Vipera aspis

Vipera aspis
Scientific classification
Kingdom: Animalia Phylum: Chordata Subphylum: Vertebrata Class: Reptilia Order: Squamata Suborder: Serpentes Family: Viperidae Subfamily: Viperinae Genus: Vipera Species: V. aspis
Binomial name
Vipera aspis (Linnaeus, 1758)
Synonyms
[Coluber] Aspis - Linnaeus, 1758 Vipera Mosis Charas - Laurenti, 1768 Vipera vulgaris - Latreille In Sonnini & Latreille, 1801 Vipera ocellata - Latreille In Sonnini & Latreille, 1801 Coluber Charasii - Shaw, 1802 [Vipera (Echidna)] Aspis - Merrem, 1820 C[hersea]. vulgaris - Fleming, 1822 Vipera aspis - Metaxa, 1823 Aspis ocellata - Fitzinger, 1826 [Pelias] Col[uber]. aspis - F. Boie, 1827 Berus Vulgaris - Gray, 1831 Vipera aspis var. ocellata - Bonaparte, 1834 Vipera aspis var. ocellata - Massalongo, 1853 V[ipera]. (Vipera) aspis - Jan, 1863 Vipera berus subspec. aspis - Camerano, 1888 Vipera aspis - Boulenger, 1896 Vipera aspis var. lineata - Düringen, 1897 [Vipera aspis] var. Delalande - Phisalix, 1902 Vipera aspis aspis - Mertens, 1925 Mesovipera aspis - Reuss, 1927 Mesovipera maculata - Reuss, 1930 (nomen nudum) Mesovipera maculata aspis - Reuss, 1930 (nomen nudum) Vipera ammodytes aspis - Schwarz, 1936 Vipera aspis delalande - Phisalix, 1968 Vipera (Rhinaspis) aspis aspis - Obst, 1983 Vipera aspis - Golay et al., 1993

Common names: asp, asp viper, European asp, aspic viper.

Vipera aspis is a venomous viper species found in southwestern Europe. Five subspecies are currently recognized, including the typical form described here.

Description

Grows to an average length of 60-65 cm. Males reach a maximum of 85 cm, females rarely more than 75 cm. Males, however, are a little slimmer than females. The tail is very short: one-seventh to one-ninth of total body length in females, and one-sixth to one-eighth in males.

The head is broad, triangular and quite distinct from the neck. The tip of the snout is slightly but distinctly upturned. The rostral scale is generally higher than it is wide, touching 2 to 3 scales on the upper side of the snout. Dorsally, the snout is flat with distinct and slightly raised sharp margins. The nasal scale is single (hardly ever divided) and separated from the rostral by a single nasorostral scale. The crown is covered with numerous small and irregular scales of different sizes that are mostly smooth, but sometimes slightly keeled. Frontal and parietal scales are usually not present, but if so, they are small and irregularly shaped, with the frontal separated from the supraoculars by 2 scale rows. The supraocular scales are large and distinct, separated by 4-7 scale rows. There are 10-12 (rarely 8-18) small circumorbital scales below the supraocular. The eye is separated from the supralabials by 2 (rarely 3) scale rows. The vertical diameter of the eye is about the same as the distance between the eye and the mouth. There are 9-13 supralabials. The 4th-5th supralabials (rarely 4th-6th or 5th-6th) are separated from the eye by 2 (rarely 3) rows of small scales, but sometimes there is a single scale between the 4th supralabial and the eye. Generally, the temporal scales are smooth, but sometimes slightly keeled.

Midbody, there are 21-23 (rarely 19 or 25) rows of dorsal scales. These are strongly keeled, except for the outermost rows that vary and are sometimes smooth. There are 134-170 ventral scales. Subspecies V. a. aspis averages fewer than 150 ventrals, while V. a. atra averages more. The anal scale is single. Males have 32-49 subcaudals, females 30-43. The subcaudal scales are paired.

The dorsal markings vary strongly, but only rarely take the form of a clear zigzag, as in V. berus.

Geographic range

France, Andorra, northeastern Spain, extreme southwestern Germany, Switzerland, Monaco, the islands of Elba and Montecristo, Sicily, Italy, San Marino and northwestern Slovenia. The original type locality was listed simply as "Gallia." However, Schwarz (1936) proposed that it be restricted to "Poitou [Frankreich]" (Poitou, France).

In August-October of 2006, a number of specimens were discovered in a wooded area near the town of Portugaal in the Netherlands (south of Rotterdam). Although they were doing quite well, the species is not native in this country. It is likely that one or more escaped or were set loose in the area.

Conservation status

This species is classified as Least Concern (LC) according to the IUCN Red List of Threatened Species (v3.1, 2001). So listed due to its wide distribution, tolerance of a broad range of habitats, presumed large population, and because it is unlikely to be declining fast enough to qualify for listing in a more threatened category.

However, subspecies V. a. aspis is categorized as Critically Endangered in Switzerland, V. a. atra is categorized as Vulnerable, and V. a. francisciredi is categorized as Endangered (Monney and Meyer, 2005).

In general, the species is also listed as protected (Appendix III) under the Berne Convention.

