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Aesculapian snake
Aesculapian snake
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Aesculapian snake
Adult Zamenis longissimus from the region of Ticino, Switzerland
Scientific classification Edit this classification
Kingdom: Animalia
Phylum: Chordata
Class: Reptilia
Order: Squamata
Suborder: Serpentes
Family: Colubridae
Genus: Zamenis
Species:
Z. longissimus
Binomial name
Zamenis longissimus
(Laurenti, 1768)
Synonyms[2]

The Aesculapian snake /ˌɛskjəˈlpiən/ (Zamenis longissimus, previously Elaphe longissima) is a species of non-venomous constrictor snake native to Europe, a member of the subfamily Colubrinae of the family Colubridae. Growing up to 2 metres (6.6 ft) in length, it is among the largest European snakes, similar in size to the four-lined snake (Elaphe quatuorlineata) and the Montpellier snake (Malpolon monspessulanus). The Aesculapian snake has been of cultural and historical significance for its role in ancient Greek, Roman, and Illyrian mythology and derived symbolism.

Description

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snake with a regular dark and light pattern along its body, getting darker towards the tail, partly coiled on a rocky surface
Juvenile with distinctive coloration

Zamenis longissimus hatches at around 30 cm (11.8 in). Adults are usually from 110 cm (43.3 in) to 160 cm (63 in) in total length (tail included), but can grow to 200 cm (79 in), with the record size being 225 cm (7.38 ft).[3] Expected body mass in adult Aesculapian snakes is from 350 to 890 g (0.77 to 1.96 lb).[4][5] It is dark, long, slender, and typically bronzy in colour, with smooth scales that give it a metallic sheen.

Juveniles can easily be confused with juvenile grass snakes (Natrix natrix) and barred grass snakes (Natrix helvetica), because juvenile Aesculapians also have a yellow collar on the neck that may persist for some time in younger adults. Juvenile Z. longissimus are light green or brownish-green with various darker patterns along the flanks and on the back. Two darker patches appear in the form of lines running on the top of the flanks. The head in juveniles also features several distinctive dark spots, one hoof-like on the back of the head in-between the yellow neck stripes, and two paired ones, with one horizontal stripe running from the eye and connecting to the neck marks, and one short vertical stripe connecting the eye with the fourth to fifth upper labial scales.

front portion of a snake on a soil border by a wall; the snake is olive-coloured above and yellow below
Lightly coloured adult

Adults are much more uniform, sometimes being olive-yellow, brownish-green, sometimes almost black. Often in adults, there may be a more or less regular pattern of white-edged dorsal scales appearing as white freckles all over the body up to moiré-like structures in places, enhancing the shiny metallic appearance. Sometimes, especially when pale in colour, two darker longitudinal lines along the flanks can be visible. The belly is plain yellow to off-white, while the round iris has amber to ochre colouration. Melanistic, erythristic, and albinotic natural forms are known, as is a dark grey form.

Although there is no noticeable sexual dimorphism in colouration, males grow significantly longer than females, presumably because of the more significant energy input of the latter into the reproductive cycle. Maximum weight for German populations has been 890 grams (1.96 lb) for males and 550 grams (1.21 lb) for females (Böhme 1993; Gomille 2002). Other distinctions, as in many snakes, include in males a relatively longer tail to total body length and a wider tail base.

Scale arrangement includes 23 dorsal scale rows at midbody (rarely 19 or 21), 211–250 ventral scales, a divided anal scale, and 60–91 paired subcaudal scales (Schultz 1996; Arnold 2002). Ventral scales are sharply angled where the underside meets the side of the body, which enhances the species' climbing ability.

Lifespan is estimated at 25 to 30 years.[3][6][7]

Geographic range

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Respective approximate European ranges of Aesculapian snake (green) and Italian Aesculapian snake (blue)

The contiguous area of the previous nominotypical subspecies, Zamenis longissimus longissimus, which is now the only recognized monotypic form, covers most of France except in the north (up to about the latitude of Paris), the Spanish Pyrenees and the eastern side of the Spanish northern coast, Italy (except the south and Sicily), all of the Balkan peninsula down to Greece and Asia Minor and parts of Central and Eastern Europe up until about the 49th parallel in the eastern part of the range (Switzerland, Austria, South Moravia (Podyjí/Thayatal in Austria) in the Czech Republic, Hungary, Slovakia, south Poland (mainly Bieszczady/Bukovec Mountains in Slovakia), Romania, south-west Ukraine).

