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Showing posts with label Elapidae. Show all posts
Showing posts with label Elapidae. Show all posts

Wednesday, September 25, 2013

Basics of Snake Fangs


Solenoglyphous fangs of a Gaboon Viper
Snake fangs are specialized, elegantly modified teeth. Some are like hypodermic needles, others are more like water slides. But all serve essentially the same purpose: to inject venom into the snake's prey. Occasionally, the fangs are also used in defense, but studies show that snakes striking in defense are far less likely to inject venom than when they're striking at a prey item, a fact that has assuaged the fears of many an ophidiophobic. I wanted to write a brief review of snake fang types, because their anatomy is very interesting and also because of their important role in classifying snakes and understanding how different groups of snakes are related to each other.

Cross-sections of fangs:
F is an aglyphous tooth.
G is an opisthoglyphous fang.
H is a proteroglyphous fang.
I is a hollow solenoglyphous fang.
From Bauchot (2006)
Many snakes produce venom, which is essentially very strong saliva, in glands in their heads (which is where you produce your saliva, too). We call these glands venom glands if they are well-developed, complete with an interior cavity, a duct connecting to a hollow fang, and compressor muscles that generate high pressures when the jaws are rapidly closed. If they lack these features, we usually call them Duvernoy's glands instead. Because there is a lot of variation among snake species in the structure of these glands and their associated teeth, there is some debate about whether or not venom glands and Duvernoy's glands are really two forms of the same thing. Either way, three groups of snakes (atractaspidines, elapids, and viperids) have independently evolved an advanced apparatus to deliver large quantities of venom during a brief strike, and many other snakes (and a few lizards) have evolved less sophisticated, but still relatively effective, modifications to their teeth in order to deliver venom after they have grabbed their prey and are "chewing" on it. The teeth of modern snakes are classically divided into four types, three of which are typically called fangs. The four tooth types have fancy names, all of which involve the Greek word glyph, one of the meanings of which is "groove". They are as follows:

Solenoglyphous

Folding of solenoglyphous fangs.
Fang is in red, maxilla green,
prefrontal orange, pterygoid yellow,
ectopterygoid purple. Vipers lack
premaxillary and palatine teeth.
From Bauchot (2006)
This most sophisticated fang type evolved once, in the ancestor to all modern vipers, which lived in Asia about 40 million years ago. Fossils suggest that solenoglyphous fangs have changed little since that time, even though vipers have undergone an incredibly successful radiation into 320 extant species found on all continents except for Australia and Antarctica. Solenoglyphous fangs are long and tubular and are attached to the snake's maxillary bone. Most snakes have several tooth-bearing bones, including four (the premaxilla, maxilla, pterygoid, and palatine) in the upper jaw, and one (the dentary) in the lower. In humans, three of these bones (the premaxilla, maxilla, and dentary) also bear teeth - your premaxilla holds your top incisors, while your maxilla holds your upper canines and molars and your dentary all your lower teeth - while the others form part of the roof of the mouth. In vipers, the maxilla bears only a single tooth (the fang) and is hinged so that the fangs can be folded back parallel to the jaws when the mouth is closed, or erected perpendicular to the jaws, the position when striking. The teeth in the pterygoids and dentaries work together to manipulate food once it gets into the mouth. Solenoglyphous fangs are strikingly similar to hypodermic needles. They have a hollow core that receives venom from the venom gland at the entrance orifice near the base and injects it from a slit-like exit orifice on the front of the fang near the tip. If the opening were at the very tip of the fang, its strength would be compromised and it would lack the sharp point needed to penetrate the target. Even under normal use, vipers shed their fangs every two months.

Modified solenoglyphous fang of
African Burrowing Asp (Atractaspis engaddensis)
A similar fang type evolved a second time about 29 million years ago in a group of African snakes, currently placed in the family Lamprophiidae, subfamily Atractaspidinae. Two genera, Atractaspis (mole vipers, burrowing asps, or stiletto snakes) and Homoroselaps (African dwarf garter or harlequin snakes), possess elongate anterior fangs, although only those of the stiletto snakes are movable. Stiletto snake fangs pivot on a socket-like joint that is more flexible than those of vipers, allowing these snakes to strike beside and behind them with their mouth closed. This is an adaptation to living underground and envenomating small mammals and other reptiles in narrow subterranean burrows. The fang morphology of atractaspidines and viperids is remarkably similar, considering that these two snake lineages last shared a common ancestor over 40 million years ago.

