Category Archives: Extinction

Going a long way with your mouth open to new tastes

by Piter Kehoma Boll

Everybody knows that human activities have driven our environment toward an unfortunate situation. The most popular forms of human impact include pollution, deforestation and overexploitation of natural resources, but certainly an important factor in remodeling ecosystems is the invasion of species.

While humans move around the world, they carry many species with them, either intentionally or not, an some of them establish successfully in the new environment, while others do not. But what makes some species become successful invaders while other are unable to do so?

It is clear for some time that having a broad niche, i.e., a broad tolerance in environmental conditions and a broad use of resources is very important to succeed in invading a new habitat. Food niche breadth, i.e., the amount of different food types one can ingest, is among the most important dimensions of the niche influencing the spread of a species.

I myself studied the food niche breadth of six Neotropical land planarians in my master’s thesis (see references below) and it was clear that the species with the broader niche are more likely to become invasive. Actually, the one with the broadest food niche, Obama nungara, is already an invader in Europe, as I already discussed here.

obama_marmorata_7

A specimen of Obama nungara from Southern Brazil that I used in my research. Photo by myself, Piter Kehoma Boll.*

But O. nungara has a broad food niche in its native range, which includes southern Brazil, and likely reflected this breadth in Europe. But could a species that has a narrow food niche in its native range broaden it in a new environment?

A recent study by Courant et al. (see references) investigated the diet of the African clawed frog, Xenopus laevis, that is an invasive species in many parts of the world. They compared its diet in its native range in South Africa whith that in several populations in other countries (United States, Wales, Chile, Portugal and France).

Xenopus_laevis

The African clawed frog Xenopus laevis. Photo by Brian Gratwicke.**

The results indicated that X. laevis has a considerable broad niche in both its native and non-native ranges, but the diet in Portugal showed a greater shift compared to that in other areas, which indicates a great ability to adapt to new situations. In fact, the population from Portugal lives in running water, while in all other places this species prefers still water.

We can conclude that part of the success of the African clawed frog when invading new habitats is linked to its ability to try new tastes, broadening its food niche beyond that from its original populations. The situation in Portugal, including a different environment and a different diet, may also be the result of an increased selective pressure and perhaps the chances are that this population will change into a new species sooner than the others.

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References:
Boll PK & Leal-Zanchet AM (2016). Preference for different prey allows the coexistence of several land planarians in areas of the Atlantic Forest. Zoology 119: 162–168.

Courant J, Vogt S, Marques R, Measey J, Secondi J, Rebelo R, Villiers AD, Ihlow F, Busschere CD, Backeljau T, Rödder D, & Herrel A (2017). Are invasive populations characterized by a broader diet than native populations? PeerJ 5: e3250.

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Land snails on islands: fascinating diversity, worrying vulnerability

by Piter Kehoma Boll

The class Gastropoda, which includes snails and slugs, is only beaten by the insects in number of species worldwide, having currently about 80 thousand described species. Among those, about 24 thousand live on land, where they are a very successful group, especially on oceanic islands.

The Hawaiian Islands alone, for example, have more than 750 snail species and there are more than 100 endemic species in the small island of Rapa in the South Pacific. This diversity is much higher than that in any continental place, but the reason for that is not completely understood.

Mandarina

A land snail of the genus Mandarina, endemic to the Ogasawara Islands, Japan. Photo by flickr user kmkmks (Kumiko).*

One of the most likely explanations for this huge diversity on islands is related to the lack of predators. The most common predators of snails include birds, mammals, snakes, beetles, flatworms and other snails. Most of those are not present in small and isolated islands, which allows an increase in land snail populations in such places. Without too much dangers to worry about, the community of land snails n islands can explore a greater range of niches, eventually leading to speciation.

