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Showing posts with label Ramphotyphlops. Show all posts
Showing posts with label Ramphotyphlops. Show all posts

Friday, October 30, 2015

Are there any countries without snakes?


Global distribution of all snake species combined
Public domain from Wikipedia
Terrestrial data from Ernst & Ernst (2011) and Cogger et al. (1998)
Sea snake data based on Campbell & Lamar (2004), Phillips (2002),
Ernst & Ernst (2011), and Spawls & Branch (1995)
Snakes are found in almost every country in the world, but there are a few places without wild1 snakes. Snake-free land generally falls into two categories: remote islands, mostly formed by volcanism or as atolls, that have never been part of a continental land mass and/or have been isolated from continents for a long time, and continental areas that are or were covered by ice within the last 26,000 years and haven't been recolonized since (for example, there are snake fossils from northern Canada, where no snakes live now, from a time when it was much warmer). There are also snake-free parts of the oceans, and probably there are some urban areas that are so disturbed that no snakes live there any more (e.g., downtown Manhattan), although they once did.

Iceland

Iceland is a volcanic archipelago just outside the Arctic Circle. Despite its high latitude, Iceland is warmed by the Gulf Stream and has a temperate climate, so snakes might actually do fairly well there, especially if they could take advantage of its plentiful geothermal features, as the high-altitude hot-spring snakes of Tibet (genus Thermophis) have done. However, Iceland has never been connected to any continent—instead, it was formed about 20 million years ago by a series of volcanic eruptions in the Mid-Atlantic Ridge, which separates the Eurasian and North American plates. It's been at about its current latitude the entire time, and, as far as anyone knows, has never been colonized by snakes. Today, the closest snakes are adders (Vipera berus) in both Scotland (470 mi away) and Norway (600 mi away), both of which are separated by a great deal of very cold ocean.

Ireland

Unlike Iceland, Ireland was once connected to other land masses. Parts of it are at least 1.7 billion years old. At the end of the Precambrian, two pieces of rock that would become Ireland could be found beneath the sea, one piece connected to the continent of Laurentia and the other piece to the smaller continent of Avalonia, both around 80° South. Over the next 50 million years, these two parts drifted northward, eventually uniting and breaking sea level near the equator about 440 million years ago, in the Silurian Period. Throughout the late Paleozoic Era, Ireland sank back under the sea and gained 65% of its modern mass as limestone deposits from huge coral reefs. At the beginning of the Mesozoic, Ireland was at the latitude of present-day Egypt and had a desert climate, and by the time snakes evolved (150 million years ago, in the late Jurassic-early Cretaceous) Ireland had separated from any other land mass, and has been connected on and off to this day. There is some debate over how recently a land bridge connected Ireland with Great Britain and, by extension, mainland Europe, with the consensus resting on the idea that Ireland was isolated by ocean by 16,000 years ago, at which time the climate was still quite cold and there was a lot more ice in Ireland than there is now. Although it's not insane to think that snakes might have colonized Ireland from Europe sometime during the 90 million years that preceded the Pleistocene Ice Ages, as they have since re-colonized Great Britain, so far no one has found any snake fossils in Ireland. But, viviparous lizards, natterjack toads, and common frogs have managed to make it to Ireland, and the slowworm has been introduced there, so it could happen one day. Likely successful colonists include adders (Vipera berus), grass snakes (Natrix natrix), or smooth snakes (Coronella austriaca) from Great Britain, France, or Scandinavia. The Irish climate is highly moderated by the gulf stream, with much milder winters than expected for such a northerly area, so snakes could do quite well there.

Cape Verde

Cape Verde is an island country consisting of 10 volcanic islands in the central Atlantic Ocean, 350 miles off the coast of the western African countries of Mauritania and Senegal. The Cape Verde Islands were all formed by the same volcanic hot spot, the oldest 26 million years ago and the youngest just 100,000 years ago. They have never been colonized by snakes from mainland Africa. There is a single reference to the Striped Sand Snake (Psammophis sibilans) on the island of Sal in a 1951 paper that, according to the authors, was an accidental introduction from Guinea-Bissau. Neither this snake nor any other has ever been recorded again from Cape Verde, although the archipelago is home to 31 endemic lizard species, more than any other island chain in the Macaronesian region.

New Zealand

New Zealand was part of Gondwana (aka Gondwanaland), the more southerly of the two supercontinents formed by the breakup of Pangaea 200-180 million years ago. Gondwana comprised the present-day continents of South America, Africa, Australia, India, and Antarctica as well as New Zealand. Today, New Zealand is the highest part of a mostly-submerged continent called Zealandia that broke away from Gondwana between 100 and 80 million years ago. Since that time, New Zealand has developed a unique flora and fauna that does not include any terrestrial snakes, which makes sense since it has been isolated since around the dawn of their evolution (and has been mostly submerged several times since). However, a steady trickle of reports of sea snakes, borne by oceanic currents beyond their normal range to New Zealand waters and beaches, was summarized in 1997, at which time an amazing 69 records of 2 species were known, dating back to 1837 (more records and a third species have been added since). About 90% are of pelagic sea snakes (Hydrophis platurus; formerly Pelamis platurus, also known as yellow-bellied sea snakes), a very widespread species that is infamous for vagrancy and recently made headlines when one washed ashore in Ventura County, California. The remaining 10% of records are of banded sea snakes (Laticauda colubrina), a species that normally sticks more closely to shores, and judging by their morphology most of these have likely come to New Zealand from Fiji or Tonga. In 1995, one specimen in the British Museum collected in New Zealand in 1925 and formerly classified as L. colubrina was re-identified as a new species from New Caledonia, L. saintgironsi, by herpetologists revising the widespread Laticauda colubrina complex.