Further isolated populations have been identified in western Germany (Schlangenbad, Odenwald, lower Salzach, plus one - near Passau - connected to the contiguous distribution area) and the northwest of the Czech Republic (near Karlovy Vary, the northernmost known current natural presence of the species).[6] Also found in a separate enclave south of Greater Caucasus along the Russian, Georgian and Turkish northeastern and eastern shores of the Black Sea.

Two further enclaves include the first around Lake Urmia in northern Iran, and on the northern slopes of Mount Ararat in east Turkey, roughly halfway between the former and the Black Sea habitats.[3] V.L. Laughlin hypothesized that parts of the species' geographical distribution may be the result of intentional placement and later release of these snakes by Romans from the temples of Asclepius, classical god of medicine, where they were important in the medical rituals and worship of the god.[8][9]

The previously recognised subspecies Zamenis longissimus romanus, found in southern Italy and Sicily, has been recently elevated to the status of a separate new species, Zamenis lineatus (Italian Aesculapian snake). It is lighter in color, with a reddish-orange to glowing red iris.

The populations previously classified as Elaphe longissima living in south-east Azerbaijan and northern Iranian Hyrcanian forests were reclassified by Nilson and Andrén in 1984 to Elaphe persica, now Zamenis persicus.

According to fossil evidence, the species' area in the warmer Atlantic period (around 8000–5000 years ago) of Holocene reached as far north as Denmark. Three specimens were collected in Denmark between 1810 and 1863 on the southern part of Zealand, presumably from a relict and now extinct population.[10] The current northwestern Czech population now is considered an autochthonous remnant of that maximum distribution based on the results of genetic analyses (it is closest genetically to the Carpathian populations). This likely applies also to the German populations. There are also fossils showing that they had UK residency during earlier interglacial periods but were driven south afterwards with subsequent glacials; these repeated climate-caused contractions and extensions of range in Europe appear to have occurred multiple times over the Pleistocene.[11]

Escaped populations in Great Britain

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There are three populations of Aesculapian snake, descendants of escapees, in Great Britain. The oldest recorded of these is on the grounds and in the vicinity of the Welsh Mountain Zoo, near Colwyn Bay, North Wales. This population has survived and consistently reproduced since at least the early 1970s,[12] and, in 2022, the population was estimated at 70 adults.[13]

A second, more recently established population was reported in 2010 along Regent's Canal, near the London Zoo, likely living on rats and mice, and thought to number a few dozen. Growth of this population may be limited due to the urban setting and potential scarcity of appropriate nesting sites. It is thought this colony has been present for years, living unseen: it is not harmful or invasive and is predicted to die out.[14] Sightings were still being reported in 2023, with the population estimated at around 40.[15]

In 2020, a third population was confirmed in Britain, this one in Bridgend, Wales. This group has thrived for approximately 20 years.[16]

As of 2022, the Aesculapian snake is believed to be the only non-native species of snake in the United Kingdom to have established breeding populations.[17]

Habitat

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In a cherry tree in Mödling, Lower Austria

The Aesculapian snake prefers forested, warm but not hot, moderately humid but not wet, hilly or rocky habitats with proper insolation and varied, not sparse vegetation that provides sufficient variation in local microclimates, helping the reptile with thermoregulation. In most of its range it is typically found in relatively intact or fairly cultivated warmer temperate broadleaf forests including the more humid variety such as along river valleys and riverbeds (but not marshes) and forest steppes. Frequented locations include places such as forest clearings in succession, shrublands at the edges of forests and forest/field ecotones, woods interspersed with meadows etc. However, it generally does not avoid human presence, being often found in places such as gardens and sheds, and even prefers habitats such as old walls and stonewalls, derelict buildings and ruins that offer a variety of hiding and basking places. The synanthropic aspect appears to be more pronounced in northernmost parts of the range where it is dependent on human structures for food, warmth and hatching grounds. It avoids open plains and agricultural deserts.

