About Orthoptera
Crickets and grasshoppers
Introduction
The order Orthoptera is divided into two major divisions: Ensifera (true crickets)
and Caelifera (true grasshoppers). Ensifera includes the families Gryllidae (crickets)
and Tettigoniidae (bush crickets; long-horn grasshoppers referring to their long
antennae). Caelifera encompasses the true grasshoppers in the family Acrididae (short-horn
grasshoppers referring to their short antennae).
Orthoptera and allied insects have an incomplete metamorphosis (they are exopterygote).
This means that they don’t have a pupal stage and that the immature stages (called
nymphs) closely resemble the adults. Female adults lay eggs
which vary in size and shape between species. The first instar (first nymphal stage)
nymphs hatch (eclose) in the spring when the temperature is suitable for development
and food is abundant, especially young, succulent vegetation. The number of nymphal
instars (discrete nymphal stages) varies between species but most Acrididae have
four nymphal instars and most Tettigoniidae have five or six. Nymphal development
takes about two months and the adults usually emerge in July.
Males and females mate after a courtship display in which
song (stridulation) plays an important role. Females
lay eggs throughout their adult lives. Each species has a preferred habitat for
egg laying. The eggs of Tettigoniidae are always laid singly and those of Acrididae
are laid in groups protected by a tough case (egg pod). It is possible to identify
egg pods to species.
The egg is the overwintering stage for most species of Orthoptera; development of
the egg is arrested during winter (diapause). Hatching is
triggered by increased temperature and humidity such as after spring rainfall. Nymphs
first appear as vermiform larvae on emergence.
Vermiform larvae
Orthoptera hatch as “vermiform larvae” - newly emerged nymphs are surrounded by
a protective embryonic cuticle (a thin membranous sleeve). Acrididae need to emerge
not only from their egg shell but also from the egg pod. Additionally some acridids
and tettigoniids lay their eggs in soil and the vermiform larva has to travel to
the soil surface. It is only at the soil surface that the embryonic cuticle is shed
and the first instar nymph emerges.
Stridulation
Orthoptera song is produced through stridulation. A typical stridulatory mechanism
consists of a file (series of pegs) and a scraper (thickened ridge). Rubbing together
of the file and scraper produces the characteristic sound of Orthoptera.
Acridid males are more effective at sound production than females. Their file is
longer and has more stridulatory pegs than females. The prominent fore wing veins
constitute the scraper. The space between the fore wings is thought to have a role
in resonance. Some short winged females (such as the Meadow Grasshopper, Chorthippus
parallelus) do not make any sound despite stridulatory movements.
Courtship display
Male acridids are thought to produce five types of song during courtship and mating.
The songs vary in intensity of sound, form of pulse and frequency of repetition.
Single males or groups of males produce ‘normal song’ to attract females. Rival
males in close proximity to a female can alternately stridulate in a ‘rivals duet’.
Females sometimes respond through stridulation as they orientate towards the male.
‘Courtship song’ follows and this form can be elaborate and very different to the
‘normal song’. Some species combine song with dance.
At the end of the courtship display males produce a short ‘assault song’ just prior
to mating. In acridids, the male grips the female with his two fore legs and curls
his abdomen beneath the female abdomen during mating. The male is hooked to the
female through special structures on the male organ. The male sperm is transferred
in a package called the spermatophore. During the process of mating the male continues
to stridulate producing a ‘copulation song’.
Egg laying and oviposition sites
Female orthoptera position and lay their eggs through structures called ovipositors.
In tettigoniids the ovipositor consists of three long valves. Acridids have short,
stout anterior and dorsal valves with the inner pair also reduced.
The acridid ovipositor is adapted for laying egg pods into the ground; the short,
stout structure is used for digging and probing prior to egg laying. After each
egg is laid the female injects a frothy secretion into the hole which mixes with
soil particles to form the outer surface of the egg pod. When all the eggs are laid
further froth is excreted to complete the egg pod.
Egg Laying
Click on picture for details
The long tettigoniid ovipositor is adapted for laying eggs deep into plant tissue
or into the ground. There is considerable variation in ovipositor form between species
and this relates to differing functions. Females select an egg-laying site after
examining the substrate with the sensory palps (mouthparts). Some species use their
mouthparts to bite through the substrate to assist oviposition. The ovipositor is
covered with sensory hairs that allow the female to assess the oviposition site
and the placement of the egg.
Tettigoniids are relatively specific in oviposition site selection. The acridids
all lay their egg pods in the soil.
