Evolution and Biodiversity

Category: defence (Page 4 of 4)

Trapped, encased, killed

Snails use their shells as a weapon against parasitic worms

a grove snail's shell can kill parasites

Parasitic roundworms that invade a snail’s shell may be trapped, encased and fixed permanently to the inner layer of that shell, as Robbie Rae shows.

Thanks to its shell, a snail is protected against damage, predators, heat and cold, drought and rain. But there is more, as Robbie Rae discovered. The snail also uses its shell as a defence system to eliminate parasitic roundworms (nematodes). These parasites attack snails since snails appeared on earth, about 400 million years ago. It is obvious that snails had to evolve a defence mechanism against these enemies, but until now, no defence mechanism was known.

Encapsulation

In his lab, Rae exposed grove snails (Cepaea nemoralis) to the nematode Phasmarhabditis hermaphrodita for several weeks. This bottom dwelling animal, less than 2 millimetres long, is able to penetrate and kill many snail and slug species, but some snails are resistant, as for instance the grove snail. Rae studied the interaction between the grove snail and the worms to find out how the snail eliminates the parasites.

worms attached to the inner layer of the shell of a grove snailIt turned out that the cells on the inner layer of the shell do the job. They adhere to an invading worm, multiply, and swarm over the parasite’s body until it is entirely covered. Engulfed by the cells, it is fused to the inside of the shell and dies. By this procedure, grove snails not only encapsulate this lethal roundworm, but they use the immune reaction also to kill other, less dangerous nematodes, as experiments showed.

In nature, this is common practice. Rae collected grove snails and white-lipped snails (Cepaea hortenis) from the wild and observed that many snails had different species of roundworms attached to their inner shell surface, up to 100 worms in one shell. Also the garden snail (Cornu aspersum) – like the other two snail species an inhabitant of Western Europe – uses its shell to eliminate invading worms by encapsulation.

Old defence

Finally, he examined a large number of snails from museum collections, to conclude that many snails of many different species had nematodes attached to their shells. Trapped worms proved to be fixed permanently; they even can be found in snails that died a few hundred years before. As this defence mechanism is found to be widespread among the large and old clade of terrestrial snails and slugs, it must have evolved about 100 million years ago. Even some slug species eliminate parasitic roundworms by this mechanism. During evolutionary history, their shells have become reduced and internalised, but in many species they retained the ability to trap, encase and kill roundworms.

The vineyard snail (Cernuella virgata) is one of the species that is unable to get rid of the roundworm Phasmarhabditis hermaphrodita. Apparently, the parasite evades its immune reaction in one way or the other. As many slug species are also susceptible to this parasite, it is formulated into a biological control agent to be used against herbivirous slugs.

Willy van Strien

Photos:
Large: grove snail, Cepaea nemoralis. Kristian Peters (Wikimedia Commons, Creative Commons CC BY-SA 3.0)
Small: nematodes fixed to the inner layer of a grove snail’s  shell. © Robbie Rae

Source:
Rae, R., 2017. The gastropod shell has been co-opted to kill parasitic nematodes. Scientific Reports 7: 4745. Doi: 10.1038/s41598-017-04695-5

Biting prey

Fish with venomous fangs have many imitators

Fangblenny Petroscirtes breviceps mimics a venomous species

Meiacanthus fish species are armed with venomous fangs that deter predators. Many nonvenomous fish species protect themselves from being attacked by mimicking the aposematic colours and the behaviour of Meiacanthus species. A large research team unravelled the evolution of the venomous fish.

A predator fish expecting to easily ingest a small Meiacanthus fish will prove to be wrong. This prey is armed with sharp teeth that inject venom into its enemy. Disoriented, the predator will release its victim – and will not go after the same fish anymore.

Meiacanthus species are the only fish with venomous fangs. They belong to the group of the saber-toothed blennies or fangblennies (Nemophini), which all have a pair of enlarged, hollow canines in the lower jaw. Nicholas Casewell, together with a large research team, has shown that these fangs must have originated in the common ancestor of these blennies. But only species of the genus Meiacanthus developed venomous fangs. They possess venom glands at the base of the fangs and grooves on the fangs to deliver the venom into the wound.

According to the researchers, the venom does not cause pain upon injection, but it reduces the blood pressure in the predator, which becomes weakened and disoriented so that the prey can escape unharmed from its mouth. Blood pressure reduction appears to be such a bad experience that the predator fish will never try to ingest a Meiacanthus again. The venom was found to contain three compounds that had never been found in fish before.

Protection

Some non-venomous fangblennies, as well as many fish species from other groups, profit from the aversion that predators have to Meiacanthus species by looking the same and behaving the same. While not mounting a defence against predators themselves, they are still protected from attacks thanks to this mimicry.

What do non-venomous fangblennies use their fangs for? To eat, probably. This holds at least for all Plagiotremus species, which feed on dermal tissue, scales, mucus, and fins of larger fish. If they look like Meiacanthus species, they can easily approach their victims, which are reluctant to attack.

