The Aesculapian snake // (now Zamenis longissimus, previously Elaphe longissima), is a species of nonvenomous snake native to Europe, a member of the Colubrinae subfamily 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.
|Adult Z. longissimus from the region of Ticino, Switzerland.|
Z. 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 (including tail), but can grow to 200 cm (79 in), with the record size being 225 cm (7.38 ft). It is dark, long, slender, and typically bronzy in color, 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 Aesculapian snakes 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 4th to 5th upper labial scales.
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 color, 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 coloration. Melanistic, erythristic, and albinotic natural forms are known, as is a dark grey form.
Although there is no noticeable sexual dimorphism in coloration, 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.
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). 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. 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.
The previously recognized 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. 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.
Escaped populations in Great BritainEdit
There are three populations of Aesculapian snake which derive from escapes in Great Britain. The oldest recorded of these is in the grounds and vicinity of the Welsh Mountain Zoo near Conwy in North Wales. This population had persisted and reproduced since at least the early 1970s. A second, more recent population was reported in 2010 to be along the Regent's Canal near London Zoo, living on rats and thought to number a few dozen, limited by the scarcity of egg-laying sites. It is suspected this colony may have been there some years, undetected. It is not a harmful invasive species, and the population was thought likely to become extinct. In 2020, a third population was confirmed in Britain being present in Bridgend, Wales. This population has persisted for approximately 20 or so years.
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 their range they are 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, they generally do not avoid human presence, being often found in places such as gardens and sheds, and even prefer 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 they are dependent on human structures for food, warmth and hatching grounds. They avoid open plains and agricultural deserts.
In the south their 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 their line of presence appears temperature-limited.
Diet and predatorsEdit
Their main food source are rodents up to the size of rats (a 130 cm adult specimen has been reported to have overpowered a 200g rat) and other small mammals such as shrews and moles. They also eat birds as well as bird eggs and nestlings. They suffocate their 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 only found rarely in adult prey.
Predators include badgers and other mustelids, foxes, wild boar (mainly by digging up and decimating hatches and newborns), hedgehogs, and various birds of prey (though there are reports of adults successfully standing their ground against feathered attackers). Juveniles may be eaten by smooth snakes and other reptilivorous snakes. Also a threat mainly to juveniles and hatches are domestic animals such as cats, dogs, and chickens, and even rats may be dangerous to inactive adult specimens in hibernation. In areas of concurrent distribution, they are also preyed upon by introduced North American raccoons and east Asian raccoon dogs.
The snakes are active by day. In the warmer months of the year, they come out in late afternoon or early morning. They are very good climbers capable of ascending even vertical, branchless tree trunks. The snakes have been observed at heights of 4–5 m and even 15–20 m in trees, and foraging in the roofs of buildings. Observed optimum temperature for activity in German populations is 20-22 °C (Heimes 1988) and they are rarely recorded below 16 °C or above 25 °C, other observations for Ukrainian populations (Ščerbak et Ščerban 1980) put minimum activity temperature from 19 °C and optimum to 21-26 °C. Above around 27 °C they try to avoid exposure to direct sunlight and cease activity with more extreme heat. The snakes will exhibit a degree of activity even during hibernation, moving around to keep a body temperature near 5 °C and occasionally emerging to bask on sunny days.
The average home range for French populations has been calculated at 1.14ha, however males will travel longer distances of up to 2 km to find females during the mating season and females to find suitable hatching sites to lay eggs.
The Aesculapian snakes are deemed secretive and not always easy to find even in areas of positive presence, or found in surprising contexts. In contact with humans, they can be rather tame, possibly due to their cryptic coloration keeping them hidden within their natural environment. They usually disappear and hide, but if cornered they may sometimes stand their ground and try to intimidate their opponent, sometimes with a chewing-like movement of the mouth and occasionally biting.
It has been speculated that the species may be actually more prevalent than thought due to spending a significant part of its time in tree canopy, however 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 the 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.
Minimum length of individuals entering the reproductive cycle has been reported at 85–100 cm, 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 jaw (Lotze 1975). 4 to 6 weeks after 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.
Apart from the recent taxonomic changes, there are currently four recognized phylogeographically traceable genetic lines in the species: the Western haplotype, Adriatic haplotype, the Danube haplotype and Eastern haplotype.
The status of the Iranian enclave population remains unclear due to its specific morphological characteristics (smaller length, scale arrangement, darker underbelly), probably pending reclassification.
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 "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 equivalents 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.
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.
The snake has been classified as Critically Endangered in the German Red List of endangered species. In most other countries including France, Switzerland, Austria, the Czech Republic, Slovakia, Hungary, Bulgaria, Poland, Ukraine and Russia it is also under protection status.
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.
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.
- IUCN Red List of Threatened Species
- "Zamenis longissimus ". The Reptile Database. www.reptile-database.org.
- Edgar P, Bird DR (2006). "Action Plan for the Conservation of the Aesculapian Snake (Zamenis longissimus) in Europe". Strasbourg: Council of Europe: Convention on the Conservation of European Wildlife and Natural Habitats. Standing Committee, 26th meeting, 27–30 November 2006.
- "Aesculapian snake, Zamenis longissimus at Reptiles & Amphibiens de France".
- Musilová R (2011). "Ekologie a status užovky stromové (Zamenis longissimus) v severozápadních Čechách [Ecology and Status of the Aesculapian Snake (Zamenis longissimus) in northwest Bohemia]" (in Czech and English). Dissertation. Prague: Czech University of Life Sciences Prague.
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- Hvass, Hans (1970). Danmarks Dyreverden, vol 5. Copenhagen: Rosenkilde og Bakker. pp. 223–228.
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- Press Office (16 May 2006). "Wild snake caught on film in north Wales". BBC.
- JOSH LOEB (2 September 2010). ""The Camden Creature" - An amphibian and reptile trust says our waterways are alive with some exotic creatures". Islington Tribune. Archived from the original on 12 February 2015.
- Clemens, David. J.; Allain, Steven J. R. (2020). "New records of Aesculapian snakes (Zamenis longissimus) in South Wales, UK". Herpetological Bulletin. 152: 30–31. doi:10.33256/152.3031. Subscription required
- Baruš V, Oliva O; et al. (1992). Fauna ČSFR - Plazi (Fauna of ČSFR - Reptiles) (in Czech). Prague: Academia.
- Wagler, J. (1830). Natürliches System der Amphibien : mit vorangehender Classification der Säugethiere und Vögel : ein Beitrag zur vergleichenden Zoologie. (Zamenis, new genus, p. 188). Available online at the Biodiversity Heritage Library (BHL).
- This page uses translations from respective articles in German, French, Russian and Polish Wikipedias.
- Arnold EN, Burton JA (1978). A Field Guide to the Reptiles and Amphibians of Britain and Europe. London: Collins. 272 pp. + Plates 1-40. ISBN 0-00-219318-3. (Elaphe longissima, pp. 199–200 + Plate 36 + Map 112 on p. 266).
- Boulenger GA (1894). Catalogue of the Snakes in the British Museum (Natural History). Volume II., Containing the Conclusion of the Colubridæ Aglyphæ. London: Trustees of the British Museum (Natural History). (Taylor and Francis, printers). xi + 382 pp. + Plates I-XX. (Coluber longissimus, pp. 52–54).
- Laurenti JN (1768). Specimen medicum, exhibens synopsin reptilium emendatam cum experimentis circa venena et antidota reptilium austricorum. Vienna: "Joan. Thom. Nob. de Trattnern". 214 pp. + Plates I-V. (Natrix longissima, new species, p. 74). (in Latin).