Table = Preferred egg laying sites for UK short-horn grasshoppers (acridids) (from
Waloff, 1950)
|
Common name
|
Scientific name
|
Egg-laying site
|
|
Field Grasshopper
|
Chorthippus brunneus
|
Soil – upper surface
|
|
Meadow Grasshopper
|
Chorthippus parallelus
|
Soil – upper surface
|
|
Heath Grasshopper
|
Chorthippus vagans
|
Soil – upper surface
|
|
Rufous Grasshopper
|
Gomphocerippus rufus
|
Soil – upper surface
|
|
Mottled Grasshopper
|
Myrmeleotettix maculatus
|
Soil – upper surface
|
|
Woodland Grasshopper
|
Omocestus rufipes
|
Soil – upper surface
|
|
Stripe-winged Grasshopper
|
Stenobothrus lineatus
|
Soil – above grass roots
|
|
Lesser Marsh Grasshopper
|
Chorthippus albomarginatus
|
Vegetation – base of grass blades
|
|
Large Marsh Grasshopper
|
Stethophyma grossum
|
Vegetation – base of grass blades
|
|
Common Green Grasshopper
|
Omocestus viridulus
|
Vegetation – base of grass blades
|
Thermoregulation and Diapause
Like all insects, orthopterans are “ectotherms”, a term which signifies that they
mostly rely on external sources of heat to raise their body temperature. The internal
temperature of ectotherms, therefore, tends to vary, often tracking the ambient
temperature of the immediate environment. To cope with this, ectotherms have developed
various ways of controlling their body temperatures, for example basking on rocks,
moving in and out of shade, and dilating or constricting peripheral blood vessels
(see photos). In addition, ectotherms often have more complex metabolisms than endotherms
(such as mammals), for example they may have many (up to ten) enzyme systems that
operate at different temperatures for an important chemical reaction.
Despite these adaptations, ectothermic animals are often more reliant on environmental
conditions than endothermic animals. Therefore, they are often constrained to certain
microclimatic conditions and, so, changes in climate can trigger corresponding changes
in the distributions of ectothermic animals. Therefore, highly mobile, ectothermic
insects, such as grasshoppers and crickets are regarded as valuable indicators of
climate change. Long-winged Coneheads (Conocephalus discolor) have been expanding
into new territories, with rising temperatures under climate change a likely factor.
Until the 1980s they were confined to the South Coast, but they can now be found
north of Leicester. Similarly Roesel’s Bush Cricket (Metrioptera roeselii)
was largely restricted to the Thames and Solent Estuaries in the mid-20th century,
but is now seen across south and central England up to the Midlands.
Spread of Long-winged Conehead
Click on map for details
Spread of Roesel’s Bush-Cricket
Click on map for details
Many insects in the UK also undergo arrested development in winter, a complex physiological
process known as diapause. There is another form of arrested development known as
acquiescence. Acquiescence ends as soon as conditions are favourable whereas diapause
is not terminated even if ambient conditions are suitable for insect activity. Therefore,
diapausing eggs do not hatch until diapause has been completed and even warm weather
does not stimulate premature hatching. Diapause is a common phenomenon in insects,
for example adult ladybirds enter diapause during winter and undergo reproductive
maturation during this period.
Mortality of Orthoptera
Temperature and rainfall are major mortality factors of the egg stage. Eggs laid
in soil are vulnerable to waterlogging and egg diapause has precise temperature
requirements. Natural enemies of Orthoptera are also important mortality factors.
Natural enemies
Microbial pathogens (fungi, bacteria, viruses and nematodes) are important natural
enemies of all Orthoptera. The prevalence of these pathogens is predicted to increase
with climate change.
A number of parasitoids (parasitic Diptera (flies) or Hymenoptera (wasps) with complex
life cycles intimately connected to the host) attack Orthoptera. Chalcid (Hymenoptera)
wasps lay their eggs into the eggs of Conocephalus dorsalis. Scelionid wasps from
the genus Scelio are egg parasites of acridids. Some species of acridid are attacked
by Blaesoxipha laticornis (Diptera: Sarcophagidae) as adults. The female
fly is viviparous - instead of laying eggs onto the host, she deposits young larvae
onto the grasshopper cuticle. The larvae invade the body cavity of the host and
emerge from behind the grasshoppers head as final instar (last stage) larvae ready
to pupate in the soil.
Ectoparasitic mites are commonly seen on the bodies of Orthoptera in mainland Europe
but rarely in the UK. Warmer UK temperatures could increase the occurrence of these
mites.
There is very little information on the predators of Orthoptera although birds,
small mammals and reptiles have been observed feeding on them. A number of invertebrate
predators are known to consume Orthoptera, including spiders, Sphecidae (hunting
wasps), Vespidae (wasps) and Asilidae (robber flies). Tettigoniid nymphs and all
stages of acridids have been seen in the low-level webs of the spider Agelena labyrinthica.
Some bush-crickets are predatory and consume grasshoppers or younger stages of their
own species.
Links
The Orthoptera Species File is
a taxonomic database of the world's Orthoptera, both living and fossil.
Wikipedia article on Tettigoniidae (bush-crickets)
Wikipedia article on Gryllidae
(crickets)
Wikipedia article on Caelifera (grasshoppers)