Map of pelagic sea snake records from New Zealand
(1837-1997)
From Gill 1997
High sea surface temperatures in 1969-1975 and again in 1988-1990 coincided with major influxes of tropical and subtropical fishes, sea turtles, and sea snakes (up to 16 a year) carried to New Zealand waters by the East Australian Current. Most records are of single animals, but in March 1985 four H. platurus were found on Tokerau Beach in Northland. About three-quarters of sea snake records are from Austral autumn (March-May), and many are from the north coast of the north island, but H. platurus has been found all around the North Island, including in the Cook Strait, and once even on the north coast of the South Island (at Pakawau, Golden Bay, in March 1974)! All L. colubrina records are from the north-east coast of the North Island, except for one at Castlepoint, Wairarapa, in August 1977. All records are of adult snakes, and most (79%) were alive when found, usually washed ashore, but occasionally swimming freely. One even swam up a stream near the sea! Even more amazingly, several sea snakes have been found alive inland from the coast, including a May 1938 record of H. platurus "some distance" from the sea at Table Cape on the Mahia Peninsula, a January 1990 record of L. colubrina "well above" the high-tide line at Whangaruru Harbour, an April 1938 record of H. platurus 200 feet from the sea on a lawn at New Plymouth, and, most incredible, a September 1945 record of L. colubrina alive at Te Aroha, near Hamilton, which is over 12 miles from an estuary over a range of hills or over 27 miles from the ocean along the Waihou River. Unlike H. platurus, which is almost incapable of moving on land, L. colubrina is reasonably good at terrestrial locomotion, which could explain the inland presence of these snakes. Alternatively, the author of the review paper suggested that the snakes could have been carried inland by birds.2

New Zealand also owns the Chatham Islands 560 miles to the east, the Kermadec Islands 620 miles to the north, and Tokelau 2000 miles to the northeast3, but no sea snakes have been reported from these islands, probably because so few people live there. Like vagrant birds, even the records from mainland New Zealand surely represent just a small percentage of the total number of marine reptiles that have reached New Zealand over the years. However, New Zealand is still widely considered to have no native snakes, since H. platurus  stop feeding at sea temperatures below 18°C and die at temperatures between 14.5 and 17°C (the average sea temperature in the coldest month in northern New Zealand is 16°C).

Kiribati

Kiribati is a Pacific Island nation that straddles the region of the central Pacific Ocean where the Equator and the International Date Line cross, making it the only country that is in all four hemispheres. It consists of four island groups totaling 32 atolls and one coral island. Of these, approximately the eastern half (the Phoenix and Line Islands) are apparently devoid of snakes; at least, they are listed as having no snakes in the most up-to-date and authoritative guide to the reptiles of the Pacific Islands. This guide takes a conservative approach in listing only species that are confirmed by a museum specimen or literature record, so it's possible that at least pelagic sea snakes are found in the waters of eastern Kiribati. What is certain is that the western half of Kiribati (Banaba and the Gilbert Islands) is home to breeding populations of banded sea snakes (Laticauda colubrina), and possibly pelagic sea snakes as well. Additionally, there is a single record of an ornate reef seasnake (Hydrophis ornatus), a species that is normally found much farther west, from the Gilbert Islands. This might represent a vagrant, but more likely it is a misidentified or mislabeled specimen. So, Kiribati has no terrestrial snakes, unless you count banded sea snakes, which mate, lay eggs, and sometimes digest food on land, but hunt, catch prey, and spend much of their time in the ocean.

Tuvalu

Tuvalu is a Pacific Island nation south of Kiribati comprising three reef islands and six atolls and totaling 10 square miles, making it the fourth smallest country in the world. Like Kiribati, Tuvalu has no terrestrial snakes unless you count L. colubrina, but unlike Kiribati it has literature records of pelagic sea snakes off its shores. Happily, Tuvalu has decided to honor this species by putting it on one of its coins! It's a commemorative coin rather than a coin that's actually part of normal circulation, but still, it's pretty cool to have a snake on your money. Tuvalu is also home to at least 9 species of lizards and the introduced cane toad, so it's possible that snakes could show up there one day. In fact, it's even possible that a native, endemic blindsnake could have escaped detection on Tuvalu (or any other Pacific island) to this day. The only reason the Federated States of Micronesia aren't on this list is because of two unexpected species of endemic blindsnakes, Ramphotyphlops adocetus and R. hatmaliyeb, described in 2012 from two small islands, one in the eastern part of FSM and the other in the western part.

