Pine processionary

Pine processionary
Pine processionary larvae marching in characteristic fashion
Scientific classification
Kingdom:	Animalia
Phylum:	Arthropoda
Class:	Insecta
Order:	Lepidoptera
Family:	Thaumetopoeidae
Genus:	Thaumetopoea
Species:	T. pityocampa
Binomial name
Thaumetopoea pityocampa Denis & Schiffermüller, 1775

The pine processionary (Thaumetopoea pityocampa) is a moth of the family Thaumetopoeidae. It is sometimes placed in the genus Traumatocampa, is one of the most destructive species to pines and cedars in Central Asia, North Africa and the countries of southern Europe. The urticating hairs of the caterpillar larvae cause harmful reactions in humans and other mammals. The species is notable for the behaviour of its caterpillars, which overwinter in tent-like nests high in pine trees, and which process through the woods in nose-to-tail columns, protected by their severely irritating hairs, as described by entomologist Jean Henri Fabre.

Life cycle

Though most pine processionary moths only live one year, some in high altitudes or more northern areas may survive for over two years. The adult moths lay their eggs near the tops of pine trees. After hatching, the larva eat pine needles while progressing through five stages of development. In order to maintain beneficial living conditions, silken nests are built over the winter. Around the beginning of April, the caterpillars leave the nests in the procession for which the species is known. They burrow underground and emerge at the end of summer. High numbers of adults are produced in years with a warm spring.

Egg

The eggs of the Moth are laid in cylindrical bodies ranging from 4 cm to 5 cm in length. The eggs are covered with scales which come from the female and mimic pine shoots.

Larva

The larva is a major forest pest, living communally in large "tents", usually in pine trees but occasionally in cedar or larch, marching out at night in single file (hence the common name) to feed on the needles. There are often several such tents in a single tree. When they are ready to pupate, the larvae march in their usual fashion to the ground, where they disperse to pupate singly on or just below the surface.

The larvae should never be handled as the abundant hairs on their bodies cause extreme irritation (urticaria) to the skin. 5th stage larvae can eject hairs when threatened or stressed; the hairs, which have the form of harpoons, then penetrate and irritate all areas of exposed skin nearby with an urticating protein. Allergic reactions may follow in susceptible individuals on subsequent exposure to the hairs.

Fabre conducted a famous study on the processionary pine larvae where a group of them were attached nose-to-tail in a circle with food just outside the circle; they continued marching in the circle for a week; he described the experiment in his 1916 book The Life of the Caterpillar. The caterpillars may follow a trail of pheromones or silk, but the main stimuli that induce following are from the hairs (setae) on the end of the abdomen of the caterpillar in front. The ant mill is a similar phenomenon.

Pupa

The moth's pupal stage occurs in a white silken cocoon under soil. The pupae measure around 20 mm and are a pale brownish-yellow color that changes into a dark reddish-brown.

Adult

Adult

As an adult, T. pityocampa has predominately light brown forewings with brown markings. The moth's hind-wings are white. Females have larger wingspans of 36 to 49 mm, compared to a male's 31 to 39 mm. The species flies from May to July.

Shelter building

'Tent' made by larvae in pine tree; frass collects at the bottom of the tent.

T. pityocampa is a highly social organism. Throughout its life cycle, a pine processionary will make several shelters. The first of these are flimsy and temporary, but in the third instar, they build a permanent nest. Once their permanent nest is built, the caterpillars become foragers staying in the vicinity of the nest. The nest has no openings, so catterpillars force themselves through the layers of the shelter. The waste from the larvae's diet accumulates at the bottom of the nest.

Impact of foraging

The pine processionary caterpillar is responsible for most of the defoliation of southern Europe. Although pines are most susceptible to the caterpillar, other trees such as larches are also vulnerable. The caterpillars can completely defoliate trees if large quantities are present.