Proteroglyphous

Proteroglyphous fangs of an Eastern Green Mamba
(Dendroaspis angusticeps). Don't try this.
From Bauchot (2006)
This fang type also evolved only once, in the ancestor to all modern elapids, which lived 25-40 mya in Asia or Africa. Proteroglyphous fangs are in the front of the mouth and are about three times shorter than solenoglyphous fangs. This is because they are not hinged. Snakes with proteroglyphous fangs typically strike their prey and hang on until the venom has taken effect, as opposed to releasing they prey and then tracking it down. Some elapids constrict their prey at the same time as envenomating it. Over 350 species of elapids exist today, including well-known groups such as cobras, mambas, death adders, taipans, coralsnakes, and sea snakes, and less-well-known species, mainly found in Australia, of which a good number are small, secretive, and not considered dangerous to humans.

Maxilla of a proteroglyphous snake showing the almost
completely closed groove along the anterior edge connecting
the two orifices, as well as the aglyphous tooth at the
rear of the maxilla. This line may be obscured in longer fangs.
From Shea et al. 1993
Unlike solenoglyphs, some proteroglyphs have other teeth on the maxilla behind the fang. However, the fang is always separated from the other teeth by a gap, called a diastema. Some elapids have more than one functional fang on each side. In both vipers and elapids, there are usually at least two fangs on each maxilla at any one time, one that is in use and one that is a reserve fang. Both fangs are draped in a layer of connective tissue and skin called the fang sheath. Some proteroglyphs have partially movable fangs, including many of the most dangerous species such as mambas, taipans, and death adders. A few, such as spitting cobras, have modified exit orifices to their fangs that are smaller and rounder than in other cobras, a modification that increases the velocity with which venom is ejected. Modifications to the muscles and the fang sheath also facilitate spitting in these cobras. A few elapids, such as sea snakes that eat only fish eggs, have lost their fangs and their venom glands, which suggests that the primary role of venom, at least among elapids, is in feeding rather than in defense.

Opisthoglyphous

Opisthoglyphous fang of Eastern Hog-nosed Snake
These are commonly known as "rear-fanged" snakes. Opisthoglyphous fangs are grooved rather than hollow and are found near the back of the maxilla, behind the normal teeth. Typically, snakes with rear fangs must chew on their prey to bring their fangs into a biting position. There is considerable variation in the size, shape, and number of opisthoglyphous fangs from species to species, and sometimes even within a species. Most opisthoglyphous fangs are connected to Duvernoy's glands, which differ from true venom glands in several important ways, most notably in that they lack associated muscles to generate the pressure needed to evacuate venom, as in solenoglyphous and proteroglyphous snakes. The pressure on the venom glands of biting solenoglyphs and proteroglyphs can exceed 30 psi, the pressure of a car tire, whereas the pressure inside the Duvernoy's glands of opisthoglyphs is generally less than 5 psi. Because Duvernoy's glands also lack a chamber for storing venom, the idea is emerging that opisthoglyphous snakes probably secrete their venom only during chewing, which explains why prolonged bites by opisthoglyphs generally have more severe effects.

Opisthoglyphous fangs of Boomslang (Dispholidus typus)
Don't do this either.
Most of these snakes are not harmful to humans, with a few notable exceptions. Boomslangs and Twigsnakes are arboreal, diurnal African colubrines that prey on lizards and birds. They have short heads, rear fangs situated comparatively close to the front of the mouth, and partially muscled Duvernoy's glands. They also have potent venoms and their bites have killed several people, including two prominent snake biologists, Karl Schmidt and Robert Mertens. Bites from other rear-fanged snakes are known to cause relatively mild, transient, and local symptoms, but clinical documentation of these bites and their effects is scattered, incomplete, and frequently anecdotal. Many are written by the victim themselves! The above notwithstanding, bites from opisthoglyphs are generally less medically important than those from proteroglyphs and solenoglyphs. As a result, snake venom research has not focused on them, so there is still much that we do not know about this group of snakes, some of which are becoming increasingly common in the pet trade. Based on what little we do know, the composition of opisthoglyph venom/Duvernoy's secretion is fairly similar to that of viperids, elapids and atractaspidines, which makes sense given that each of these groups is more closely related to certain opisthoglyphs than they are to one another.