In the south its range seems to coincide with the borderline between deciduous broadleaf forests and Mediterranean shrublands, with the latter presumably too dry for the species. In the north its line of presence appears temperature-limited.[3][7]

Diet and predators

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Swallowing a small mammal

The main food source of Zamenis longissimus is small mammals such as shrews, moles, and rodents up to the size of rats. A 130 cm (51 in) adult specimen has been reported to have overpowered a 200 g (7.1 oz) rat. It also eats birds as well as bird eggs and nestlings. It suffocates its prey by constriction, though harmless smaller mouthfuls may be eaten alive without constriction, or simply crushed on eating by jaws. Juveniles mainly eat lizards and arthropods, later small rodents. Other snakes and lizards are taken, but adults are rarely taken.

Predators include badgers and other mustelids, foxes, wild boar (mainly by digging up and eating egg clutches and hatchlings), hedgehogs, and various birds of prey (though there are reports of adults successfully standing their ground). Juveniles may be eaten by smooth snakes and other reptilivorous snakes. Domestic animals such as cats, dogs, and chickens are a threat mainly to juveniles and hatchlings; rats may be dangerous to inactive adults in hibernation. In areas of concurrent distribution, the snake is also preyed upon by introduced North American raccoons and east Asian raccoon dogs.[3][6][7][18]

Behaviour

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Zamenis longissimus is active by day (diurnal). In the warmer months of the year, it comes out in late afternoon or early morning. It is a very good climber capable of ascending even vertical, branchless tree trunks. It has been observed at heights of 4 to 5 m (13 to 16 ft) and even 15 to 20 m (49 to 66 ft) in trees, and foraging in the roofs of buildings. Observed optimum temperature for activity in German populations is 20–22 °C (68–72 °F) (Heems 1988) and it is rarely recorded below 16 °C (61 °F) or above 25 °C (77 °F), other observations for Ukrainian populations (Skarbek et Ščerban 1980) put minimum activity temperature from 19 °C (66 °F) and optimum to 21–26 °C (70–79 °F). Above around 27 °C (81 °F) it tries to avoid exposure to direct sunlight and ceases activity with more extreme heat. It will exhibit a degree of activity even during hibernation, moving around to keep a body temperature near 5 °C (41 °F) and occasionally emerging to bask on sunny days.

The average home range for French populations has been calculated at 1.14 ha (2.8 acres), however males will travel longer distances of up to 2 km (1.2 mi) to find females during the mating season and females to find suitable hatching sites to lay eggs.

The Aesculapian snake is deemed secretive and not always easy to find even in areas of positive presence, or found in surprising contexts.[3][6][7][18] In contact with humans, it can be rather tame, possibly due to its cryptic coloration keeping it hidden within its natural environment. It usually disappears and hides, but if cornered it may sometimes stand its ground and try to intimidate its opponent, sometimes with a chewing-like movement of the mouth and occasionally biting.[6]

It has been speculated that the species may be more prevalent than thought due to spending a significant part of its time in tree canopy, but no reliable data exist as to what part that would be. In France it is said to be the only snake species that occurs inside dense, shadowy forests with minimum undergrowth, presumably because of using foliage for basking and foraging. In other parts of its geographic range it has been reported to only use the canopy on a more substantial basis in largely uninhabited areas, such as the natural beech forests of the East Slovak and Ukrainian Carpathians, with similar characteristics.[3][7]

Reproduction

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Minimum length of individuals of Zamenis longissimus entering the reproductive cycle has been reported at 85–100 cm (33–39 in), which corresponds to sexual maturity age of about 4–6 years. Breeding occurs annually after hibernation in spring, typically from mid-May to mid-June. In this time the snakes actively seek each other and mating begins. Rival males engage in ritual fights the aim of which is to pin down the opponent's head with one's own or coils of one's body; biting may occur but is not typical. The actual courtship takes the form of an elegant dance between the male and female, with anterior portions of the bodies raised in an S-shape and the tails entwined. The male may also grasp the female's head with its jaws (Lotze 1975). 4 to 6 weeks after mating, about 10 eggs are laid (extremes are from 2 to 20, with 5–11 on average) in a moist, warm spot where organic decomposition occurs, usually under hay piles, in rotting wood piles, heaps of manure or leaf mold, old tree stumps and similar places. Particularly in the northern parts of the range, preferred hatching grounds often are used by multiple females and are also shared with grass snakes. The eggs incubate for around 8 (6 to 10) weeks before hatching.[3][6]

Taxonomy

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Apart from recent taxonomic changes, there are currently four recognised phylogeographically traceable genetic lines in the species Zamenis longissimus: the Western haplotype, the Adriatic haplotype, the Danube haplotype, and the Eastern haplotype.

