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| Spitting cobras have been known for centuries, as you can see from this report published in the Journal of the Bombay Natural History Society in 19001 |
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| A clever comic from birdandmoon highlighting the fact that king cobras are not true cobras |
Cobras are some of the most iconic snakes in the world, instantly recognizable by their hoods even to those who have never seen one. They are also among the most dangerous snakes—fast-moving, with potent neurotoxic venom, cobra bites cause injury or death to many people in Asia and Africa. Cobras are elapids, together with coralsnakes, mambas, kraits, seasnakes, and numerous terrestrial Australian snakes both well-known and obscure. What unites these ~350 species of snakes is their short, immovable, and hollow ("proteroglyphous") fangs. Elapids probably evolved in Asia between 25 and 30 million years ago. By 16 million years ago, cobras were found in Europe, where they no longer live, and in Asia and Africa, where they are still found today. The core cobra clade consists of three small genera (Hemachatus, Aspidelaps, and Walterinnesia) and one large one, Naja. Other hooded snakes that are usually called "cobras" include tree cobras (genus Pseudohaje), whose placement remains uncertain, and the king cobra (Ophiophagus hannah), which is probably more closely related to mambas than it is to true cobras. Ironically, most people, if asked for a species of cobra, would almost certainly come up with the king first. But, probably they would think of a spitting cobra second, and with good reason from an evolutionary perspective, as we shall see.
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| Mozambique Spitting Cobra (Naja mossambica) |
Almost all spitting cobras belong to the genus Naja, a large genus that comes from the Sanskrit word for snake, nāga. Literature buffs will recognize the name of the cobras in Kipling's Rikki Tikki Tavi, which led to the name of the snake Nagini in the Harry Potter books. Over the past 50 years, the number of species within the genus Naja has risen from six to 292, and more will probably become recognized in the future. At least 15 of these species can spit their venom through the air. The best of them are capable of aiming at targets the size of a human face with >90% accuracy up to 8 feet away. This adaptation represents the only purely defensive use of venom by any snake. Vipers and other venomous snakes occasionally eject venom from their fangs into the air, particularly when being handled, but these snakes are not aiming at anything, so they are not really using their venom defensively. Spitting in cobras is an adaptation that involves changes to the morphology of the fangs, their head musculature, and the chemistry of their venom.
All snake fangs are modified teeth provisioned with grooves that vary in depth and degree of closure. In vipers and elapids, the grooves are completely closed, forming hollow tubes, along the front edge of which a narrow suture can still be seen where the ridges forming the tube have come together in the developing embryo. In spitting cobras, the inside of this tube contains ridges, which act like rifling in a gun barrel to impart spin on the venom. The discharge orifice, located near but not at the point of the tooth (like a hypodermic needle), is large and elliptical in non-spitting cobras but small and round in spitting cobras, which has the same velocity-increasing effect as putting your thumb most of the way over the end of a garden hose. A sharp 90° bend at the distal end directs the jet of venom forward or slightly upward, instead of downward as in most snakes, and venom stream spins towards the exit orifice, which prevents the flow from slowing down as it goes through the sharp bend at the exit (similar strategies are used in pressure washers). These adaptations of the fang enable a cobra to spit venom in defense but do not prevent venom injection when biting, which is used both defensively and for killing prey. In fact, spitting cobras can meter the duration of their venom pulse, which is normally about five times longer during biting (1/4th of a second) than during spitting (1/20th of a second). This affects the quantity of venom ejected, which varies considerably from bite to bite and may consist of up to 100 times more venom than the fairly consistent 1.9-3.7 milligrams (~1/10th of a milliliter) of venom per spit. Most estimates suggest that a single cobra has enough venom to spit about 40-50 times consecutively. The fluid dynamics of such tiny volumes over relatively long distances are complex, and spitting cobra venom has shear-reducing properties, such as high surface tension and viscosity, which hold the droplets together as they fly through the air. Some species of spitting cobra eject their venom as a spray, whereas others eject two pressurized parallel streams. Reports of the maximum distance achievable by a spitting cobra vary from surely exaggerated distances of 12 feet or more to more believable (though still impressive) distances of five to eight feet.
