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Anguinae
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| Anguinae Temporal range:
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|---|---|
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| An eastern glass lizard (Ophisaurus ventralis). | |
Scientific classification 
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| Kingdom: | Animalia |
| Phylum: | Chordata |
| Class: | Reptilia |
| Order: | Squamata |
| Suborder: | Anguimorpha |
| Family: | Anguidae |
| Subfamily: | Anguinae |
| Genera | |
Anguinae is a subfamily of legless lizards in the family Anguidae, commonly called glass lizards, glass snakes or slow worms. The first two names come from the fact their tails easily break or snap off. Members of Anguinae are native to North America, Europe, Asia, and North Africa.
Evolution
[edit]They first appeared in Europe during the early Eocene, approximately 48.6 million years ago, originating from North American ancestors that crossed over from Greenland via the Thule Land Bridge and spread toward Asia sometime after the drying of the Turgai Strait at the beginning of the Oligocene, and then across the Bering Land Bridge to North America during the Miocene.[1]
Description
[edit]Very vestigial hindlegs are present in Hyalosaurus and Pseudopus, but are entirely absent in the other genera.[1] Members of the group largely feed on insects and other invertebrates.[2] The largest living species, the Sheltopusik (Pseudopus apodus),[3] can reach lengths of 120 centimetres (47 in).[4]
Taxonomy
[edit]The subfamily contains the following genera:
- Dopasia (7 species), native to eastern Asia
- Hyalosaurus (1 species), native to North Africa
- Ophisaurus (6 species), native to eastern North America
- Pseudopus (1 extant species, the Sheltopusik), native to Europe and Asia
- Anguis - slowworms (5 species), native to Europe and Western Asia
Relationships after Lavin & Girman, 2019:[1]
| Anguinae | |
References
[edit]- ^ a b c Lavin, & Girman, D. J. (2019). Phylogenetic relationships and divergence dating in the Glass Lizards (Anguinae). Molecular Phylogenetics and Evolution., 133, 128–140.
- ^ "Anguidae". Animal Diversity Web. Retrieved 2017-05-02.
- ^ Lambertz, Markus; Arenz, Nils; Grommes, Kristina (2018-04-05). "Variability in pulmonary reduction and asymmetry in a serpentiform lizard: The sheltopusik, Pseudopus apodus (Pallas, 1775)". Vertebrate Zoology. 68 (1): 21–26. doi:10.3897/vz.68.e32216. ISSN 2625-8498.
- ^ Glavaš, Olga Jovanović; Počanić, Paula; Lovrić, Vanja; Derežanin, Lorena; Tadić, Zoran; Lisičić, Duje (2020-03-01). "Morphological and ecological divergence in two populations of European glass lizard, Pseudopus apodus (Squamata: Anguidae)". Zoological Research. 41 (2): 172–181. doi:10.24272/j.issn.2095-8137.2020.025. ISSN 2095-8137. PMC 7109015. PMID 32125102.
