common name: sharpshooters, leafhoppers
scientific name: Cicadellidae (Insecta: Hemiptera: Auchenorrhyncha: Cicadellidae)
Introduction - Description and Systematics - Life History - Diet - Economic Importance - Natural Enemies - Selected References
Sharpshooter is a term commonly used to describe a group of leafhoppers in the family Cicadellidae. There have been several explanations for the use of this term. Riley and Howard (1893) first used 'sharpshooter' to describe the feeding damage of the glassy-winged sharpshooter, Homalodisca coagulata (Say), on cotton. This damage was caused by the piercing-sucking mouthparts of H. coagulata that appeared to be caused by a 'minute bullet'. They also reported 'rapid and forcible
ejection of minute drops of fluid' as another explanation for the use of this term. The term sharpshooter is also attributed to the hiding behavior of these insects when alarmed. Disturbed sharpshooters will slip quickly behind branches and stems to avoid predators, an action not unlike the behavior of army sharpshooter riflemen who would hide behind the trunks of trees to avoid detection by the opposition as they passed by their position.
Sharpshooters are leafhoppers in the tribes Proconiini and Cicadellini within the family Cicadellidae in the
suborder Auchenorrhyncha of the Hemiptera. Worldwide, there are nearly 20,000 described
species, making the Cicadellidae the 10th largest insect family. Presently, there are 300 genera within the two tribes. Because leafhopper diversity is directly related to plant diversity, many
more new species will be undoubtedly be described as entomologists continue to explore pristine
tropical regions.
Like all true bugs, sharpshooters have piercing-sucking mouthparts, which they use to tap into
and feed upon xylem or phloem (sap) tissue of plants. Most leafhoppers have cryptic coloration
(camouflage) and are often brown, green, or yellow which enables them to blend into their
surroundings. Sharpshooters are expert jumpers with powerful hind legs lined with a row of
distinct spines on the tibia. The adults have two pairs of wings and are strong flyers. The nymphs
of sharpshooters are wingless but are capable of powerful leaps to search for food and to avoid
predators. Sharpshooters have large eyes for excellent visual acuity to avoid detection and
capture by potential predators. Additionally, they can detect the reflectance spectrum of several
colors, with hues of yellow being the most attractive (Tipping et al. 2004).
neonate H. coagulata
fifth instar H. insolita nymph
fourth instar P. irrorata nymph
Sharpshooters are among the largest of leafhoppers found in North America with several species
nearly 30 mm in length. Some of the sharpshooters commonly found in Florida and throughout
the southeastern U.S. are represented by the genera Cuerna, Homalodisca, Oncometopia and
Paraulacizes (Turner and Pollard 1959).
adult C. costalis
adult H. coagulata
adult H. insolita
adult O. nigricans
adult P. irrorata
Sharpshooters develop through a gradual metamorphosis. Females insert their eggs into plant
tissue, usually leaves, with a sharp knifelike structure called an ovipositor (a structure that
deposits eggs). Several species of sharpshooters produce a white chalky material known as
brochosomes that is placed on the wing covers. After the eggs have been deposited into the plant,
females then scrape this material to 'powder' the area (Rakitov 2004). There are five nymphal
instars that are morphologically similar but increase in size with each stage. The adult stage
initially emerges with small wings that require a few hours to fully expand and harden. The
number of generations varies between sharpshooter species but is usually one to two per year.
H. coagulata egg mass
H. insolita egg mass
brochosomes on forewings of H. coagulata
eclosion of adult O. nigricans (1 of 4)
eclosion of adult O. nigricans (2 of 4)
eclosion of adult O. nigricans (3 of 4)
eclosion of adult O. nigricans (4 of 4)
video of female H. coagulata ovipositing
video of female H. coagulata depositing brochosomes
The diet of the majority of sharpshooters consists exclusively of nutrient-poor xylem
fluid from a great variety of plant species (Andersen et al. 1989). This fluid is comprised of over
95% water with small amounts of organic and inorganic molecules. Amino acids such as
glutamine, arginine and asparagine, as well as organic acids such as citric, malic and oxalic acids
are often present but occur in concentrations that are magnitudes lower than the nutrients found in
other plant tissues. Because xylem fluid is under a negative pressure, leafhoppers must extract it
with a cibarium pump (sucking apparatus) that is powered by large dilator muscles that have their
origins in the bulging front region of the head.
