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Naja is a of commonly known as (or " true cobras"). Various species occur throughout , , , and . Several other elapid species are often called "cobras", such as the and the , but they are not "true cobras", in that they do not belong to the genus Naja.

(1995). 9780883590294, Ralph Curtis Books. 192 pp.. .
(1993). 9780916984281, Society for the Study of Amphibians & Reptiles. 522 pp.. .
(2006). 9783936027938, Hollywood Import & Export. .

Until recently, the genus Naja had 20 to 22 , but it has undergone several taxonomic revisions in recent years, so sources vary greatly. Wide support exists, though, for a 2009 revision that synonymised the genera and Paranaja with Naja. According to that revision, the genus Naja now includes 38 species.


Etymology
The origin of the , Naja, is from the nāga (with a hard "g") meaning "snake". Some hold that the Sanskrit word is cognate with English "snake", Germanic: *snēk-a-, Proto-IE: *(s)nēg-o-, but Manfred Mayrhofer calls this etymology "not credible", and suggests a more plausible etymology connecting it with Sanskrit nagna, "hairless" or "naked".
(1996). 9783825345501, Universitätsverlag C. Winter.
(in German).


Description
Naja species vary in length, and most are relatively slender-bodied snakes. Most species are capable of attaining a total length (tail included) of . Maximum lengths for some of the larger species of cobras are around , with the ( Naja melanoleuca) arguably being the longest species. All have a characteristic ability to raise the front quarter of the body off the ground and flatten the neck to appear larger to a potential predator. Fang structure is variable. All species except the Indian cobra ( ), Egyptian cobra ( ) and Caspian cobra ( ) have some degree of adaptation to .


Venom
All species in the genus Naja are capable of delivering a fatal bite to a human. Most species have strongly venom, which attacks the nervous system, causing paralysis, but many also have features that cause swelling and , and have a significant anticoagulant effect. Some also have components to their venom.

Several Naja species, referred to as , have a specialized venom delivery mechanism, in which their , instead of ejecting venom downward through an elongated discharge orifice (similar to a hypodermic needle), have a shortened, rounded opening in the front surface, which ejects the venom forward, out of the mouth. While typically referred to as "spitting", the action is more like squirting. The range and accuracy with which they can shoot their venom varies from species to species, and it is used primarily as a defense mechanism. The venom has little or no effect on unbroken skin, but if it enters the eyes, it can cause a severe burning sensation and temporary or even permanent blindness if not washed out immediately and thoroughly.

A recent study showed that all three spitting cobra lineages have evolved higher pain-inducing activity through increased phospholipase A2 levels, which potentiate the pain-inducing action of the cytotoxins present in most cobra venoms. The timing of the origin of spitting in African and Asian Naja species corresponds to the separation of the human and evolutionary lineages in Africa and the arrival of in Asia. The authors therefore hypothesize that the arrival of bipedal, tool-using primates may have triggered the evolution of spitting in cobras.

The ( N. oxiana) of Central Asia is the most venomous Naja species. According to a 2019 study, the via intravenous injection value for Naja oxiana (Iranian specimens) was estimated to be 0.14 mg/kg (0.067-0.21 mg/kg) more potent than the Pakistani Naja naja karachiensis and Naja naja indusi found in far north and northwest India and adjacent Pakistani border areas (0.22 mg/kg), the Naja kaouthia (0.2 mg/kg), and Naja philippinensis at 0.18 mg/kg (0.11-0.3 mg/kg). (1984) listed a subcutaneous value of 0.2 mg/kg (0.16-0.47 mg/kg) for N. oxiana. The crude venom of N. oxiana produced the lowest known lethal dose (LCLo) of 0.005 mg/kg, the lowest among all cobra species ever recorded, derived from an individual case of envenomation by intracerebroventricular injection. The 's was estimated to be 0.17 mg/kg via IV according to Christensen (1968). The ( N. philippinensis) has an average murine of 0.18 mg/kg IV ( Tan et al, 2019). Minton (1974) reported 0.14 mg/kg IV for the Philippine cobra.

(1974). 9780398030513, C.C. Thomas.
256 pp. The ( Naja samarensis), another cobra species endemic to the southern islands of the Philippines, is reported to have a of 0.2 mg/kg, similar in potency to the ( Naja kaouthia) which also have a of 0.2 mg/kg. The that are with N. oxiana, in Pakistan and far northwest India, also have a high potency of 0.22 mg/kg.