 | This lizard from family Anguidae article is a stub. You can help Wikipedia by expanding it. |
Anguinae
View on Grokipediafrom Grokipedia
Overview
Etymology and Common Names
The subfamily Anguinae derives its name from the type genus Anguis, which originates from the Latin term anguis meaning "snake," a reference to the elongated, limbless body plan that superficially resembles serpents, though these are lizards within the family Anguidae.[7][8] Members of Anguinae are widely known by common names such as glass lizards and glass snakes, which stem from the distinctive ability of these animals to perform caudal autotomy, where the tail fractures easily at predetermined points, mimicking the brittle shattering of glass.[9] In parts of Europe, particularly for species in the genus Anguis, they are referred to as slow worms, a name tracing back to Old English slāwyrm (slow worm), likely alluding to their sluggish locomotion and worm-like form.[10] Regional linguistic variations further highlight cultural perceptions of these lizards; for instance, Pseudopus apodus is called "sheltopusik" in Eastern Europe, borrowed from the Russian želtopuzik (yellow-bellied), describing the species' pale yellow underside.[11] These informal names emerged alongside formal taxonomic descriptions in the 19th century, as early herpetologists like John Edward Gray documented the family's traits in works establishing Anguidae.General Characteristics
Anguinae is a subfamily within the lizard family Anguidae, comprising limbless or nearly limbless species that exhibit highly elongated bodies adapted to a serpentine form. These lizards are united by their reduction or complete loss of limbs, resulting in a streamlined morphology that facilitates movement through soil or vegetation, while retaining key lizard traits such as osteoderms embedded in the skin for protection.[3] A defining feature of Anguinae is their snakelike appearance combined with distinct lizard characteristics, including external ear openings and movable eyelids, which clearly differentiate them from true snakes in the order Squamata.[12] This combination allows for auditory detection and visual accommodation not found in ophidian reptiles, underscoring their evolutionary position as anguimorph lizards rather than derived serpents.[13] The subfamily's diversity includes about 20 extant species across five genera—Anguis, Dopasia, Hyalosaurus, Ophisaurus, and Pseudopus—with members predominantly occupying terrestrial and fossorial niches in various ecosystems.[14] These habitats reflect their burrowing tendencies and ground-dwelling behaviors, enabling them to exploit microenvironments where limbless locomotion provides an advantage.[3]Taxonomy
Classification History
The subfamily Anguinae was established in the 19th century by John Edward Gray in his 1825 synopsis of reptile genera, where it was recognized as a distinct group within the newly defined family Anguidae based on shared morphological traits such as elongated, limbless bodies and fragile tails among genera like Anguis and Ophisaurus. Initially, Anguinae was grouped closely with other anguids, including forms now placed in Gerrhonotinae, reflecting limited understanding of internal family relationships at the time.[15] Mid-20th-century revisions refined the classification, with McDowell and Bogert (1954) formally proposing four subfamilies within Anguidae—Glyptosaurinae, Gerrhonotinae, Diploglossinae, and Anguinae—based on osteological features like skull structure and osteoderm patterns, solidifying Anguinae's status as a legless clade. However, debates arose, as Hoffstetter (1962) argued for merging Anguinae with Diploglossinae due to similarities in osteoscutes and the absence of a lateral skin fold, questioning the subfamily's distinctiveness in earlier morphological treatments.[15] Meszoely (1970) further reviewed these boundaries in the context of fossil evidence, retaining Anguinae as separate while noting its primitive traits linking it to early anguid evolution.[16] Molecular phylogenetics in the late 1990s and 2000s confirmed the monophyly of Anguinae, with Macey et al. (1999) using mitochondrial and nuclear DNA sequences to resolve relationships among anguids and related families, placing Anguinae as a cohesive clade of legless forms distinct from limbed subfamilies.[17] Wiens and Chippindale (2001) reinforced this through a combined morphological and molecular analysis of body-form evolution, demonstrating multiple independent limb losses but affirming Anguinae's unified evolutionary history within Anguidae.[18] Recent studies, including Lavin and Girman (2019), have further separated Anguinae from Anniellinae using multi-locus nuclear and mitochondrial data, highlighting Anniellinae's fossorial adaptations versus Anguinae's grass-swimming ecomorphology and establishing the former as a North American endemic clade. Current consensus, derived from integrated cladistic and molecular analyses, positions Anguinae as a distinct Northern Hemisphere clade originating in Europe during the Eocene, with subsequent dispersals to Asia and North America.Genera and Species
