File: <cicindel.htm>
|
COLEOPTERA, Cicindelidae
(Latreille 1804) Description &
Statistics
Cicindelidae
are a moderately large family with ca. 36 genera and 2009 species known as of
1993. They are well represented in the
New World, but are absent from certain areas such as Australia. Important morphological characters of
these "tiger beetles" include a prognathous head with long, thin
sickle-shaped mandibles; clypeus broad, extending laterally beneath the
antennal base; eyes protruding laterally, rendering the head wider than the
pronotum. Their legs are long and
slender, and the body is medium sized (10-15 mm), often brightly colored with
metallic luster. All
active stages of cicindelids are predaceous.
The larvae live in vertical tunnels in hard-packed soil or sand. They hold themselves in position at the
mouths of these tunnels by aid of hooks on the dorsal side of the 5th
abdominal segment. These hooks also
serve to hold the larvae in their tunnels should their prey, usually insects,
prove difficult to pull down into the depths. Adults are active and fast runners. They are found along roadways and paths, stream banks and other
open sunny places. A few exotic
species live in termite nests; other tropical exotics are arboreal. A few species have been transported to
other countries for biological control with no practical results. Further Description.--
Cicindelids are called "tiger beetles" because of the markings of
the elytra in some species and the way in which adults attack their
prey. They are also conspicuous
because of the metallic color of the elytra of many species and their agility
in flight and running. Most species
are terrestrial, some are arboreal and other semi-aquatic. All species are believed to be predaceous
as both adults and larvae, and their food consists of a wide variety of
insects and other small animals. The
adults, because of their greater activity, have a greater variety of food
than larvae, which are dependent on what they find in their comparatively
limited range. Several species are
associated with termite nests, although their exact status is not always
certain. Early biological studies
were performed by Shelford (1909), Hamilton (1925), Balduf (1935) and Clausen
(1940). Terrestrial cicindelidae inhabit exposed
locations such as paths, sandy areas and roadways. When ovipositing, the female excavates small cavities, <1/2
in. deep, in soil, and lay single their ovate and translucent eggs. The larvae show several morphological modification
that suit them for predation and movement in their burrows. The head and pronotum are large and
heavily sclerotized. The mandibles
are very large and powerful, being bent upward so that they serve for more
than just seizing and holding prey (Clausen 1940). Ventrally, the head is decidedly convex. The legs have long sharp claws, which in
conjunction with the heavy, forwardly directed hooks on the dorsum of the 5th
abdominal segment and with the S-shaped body, allow for quick movement in the
burrow and also serve to brace the larva in case of a struggle with a
powerful prey. The
burrow's depth is dependent on the type of soil in which it is constructed,
and it varies among species and with the age of the larva. Some species make burrows in sand that are
1-2 m. deep, although most do not exceed 1/2 m. The burrows are generally perpendicular to the ground
surface. The larva lies with its head
at the entrance of the burrow, the claws and dorsal hooks embedded in the
walls, and strikes out with a very rapid movement when an insect or other
animal of suitable size ranges close. Overwintering
is most frequently as larvae, though some species hibernate as adults at the
bottom of the closed burrow. Prior to
pupation, the larva closes the entrance to form a special pupation chamber
either at the bottom of the burrow ar at one side of the main shaft. In the tropics, the life cycle usually
takes one year, while in colder climates it may be 3-4 years. Arboreal
species of Tricondyla and Collyris in Java differ from
those inhabiting soil principally in the location of their burrows. These are formed instead in young twigs of
plants. The initial entry hole
through the bark and into the pith is made by the parent female with her
ovipositor. This hole is plugged by
the female after the egg is laid. The
burrow is increased in size as the larva develops. Coffee trees are susceptible to injury of this type, and ants
that tend various scale insects, notably Coccus
viridis and Pseudococcus spp. are thought
to be the main food of the species occurring in twig burrows (Clausen
1940/1962). References: Please refer to
<biology.ref.htm>, [ Additional references may be found at: MELVYL Library ] Evans, M. G. E. 1965.
Proc. Royal Ent. Soc. London 40:
61-6. Willis, H. L. 1968.
J. Kansas Ent. Soc. 41:
303-17. |