Nauru

Nauru is a relatively isolated Pacific Island nation and is one of the only countries smaller than Tuvalu (at 8.1 square miles, only Monaco and Vatican City, both in Europe, are smaller). Unlike many Pacific Island nations, Nauru is a single island. Nauru has no native terrestrial snakes, but it does have H. platurus off its shores, and it also has what is likely an introduced species, the ubiquitous Indotyphlops braminus or Brahminy Blindsnake, the only unisexual species of snake. It's actually amazing to me that we're on the seventh entry and haven't encountered this species yet, considering how widespread it is globally. The original native range of I. braminus is unknown, but it probably evolved in continental Asia. Because a single individual constitutes a reproductively-competent population, it has since spread all over the world, and it's unclear how long it has been established on Nauru or elsewhere in the Pacific. Many similarly-widespread species in the Pacific owe their distribution to human-assisted transport, the precise timeline of which is difficult to determine. Given the harm done to Nauru's environment by phosphate mining during the 20th century, it's unlikely that any native terrestrial snake would have survived.

Marshall Islands

The Marshall Islands (see above map) have close political ties with the USA, but they are self-governing. They are located north of Kiribati, west of the FSM, and south of Wake Island. The authoritative guide to the reptiles of the Pacific Islands lists only I. braminus from the Marshall Islands, but other sources suggest that at least a few brown treesnakes (Boiga irregularis), infamously introduced to Guam, have been found there as well, and it's possible that H. platurus and possibly other sea snakes are found off its shores. Both the Gilbert Islands in Kiribati to the south and Pohnpei and Kosrae in FSM to the west have L. colubrina, although an official page states that the Marshall Islands have no sea snakes. So, as far as we know the Marshall Islands have no snakes that are native and terrestrial (unless you count I. braminus as native, considering that we don't know how long it's been there).

Vatican City

The Vatican is a walled enclave within the city of Rome, Italy, with an area of 110 acres and a population of 842, making it the smallest internationally-recognized independent state in the world, both by area and population. I couldn't find any references confirming or denying the presence of wild snakes in the Vatican, but other wildlife seem to be pretty minimal, which makes sense considering that Rome has been a large city for thousands of years. But, snakes and other wildlife can hang on in some amazingly urbanized places, so I wouldn't completely rule out the presence of a few of the eight species of snakes that can surely be found in the surrounding Italian countryside. Monaco, another European microstate with a very dense population and a high degree of urbanization, is another possibility for a snake-less nation, although, given Monaco's reputation as a playground for the rich and famous (30% percent of its population are millionaires), there are certainly some who meet an alternate definition of the word "snake" within its walls.

Cover of a joke book that's blank inside
So there you have it: a maximum of ten countries out of 196 "without snakes", depending on where you want to draw the line. If we start expanding into territories or disjunct sections of larger countries, the list grows considerably, including places like Greenland, the Falkland Islands, Bermuda, Hawaii4, Wake Island, Johnston Atoll, Howland & Baker Islands, the Marquesas Islands, the Pitcairn Islands, Sala y Gomez, Isla Malpelo, St. Helena, the Faroe Islands, the Isle of Man, many Arctic and Antarctic islands, and Antarctica itself, which is owned by no country. And of course, as you can see from the map at the top, there are also large mainland areas of northern Europe, Asia, and North America, as well as the southern tip of Patagonia, that are too cold for snakes (although Vipera berus gets above the Arctic Circle in Scandinavia), not to mention the Atlantic, Arctic, and Antarctic Oceans5.

In the course of the research I did for this post, I found many travel articles promoting the snakelessness of some of these places as overwhelmingly positive, as I'm sure it is for many ophidiophobic travelers. But, the risk that snakes pose is way, way smaller than the fear we have of them, and in my mind the real danger is that many people see eradication of snakes as a positive thing, despite the fact that many of them are in real danger of extinction. Mauritius barely made it off this list, with one of two native species extinct and the other hanging on thanks only to captive breeding and reintroduction efforts. St. Kitts & Nevis could lose its only native snake, the Saba or orange-bellied Racer (Alsophis rufiventris), and native snakes have gone extinct or become critically endangered on many other islands throughout the Pacific and Caribbean due to centuries of forest clearance, overgrazing, development, and the introduction of invasive species, not to mention the many continental snake species threatened by sprawling development and habitat fragmentation. So, please, let's keep this list from growing.



1 Given the growing popularity of herpetoculture, I'd be willing to bet that there are captive snakes in every country, although a few countries have stringent laws banning any captive snakes, including as pets as well as in zoos and research facilities.



2 Studies have shown that, although many Pacific birds avoid pelagic sea snakes, naive Atlantic birds will try eat them (only to throw them up, since they are apparently poisonous as well as venomous). New Zealand's birds might be sufficiently naive to try to eat one.



3 Zug's Reptiles and Amphibians of the Pacific Islands lists Tokelau as having no snakes, not even sea snakes, but does not cover the Chatham or Kermadec Islands.



4 Hawaii has introduced Brahminy Blindsnakes and, unlike many Pacific Islands, it is known that these colonized the island chain more recently, in 1930, when they were imported from the Philippines in potted palm trees. Hawaii also has pelagic sea snakes and there are a few records of introduced brown treesnakes and boa constrictors, but neither species has established a breeding population (yet).



5 A study evaluating the probability that pelagic sea snakes could enter the Caribbean and Atlantic through the Panama canal, as lionfish have, concluded that there were no real barriers to their colonization of the eastern side of the Americas, but so far this has not happened.


ACKNOWLEDGMENTS

Thanks to Kerry Nelson for doing some of the background research for this post as part of a discussion in the Wild Snakes: Education & Discussion Facebook group.