Unlike vipers, cobras cannot move their fangs, so in order to accurately hit their targets, they move their heads instead. When a spitting cobra spits, it opens its mouth slightly and contracts the muscles around the venom glands so that a small amount of venom is forced out of the glands and down the venom canal of the fangs. At the same time, the upper lip scales and the fang sheaths are levered up out of the way and the maxilla levered down, removing soft tissue barriers between the venom glands and the fangs as well as between the exit orifices of the fangs and the air around them3. Most often, the spit is accompanied by slight movements of the head in response to change in direction of the target, which disperse the venom over an area about the size of a human face. Measurements indicate that more head rotation corresponds to a larger area covered by the venom stream, allowing cobras to adjust for target size and distance. Splattering of the venom when it hits the target and partial disintegration of the venom stream as it travels through the air increase the chance that at least some of the venom will hit the target's eye. Consequently, cobras only need to aim at the center of the face, rather than precisely at the eyes, in order to hit the eyes 90-100% of the time. They adjust for target movement by using a strategy familiar to any Space Invaders or Galaga player: firing not at where you are but at where you're going to be. Chameleons, archer fish and spitting spiders do the same kind of thing. In some species venom spitting is often accompanied by an audible hiss as the cobra exhales, but in contrast to early reports that spitting cobras propelled their venom with their breath, this is not an essential part of the spitting process. In one experiment, spitting cobras restrained in tubes did not seem to suffer from reduced spitting ability or range. How do they choose their targets? Cobras have good vision and moving human faces are the stimuli that normally elicit spitting, although in lab experiments they will also spit at masks, photos of human faces, and even plain ovals without eyes, as long as they are moving, but not at moving triangles. Adult cobras will not spit at stationary human faces or moving human hands, although newly hatched cobras will spit at nearly anything, even if it is beyond their maximum target distance, including human hands, unhatched eggs, other baby cobras, and even their own reflection. Hatchling cobras also spit more of their venom, proportionally, and rotate their heads in a more pronounced fashion; their spitting performance improves following their first shed. Like many stereotypical snake defensive behaviors, most spitting cobras apparently habituate to humans when in captivity and are disinclined to spit after a while, although some spit without hesitation and willingness to express defensive behavior is very variable from individual to individual.
Although the color and consistency of spat venom does not change noticeably with repeated spitting, the venom chemistry of at least one species, Red Spitting Cobras (Naja pallida), changed over 10 minutes of repeated spitting. The quantity of venom remained the same and the toxin concentration rose over the first 20 spits, but both decreased afterward. The first five spits contained a protein that was not found in later spits, which might be involved in venom storage. Although this protein is non-toxic, most of the other molecules in spitting cobra venom are not. African spitting cobra venom is rich in cytotoxins and PLA2s, which cause tissue damage; spitting cobra cytotoxins lack certain acidic proteins, which frees them to damage tissues in the eyes. If even a small quantity of venom contacts the eye it causes instant, intense pain and damage to the cornea and mucous membranes. If left untreated, it can lead to blindness. Treating spitting cobra venom in your eyes involves flushing it out with water for 15-20 minutes. Anti-inflammatory eye drops are sometimes prescribed.
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| Sumatran Spitting Cobra (Naja sumatrana) |
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| Rinkhals (Hemachatus haemachatus) |
The 29 living species of Naja fall into four groups: a basal Asian clade of eleven species (subgenus Naja, including six accomplished spitting members, two non-spitters, and three species of intermediate spitting ability), an African spitting group of eight species (subgenus Afronaja), and two African non-spitting groups of six and four species, respectively (subgenus Uraeus, found mostly in open areas, and subgenus Boulengerina, found mostly in forests). This pattern of species relationships suggests that spitting evolved more than once! In Asia, the six spitting cobras (Naja siamensis, N. sumatrana, N. sputatrix, N. mandalayensis, N. samarensis, and N. philippinensis4) are probably one another's closest relatives, and their closest cousins are a group of three cobra species (Naja atra, N. kaouthia, and N. sagittifera) with somewhat modified fangs and intermediate spitting ability. They can spit their venom, but they do so rarely and with less accuracy than the "true" spitters. The remaining Asian cobras, Naja naja and Naja oxiana, do not spit their venom but nevertheless are more closely related to Asian spitting cobras than to other cobras. This means that venom spitting arose independently in the common ancestor of the seven species of African spitting cobras (N. pallida, N. nubiae, N. katiensis, N. nigricollis, N. ashei, N. mossambica, and N. nigricincta), which form a monophyletic group sometimes referred to as Afronaja. Their cousins, the other African Naja (i.e., subgenera Uraeus and Boulengerina), do not spit. Finally, a member of one of those small genera, a very interesting cobra known as the rinkhals (Hemachatus haemachatus) also spits its venom, indicating that venom spitting has evolved three times in cobras (or, alternatively, been lost twice, in Naja naja/N. oxiana and in the common ancestor of Uraeus and Boulengerina, with a third partial loss in N. atra & kin). Because the details of spitting behavior and morphology differ slightly among the three groups of spitting cobras, the former hypothesis is more likely.