The status of the Iranian enclave population remains unclear due to its specific morphological characteristics (smaller length, different scale arrangement, darker underbelly), probably pending reclassification.[18]

History

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Asclepius/Aesculapius with rod and snake

The Aesculapian snake was first described by Josephus Nicolaus Laurenti in 1768 as Natrix longissima, later it was also known as Coluber longissimus and for the most part of its history as Elaphe longissima. The current scientific name of the species based on revisions of the large genus Elaphe is Zamenis longissimus. Zamenis is from Greek ζαμενής[19] "angry", "irritable", "fierce", longissimus comes from Latin and means "longest"; the snake is one of the longest over its range. The common name of the species, Aesculape in French and its equivalent in other languages, refers to the classical god of healing (Greek Asclepius and later Roman Aesculapius) whose temples the snake was encouraged around. It is surmised that the typical depiction of the god with his snake-entwined staff features the species. Later from these, modern symbols developed of the medical professions as used in a number of variations today. The species, along with four-lined snakes, is carried in an annual religious procession in Cocullo in central Italy, which is of separate origin and was later made part of the Catholic calendar.

Conservation

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Though the Aesculapian snake occupies a relatively broad range and is not endangered as a species, it is thought to be in general decline largely due to anthropic disturbances. The snake is especially vulnerable in fringe parts and northern areas of its distribution where, given the historic retreat as a result of climatic changes since the Holocene climatic optimum, local populations remain isolated both from each other and from the main distribution centers, with no exchange of genetic material and no reinforcement through migration as a result. In such areas active local protection is due. [citation needed]

The snake has been classified as Critically Endangered in the German Red List of endangered species.[citation needed] In most other countries including France, Switzerland, Austria, the Czech Republic, Slovakia, Hungary, Bulgaria, Poland, Ukraine and Russia it is also under protection status.[citation needed]

Among the key concerns is human-caused habitat destruction, with a series of respective recommendations concerning forestry and agriculture as to the protection through non-intervention of the species' core distribution centers, including targeted protection of potential hatching and hibernation places like old growth zones and fringe ecotones near woodland areas.[citation needed]

A significant threat also are roads both in terms of new construction and rising traffic, with a risk of further fragmentation of populations and loss of genetic exchange.[3]

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See also

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References

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Further reading

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Revisions and contributorsEdit on WikipediaRead on Wikipedia
from Grokipedia
The Aesculapian snake (Zamenis longissimus) is a large, non-venomous colubrid snake native to southern and , characterized by its slender, elongated body that can reach up to 2 meters in length, smooth scales with a metallic or olive-brown sheen, and a small head with round pupils. Named after , the Greek god of medicine, due to its resemblance to the serpent entwined on his staff, it inhabits a range from northwestern and eastward to northwestern and the , with fragmented populations extending to northern limits in , , and the where it has been introduced. Juveniles display darker, mottled patterns that fade to a uniform coloration in adults, aiding in forested environments. This species prefers warm, sunny habitats such as broadleaf woodlands, river valleys, shrublands, and rocky areas, often near human settlements where it exploits structures for shelter and hunting. It is partly arboreal, frequently climbing trees and bushes, and exhibits diurnal activity, basking in to regulate its body temperature as an . The diet primarily consists of small mammals like , birds and their eggs, and , which it subdues through rather than . Reproduction is oviparous, with females laying 4–10 eggs in summer that hatch after about two months, and sexual maturity is reached at 4–5 years. Despite its wide distribution, the Aesculapian snake faces localized threats including , road mortality, and persecution due to misidentification with venomous species, though its overall population remains stable. Classified as Least Concern by the IUCN, it benefits from adaptability to human-modified landscapes but requires conservation efforts in northern disjunct populations to preserve . Notable for its role in ecosystems as a predator and its cultural symbolism in , the continues to be studied for insights into thermophilous across .