A: python, B: viper, C: rear-fanged colubroid, D: cobra
The f  marks the portion of the maxilla where the fang develops.
E shows the elongation of the posterior part of the
maxilla pushing forward the developing fang of a
night adder (d.a.o. = days after oviposition)
From Vonk et al. 2008
Unlike the first two groups, opisthoglyphous fangs appear to have evolved more than once, in snakes as diverse as Quill-snouted Snakes, Neck-banded Snakes, and Boomslangs. At least, that's what we used to think. Actually, it is likely that both solenoglyphous and proteroglyphous fangs evolved from opisthoglyphous fangs, as revealed by an ingenious study that used evidence from embryology and genetics to reveal the evolutionary origins of the three types of snake fangs. In a snake embryo, tubular fangs are formed by the infolding of ridges on the front and back sides of the fang, such as those that form the groove of opisthoglyphous fangs. Furthermore, front fangs develop from the rear part of the upper jaw, and are strikingly similar in their formation to rear fangs. They are pushed into the front of the mouth by disproportionate growth of the initially small part of the maxilla that is behind them. Finally, in the anterior part of the maxilla of front-fanged snakes, expression of a gene called sonic hedgehog, which is responsible among other things for the formation of teeth, is suppressed.


Relative size of the venom gland (VG) in
A: rear-fanged colubrid (Helicops leopardinus),
B: boomslang, C: homalopsid,
D: cornsnake, E: African egg-eater
SG = supralabial salivary gland
From Fry et al. 2008
Although developmental similarity is not conclusive proof of structural homology (similarity due to inheritance rather than due to other factors), these findings are consistent with the hypothesis that solenoglyphous, proteroglyphous, and at least some opisthoglyphous fangs are homologous structures. The hypothetical evolutionary trajectory was thus: some snakes evolved grooved fangs in the rear of their mouth. In a few cases (viperids, elapids, and atractaspidines), they subsequently lost the preceding teeth as what was formerly a rear fang became a tubular front fang. Other snakes retained their anterior teeth (at least some non-front-fanged colubroids), and still others developed fangs but then lost them (aglyphs such as ratsnakes). Evidence for this surprising final part comes from the formation of the maxilla and its teeth, which takes place in a single piece in pythons, but from two pieces in all fanged snakes as well as in ratsnakes, a pattern which supports a single evolutionary origin and subsequent loss of fangs. Additionally, vestigial Duvernoy's glands have been found in ratsnakes, egg-eaters, pareatid slug-eaters, and other nonvenomous aglyphs, a discovery that has led to the misleading generalization that all snakes are venomous and much subsequent misunderstanding among the non-scientific community. Toxic saliva does not a venomous animal make, as evidenced by the fact that even human saliva injected subcutaneously will produce pain and swelling.

Aglyphous

Both boas and pythons have only
aglyphous teeth, which is about
the only thing this film got right.
This word is used to describe unmodified teeth, essentially non-fangs. All snakes, even those that possess fangs of the first three types, have aglyphous teeth which they use for gripping their prey as they manipulate it during swallowing. As I just mentioned, many advanced snakes that today have only aglyphous teeth probably evolved from fanged ancestors. Several of these snakes, such as North American kingsnakes, ratsnakes, and bullsnakes, have atrophied Duvernoy's glands that lack toxin-producing serous cells. These snakes employ other sophisticated techniques, such as constriction, which is also used by more primitive snakes like boas and pythons (which did not evolve from fanged ancestors).

There are very few dangerous species of aglyphs, but one, Rhabdophis tigrinus, is becoming well-known as one of the only snakes capable of sequestering toxins from its prey for use in its own defense. This species has enlarged posterior maxillary teeth that lack grooves, so they are by definition aglyphous. However, it has relatively potent venom and has caused the deaths of several people. Among colubroids, the distinction between opisthoglyphs and aglyphs has never been entirely clear, but I'm distinguishing between them here because they are two of the four traditionally recognized types of snake teeth. Although the four types of snake teeth in this article are commonly discussed, a more accurate classification for snake teeth might be to divide them into tubular (the fangs of viperids, elapids, and atractaspidines), grooved (the rear fangs of non-front-fanged colubroids), and ungrooved (all other snake teeth).

