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Vol. 3: Insects

Order: Neuroptera

Species accounts

Beaded lacewing

Spermophorella maculatissima

FAMILY

Berothidae

TAXONOMY

Spermophorella maculatissima Tillyard, 1916, Brisbane, Queensland, Australia.

REPRODUCTIVE BIOLOGY

Adult females lay solitary eggs on long, silken stalks. It is thought that the first instar triungulin larvae seek out and enter a suitable termite colony, where they can remain undetected by the termites. The larvae undergo hypermetamorphic development.

CONSERVATION STATUS

Not listed by the IUCN.

SIGNIFICANCE TO HUMANS

OTHER COMMON NAMES

None known.

PHYSICAL CHARACTERISTICS

Relatively small lacewings. Short, narrow body, with wings held vertically over the abdomen. Wings have speckled black, brown, and white pattern on wing veins to aid in camouflage. Body and wing veins are covered with long setae. Newly hatched larvae are elongate with short jaws. Later instars unknown.

DISTRIBUTION

Queensland, Australia.

HABITAT

None known.

Green lacewing

Mallada albofascialis

FAMILY

Chrysopidae

TAXONOMY

Mallada albofascialis Winterton, 1995, Brisbane, Queensland, Australia.

Arid regions, particularly in open sclerophyll forests.

OTHER COMMON NAMES

 

BEHAVIOR

Adults remain motionless during the day, with the antennae held out in front of the head. They sway their bodies when potential predators are near.

FEEDING ECOLOGY AND DIET

Adults probably are generalist feeders. The larvae of all known berothids are obligate predators on subterranean termites. Larvae presumably use an allomone to subdue their termite prey.

First and third instars are active feeders, whereas the second instar is a sedentary, resting stage.

None known.

PHYSICAL CHARACTERISTICS

Relatively small lacewings. The body is elongate and delicate, with broad wings that have characteristic open, “chrysopidtype” venation. The body is light to dark green in color, with red patches on the prothorax and head. The face also has a dis-

Euclimacia torquata

 

Myrmeleon formicarius

Megalithone tillyardi

Spermophorella maculatissima

Mallada albofascialis

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Order: Neuroptera

tinctive white area above the mouth. The larva has an elongate body and carries a trash packet within special curved hairs on its back, used for camouflage.

DISTRIBUTION

Northern Territory and coastal Queensland, Australia.

HABITAT

Forested areas.

BEHAVIOR

Nothing is known.

FEEDING ECOLOGY AND DIET

Adults feed on honeydew and flower nectar. The larva is an arboreal generalist predator feeding on a variety of soft-bodied arthropods, especially mealybugs (Hemiptera: Margarodidae).

REPRODUCTIVE BIOLOGY

Adult females lay eggs on long silken stalks in patches of 10–15 eggs.

CONSERVATION STATUS

Not listed by the IUCN.

SIGNIFICANCE TO HUMANS

None known.

Moth lacewing

Megalithone tillyardi

FAMILY

Ithonidae

TAXONOMY

Megalithone tillyardi Riek, 1974, Cunningham’s Gap, Queensland, Australia.

OTHER COMMON NAMES

None known.

PHYSICAL CHARACTERISTICS

The moth lacewing is a relatively large, robust insect with an appearance similar to that of a dull hepialid moth. The wings and body are dull brown, and the body is covered with numerous long hairs. The wings are folded over the body. The larva is fossorial and scarabaeiform in body shape.

DISTRIBUTION

Southeastern Queensland and northern New South Wales, Australia.

HABITAT

Higher elevations, often on sandy soils.

BEHAVIOR

Adults emerge in masses to form large mating aggregations or swarms composed of many more males than females.

FEEDING ECOLOGY AND DIET

It is not clear if adults feed, but the larvae eat root exudates of plants. Ithonids have been recorded erroneously as predators of scarab larvae.

REPRODUCTIVE BIOLOGY

The female has a genital plug upon emergence, which is apparently displaced during copulation.

Vol. 3: Insects

CONSERVATION STATUS

Not listed by the IUCN. The conservation status of the moth lacewing is difficult to assess, because larvae are fossorial and adult swarms are infrequent. Habitat destruction appears to be the main threat to individual populations.