Unfortunately, as always, the lack of danger leads to recklessness. Without predators to worry about, insular land snails tend to lay fewer eggs than their mainland relatives. If there is no danger of having most of your children eaten, why would you have that many? It is better to lay larger eggs, putting more resources on fewer babies, and so assure that they will be strong enough to fight against other snail species. Afterall, the large number of species in such a small place as an island likely leads to an increased amount of competition between species.

But why is this recklessness? Well, because you never known when a predator will arrive. And they already arrived… due to our fault.

The diversity of insular land nails was certainly affected by habitat loss promoted by humans, but also by predators that we carried with us to the islands, whether intentionally or not. These predators include rats, the predatory snail Euglandina rosea and the land flatworm Platydemus manokwari, the latter being most likely the worst of all.

800px-platydemus_manokwari

The flatworm Platydemus manokwari in the Ogasawara Islands. Photo by Shinji Sugiura.

This flatworm arrived at the Chichijima Island, part of the Ogasawara Islands in the Pacific Ocean, in the early 1990s and in about two decades it led most land snail species on the island to extinction and many more are about to face the same fate on this island and on others. Not being prepared for predators, these poor snails cannot reproduce fast enough to replace all individuals eaten by the flatworm.

We have to act quickly if we want to save those that are still left.

See also: The New Guinea flatworm visits France – a menace.

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ResearchBlogging.orgReferences and further reading:

Chiba, S., & Cowie, R. (2016). Evolution and Extinction of Land Snails on Oceanic Islands. Annual Review of Ecology, Evolution, and Systematics, 47 (1), 123-141 DOI: 10.1146/annurev-ecolsys-112414-054331

Sugiura, S., Okochi, I., & Tamada, H. (2006). High Predation Pressure by an Introduced Flatworm on Land Snails on the Oceanic Ogasawara Islands. Biotropica, 38 (5), 700-703 DOI: 10.1111/j.1744-7429.2006.00196.x

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Friday Fellow: Amphibian chytrid fungus

by Piter Kehoma Boll

Today I’m bringing you a species that is probably one of the most terrible ones to exist today, the amphibian chytrid fungus, Batrachochytrium dendrobatidis, also known simply as Bd.

batrachochytrium_dendrobatidis

Several sporangia of Batrachochytrium dendrobatidis (spherical structures) growing on a freshwater arthropod. Photo by AJ Cann.*

The amphibian chytrid fungus, as its name says, is a chytrid, a fungus of the division Chytridiomycota, which include microscopic species that usually feed by degrading chitin, keratin in other such materials. In the case of the amphibian chytrid fungus, it infects the skin of amphibians and feeds on it. It grows through the skin forming a network of rhizoids that originate spherical sporangia that contains spores.

The infection caused by the amphibian chytrid fungus is called chytridiomycosis. It causes a series of symptoms, including reddening of the skin, lethargy, convlusions, anorexia and excessive thickening and shedding of the skin. This thickening of the skin leads to problems in taking in nutrients, releasing toxins and even breathing, eventually leading to death.

chytridiomycosis

An individual of the species Atelopus limosus infected by the amphibian chytrid fungus. Photo by Brian Gratwicke.**

Since its discovery and naming in 1998, the amphibian chytrid fungus has devastated the populations of many amphibian species throughout the world. Some species, such as the golden toad and the Rabb’s fringe-limbed treefrog, were recently extinct by this terrible fungus. This whole drastic scenario is already considered one of the most severe examples of Holocene extinction. The reason for such a sudden increase in the infections is unknown, but it may be related to human impact on the environment.

We can only hope to find a way to reduce the spread of this nightmare to biodiversity.

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ResearchBlogging.org
References:

Fisher, M., Garner, T., & Walker, S. (2009). Global Emergence of Batrachochytrium dendrobatidis and Amphibian Chytridiomycosis in Space, Time, and Host Annual Review of Microbiology, 63 (1), 291-310 DOI: 10.1146/annurev.micro.091208.073435

Wikipedia. Batrachochytridium dendrobatidis. Available at <https://en.wikipedia.org/wiki/Batrachochytrium_dendrobatidis&gt;. Access on March 4, 2017.