Other highly venomous species are the forest cobras and/or water cobras ( Boulengerina subgenus). The murine intraperitoneal of and venoms were 0.143 mg/kg (range of 0.131 mg/kg to 0.156 mg/kg) and 0.120 mg/kg, respectively. Christensen (1968) also listed an IV of 0.17 mg/kg for N. annulata.

(1968). 9781483229492, Academic Press. .
The Chinese cobra ( N. atra) is also highly venomous. Minton (1974) listed a value of 0.3 mg/kg intravenous (IV), while Lee and Tseng list a value of 0.67 mg/kg (SC). The of the ( N. nivea) according to Minton, 1974 was 0.35 mg/kg (IV) and 0.4 mg/kg (SC). The ( N. senegalensis) has a murine of 0.39 mg/kg (Tan et al, 2021) via IV. The ( N. haje) of locality had an IV of 0.43 mg/kg (0.35–0.52 mg/kg).

Medical importance
The Naja species are a medically important group of snakes due to the number of bites and fatalities they cause across their geographical range. They range throughout (including some parts of the Sahara where Naja haje can be found), , , , , and . Roughly 30% of bites by some cobra species are dry bites, thus do not cause envenomation (a dry bite is a bite by a venomous snake that does not inject venom). Brown (1973) noted that cobras with a higher rates of 'sham strikes' tend to be more venomous, while those with a less toxic venom tend to envenomate more frequently when attempting to bite. This can vary even between specimens of the same species. This is unlike related elapids, such as those species belonging to (mambas) and (kraits), with mambas tending to almost always envenomate and kraits tending to envenomate more often than they attempt 'sham strikes'.
(1973). 9780398028084, Charles C. Thomas. .

Many factors influence the differences in cases of fatality among different species within the same genus. Among cobras, the cases of fatal outcome of bites in both treated and untreated victims can be quite large. For example, mortality rates among untreated cases of envenomation by the cobras as a whole group ranges from 6.5–10% for N kaouthia.

(1995). 9780203719442, CRC Press. .
to about 80% for N. oxiana. Mortality rate for Naja atra is between 15 and 20%, 5–10% for N. nigricollis, 50% for N. nivea, 20–25% for N. naja, In cases where victims of cobra bites are medically treated using normal treatment protocol for elapid type envenomation, differences in prognosis depend on the cobra species involved. The vast majority of envenomated patients treated make quick and complete recoveries, while other envenomated patients who receive similar treatment result in fatalities. The most important factors in the difference of mortality rates among victims envenomated by cobras is the severity of the bite and which cobra species caused the envenomation. The Caspian cobra ( N. oxiana) and the Philippine cobra ( N. philippinensis) are the two cobra species with the most toxic venom based on studies on mice. Both species cause prominent and progression of life-threatening symptoms following envenomation. Death has been reported in as little as 30 minutes in cases of envenomation by both species. N. philippinensis purely neurotoxic venom causes prominent neurotoxicity with minimal local tissue damage and pain and patients respond very well to antivenom therapy if treatment is administered rapidly after envenomation. Envenomation caused by N. oxiana is much more complicated. In addition to prominent neurotoxicity, very potent and components are in this species' venom. Local effects are marked and manifest in all cases of envenomation: severe pain, severe swelling, bruising, blistering, and tissue necrosis. Renal damage and cardiotoxicity are also clinical manifestations of envenomation caused by N. oxiana, though they are rare and secondary. The untreated mortality rate among those envenomed by N. oxiana approaches 80%, the highest among all species within the genus Naja.
(1990). 9789971622176, National University of Singapore.
Antivenom is not as effective for envenomation by this species as it is for other Asian cobras within the same region, like the Indian cobra ( N. naja) and due to the dangerous toxicity of this species' venom, massive amounts of antivenom are often required for patients. As a result, a monovalent antivenom serum is being developed by the Razi Vaccine and Serum Research Institute in Iran. Response to treatment with antivenom is generally poor among patients, so mechanical ventilation and endotracheal intubation is required. As a result, mortality among those treated for N. oxiana envenomation is still relatively high (up to 30%) compared to all other species of cobra (<1%).
(1984). 9780916984229, Society for the Study of Amphibians & Reptiles.
156 pp.