REFERENCES

Edwards, R. J., and A. J. Brooks. 2008. The Island of Ireland: Drowning the Myth of an Irish Land-bridge? Pages 19-34 in J. J. Davenport, D. P. Sleeman, and P. C. Woodman, editors. Mind the Gap: Postglacial Colonisation of Ireland. Special Supplement to The Irish Naturalists’ Journal <link>

Gill, B. J. 1997. Records of turtles and sea snakes in New Zealand, 1837-1996. New Zealand Journal of Marine and Freshwater Research 31:477-486 <link>

Heatwole, H., S. Busack, and H. Cogger. 2005. Geographic variation in sea kraits of the Laticauda colubrina complex (Serpentes: Elapidae: Hydrophiinae: Laticaudini). Herpetological Monographs 19:1-136 <link>

Hecht, M. K., C. Kropach, and B. M. Hecht. 1974. Distribution of the yellow-bellied sea snake, Pelamis platurus, and its significance in relation to the fossil record. Herpetologica 30:387-396 <link>

McKeown, S. 1996. A Field Guide to Reptiles and Amphibians in the Hawaiian Islands. Diamond Head Publishing.

Vasconcelos, R., J. C. Brito, S. Carranza, and D. J. Harris. 2013. Review of the distribution and conservation status of the terrestrial reptiles of the Cape Verde Islands. Oryx 47:77-87 <link>

Wynn, A. H., R. P. Reynolds, D. W. Buden, M. Falanruw, and B. Lynch. 2012. The unexpected discovery of blind snakes (Serpentes: Typhlopidae) in Micronesia: two new species of Ramphotyphlops from the Caroline Islands. Zootaxa 3172:39–54 <link>

Zug, G. R. 2013. Reptiles and Amphibians of the Pacific Islands: A Comprehensive Guide. University of California Press, Berkeley, California, USA <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, July 7, 2015

Snakes that decapitate their food

Crab-eating Snake (Fordonia leucobalia) eating a crab
A few years ago I wrote an article about southeast Asian crab-eating snakes, the only snakes (at the time) known to break apart their food instead of swallowing it whole. Although I ended that article by wondering how many more strange snake dietary adaptations we might discover, I didn't actually anticipate writing a sequel to that article—it was so unique that the BBC filmed it for their series Life in Cold Blood, and I doubted that anyone would discover another snake that tore apart its prey. You can imagine my surprise when recently I was asked to review a paper about another snake that breaks its food apart! I was also delighted that this snake was a scolecophidian, because I feel that they are underrepresented both on this blog and in snake biology in general. It is a bit unsatisfying that it is the Brahminy Blindsnake (Indotyphlops braminus, formerly known as Ramphotyphlops braminus), the best studied scolecophidian by far by virtue of its enormous range and unusual breeding habits, but I think this exciting discovery could become extended to some or most of the other >400 species of blindsnakes.

A blindsnake with decapitated termite heads
stuck to the back of its head
Late last year, herpetologist Yosuke Kojima, a postdoctoral researcher at Kyoto University, and entomologist Takafumi Mizuno, a graduate student at Kyoto Institute of Technology, made a chance finding. They had been close friends since elementary school and shared an interest in behavioral and chemical ecology. Together, they planned some experiments to learn more about interactions between blindsnakes and their primary prey, ants. Mizuno's lab also kept colonies of termites (in this case, Reticulitermes speratus), which are also eaten by blindsnakes. Blindsnakes are unusual in that they eat many small prey at a time rather than a few large prey infrequently. Blindsnakes often eat 20 or more prey items at a time, and the maximum number of prey items ingested by a single individual is 1,431 for Anilios (Ramphotyphlops) nigrescens from Australia. Because blindsnakes often gorge themselves when feeding in an ant or termite nest, they often eat very quickly, using a raking technique of the mandibles (in leptotyphlopids) or of the maxillae (in typhlopids). Nate Kley's lab at Stony Brook University has taken some fantastic videos of blindsnake feeding techniques.

Time-sequence of a blindsnake ingesting and decapitating
a termite worker. From Mizuno & Kojima 2015
Supplementary video here
As Mizuno fed termites to the blindsnakes, he observed something very unusual. The blindsnakes typically grabbed and swallowed the termites backwards. Most snakes usually swallow their prey head-first, so this was weird enough. But, it gets weirder. Often, when the snake had maneuvered a termite so that only its head stuck out of the snake's mouth, it would rub its face on the bottom of the tank, decapitating the termite. All of the termite soldiers and about half of the termite workers offered to the blindsnakes were decapitated. Occasionally, a snake would regurgitate a termite that it had consumed whole, decapitate it, and re-consume the body. Decapitated termite heads became attached to the back of the snake’s head or were scattered around the bottom of the cage. The snakes never ate the decapitated heads. There did not appear to be a cost to decapitation—whether a snake decapitated a termite or not, the time required to completely ingest it was about 3 seconds. However, twice blindsnakes were observed swallowing termites head-first, which took only about 1-1.5 seconds. This may not seem like a big difference, but when you're eating hundreds or thousands of prey items in one sitting, it can add up!

