worm.
[54]
Artenporträt Blindschleiche - NABU
Blindschleichen sind leicht zerbrechliche Wesen. Ein unbedachter Griff und die mühelos zu fangenden Tiere brechen entzwei. Während sich das längere Ende ...
[55]
[PDF] Table 7: Species changing IUCN Red List Status (2022–2024)
Jun 27, 2024 · Anguis cephallonica. Peloponnese Slow Worm. NT. LC. N. 2024-1. REPTILES. Bungarus multicinctus. Many-banded Krait. LC. VU. N. 2024-1. REPTILES.
[56]
[PDF] European Red List of Reptiles - IUCN Portals
All species had their global status assessed according to the 2001 IUCN Red List Categories ... Anguis cephalonnica. NT. NT. Yes. Yes. SQUAMATA. ANGUIDAE. Anguis ...
[57]
Slow Worm - Rīga ZOO
The Anguis fragilis is found in Albania, Andorra, Austria, Belgium, Bosnia and Herzegovina, Bulgaria, Croatia, Czechia, Denmark, France, Germany, Hungary ...Missing: legal | Show results with:legal<|control11|><|separator|>
[58]
[PDF] Effect of habitat fragmentation on the genetic structure of slow-worm ...
Even so the slow-worm is included in the. “annexe III”, protected species of the “Bern Convention on the Conservation of European Wildlife and. Natural Habitats ...
[59]
Snake FAQs - Amphibian and Reptile Conservation
Jun 19, 2016 · Slow-worms though mistaken for snakes, are actually a species of legless lizard. ... Check identification again - it is much more likely to be a ...
[60]
[PDF] slow-worms (Anguis fragilis) - Kent Academic Repository
In the United Kingdom, 1,115 animal species have been assessed and assigned a conservation status (IUCN 2017b). Approximately 7.35% of these species are ...<|control11|><|separator|>
[61]
Translocation of slow-worms (Anguis fragilis) as a mitigation strategy
This paper describes a case study in which translocation was used as a mitigation measure for the slow-worm (Anguis fragilis) a cryptic legless lizard.Missing: legal | Show results with:legal
[62]
The effect of the climate crisis on UK reptile populations - Froglife
Feb 22, 2021 · Climate change is already affecting reptile prey populations and will continue to do so. For example Ewald et al. (2015) identified numerous ...