Wikipedia. Chytridiomycosis. Available at <https://en.wikipedia.org/wiki/Chytridiomycosis&gt;. Access on March 4, 2017.

Wikipedia. Decline in amphibian populations. Available at <https://en.wikipedia.org/wiki/Decline_in_amphibian_populations&gt;. Access on March 4, 2017.

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Shaking dinosaur hips and messing with their heads

by Piter Kehoma Boll

This week brought astonishing news regarding the phylogeny of dinosaurus, as you perhaps have heard or read. New anatomical evidences have completely rebuilt the basis of the dinosaur family tree and I’m here to explain a little bit of what happened.

As we all know, Dinosaurs include a great variety of beasts, from the meat-eating theropods to the long-necked sauropods and from the horned ceratopsians to the armored ankylosaurs, among many others.

largestdinosaursbysuborder_scale

Silhouette of a human compared to the largest known dinosaurs of each major group. Picture by Matt Martyniuk.*

For more than a century now, dinosaurus have been divided into two groups, called Ornithischia and Saurischia. Ornithischia (“bird-hipped”) includes dinosaurus whose pelvic bones are more similar to what is found in birds, with a pubis directed backward. Saurischia (“lizard-hipped”), on the other hand, have a pubis directed forward, as in reptiles in general. This grouped the theropods and the sauropods in the same group as Saurischia while other dinosaurus were grouped as Ornithischia. But birds are actually theropods, thus being lizard-hipped dinosaurus and not bird-hipped dinosaurus! Confusing, isn’t it? So let’s take a look at their hips:

Pelvic_bones

Comparison of the hips of a crocodile (Crocodylus), a sauropod (Diplodocus), a non-avian theropod (Tyrannosaurus), a bird (Apteryx), a thyreophoran (Stegosaurus), and an ornithopod (Iguanodon). Red = pubis; Blue = ischium; Yellow = ilium. Picture by myself, Piter K. Boll.**

As you can see, the primitive state, found in crocodiles, sauropods and early theropods, is a pubis pointing forward. A backward-pointing pubis evolved at least twice independently, both in more advanced theropods (such as birds) and the ornithischian dinosaurus. But could we be so certain that Tyrannosaurus and Diplodocus are more closely related to each other (forming a clade Saurischia) just because of their hips? Afterall, this is a primitive hip, so it is very unlikely to be a synapomorphy (a shared derived character). Nevertheless, it continued to be used as a character uniting sauropods and theropods.

A new paper published by Nature this week, however, showed new evidences that point to a different relationship of the groups. After a detailed analysis of the bone anatomy, Matthew G. Baron, David B. Norman and Paul M. Barrett have found 20 characters that unite theropods with ornithischians and not with sauropods. Among those we can mention the presence of a foramen (a hole) at the anterior region of the premaxillary bone that is inside the narial fossa (the depression of the bone that surrounds the nostril’s opening) and a sharp longitudinal ridge along the maxilla.

skulls

The skulls of both ornithischians and theropods (above) show an anterior premaxillary foramen in the narial fossa (shown in yellow) and and a sharp ridge on the maxilla (shown in green), as well as other characters that are not present in sauropodomorphs and herrerasaurids (below). Composition using original pictures by Carol Abraczinskas and Paul C. Sereno (Heterodontosaurus), Wikimedia user Ghedoghedo (Eoraptor and Herrerasaurus), and flickr user philosophygeek (Plateosaurus).**

In his blog Tetrapod Zoology, Dr. Darren Naish comments the new classification and points out some problems that arise with this new view. One of them is the fact that both theropods and sauropodomorphs have pneumatic (hollow) bones, while ornithischians do not. If the new phylogeny is closer to the truth, that means that pneumacity evolved twice independently or evolved once and was lost in ornithischians.