Aglyphous (ungrooved) teeth and rear fangs of
Rhabdophis tigrinus
From Mittleman & Goris 1974
Happily for snake biologists like myself, the evolution of fangs opened the door for a massive evolutionary radiation of advanced snakes (>2800 species, or >80% of all living snake species). Although sophisticated venom delivery systems, of which fangs are just one of many integral parts, were clearly evolutionary advantageous, they have obviously also been costly at times, leading to their loss in ratsnakes, egg-eaters, and other lineages of advanced snakes. Also worth noting is that many lineages of basal snakes have got along just fine without venom, so there is not an inherent superiority of being venomous as the word "advanced" seems to imply. Rather, some have suggested that during periods of transition from forest to grassland, such as that which took place simultaneous to the dramatic colubroid radiation during the Miocene, snake taxa that were characterized by slow locomotion and constriction (boas & pythons) were supplanted by those characterized by rapid locomotion (many aglyphous colubrids) or passive immobilization (tubular- and grooved-fanged vipers, elapids, and atractaspidines that could use venom to catch their prey). Of course, both slow locomotion and constriction have subsequently been re-evolved among the colubroids, but there has been a lot of time since the Miocene.

ACKNOWLEDGMENTS

Thanks to Daniel Rosenberg (boomslang fang) and Nick Kiriazis (hognose fang) for use of their photographs.

REFERENCES

Bauchot R, editor. 2006. Snakes: A Natural History. New York, New York: Sterling Publishers. <link>


Cundall, D., (2002) Envenomation strategies, head form, and feeding ecology in vipers. In: Biology of the Vipers: 149-162. G. W. Schuett, M. Höggren, M. E. Douglas & H. W. Greene (Eds.). Eagle Mountain Publishers, Eagle Mountain, UT <link>



Greene, H. W. (1997) Snakes: The Evolution of Mystery in Nature. Berkeley: University of California Press <link>



Fry BG, Scheib H, van der Weerd L, Young B, McNaughtan J, Ramjan SR, Vidal N, Poelmann RE, Norman JA, 2008. Evolution of an arsenal: structural and functional diversification of the venom system in the advanced snakes (Caenophidia). Mol Cell Proteomics 7:215-246 <link>



Hayes, W. K., S. S. Herbert, G. C. Rehling & J. F. Gennaro, (2002) Factors that influence venom expenditure in viperids and other snake species during predator and defensive contexts. In: Biology of the Vipers: 207-234. G. W. Schuett, M. Höggren, M. E. Douglas & H. W. Greene (Eds.). Eagle Mountain Publishers, Eagle Mountain, UT <link>



Jackson K, 2002. How tubular venom‐conducting fangs are formed. J Morphol 252:291-297 <link>



Kardong, K. V. & T. L. Smith, (2002) Proximate factors involved in rattlesnake predatory behavior: a review. In: Biology of the Vipers: 253-266. G. W. Schuett, M. Höggren, M. E. Douglas & H. W. Greene (Eds.). Eagle Mountain Publishers, Eagle Mountain, UT <link>



Kardong KV, 1996. Snake toxins and venoms: an evolutionary perspective. Herpetologica 52:36-46 <link>



Kuch, U., J. Müller, C. Mödden & D. Mebs (2006). Snake fangs from the Lower Miocene of Germany: evolutionary stability of perfect weapons. Naturwissenschaften 93, 84-87



LaDuc, T. J., (2002) Does a quick offense equal a quick defense? Kinematic comparisons of predatory and defensive strikes in the Western Diamond-backed Rattlesnake (Crotalus atrox). In: Biology of the Vipers: 267-278. G. W. Schuett, M. Höggren, M. E. Douglas & H. W. Greene (Eds.). Eagle Mountain Publishers, Eagle Mountain, UT <link>



Mittleman M, Goris R, 1974. Envenomation from the bite of the Japanese colubrid snake Rhabdophis tigrinus (Boie). Herpetologica 30:113-119 <link>