close up of H. coagulata head
close up of P. irrorata head
To successfully develop and reproduce by feeding solely on nutritionally poor xylem fluid,
sharpshooters have high consumption rates coupled with an efficient digestive tract that features a
re-circulating loop called a filter chamber. They are extremely efficient at assimilating what they
have ingested and their waste is 99% water with small amounts of ammonia. Sharpshooters have
been recorded to consume, process, and excrete 17 ml per day (Tipping unpublished data). That
is the equivalent of a person drinking nearly 400 gallons of water! The filter chamber allows for
greater efficiency in absorbing nutrients from the dilute xylem fluid.
video of O. nigricans excreting
In addition, the chemical composition of xylem fluid varies widely between plant species as well as
within a single plant over the course of the season. Sharpshooters tend to find and congregate on
certain plants during different times of the season to maximize nutrient consumption (Mizell and
French 1987). As the nymphs and adults disperse to find adequate nutrients for development,
maintenance, and reproduction, they determine host suitability by tasting.
Because sharpshooters disperse relatively long distances as both nymphs and adults in their search
for adequate nutrition required for development, maintenance, and reproduction, they feed on a
great variety of plants. Sharpshooters can cause physical damage to plants by the insertion of
their mouthparts or by robbing the plant of important nutrients. More importantly however, is
their ability to vector (transmit) infectious pathogens from plant to plant. Some of these
pathogens include viruses, bacteria, and other microorganisms (McClure et al. 1982, Purcell and
Suslow 1984). One of the most important disease organisms vectored by sharpshooters is the
bacterium Xylella fastidiosa Wells et al. Xylella is the causative agent for a variety of
economically important diseases including phony peach, plum leaf scald, almond leaf scorch,
citrus variegated chlorosis (in Brazil) and Pierce's disease of grape (Wells et al. 1987, Mizell et al. 2003). The bacterium blocks the water-conducting xylem tissue causing
scorch symptoms in diseased plants. Sharpshooters can acquire the bacterium after they feed on
an infected plant. The bacterium can survive and colonize the inner linings of the mouthparts (Timmer et al. 1983).
Once they have acquired Xylella, adult sharpshooters can vector it for the remainder of their lives.
However, the nymphs lose the bacteria when they moult (shed their skin) the inner linings of the
mouthparts but can reacquire the pathogen by feeding on an infected plant.
Pierce's disease of grape symptoms
The natural enemies of sharpshooters include predatory insects such as mantids and dragonflies.
Free living and snare building spiders also capture and eat sharpshooters. In Florida, anoles have
been observed eating sharpshooters. Small parasitic wasps in the genus Gonatocerus are
important natural enemies of sharpshooters because they attack the egg stage of several species
(Lopez et al. 2004). The larvae of these minute wasps develop inside the eggs of the
sharpshooter, and kill the developing embryo.
parasitic Gonatocerus wasps
parasitic Gonatocerus wasps
H. coagulata egg mass parasitized by Gonatocerus wasps
In North Florida, several species of fungal pathogens reach epizootic levels in two species of
sharpshooters, Homalodisca coagulata and Oncometopia nigricans. A new species of the genus
Hirsutella has been found to be the principle pathogen (Boucias and Mizell unpublished). During
cool, wet conditions, many sharpshooters can be found mycosed (attacked by fungi) and
mummified in the field.
dead and mummified H. coagulata
dead and mummified O. nigricans
dead and mummified H. coagulata
Strepsipterans, or twisted-wing parasites, are an unusual group of insects that parasitize a variety
of insects including sharpshooters. Strepsipterans have an unusual life cycle with adult
females remaining inside the host but protruding a structure called a cephalathorax. Males emerge
from pupal cases that also protrude from the host and seek out mature females for mating. The
eggs remain within the body of the female until they eclose. The larvae are called triungulins
(walking mobile stage) and escape the bodies of both the female and the host. After the
triungulins enter a new host they lose their legs and appear maggot-like. Oncometopia nigricans
is often stylopized (attacked by a strepsipteran) by an unidentified species of Halictophagidae.