Habitat

This species has a few clearly defined and relatively specific habitat requirements. It needs warm areas that are exposed to the sun, structured vegetation and comparatively dry soils. In Italy and France, it is often found in areas with low mountains or hills, notably in limestone regions, but sometimes occurs in lower plains. It has a preference for vegetated areas or environments with at least some cover. Here it can be found on sunny slopes, on scrublands, in glades, in mountain meadows, forest clearings, at the borders of woods, in rubbish dumps and in stone quarries. In Italy, it occurs in mesic chestnut/oak woodlands and often near streams. Although it is not really associated with high altitudes, in the Pyrenees it it has been found at well over 2,100 m above sea level.

Venom

A bite from this species can be more severe than from V. berus and is very painful. According to Stemmler (1971), about 4% of all untreated bites are fatal. Lombardi and Bianco (1974) mention that this species is responsible for 90% of all cases of snakebite in Italy.

The toxicity of the venom varies. Stemmler (1971) states that the population in Passwang district, Switzerland have the strongest venom. Compared to venoms from other species, it is relatively toxic. Brown (1973) gives LD₅₀ values of 1.0 mg/kg IV and 1.0-2.0 mg/kg SC. Tu et al. (1969) reports 4.7 mg/kg IM. Venom yield is relatively low. Boquet (1964) reported a daily extraction figure of 9-10 mg.

Envenomation symptoms include rapidly spreading acute pain, followed by edema and discoloration. Severe haemorrhagic necrosis may occur within a few hours. Vision may be severely impaired, most likely due to degradation of blood and blood vessels in the eyes. The venom has both coagulant and anticoagulant effects. Anticoagulant activity is apparently stronger than that of Daboia russelii. The venom may also affect glomerular structure, which can lead to death due to renal failure.

According to Cheymol et al. (1973), the venom does not affect neuromuscular contractions in in vitro preparations. Lack of this neurotoxic affect would indicate that fatal cases involving the cardiovascular system are the result of direct muscle injury or reduced oxygen exchange. On the other hand, Gonzalez (1991) reported that in two cases the victims developed neurotoxic symptoms, including difficulty in breathing and swallowing, as well as paralysis of the bitten limbs.

Subspecies

Subspecies	Authority	Geographic range
V. a. aspis	(Linnaeus, 1758)	Found in most of France, except those areas bordering the English Channel. On the Atlantic coast, it is found in Île de Ré and Oléron, but not south of the Gironde estuary. Mostly absent east of the Moselle River and from much of the Mediterranean region, but does occur near Montpellier and in Alpes-Maritimes. A disjunct subpopulation exists in the Pyrenees, notably in Spain southwest of Bilbao. In Germany it occurs in the southern Black Forest along the Swiss border, bus is rare in this area. It is common northwestern Italy and western Switzerland.
V. a. atra	Meisner, 1820	Parts of Switzerland.
V. a. francisciredi	Laurenti, 1768	Central Italy.
V. a. hugyi	Schinz, 1833	The south of Italy.
V. a. zinnikeri	Kramer, 1958	Gascony, Andorra and nearby Spain.

See also

• Vipera.
• List of viperine species and subspecies.
• True vipers - Common names.
• True vipers - Synonymy.
• Snakebite.

Other references

• Boquet P. 1964. Venins de serpentes. Part I: Physio-pathologie de l'envenimation et properties biologiques des venins. Topxicon2:4-41.
• Cheymol J, Boquet P, Detrait J, Roch-Arveller M. 1973. Comparaison des principales proprietes pharmacologiques de differents venins d'Echis carinatus. Arch Int Pharmaco 205:293-304.
• Gonzalez D. 1991. Snakebite problems in Europe. In: Tu AT, editor. Handbook of Natural Toxins. New York: Marcel Dekker. pp 687-751.
• Guillemin I, Bouchiert C, Garrigues T, Wisner A, Choumet V. 2003. Sequences and structural organization of phosphilopase A2 genes from Vipera aspis aspis, V. aspis zinnikeri and Vipera berus berus venom. Eur. J. Biochem. 270:2697-2706. PDF at FEBS Journal. Accessed 9 October 2006.
• Monney JC, Meyer A. 2005. Rote Liste der gefährdeten Reptilien der Schweiz. Hrsg. Bundesamt für Umwelt, Wald und Landschaft BUWAL, Bern und Koordinationsstelle für Amphibien- und Reptilienschutz der Schweiz, Bern. BUWAL-Reihe. 50 pp.
• Stemmler O. 1971. Die Reptilien der Schweiz mit besonderer Berucksichtigung der Basler Region. Veroff Nat Mus Basel, Number 5.
• Tu AT, Homma M, Hong B. 1969. Hemorrhagic, myonecrotic, thrombotic and proteolytic activities of viper venoms. Toxicon 6:175-8.

External links

• Species Vipera aspis at the Species2000 Database
• Vipera aspis at Amphibians and Reptiles of Europe. Accessed 9 October 2006.
• Vipera aspis at Club100. Accessed 9 October 2006.
• Asp viper, Vipera aspis at Reptiles & Amphibians of France. Accessed 30 October 2006.