Why do some cobras spit their venom? Herpetologist Thomas Barbour, who published one of the first studies on spitting cobras, thought that spitting cobras evolved venom spitting for much the same reason that rattlesnakes were thought to have evolved their rattles—to alert large ungulates to their presence and avoid getting stepped on. He was speculating in the absence of any direct evidence when he wrote in 1922 that "The African veldt is the only other region in the world where snakes abound and where hoofed animals grazed in numbers comparable with those of the western American plains. Snakes probably found the heavy antelopes equally dangerous though unwitting foes and many antelopes probably suffered from snake bite. No rattle was evolved, however but some of the common veldt-ranging snakes secured protection in another way. Several common cobras and cobra-allies learned to expel their poison in a fine spray for very considerable distances, and with a fairly shrewd aim at the eye."
Nearly 100 years after Barbour, we have just as little direct evidence—published field observations of spitting cobras interacting with their non-human predators are non-existent. The main reason we now think that the evolutionary cause of these adaptations isn't so simple is that spitting is too old. Molecular dating methods suggest that African spitting cobras evolved about 15 million years ago, whereas the spread of open grasslands and their characteristic megafauna (elephants, etc.) didn't happen until about 5 million years ago. Asian spitting cobras don't inhabit open grasslands, so this hypothesis seems unlikely to explain their evolution either. African spitting cobras are eaten by birds and other snakes, against which spitting venom would be a relatively ineffective weapon, and in captive experiments cobras do not spit at mounted bird specimens. Given what we know about face targeting, it's possible that spitting may represent a defense that is specifically adapted for use against primates [Edit: Harry Greene hinted at this idea in his recent book, Tracks and Shadows]. Barbour's comment that "...[venom spitting] must antedate man's coming, for contact between man and the snakes can hardly be conceived as sufficiently frequent to account for the modification" may be technically correct, but the evolution of spitting cobras coincides roughly with the evolution of apes in Asia and Africa, which (as we all know) are diurnal primates with forward-facing eyes, some of which are omnivorous and many of which (ourselves included) habitually kill snakes either for food or in defense. Could it be that spitting cobras evolved their venom spitting capacity to deal with threats from our own ancestors? Only further research into the co-evolution of apes and snakes can tell us. Perhaps this is why, although certain toads, salamanders, insects, and scorpions can also eject their toxin defensively, spitting cobras are by far the longest- and best-known organisms to do so. Clearly, much remains to learn about them and their fascinating habits.