SIGNIFICANCE TO HUMANS

Swarms have been recorded hitting the metal roofs of houses and sounding like a hail storm. While they are rare, swarms are a nuisance to humans, because adults also enter houses and gather in dark places. Such plagues are known to last as long as three weeks.

Mantid lacewing

Euclimacia torquata

FAMILY

Mantispidae

TAXONOMY

Euclimacia torquata Navás, 1914, Queensland, Australia.

OTHER COMMON NAMES

None known.

PHYSICAL CHARACTERISTICS

Medium-size lacewings. The body is robust, with relatively narrow wings that are darkly pigmented along the anterior portion. This species has strongly contrasting black, yellow, and orange coloration, enabling it to be an effective wasp mimic. The front legs are raptorial. The immature stages are unknown.

DISTRIBUTION

Queensland, Australia, and Papua New Guinea.

HABITAT

Forested areas.

BEHAVIOR

Adults fly and walk in a way similar to paper wasps, as a defense against predators.

FEEDING ECOLOGY AND DIET

Adults are generalist predators, using their raptorial forelegs to capture prey. Based on evidence from other mantid lacewings, the larva is presumably a specialized predator of spider egg sacs and probably also is highly host specific.

REPRODUCTIVE BIOLOGY

Nothing is known.

CONSERVATION STATUS

Not listed by the IUCN.

SIGNIFICANCE TO HUMANS

None known.

Antlion

Myrmeleon formicarius

FAMILY

Myrmeleontidae

TAXONOMY

Myrmeleon formicarius Linnaeus, 1767, Europe.

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Grzimek’s Animal Life Encyclopedia

Vol. 3: Insects

OTHER COMMON NAMES

English: Doodlebug.

PHYSICAL CHARACTERISTICS

Large, very long lacewing. The head and thorax are short and stout, and the abdomen is very elongate. Body is brown with tan markings; antennae are thickened apically. Wings very elongate, narrow, and hyaline. Venation is mottled brown, black, and white. Larvae are robust and ovoid-shaped with large curved jaws. Body is adapted for burrowing backward through sandy soil.

DISTRIBUTION

Western Europe.

HABITAT

A wide variety of habitats, especially sandy desert or savanna regions.

BEHAVIOR

Adults are active at night and sit on foliage during the day. The elongated body and brown coloration of the adult serve as crypsis as they lie flat against a twig or branch. Larvae quickly burrow deep into the sand to avoid predation when the pit is disturbed by anything larger than a small prey item.

FEEDING ECOLOGY AND DIET

Adults are generalist predators, capturing prey on the wing. Larvae construct conical pits in fine, sandy soil by flicking sand out of the pit with rapid upward movements of the head. The larva waits at the bottom of the pit with only its large jaws exposed. When a suitable prey falls into the pit, the larva quickly seizes the prey by impaling it and injects paralyzing venom before dragging it below the sand surface.

REPRODUCTIVE BIOLOGY

The adult female lays egg in sandy soil. Larvae burrow through the soil and form conical pits, typically under overhangs or in caves, to avoid precipitation that may disturb the pit and drown the larva. When development is complete, the larva spins a spherical cocoon from silk produced from the anus, which is impregnated with sand particles.

CONSERVATION STATUS

Not threatened.

SIGNIFICANCE TO HUMANS

Antlion larvae, or “doodlebugs,” have long been established in human folklore, particularly in children’s chants or charms, typically from countries around the world that have been influenced by Europeans. Many charms referring to doodlebugs specifically cite the conical pits formed by the larva or their peculiar reverse-burrowing behavior.

Spoonwing lacewing

Nemoptera sinuata

FAMILY

Nemopteridae

TAXONOMY

Nemoptera sinuata Olivier, 1811, eastern Mediterranean.

Order: Neuroptera

Nemoptera sinuata

Norfolius howensis

OTHER COMMON NAMES

None known.

PHYSICAL CHARACTERISTICS

Large to medium-size lacewings. The body is elongate and robust, with relatively broad, rounded forewings. The hind wings are highly modified, narrow, and petiolate basally and slightly dilated apically, so that the wing is somewhat spoon-shaped. Wings are strikingly marked with irregular yellow and black banding. The forewings are held above the body, while the hind wings project posteriorly. The larvae are broad and oval shaped, with short necks and short jaws.

DISTRIBUTION

Europe and the Mediterranean region.

HABITAT

Open grasslands and forests.