The subfamily Anguinae includes five extant genera encompassing a total of 20 recognized species, with no new species additions following taxonomic reviews conducted after 2020.[14] The genus Anguis, containing five species, is distributed across Europe and western Asia. Representative species include Anguis fragilis, the common slowworm, native to much of temperate Europe. Species in this genus are distinguished by their smooth dorsal and ventral scales, contributing to a sleek, uniform appearance.[19][20] Dopasia, with seven species, is endemic to eastern Asia, ranging from India through China to Southeast Asia. These lizards exhibit elongated bodies adapted to forested and grassland habitats, though specific scale traits vary minimally across the genus.[21] The monotypic genus Hyalosaurus consists of a single species, Hyalosaurus koellikeri, restricted to North Africa, particularly Morocco and Algeria. This species is notable for its fragile tail, a characteristic shared with other anguines, but lacks unique scale distinctions highlighted in related genera.[22] Ophisaurus comprises six species found in eastern North America and parts of Asia. An example is Ophisaurus ventralis, the eastern glass lizard, occurring in the southeastern United States. Members of this genus feature granular ventral scales, aiding in locomotion over varied substrates.[23][24] Finally, the monotypic Pseudopus includes Pseudopus apodus, the European legless lizard, distributed across southeastern Europe and central Asia. This is the largest species in the subfamily, with robust body scaling intermediate between smooth and granular types.[25]Evolutionary History
Origins and Dispersal
The subfamily Anguinae originated in Europe during the early Eocene, approximately 48.6 million years ago, with the earliest fossil records appearing in multiple localities across the continent, including Belgium, France, and Great Britain.[26] These initial European populations are believed to have descended from North American ancestors within the Anguidae family, which dispersed across the North Atlantic via the Thulean land bridge connecting Greenland and Spitsbergen during the Paleocene to early Eocene, facilitated by warm climatic conditions that maintained the bridge until the mid-Eocene.[27] Phylogenetic analyses support the monophyly of Anguinae and confirm this transatlantic migration as a key event in their early diversification.[28] Subsequent dispersal events shaped the broader distribution of Anguinae. Following their establishment in Europe, the lineage spread eastward into Asia during the early Oligocene, around 33 million years ago, coinciding with the drying of the Turgai Strait, which had previously acted as a marine barrier between Europe and Asia; this event enabled terrestrial connectivity and faunal exchange across Eurasia.[27] Fossil evidence from Turkish localities, such as Kocayarma (dated to MP 23–27, approximately 33–32.2 Ma), documents the presence of early anguines like Ophisaurus in western Asia shortly after this barrier's closure, marking the initial phase of Asian colonization.[27] A later recolonization of North America occurred during the early Miocene, around 20 million years ago, primarily through the Bering Land Bridge, which linked eastern Asia and western North America during periods of lowered sea levels and cooler climates. The earliest North American fossils of Anguinae, including Ophisaurus from Hemingfordian (early Miocene) deposits in the Texas Gulf Coastal Plain, align with this dispersal route from Asian populations. These migrations were driven by major paleoclimatic shifts, including global cooling and the episodic formation of land bridges, which alternately promoted connectivity and isolation. The resulting disjunct distribution— with extant species primarily in Europe and Asia versus a separate North American clade—reflects vicariance processes, such as the uplift of tectonic barriers like the Tibetan Plateau in the late Oligocene to Miocene, which fragmented Eurasian populations and prevented further gene flow.[28]Fossil Record