1 The cobra in this account was undoubtedly Naja mandalayensis, which was described by Joe Slowinski & Wolfgang Wüster 100 years later. Before 2000, no spitting cobras were known from Burma. Cobra specimens with fangs highly modified for spitting from northeastern India may represent a seventh species of undescribed Asian spitting cobra.↩
2 This number includes species of cobras formerly placed in the genera Boulengerina and Paranaja, both of which have been synonymized with Naja in the last 15 years. In part, the reason for this change is that, when scientists realized that some species of Naja were more closely related to Boulengerina and Paranaja than they were to other Naja (i.e., that Naja was paraphyletic), they were reluctant to split up the genus Naja because they didn't want to change the name of medically-important snakes and create potential confusion. However, a few sources use Afronaja and other other subgenera as full genera anyway.↩
3 The fang sheath is soft tissue that completely surrounds the fang at rest, including at the top, which keeps the venom from dribbling out. In other venomous snakes, physical contact with a target is required for displacement of the fang sheath and release of venom, but spitting cobras have co-opted the movements normally used for jaw-walking over a prey item (the ‘pterygoid walk’) to free their fangs for spitting in the absence of any external physical contact. This has been termed the "buccal buckle" (pronounced "buckle buckle") by the research group of Bruce Young, of Kirksville College, which has studied several aspects of the functional morphology of spitting in cobras.↩
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| The largest Giant Spitting Cobras (Naja ashei) can top 9 feet. This species was described in 2007. From Wüster & Broadley 2007 |
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| A rinkhals (Hemachatus haemachatus) spits its venom |
1 The cobra in this account was undoubtedly Naja mandalayensis, which was described by Joe Slowinski & Wolfgang Wüster 100 years later. Before 2000, no spitting cobras were known from Burma. Cobra specimens with fangs highly modified for spitting from northeastern India may represent a seventh species of undescribed Asian spitting cobra.↩
2 This number includes species of cobras formerly placed in the genera Boulengerina and Paranaja, both of which have been synonymized with Naja in the last 15 years. In part, the reason for this change is that, when scientists realized that some species of Naja were more closely related to Boulengerina and Paranaja than they were to other Naja (i.e., that Naja was paraphyletic), they were reluctant to split up the genus Naja because they didn't want to change the name of medically-important snakes and create potential confusion. However, a few sources use Afronaja and other other subgenera as full genera anyway.↩
3 The fang sheath is soft tissue that completely surrounds the fang at rest, including at the top, which keeps the venom from dribbling out. In other venomous snakes, physical contact with a target is required for displacement of the fang sheath and release of venom, but spitting cobras have co-opted the movements normally used for jaw-walking over a prey item (the ‘pterygoid walk’) to free their fangs for spitting in the absence of any external physical contact. This has been termed the "buccal buckle" (pronounced "buckle buckle") by the research group of Bruce Young, of Kirksville College, which has studied several aspects of the functional morphology of spitting in cobras.↩
4 Naja philippinensis is the only spitting cobra species with pronounced sexual dimorphism in discharge orifice size—females have longer orifices less well-adapted for spitting, whereas males have small round orifices. The evolutionary causes and consequences of this dimorphism are not understood.↩
This post is part of a Reptile and Amphibian Blogging Network (RAmBlN) online event called #CrawliesConverge. We are writing about convergent evolution in reptiles and amphibians. Find our event schedule here, or follow on Twitter or Facebook.
ACKNOWLEDGMENTS