Taxonomy and identification

Taxonomy

The Aesculapian snake is classified as Zamenis longissimus (Laurenti, 1768), a within the Colubridae and subfamily Colubrinae. It was originally described as Coluber longissimus and later placed in the Elaphe as Elaphe longissima, a that persisted until 2002 when molecular phylogenetic analyses revived the genus Zamenis to reflect monophyletic groupings among Old World ratsnakes. The Zamenis currently includes six , distinguished from closely related genera such as Elaphe (true ratsnakes) and Hierophis (whip snakes) through genetic markers and subtle morphological differences, including vertebral scale row counts and hemipenial morphology that align Zamenis in a distinct within Colubrinae. Phylogenetically, Z. longissimus belongs to the western Palearctic radiation of colubrids, with studies revealing deep divergences among populations that trace back to Pleistocene refugia. Fossil evidence, including subfossil remains from , indicates the species' presence since the Middle Pleistocene, approximately 500,000 years ago, supporting its role as a of warmer periods during glacial cycles. Phylogeographic analyses further show post-glacial expansion from Balkan and Italian refugia during the Pleistocene-Holocene transition around 11,700 years ago, with limited leading to regional genetic lineages. Current taxonomy recognizes Z. longissimus as monotypic, with no valid , though historical proposals based on geographic variation in scalation and coloration (such as darker dorsal patterns in southern populations) have not been upheld by recent genetic data.

Physical description

The Aesculapian snake (Zamenis longissimus) is a medium to large colubrid with a relatively slender, cylindrical body and a long, tapering tail that comprises 20–25% of its total length. Adults typically measure 1.4–1.6 m in total length, though individuals in can reach up to 2.25 m, while northern populations rarely exceed 1.8 m. Juveniles hatch at lengths of 12–37 cm. The dorsal scales are smooth on the anterior third of the body and lightly keeled on the posterior two-thirds, arranged in 23 rows at mid-body (rarely 21 or 19), with 211–250 ventral scales, a divided anal scale, and 60–91 paired subcaudal scales. The head is long and slender, only slightly distinct from the , featuring a moderate-sized eye with a round pupil and iris. There are typically 8 supralabials, of which the 4th and 5th contact the eye, along with a single preocular and a series of small subocular scales. The ventral scales are sharply angled, aiding in locomotion. Coloration in adults is fairly uniform, ranging from grey-brown and yellow-brown to dorsally, often with the anterior third lighter and white-edged scales that may form faint bands; the upper labials are , with two yellow patches on the head, and the ventral surface is yellow to whitish, sometimes with grey spots. Juveniles exhibit brighter coloration with 4–7 rows of brown spots or crossbars, more distinct yellow head markings, and dark postocular stripes. Rare color variants include melanistic, erythristic, and albino forms, as well as the dark subgrisea morphotype found in and on the island of , . Sexual dimorphism is evident in size, with males growing significantly longer and more slender than females, though no notable differences in coloration occur; males also possess hemipenes. Regional variations include a tendency toward more yellowish hues in southern populations, which may align with subspecies distinctions in coloration.

Distribution and habitat

Geographic range

The Aesculapian snake (Zamenis longissimus) is native to central and , with its range spanning from northwestern and northern in the west to southwestern , , and the in the east. The southern limit extends through , , and , while the northern boundary reaches isolated populations in , , and the . Additional native occurrences are documented in , , , , , , , , , , , and . The species' range also includes parts of western , such as northern , the region (Georgia, ), , and northwestern . Post-glacial recolonization shaped the current distribution, with the species expanding northward from refugia in the and (or possibly Iberia for the western clade) following the . During the approximately 5,000–8,000 years ago, populations reached farther north into , including historical presence in , though these northern groups later went extinct due to cooling climates. Subfossil evidence supports a broader mid-Holocene range, with relic populations persisting today in fragmented northern habitats. Introduced populations have established outside the native range, primarily from escaped or released pets. In Great Britain, feral groups persist in , (originating in the 1960s near the zoo), in (from the 1970s), and in Dorset. Small, localized introduced populations also occur in the . Population densities vary across the range, with higher concentrations in Mediterranean core areas compared to sparser distributions at northern periphery sites, where individuals may number only a few dozen in total for isolated groups. and pose ongoing threats, restricting natural northward expansion and isolating peripheral populations.