Willy van Strien

Photo:
Petroscirtes breviceps, with nonvenomous fangs in the lower jaw. ©Alex Ribeiro
CT-scan of the venomous species Meiacanthus grammistes. ©Anthony Romilio (University of Queensland, Australia)

Source:
Casewell, N.R., J.C. Visser, K. Baumann, J. Dobson, H. Han, S. Kuruppu, M. Morgan, A. Romilio, V. Weisbecker, S.A. Ali, J. Debono, I. Koludarov, I.Que, G.C. Bird, G.M. Cooke, A. Nouwens, W.C. Hodgson, S.C. Wagstaff, K.L. Cheney, I. Vetter, L. van der Weerd, M.K. Richardson & B.G. Fry, 2017. The evolution of fangs, venom, and mimicry systems in blenny fishes. Current Biology, March 30 online. Doi: 10.1016/j.cub.2017.02.067

Micro army

Cloud of semiautonomous pincers protects sea urchin

Collector sea urchin released a cloud of pincers

When a hungry fish approaches, the collector sea urchin releases a cloud of small biting, venomous pincers that deter its enemy before it has attacked. This peculiar defensive strategy is revealed by Hannah Sheppard-Brennand and colleagues.

In addition to their prominent spines, sea urchins and sea stars possess numerous smaller appendages as well: little pincer-like heads on a movable stalk, called pedicellariae. The pincers have different functions, such as catching food or removing debris – and tormenting predators. For in spite of the unattractive appearance that sea urchins and sea stars have, predators such as fish will pick at their tube feet and other soft tissue. Some species have pedicellariae with teethed jaws and a venom sac to deal with such predators, and anyone who once stepped on such a sea urchin will remember the painful experience.

Cloud

One species, the collector sea urchin Tripneustes gratilla, deploys these venomous pedicellariae in an unique way, as Hannah Sheppard-Brennand and colleagues show: when harassed, this sea urchin will release a cloud of them in the surrounding water. Upon release, the pincer-like heads behave semi autonomously; they are mobile, have sensory structures and will bite and deliver their venom when they touch a supposed enemy.

Safe

Fish are deterred by such a swarm, as lab experiments revealed, and they will leave before they have bitten the sea urchin. Protected by his unique defensive army, the collector sea urchin is able to forage safely on grass and eelgrass during the day, when other sea urchin species have to take shelter, as well as during the night.

Willy van Strien

Photo:
Collector sea urchin Tripneustes gratilla with a cloud of released pedicellaria heads. © Hannah Sheppard Brennand

Source:
Sheppard-Brennand, H., A.G.B. Poore & S.A. Dworjanyn, 2017. A waterborne pursuit-deterrent signal deployed by a sea urchin. The American Naturalist 189, online March 27. Doi: 10.1086/691437

Tiny scarecrow

Red-winged blackbird flinches from whistling caterpillar

red-winged blackbird s scared by whistling caterpillar

It is funny when the tiny caterpillar of the walnut sphinx Amorpha juglandis suddenly emits a high-pitched noise. Thus sound scares birds, as Amanda Dookie and colleagues witnessed, so that they will refrain from picking the caterpillar. Why are birds startled by this whistling caterpillar?

caterpillars od walnut sphinx can make whistling soundsNormally birds are not afraid of a caterpillar, but caterpillars of the moth Amorpha juglandis can scare them, Amanda Dookie and colleagues report, by starting to scream when they are touched – a most peculiar behaviour.

A few years ago, Veronica Bura investigated how the caterpillars produce their high pitched sound. Their respiratory system consists of a network of tubes with on each side a row of openings, the spiracles. When screaming, Bura assessed, walnut sphinx caterpillars contract the front end of their bodies, close all spiracles except the rear pair and expulse the air forcefully through these openings, producing a whistling sound. The posterior spiracles are enlarged compared to the others, which probably is an adaptation for sound production. Often the caterpillars also thrash their heads to defend themselves while whistling, and Dookie wanted to know if the whistle sound in itself is enough to frighten birds, and how great the startling effect is.

Startle response

To find out, she exposed a number of male red-winged blackbirds to playbacks of caterpillar whistles that had been recorded before. Just like the walnut sphinx, red-winged blackbirds are to be found throughout North America. The experimental birds were housed in individual cages and provided mealworms on a small platform for four days before the tests started. Then the platform was equipped with a sensor and a speaker, and as soon as a bird touched the dish during a test, the whistling sound was played back.

That had a huge effect: the sound evoked a startle response in all birds. Most flew away, hopped backwards or clapped their wings. After a while they tried again to pick a mealworm and then they heard the whistle sound again. The birds got habituated a bit and the startle response decreased over time, but when they were exposed to the sound after two days of rest, they were as frightened as they had been the first time.

Danger

Can the caterpillars protect themselves from hungry birds by whistling? Probably so. In the wild, the birds scurry around and when they are scared by a noisy caterpillar, they will abandon that prey and move on in search of another.

But why are birds scared by a whistling caterpillar that is not dangerous or venomous, as far as is known? The birds may associate the short, high-pitched sound with danger, the researchers propose, because the sound is similar to the alarm call that many birds emit when they are threatened. A fright response to such alarm call is hard-wired in birds, and this seems to be exploited by the caterpillars when they mimic the call.

Willy van Strien

Photos:
Large: red-winged blackbird Agelaius phoeniceus. Janet Beasly (Wikimedia Commons, Creative Commons CC BY-SA 2.0)
Small: caterpillar of walnut sphinx, Amorpha juglandis. © Jayne Yack

Sources:
Dookie, A.L., C.A. Young, G. Lamothe, L.A. Schoenle & J.E. Yack, 2017. Why do caterpillars whistle at birds? Insect defence sounds startle avian predators. Behavioural Processes, 138: 58-66. Doi: 10.1016/j.beproc.2017.02.002
Bura, V.L., V.G. Rohwer, P.R. Martin & J.E. Yack, 2011. Whistling in caterpillars (Amorpha juglandis, Bombycoidea): sound-producing mechanism and function. The Journal of Experimental Biology 214: 30-37. Doi:10.1242/jeb.046805

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