Intact termite heads in the feces of a blindsnake
From Mizuno & Kojima 2015
Why do blindsnakes remove the heads of their prey? One reason might be that termite heads contain glands full of toxic chemicals called terpenes. But, unlike predators that remove the skin of various amphibians to avoid the toxins in their skin glands, blindsnakes don't always remove the heads of their prey, suggesting that they aren't that susceptible to terpene poisoning. It's even been suggested that some blindsnakes might be sequestering defensive chemicals from the ants and termites that they eat, just as gartersnakes sequester tetrodotoxin from newts, in which case they might actually prefer the part of the termite with more chemicals. A more likely hypothesis is that the heads are less digestible than the termites' bodies. Between 26 and 100% of the termite heads consumed by blindsnakes in Mizuno & Kojima's experiment remained undigested in the snakes' feces. Additionally, the snakes preferred to eat the worker termites rather than the more heavily-armored soldier termites, and the few soldier termites they did eat were newly-molted. Removing the termites' scleritized heads might allow blindsnakes to pack more soft, squishy bodies into their stomachs, maximizing the nutrition they get out of their meals. It's a bit like you or me peeling a banana or an orange, or removing the husk from a coconut. Since soldier termites have pinching mandibles, removing their heads might also prevent the blindsnakes from being bitten from the inside, which is a bit like you or me...removing the horns of a cow before eating it, if we ate cows alive and whole, I guess?

Evidently the raking maxillae of typhlopids
are sufficiently dexterous to manipulate
prey inside the mouth to position them
for decapitation.
From Kley 2001
Since snakes don't have hands, they've got to remove any indigestible parts using the only maneuverable part they do have—their jaws. Unlike other blindsnakes (which use bilaterally synchronous jaw movements similar to those of all other vertebrates) but like alethinophidians, typhlopid blindsnakes can move the left and right sides of their highly mobile upper jaws independently and asynchronously. Despite its sophistication, the ratcheting movements of their maxillary raking mechanism are insufficient, by themselves, to allow them to decapitate their prey. We must await further functional-morphological studies to assess the role of the toothless lower jaw, which could act as a wedge or blade, in this process. Since snakes cannot really "bite", arthropods, with their jointed limbs and bodies, might be the only type of prey that a snake could pull apart. There are a fair number of snakes that eat arthropods, but most of them are relatively obscure. Besides the crab-eating snakes, one might look for prey-dismembering behavior in sonorines, a tribe of desert-dwelling snakes from southwestern North America, other North American snakes such as the colubrines Tantilla and Opheodrys and the natricine Regina, the dwarf racers of Africa and the Middle East (genus Eirenis), the centipede-snakes of Africa (genus Aparallactus), or certain kukrisnakes (genus Oligodon). In addition to the typhlopid blindsnake in this study, two short notes from the 1950s and 60s document similar decapitation behaviors in two different species of leptotyphlopids (Epictia goudotii [formerly Leptotyphlops phenops] from Central America and Rena dulcis [formerly L. dulcis] from Texas), despite their radically different jaw morphology. I won't be surprised if it turns up in other scolecophidian families as well, since this most-basal group of living snakes probably co-evolved with the early radiation of ants and termites, their favorite prey.

ACKNOWLEDGMENTS

Thanks to Brendan Schembri for the use of his photo, and to Takafumi Mizuno and Yosuke Kojima for giving me the opportunity to write about their discovery in advance of its publication and for translating it into Japanese.

REFERENCES

Kley, N.J. 2001. Prey transport mechanisms in blindsnakes and the evolution of unilateral feeding systems in snakes. American Zoologist 41:1321-1337 <link>

Mizuno, T. and Y. Kojima. In press. A blindsnake that decapitates its termite prey. Journal of Zoology 10.1111/jzo.12268 <link>

Prestwich, G.D., B. Bierl, E. Devilbiss, and M. Chaudhury. 1977. Soldier frontal glands of the termite Macrotermes subhyalinus: Morphology, chemical composition, and use in defense. Journal of Chemical Ecology 3:579-590 <link>

Reid, J.R. and T.E. Lott. 1963. Feeding of Leptotyphlops dulcis dulcis (Baird and Girard). Herpetologica 19:141-142  <link>

Savitzky, A.H., A. Mori, D.A. Hutchinson, R.A. Saporito, G.M. Burghardt, H.B. Lillywhite, and J. Meinwald. 2012. Sequestered defensive toxins in tetrapod vertebrates: principles, patterns, and prospects for future studies. Chemoecology 22:141-158 <link>

Shine, R. and J.K. Webb. 1990. Natural history of Australian typhlopid snakes. Journal of Herpetology 24:357-363 <link>

Smith, H.M. 1957. Curious feeding habit of a blind snake, Leptotyphlops. Herpetologica 13:102 <link>

Stokes, A.N., A.M. Ray, M.W. Buktenica, B.G. Gall, E. Paulson, D. Paulson, S.S. French, E.D.B. III, and J. E.D. Brodie. 2015. Otter predation on Taricha granulosa and variation in tetrodotoxin levels with elevation. Northwestern Naturalist 96:13-21 <link>

Vidal, N., J. Marin, M. Morini, S. Donnellan, W.R. Branch, R. Thomas, M. Vences, A. Wynn, C. Cruaud, and S.B. Hedges. 2010. Blindsnake evolutionary tree reveals long history on Gondwana. Biology Letters 6:558-561 <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.