Pyron, R. A., F. T. Burbrink, G. R. Colli, A. N. M. de Oca, L. J. Vitt, C. A. Kuczynski & J. J. Wiens (2011). The phylogeny of advanced snakes (Colubroidea), with discovery of a new subfamily and comparison of support methods for likelihood trees. Mol. Phylogenet. Evol. 58, 329-342 <link>



Savitzky AH, 1980. The role of venom delivery strategies in snake evolution. Evolution 34:1194-1204 <link>



Shea G, Shine R, Covacevich JC, 1993. Elapidae. In: Glasby C, Ross G, Beesley P, editors. Fauna of Australia. Canberra: AGPS <link>



Vonk FJ, Admiraal JF, Jackson K, Reshef R, de Bakker MA, Vanderschoot K, van den Berge I, van Atten M, Burgerhout E, Beck A, 2008. Evolutionary origin and development of snake fangs. Nature 454:630-633 <link>



Weinstein SA, Warrell DA, White J, Keyler DE, 2011. "Venomous" Bites from Non-Venomous Snakes: A Critical Analysis of Risk and Management of "Colubrid" Snake Bites. Amsterdam: Elsevier <link>



Weinstein SA, White J, Keyler DE, Warrell DA, 2013. Non-front-fanged colubroid snakes: A current evidence-based analysis of medical significance. Toxicon. 69, 103-113 <link>



Weinstein S, White J, Westerström A, Warrell DA, 2013. Anecdote vs. substantiated fact: the problem of unverified reports in the toxinological and herpetological literature describing non-front-fanged colubroid (“colubrid”) snakebites. Herpetological Review 44:23-29.



Wüster, W., L. Peppin, C. Pook & D. Walker (2008). A nesting of vipers: Phylogeny and historical biogeography of the Viperidae (Squamata: Serpentes). Mol. Phylogenet. Evol. 49, 445-459 <link>



Young BA, Dunlap K, Koenig K, Singer M, 2004. The buccal buckle: the functional morphology of venom spitting in cobras. J Exp Biol 207:3483-3494 <link>



Creative Commons License

Life is Short, but Snakes are Long by Andrew M. Durso is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License.

Tuesday, May 28, 2013

Basics of Snake Taxonomy


A while back, medical-doctor-turned-snake-blog-post-translator-extraordinaire1 Alvaro Pemartin asked me to write an article covering basic snake taxonomy. Taxonomy is the branch of biology that deals with naming and classifying organisms. Biologists still use the Linnean hierarchical system for taxonomy, which is convenient for grouping organisms, but there is a move towards using phylogenetic systematics and the evolutionary species concept in taxonomy, particularly in the sense that recognizing and giving names to non-monophyletic groups is discouraged.2 We'll primarily stick with the Linnean system in this article, which uses particular suffixes to denote the taxonomic level (for example, all animal families end in '-idae' and all subfamilies end in '-inae'). However, I've also included some cladograms, which are the most useful figures for understanding evolutionary relationships. If you haven't read one before, you can read up on them here, here, or here, but just know that they essentially work just like a family tree.

Snake Diversity

My only criticism of this film:
not enough snakes
There are about 3,400 species of snakes in the world. All are placed in the suborder Serpentes (aka Ophidia) of the order Squamata, which also includes lizards, from which snakes evolved about 190 million years ago during the Jurassic Period. Extant (modern or living) snakes are divided into two major groups, the blindsnakes (aka threadsnakes or scolecophidians) and the advanced or true snakes (alethinophidians). Advanced snakes are also divided into two non-monophyletic groups, the "older snakes" (henophidians) and the "recent snakes" (caenophidians). The vast majority of all living snakes, about 77% or 2,650 species, are caenophidians, including most of the snakes you've probably heard of: rattlesnakes, cobras, kingsnakes, and many others. A few well-known snakes are henophidians, namely boas and pythons. Most scolecophidians are poorly known. Let's break down each of these groups in slightly more detail.