The fossil record of Anguinae, the subfamily of limbless anguid lizards, provides critical evidence for their evolutionary diversification, with the earliest unambiguous records dating to the Eocene epoch in Europe. Indeterminate Anguimorpha fossils, including those attributable to early anguines, have been recovered from the middle Eocene Messel Pit in Germany, a renowned Lagerstätte preserving exceptionally detailed specimens that reveal primitive limbless morphologies such as elongated vertebral columns and reduced limb girdles. These finds, including the genus Ophisauriscus (e.g., O. quadrupes), demonstrate early adaptations for a serpentine body plan, with osteoderms and trunk vertebrae indicating a transition toward the limbless condition characteristic of modern anguines.[29][30] Subsequent Paleogene and Neogene deposits across Europe and Asia yield more diverse anguine taxa, highlighting their dispersal and radiation. In Europe, Oligocene and Miocene sites in France, Belgium, and Great Britain preserve vertebrae and dentaries of early Ophisaurus and Anguis species, showing progressive elongation of the axial skeleton and loss of functional limbs. Notable among these is Pseudopus pannonicus, the largest known anguine, with abundant fossils from late Miocene to Pliocene localities in Central and Eastern Europe, including over 1,800 specimens from Hungarian sites that exhibit robust skulls and massive osteoderms adapted for burrowing or surface locomotion. A recently described species, Fontisaurus tarumbaire, from the Late Miocene (Vallesian, ~10.3–9.4 Ma) of the Vallès-Penedès Basin in northeastern Spain, represents a new genus with a large articulated skull showing unique parietal features; phylogenetic analyses place it within Anguinae and suggest higher generic diversity in European Neogene anguines, with divergence from sister clades dating to the early Eocene (~50 Ma).[31] In Asia, Paleogene records include Pseudopus-like forms from indeterminate anguine remains in early Eocene to Oligocene sediments, while the first definitive Ophisaurus appears in the Miocene of the Northern Caucasus, supporting an eastward migration via Anatolian land bridges.[32][33][34] North American fossils further illustrate anguine biogeography, with Miocene Ophisaurus remains from disarticulated vertebrae and dentaries in Colorado and Saskatchewan deposits, marking the genus's transatlantic dispersal likely via Beringian routes. These specimens, dating to the late Miocene (e.g., Hemphillian stage), feature smooth osteoderms and recurved teeth akin to modern glass lizards, providing evidence of ecological convergence in grassland habitats. Overall, approximately 10 extinct anguine species have been described from these Cenozoic sites, including Ophisauriscus quadrupes, Ophisaurus fejfari, and Pseudopus pannonicus, offering insights into the subfamilys diversification amid climatic shifts and habitat fragmentation. These fossils underscore early limbless adaptations as key to their survival and spread across Holarctic continents.[3][35]Physical Description
Body Morphology
Members of the subfamily Anguinae display considerable variation in body size, with total lengths ranging from about 30 cm in smaller adult species to over 140 cm in larger species like Pseudopus apodus.[36][37] The tail typically constitutes a significant portion of the overall length, often comprising up to two-thirds or more of the total, which contributes to their serpentine appearance.[38] The scalation of Anguinae is characterized by smooth dorsal scales arranged in longitudinal rows, providing a sleek covering that facilitates movement through vegetation.[39] Ventral scales are arranged transversely and are smaller compared to those of snakes, often numbering in the dozens across the width of the belly.[12] Underlying these scales are osteoderms, thin bony plates embedded in the dermis that reinforce the integument across the head, body, tail, and any vestigial limb regions.[40] Skeletally, Anguinae possess an elongated skull adapted to their limbless or limb-reduced form, with features such as reduced supratemporal arches and specialized dentition varying by genus.[41] Limbs are absent in most genera, but vestigial hindlimbs persist in Hyalosaurus and Pseudopus, consisting of reduced elements like tiny femur and tibia-fibula that do not protrude significantly externally.[42][43][44] The vertebral column is notably flexible, comprising a high number of precaudal and caudal vertebrae—often exceeding 100 in total—which supports the elongated trunk and tail while allowing serpentine locomotion.[45]Adaptations for Limblessness
Anguinae species exhibit several anatomical modifications that compensate for the absence of limbs, enabling effective locomotion, burrowing, and sensory perception in their environments. Their elongated bodies, often exceeding 1 meter in total length in larger species, facilitate serpentine movement and soil penetration, with the integument reinforced by osteoderms—dermal bone plates embedded in the scales—that provide structural rigidity while allowing flexibility.[46] A key adaptation is caudal autotomy, where the tail, comprising up to two-thirds of the total body length, detaches readily at preformed fracture planes to distract predators during escape.[47] This brittle tail structure, enhanced by the osteoderms, can fracture into multiple segments, but regeneration is limited, typically producing a shorter, paler, and less elongated replacement that takes several months to form and offers reduced functionality.