Tuesday, April 22, 2014

The most widespread snake in the world


Global distribution of snakes
Snakes are found in almost all parts of the world, with the exception of New Zealand and Ireland, the polar regions, the Atlantic Ocean, and some very urban areas. Many species are very widespread. Pelagic Sea Snakes (Pelamis platurus) are probably found over the greatest percentage of the Earth's surface, although they are entirely marine. On land, Ring-necked Snakes (Diadophis punctatus) and Racers (Coluber constrictor) are found throughout North America, European Adders (Vipera berus) from Spain to Kamchatka and above the Arctic Circle, Grass Snakes (Natrix natrix) from Great Britian to Mongolia, and Gaboon Vipers (Bitis gabonica) from Africa's Gold Coast to its Great Rift Valley. However, the title of "most widespread snake in the world" goes to the tiny Brahminy Blindsnake (Ramphotyphlops braminus), named after Hinduism's Brahmin caste.

Map of locations of Brahminy Blindsnakes
Modified from DiscoverLife and Kraus's database
Most dots represent introduced localities
Brahminy Blindsnakes are found on nearly every continent and on countless islands, mostly in the tropics. They are so successful at least in part because they are the only unisexual species of snake. There are no male Brahminy Blindsnakes. There never have been and there never will be. Instead, each female lays about 4 rice-grain-sized eggs a year, which hatch into sewing-needle-sized daughters identical to each other and to their mother. If that doesn't sound very fecund, it's because it isn't - it doesn't have to be! In spite of their low reproductive output, Brahminy Blindsnakes have spread over most of the world, because just a single individual is capable of founding a new population. In fact, we don't even really know where the original native range of the Brahminy Blindsnake was. It is most common in southern Asia, where it was first discovered in 1796, so it's likely that it originated somewhere around there, but it's difficult to say for sure. Usually, biologists can exploit differences in the genetics or morphology of a widespread species to figure out where it came from. Attempts to uncover the geographic origin of Brahminy Blindsnakes have been unsuccessful because all Brahminy Blindsnakes are clones of one another, so there is almost no variation to analyze!

How did this species evolve? The leading theory for most unisexual species of reptiles, amphibians, and fishes involves a hybrid origin, where two or more "parent" species contribute genes. In most unisexual amphibians and fishes, sperm from a male (often of one of the parent species, but sometimes any sperm will do) is required to initiate development of the eggs but does not contribute genetic material. This is not the case for lizards or for the Brahminy Blindsnake, which are truly parthenogenetic. Which were the parent species of the Brahminy Blindsnake? We don't know. Of the 400-odd blindsnake species, the Brahminy Blindsnake is probably one of the best known due to its wide distribution and peculiar reproductive habits. Some recent phylogenies have shown that it is closely related to the South Indian Blindsnake (Typhlops pammeces), and others to an undescribed species of Sri Lankan blindsnake, both consistent with the hypothesis that south Asia is the species' center of origin. One very recent analysis suggested reclassifying all three species into a new genus, Indotyphlops. Because up to a quarter of all blindsnake species are still undescribed, it's possible that the parent species are as-yet unknown to science.

Image from O'Shea et al 2013
You guessed it, that's a Brahminy Blindsnake
These days Brahminy Blindsnakes mostly get around through the horticulture trade, although in the past they may have hitchhiked along with Pacific Islanders. Snakes are generally good dispersers, with the ability to go without food for long periods of time and squeeze into tight spaces, which might help explain why they have successfully colonized most of the world. Of all the fantastic voyages Brahminy Blindsnakes must have undergone, one of the most amazing is that documented by herpetologist and TV personality Mark O'Shea in East Timor. He and his team found a live Brahminy Blindsnake coming out of the back end of a toad, demonstrating the snakes' resilience to even the most caustic of environments.

Most of the time, an introduced species has about a 50/50 chance of successfully establishing itself in a new environment. Given how widespread Brahminy Blindsnakes are and their infamy as invaders, you might ask whether an introduced population of Brahminy Blindsnakes has ever failed to become established? A comprehensive database of reptile introductions includes only two such instances, one in southern Arizona and one in New Zealand. In Arizona, a population has subsequently become established despite the arid climate, but New Zealand is probably too cold for blindsnakes, and they take introduced species very seriously there. Nevertheless, the Brahminy Blindsnake will probably continue to spread, at least throughout the tropical regions of the world. The literature is full of first reports of this species, so much so that at least one was reported twice! Amazingly, both specimens were bicycle casualties collected in the same suburb of Cairo, leading the second author to title his article "How many times can a flower-pot snake be run over for the first time?"


ACKNOWLEDGMENTS

Thanks to Todd Pierson for his photograph and to Phil Rosen, Jeff Servoss, Don Swann, Michael Lau, and Skip Lazell for bringing me up to date on the latest in blindsnake biology.

REFERENCES

Baha el Din, S. M. 2001. On the first report of Ramphotyphlops braminus from Egypt: how many times can a flower-pot snake be run over for the first time? Herpetological Review 32:11.

Hedges, S., A. Marion, K. Lipp, J. Marin, and N. Vidal. 2014. A taxonomic framework for typhlopid snakes from the Caribbean and other regions (Reptilia, Squamata). Caribbean Herpetology 49:1-61 <link>

Kamosawa, M. and H. Ota. 1996. Reproductive biology of the brahminy blind snake (Ramphotyphlops braminus) from the Ryukyu archipelago, Japan. Journal of Herpetology 30:9-14.

