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NEUROPTERA, Hemerobiidae (Westwood 1840 -- <Images> & <Juveniles> Please refer also to the following links for details on this
group: Hemerobiidae = Link 1 Description & Statistics
Hemerobiidae are known as "brown lacewings" and are
distributed worldwide. There are
around 60 species known in North America.
Diagnostic characters include forked costal cross-veins, filiform or
moniliform antennae and the forewing having two or more R-s veins. Hemerobiids resemble chrysopids as
far as their predaceous habits are concerned, but they may be distinguished
on the basis of several subtle characteristics as follows: Hemerobiid larvae never carry trash as do
some chrysopid larvae; the eggs are not stalked and are attached by their
sides to leaves and bark (Withycombe 1922, 1923). Eggs are whitish, grayish or even pink and elongate-oval, with
the chorion often pitted. They bear a
knob-like or disk-like micropyle, often of considerable size (Clausen
1940/62). The chorion is densely
studded with glossy papillate projections.
The egg breaker is saw-shaped.
Eggs of H. pini are pale cream colored, that
changes to brown before hatching (Clausen 1940/62). There are three active larval
instars, all quite similar to the larvae of Chrysopidae. Only 1st instar larvae have the
trumpet-shaped tarsal claws, while they occur on all instars of
Chrysopidae. No species carries a
trash packet on the dorsum of the body and thus none has the hooked setae. The cocoon is loosely woven,
double-walled, elliptical in outline, and generally is formed in protected
spots, such as under bark, rather than exposed on bark or foliage. Cocoons differ markedly from the nearly
spherical parchment-like ones of Chrysopidae. The pupal skin is cast outside the cocoon. All species are predaceous, attacking
mainly aphids, but also chermids, mealybugs and white flies, and sometimes
diaspine scales. Several species are
restricted to certain types of trees and thus feed only on insects that live
on those trees. Withycombe (1922, 1923) gave early
accounts on the behavior of a number of Hemerobius
spp.. Hemerobius pygmaeus
Ramb. is confined entirely to oak, while H.
atrifrons McL. and H. pini
Steph. are found only on conifers (Killington 1932). Killington (1936, 1937) gave detailed
information on immatures and behavior of several species. There are several generations
annually, the number varying with climate.
Sympherobius amicus has 8 generations in Israel, with the minimum cycle taking only
23.5 days. Hemerobius pygmaeus and
several others have only a single generation in England. The average duration of the egg, larval
and cocoon stages in summer in temperate regions is ca. 5-12, 10-18 and 12-16
days, respectively. Most species
hibernate as either larvae or pupae within the cocoons, though H. stigma
Steph. can be found as adults during winter and H. pygmaeus occurs only
as free larvae in sheltered places. Wesmaelius concinnus Steph. hibernates in the egg in England, this stage
persisting for 7 months. There are two color forms of adults
in many species, the normal summer form being brown, while that found during
winter is grayish-brown or spotted (Withycombe (1922, 1923). Bodenheimer (1928) recorded an
average production of 250 eggs by a series of females and a maximum of 589 by
one individual. Smith (1923) studied
the behavior of a series of North American species and found that the
gestation period took ca. 5 days. A
maximum production of 460 eggs was obtained from Hemerobius humuli L.,
though this was from a field-collected female and may not represent the total
capacity. Micromus posticus Wlk.
lays up to 58 eggs per day. Clausen
(1940) regarded the reproductive capacity to be somewhat higher than in
Chrysopidae. Several species have been imported
for biological control of forest pests in Canada and other countries. Bodenheimer (1928) claimed effective
control of Pseucococcus citri Risso in Israel through the
liberation of large numbers of native Sympherobius
amicus Nav. Several species of Hemerobius were introduced into Australia, New Zealand and Canada
for control of Chermidae attacking forest trees. References:
Please refer to <biology.ref.htm>, [Additional references may be
found at: MELVYL Library] Banks, N.
1906. A revision of the
nearctic Hemerobiidae. Trans. Ent.
Soc. Amer. 32: 21-51. Killington, J. F. 1932.
Notes on the life-history of Hemerobius
pini Steph. Trans. Ent. Soc. So. England 8: 41-4. |