Midwinter foraging and thermoregulation

The biologist Terrence Fitzgerald has written, "Colonies are active throughout the winter months. Activity records of colonies foraging in pine forests in mountainous regions near Barcelona, Spain, obtained with infrared activity monitors, show that the caterpillars leave their nests soon after sunset and travel to distant feeding sites on the branches of the host tree. There, they feed overnight then return to the nest at dawn." The caterpillars have been observed foraging on the coldest nights and can move at sub-zero temperatures. The nests are positioned so that they can be warmed by the sun. The caterpillars rest during the day and the heat in the nest helps them to digest their food. When they emerge from their nests in late March, they are fully grown and leave their nest processing towards pupation sites in the ground.

Trail marking and processionary behaviour

The caterpillars lay down a pheromone trail from the tip of the abdomen as they advance over the branches of the host tree. Although the caterpillars also secrete silk and mark their pathways with the material, it plays little or no role in trail following. Most likely, silk helps the caterpillars grip on smooth plant surfaces. The caterpillars can distinguish old from new trails. Caterpillars preferentially follow trails marked by larger numbers of caterpillars. Trail marking enables the caterpillars to aggregate at feeding sites and allows them to find their way back to nest after feeding. When they move over the branches, caterpillars may travel head to tail in small groups or alone. In either case, they rely on the trail marker to find their way.

The most spectacular processions are formed when the caterpillars are fully grown and abandon the host tree in search of pupation sites, when as many as three hundred caterpillars may travel long distances from the natal tree looking for soft soil in which to bury themselves and form cocoons. During processions, stimuli from setae on the tip of the abdomen of the caterpillar in front serve to hold processions together, taking priority over the trail pheromone or silk. A caterpillar can readily be induced to follow a model made of a wooden dowel covered with the integument of the abdomen of a killed caterpillar, or induced to run in circles.

Anti-predator defence

Towards the end of their larval development, pine processionary caterpillars are highly irritating to the skin. Contact with the hairs of the caterpillar can cause rashes and eye irritation. Some individuals may have an allergic reaction to the caterpillar's hairs.

When the paws and other body parts of a dog come into contact with the caterpillars' hairs, they become severely irritated. In response, the dog licks the affected area, leaving the dog's tongue severely irritated. The tongue may become necrotic, and it may be necessary to amputate the tongue to prevent sepsis and spread of necrosis. Severe reactions to the hairs may cause kidney failure in the dog, and death may occur.

Natural controls

Mantis religiosa eating Thaumetopoea pityocampa larvae in the Pyrenees.

The pine processionary is an economic pest in coniferous forests in southern Europe. It is controlled to some extent by predators, parasites and viruses which attack the moth at different stages of its life-cycle:

• Eggs are eaten by the orthopteran Ephippiger ephippiger.
• Larvae are eaten by birds such as great tit (Parus major) and great spotted cuckoo (Clamator glandarius).
• Larvae are parasitised by solitary wasps (Ichneumonidae, Braconidae) and some species of horse-fly (Tachinidae).
• Larvae are eaten by Calosoma ground beetles
• Pupae are eaten by hoopoes (Upupa epops).
• Adults are eaten by bats.
• Larvae may be infected by the processionary moth virus Smithiavirus pityocampae.

Artificial control

Efforts to control the pine processionary have included biological control using Bacillus thuringiensis, which is effective on eggs and first or second stage caterpillars (in September or October), or insecticides such as diflubenzuron, an insect growth regulator, which can be sprayed from aircraft. Monitoring can include the use of pheromone traps. Older methods used insecticides in oil, inserted directly into nests, or mechanical removal of nests.