Kraus, F. 2009. Alien reptiles and amphibians: a scientific compendium and analysis series. Springer, Dordrecht <link>

Nussbaum, R. A. 1980. The brahminy blind snake (Ramphotyphlops braminus) in the Seychelles Archipelago: distribution, variation, and further evidence for parthenogenesis. Herpetologica 36:215-221 <link>

O'Shea, M., A. Kathriner, S. Mecke, C. Sanchez, and H. Kaiser. 2013. ‘Fantastic Voyage’: a live blindsnake (Ramphotyphlops braminus) journeys through the gastrointestinal system of a toad (Duttaphrynus melanostictus). Herpetology Notes 6:467-470 <link>

Ota, H., T. Hikida, M. Matsui, A. Mori, and A. H. Wynn. 1991. Morphological variation, karyotype and reproduction of the parthenogenetic blind snake, Ramphotyphlops braminus, from the insular region of East Asia and Saipan. Amphibia-Reptilia 12:181-193.

Wynn, A. H., C. J. Cole, and A. L. Gardner. 1987. Apparent triploidy in the unisexual brahminy blind snake, Ramphotyphlops braminus. American Museum Novitates 2868:1-7 <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.

Thursday, February 13, 2014

Snakes that Give Virgin Birth

In continuing association with the group that brought you the #SnakesAtYourService December blog carnival, this post is part of the new Reptile & Amphibian Blogging Network's first event, #HerpsAdapt. Starting on February 12th (in honor of Charles Darwin’s birthday), this event will showcase the remarkable evolutionary abilities of reptiles and amphibians.



One of several excellent new science mnemonics
from the popular webcomic xkcd
Virgin birth (a form of asexual reproduction) has fascinated humans for centuries. Recently, biologists have uncovered many of the mysteries associated with the ability of some animals to produce offspring without ever mating. This phenomenon is common in bacteria, most fungi, many plants, and some invertebrate animals, where it takes many forms. It is relatively uncommon in vertebrates, although a few species of fishes, amphibians, and reptiles reproduce using a form of asexual reproduction called parthenogenesis, which is when an embryo develops from an unfertilized egg cell. Parthenogenesis can be facultative or obligate. Species with facultative parthenogenesis can also reproduce sexually (and usually do), whereas species with obligate parthenogenesis cannot and are usually all-female. Both types of parthenogenesis are found in snakes, and several new examples have been documented in the past few years.

Brahminy Blindsnake (Ramphotyphlops braminus)
Only one species of snake is known to have obligate parthenogenesis. It is a member of the Scolecophidia, or blindsnakes, called the Brahminy Blindsnake or Flowerpot Snake (Ramphotyphlops braminus). This tiny egg-laying species is made up only of females and is extremely widespread, partially thanks to the ability of just a single individual to colonize new areas. Unlike mammals, most reptiles (and birds) have a ZW chromosomal sex determination system, so instead of the males being XY and the females XX (click here for a review), male snakes are ZZ and female snakes are ZW. However, in common with other obligate parthenogenetic species, Brahminy Blindsnakes are triploid, meaning that they have three sets of chromosomes rather than two. Examination of the karyotype (a picture of one complete set of chromosomes) of Brahminy Blindsnakes has revealed evidence of hybridization, which has also played a role in the origin of other polyploid obligate parthenogenetic vertebrates, including certain lizards, salamanders, and fishes.

Boa constrictor (Boa constrictor)
Facultative parthenogenesis has been documented in a number of species of snakes that normally reproduce sexually. Most of the time this takes place when someone has kept a female snake in captivity for a long period of time. Although it can be difficult to distinguish parthenogenesis from long-term sperm storage, which is possible in snakes over periods of up to at least 5 years, new molecular methods have allowed biologists to differentiate offspring that were produced parthenogenetically from those that were produced from sexual reproduction following prolonged sperm storage. Looking back at supposed cases of lengthy sperm storage may reveal facultative parthenogenesis in unexpected places.

In snakes, there are a wide variety of cellular mechanisms by which parthenogenesis can occur. Evidence for the exact type of facultative parthenogenesis can be gained by examining the sex and karyotype of the offspring, and appears to be correlated with the higher taxonomic group. Captive booid snakes such as rainbow boas (Epicrates maurus) and boa constrictors (Boa constrictor) have given birth to viable female offspring that have a WW sex chromosome pair, which is different from any other known chromosome combination. Why the parthenogenetically-produced offspring of these species are not a 50:50 mix of ZW and WW (the two combinations a female boa is capable of making via meiosis) is unknown.

Burmese Python (Python bivittatus)
Burmese python (Python bivittatus) females are capable of making exact ZW female clones of themselves, using a mechanism that is functionally similar to but distinct from that used by obligate parthenogenetic species like the Brahminy Blindsnake. The python offspring are all females and are mostly viable, having suffered no loss of genetic information. In both boas and pythons, the sex chromosomes are monomorphic, meaning that the Z and the W chromosome are approximately equal in size and indistinguishable from one another. It has been suggested that this method of reproduction might help species circumvent limitations on lifespan and establish new populations when individuals are isolated for long periods of time, although this claim will require more evidence to evaluate because parthenogenesis has not been observed in wild boas or pythons. However, new data from molecular ecologist Warren Booth has resulted in a reinterpretation of some of the conclusions of the original description of parthenogenesis in pythons [edit: specifically, Booth & colleagues suggested that the mode is in fact similar in boas and pythons, but that the female python who gave birth to exact clones was herself born via parthenogenesis - which is still exciting because it proves the reproductive competency of parthenogenetically-produced offspring].