REFERENCES
Barbour, T. 1922. Rattlesnakes and spitting snakes. Copeia 105:36-38 <link>
Berthé, R., S. de Pury, H. Bleckmann, and G. Westhoff. 2009. Spitting cobras adjust their venom distribution to target distance. Journal of Comparative Physiology A 195:753–757 <link>
Berthé, R.A., G. Westhoff, and H. Bleckmann. 2013. Potential targets aimed at by spitting cobras when deterring predators from attacking. Journal of Comparative Physiology A 199:335-340 <link>
Bogert, C.M. 1943. Dentitional phenomena in cobras and other elapids, with notes on adaptive modifications of fangs. Bulletin of the American Museum of Natural History 81:285-360 <link>
Cascardi, J., B.A. Young, H.D. Husic, and J. Sherma. 1999. Protein variation in the venom spat by the red spitting cobra, Naja pallida (Reptilia: Serpentes). Toxicon 37:1271-1279 <link>
Berthé, R., S. de Pury, H. Bleckmann, and G. Westhoff. 2009. Spitting cobras adjust their venom distribution to target distance. Journal of Comparative Physiology A 195:753–757 <link>
Berthé, R.A., G. Westhoff, and H. Bleckmann. 2013. Potential targets aimed at by spitting cobras when deterring predators from attacking. Journal of Comparative Physiology A 199:335-340 <link>
Bogert, C.M. 1943. Dentitional phenomena in cobras and other elapids, with notes on adaptive modifications of fangs. Bulletin of the American Museum of Natural History 81:285-360 <link>
Cascardi, J., B.A. Young, H.D. Husic, and J. Sherma. 1999. Protein variation in the venom spat by the red spitting cobra, Naja pallida (Reptilia: Serpentes). Toxicon 37:1271-1279 <link>
Chu ER, Weinstein SA, White J, Warrell DA (2010) Venom ophthalmia caused by venoms of spitting elapid and other snakes: Report of ten cases with review of epidemiology, clinical features, pathophysiology and management. Toxicon 56:259-272 <link>
Goring Jones, M.D. 1900. Can a cobra eject its poison? Journal of the Bombay Natural History Society 8:376 <link>
Hayes, W., S. Herbert, J. Harrison, and K. Wiley. 2008. Spitting versus biting: differential venom gland contraction regulates venom expenditure in the Black-Necked Spitting Cobra, Naja nigricollis nigricollis. Journal of Herpetology 42:453-460 <link>
Keogh, J.S. 1998. Molecular phylogeny of elapid snakes and a consideration of their biogeographic history. Biological Journal of the Linnean Society 63:177-203 <link>
Petras, D., L. Sanz, Á. Segura, M. Herrera, M. Villalta, D. Solano, M. Vargas, G. León, D.A. Warrell, and R.D.G. Theakston. 2011. Snake venomics of African spitting cobras: toxin composition and assessment of congeneric cross-reactivity of the pan-African EchiTAb-Plus-ICP antivenom by antivenomics and neutralization approaches. Journal of Proteome Research 10:1266-1280 <link>
Rasmussen, S., B. Young, and H. Krimm. 1995. On the ‘spitting’ behaviour in cobras (Serpentes: Elapidae). Journal of Zoology 237:27-35 <link>
Slowinski, J.B. and W. Wüster. 2000. A new cobra (Elapidae: Naja) from Myanmar (Burma). Herpetologica 2000:257-270 <link>
Szyndlar, Z. and J.C. Rage. 1990. West Palearctic cobras of the genus Naja (Serpentes: Elapidae): interrelationships among extinct and extant species. Amphibia-Reptilia 11:385–400 <link>
Triep, M., D. Hess, H. Chaves, C. Brücker, A. Balmert, G. Westhoff, and H. Bleckmann. 2013. 3D Flow in the Venom Channel of a Spitting Cobra: Do the Ridges in the Fangs Act as Fluid Guide Vanes? PLoS ONE 8:e61548 <link>
Wallach, V., W. Wüster, and D.G. Broadley. 2009. In praise of subgenera: taxonomic status of cobras of the genus Naja Laurenti (Serpentes: Elapidae). Zootaxa 2236:26-36 <link>
Westhoff, G., K. Tzschätzsch, and H. Bleckmann. 2005. The spitting behavior of two species of spitting cobras. Journal of Comparative Physiology A 191:873-881 <link>
Goring Jones, M.D. 1900. Can a cobra eject its poison? Journal of the Bombay Natural History Society 8:376 <link>
Hayes, W., S. Herbert, J. Harrison, and K. Wiley. 2008. Spitting versus biting: differential venom gland contraction regulates venom expenditure in the Black-Necked Spitting Cobra, Naja nigricollis nigricollis. Journal of Herpetology 42:453-460 <link>