Habitat preferences

The Aesculapian snake (Zamenis longissimus) primarily inhabits woodlands, forest edges, and riverine areas, where it favors environments with a mix of open clearings and dense vegetation for shelter and movement. It also occupies abandoned ruins, stone walls, and farmlands, particularly those with shrubs and hedgerows that support its semi-arboreal lifestyle, allowing it to climb trees and bushes for and refuge. These preferences align with its physical adaptations, such as a slender body and smooth scales, which facilitate navigation in vegetated and elevated microhabitats. Within these habitats, the snake selects microhabitats that provide moist, sunny spots for basking to regulate body , often near water bodies like river valleys to maintain levels essential for its ectothermic . Ground cover such as leaf litter, grassy edges, and stone structures offers hiding places from predators and suitable conditions for , with studies showing a strong association with ecotones—transitional zones between forests and open areas—where 98% of observations occur within 10 meters of such edges. Anthropogenic features like heaps and buildings are frequently used for shelter, especially in northern populations facing constraints. The species occurs from up to 2,000 meters in mountainous regions, thriving in warm, moderately humid conditions but avoiding dense coniferous forests in favor of open broadleaf woodlands. Seasonally, it shifts toward more arboreal habits in summer to access cooler, shaded perches in trees and shrubs, while becoming predominantly ground-dwelling during cooler months for overwintering in burrows or man-made structures. This flexibility extends to human-modified landscapes, including orchards and vineyards, where it tolerates fragmented habitats as long as edge structures and sunny exposures persist, contributing to its persistence in altered environments.

Ecology and behavior

Diet and foraging

The Aesculapian snake (Zamenis longissimus) is an opportunistic carnivore with a diet dominated by small vertebrates. Primary prey consists of small mammals, particularly rodents such as mice (Apodemus spp.), voles (Microtus spp.), and rats, as well as shrews (Sorex spp.) and moles; adults have been documented consuming rodents up to the size of rats. Secondary prey includes birds and their eggs or nestlings, lizards (such as lacertids like Podarcis muralis), and occasionally amphibians or invertebrates. Juveniles, measuring 27.5–67.5 cm in length, primarily target smaller items like lizards and invertebrates (e.g., beetles and earthworms), transitioning to larger vertebrates as they grow. As a non-venomous constrictor, the Aesculapian snake employs a hunting strategy involving strikes followed by coiling around prey to suffocate it through . It is predominantly diurnal, active during warmer periods when temperatures range from 16–25°C, and relies on a combination of visual cues and chemical detection via its to locate prey. Excellent climbing abilities enable it to forage arboreally in canopies or on structures to access birds and eggs, while on the ground it targets terrestrial mammals. Prey size correlates positively with the snake's body mass, and adults can ingest items nearly as wide as their head through jaw flexibility, where the mandibles disarticulate at the to accommodate larger meals. Feeding occurs opportunistically from early April to early November, with no significant seasonal variation in prey composition observed across studies; small mammals remain predominant year-round during the active season. Ecologically, the species plays a key trophic role in controlling populations, particularly in agricultural areas where it helps regulate pest species like voles and mice, providing economic benefits to farmers.

Predators and defenses

The Aesculapian snake (Zamenis longissimus) faces predation primarily from such as buzzards and hawks, as well as corvids like and ravens, which target both adults and juveniles in open or forested habitats. Mammalian predators include foxes, badgers, wild boars, and small mustelids such as stoats, with wild boars particularly noted for disturbing nests and preying on eggs or newborns. In some regions, larger snakes like the western whip snake (Hierophis viridiflavus) or (Coronella austriaca) occasionally prey on adults. Juveniles are especially vulnerable to a broader array of small carnivores, including hedgehogs, rats, and domestic cats, as well as , due to their smaller size and less developed defenses. Road mortality represents a significant anthropogenic threat to juveniles, as busy roadways fragment habitats and increase encounters with vehicles during dispersal. To counter these threats, the Aesculapian snake employs several anti-predator strategies, including rapid into trees or vegetation to evade ground-based pursuers, leveraging its arboreal . When threatened, individuals may release a foul-smelling cloacal to deter attackers, a form of known as musking. Other behaviors include tail vibration to mimic a rattlesnake's warning or distract predators from the head, hissing, bluff strikes, and thanatosis—feigning death by lying motionless with the mouth agape—sometimes accompanied by (self-inflicted bleeding from the ) to appear unpalatable. If captured, the snake may resort to mild as a last resort. Camouflage plays a key role in avoidance, with the snake's olive-green to brown coloration and keeled scales allowing it to blend seamlessly into foliage, leaf litter, or tree bark. Human-related predation often stems from persecution, as the snake is frequently misidentified as a venomous viper and killed on sight in rural areas.