Sources

• Arnaldo P, C. S., Lopes D. (2010). Effects of defoliation by the pine processionary moth, Thaumetopoea pityocampa on biomass growth of young stands of Pinus pinaster in Northern Portugal. iForest, [online: November 15]. Retrieved June 21, 2013 doi: 10.3832/ifor0553-003.
• Brindley, H. H. (1910). "Further notes on the procession of Cnethocampa pinivora". Proc. Cambridge Phil. Soc. 15: 576–587.
• Bryner, R. (2000): Thaumetopoea pityocampa. — In: Pro Natura – Schweizerischer Bund für Naturschutz (Hrsg.) (2000): Schmetterlinge und ihre Lebensräume. Arten, Gefährdung, Schutz. Schweiz und angrenzende Gebiete. Band 3: 521-524. Egg (Fotorotar AG).
• Chinery, Michael. Collins Guide to the Insects of Britain and Western Europe. Collins, 1986. (Reprinted 1991)
• Dajoz, R. 2000. Insects and Forests. The Role and Diversity of Insects in the Forest Environment. Lavoisier publishing, Paris.
• Demolin, G (1962). "Comportement des chenilles de Thaumetopoea pityocampa au cours des processions de nymphose". C. R. Acad. Sci. 254: 733–744.
• Demolin, G. 1971. Incidences de quelques facteurs agissant sur le comportment social des chenilles de Thaumetopoea pityocampa Schiff. (Lepidoptera) pendant la période des processions de nymphose. Répercussion sur l’efficacité des parasites. Ann. Zool. –Ecol. anim., no hors série: 33–56.
• Ducombs, G.; Lamy, M.; Mollard, S.; Guillard, J. M.; Maleville, J. (1981). "Contact dermatitis from processional pine caterpillar (Thaumetopoea pityocampa Schiff., Lepidoptera)". Contact Dermatitis. 7: 287–288. doi:10.1111/j.1600-0536.1981.tb04081.x.
• Edwards, T. G. (1910). "On the procession and pupation of the larva of Cnethocampa pinivora". Proceedings of the Cambridge Philosophical Society. 15: 431–436.
• Fabre, J-H. 1898. Souvenirs Entomologiques 6:298–392.
• Fabre, J-H. 1916. The Life of the Caterpillar. Dodd, Mead. New York.
• Fitzgerald, T. D. (2003). "The role of a trail pheromone in the foraging and processionary behavior of Thaumetopoea pityocampa". J. Chem. Ecol. 29 (3): 513–532.
• Fitzgerald, T. D. 2008. Lethal Fuzz. Natural History Magazine 117:28–33 (September).
• Halperin, J (1990). "Life history of Thaumetopoea spp. (Lep., Thaumetopoeidae) in Israel". J. Appl. Ent. 110: 1–6. doi:10.1111/j.1439-0418.1990.tb00088.x.
• Lamy, M.; Pastureaud, M-H.; Novak, F.; Ducombs, G.; Vincendeau, P.; Maleville, J.; Texier, L. (1986). "Thaumetopoein: an urticating protein from the hairs an integument of the pine procession caterpillar (Thaumetopoea pityocampa Schi ff., Lepidoptera,Thaumetopoeidae)". Toxicon. 24: 347–356. doi:10.1016/0041-0101(86)90194-7.
• Mallmann, R. J. (1962). "Observations sur les réactions tactiles de la chenille processionnaire du pin, Thaumetopoea pityocampa Schiff". Insectes Sociaux. 9: 335–345. doi:10.1007/bf02229633.
• Réaumur, M. 1736. Mémoires pour l'histoire des Insectes, II. Paris.
• Vega, J. M.; Mo; Armentia, A.; Fernández, J.; Vega, J.; De La, Fuente; Sanchez, P.; Sánchís, E. (1999). "Allergy to the pine processionary caterpillar (Thaumetopoea pityocampa)". Clinical and Experimental Allergy. 29: 1418–1423. doi:10.1046/j.1365-2222.1999.00626.x.

External links

Biology

• INRA website: La Processionaire du Pin (in French)
• La Processionnaire du Pin revue Stantari août 2008 (in French)
• Pine processionary Caterpillar by Terrence D. Fitzgerald.

Informal advice

• Wildlife in France