Taxonomy
The genus contains several of closely related and often similar-looking species, some of them only recently described or defined. Several recent taxonomic studies have revealed species not included in the current listing in ITIS:

  • (Bocage, 1879), Anchieta's cobra, is regarded as a subspecies of by Mertens (1937) and of by Broadley (1995). It is regarded as a full species by Broadley and Wüster (2004).
  • Scortecci, 1932, the Arabian cobra, has long been considered a subspecies of N. haje, but was recently raised to the status of species.
  • Broadley and Wüster, 2007, Ashe's spitting cobra, is a newly described species found in and also a highly aggressive snake; it can spit a large amount of venom.
  • Bogert, 1940, was long regarded as a subspecies of N. nigricollis, but was recently found to be a full species (with N. n. woodi as a subspecies).
  • Naja senegalensis Trape et al., 2009, is a new species encompassing what were previously considered to be the West African savanna populations of N. haje.
  • Naja peroescobari Ceríaco et al. 2017, is a new species encompassing what was previously considered the São Tomé population of N. melanoleuca.
  • Broadley et al., 2018, is a new species encompassing what were previously considered to be the West African forest populations of N. melanoleuca.
  • Broadley et al., 2018, is a new species encompassing what were previously considered to be the West African savanna populations of N. melanoleuca.
  • Laurent, 1955, previously regarded as a subspecies of N. melanoleuca, was recently recognized as a full species.

Two recent molecular phylogenetic studies have also supported the incorporation of the species previously assigned to the genera and Paranaja into Naja, as both are closely related to the ( Naja melanoleuca).; ; ; Branch, W.R.; ; ; (2005). "Molecular systematics of African Colubroidea (Squamata: Serpentes)". pp. 221–228. In: ; ; (editors) (2005). African Biodiversity: Molecules, Organisms, Ecosystems. Proceedings of the 5th International Symposium on Tropical Biology. Bonn: Museum Koenig. In the most comprehensive phylogenetic study to date, 5 putative new species were initially identified, of which 3 have since been named.

The controversial amateur herpetologist proposed the genus Spracklandus for the African spitting cobras. (2009). " Naja, Boulengerina and Paranaja". Australasian Journal of Herpetology 7: 1–15. Wallach et al. suggested that this name was not published according to the Code and suggested instead the recognition of four subgenera within Naja: Naja for the Asiatic cobras, Boulengerina for the African forest, water and burrowing cobras, Uraeus for the Egyptian and Cape cobra group and Afronaja for the African spitting cobras. International Commission on Zoological Nomenclature issued an opinion that it "finds no basis under the provisions of the Code for regarding the name Spracklandus as unavailable".

Asiatic cobras are believed to further be split into two groups of southeastern Asian cobras ( N. siamensis, N. sumatrana, N. philippinensis, N. samarensis, N. sputatrix, and N. mandalayensis) and western and northern Asian cobras ( N. oxiana, N. kaouthia, N. sagittifera, and N. atra) with Naja naja serving as a basal lineage to all species. (preprint).