Scolecophidians

Ramphotyphlops braminus,
a parthenogenetic blindsnake
There are about 400 species of scolecophidians, divided into five families and found mostly in the tropics. They are commonly called blindsnakes, because many have vestigial eyes as a result of their fossorial lifestyle, or threadsnakes, because most are very thin. Most have unspecialized ventral scales, shed in thick rubbery rings, and have a spine at their tail tip. Many eat termites and ants. Most are probably oviparous, or egg-laying, but their reproductive biology is poorly known. Scolecophidians diverged from alethinophidians about 125 million years ago during the Cretaceous Period. You can read more about a fascinating mutualism between a blindsnake and an owl here, or about basic blindsnake biology here.


Phylogenetic tree showing currently accepted hypotheses of snake relationships. Figure from Lee et al 2007.
Thick lines are supported by both morphological and molecular studies, thin solid lines are supported
primarily by similarity of morphology, dotted lines are supported primarily by molecular analyses.




"Henophidians"

Anilius scytale
Red Pipesnake
"Henophidians" are a diverse, if species-poor, group of snakes. I mentioned earlier that they are non-monophyletic, meaning that some henophidians are more closely related to caenophidians than others, which is why the name of their group is in quotation marks. All henophidians shared a common ancestor about 98 million years ago, during the Cretaceous Period. There is some pretty major uncertainty about how henophidians are related to one another, but many taxonomies divide them into four superfamilies (which end in '-oidea' under the Linnean system). The most primitive, the Uropeltoidea, is comprised of five families (Aniliidae, Tropidophiidae, Anomochilidae, Cylindrophiidae, and Uropeltidae) that lack the ability to open their mouths very widely. These snakes have stout skulls with few lizard-like teeth, short tails, and poorly developed ventral scales. Most are viviparous, meaning that they give birth to live young, except the anomochilids, which are oviparous. There is better evidence linking the former two and latter three groups than there is for combining all five families together into a single superfamily. Also, two enigmatic species in the genus Xenophidion might belong somewhere in here.

Calabaria reinhardtii,
the Cameroon Burrowing Boa,
the only oviparous booid
The rest of the henophidians together with the caenophidians are often called the macrostomatans, because they have the ability to open their mouths (Greek: stomata) very wide and consume very large (Greek: macro) prey items. The most primitive of these are the oviparous Pythonoidea, a superfamily including true pythons (Pythonidae) as well as two small lesser-known groups respectively known as the Asian and Neotropical sunbeam snakes, the xenopeltids and the loxocemids. Pythonoids and a superficially similar but surprisingly unrelated group, the  viviparous booids (consisting of true boas and their less well-known relatives, the ungaliophine dwarf boas and the erycine sand boas),  diverged from other henophidians about 75 million years ago. Finally, the most advanced henophidians, the oviparous splitjaw snakes (aka Round Island "boas" or bolyeriids), diverged just slightly later than or around the same time as the true boas. Because the splitjaw snakes constitute only a single family and were historically considered boas, you don't usually hear them referred to as a fourth superfamily.

Caenophidians


Acrochordus granulatus
Little Filesnake
This huge group is divided into two superfamilies, called Acrochordoidea and Colubroidea. The first is small, containing only three species of Acrochordus, the filesnakes of southeast Asia and north Australia. These diverged from other caenophidians about 60 million years ago. The second is huge and there is some uncertainty about the relationships therein, although thanks to recent work by Alex Pyron and his colleagues, the picture is becoming more clear. Traditionally, colubroids have been divided into groups based on their tooth morphology: those with fixed fangs were placed into Elapidae, those with folding fangs into Viperidae, and those without fangs lumped into Colubridae. The first two of these groups have proven to be for the most part monophyletic, certain exceptions notwithstanding. However, a more nuanced and accurate view of colubroid snake taxonomy is emerging thanks to a combination of molecular tools and decades of careful work by snake morphologists. Ready for it? Here it is:

Figure from Pyron et al. 2011
These snakes are exciting! These snakes have venom, excellent color vision, and sophisticated chemosensory, prey acquisition, and antipredator abilities. Also they have spines on their hemipenes. Also they are awesome. Can you tell which group is my favorite?