[48] Sensory capabilities are well-developed to support foraging and navigation without limbs. The vomeronasal organ, or Jacobson's organ, is highly specialized for chemoreception, with lizards rapidly flicking their forked tongues to collect airborne and substrate-borne chemical cues, which are then transferred to the organ for analysis of prey scents and conspecific signals.[49] Unlike snakes, Anguinae retain functional movable eyelids that protect and lubricate the eyes during surface activity and burrowing, alongside external ear openings that enable auditory detection of vibrations and sounds.[46] Additional structural features support a semifossorial lifestyle. The cranium is reinforced with thickened, fused bony elements and a shortened snout, adaptations that withstand the compressive forces encountered during head-first burrowing into loose soil or leaf litter.[50]Distribution and Habitat
Geographic Range
The subfamily Anguinae displays a disjunct distribution across the Northern Hemisphere, primarily in temperate and subtropical regions, with no recorded presence in South America or Australia.[3] In eastern North America, the genus Ophisaurus predominates, encompassing four species (O. attenuatus, O. compressus, O. mimicus, and O. ventralis) that range from the southeastern United States, including Florida and Georgia, northward to parts of the Midwest and Great Lakes region.[46][49] European and western Asian ranges are occupied by the genera Anguis (five species, such as A. fragilis and A. colchica, extending from western Europe through the Balkans to the Caucasus and Anatolia) and Pseudopus (one species, P. apodus, distributed from southeastern Europe, including the Balkans and Greece, eastward to Iran and central Asia).[51][25][52] The genus Dopasia (seven species, including D. gracilis) is restricted to eastern and southeastern Asia, with occurrences in southern China, northeastern India, northern Myanmar, Thailand, Laos, Vietnam, possibly Bhutan, Indonesia (Borneo and Sumatra), Malaysia (Borneo), and Taiwan.[53][54] In North Africa, the genus Hyalosaurus (one species, H. koellikeri) is endemic to the Maghreb region, specifically Morocco and Algeria, marking the southernmost extent of the subfamily.[55][43] This fragmented pattern spans roughly 50 million km² across the Holarctic realm and the northern fringes of the Afrotropical region, reflecting ancient vicariance events.[3] No major range expansions or contractions have been documented since 2000, though local extirpations persist in habitat fragments due to agricultural intensification and urbanization, particularly in European populations of Anguis.[51]Habitat Preferences
Anguinae species exhibit a broad range of habitat preferences, primarily favoring temperate to subtropical environments that provide ample cover and suitable substrates for their limbless locomotion. Common habitats include grasslands, forests, and scrublands, where loose soil and vegetation facilitate burrowing and concealment. These lizards are predominantly fossorial, often inhabiting areas with friable soils that allow them to tunnel for shelter and thermoregulation.[3] Microhabitats within these areas are critical for Anguinae survival, with individuals frequently found under leaf litter, rocks, logs, or in compost heaps, which offer protection from predators and maintain necessary humidity levels. They are humidity-dependent, thriving in moist conditions and generally avoiding arid extremes that could desiccate their fragile bodies; for instance, activity peaks on cool, humid days in shrub-dominated landscapes. These preferences align with their limbless adaptations for burrowing, enabling efficient navigation through dense, cluttered substrates.[56][57][58] Habitat variations occur across genera and regions, reflecting local ecological niches. In the temperate meadows and woodland edges of Europe, Anguis species, such as the common slow worm (Anguis fragilis), prefer dense vegetation in hedgerows, heathlands, and even urban gardens for basking and foraging cover. Conversely, North American Ophisaurus lizards, like the slender glass lizard (Ophisaurus attenuatus), favor sandy pine barrens and open grasslands in the southeastern United States, where pine flatwoods and dry, open woodlands provide ideal loose substrates for fossorial life. Dopasia taxa in Southeast Asia extend into forested agricultural areas at elevations up to approximately 1,600 meters, utilizing forest floors and understories for cover and foraging in humid, vegetated zones.[59][49][60][61]Behavior and Ecology
Locomotion and Foraging
