Introduction
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 vitripennis (Germar), on cotton. This damage, which appeared to be caused by a "minute bullet," was caused by the piercing-sucking mouthparts of H. vitripennis. 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.
Description and Systematics
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).
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).
Life History
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 which 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.
Diet
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.
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.
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.
Economic Importance
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. 1987). 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.
Natural Enemies
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.
In North Florida, several species of fungal pathogens reach epizootic levels in two species of sharpshooters, Homalodisca vitripennis 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.
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.
Selected References
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.
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.
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.
Mizell III RF, Andersen PC, Tipping C, Brodbeck BV. (2003). Xylella fastidiosa diseases and their leafhopper vectors. EDIS. https://edis.ifas.ufl.edu/in174 (12 October 2004).
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.
Timmer LW, Brlansky RH, Lee RF, Raju BC. 1983. A fastidious xylem-limited bacterium infecting ragweed. Phytopathology 73: 975-979.
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.
Riley CV, Howard LO. 1893. The glassy-winged sharpshooter. Insect Life 5: 150-154.
Takiya DM, McKamey SH, Cavichiloi RR. 2006. Validity of Homalodisca and of H. vitripennis as the name for glassy-winged sharpshooter (Hemiptera: Cicadellidae: Cicadellinae). Annals of the Entomological Society of America 99: 648-655.
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.
Tipping C, Triapitsyn SV, Mizell III RF. 2005. A new host record for the egg parasitoid Paracentrobia americana (Girault) (Hymenoptera: Trichogrammatidae) of the Proconiine sharpshooter Homalodisca insolita (Walker) (Hemiptera: Clypeorryncha: Cicadellidae). Florida Entomologist 88: 217-218.
Tipping C, Triapitsyn SV, Mizell III RF. 2006. First record of an egg parasitoid for the North American Proconiine sharpshooter Paraulacizes irrorata (Hemiptera: Cicadellidae), with notes on rearing techniques. Florida Entomologist 89: 288-289.
Turner WF, Pollard HN. 1959. Life histories and behaviors of five insect vectors of phony peach disease. USDA Technical Bulletin 1188. 28 pps.
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.