Dendrelaphis punctulatus
Common Treesnake
The traditional three-family tooth-morphology arrangement of colubroids has been replaced by the seven family arrangement seen above.3 Three of those seven families include several subfamilies. The most primitive colubroids are the xenodermatids, or odd-scaled snakes, which diverged from the others about 47 mya. The snail-eating pareatids are next, a group you'll be familiar with if you've been following this blog since the beginning. Next diverged the viperids or vipers, about 35 million years ago. There are three subfamilies of vipers: the old world viperines, the widespread crotalines (or pit vipers), and the monotypic Azemiopsinae, or Fea's Viper. True colubrids are still a large group, even though many species have been removed to the "new" families. The subfamilies are large and diverse, although most lack dangerous venom (a few species notwithstanding). You can read the story of the evolution of some of the subfamilies here. There are many well-known colubrids, including ratsnakes, kingsnakes, racers, hog-nosed snakes, and many others. Homalopsids, including some that chew their food, are a small but interesting group of semi-aquatic snakes found in southeast Asia. The front-fanged elapids (including cobras and coral snakes) have retained their monophyly, and little support has been found for recognizing the sea snakes as a separate family. Finally, we have the Lamprophiidae, a new family erected to contain former colubrids that turned out to be closer relatives of elapids. Lamprophiids also represent several interesting subfamilies, including the side-stabbing atractaspines, scale-polishing psammophines, and Malagasy pseudoxyrhophiines. I think Darren Naish would agree that there's plenty of fodder for future articles in these groups.

One a closing note, some non-snakes that are commonly mistaken for snakes, primarily because they have no legs, include:
  • Legless lizards: There are several groups of legless lizards. The North American glass lizards are among the most familiar. All have external ear openings and most have eyelids. In one sense, snakes are but one very diverse group of legless lizards.
  • Amphisbaenians: These are also technically lizards, but under some older taxonomies they are referred to as a separate group of reptiles, because they have a vestigial right lung and have a unique skeletal structure.
  • Caecilians: These most primitive of amphibians have slimy skin and are found underground in the world's tropics. Many are common prey of coral snakes.
  • Eels: Elongate fishes that actually do have limbs in the form of fins. There are several groups of fishes that are all colloquially called eels, including spiny eels, fire eels, electric eels, and true eels (Anguilliformes). Some amphibians are also sometimes called eels, including amphiumas or conger eels, sirens or mud eels, and rubber eels, a kind of caecilian.
  • Worms: There are several different major groups of worms, including roundworms (nematodes), flatworms (platyhelminths), and segmented worms (annelids).
Snake taxonomy is a complicated field and there is still much disagreement among experts. I have made several oversimplifications above, so if this is your area of expertise feel free to chime in with a comment or two. I hope you're looking as forward to reading more about many of these groups as I am looking forward to writing about them.




1 His wife tells me that mediocre is actually more accurate




2 A monophyletic group is one that contains a common ancestor and all of its descendants. Examples include groups like animals, vertebrates, mammals, birds, amphibians, primates, and snakes. A non-monophyletic group is one that either omits some descendants (e.g., "reptiles", which does not include birds, or "fishes", which does not include tetrapods) or omits the common ancestor (e.g., warm-blooded vertebrates, which includes mammals and birds but not their cold-blooded common ancestor).


ACKNOWLEDGMENTS

Thanks to ptrick127, Gary Nafis, Tein-Shin Tsai, and Stephen Zozaya for use of their photos.

REFERENCES

Lee, M. S. Y., A. F. Hugall, R. Lawson, and J. D. Scanlon. 2007. Phylogeny of snakes (Serpentes): combining morphological and molecular data in likelihood, Bayesian and parsimony analyses. Systematics and Biodiversity 5:371-389 <link>

Pyron, R. A., F. Burbrink, and J. J. Wiens. 2013. A phylogeny and revised classification of Squamata, including 4161 species of lizards and snakes. BMC Biology 13. DOI: 10.1186/1471-2148-13-93 <link>

Pyron, R. A., F. T. Burbrink, G. R. Colli, A. N. M. de Oca, L. J. Vitt, C. A. Kuczynski, and J. J. Wiens. 2011. The phylogeny of advanced snakes (Colubroidea), with discovery of a new subfamily and comparison of support methods for likelihood trees. Molecular Phylogenetics and Evolution 58:329-342 <link>

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Life is Short, but Snakes are Long by Andrew M. Durso is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License.