Daily and seasonal behavior

The Aesculapian snake (Zamenis longissimus) is primarily diurnal, emerging from shelters in the morning to bask and thermoregulate, with activity peaking from late morning through the afternoon. Observations indicate that snakes become active between 0800 and 0900 hours and remain so until 1800–1900 hours during warmer months, though they may shift to crepuscular or nocturnal patterns in extreme heat. Thermoregulatory behaviors, such as basking on rocks or vegetation, dominate early daily activity to achieve optimal body temperatures. As semi-arboreal , Aesculapian snakes frequently climb trees and shrubs up to 10 meters high for , escape, or resting, leveraging their slender build and . Home ranges typically span 5–20 hectares, varying by quality and sex, with males exhibiting greater mobility and longer dispersal distances than females during the active season. Individuals maintain fidelity to core areas but show seasonal shifts, with most movements occurring within 100 meters of refuges. Seasonally, activity intensifies from through , coinciding with warmer temperatures and prey availability, before declining in autumn as snakes prepare for brumation. Brumation occurs from October to March in underground burrows, rock crevices, or tree hollows, where snakes maintain a low level of activity to regulate body temperature around 5°C and may briefly on mild, sunny days. is triggered by temperatures exceeding 10°C, often in late March or early depending on regional climate. Aesculapian snakes are solitary outside of brief mating interactions, showing no evidence of territorial aggression or group formations. Activity decreases during rainy or overcast conditions, with snakes retreating to shelters to avoid excessive moisture and maintain thermal balance; conversely, warmer years may enhance dispersal and overall mobility.

Reproduction and life cycle

Mating and breeding

The mating season of the Aesculapian snake (Zamenis longissimus) occurs annually after , typically from mid-May to mid-June, coinciding with peaks in seasonal activity. During this period, males actively search for receptive females, often traveling distances up to 2 km, guided by chemical cues including pheromones released by females to signal readiness. Courtship involves ritualized behaviors between males competing for access to females, including displays where rivals raise their anterior bodies in an S-shape, intertwine tails, and attempt to push or pin down the opponent's head through twisting and shoving motions. The victorious male then engages in with the female, grasping her neck and aligning bodies for copulation, which lasts 10–45 minutes. Oviposition follows 4–6 weeks after , with females laying clutches of 5–11 elongated eggs in late or , typically in warm, moist microhabitats such as rotting wood, heaps, piles, or leaf litter where provides suitable incubation temperatures. Clutch size positively correlates with female body size, ranging from 6–12 eggs in observed populations, with an average of about 9. Larger females produce relatively larger clutches, reflecting a in reproductive . Eggs are soft-shelled and , often laid communally in favored sites. There is no extended ; females may coil briefly around the clutch immediately after laying but abandon the eggs soon thereafter, leaving them to develop independently through external incubation. is reached at a snout-vent length of approximately 85–100 cm, corresponding to an age of 4–6 years, though smaller individuals below 85 cm for females and 74 cm for males typically do not reproduce. Annual breeding occurs in about 77–82% of adult females.