He also mentions that both ornithischians and theropods had hair-like or quill-like structures on their skin. In theropods this eventually led to feathers. Could this be another synapomorphy uniting these groups? Maybe… but when we think that pterosaurs also had “hairs”, one could also conclude that a “hairy” integumentary structure was already presented in the common ancestor of dinosaurus. In this case, perhaps, we only had not found it yet on sauropods. Now imagine a giant Argentinosaurus covered with feathers!

One concern that appeared with this new organization is whether sauropodomorphs would still be considered dinosaurs. The term “dinosaur” was coined by Richard Owen in 1842 to refer to the remains of the three genera known at the time, Iguanodon, Hylaeosaurus and Megalosaurus, the first two being ornithischians and the latter a theropod. As a consequence, the original definition of dinosaur did not include sauropods. Similarly, the modern phylogenetic definition of dinosaur was “the least inclusive clade containing Passer domesticus (the house sparrow) and Triceratops horridus“. In order to allow Brachiosaurus and his friends to continue sitting  with the dinosaurs, Baron et al. suggested to expand the definition to include Diplodocus carnegii. So, dinosaurus would be the least inclusive clade containing P. domesticusT. horridus and D. carnegii.

In this new family tree, the name Saurischia would still be used, but to refer only to the sauropodomorphs and some primitive carnivores, the herrerasaurids. The new clade formed by uniting theropods and ornithischians was proposed to be called Ornithoscelida (“bird-legged”), a name coined in 1870 to refer to the bird-like hindlimbs of both theropods and ornithopods (the subgroup of ornithischians that includes dinosaurs such as Iguanodon and the duck-billed dinosaurs).

What can we conclude with all that? Nothing will change if you are just a dinosaur enthusiast and do not care about what’s an ornithischian and a saurischian. Now if you are a phylogeny fan, as I am, you are used to sudden changes in the branches. Most fossils of basal dinosaurs are incomplete, thus increasing the problem to know how they are related to each other. Perhaps this new view will last, perhaps new evidence will change all over again the next week.

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ResearchBlogging.orgReferences and further reading:

Baron, M., Norman, D., & Barrett, P. (2017). A new hypothesis of dinosaur relationships and early dinosaur evolution Nature, 543 (7646), 501-506 DOI: 10.1038/nature21700

Naish, D. (2017). Ornithoscelida Rises: A New Family Tree for DinosaursTetrapod Zoology.

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Friday Fellow: Blue whale

by Piter Kehoma Boll

We’ve talked about the cutest and the leggiest, so now it’s time to introduce the largest, at once.

I think most of us know already that the largest animal ever is our beloved blue whale, Balaenoptera musculus. It can reach 30 m in length and weigh more than 180 tonnes. It’s really big, but probably not as big as many people think. There are some popular legends, like that the heart of a blue whale is the saze of a car or that a human could swim inside its aorta, which are not actually true.

It's almost impossible to find a good photo of the entire body of a blue whale. Afterall, it's huge and lives underwater!

It’s almost impossible to find a good photo of the entire body of a blue whale. Afterall, it’s huge and lives underwater!

But what else can we say about the blue whale? It is a rorqual, a name used to designate whales in the family Balaenopteridae and, as all of them, its main and almost exclusive food is krill, a small crustacean very abundant in all oceans. And krill needs to be abundant in order to provide the thousands of tonnes that all whales in the oceans need to eat every day. A single blue whale eats up to 40 million krill in a day, which equals to roughly 3.5 tonnes. A blue whale calf (young) is born measuring around 7 m in length and drinks around 500 liters of milk per day!

Blue whales were abundant in nearly all oceans until the beginning of the 20th century, when they started to be hunted and were almost extinct. Nowadays, the real population size is hard to estimate, but may encompass as few as 5,000 specimens, much less than the estimated hundreds of thousands in the 19th century. Due to such a drastic reduction in the population, the blue whale is currently listed as “endangered” in IUCN’s Red List.