Keogh, J.S. 1998. Molecular phylogeny of elapid snakes and a consideration of their biogeographic history. Biological Journal of the Linnean Society 63:177-203 <link>
Petras, D., L. Sanz, Á. Segura, M. Herrera, M. Villalta, D. Solano, M. Vargas, G. León, D.A. Warrell, and R.D.G. Theakston. 2011. Snake venomics of African spitting cobras: toxin composition and assessment of congeneric cross-reactivity of the pan-African EchiTAb-Plus-ICP antivenom by antivenomics and neutralization approaches. Journal of Proteome Research 10:1266-1280 <link>
Rasmussen, S., B. Young, and H. Krimm. 1995. On the ‘spitting’ behaviour in cobras (Serpentes: Elapidae). Journal of Zoology 237:27-35 <link>
Slowinski, J.B. and W. Wüster. 2000. A new cobra (Elapidae: Naja) from Myanmar (Burma). Herpetologica 2000:257-270 <link>
Szyndlar, Z. and J.C. Rage. 1990. West Palearctic cobras of the genus Naja (Serpentes: Elapidae): interrelationships among extinct and extant species. Amphibia-Reptilia 11:385–400 <link>
Triep, M., D. Hess, H. Chaves, C. Brücker, A. Balmert, G. Westhoff, and H. Bleckmann. 2013. 3D Flow in the Venom Channel of a Spitting Cobra: Do the Ridges in the Fangs Act as Fluid Guide Vanes? PLoS ONE 8:e61548 <link>
Wallach, V., W. Wüster, and D.G. Broadley. 2009. In praise of subgenera: taxonomic status of cobras of the genus Naja Laurenti (Serpentes: Elapidae). Zootaxa 2236:26-36 <link>
Westhoff, G., K. Tzschätzsch, and H. Bleckmann. 2005. The spitting behavior of two species of spitting cobras. Journal of Comparative Physiology A 191:873-881 <link>
Westhoff, G., M. Boetig, H. Bleckmann, and B.A. Young. 2010. Target tracking during venom ‘spitting’by cobras. Journal of Experimental Biology 213:1797-1802 <link>
Wüster, W. and D.G. Broadley. 2007. Get an eyeful of this: a new species of giant spitting cobra from eastern and north-eastern Africa (Squamata: Serpentes: Elapidae: Naja). Zootaxa 1532:51-68 <link>
Wüster, W., S. Crookes, I. Ineich, Y. Mané, C.E. Pook, J.F. Trape, and D.G. Broadley. 2007. The phylogeny of cobras inferred from mitochondrial DNA sequences: Evolution of venom spitting and the phylogeography of the African spitting cobras (Serpentes: Elapidae: Naja nigricollis complex). Molecular Phylogenetics and Evolution 45:437-453 <link>
Wüster, W. and R.S. Thorpe. 1992. Dentitional phenomena in cobras revisited: spitting and fang structure in the Asiatic species of Naja (Serpentes: Elapidae). Herpetologica:424-434 <link>
Wüster, W. and D.G. Broadley. 2007. Get an eyeful of this: a new species of giant spitting cobra from eastern and north-eastern Africa (Squamata: Serpentes: Elapidae: Naja). Zootaxa 1532:51-68 <link>
Wüster, W., S. Crookes, I. Ineich, Y. Mané, C.E. Pook, J.F. Trape, and D.G. Broadley. 2007. The phylogeny of cobras inferred from mitochondrial DNA sequences: Evolution of venom spitting and the phylogeography of the African spitting cobras (Serpentes: Elapidae: Naja nigricollis complex). Molecular Phylogenetics and Evolution 45:437-453 <link>
Wüster, W. and R.S. Thorpe. 1992. Dentitional phenomena in cobras revisited: spitting and fang structure in the Asiatic species of Naja (Serpentes: Elapidae). Herpetologica:424-434 <link>
Young, B.A., M. Boetig, and G. Westhoff. 2009. Functional bases of the spatial dispersal of venom during cobra “spitting”. Physiological and Biochemical Zoology 82:80-89 <link>
Young, B.A., M. Boetig, and G. Westhoff. 2009. Spitting behaviour of hatchling red spitting cobras (Naja pallida). The Herpetological Journal 19:185-191 <link>
Young, B.A., K. Dunlap, K. Koenig, and M. Singer. 2004. The buccal buckle: the functional morphology of venom spitting in cobras. Journal of Experimental Biology 207:3483-3494 <link>
Young, B.A., M. Boetig, and G. Westhoff. 2009. Spitting behaviour of hatchling red spitting cobras (Naja pallida). The Herpetological Journal 19:185-191 <link>
Young, B.A., K. Dunlap, K. Koenig, and M. Singer. 2004. The buccal buckle: the functional morphology of venom spitting in cobras. Journal of Experimental Biology 207:3483-3494 <link>
Life is Short, but Snakes are Long by Andrew M. Durso is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License.