Russell's Viper (Daboia russelii) is one of several species in the genus Daboia, which includes one or two North African species (mauritanica, deserti) formery included in Macrovipera, the Levantine D. palaestinae (formerly Vipera palaestinae), and the South Asian (Daboia russelii), which reaches the Middle East only peripherally in Pakistan. Daboia is characterized by a raised numbers of body scales. (Stümpel and Joger 2009 and references therein)
According to Leviton et al. (2003), Russell's Viper (Daboia russelii) occurs in Myanmar (Ayeyarwady, Bago, Magway, Mandalay, Sagaing , and Yangon Divisions and Shan State), as well as southern China, Taiwan, India, Pakistan, Sri Lanka, Bangladesh, Thailand, and Indonesia (Java east to Lomblen Island [=Lembata]). This species has not been recorded from Malaysia or Sumatra.. It primarily inhabits lowland areas. Thorpe et al. (2007) studied the phylogeography of Russell's Viper (using a combination of mitochondrial genetic data, morphometrics, and color pattern) and concluded that two distinct species should be recognized: D. russelii throughout South Asia, west of the Bay of Bengal, and D. siamensis in Southeast Asia, east of the Bay of Bengal.
In Myanmar, Russell's Vipers are common throughout the central dry zone and Ayeyarwady (= Irrawaddy) Delta, where they are often encountered in agricultural areas and paddies as well as in open grasslands. These snakes are active at night.
This may be the most common of the dangerously venomous snakes in southern Asia, where it accounts for more than half of all reported snakebites. Hiremath et al. (2014) note that Russell's Viper is one of the four snake species long believed to account for the large majority of snakebite cases in India, often known as "the Big Four"--the other three species being another viper, Saw-scaled Viper (Echis carinatus), and two elapids, Indian Cobra (Naja naja) and Common Krait (Bungarus caeruleus) (with bites from other dangerously venomous snakes such as King Cobra, Ophiophagus hannah, being relatively rare). Hiremath et al. compare the impacts of the venoms of these four types of snakes on blood coagulation. (Note, however, that Simpson et al  have argued that the "Big Four" concept has resulted in significantly misdirected epidemiological and treatment efforts, e.g., through the misdiagnosis of envenomations actually attributable to the Hump-nosed Pit Viper (Hypnale hypnale). Hung et al. (2002) reviewed Russel's Viper snakebites in Taiwan and noted that symptoms appear to differ from those reported from some other parts of Asia.
Several color pattern variants have been recognized as subspecies: D. r. siamensis from southern China, central and southern Myanmar, and central Thailand; D. r. formosensis from eastern China and Taiwan; and the nominate form from India, Pakistan, and Bangladesh. Its unusual distribution (eespecially its erratic distribution in Indonesia) suggests that it has been moved over long distances in the course of commercial exchange, likely during the 18th and 19th centuries. Russell’s Viper is a prolific breeder and young could plausibly have been moved along with plants or other goods in the early days of colonial expansion.
Although this species was named in honor of Patrick Russell, the original description used just one “l” in the specific epithet, which Leviton et al. (2003) therefore consider to be the correct spelling. Mallow et al. (2003) provide additional information on this species.
(Leviton et al. 2003 and references therein)
Tun-Pe et al. (1995) studied the properties of the venom of Russell’s Vipers of varying ages.
Kavitha et al. (2014a) reported on the presence of Sparganum cestode larvae parasitizing two Russell's Vipers in southern India. Kavitha et al. (2014b) reported the presence of Kalicephalus hookworms (Nematoda: Diaphanocephalidae) in the stomach and intestine of a captive Russell's Viper.
Patel and Tank (2014) describe both the typical body coloration, as well as that of a rare whitish color morph.
Leviton et al. (2003) provide a technical description of Russell's Viper: No sensory pit between nostril and eye. Head very distinct from neck, above covered by small, keeled, imbricate scales, 6-9 between narrow supraoculars; nostril large, in large nasal shield which, below is fused to the rostral; eye, with vertically elliptic pupil, is surrounded by 10-15 small scales, 3-4 rows of small scales separating the circumocular scales from the upper labials; temporals small; 10-12 upper labials; 27-33 longitudinal rows of scales at midbody, all except outermost row strongly keeled; ventrals 153-180; subcaudals 41-64, all paired; color above light brown with three longitudinal series of large black-margined brown spots or blotches, the vertebral series often merging to form a chain-like longitudinal strip, occasionally an additional longitudinal series of small dark spots between the vertebral and lateral series. Yellowish white below occasionally with dark brown markings. Total length to 1600 mm not uncommon.