Cottonmouth (Agkistrodon piscivorus)
In contrast, facultative parthenogenesis in caenophidians is fraught with difficulties. Most of the offspring produced this way are not viable because they have suffered a loss of some genetic information. Many are stillborn or have deformities or other abnormalities. All are males, and the litters are unusually small. Nevertheless, parthenogenesis has been documented in both captive and wild Cottonmouths (Agkistrodon picivorus) and Copeprheads (Agkistrodon contortrix), and in captive Eastern Diamondback (Crotalus adamanteus), Timber (C. horridus), and Aruba Island (C. unicolor) Rattlesnakes, four species of gartersnakes (Thamnophis couchii, T. elegans, T. marcianus, and T. atratus), and Arafura filesnakes (Acrochordus arafurae). Most of these species are commonly kept in captivity, and they span the gamut from the most basal caenophidians to the most derived, but the infrequent occurrence and low viability of facultative parthenogenesis in these species suggests that although all caenophidians may be capable of parthenogenesis, it is probably not very ecologically or evolutionarily significant. The reproductive potential of the few captive-born parthenogenetically-produced Copperheads that have survived is currently being assessed.

The next steps in this area of herpetology are to discover more about the different cellular and developmental mechanisms that control and influence parthenogenesis, document parthenogenesis in species and taxonomic groups where it is not so far known, and understand more about the hybrid origins of obligate parthenogenetic species. We still don't know what is required to induce parthenogenetic reproduction in either facultative or obligate species - some lizards require copulation with other females, and many salamanders require egg activation by the sperm of a male salamander of a different species. Who knows what bizarre adaptations parthenogenetic snakes await discovery?

Next month: the story of the most widespread snake in the world!

Update: In August 2014 a captive Green Anaconda joined the ranks of boid snakes known to be capable of facultative parthenogenesis, although as of November the observation was still awaiting confirmation via genetic methods. I also learned recently that parthenogenetic snakes play a starring role in a new curriculum for teaching mitosis and meiosis to introductory biology students.

ACKNOWLEDGMENTS

Thanks to xkcd, JD Willson, Todd Pierson, and Pierson Hill for their drawings and photographs.

REFERENCES

Booth, W., D. H. Johnson, S. Moore, C. Schal, and E. L. Vargo. 2011. Evidence for viable, non-clonal but fatherless Boa constrictors. Biology Letters 7:253-256 <link>

Booth, W., L. Million, R. G. Reynolds, G. M. Burghardt, E. L. Vargo, C. Schal, A. C. Tzika, and G. W. Schuett. 2011. Consecutive virgin births in the New World boid snake, the Colombian Rainbow Boa, Epicrates maurus. Journal of Heredity 102:759–763 <link>

Booth, W. and G. W. Schuett. 2011. Molecular genetic evidence for alternative reproductive strategies in North American pitvipers (Serpentes: Viperidae): long-term sperm storage and facultative parthenogenesis. Biological Journal of the Linnean Society 104:934–942 <link>

Booth, W., G. W. Schuett, A. Ridgway, D. W. Buxton, T. A. Castoe, G. Bastone, C. Bennett, and W. McMahan. 2014. New insights on facultative parthenogenesis in pythons. Biological Journal of the Linnean Society 10.1111/bij.12286 <link>

Booth, W., C. F. Smith, P. H. Eskridge, S. K. Hoss, J. R. Mendelson, and G. W. Schuett. 2012. Facultative parthenogenesis discovered in wild vertebrates. Biology Letters 8:983-985 <link>

Germano, D. J. and P. T. Smith. 2010. Molecular evidence for parthenogenesis in the Sierra garter snake, Thamnophis couchii (Colubridae). The Southwestern Naturalist 55:280-282 <link>

Groot, T., E. Bruins, and J. Breeuwer. 2003. Molecular genetic evidence for parthenogenesis in the Burmese python, Python molurus bivittatus. Heredity 90:130-135 <link>

Kearney, M., M. K. Fujita, and J. Ridenour. 2009. Lost sex in the reptiles: constraints and correlations. Pages 447-474 in I. Schön, K. Martens, and P. van Dijk, editors. Lost Sex: The Evolutionary Biology of Parthenogenesis. Springer, Dordrecht, Holland <link>

Reynolds, R. G., W. Booth, B. M. Fitzpatrick, G. W. Schuett, and G. M. Burghardt. 2012. Successive virgin births of viable male progeny in the checkered gartersnake, Thamnophis marcianus. Biological Journal of the Linnean Society 107:566–572 <link>

Schuett, G., P. Fernandez, W. Gergits, N. Casna, D. Chiszar, H. Smith, J. Mitton, S. Mackessy, R. Odum, and M. Demlong. 1997. Production of offspring in the absence of males: evidence for facultative parthenogenesis in bisexual snakes. Herpetological Natural History 5:1-10 <link>

Wright, R. 2014. Why Meiosis Matters: The case of the fatherless snake. CourceSource 1:1-6 <link>

Wynn, A. H., C. J. Cole, and A. L. Gardner. 1987. Apparent triploidy in the unisexual brahminy blind snake, Ramphotyphlops braminus. American Museum Novitates 2868:1-7 <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.