Species
N. anchietaeBocage, 18790Anchieta's cobra (Angolan Cobra)Angola, Botswana, Namibia, Zambia, eastern Zimbabwe
N. annulataBuchholz & , 18761Banded water cobraCameroon, the Central African Republic, the Democratic Republic of the Congo (Zaire), the Republic of Congo, Equatorial Guinea, Gabon, Rwanda, and the province of Cabinda in Angola
N. annuliferaW. Peters, 18540Botswana, Malawi, Mozambique, South Africa, Swaziland, Zambia, Zimbabwe
, 19760 Miocene-aged strata of Morocco
N. arabica, 19320Oman, Saudi Arabia, Yemen
N. asheiWüster & Broadley, 20070Ashe's spitting cobra (giant spitting cobra)southern Ethiopia, Kenya, Somalia, eastern Uganda
N. atraCantor, 18420southern China, northern Laos, Taiwan, northern Vietnam
N. christyi(Boulenger, 1904)0Congo water cobrathe Democratic Republic of the Congo (Zaire), the Republic of Congo, and the province of Cabinda in Angola
N. fuxi, , & , 20220Brown banded cobraChina, Myanmar, Laos, Thailand, Vietnam
N. guineensisBroadley, Trape, , & Wüster, 20180Black forest cobraGhana, Guinea, Guinea-Bissau, the Ivory Coast, Liberia, Sierra Leone, Togo
N. haje, 17580Tanzania, Kenya, Somalia, Ethiopia, Uganda, South Sudan, Sudan, Cameroon, Nigeria, Niger, Burkina Faso, Mali, Senegal, Mauritania, Morocco, Algeria, Tunisia, Libya, and Egypt
, 1985 Miocene-aged strata of Spain
N. kaouthiaLesson, 18310Bangladesh, Bhutan, Burma, Cambodia, southern China, eastern India, Laos, northwestern Malaysia, Nepal, Thailand, southeastern Tibet, Vietnam
N. katiensis, 19220 (Katian spitting cobra)Benin, Burkina Faso, Cameroon, Ghana, Guinea, the Ivory Coast, Mali, Gambia, Mauritania, Niger, Nigeria, Senegal, Togo
N. mandalayensisSlowinski & Wüster, 20000Mandalay spitting cobra (Burmese spitting cobra)Myanmar (Burma)
N. melanoleucaHallowell, 18570Angola, Benin, Cameroon, the Central African Republic, the Republic of Congo, the Democratic Republic of the Congo (Zaire), Equatorial Guinea, Gabon, Nigeria
N. mossambicaW. Peters, 18540Mozambique spitting cobraextreme southeastern Angola, Botswana, Malawi, Mozambique, Somalia, northeastern Namibia, South Africa, Swaziland, Tanzania (including Pemba Island), Zambia, Zimbabwe
N. multifasciata(, 1902)0Many-banded cobraCameroon, Congo, the Democratic Republic of the Congo (Zaire), Gabon
N. naja(Linnaeus, 1758)0 (spectacled cobra)Bangladesh, Bhutan, India, Nepal, Pakistan, Sri Lanka
N. nana& Trape, 20200Dwarf water cobraDemocratic Republic of Congo
N. nigricinctaBogert, 19401Zebra spitting cobraAngola, Namibia, South Africa
N. nigricollis, 18430Black-necked spitting cobraAngola, Benin, Burkina Faso, Burundi, Cameroon, the Central African Republic, Chad, the Democratic Republic of the Congo (Zaire) (except in the central region), Congo, Ethiopia, Gabon, Gambia, Ghana, Guinea-Bissau, Guinea, the Ivory Coast, Kenya, Liberia, Mali, Mauritania, Namibia, Niger, Nigeria, Rwanda, Senegal, Sierra Leone, Sudan, Tanzania, Somalia, Togo, Uganda, Zambia
N. nivea(Linnaeus, 1758)0 (yellow cobra)Botswana, Lesotho, Namibia, South Africa
N. nubiaeWüster & Broadley, 20030Nubian spitting cobraChad, Egypt, Eritrea, Niger, Sudan
N. obscura& Trape, 20230Egypt
N. oxiana(, 1831)0Afghanistan, northwestern India, Iran, Kyrgyzstan, Pakistan, Tajikistan, Turkmenistan, Uzbekistan
N. pallidaBoulenger, 18960Red spitting cobraDjibouti, Ethiopia, Kenya, Somalia, Tanzania
N. peroescobariCeríaco, Marques, & Bauer, 20170São Tomé forest cobra, cobra pretaSão Tomé and Príncipe (São Tomé)
N. philippinensisTaylor, 19220the Philippines (Luzon, Mindoro)
(Hofstetter, 1939)0Miocene-aged strata of France, Germany, Austria, Russia, Hungary, Greece and Ukraine.
N. sagittiferaWall, 19130India (the Andaman Islands)
N. samarensisW. Peters, 18610the Philippines (Mindanao, Bohol, Leyte, Samar, Camiguin)
N. savannulaBroadley, Trape, Chirio & Wüster, 20180West African banded cobraBenin, Burkina Faso, Cameroon, Chad, Gambia, Ghana, Guinea, the Ivory Coast, Mali, Niger, Nigeria, Senegal, Togo
N. senegalensisTrape, Chirio & Wüster, 20090Benin, Burkina Faso, Ghana, Guinea, Guinea-Bissau, the Ivory Coast, Mali, Niger, Nigeria, Senegal
N. siamensisLaurenti, 17680Indochinese spitting cobraCambodia, Laos, Thailand, Vietnam
N. sputatrix, 18270Javan spitting cobraIndonesia (Java, the Lesser Sunda Islands, East Timor)
N. subfulvaLaurent, 19550Brown forest cobraAngola, Burundi, Cameroon, the Central African Republic, Chad, the Republic of Congo, the Democratic Republic of the Congo (Zaire), Ethiopia, Kenya, Malawi, Mozambique, Nigeria, Rwanda, Somalia, South Africa, South Sudan, Tanzania, Uganda, Zambia, Zimbabwe
N. sumatranaJ. Müller, 18870Equatorial spitting cobraBrunei, Indonesia (Sumatra, Borneo, Bangka, Belitung), Malaysia, the Philippines (Palawan), southern Thailand, Singapore
  • Not including the nominate subspecies
Extinct
T

  • : A binomial authority in parentheses indicates that the species was originally described in a genus other than Naja.


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