But let's see a blue whale in all of its blueness.

But let’s see a blue whale in all of its blueness.

Occasionally, blue whales can hybridize with fin whales (Balaenoptera physalus) and perhaps even with humpback whales (Megaptera novaeangliae), a species classified in a different genus! Some recent genetic analyses, however, indicate that the Balaenoptera genus is polyphyletic and the blue whale may become known as Rorqualus musculus.

Different from other whales, blue whales usually live alone or in pairs, but never form groups, even though they may sometimes gather in places with high concentrations of food.

Like other cetaceans, especially other baleen whales, the blue whale sings. The song, however, is not as complex and dynamic as the ones produced by the related humpback whale. An intriguing fact that was recently discovered is that the frequency of the blue whale song is getting lower and lower at least since the 1960s. There is no good hypothesis to explain this phenomenon yet, but several ones have been proposed, such as the increase in background noise due to human activities or the increase in population density due to the decrease in whaling.

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References:

Hassanin, A.; Delsuc, F.; Ropiquet, A.; Hammer, C.; van Vuuren, B. J.; Matthee, C.; Ruiz-Garcia, M.; Catzeflis, F.; Areskoug, V.; Nguyen, T. T.; Couloux, A. 2012. Patter and timing of diversification of Cetartiodactyla (Mammalia, Laurasiatheria), as revealed by a comprehensive analysis of mitochondrial genomes.  Comptes Rendus Biologies, 335: 32-50.

Mellinger, D. K.; Clark, C. W. 2003. Blue whale (Balaenoptera musculus) sounds from the North Atlantic. Journal of the Acoustical Society of America, 114(2): 1108-1119.

Wikipedia. Blue whale. Available at: <https://en.wikipedia.org/wiki/Blue_whale&gt;. Access on January 27, 2016.

 

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The Story of the Dwarf Rhea

by Rafael Nascimento

The family Rheidae is nowadays represented by two or three (according to different authors) species of rheas, large running flightless birds, similar to the African ostriches, but having three toes on each foot instead of two. The largest one, the common rhea Rhea americana, has five subspecies distributed from northeastern Brazil to eastern Argentina and including Bolivia, Paraguay and Uruguay. The other forms, earlier put in a separate genus, Pterocnemia, are R. pennata and R. tarapacensis (commonly known as Darwin’s rhea and Puna rhea, respectively). Darwin’s rhea, which helped the British naturalist in the elaboration of his theory of natural selection, lives in the Argentinean and Chilean Patagonia. The systematic situation of the Puna rhea (and its possible subspecies), which is found in the area where Peru, Bolivia, Chile and Argentina meet, is not yet clear, and currently it is considered a distinct form based on some physical features, but more clarifying studies are necessary.

Beside these current forms and some fossil species, such as Opisthodactylus horacioperezi and Hinasuri nehensis, respectively from the Argentinian Miocene and Pliocene, another species was described in 1894 by the British Naturalist Richard Lydekker based on a small egg: Rhea nana – therefore representing a possible fourth rhea species living in historical times.

Richard Lydekker, ca 1900.

Richard Lydekker, ca 1900.

Following you can see the original text published in the journal Proceedings of the Zoological Society of London from 1894, with comments regarding this possible new species:

“Mr. R. Lydekker exhibited photographs and a model of a unique egg, the original of which had been obtained many years ago in Southern Patagonia, and now preserved in the Museum at La Plata. If not an abnormal specimen, it could not be assigned to any known species of bird.

When travelling in the district where the specimen was obtained, Dr. P. Moreno, Director of the Museum at La Plata, many years ago saw numbers of small Ratite birds, which he at first took to be small Rheas. By the natives, to whom they were well known, he was, however, assured that they were adult birds, allied to the Rheas. Desirous of confirming this information, Dr. Moreno applied to a friend acquainted with the district; who replied that not only did he well know the birds, but that he possessed an egg, that egg being the original specimen of which a model was now exhibited.