Anguinae lizards, being limbless, utilize a variety of serpentine locomotion modes adapted to their terrestrial and semi-fossorial lifestyles, including lateral undulation, slide-pushing, and concertina movement. Lateral undulation, the most common mode on open or rough ground surfaces, involves propagating waves along the body to generate propulsion through lateral contact points, enabling maximum speeds of up to 0.55 m/s for the center of gravity in species like Ophisaurus apodus.[62] Slide-pushing occurs on smoother substrates at moderate speeds around 0.13 m/s, relying on friction from body bends and tail swings for forward thrust.[62] Concertina locomotion, characterized by alternating extension and contraction of body loops, is employed in confined spaces like burrows or narrow channels, but at slower rates of approximately 0.03 m/s.[62] These locomotion strategies facilitate foraging as ambush predators, where individuals often remain stationary or move slowly to detect and strike at prey, though some active searching occurs in open habitats.[49] Their diet consists primarily of invertebrates such as insects (e.g., grasshoppers, larvae), snails, slugs, earthworms, and millipedes, supplemented occasionally by small vertebrates like lizards, eggs, or nestling birds in species like Ophisaurus attenuatus.[63][49] Prey detection relies on chemosensory adaptations, including frequent tongue flicking to sample airborne or substrate odors via the vomeronasal organ, allowing precise location of hidden or slow-moving targets like earthworms in soil.[36] Activity patterns in Anguinae vary from diurnal to crepuscular, with individuals most active during mild daytime hours for basking and foraging, shifting to nocturnal behavior in hotter conditions to avoid overheating.[49] In colder climates, they exhibit seasonal torpor or hibernation, retreating underground from late fall to early spring to conserve energy, emerging in warmer months when prey availability increases.[36]Reproduction and Life History
Members of the Anguinae subfamily exhibit varied reproductive strategies, with some species being viviparous or ovoviviparous, producing live young after internal development, while others are oviparous, laying eggs that the female may guard until hatching.[64] For instance, the slow worm (Anguis fragilis) is viviparous, with females giving birth to litters typically ranging from 5 to 12 neonates, though sizes up to 20 have been recorded in some populations.[65][66] Breeding is generally seasonal, occurring in spring, with mating from mid-March to mid-May and births in late summer (August to September) following a gestation period of 8 to 12 weeks.[65][66] In contrast, species like the slender glass lizard (Ophisaurus attenuatus) are oviparous, laying clutches of 5 to 17 eggs in June or July after spring mating, with females attending the nest site until hatching in late summer.[49][67] Sexual maturity is typically reached at 2 to 4 years of age, depending on species and environmental conditions; for example, female A. fragilis mature between 2 and 3 years at a snout-vent length of 135 to 150 mm, while O. attenuatus individuals attain maturity at 3 to 4 years.[65][49] Lifespans vary widely, ranging from 10 to 30 years in the wild, with some species achieving greater longevity in captivity; A. fragilis averages 20 to 30 years in nature and up to 54 years in captivity, whereas O. attenuatus lives about 10 years but can reach 30 years.[36][68] Growth rates differ among species, often slower in Anguis due to their temperate habitats and biennial reproductive cycles in some populations, compared to faster growth in more arid-adapted forms like Pseudopus apodus, which matures at 2 to 3 years.[65][69] Parental care is minimal across Anguinae, limited to egg attendance in oviparous species until hatching, with no post-birth or post-hatching investment; neonates are fully independent upon emergence or birth, dispersing immediately to forage on their own.[64][49] This independence aligns with their limbless, fossorial lifestyles, where early autonomy enhances survival in fragmented habitats.[65]Defense and Predation
Anguinae species face predation from a variety of vertebrates, including birds of prey such as hawks, mammals like foxes and badgers, and snakes.[38][70] Their limbless body form increases vulnerability compared to limbed lizards, as it limits escape options like climbing or rapid maneuvers, forcing reliance on passive and active defenses.[71] The primary defense mechanism in Anguinae is caudal autotomy, where the tail—often comprising over half the total body length—detaches easily when grasped by a predator, sometimes shattering into multiple wriggling segments to distract the attacker and facilitate escape.[38][71] This fragile tail structure, composed of specialized vertebrae and muscles, regenerates over months but remains shorter and less functional than the original.[36] Additional tactics include thanatosis, or death-feigning, observed in species like Anguis graeca, where individuals enter tonic immobility, inverting their body and remaining motionless for minutes to mimic a dead carcass and deter further interest from predators.[72] Camouflage provided by their scalation and cryptic coloration, such as uniform brown or greenish patterns that blend with grassy or leafy substrates, further aids in evasion by allowing individuals to remain undetected.[49] Predation exerts significant pressure on Anguinae populations, particularly juveniles, which are smaller and more conspicuous to smaller predators like birds and lizards, leading to high mortality rates that shape recruitment and overall dynamics.[73] For instance, in Anguis species, juvenile survivorship is reduced by avian and reptilian attacks, influencing age structure and density in local populations.[74]Conservation Status
