common name: citrus flatid planthopper
scientific name: Metcalfa pruinosa (Say) (Insecta: Hemiptera: Flatidae)
True to its name, the citrus flatid planthopper, Metcalfa pruinosa (Say), is found on citrus, but
also is found on a wide variety of woody plants, many of which are used in the ornamental
trade. This planthopper seldom causes economic damage to most plants except to those
weakened by some other factor such as freeze damage. The unsightly white, flocculent, waxy
material made by the nymphs impairs the sales quality of affected plants, partly because buyers
sometimes mistake these deposits for those of mealybugs or the cottony-cushion scale.
adult
The catalogue on Flatidae by Metcalf (1957) covers the literature through 1955 and gives
approximately seven pages of annotated citations to this planthopper. Previous to 1951
pruinosa (Say) was listed primarily in the genus Ormenis; however, the species was described
in Flata and later referred to several times in Poeciloptera or Melormenis.
M. pruinosa is common in eastern North America, ranging from Ontario and Quebec to
Florida, west to the Great Plains states, south to Texas, New Mexico, Arizona, California, and
Mexico. In Florida, M. pruinosa has been collected in all regions, but no specimens are at
hand from the southern tip area. Metcalf and Bruner (1948) reported M. pruinosa
widely distributed in Cuba.
Usually, adults of M. pruinosa are 5.5 to 8 mm in length and 2 to 3 mm in width at the widest
point. This species, along with certain other flatids, might be mistaken for a moth at first
glance. Flatids have broadly triangular front wings that are held close to the body in a vertical
position and give the insects a wedge-shaped, laterally compressed appearance from above.
The front wings (tegmina) have a well developed, transversely veined costal cell and a
granulate clavus; the hind tibiae normally have two lateral spines in addition to those at the
apex. The superficially similar acanaloniid planthoppers lack the transversely veined costal
cell, granulate clavus, and the lateral spines of the hind tibiae.
adult
The color of adult M. pruinosa varies considerably from brown to gray, due chiefly to the
presence or absence of a bluish white waxy powder. A characteristic pair of dark spots is
located in the basal half of each forewing.
Nymphs are less than twice as long as wide, and vary in size depending upon the growth stage.
A mature nymph is approximately 4 mm long, not counting waxy filaments which break
easily.
nymph
The following illustrations in literature may be of particular interest: genitalia drawings of M.
pruinosa are in Metcalf and Bruner (1948); habitus and genitalia drawings in Osborn (1938); a
color profile drawing of the adult in Metcalf (1923); egg puncture and adult photographs in
Dozier (1928); infestation on grapefruit photograph in Wene (1950); eggs, young nymphs,
mature nymphs, and adult photographs in Dean and Bailey (1961).
Dean and Bailey (1961) reported on the life history of this planthopper in the Lower Rio
Grande Valley and summarized the findings of previous workers. M. pruinosa overwinters in
the egg stage, with hatching starting early in March in the Weslaco, Texas, area. First adults
in the field were taken 69 days after the hatching date. Greater numbers were taken in June
than in later months. Only one generation was observed each year. Eggs were found scattered
singly in the bark of dead citrus twigs. Adults apparently can live several weeks. In Florida,
the Division of Plant Industry has records of nymphs from April to June and adult records
from May to October. In the Niagara peninsula, Ontario, Canada, nymphs were reported in
sour cherry orchards from May to late July, and adults from late July to September.
In Florida adults have been taken repeatedly in Steiner traps and in black-light traps. The
presence of this planthopper is revealed by the long, curled filaments of waxy exudate on the
undersides of succulent leaves or on the terminals of branches. This woolly material often
obscures the nymph producing it.
The whitish, comparatively flat planthopper can be separated easily from sedate mealybugs and
cottony-cushion scales by placing a pencil point at the caudal end; the planthopper will jump
like a leafhopper nymph. Leafhoppers do not surround themselves with flocculent exudate and
have one or more rows of small spines extending the length of hind tibiae; planthoppers have
only a few stout spines on hind tibiae.