Assuming the egg to be a normal one, Mr. Lydekker was of opinion that, taken in connexion with the evidence of two independent witnesses who had been the birds, it pointed to the existence in Southern Patagonia of a small unknown Ratite bird more or less nearly allied to the Rheas.”

Illustration of Darwin's Rhea by John Gould, 1841.

Illustration of Darwin’s Rhea by John Gould, 1841.

Until today, however, no other similar egg or adult bird of a species different from the three already mentioned has been found. When we deal with potentially extinct species, only know by scarce reports or aberrant specimens, one must watch the data through a skeptical point of view. We need to be certain that those are not variations within the species or a witness confusion. The lack of extensive comparative material due to the date of the descriptions must also be taken into account, as well as the constant advancements in our understanding of science.

Normal egg of R. pennata, at Museum Wiesbaden (Germany). Photo by Klaus Rassinger/Gerhard Cammerer.

Normal egg of R. pennata, at Museum Wiesbaden (Germany). Photo by Klaus Rassinger/Gerhard Cammerer.

This egg is currently treated as an aberrant form of a Rhea pennata egg. The model cited by Lydekker, made of wax, is found in the Tring Natural History Museu, England.

del Hoyo, J., Collar, N. & Garcia, E.F.J. (2015) Puna Rhea (Rhea tarapacensis). In: del Hoyo, J., Elliott, A., Sargatal, J., Christie, D.A. & de Juana, E. (eds.). Handbook of the Birds of the World Alive. Lynx Edicions, Barcelona. (retrieved from http://www.hbw.com/node/467080 on 24 December 2015).

Folch, A., Jutglar, F., Garcia, E.F.J. & Boesman, P. (2015) Greater Rhea (Rhea americana). In: del Hoyo, J., Elliott, A., Sargatal, J., Christie, D.A. & de Juana, E. (eds.). Handbook of the Birds of the World Alive. Lynx Edicions, Barcelona. (retrieved from http://www.hbw.com/node/52399 on 24 December 2015).

Folch, A., Christie, D.A., Jutglar, F. & Garcia, E.F.J. (2015) Lesser Rhea (Rhea pennata). In: del Hoyo, J., Elliott, A., Sargatal, J., Christie, D.A. & de Juana, E. (eds.). Handbook of the Birds of the World Alive. Lynx Edicions, Barcelona. (retrieved from http://www.hbw.com/node/52400 on 24 December 2015).

Hume, J. P.; Walters, M. (2012) Extinct Birds. T & AD Poyser. Londres.

Knox, A. G.; Walters M. P. (1994) Extinct and Endangered Birds in the collections of The Natural History Museum. British Ornithologists’ Club Occasional Publications.

Lydekker, R. (1894) Exhibition of, and remarks upon, a photograph and model of an egg from Southern Patagonia in the La Plata Museum. Proceedings of the Zoological Society of London (1894): 654.

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The New Guinea flatworm visits France – a menace

by Piter Kehoma Boll

ResearchBlogging.orgFor as long as life exists, it spreads. Organisms move (even if only as gametes or spores) and conquer new environments if they fit. If it wasn’t so, life wouldn’t be found all over the world. Recently, however, due to human dispersion, species are much more likely to reach places far away from where they were born. We considered a species living outside its native area as exotic. And there are a lot of them. I wonder if there is any place where no exotic species exist.

In my first post in this blog, I talked about how exotic species are not always a threat to native ecosystems. But many of them are, indeed, dangerous to local diversity. The ISSG (Invasive Species Specialist Group) lists what are considered the 100 worst invasive species. Strangely, they fail to mention the top worst invasive species, Homo sapiens.

Among those 100 species, a very famous one is the giant African land snail, Achatina fulica. Native to East Africa, it has been introduced worldwide and is a major pest in gardens and agricultural sites, and can also be an intermediate host of several parasites that infect humans.