- Patel, H. and S.K. Tank. 2014. Cases of unusual colour morph in Russell’s Viper Daboia russelii (Shaw & Nodder, 1797) from Gujarat, India. Reptile Rap #16: 27-30.
- Kularatne, S.A.M., A. Silva, K. Weerakoon, et al. 2014. Revisiting Russell’s Viper (Daboia russelii) Bite in Sri Lanka: Is Abdominal Pain an Early Feature of Systemic Envenoming? PLoS ONE 9(2): e90198. doi:10.1371/journal.pone.0090198
- Leviton, A.E., G.O.U. Wogan, M.S. Koo, G.R. Zug, R.S. Lucas, and J.V. Vindum. 2003. The dangerously venomous snakes of Myanmar: illustrated checklist with keys. Proceedings of the California Academy of Sciences 54(24): 407-462.
- Hiremath, V., M. Yariswamy, et al. 2014. Differential action of Indian BIG FOUR snake venom toxins on blood coagulation.Toxin Reviews 33 (1-2): 23-32.
- Hung, D.-Z., M.-L. Wu, et al. 2002. Russell’s viper snakebite in Taiwan: differences from other Asian countries. Toxicon 40: 1291-1298.
- Kavitha, K.T., B.R. Latha, et al. 2014a. Sparganosis in Russell’s viper snake: a case report. J Parasit. Dis. 38(4): 394-395.
- Kavitha, K.T., B.R. Latha, et al. 2014b. Kalicephalus sp. in a captive Russell’s viper: a case report. J Parasit. Dis. 38(3) :293–296.
- Mallow, D., D. Ludwig, and G. Nilson. 2003. The Vipers: Natural History & Toxicology of Old World Vipers. Kreiger Publishing Co. Malabar, Florida. 259 pp.
- Simpson, I.D. and R.L. Norris. 2007. Snakes of Medical Importance in India: Is the Concept of the ‘‘Big 4’’ Still Relevant and Useful? Wilderness and Environmental Medicine 18: 2-9.
- Stümpel, N. and U. Joger. 2009. Recent advances in phylogeny and taxonomy of Near and Middle Eastern Vipers – an update. ZooKeys 31: 179–191. doi: 10.3897/zookeys.31.138
- Thorpe, R.S., C.E. Pook, and A. Malhotra. 2007. Phylogeography of the Russell’s viper (Daboia russelii) complex in relation to variation in the colour pattern and symptoms of envenoming. Herpetol J 17: 209–18.
- Tun-Pe, Nu-Nu-Lwin, Aye-Aye-Myint, et al. .1995. Biochemical and biological properties of the venom from Russell’s Viper (Daboia russelli siamensis ) of different ages. Toxicon 33(6): 817-821.
Daboia is a monotypic genus of venomous Old World viper. The single species, D. russelii (Russel's viper) is found in Asia throughout the Indian subcontinent, much of Southeast Asia, southern China and Taiwan. The species was named in honor of Patrick Russell (1726–1805), a Scottish herpetologist who first described many of India's snakes; and the name of the genus is from the Hindi word meaning "that lies hid," or "the lurker." Daboia russelii is one of the "big four" snakes responsible for causing the most snakebite incidents and deaths in South Asia (mostly India). They have a wide distribution and occur frequently in highly-populated areas. Two subspecies are currently recognized, D. r. siamensis and D. r. russelii.