Development and growth

The eggs of the Aesculapian snake (Zamenis longissimus) undergo incubation for approximately 6–10 weeks, typically at temperatures between 25–30°C, with occurring in late to early September. Upon hatching, juveniles measure 20–30 cm in total length and exhibit brighter, more patterned coloration compared to adults, featuring longitudinal rows of spots that aid in . These hatchlings are fully independent from birth, dispersing immediately from the nest site without . Juveniles experience rapid growth during their first year, potentially reaching up to 50 cm in as they establish patterns and avoid threats. Growth slows after , which is attained at 4–6 years of age when individuals reach 74–85 cm, depending on sex. In , lifespan averages 20–30 years, though individuals in captivity can exceed this with proper care. The first (skin shedding) occurs 1–2 weeks post-hatching, often coinciding with the onset of feeding. Juvenile mortality is notably high, estimated at 50–70%, primarily due to predation by mammals, birds, and other snakes, as well as during the initial dispersal phase. The employs an iteroparous life history , with adults capable of annual breeding after reaching maturity, contributing to population persistence despite early-life vulnerabilities.

Conservation and human relations

Conservation status

The Aesculapian snake (Zamenis longissimus) is classified as Least Concern on the global and European , with assessments indicating a wide distribution and no major threats across its core range. This status was established in the 2009 reptile assessment and reaffirmed in regional evaluations, reflecting stable populations in Mediterranean habitats. However, at northern range edges, the faces heightened risks, with classifications as severely endangered in and critically endangered in isolated Czech populations due to limited suitable habitats. Key threats include from agricultural expansion and , which isolate populations and reduce foraging areas. Illegal collection for the pet trade, particularly of juveniles, further pressures small groups, while mortality is significant near human infrastructure, with studies documenting elevated death rates along busy roads. may disrupt cycles by altering winter temperatures and , potentially affecting emergence timing and survival in marginal northern areas, though direct impacts remain under study. Population trends are stable in the core Mediterranean range, supported by broad habitat availability, but declining in northern isolates, where small groups—estimated in the low hundreds across sites like Germany's Neckar Valley—face risks from stochastic events. These peripheral populations, relics of post-glacial distributions, exhibit low and vulnerability to habitat loss. The is protected under Annex IV of the EU , requiring strict measures against capture or harm across member states. National protections apply in countries such as and , where it is listed as a protected wild species with bans on exploitation. The 2005 European outlines habitat restoration and monitoring priorities. In the , introduced populations in and are monitored to assess ecological impacts and potential persistence amid . As of 2025, UK authorities are evaluating the species' non-native status, with research suggesting climate change may enable naturalization of introduced populations. Monitoring relies on radio-tracking to map movements and site fidelity in fragmented landscapes, revealing preferences for woodland edges and human-modified areas. initiatives, such as reporting apps, contribute to population estimates and threat identification in .

Interactions with humans

The Aesculapian snake (Zamenis longissimus) derives its common name from Aesculapius, the Roman god of medicine and healing, reflecting its prominent role in ancient Greco-Roman mythology as a symbol of renewal and therapeutic power. In these traditions, the snake entwined around Aesculapius's staff—known as the —represents the shedding of skin as a for rebirth and the restoration of health, influencing enduring medical iconography. Fossil evidence indicates the species was present in Britain during prehistoric warmer interglacial periods, but it became extinct there long before human settlement, with current UK populations resulting from 19th–20th century introductions. In medieval European folklore, particularly drawing from classical sources like Pliny the Elder, Aesculapian snakes were viewed as beneficial household guardians that detected and eradicated pests, earning a reputation as natural healers or controllers of vermin in agrarian communities. In contemporary contexts, the Aesculapian snake is often misperceived as venomous in rural areas of its range, resulting in deliberate killings by humans despite its harmless nature. Conversely, it enjoys popularity among reptile enthusiasts in , where it is kept as a ; trade and possession are legal within the but subject to strict regulations under the Bern Convention and national wildlife laws to prevent . The trade, while boosting awareness, contributes to localized collection pressures on wild populations. Economically, the snake provides indirect benefits to through its predation on , reducing crop damage without the need for chemical interventions, though unfounded myths persist regarding attacks on , which exceed its dietary preferences for small mammals and birds. Introduced populations in the trace their origins to 19th-century imports for zoological collections and medicinal displays, with escapes from facilities like establishing self-sustaining colonies along the and in since the mid-20th century. These groups, numbering in the dozens, are actively monitored by authorities to assess ecological risks and contain spread, reflecting broader efforts to balance human-facilitated introductions with native protection.

References

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