The giant African land snail Achatina fulica. Photo by Eric Guinther. Extracted from commons.wikimedia.org

The giant African land snail Achatina fulica. Photo by Eric Guinther*. Extracted from commons.wikimedia.org

As an attempt to control the populations of Achatina fulica, some “genius” decided to introduce one more exotic species in the areas where A. fulica was a pest: a voracious generalist predator of land snails.

Let's fight against an exotic pest with another exotic pest!

Let’s fight against an exotic pest with another exotic pest!

As a result, the predator snail Euglandina rosea, known as the rosy wolfsnail or cannibal snail, was introduced in areas infested by A. fulica. But E. rosea is native to North America while A. fulica is native to East Africa. In order to be effective, E. rosea had to be a generalist predator, feeding on any kind of snails. And that’s what it does…

The rosy wolfsnail Euglandina rosea. Photo by Tim Ross. Extracted from commons.wikimedia.org

The rosy wolfsnail Euglandina rosea. Photo by Tim Ross. Extracted from commons.wikimedia.org

Euglandina rosea started to prey on A. fulica, but… ops! It also attacked native land snails and led several species to extinction in Pacific Islands. It became a pest even worse than the giant African land snail…

Not satisfied by the damage caused by this predator, people decided to introduce one more species in order to control A. fulica. And the chosen one was another voracious generalist predator of land snails, the New Guinea flatworm Platydemus manokwari. As its name suggest, thee New Guinea flatworm is native to New Guinea, again a different place, and so, in order to feed on the giant African land snail, it had to feed on any kind of land snail. Thus, it became a pest as harmful as the previous one and led several species of land snails to extinction in Pacific Islands.

Until very recently it was thought that the New Guinea flatworm infestation was restricted to the Indo-Pacific Region, not so far from home. However, a recent paper by Justine et al. (2014) reports its presence in a hothouse in Caen, northern France. This report extends significantly its occurrence over the world and indicates that it may be much more spread than previously thought. Unfortunately, people are more interesting in preserving their gardens than preserving biodiversity. So those predatory pests will probably keep being introduced as biological controls, even though they pose a threat to ecosystems.

The New Guinea Flatworm Platydemus manokwari. Photo by Pierre Gros, taken from Justine et al., 2014, via commons.wikimedia.org.

Bonjour tout le monde! I came to visit Paris! The New Guinea Flatworm Platydemus manokwari. Photo by Pierre Gros**, taken from Justine et al., 2014, via commons.wikimedia.org.

Fortunately, in France, P. manokwati seems to be restricted to greenhouses. Let’s hope that it won’t be found somewhere else.

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References:

Albuquerque, F., Peso-Aguiar, M., & Assunção-Albuquerque, M. 2008. Distribution, feeding behavior and control strategies of the exotic land snail Achatina fulica (Gastropoda: Pulmonata) in the northeast of Brazil. Brazilian Journal of Biology, 68 (4), 837-842 DOI: 10.1590/S1519-69842008000400020

ISSG, Invasive Species Specialist Group. 100 of the World’s Worst Invasive Alien Species. Availabe at: < http://www.issg.org/database/species/search.asp?st=100ss >. Access on April 04, 2014.

Justine, J., Winsor, L., Gey, D., Gros, P., & Thévenot, J. 2014. The invasive New Guinea flatworm in France, the first record for Europe: time for action is now. PeerJ, 2 DOI: 10.7717/peerj.297

Sugiura, S., Okochi, I., & Tamada, H. 2006. High Predation Pressure by an Introduced Flatworm on Land Snails on the Oceanic Ogasawara Islands. Biotropica, 38 (5), 700-703 DOI: 10.1111/j.1744-7429.2006.00196.x

Sugiura, S., & Yamaura, Y. 2008. Potential impacts of the invasive flatworm Platydemus manokwari on arboreal snails. Biological Invasions, 11 (3), 737-742 DOI: 10.1007/s10530-008-9287-1

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