BEHAVIOR

Adults are active during the day, feeding at flowers.

FEEDING ECOLOGY AND DIET

Adults feed at flowers on pollen and nectar. Larvae lie buried in the sand, remaining inactive for long periods of time. When prey movement is detected, larvae approach slowly and attack with a single impaling of the prey with their jaws, during which time it is presumed that paralyzing venom is injected. Larvae are occasionally cannibalistic.

REPRODUCTIVE BIOLOGY

Females lay eggs in sand. Larval development is prolonged and probably univoltine in nature. Adults are active in late spring.

CONSERVATION STATUS

Not listed by the IUCN.

SIGNIFICANCE TO HUMANS

None known.

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Order: Neuroptera

Norfolius

Norfolius howensis

FAMILY

Nymphidae

TAXONOMY

Myiodactylus howensis Tillyard, 1917, Lord Howe Island, New South Wales, Australia.

OTHER COMMON NAMES

None known.

PHYSICAL CHARACTERISTICS

Medium-size to large lacewings, with large, broad wings. Body is elongate and yellow-green in color, with a series of brown spots along the dorsal surface of thorax and abdomen. Antennae are long and yellow. Wings are transparent, with densely reticulate venation and black spots located on the pterostigma. Larva is discoid, with a quadrangular head and large, scythe-like jaws.

DISTRIBUTION

Eastern coastal regions of mainland Australia and Lord Howe Island (Australia).

Vol. 3: Insects

HABITAT

Dense forested areas.

BEHAVIOR

Nothing is known.

FEEDING ECOLOGY AND DIET

Adult and larva are generalist predators. Larva is a sedentary leaf litter dweller.

REPRODUCTIVE BIOLOGY

Nothing is known.

CONSERVATION STATUS

Not listed by the IUCN. Norfolius is not uncommon in densely forested (e.g., rainforest) areas along coastal eastern Australia. Habitat destruction appears to be the only real threat to this species.

SIGNIFICANCE TO HUMANS

None known.

Resources

Books

Aspöck, H., U. Aspöck, and H. Hölzel. Die Neuropteren Europas. 2 vols. Krefeld, Germany: Goecke and Evers, 1980.

McEwen, P. K., T. R. New, and A. E. Whittington, eds.

Lacewings in the Crop Environment. Cambridge, U.K., and New York: Cambridge University Press, 2001.

New, T. R. “Planipennia (Lacewings).” In Handbuch der Zoologie: Eine Naturgeschichte der Stämme des Tierreiches. Vol. 4, Arthropoda: Insecta, edited by Max Beier, Maximilian Fischer, Johann-Gerhard Helmcke, Dietrich Starch, and Heinz Wermuth. Berlin and New York: W. de Gruyter, 1989.

—. “Neuroptera (Lacewings).” In The Insects of Australia, edited by CSRIO. 2nd edition. Vol. 1. Carlton, Australia: Melbourne University Press, 1991.

Periodicals

Aspöck, U. “Male Genital Sclerites of Neuropterida: An Attempt at Homologisation (Insecta: Holometabola).” Zoologischer Anzeiger 241, no. 2 (2002): 161–171.

Aspöck, U., J. D. Plant, and H. L. Nemeschkal. “Cladistic Analysis of Neuroptera and Their Systematic Position

within the Neuropterida (Insecta: Holometabola: Neuropterida: Neuroptera).” Systematic Entomology 26 (2001): 73–86.

Oswald, J. D. “Revision and Cladistic Analysis of the World Genera of the Family Hemerobiidae (Insecta: Neuroptera).”

Journal of the New York Entomological Society 101 (1993): 143–299.

Oswald, J. D., and N. D. Penny. “Genus-Group Names of the Neuroptera, Megaloptera and Raphidioptera of the World.”

Occasional Papers of the California Academy of Sciences 147 (1991): 1–94.

Withycombe, C. L. “Some Aspects of the Biology and Morphology of the Neuroptera, With Special Reference to the Immature Stages and Their Possible Phylogenetic Significance.” Transactions of the Entomological Society of London (1924) 303–411.

Other

Oswald, J. D. “NeuroWeb: The Neuropterists’ Home Page.”

[3 Apr. 2003] <http://insects.tamu.edu/research/

neuropterida/neuroweb.html>.

Shaun L. Winterton, PhD

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