The planthopper antennae arise on the side of the head beneath the eyes, instead of the front of
head between the eyes, as on treehoppers, spittlebugs, leafhoppers and cicadas. No
identification keys exist whereby the citrus flatid planthopper nymphs can be separated from its
near relatives, but circumstantial evidence is often sufficient to permit tentative determinations.
Not only are identification manuals apparently rare or non-existent on planthopper nymphs at
the specific and generic levels, but they are inadequate at the family level.
M. pruinosa is the only member of its genus reported in the United States and is the only U.S.
flatid of its general shape and size that has the basic dark color. The more closely related
flatids usually are greenish. Outside of the U.S., particularly in Cuba, there are several
species which might be confused with M. pruinosa. A subspecies, Metcalfa pruinosa cubana
(Metcalf and Bruner), is listed for Cuba. The writer has not examined this subspecies nor
other pertinent Antillean material.
M. pruinosa has been reported on a long list of plants, including many forest trees, orchard
and citrus trees, grape and other vines, numerous shrubs, and some herbs. Among the more
important hosts in Florida are camellias, azaleas, viburnum, magnolias, hollies, seagrape,
cherry laurel, peach, orange and grapefruit. Dean and Bailey (1961) found M. pruinosa
favored grapefruit over orange as a host in the lower Rio Grande Valley of Texas.
M. purinosa ordinarily does very little damage to plants; however Wene (1950) found it
destroying very small buds in a lime grove which had been defoliated by a recent freeze in the
Mission, Texas, area. Furthermore there was a considerable amount of fruit drop in a few
heavily infested groves freeze-damaged three months previously. Wene and Riherd (1953)
reported pruinosa destroying part of a hedge of Amour River privet, Ligustrum amurense, near
Donna, Texas. Sooty-mold fungus commonly develops in the honeydew excreted by the citrus
flatid. Limited virus transmission tests have shown M. pruinosa a nonvector of tristeza, peach
yellows, and blueberry stunt. Apparently, it is rare for flatids to transmit virus diseases.
However, it is of possible interest to the citrus industry that an Asiatic flatid, Geisha
distinctissima (Wlk.) is the vector of a virus which causes dwarf disease of satsuma orange in
Japan.
Usually no chemical control measures are necessary.
A dryinid wasp parasite, Psilodryinus typhlocybae (Ashmead), has been reported as common on
nymphs of the citrus flatid planthopper and its relatives.
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Dean HA, Bailey JC. 1961. A flatid planthopper, Metcalfa pruinosa. Journal of Economic
Entomology 54: 1104-1106.
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Dozier HL. 1928. The Fulgoridae or plant-hoppers of Mississippi, including those of
possible occurrence; a taxonomic, biological, ecological, and economic study. Technical
Bulletin of the Mississippi Agricultural Experiment Station 14: 112-114.
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Metcalf ZP. 1923. J. Elisha Mitchell Science Society 38: 152.
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Metcalf ZP. 1957. General Catalog Homoptera, Fasc. 4, Part 13, Flatidae and
Hypochthonellidae, 342-350.
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Metcalf ZP, Bruner SC. 1948. Cuban Flatidae with new species from adjacent regions.
Annals of the Entomological Society of America 41: 96.
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Osborn, H. 1938. The Fulgoridae of Ohio. Bulletin of the Ohio Biological Survey 6: 318.
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Wene GP. 1950. The citrus fulgorid. Annual Proceedings of the Lower Rio Grande Valley
Citrus and Vegetable Institute 4: 90-93.
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Wene GP, Riherd PT. 1954. Control of puss caterpillar and fulgorids attacking ornamentals
during 1953. Texas Avocado Society Year Book for 1953: 45-46.
Author: F.W. Mead (retired), Florida Department of Agriculture and Consumer Services, Division of Plant Industry.
Originally published as DPI Entomology Circular 85.
Photographs: Lyle J. Buss, University of Florida
Project Coordinator: Thomas R. Fasulo, University of Florida
Publication Number: EENY-329
Publication Date: June 2004
Copyright 2004 University of Florida
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Department of Entomology and Nematology
Division of Plant Industry
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