(Modified from Wikipedia 2013)
Distribution: Pakistan, India (Punjab Himachal Pradesh, Maharashtra, Uttar Pradesh, Bihar, Northern Bengal), Sri Lanka (elevation up to 1500 m), Bangladesh, Indonesia (Java, Komodo, Flores, Lomblen, Endeh), Myanmar (= Burma), Thailand, Cambodia, Vietnam, Laos China (Kwangtung), Taiwan siamensis: China (Kwantung), Myanmar (= Burma), Indonesia (E Java, Komodo, Flores, Lomblen, Endeh), Thailand, Taiwan, Cambodia (fide WELCH 1994)
Type locality: Coromandel Coast [India]
Life History and Behavior
Lifespan, longevity, and ageing
Molecular Biology and Genetics
Statistics of barcoding coverage: Vipera russelli
Public Records: 0
Specimens with Barcodes: 1
Species With Barcodes: 1
Statistics of barcoding coverage: Vipera russelli russelli
Public Records: 0
Specimens with Barcodes: 2
Species With Barcodes: 1
Daboia is a monotypic genus of venomous Old World viper. The single species, D. russelii, is found in Asia throughout the Indian subcontinent, much of Southeast Asia, southern China and Taiwan. The species was named in honor of Patrick Russell (1726–1805), a Scottish herpetologist who first described many of India's snakes; and the name of the genus is from the Hindi word meaning "that lies hid", or "the lurker." Apart from being a member of the big four snakes in India, Daboia is also one of the species responsible for causing the most snakebite incidents and deaths among all venomous snakes on account of many factors, such as their wide distribution, generally aggressive demeanor, and frequent occurrence in highly populated areas.
This snake can grow to a maximum total length (body + tail) of 166 cm (5.5 ft) and averages about 120 cm (4 ft) on mainland Asian populations, although island populations do not attain this size. It is more slenderly built than most other vipers. Ditmars (1937) reported the following dimensions for a "fair sized adult specimen":
|Total length||4 ft., 1 inch||124 cm|
|Length of tail||7 inches||18 cm|
|Girth||6 inches||15 cm|
|Width of head||2 inches||5 cm|
|Length of head||2 inches||5 cm|
The head is flattened, triangular and distinct from the neck. The snout is blunt, rounded and raised. The nostrils are large, each in the middle of a large, single nasal scale. The lower edge of the nasal touches the nasorostral. The supranasal has a strong crescent shape and separates the nasal from the nasorostral anteriorly. The rostral is as broad as it is high.
The crown of the head is covered with irregular, strongly fragmented scales. The supraocular scales are narrow, single, and separated by 6–9 scales across the head. The eyes are large, flecked with yellow or gold, and each is surrounded by 10–15 circumorbital scales. There are 10–12 supralabials, the 4th and 5th of which are significantly larger. The eye is separated from the supralabials by 3–4 rows of suboculars. There are two pairs of chin shields, the front pair of which is notably enlarged. The two maxillary bones support at least two and at the most five or six pairs of fangs at a time: the first are active and the rest replacements. The fangs attain a length of 16.5 mm (0.65 in) in the average specimen.
The body is stout, the cross-section of which is rounded to circular. The dorsal scales are strongly keeled; only the lowest row is smooth. Mid-body, the dorsal scales number 27–33. The ventral scales number 153–180. The anal plate is not divided. The tail is short — about 14% of the total length — with the paired subcaudals numbering 41–68.
Dorsally, the color pattern consists of a deep yellow, tan, or brown ground color, with three series of dark brown spots that run the length of the body. Each of these spots has a black ring around it, the outer border of which is intensified with a rim of white or yellow. The dorsal spots, which usually number 23–30, may grow together, while the side spots may break apart. The head has a pair of distinct dark patches, one on each temple, together with a pinkish, salmon, or brownish V or X marking that forms an apex towards the snout. Behind the eye, there is a dark streak, outlined in white, pink, or buff. The venter is white, whitish, yellowish or pinkish, often with an irregular scattering of dark spots.
In English, common names of Daboia include Russell's viper, chain viper, Indian Russell's viper, common Russell's viper, seven pacer, chain snake, and scissors snake. Previously, another common name was used to described a subspecies that is now part of the synonymy of this form: Sri Lankan Russell's viper for D. r. pulchella.
In South Asia, it is known as daboia (दबौया) in Hindi, Punjabi, and Urdu; bora, chandra bora, or uloo bora in Bengali; chitalo or khadchitalo in Gujarati; kolakumandala or mandaladha haavu (ಮಂಡಲದ ಹಾವು) in Kannada; gunas on Kashmiri; raktamandali,chenathandan, vattakoora, rakta anali, or thavitta (അണലി) in Malayalam; ghonas (घोणस, घोण्या), Tawarya in Marathi; chandan boda in Oriya; koraile in Sindhi; thith polonga (තිත් පොලඟා) in Sinhala; retha aunali or kannadi viriyan (கண்ணாடி விரியன்) in Tamil; కాటుక రేకుల పాము (katuka rekula paamu). or రక్తపింజర (raktha penjara/penjari) in Telugu; and pili kandhodi in Tulu.