These parasites do not kill the sharpshooter host, however they have been reported to reduce the
fecundity of infested females. Generally, a single strepsipteran is found within a host, although;
on rare occasions, more than one may be present in a single host.
strepsipteran parasites in O. nigricans
- Andersen PC, Brodbeck BV, Mizell III RF. 1989. Metabolism of amino acids, organic acids and
sugars extracted from the xylem fluid of four host plants by Homalodisca coagulata.
Entomologia Experimentalis et Applicata 50: 149-159.
-
Lopez R, Mizell III RF, Andersen PC, Brodbeck BV. 2004. Overwintering biology, food
supplementation and parasitism of eggs of Homalodisca coagulata (Say) (Homoptera:
Cicadellidae) by Gonatocerus ashmeadi Girault and Gonatocerus morilli (Howard)
(Hymenoptera: Mymaridae). Journal of Entomological Science 39: 214-222.
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McClure MS, Andreadis TG, Levy GH. 1982. Manipulating orchard ground cover to reduce
invasion by leafhopper vectors of peach X-disease. Journal of Economic Entomology 75: 64-68.
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Mizell III RF, French WJ. 1987. Leafhopper vectors of phony peach disease: Feeding site
preference and survival on infected and uninfected peach, and seasonal response to selected host
plants. Journal of Entomological Science 22: 11-22.
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Mizell III RF, Andersen PC, Tipping C, Brodbeck BV. (2003). Xylella fastidiosa diseases and
their leafhopper vectors. EDIS.
http://edis.ifas.ufl.edu/IN174 (12 October 2004).
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Purcell AH, Suslow KG. 1984 Surveys of leafhoppers (Homoptera: Cicadellidae) and pear psylla
(Homoptera: Psyllidae) in pear and peach orchards and the spread of peach yellow leaf roll
disease. Journal of Economic Entomology 77: 1489-1494.
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Timmer LW, Brlansky RH, Lee RF, Raju BC. 1983. A fastidious xylem-limited bacterium
infecting ragweed. Phytopathology 73: 975-979.
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Rakitov RA. 2004. Powdering of egg nests with brochosomes and related sexual dimorphism in
leafhoppers (Hemiptera: Cicadellidae). Zoological Journal of the Linnaean Society 140: 353-381.
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Riley CV, Howard LO. 1893. The glassy-winged sharpshooter. Insect Life 5: 150-154.
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Tipping C, Mizell III RF, Andersen PC. 2004. Dispersal adaptations of immature stages of three
species of leafhopper (Hemiptera: Auchenorrhyncha: Cicadellidae). Florida Entomologist 87: 372-379.
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Turner WF, Pollard HN. 1959. Life histories and behaviors of five insect vectors of phony peach
disease. USDA Technical Bulletin 1188. 28pgs.
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Wells JM, Raju BC, Hung HY, Weisburg WG, Paul LM, Brenner DJ. 1987. Xylella fastidiosa
gen. nov., sp. nov: gram-negative, xylem-limited, fastidious plant bacteria related to Xanthomonas
spp. International Journal of Systematic Bacteriology 37: 136-143
Authors: Chris Tipping and Russell F. Mizell III, University of Florida
Photographs: C. Tipping, University of Florida; and J. Lu, Florida A&M University
Raw analog video: R. Mizell, digitized and edited: C. Tipping, University of Florida
Project Coordinator: Thomas R. Fasulo, University of Florida
Publication Number: EENY-334
Publication Date: October 2004
Copyright 2004 University of Florida
Featured Creatures
Department of Entomology and Nematology
Division of Plant Industry
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