Major Threats
Anguinae species face several anthropogenic and environmental pressures that contribute to population declines across their ranges. Habitat loss and degradation, primarily driven by agricultural expansion and urbanization, represent the most pervasive threats. In Europe, populations of the slow worm (Anguis fragilis) have experienced significant declines due to the conversion of grasslands and forested edges into farmland and built environments, with urban development disrupting essential refugia for these fossorial lizards.[36] Similarly, logging and land conversion affect species like the European glass lizard (Pseudopus apodus) in parts of its Eurasian range, reducing available moist, vegetated habitats critical for thermoregulation and foraging.[75] Road mortality exacerbates habitat fragmentation, posing a direct lethal risk to mobile individuals during dispersal or foraging. For A. fragilis, vehicle collisions on rural and suburban roads contribute to localized population reductions, particularly in fragmented landscapes where barriers limit connectivity between habitat patches.[76] In addition, there is some illegal collection for the exotic pet trade targeting larger species such as P. apodus, though the extent of this pressure is unknown. Climate change introduces further vulnerabilities, especially for fossorial Anguinae reliant on stable soil moisture. Drying trends and increased aridity in parts of Asia and North Africa, linked to shifting precipitation patterns, threaten species by altering underground microhabitats and exacerbating habitat desiccation. For instance, the Moroccan glass lizard (Hyalosaurus koellikeri) in northwestern Africa is impacted by desertification processes that degrade forested and semi-arid zones through reduced rainfall and soil erosion.[77] Species in Asia, such as those in the genus Dopasia, face similar habitat-related threats but are assessed as Least Concern globally.[78] Overall, all Anguinae taxa are assessed as Least Concern by the IUCN as of 2025, reflecting their relatively wide distributions, but localized declines underscore the need for threat mitigation.[79][25][55]Protection and Management
Species within the Anguinae subfamily, primarily glass lizards (Ophisaurus spp.) in North America and slow-worms (Anguis fragilis) in Europe, receive varying levels of protection depending on regional legislation and conservation priorities, often focusing on habitat preservation amid threats like development and habitat fragmentation.[80] In the United States, the mimic glass lizard (Ophisaurus mimicus) faces imminent extinction risk from habitat loss in longleaf pine ecosystems, predation, road mortality, and climate change impacts on fire regimes, prompting a petition for Endangered Species Act listing filed on October 15, 2025, by the Center for Biological Diversity to enhance federal protections and forest management.[81] The slender glass lizard (Ophisaurus attenuatus), while globally secure, is state-endangered in Wisconsin, where management includes habitat avoidance during development, population surveys, and monitoring as a Species of Greatest Conservation Need under the Wisconsin Wildlife Action Plan.[82] Translocation has been employed as a mitigation strategy for Anguinae species encountering development threats; for instance, slow-worms (Anguis fragilis) in the UK have been successfully relocated to suitable habitats to minimize population impacts from construction.[83] In the UK, slow-worms are legally protected under the Wildlife and Countryside Act 1981 against intentional killing, injury, or commercial trade, with management recommendations emphasizing the creation of refuges like log piles and scrubby grasslands, alongside non-toxic pest control to reduce secondary poisoning risks from domestic cats and introduced predators.[84][73] Broader efforts for Anguinae conservation prioritize restoring fire-maintained habitats, such as longleaf pine-wiregrass systems in the southeastern US, to support population persistence on public and private lands.[85]References
- https://en.wiktionary.org/wiki/Anguinae
- https://en.wiktionary.org/wiki/slowworm
- https://en.wiktionary.org/wiki/sheltopusik