D. russelii is found in India, Pakistan, Sri Lanka, Bangladesh, Nepal, Myanmar, Thailand, Cambodia, China (Guangxi, Guangdong), Taiwan and Indonesia (Endeh, Flores, east Java, Komodo, Lomblen Islands). The type locality is listed as "India". More specifically, this would be the Coromandel Coast, by inference of Russell (1796).
Brown (1973) mentions that it can also found in Vietnam, Laos and on the Indonesian island of Sumatra. Ditmars (1937) reportedly received a specimen from Sumatra as well. However, the distribution of this species in the Indonesian archipelago is still being elucidated.
Within its range it can be very common in some areas, but scarce in others. In India, is abundant in Punjab, very common along the West Coast and its hills, in southern India and up to Bengal. It is uncommon to rare in the Ganges valley, northern Bengal and Assam. It is prevalent in Myanmar.
It is not restricted to any particular habitat, but does tend to avoid dense forests. The snake is mostly found in open, grassy or bushy areas, but may also be found in second growth forests (scrub jungles), on forested plantations and farmland. It is most common in plains, coastal lowlands and hills of suitable habitat. Generally not found at altitude, but has been reported as far up as 2300–3000 m (7,500-9,800 ft). Humid environments, such as marshes, swamps, and rain forests, are avoided.
This species is often found in highly urbanized areas and settlements in the countryside, the attraction being the rodents commensal with man. As a result, those working outside in these areas are most at risk of being bitten. It should be noted, however, that D. russelii does not associate as closely with human habitation as Naja and Bungarus (cobras and kraits).
Adults are reported to be slow and sluggish unless pushed beyond a certain limit, after which they can become very aggressive. Juveniles, on the other hand, are generally more nervous.
When threatened they form a series of S-loops, raise the first third of the body and produce a hiss that is supposedly louder than that of any other snake. When striking from this position, they can exert so much force that even a large individual can lift most of its body off the ground in the process. These snakes are strong and may react violently to being picked up. The bite may be a snap, or they may hang on for many seconds.
Although this genus does not have the heat-sensitive pit organs common to the Crotalinae, it is one of a number of viperines that are apparently able to react to thermal cues, further supporting the notion that they too possess a heat-sensitive organ. The identity of this sensor is not certain, but the nerve endings in the supranasal sac of these snakes resemble those found in other heat-sensitive organs.
This species is ovoviparous. Mating generally occurs early in the year, although gravid females may be found at any time. The gestation period is more than six months. Young are produced from May to November, but mostly in June and July. It is a prolific breeder. Litters of 20–40 are common, although there may be fewer offspring and as little as one. The reported maximum is 65 in a single litter. At birth, juveniles are 215–260 mm (8.5–10.2 in) in total length. The minimum total length for a gravid female is about 100 cm (39 in). It seems that sexual maturity is achieved in 2–3 years. In one case, it took a specimen nearly 4.5 hours to give birth to 11 young.
It feeds primarily on rodents, especially murid species. However, it will eat just about anything; including rats, mice, shrews, squirrels, land crabs, scorpions, lizards and other arthropods. Juveniles are crepuscular, feeding on lizards and foraging actively. As they grow and become adults, they begin to specialize in rodents. Indeed, the presence of rodents and lizards is the main reason they are attracted to human habitation.
Some herpetologists believe that, because D. russelii is so successful as a species and has such a fearful reputation within its natural environment, another snake has even come to mimic its appearance. Superficially, the rough-scaled sand boa, Gongylophis conicus, has a color pattern that often looks a lot like that of D. russelii, even though it is completely harmless.
The quantity of venom produced by individual specimens is considerable. Reported venom yields for adult specimens range from 130–250 mg to 150–250 mg to 21–268 mg. For 13 juveniles with an average total length of 79 cm (31 in), the average venom yield was 8–79 mg (mean 45 mg).
The LD50 in mice, which is used as a possible indicator of snake venom toxicity, is as follows: 0.133 mg/kg intravenous, 0.40 mg/kg intraperitoneal, about 0.75 mg/kg subcutaneous. For most humans, a lethal dose is approximately 40–70 mg. In general, the toxicity depends on a combination of five different venom fractions, each of which is less toxic when tested separately. Venom toxicity and bite symptoms in humans vary within different populations and over time.
Envenomation symptoms begin with pain at the site of the bite, immediately followed by swelling of the affected extremity. Bleeding is a common symptom, especially from the gums and in the urine, and sputum may show signs of blood within 20 minutes post-bite. There is a drop in blood pressure, and the heart rate falls. Blistering occurs at the site of the bite, developing along the affected limb in severe cases. Necrosis is usually superficial and limited to the muscles near the bite, but may be severe in extreme cases. Vomiting and facial swelling occur in about one-third of all cases. Kidney failure (renal failure) also occurs in approximately 25-30 percent of untreated bites. Severe disseminated intravascular coagulation also can occur in severe envenomations. Early medical treatment and early access to antivenom can prevent and drastically reduce the chance of developing the severe/potentially lethal complications.
Severe pain may last for 2–4 weeks. Locally, it may persist depending on the level of tissue damage. Often, local swelling peaks within 48–72 hours, involving both the affected limb and the trunk. If swelling up to the trunk occurs within 1–2 hours, massive envenomation is likely. Discoloration may occur throughout the swollen area as red blood cells and plasma leak into muscle tissue. Death from septicaemia, kidney, respiratory or cardiac failure may occur 1 to 14 days post-bite or even later.
A study in The Lancet journal showed that out of a sample of people bitten by Daboia russelii who survived, 29% of them suffered severe damage to their pituitary glands, which later resulted in hypopituitarism. Other scientific studies support the hypothesis that D. russelii bites can cause hypopituitarism.
Because this venom is so effective at inducing thrombosis, it has been incorporated into an in vitro diagnostic test for blood clotting that is widely used in hospital laboratories. This test is often referred to as Dilute Russell's viper venom time (dRVVT). The coagulant in the venom directly activates factor X, which turns prothrombin into thrombin in the presence of factor V and phospholipid. The venom is diluted to give a clotting time of 23 to 27 seconds and the phospholipid is reduced to make the test extremely sensitive to phospholipid. The dRVVT test is more sensitive than the aPTT test for the detection of lupus anticoagulant (an autoimmune disorder), because it is not influenced by deficiencies in clotting factors VIII, IX or XI.
|Subspecies||Taxon author||Common name||Geographic range|
|D. russelii||(Shaw, 1797)||Indian Russell's viper||Across the Indian subcontinent through Pakistan and Bangladesh to Sri Lanka.|
|D. siamensis||(M.A. Smith, 1917)||Eastern Russell's viper (Sometimes treated as a species)||From Myanmar through Thailand, Cambodia, Indonesia and southern China. Also found in Taiwan.|
Using morphological and mitochondrial DNA data, Thorpe et al. (2007) provided evidence that the eastern subspecies should be considered a separate species, Daboia siamensis
A number of other subspecies may be encountered in literature, including:
- D. s. formosensis (Maki, 1931) – found in Taiwan (considered a synonym of D. siamensis).
- D. s. limitis (Mertens, 1927) – found in Indonesia (considered a synonym of D. siamensis).
- D. r. pulchella Gray, 1842 – found in Sri Lanka (considered a synonym of D. r. russelii).
- D. r. nordicus (Deraniyagala, 1945) – found in northern India (considered a synonym of D. r. russelii).
The correct spelling of the species, D. russelii has been, and still is, a matter of debate. Shaw & Nodder (1797), in their account of the species Coluber russelii, named it after Dr. Patrick Russell, but apparently misspelled his name, using only one "L" instead of two. Russell (1727–1805) was the author of An Account of Indian Serpents (1796) and A Continuation of an Account of Indian Serpents (1801). McDiarmid et al. (1999) are among those who favor the original misspelled spelling, citing Article 32c (ii) of the International Code of Zoological Nomenclature. Others, such as Zhao and Adler (1993) favor russellii.
In the future, more species may be added to Daboia. Obst (1983) reviewed the genus and suggested that it be extended to include Macrovipera lebetina, Vipera palaestinae and V. xanthina. Groombridge (1980, 1986) united V. palaestinae and Daboia as a clade based on a number of shared apomorphies, including snout shape and head color pattern. Lenk et al. (2001) found support for this idea based on molecular evidence, suggesting that Daboia not only include V. palaestinae, but also M. mauritanica and M. deserti.
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- Viperinae by common name
- Viperinae by taxonomic synonyms
- Dilute Russell's viper venom time
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